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Full text of "Electrodynamics of Continuous Media"

Landau Electrodynamics of Continuous Media ^ ■ o a 3 n 3 c c o Per,:,:: man Course of Theoretical Physics Volume 8 L. D. Landau (Deceased) and E. M. Lifshitz Institute of Physical Problems USSR Academy of Sciences MCMXCVn COURSE OF THEORETICAL PHYSICS Volume 8 ELECTRODYNAMICS OF CONTINUOUS MEDIA COURSE OF THEORETICAL PHYSICS Vol. 1. Mechanics Vol. 2. The Classical Theory of Fields Vol. 3. Quantum Mechanics — Non-relativistic Theory Vol. 4. Relativistic Quantum Theory Vol. 5. Statistical Physics Vol. 6. Fluid Mechanics Vol. 7. Theory of Elasticity Vol. 9. Physical Kinetics ELECTRODYNAMICS OF CONTINUOUS MEDIA by L. D. LANDAU and E. M. LIFSHITZ INSTITUTE OF PHYSICAL PROBLEMS, U.S.S.R. ACADEMY OF SCIENCES Volume 8 of Course of Theoretical Physics Translated from the Russian by J. B. SYKES and J. S. BELL PERGAMON PRESS Oxford • London • New York • Paris PERGAMON PRESS LTD. Headington Hill Hall, Oxford 4 and 5 Fitzroy Square, London, W.l PERGAMON PRESS INC. 122 East 55th Street, New York 22, N.Y. GAUTHIER-VILLARS ED. 55 Quai des Grands- Augustins, Paris, 6 e PERGAMON PRESS G.m.b.H. 75 Kaiserstrasse, Frankfurt am Main Distributed in the Western Hemisphere by THE MACMILLAN COMPANY • NEW YORK pursuant to a special arrangement with Pergamon Press Limited Copyright © 1960 Pergamon Press Ltd. First published in English 1960 Second impression 1963 Library of Congress Card Number 60-14731 Printed in Great Britain by J. W. Arrowsmith Ltd., Bristol CONTENTS Page Preface i x Notation x I. ELECTROSTATICS OF CONDUCTORS §1. The electrostatic field of conductors 1 §2. The energy of the electrostatic field of conductors 3 §3. Methods of solving problems in electrostatics 9 §4. A conducting ellipsoid 20 §5. The forces on a conductor 31 II. ELECTROSTATICS OF DIELECTRICS §6. The electric field in dielectrics 36 §7. The dielectric permeability 38 §8. A dielectric ellipsoid 42 §9. The dielectric permeability of a mixture 45 §10. Thermodynamic relations for dielectrics in an electric field 47 §11. The total free energy of a dielectric 52 §12. Electrostriction of isotropic dielectrics 55 §13. Dielectric properties of crystals 58 §14. The sign of the dielectric susceptibility 63 §15. Electric forces in a fluid dielectric 64 §16. Electric forces in solids 69 §17. Piezoelectrics 73 §18. Thermodynamic inequalities 79 §19. Ferroelectrics 83 III. CONSTANT CURRENT §20. The current density and the conductivity 92 §21. The Hall effect 96 §22. The contact potential 99 §23. The galvanic cell 101 §24. Electrocapillarity 103 §25. Thermoelectric phenomena 104 §26. Diffusion phenomena 110 IV. CONSTANT MAGNETIC FIELD §27. Constant magnetic field 113 §28. Magnetic symmetry of crystals 116 §29. The magnetic field of a constant current 119 §30. Thermodynamic relations in a magnetic field 126 §31. The total free energy of a magnetic substance 129 §32. The energy of a system of currents 131 vi Contents Page §33. The self-inductance of linear conductors 136 §34. Forces in a magnetic field 141 §35. Gyromagnetic phenomena 144 V. FERROMAGNETISM §36. Ferromagnetics near the Curie point 146 §37. The magnetic anisotropy energy 149 §38. Magnetostriction of ferromagnetics 155 §39. The domain structure of ferromagnetics 158 §40. The antiferromagnetic Curie point 165 VI. SUPERCONDUCTIVITY §41. The magnetic properties of superconductors 167 §42. The superconductivity current 169 §43. The critical field 173 §44. The intermediate state 178 VII. QUASI-STATIC ELECTROMAGNETIC FIELD §45. Eddy currents 186 §46. The skin effect 195 §47. The complex resistance 197 §48. Capacity in a quasi-steady current circuit 202 §49. Motion of a conductor in a magnetic field 205 §50. Excitation of currents by acceleration 210 VIII. MAGNETIC FLUID DYNAMICS §51. The equations of motion for a fluid in a magnetic field 213 §52. Hydromagnetic waves 218 §53. Tangential and rotational discontinuities 224 §54. Shock waves 229 §55. The spontaneous magnetic field in turbulent motion of a conducting fluid 234 IX. THE ELECTROMAGNETIC WAVE EQUATIONS §56. The field equations in a dielectric in the absence of dispersion 239 §57. The electrodynamics of moving dielectrics 243 §58. The dispersion of the dielectric permeability 247 §59. The dielectric permeability at very high frequencies 251 §60. The dispersion of the magnetic permeability 251 §61. The field energy in dispersive media 253 §62. The relation between the real and imaginary parts of e(o>) 256 §63. A plane wave of a single frequency 263 §64. Transparent media 266 X. THE PROPAGATION OF ELECTROMAGNETIC WAVES §65. Geometrical optics 269 §66. Reflection and refraction of electromagnetic waves 272 §67. The surface impedance of metals 279 Contents vii Page §68. The propagation of waves in an inhomogeneous medium 284 §69. The reciprocity principle 288 §70. Electromagnetic oscillations in hollow resonators 290 §71. The propagation of electromagnetic waves in waveguides 293 §72. The scattering of electromagnetic waves by small particles 299 §73. The absorption of electromagnetic waves by small particles 303 §74. Diffraction by a wedge 304 §75. Diffraction by a plane screen 308 XI. ELECTROMAGNETIC WAVES IN ANISOTROPIC MEDIA §76. The dielectric permeability of crystals 313 §77. A plane wave in an anisotropic medium 315 §78. Optical properties of uniaxial crystals 321 §79. Biaxial crystals 324 §80. Double refraction in an electric field 329 §81. Mechanical-optical effects 330 §82. Magnetic-optical effects 331 §83. Natural optical activity 337 XII. THE PASSAGE OF FAST PARTICLES THROUGH MATTER §84. Ionisation losses by fast particles in matter: the non-relativistic case 344 §85. Ionisation losses by fast particles in matter: the relativistic case 349 §86. Cherenkov radiation 357 XIII. ELECTROMAGNETIC FLUCTUATIONS §87. Current fluctuations in linear circuits 360 §88. Electromagnetic field fluctuations 361 §89. Black-body radiation in a transparent medium 367 §90. Forces of molecular attraction between solid bodies 368 XIV. SCATTERING OF ELECTROMAGNETIC WAVES §91. The general theory of scattering in isotropic media 377 §92. The principle of detailed balancing applied to scattering 383 §93. Scattering with small change of frequency 385 §94. Rayleigh scattering in gases and liquids 387 §95. Critical opalescence 393 §96. Scattering in amorphous solids 395 XV. DIFFRACTION OF X-RAYS IN CRYSTALS §97. The general theory of X-ray diffraction 398 §98. The integral intensity 404 §99. Diffuse thermal scattering of X-rays 407 Appendix 410 Index 413 PREFACE The present volume in the Course of Theoretical Physics deals with the theory of electromagnetic fields in matter and with the theory of the macroscopic electric and magnetic properties of matter. These theories include a very wide range of topics, as may be seen from the Contents. In writing this book we have experienced considerable difficulties, partly because of the need to make a selection from the extensive existing material, and partly because the customary exposition of many topics to be included does not possess the necessary physical clarity, and sometimes is actually wrong. We realise that our own treatment still has many defects, which we hope to correct in future editions. We are grateful to Professor V. L. Ginzburg, who read the book in manuscript and made some useful comments. I. E. Dzyaloshinski! and L. P. Pitaevskii gave great help in reading the proofs of the Russian edition. Thanks are due also to Dr Sykes and Dr Bell, who not only carried out excellently the arduous task of translating the book, but also made some use- ful comments concerning its contents. L. D. Landau Moscow E. M. Lifshitz June, 1959 NOTATION Electric field E Electric induction D Magnetic field H Magnetic induction B External electric field © External magnetic field # Dielectric polarisation P Magnetisation M Total electric moment of a body ^ Total magnetic moment of a body J€ Dielectric permeability e Magnetic permeability fi Current density j Conductivity a Absolute temperature (in energy units) T Thermodynamic quantities : per unit volume for a body entropy S S? internal energy U tfl free energy F & thermodynamic potential <X> cp Chemical potential £ A complex periodic time factor is always taken as e~ iwt . The summation convention always applies to three-dimensional (Latin) and two-dimensional (Greek) suffixes occurring twice in vector and tensor expressions. CHAPTER I ELECTROSTATICS OF CONDUCTORS §1. Tike electrostatic field of conductors Like all macroscopic theories, the theory of electromagnetic fields in matter deals with physical quantities averaged over elements of volume which are "physically infinitesimal", ignoring the microscopic variations of the quan- tities which result from the molecular structure of matter. For example, instead of the actual "microscopic" value of the electric field e, we discuss its averaged value, denoted by E: e = E. (1.1) The fundamental equations of the electrodynamics of continuous media are obtained by averaging the equations for the electromagnetic field in a vacuum. This method of obtaining the macroscopic equations from the microscopic was first used by H. A. Lorentz. The form of the equations of macroscopic electrodynamics and the significance of the quantities appearing in them depend essentially on the physical nature of the medium, and on the way in which the field varies with time. It is therefore reasonable to derive and investigate these equations separately for each type of physical object. It is well known that all bodies can be divided, as regards their electric properties, into two classes, conductors and dielectrics, differing in that any electric field causes in a conductor, but not in a dielectric, the motion of charges, i.e. an electric current, t Let us begin by studying the constant electric fields produced by charged conductors, that is, the electrostatics of conductors. First of all, it follows from the fundamental property of conductors that, in the electrostatic case, the electric field inside a conductor must be zero. For a field E which was not zero would cause a current; the propagation of a current in a conductor involves a dissipation of energy, and hence cannot occur in a stationary state (with no external sources of energy). Hence it follows, in turn, that any charges in a conductor must be located on its surface. The presence of charges inside a conductor would necessarily cause an electric field in it; J they can be distributed on its surface, however, t It should be mentioned that the conductor is here assumed to be homogeneous (in composition, temperature, etc.)- In an inhomogeneous conductor, as we shall see later, there may be fields which cause no motion of charges. % This is clearly seen from equation (1.8) below. 1 2 Electrostatics of Conductors §1 in such a way that the fields which they produce in its interior are mutually balanced. Thus the problem of the electrostatics of conductors amounts to determining the electric field in the vacuum outside the conductors and the distribution of charges on their surfaces. At any point far from the surface of the body, the mean field E in the vacuum is almost the same as the actual field e. The two fields differ only in the immediate neighbourhood of the body, where the effect of the irregular molecular fields is noticeable, and this difference does not affect the averaged field equations. The exact microscopic Maxwell's equations in the vacuum are dive = 0. (1.2) curie = -(l/c)8h/dt, (1.3) where h is the microscopic magnetic field. Since the mean magnetic field is assumed to be zero, the derivative dhjdt also vanishes on averaging, and we find that the constant electric field in the vacuum satisfies the usual equations div E = 0, curl E = 0, (1.4) i.e. it is a potential field with a potential <f> such that E= -grad^, (1.5) and <j> satisfies Laplace's equation A<f> = 0. (1.6) The boundary conditions on the field E at the surface of a conductor follow from the equation curl E = 0, which, like the original equation (1.3), is valid both outside and inside the body. Let us take the #-axis in the direction of the normal to the surface at some point on the conductor. The component E z of the field takes very large values in the immediate neigh- bourhood of the surface (because there is a finite potential difference over a very small distance). This large field pertains to the surface itself and de- pends on the physical properties of the surface, but is not involved in our electrostatic problem, because it falls off over distances comparable with the distances between atoms. It is important to note, however, that, if the surface is homogeneous, the derivatives dE z jdx, BE z fdy along the surface remain finite, even though E z itself becomes very large. Hence, since (curl E) x = dE z \dy—dE y \dz = 0, we find that dE y \dz is finite. This means that E y is continuous at the surface, since a discontinuity in E y would mean an infinity of the derivative dE y \dz. The same applies to E z , and since E = inside the conductor, we reach the conclusion that the tangential components of the external field at the surface must be zero: E t = 0. (1.7) Thus the electrostatic field must be normal to the surface of the conductor at every point. Since E = — grad <f>, this means that the field potential must be constant on the surface on any particular conductor. In other words, §2 The energy of the electrostatic field of conductors 3 the surface of a homogeneous conductor is an equipotential surface of the electrostatic field. The component of the field normal to the surface is very simply related to the charge density on the surface. The relation is obtained from the general electrostatic equation div e = Airp, which on averaging gives div E = 4rr/5, (1.8) p being the mean charge density. The meaning of the integrated form of this equation is well known: the flux of the electric field through a closed surface is equal to the total charge inside that surface, multiplied by 4ir. Applying this theorem to a volume element lying between two infinitesimally close unit areas, one on each side of the surface of the conductor, and using the fact that E = on the inner area, we find that E n = Att<j, where a is the surface charge density, i.e. the charge per unit area of the surface of the conductor. Thus the distribution of charges over the surface of the conductor is given by the formula W = E n = -d<f>j8n, (1.9) the derivative of the potential being taken along the outward normal to the surface. The total charge on the conductor is «=-!<£ ^d/, (1.10) A-n J on the integral being taken over the whole surface. The potential distribution in the electrostatic field has the following re- markable property: the function <f>(x, y, z) can take maximum and minimum values only at boundaries of regions where there is a field. This theorem can also be formulated thus : a test charge e introduced into the field cannot be in stable equilibrium, since there is no point at which its potential energy e$ would have a minimum. The proof of the theorem is very simple. Let us suppose, for example, that the potential has a maximum at some point A not on the boundary of a region where there is a field. Then the point A can be surrounded by a small closed surface on which the normal derivative d<f>\dn < everywhere. Consequently, the integral over this surface j(dcpldn) df < 0. But by La- place's equation §(d<f>]dn) df=JA<f> dV = 0, giving a contradiction. §2. The energy of the electrostatic field of conductors Let us calculate the total energy % of the electrostatic field of charged conductors, t ^ = _Lf£2 dF) (2.1) 07T J t The square E 2 is not the same as the mean square e 2 _oi the actual field near the surface of a conductor or inside it (where E = but, of course, e 2 *£ 0). By calculating the integral (2.1) we ignore the internal energy of the conductor as such, which is here of no interest, and the affinity of the charges for the surface. 4 Electrostatics of Conductors §2 where the integral is taken over all space outside the conductors. We trans- form this integral as follows : <V = -— |E.grad<£dF= -— fdiv (<f>E) dV+— [ <f> div E dV. 07TJ StT J S7T J The second integral vanishes by (1.4), and the first can be transformed into integrals over the surfaces of the conductors which bound the field and over an infinitely remote surface. The latter of these vanishes, because the field diminishes sufficiently rapidly at infinity. Denoting by <f> a the constant value of the potential on the <zth conductor, we havet = ^2f^» d /= 8 ^2^f £ » d /- 07T ^""' J 877 a a Finally, since the total charges e a on the conductors are given by (1.10) we obtain ^ = 12%^ (2.2) which is analogous to the expression for the energy of a system of point charges. The charges and potentials of the conductors cannot both be arbitrarily prescribed; there are certain relations between them. Since the field equa- tions in a vacuum are linear and homogeneous, these relations must also be linear, i.e. they must be given by equations of the form e a = S Cab <f>b, (2.3) where the quantities C aa , C a b have the dimensions of length and depend on the shape and relative position of the conductors. The quantities C aa are called capacity coefficients, and the quantities C ab (a ^ b) are called electro- static induction coefficients. In particular, if there is only one conductor, we have e = C<f>, where C is the capacity, which in order of magnitude is equal to the linear dimension of the body. The converse relations, giving the potentials in terms of the charges, are <f> a = S C-\ b e b , (2.4) where the coefficients C _1 a & form a matrix which is the inverse of the matrix Cab- Let us calculate the change in the energy of a system of conductors caused by an infinitesimal change in their charges or potentials. Varying the original f In transforming volume integrals into surface integrals, both here and later, it must be borne in mind that E n is the component of the field along the outward normal to the con- ductor. This direction is opposite to that of the outward normal to the region of the volume integration, namely the space outside the conductors. The sign of the integral is therefore changed in the transformation. §2 The energy of the electrostatic field of conductors 5 expression (2.1), we have 8% = (1/4tt) j E-SE dV. This can be further transformed by two equivalent methods. Putting E = — grad <f> and using the fact that the varied field, like the original field, satisfies equations (1.4) (so that div SE = 0), we can write 8<% = fgrad<£.8EdF= ( div (<f> 8E) dV = — 2 $ a j 8En d /> that is 8<% = ^<f> a 8e a , ( 2 - 5 ) o which gives the change in energy due to a change in the charges. This result is obvious; it is the work required to bring infinitesimal charges 8e a to the various conductors from infinity, where the field potential is zero. On the other hand, we can write S<^ = ( E- grad 8<f> dV = ( div (E 8<f>) dV 4ttJ Att J = — 2 fy" f En d /' that is 8% = Xe a 8<f> a , (2.6) which expresses the change in energy in terms of the change in the potentials of the conductors. Formulae (2.5) and (2.6) show that, by differentiating the energy <% with respect to the charges, we obtain the potentials of the conductors, and the derivatives of <% with respect to the potentials are the charges : dW/de a = <£«, d%ld<i> a = e a . (2.7) But the potentials and charges are linear functions of each other. Using (2.3) we have d 2 <%ld<f> a d<f> b = debjd<j> a = Cba, and by reversing the order of differentiation we get C a &. Hence it follows that Cab = Cba, (2.8) and similarly C~ x a b = C~ x ba- The energy % can be written as a quadratic form in either the potentials or the charges : % = \ \ Cab Mb = \ \C-^ a b e a e b . (2.9) ' a,b a,b v This quadratic form must be positive definite, like the original expression (2.1). From this condition we can derive various inequalities which the 6 Electrostatics of Conductors §2 coefficients C a & must satisfy. In particular, all the capacity coefficients are positive : C aa > (2.10) (and also C~\ a > 0).t All the electrostatic induction coefficients, on the other hand, are negative : Cab <0 (fl^ b). (2.11) That this must be so is seen from the following simple arguments. Let us suppose that every conductor except the <zth is earthed, i.e. their potentials are zero. Then the charge induced by the charged ath conductor on another (the 2>th, say) is et, = Cb a <f>a- It is obvious that the sign of the induced charge must be opposite to that of the inducing potential, and therefore C a b < 0. This can be more rigorously shown from the fact that the potential of the electrostatic field cannot reach a maximum or minimum outside the conduc- tors. For example, let the potential <£ a of the only conductor not earthed be positive. Then the potential is positive in all space, its least value (zero) being attained only on the earthed conductors. Hence it follows that the normal derivative d$\dn of the potential on the surfaces of these conductors is positive, and their charges are therefore negative, by (1.10). Similar arguments show that C~\b > 0. The energy of the electrostatic field of conductors has a certain extremum property, though this property is more formal than physical. To derive it, let us suppose that the charge distribution on the conductors undergoes an infinitesimal change (the total charge on each conductor remaining unaltered), in which the charges may penetrate into the conductors; we ignore the fact that such a charge distribution cannot in reality be stationary. We consider the change in the integral °ti = (1/8tt) j E 2 dV, which must now be extended over all space, including the volumes of the conductors themselves (since after the displacement of the charges the field E may not be zero inside the conductors). We write h% = -—fgrad^-SEdF = -— fdiv(08E)dr+~ f^divSEdF. 4-77 J 47T J The first integral vanishes, being equivalent to one over an infinitely remote surface. In the second integral, we have by (1.8) divSE = Airhp, so that htfl = / <f>Bp dV. This integral vanishes if <f> is the potential of the true electro- static field, since then <f> is constant inside each conductor, and the integral jSpdV over the volume of each conductor is zero, since its total charge remains unaltered. t We may also mention that another inequality which must be satisfied if the form (2.9) is positive is CaaCbb > Cab 2 - §2 The energy of the electrostatic field of conductors 7 Thus the energy of the actual electrostatic field is a minimumf relative to the energies of fields which could be produced by any other distribution of the charges on or in the conductors (Thomson's theorem). From this theorem it follows, in particular, that the introduction of an uncharged conductor into the field of given charges (charged conductors) reduces the total energy of the field. To prove this, it is sufficient to compare the energy of the actual field resulting from the introduction of the un- charged conductor with the energy of the fictitious field in which there are no induced charges on that conductor. The former energy, since it has the least possible value, is less than the latter energy, which is also the energy of the original field (since, in the absence of induced charges, the field would penetrate into the conductor, remaining unaltered). This result can also be formulated thus : an uncharged conductor remote from a system of given charges is attracted towards the system. Finally, it can be shown that a conductor (charged or not) brought into an electrostatic field cannot be in stable equilibrium under electric forces alone. This assertion generalises the theorem for a point charge proved at the end of §1, and can be derived by combining the latter theorem with Thomson's theorem. We shall not pause to give the derivation in detail. Formulae (2.9) are useful for calculating the energy of a system of con- ductors at finite distances apart. The energy of an uncharged conductor in a uniform external field ©, which may be imagined as due to charges at infinity, requires special consideration. According to (2.2), this energy is % = ^e<f) y where e is the remote charge which causes the field, and <j> is the potential at this charge due to the conductor. °ll does not include the energy of the charge e in its own fieldj since we are interested only in the energy of the conductor. The charge on the conductor is zero, but the external field causes it to acquire a dipole electric moment, which we denote by 0*. The potential of the electric dipole field at a large distance r from it is <f> = ^«r/r 3 . Hence % = e&'rjlfi. But — er/r 3 is just the field © due to the charge e. Thus # = -£ 0>©. (2.12) Since all the field equations are linear, it is evident that the components of the dipole moment &> are linear functions of the components of the field ©. The coefficients of proportionality between $P and ® have the dimen- sions of length cubed, and are therefore proportional to the volume of the conductor : &i = Vaa&t, (2.13) where the coefficients a^ depend only on the shape of the body. The quantities Vane form a tensor, which may be called the polarisability tensor of the body. f We shall not give here the simple arguments which demonstrate that the extremum is a minimum. 8 Electrostatics of Conductors §2 This tensor is symmetrical: a^ = olm, a statement which will be proved in §11. Accordingly, the energy (2.12) is % = -iFottfoCfe. (2.14) PROBLEMS Problem 1. Express the mutual capacity C of two conductors (with charges ±e) in terms of the coefficients Cab. Solution. The mutual capacity of two conductors is defined as the coefficient C in the relation e = C(<f>2—<f>i), and the energy of the system is given in terms of C by % — %e 2 jC. Comparing with (2.9), we obtain 1/C = C-hi-2C-h2+C-hi = (Cll + 2C 12 +C22)/(CllC22-Cl22). Problem 2. A point charge e is situated at O, near a system of earthed conductors, and induces on them charges e a . If the charge e were absent, and the ath conductor were at potential <f>' a , the remainder being earthed, the field potential at O would be <f>'o. Express the charges e a in terms of <f>' a and <f>'o- Solution. If charges e a on the conductors give them potentials <f> a , and similarly for e' a and <j>' a , it follows from (2.3) that £ 4>ae a = S <j>aCab<f>'b = 2 <f>'aCa- a a,b a We apply this relation to two states of the system formed by all the conductors and the charge e (regarding the latter as a very small conductor). In one state the charge e is present, the charges on the conductors are e a , and their potentials are zero. In the other state the charge e is zero, and one of the conductors has a potential <j>' a ^ 0. Then we have e4>'o+e a <f>'a — 0, whence e a = —e<f>'ol<l>'a- For example, if a charge e is at a distance r from the centre of an earthed conducting sphere of radius a(< r), then <f>'o = <f>' a alr, and the charge induced on the sphere is e a = —ea/r. As a second example, let us consider a charge e placed between two concentric conducting spheres of radii a and b, at a distance r from the centre such that a < r < b. If the outer sphere is earthed and the inner one is charged to potential <f>' a> the potential at distance r is l/r-1/6 90 = <f> a— — • 1/a — l/b Hence the charge induced on the inner sphere by the charge e is e a = —ea(b—r)lr(b—a). Similarly the charge induced on the outer sphere is eb = —eb(r—a)lr(b—a). Problem 3. Two conductors, of capacities Ci and Cz, are placed at a distance r apart which is large compared with their dimensions. Determine the coefficients Cab- Solution. If conductor 1 has a charge ei, and conductor 2 is uncharged, then in the first approximation <f>i = ei/Ci, fa = ei/r ; here we neglect the variation of the field over conductor 2 and its polarisation. Thus C~hi = 1/Ci, C" 1 ^ = 1/r, and similarly C" 1 2 2 = I/C2. Hence we findf ~ „ /« , CiCaX „ C1C2 „ I CiC 2 \ Ca = C,(l+ — ), Q. = - — C 22 - C 2 (l+ -^- a ). t The subsequent terms in the expansion are in general of order (in 1/r) one higher than those given. If, however, r is taken as the distance between the "centres of charge" of the two bodies (for spheres, between the geometrical centres), then the order of the subsequent terms is two higher. §3 Methods of solving problems in electrostatics 9 Problem 4. Determine the capacity of a ring (radius b) of thin conducting wire of circular cross-section (radius a <^ b). Solution. Since the wire is thin, the field at the surface of the ring is almost the same as that of charges distributed along the axis of the wire (for a right cylinder, it would be exactly the same). Hence the potential of the ring is <f>a = — i — 2irb J r ' where r is the distance from a point on the surface of the ring to an element d/ of the axis of the wire, the integration being over all such elements. We divide the integral into two parts corresponding to r < A and r > A, A being a distance such that a «^ A <^ b. Then for r < A the segment of the ring concerned may be regarded as straight, and therefore dZ r dl ^ 2 log(2A/a). #7-f Vtf 2 +a 2 ) A>r -A In the range r > A the thickness of the wire may be neglected, i.e. r may be taken as the distance between two points on its axis. Then dl n f bd<f> „, . i, = -2 log tan i<f> , 2b sin if • tf-'J where <f> is the angle subtended at the centre of the ring by the chord r, and the lower limit of integration is such that 2b sin b<f>o = A, whence ^o = A/6. When the two parts of the integral are added, A cancels, and the capacity of the ring is c = <£« log(86/a) §3. Methods of solving problems in electrostatics The general methods of solving Laplace's equation for given boundary conditions on certain surfaces are studied in mathematical physics, and we shall not give a detailed description of them here. We shall merely mention some of the more elementary procedures and solve various problems of intrinsic interest, t (1) The method of images. The simplest example of the use of this method is to determine the field due to a point charge e outside a conducting medium which occupies a half-space. The principle of the method is to find fictitious point charges which, together with the given charge or charges, produce a field such that the surface of the conductor is an equipotential surface. In the case just mentioned, this is achieved by placing a fictitious charge e' = —e at a point which is the image of e in the plane which bounds the conducting medium. The potential of the field due to the charge e and its image e' is * = e ^~~\ (3 * 1} t The solutions of many more complex problems are given by W. R. Smythe, Static and Dynamic Electricity, 2nd ed., McGraw-Hill, New York, 1950; G. A. Grinberg, Selected Problems in the Mathematical Theory of Electric and Magnetic Phenomena (Izbrannye voprosy matematicheskoi teorii elektricheskikh i magnitnykh yavlenii), Moscow, 1948. 10 Electrostatics of Conductors §3 where r and r' are the distances of a point from the charges e and e'. On the bounding plane, r = r' and the potential has the constant value zero, so that the necessary boundary condition is satisfied and (3.1) gives the solu- tion of the problem. It may be noted that the charge e is attracted to the conductor by a force e 2 /(2a) 2 (the image force; a is the distance of the charge from the conductor), and the energy of their interaction is — e 2 \Aa. The distribution of surface charge induced on the bounding plane by the point charge e is given by 1 \d<l>~\ e a It is easy to see that the total charge on the plane is Jad/ = —e, as it should be. The total charge induced on an originally uncharged insulated conductor by other charges is, of course, zero. Hence, if in the present case the conduct- ing medium (in reality a large conductor) is insulated, we must suppose that, besides the charge —e> a charge +e is also induced, which, however, has no finite density, being distributed over the large surface of the conductor. Next, let us consider a more difficult problem, that of the field due to a point charge e near a spherical conductor. To solve this problem, we use the following result, which can easily be proved by direct calculation. The potential of the field due to two point charges e and —e', namely <f> = e/r—e'/r', vanishes on the surface of a sphere whose centre is on the line joining the charges (but not between them). If the radius of the sphere is R and its centre is distant / and /' from the two charges, then ///' = {e/e') 2 , R 2 = //'. Let us first suppose that the spherical conductor is maintained at a con- stant potential <f> = 0, i.e. it is earthed. Then the field outside the sphere due to the point charge e at A (Fig. 1), at a distance /from the centre of the sphere, is the same as the field due to two charges, namely the given charge e and a fictitious charge —e' at A' inside the sphere, at a distance /' from its centre, where /' = R 2 /l, e' = eRjl (3.3) The potential of this field is e eR * - 7-J? W r and r' being as shown in Fig. 1. A non-zero total charge —e' is induced on the surface of the sphere. The energy of the interaction between the charge and the sphere is * = -i "'IV-l') = -%e 2 RI(l 2 -R 2 ), (3.5) and the charge is attracted to the sphere by a force F = —d%jdl — -e 2 lRj(l 2 -R 2 ) 2 . §3 Methods of solving problems in electrostatics 11 If the total charge on the spherical conductor is kept equal to zero (an insulated uncharged sphere), a further fictitious charge must be introduced, such that the total charge induced on the surface of the sphere is zero, and the potential on that surface is still constant. This is done by placing a charge + e' at the centre of the sphere. The potential of the required field is then given by the formula (3.6) OA--1 OA''-l' Fig. 1 The energy of interaction in this case is qt = lee'[ 1 = . (3.7) Finally, if the charge e is at A' (Fig. 1) in a spherical cavity in a conducting medium, the field inside the cavity must be the same as the field due to the charge e at A' and its image at A outside the sphere, regardless of whether the conductor is earthed or insulated: r Ir (2) The method of inversion. There is a simple method whereby in some cases a known solution of one electrostatic problem gives the solution of another problem. This method is based on the invariance of Laplace's equation with respect to a certain transformation of the variables. In spherical co-ordinates Laplace's equation has the form 1 a / 2 d<f>\ 1 r 2 dr\ drj r 2 where An denotes the angular part of the Laplacian operator. It is easy to see that this equation is unaltered in form if the variable r is replaced by a new variable r' such that r = R 2 \r' (3.9) 12 Electrostatics of Conductors §3 (the inversion transformation) and at the same time the unknown function <f> is replaced by $ such that <f> = r'<f>'/R. (3.10) Here R is some constant having the dimensions of length (the radius of inversion). Thus, if the function <f>{t) satisfies Laplace's equation, then so does the function f(r') = R<f>(R 2 r'lr' 2 )/r'. (3.11) Let us assume that we know the electrostatic field due to some system of conductors, all at the same potential <j>o, and point charges. The potential <£(r) is usually defined so as to vanish at infinity. Here, however, we shall define <f>(r) so that it tends to — <£o at infinity. Then <f> = on the conductors. We may now ascertain what problem of electrostatics will be solved by the transformed function (3.11). First of all, the shapes and relative posi- tions of all the conductors of finite size will be changed. The boundary condition of constant potential on their surfaces will be automatically satis- fied, since <j>' = if <j> — 0. Furthermore, the positions and magnitudes of all the point charges will be changed. A charge e at a point ro moves to r'o = i? 2 ro/ro 2 and takes a value e' which can be determined as follows. As r -> tq the potential ^(r) tends to infinity as ej\8r\, where Sr = r— ro. Differentiating the relation r = R 2 r'jr' 2 , we find that the magnitudes of the small differences Sr and Sr' =. r'— r' are related by (Sr) 2 = i? 4 (Sr') 2 /r' 4 . Hence, as r' ->r' , the function <f>' tends to infinity as e/?/r'o|8r| = er'olR\8r'\, corresponding to a charge e' = er' JR = eR/r . (3.12) Finally, let us examine the behaviour of the function ^'(r') near the origin. For r' = we have r -> oo and <£(r) -> —<f>o. Hence, as r' -> 0, the func- tion <£' tends to infinity as —Rfajr'. This means that there is a charge e = —R<f> at the point r' = 0. We shall give, for reference, the way in which certain geometrical figures are transformed by inversion. A spherical surface of radius a and centre ro is given by the equation (r— ro) 2 = a 2 . On inversion, this becomes ([i? 2 r'/r' 2 ]— ro) 2 = a 2 , which, on multiplying by r' 2 and rearranging, can be written (r'— r'o) 2 = a' 2 , where r'o = -R 2 rol(a 2 -r 2 ) } a' = aR 2 l\a 2 -r 2 \. (3.13) Thus we have another sphere, of radius a' and centre r'o- If the original sphere passes through the origin (a = ro), then a' = oo. In this case the sphere is transformed into a plane perpendicular to the vector ro and distant r'o— a' ~ R 2 l(a + r ) = R 2 /2a from the origin. (3) The method of conformal mapping. A field which depends on only two Cartesian co-ordinates (x and y, say) is said to be two-dimensional. §3 Methods of solving problems in electrostatics 13 The theory of functions of a complex variable is a powerful means of solving two-dimensional problems of electrostatics. The theoretical basis of the method is as follows. An electrostatic field in a vacuum satisfies two equations : curl E = 0, div E = 0. The first of these makes it possible to introduce the field poten- tial, defined by E = — grad <f>. The second equation shows that we can also define a vector potential A of the field, such that E = curl A. In the two-dimensional case, the vector E lies in the .ry-plane, and depends only on x and y. Accordingly, the vector A can be chosen so that it is perpendicu- lar to the xy-plane. Then the field components are given in terms of the derivatives of <f> and A by E x = -d<f>/dx = dA/dy, E y = -8<j>/8y = -dA/dx. (3.14) These relations between the derivatives of tf> and A are, mathematically, just the well-known Cauchy-Riemann conditions, which express the fact that the complex quantity w = <f>-iA (3.15) is an analytic function of the complex argument z = x + iy. This means that the function w(z) has a definite derivative at every point, independent of the direction in which the derivative is taken. For example, differentiating along the #-axis, we find dwjdz = 8^j8x—i8Aj8x, or dw/dz = -E x + iE y . (3.16) The function w is called the complex potential. The lines of force are defined by the equation dx/E x = dy\E y . Expressing E x and Ey as derivatives of A, we can write this as (8A/ 8x)dx +(8A/ 8y)dy = dA = 0, whence A{x,y) = constant. Thus the lines on which the imaginary part of the function zo(z) is constant are the lines of force. The lines on which its real part is constant are the equipotential lines. The orthogonality of these families of lines is ensured by the relations (3.14), according to which 86 8 A 86 d A dx dx dy dy Both the real and the imaginary part of an analytic function zv(z) satisfy Laplace's equation. We could therefore equally well take im w as the field potential. The lines of force would then be given by re w = constant. Instead of (3.15) we should have w = A+i(f>. The flux of the electric field through any section of an equipotential line is given by the integral § E n dl = — § (d<j>l dri)dl, where dl is an element of length of the equipotential line and n the direction of the normal to it. According to (3.14) we have d<f>jdn = —8A/81, the choice of sign denoting that / is measured to the left when one looks along n. Thus § E n dl = § (8Aldl)dl = A2—A1, where A2 and A\ are the values of A at the ends 14 Electrostatics of Conductors §3 of the section. In particular, since the flux of the electric field through a closed contour is Aire, where e is the total charge enclosed by the contour (per unit length of conductors perpendicular to the plane), it follows that e = (1/4tt)A^, (3.17) where AA is the change in A on passing counterclockwise round the closed equipotential line. The simplest example of the complex potential is that of the field of a charged straight wire passing through the origin and perpendicular to the plane. The field is given by E r = 2e/r, E d = 0, where r,6 are polar co- ordinates in the xy-plane, and e is the charge per unit length of the wire. The corresponding complex potential is to = - 2e log z = - 2e log r - lied. (3.18) If the charged wire passes through the point (xo, yo) instead of the origin, the complex potential is to = -2e\og{z-zo\ (3.19) where zq = xq + iyo. Mathematically, the functional relation w = w(z) constitutes a conformal mapping of the plane of the complex variable z on the plane of the complex variable w. Let C be the cross-sectional contour of a conductor in the ary-plane, and <f>o its potential. It is clear from the above discussion that the problem of determining the field due to this conductor amounts to finding a function w(z) which maps the contour C in the -sr-plane on the line to = (f>o, parallel to the axis of ordinates, in the w-plane. Then re w gives the potential of the field. (If the function zv(z) maps the contour C on a line parallel to the axis of abscissae, then the potential is im w.) Fig. 2 (4) The wedge problem. We shall give here, for reference, formulae for the field due to a point charge e placed between two intersecting conducting half-planes. Let the z-axis of a system of cylindrical co-ordinates (r, 6, z) be along the apex of the wedge, the angle 6 being measured from one of the planes, and let the position of the charge e be (a, y, 0) (Fig. 2). The angle a between the planes may be either less or greater than ir\ in the latter case we have a charge outside a conducting wedge. (3.21) §3 Methods of solving problems in electrostatics 15 The field potential is given byt e N sinh(7r£/a) sinh(7r£/a) | aV(2<w) J Icosh (Tr^/a) - cos [tt(0 - y)/a] cosh (tt £/a) - cos [tt(0 + y)/a] I d£ (3 ' 20) x , cosh 7) — (a 2 + r 2 + z 2 )/2ar, rj > 0. -v/(cosh £ — cosh 17) The potential <f> = on the surface of the conductors, i.e. for 6 = or a. In particular, for a = 2tt we have a conducting half-plane in the field of a point charge. In this case the integral in (3.20) can be evaluated explicitly, giving e(l J-cos%(0-y)\ 1 J-co&l{d + Y )\\ <j> = — { — cos -1 cos -1 — )}, r AR \ cosh £77 J R \ cosh £77 J) R2 = a 2 + r 2 + z 2 -2arcos(y-6), R'2 = a 2 + r 2 + z 2 -2arcos(y+6). In the limit as the point (r, 6, z) tends to the position of the charge e, the potential (3.21) becomes 4> = d>' + elR, where d>' = — — [l+-^^l. (3.22) 2?ra L sin yj The second term is just the Coulomb potential, which becomes infinite as R -> 0, while <f>' is the change caused by the conductor in the potential at the position of the charge. The energy of the interaction between the charge and the conducting half-plane is * = W= - — U + -T- 1 . (3-23) 47T# L sin y J PROBLEMS Problem 1. Determine the field near an uncharged conducting sphere of radius R placed in a uniform external electric field (&. Solution. We write the potential in the form ^ = <£o+^i, where ^0 = — ©«r is the potential of the external field and <f>i is the required change in potential due to the sphere. By symmetry, the function <f>i can depend only on the constant vector (£. The only such solu- tion of Laplace's equation which vanishes at infinity is ^1 = — constant X(£«grad(l/r) = constant X©T/r 3 , the origin being taken at the centre of the sphere. On the surface of the sphere <f> must be constant, and so the constant in <f>i is R s , whence / R 3 \ I R 3 \ *=-ffi.r(l--) = -(£rcos0(l---), where is the angle between © and r. The distribution of charge on the surface of the sphere is given by a (l/47r)[a^/3r] r -R = (3(£/4w) cos 0. f This formula was first given by H. M. Macdonald (1895). Its derivation is given by him in Electromagnetism, Bell, London, 1934, p. 79. 16 Electrostatics of Conductors §3 The total charge e — 0. The dipole moment of the sphere is most easily found by comparing 4>i with the potential P-r/r 3 of an electric dipole field, whence & = R 3 (&. Problem 2. The same as Problem 1, but for an infinite cylinder in a uniform transverse field. Solution. We use polar co-ordinates in a plane perpendicular to the axis of the cylinder. The solution of the two-dimensional Laplace's equation which depends only on a constant vector is <f>i = constant X (£*grad (log r) = constant X ffi«r/r 2 . Adding ^o = — ©«r and putting the constant equal to R 2 , we have = -(£r <(-£)■ The surface charge density is a = ((£/2w) cos d. The dipole moment per unit length of the cylinder can be found by comparing ^ with the potential of a two-dimensional dipole field, namely 2^-grad (log r) = 2^-r/r 2 , so that ^ = £R 2 (g. Problem 3. Determine the field near a wedge-shaped projection on a conductor. Solution. We take polar co-ordinates r, d in a plane perpendicular to the apex of the wedge, the origin being at the vertex of the angle do of the wedge. The angle d is measured from one face of the wedge, the region outside the conductor being ^ d < lit— do. Near the apex of the wedge, the potential can be expanded in powers of r, and we shall be interested in the first term of the expansion (after the constant term), which contains the lowest power of r. The solutions of the two-dimensional Laplace's equation which are proportional to r n are r n cos nd and r n sin nd. The solution having the smallest n which satisfies the con- dition <f> = constant for 0=0 and = 27r— 0o (i.e. on the surface of the conductor) is <f> = constant X r n sin nd, n = ir/(2n— do). The value of the constant can be determined only by solving the problem for the whole field. The field varies as r n_1 . For do < -n (n < 1), therefore, the field becomes infinite at the apex of the wedge. In particular, for a very sharp wedge (do <^ 1 , n = £) E increases as r~* as r -> 0. Near a wedge-shaped concavity in a conductor ($o > ir, n > 1) the field tends to zero. Problem 4. Determine the field near the end of a sharp conical point on the surface of a conductor. Solution. We take spherical co-ordinates, with the origin at the vertex of the cone and the polar axis along the axis of the cone. Let the angle of the cone be 2#o -^ 1 , so that the region outside the conductor corresponds to polar angles in the range do < d < it. We seek a solution for the variable part of the potential, which is symmetrical about the axis, in the form * = f/(0), (1) with the smallest possible value of n. Laplace's equation 1 d I a H\ l d I n H\ ^^r^i+^n^^r^^^ ' after substitution of (1), gives 1 sin 9 d e ( 8ta9 s) + " ( " +1)/ -°- (2) The condition of constant potential on the surface of the cone means that we must have /(0o) = 0. For small do we seek a solution by assuming that n <^ 1 and f(d) is of the form constant X [1+^(0)1, where ifi <^. 1. (For do -> 0, i.e. an infinitely sharp point, we should expect that <f> tends to a constant almost everywhere near the cone.) The equation for ifi is 1 d / . A+ sin d dd (-3- (3) §3 Methods of solving problems in electrostatics 17 The solution having no singularities outside the cone (in particular, at — w) is i/>(0) — 2« log sin £0. For ~ do <^ 1, ^ is no longer small. Nevertheless, this expression remains valid, since the second term in equation (2) may be neglected because is small. To determine the con- stant n in the first approximation we must require that the function/ =1+^ vanishes for = do. Thusf « = —1/2 log 6o. The field increases to infinity as r~"< 1_B > in the neighbour- hood of the vertex, i.e. essentially as 1/r. Problem 5. The same as Problem 4, but for a sharp conical depression on the surface of a conductor. Solution. The region outside the conductor now corresponds to the range < < 0o. As in Problem 4, we seek <f> in the form (1), but now n ^> 1. Since <^ 1 for all points in the field, equation (2) of Problem 4 becomes This is Bessel's equation, and the solution having no singularities in the field is Jo(n0). The value of n is determined as the smallest root of the equation Jo(nOo) = 0, whence n = 2*4/0o. Problem 6. Determine the energy of the attraction between an electric dipole and a plane conducting surface. Solution. We take the *-axis perpendicular to the surface of the conductor, and passing through the dipole ; let the dipole moment vector 3* lie in the «y-plane. The image of the dipole is at the point — * and has a moment &' x = &x, &'v = —&y- The required energy of attraction is half the energy of the interaction between the dipole and its image, and is % = -(2&> x *+&y 2 )ll6x?. Problem 7. Determine the mutual capacity per unit length of two parallel infinite con- ducting cylinders of radii a and b, their axes being at a distance c apart.J Fig. 3 Solution. The field due to the two cylinders is the same as that which would be produced (in the region outside the cylinders) by two charged wires passing through certain points A and A' (Fig. 3). The wires have charges ±«' per unit length, equal to the charges on the cylinders, and the points A and A' lie on OO' in such a way that the surfaces of the cylinders are equipotential surfaces. For this to be so, the distances OA and O'A' must be such f A more rigorous calculation gives the formula n == 1/2 log (2/0o), containing a coefficient in the (large) logarithm, which cannot really be obtained by the simple method given here. J The corresponding problem for two, spheres cannot be solved in closed form. The difference arises because, in the field of two parallel wires bearing equal and opposite charges, all the equipotential surfaces are circular cylinders, whereas in the field of two equal and opposite point charges the equipotential surfaces are not spheres. 18 Electrostatics of Conductors §3 that OA • OA' = a 2 , O'A' • O'A = b\ i.e. di{c-d%) = a 2 , dz(c-di) = 6 2 . Then, for each cylinder, the ratio r\r' of the distances from A and A' is constant. On cylinder 1 , r\r' — ajOA' = al(c—dz) = di/a, and on cylinder 2, r'/r = dvjb. Accordingly, the potentials of the cylin- ders are fa = —2elog {r\r') = —2elog(dila), fa = 2e log (<&/&), ^2—^1 = 2e log (didzlab). Hence we find the required mutual capacity C = el(<f>2—<f>i) : 1/C = 2 log (did z /ab) = 2 cosh" 1 [(c 2 -a 2 -6 2 )/2a6]. In particular, for a cylinder of radius a at a distance h (> a) from a conducting plane, we put c = b+h and take the limit as b -> 00, obtaining 1/C = 2 cosh -1 (A/a). If two hollow cylinders are placed one inside the other (c < b—d), there is no field outside, while the field between the cylinders is the same as that due to two wires of charges ±« passing through A and A' (Fig. 4). The same method gives 1/C = 2 cosh" 1 [(a 2 +6 2 -c 2 )/2afe]. Problem 8. The boundary of a conductor is an infinite plane with a hemispherical pro- jection. Determine the charge distribution on the surface. 00=c Fig. 4 Solution. In the field determined in Problem 1, whose potential is ,R 3 \ /, R3 \ 9 = constant X2II —I, the plane z = with a projection r = jR is an equipotential surface, on which <f> = 0. Hence it can be the surface of a conductor, and the above formula gives the field outside the con- ductor. The charge distribution on the plane part of the surface is given by 47rLad z _o \ r 3 /' we have taken the constant in <f> as — Ariroo, so that cto is the charge density far from the pro- jection. On the surface of the projection we have 1 rafi 2 ■ 1 I = A an 6 1 1 Z = 3go— . r\r-R R Problem 9. Determine the dipole moment of a thin conducting cylindrical rod, of length 2/ and radius a <^ /, in an electric field © parallel to its axis. Solution. Let t(z) be the charge per unit length induced on the surface of the rod, and z the co-ordinate along the axis of the rod, measured from its midpoint. The condition of constant potential on the surface of the conductor is 2rr I K . - C f r( z')dz' d<f> -^rJi — r — =?' -i 2tt J J -I R* = (*'-*) 2 +4a 2 sin 2 i?, §3 Methods of solving problems in electrostatics 19 where <f> is the angle between planes passing through the axis of the cylinder and through two points on its surface at a distance R apart. We divide the integral into two parts, putting r(z') == t(z) + [t(z')— t(z)]. Since l^> a, we have for points not too near the ends of the rod t(z) f r dz'd<f> ^ t(^ r V—z* , , /A , MP-z*) 2tt J J R ~ 2ir J a 2 sin 2 \$ d<f> = t(z) log ■ using the result that J log sin <f>d<f> = —w log 2. In the integral which contains the diff- erence t(z')—t(z), we can neglect the a 2 term in R, since it no longer causes the integral to diverge. Thus (&z = t(z) log MP-z*) + T(Z')-T(Z) dz\ The quantity t is almost proportional to z, and in this approximation the integral gives — 2t(z), the result being r(z) = &z log[4(/ 2 -^ 2 )/a 2 ]-2 This expression is invalid near the ends of the rod, but in calculating the dipole moment that region is unimportant. In the above approximation we have -l where L = log(2//a)— 1 is large, or (with the same accuracy) ~ 3 1og(4//a)-7' Problem 10. Determine the capacity of a hollow conducting cap of a sphere. Solution. We take the origin O at a point on the rim of the cap (Fig. 5), and carry out the inversion transformation r = / 2 /r', where / is the diameter of the cap. The cap then becomes the half-plane shown by the dashed line in Fig. 5, which is perpendicular to the radius AO of the cap and passes through the point B on its rim. The angle y = it— 6, where 20 is the angle subtended by the diameter of the cap at the centre of the sphere. Fig. 5 If the charge on the cap is e and its potential is taken as zero, then as r -*■ oo the potential ^ ->— ^o+e/r. Accordingly, in the transformed problem, as r' -»■ the potential is <f>' ->■ l<f>/r' == — I fall* + eft, where the first term corresponds to a charge e' = — l<t>o at the origin. 20 Electrostatics of Conductors §4 According to formula (3.22), we have Y r' 2tt/\ sinfl/ (the potential near a charge e' at a distance / from the edge of a conducting half-plane at zero potential). Comparing the two expressions, we have for the required capacity C = e[<f>o It 6 \ R C = H 1+ "^^ = -0»in 0+0), 2tt\ sin 6/ it where R is the radius of the cap. Problem 11. Determine the correction due to edge effects on the value C = Sftird for the capacity of a plane condenser (S being the area of the plates, and d <^ \/S the distance between them). .<p-<^>Q/'d (a) -d[ ^=0 (b) Fig. 6 Solution. Since the plates have free edges, the distribution of charge over them is not uniform. To determine the required correction in a first approximation, we consider points which are at distances x from the edge such that d <^ x <^ -\/S. For example, taking the upper layer (at potential <f> = ifo, Fig. 6a) and neglecting its distance id from the mid- plane (the equipotential surface <f> = 0), we have the problem of the field near the boundary between two parts of a plane having different potentials (Fig. 6b). The solution is elemen- tary f, and the excess charge (relative to the value of a far from the edge) is A a = Enftir — <f>o/Sir s x, so that the total excess charge is L / Aa dx = (<j>oL/8ir 2 ) log (\^S/d), where L is the perimeter of the plate. In calculating the logarithmically divergent integral, we have taken the limits as those of the region d <^.x <^ \/S. Hence we find the capacity} S L , VS C = 1 log — — . 4-nd Sit 2 * d §4. A conducting ellipsoid The problem of the field of a charged conducting ellipsoid and that of an ellipsoid in a uniform external field are solved by the use of ellipsoidal co- ordinates. These are related to Cartesian co-ordinates by the equation X V Z + 1J—-+-* = 1 (a> b> c). (4.1) a? + u b 2 + u c 2 + u t See §22. In formula (22.2) for the potential we must here put ^ a & == ii>o> ol = tt. X A more exact calculation (determining the coefficient in the argument of the logarithm) demands considerably more elaborate methods, and the result depends on the shape of the plates. If these are circular, of radius R, we obtain Kirchhoff's formula R? R / 16nR „ R* R/ IbrrR \ §4 A conducting ellipsoid 21 This equation, a cubic in u, has three different real roots |, rj, £, which lie in the following ranges: £ > -c\ -c 2 ^^^ -b 2 y -b 2 > C> -a 2 . (4.2) These three roots are the ellipsoidal co-ordinates of the point x, y, z. Their geometrical significance is seen from the fact that the surfaces of constant £, rj and £ are respectively ellipsoids and hyperboloids of one and two sheets, all confocal with the ellipsoid x 2 /a 2 +y 2 /b 2 + z 2 lc 2 = 1. (4.3) One surface of each of the three families passes through each point in space, and the three surfaces are orthogonal. The formulae for transforma- tion from ellipsoidal to Cartesian co-ordinates are given by solving three simultaneous equations of the type (4.1), and aret (|+a% + a 2 )(£ + a 2 ) ~VL (b 2 -a 2 )(c 2 -a 2 ) J' y VL (c 2 -b 2 \(a 2 -W) y ~VL (a 2 -C 2 )(b 2 -C 2 ) J* (4.4) {c 2 -b 2 ){a 2 -b 2 ) (i + c^n+fU+f) (a 2 -c 2 ){b 2 -c 2 ) The element of length in ellipsoidal co-ordinates is d/2 = h&ip + WdrP + WdP, hi = V[(i-r))^-0V2R s , h = V[(v-CXn-mi2Rv \ (4-5) h = V[{t ~ m ~ l)\l^ Ru 2 = (u + a 2 )(u + b 2 )(u + c 2 ), u = i, 7], £. Accordingly, Laplace's equation in these co-ordinates is 4 A<t> = x (t-nM-€Kv-Q If two of the semiaxes a, b, c become equal, the system of ellipsoidal co- ordinates degenerates. Let a = b > c. Then the cubic equation (4.1) becomes a quadratic, 2 2 9 +-^— = 1, P 2 = x 2 +y\ (4.7) a 2 + u c 2 + u t Strictly speaking, the ellipsoidal co-ordinates should be taken not as £, 17, £ themselves but as V(« 2 + £), V(b 2 + if}, V(c 2 + £)• Then the double signs would not appear in (4.4), and the two systems of co-ordinates would be in one-to-one correspondence, as they should be. 22 Electrostatics of Conductors §4 with two roots whose values lie in the ranges £ ^ — c 2 , —c 2 > rj ^ —a 2 . The co-ordinate surfaces of constant £ and r\ become respectively confocal oblate spheroids and confocal hyperboloids of revolution of one sheet (Fig. 7). As the third co-ordinate we can take the polar angle <f> in the xy-plane (# = p cos <f>, y — p sin <j>). For a = b the ellipsoidal co-ordinate £ de- generates to a constant, — a 2 . Its relation to the angle <f> is given by the way in which it tends to —a 2 as b tends to a, namely cos<£ = V[(« 2 + 0/(« 2 -* 2 )] as 6 ^«. ( 4 - 8 ) Fig. 7 This is easily seen from (4.4) or directly from (4.1). The relation between the co-ordinates z, p and £, 17 is given, according to (4.4), by -*y[ (£+c% + c 2 ) i*2 /72 ]■ '-yi (£+«%+« 2 ) t2 — />2 (4.9) The co-ordinates £, 17, <£ are called oblate spheroidal co-ordinates, t Similarly, for a > b = c ellipsoidal co-ordinates become prolate spheroidal co-ordinates. Two co-ordinates £ and £ are roots of the equation x 2 p 2 a 2 + u b 2 + u p2 = y2 _|_ #2^ (4.10) where £ ^ — & 2 , — b 2 > £ ^ —a 2 . The surfaces of constant £ and £ are prolate spheroids and hyperboloids of revolution of two sheets (Fig. 8). The co-ordinate 17 degenerates to a constant, — b 2 , for c ->b, and we have cos<£ = VW + i)l{b 2 -c 2 )], (4.11) where <f> is the polar angle in the yz-plane. The relation between the co- ordinates x, p and £, £ is given by ■(i + a 2 )(C + a 2 )l /r(| + & 2 )(£ + & 2 )| _,_ /r(f+« a )(£+flvi /r 62_«2 ! 1- (4.12) t We here use the definition of spheroidal co-ordinates such that they are the limit of ellipsoidal co-ordinates. Other definitions are used in the literature, but are easily related to ours. §4 A conducting ellipsoid In a system of oblate spheroidal co-ordinates the foci of the spheroids and hyperboloids lie on a circle of radius <\/{a 2 —c 2 ) in the xy-plane; in Fig. 7 AA! is a diameter of this circle. Let us draw a plane passing through the #-axis and some point P. It intersects the focal circle at two points; let their distances from P be r±, r 2 . If the co-ordinates of P are p, z, then ri 2 =[p- V(" 2 ~ c 2 )f + * 2 , r 2 2 = [p + V(« 2 ~ c 2 )] 2 + z 2 . Fig. 8 The spheroidal co-ordinates |, r\ are given in terms of r\, r 2 by £ = h(r 1 + r 2 ) 2 -a 2 , V = i(r 2 -ri) 2 -a 2 . (4.13) In a system of prolate spheroidal co-ordinates the foci are the points x = ±-\Z(a 2 —b 2 ) on the #-axis (the points A, A' in Fig. 8). If r\ and r% are the distances of these foci from P, then n 2 = p 2 + [z - *J(a 2 - b 2 )f, r 2 2 = p 2 + [z + V(« 2 ~ b 2 )] 2 , and the spheroidal co-ordinates £, £ are given in terms of r±, r 2 by the same formulae (4.13), with £ in place of rj. Let us now turn to the problem of the field of a charged ellipsoid whose surface is given by the equation (4.3). In ellipsoidal co-ordinates this is the surface £ = 0. It is therefore clear that, if we seek the field potential as a function of £ only, all the ellipsoidal surfaces £ = constant, and in particu- lar the surface of the conductor, will be equipotential surfaces. Laplace's equation (4.6) then becomes whence d£< m «) - •• 00 d£ 24 Electrostatics of Conductors §4 The upper limit of integration is taken so that the field is zero at infinity. The constant A is most simply determined from the condition that at large distances r the field must become a Coulomb field and <f> ^ c/r, where e is the total charge on the conductor. When r ->- oo, £ ->■ oo, and £ £ r 2 , as we see from equation (4.1) with u = £. For large £ we have 1?£ £ £ 3/2 , and <£ £ 2A\yJ% = 2.4/r. Hence 2^4 = £, and therefore ^ = *'Jf (4 * 14) g % The integral is an elliptic integral of the first kind. The surface of the con- ductor corresponds to £ = 0, and so the capacity of the conductor is given by 1 ?dg c - *fc (4 - 15) The distribution of charge on the surface of the ellipsoid is determined by the normal derivative of the potential : a= -± \ d l] = _±r±iii From equations (4.4) we easily see that for £ = x 2 y 2 z 2 r)£ — + TT + — = 1 47T vW) *4 64 ^4 a 2^2 c 2 Hence ^nabc (x 2 y 2 z 2 \ -* ^4 + 64 + "?/ (4.16) For a spheroid the integrals (4.14), (4.15) degenerate and can be expressed in terms of elementary functions. For a prolate spheroid (a > b = c) the field potential is e la 2 — b 2 = tanh-i / , (4.17) r ^{a 2 -b 2 ) V | + fl 2 v ' and the capacity is V(« 2 -& 2 ) C = — -. (4.18) cosh _1 (a/6) For an oblate spheroid (a = 6 > c) we have e /a 2 -c 2 ' V(« 2 -^ 2 ) <£ = tan-i / , C = VV t/ ' (4.19) Y V"(« 2 -^ 2 ) V £ + c 2 cos-i(c/fl) §4 A conducting ellipsoid 25 In particular, for a circular disc {a = b, c = 0) C = laj-n. (4.20) Let us now consider the problem of an uncharged conducting ellipsoid in a uniform external electric field ©. Without loss of generality we may take the field <£ to be along one of the axes of the ellipsoid. In any other case this field may be resolved into components along the three axes, and the resultant field is a superposition of those arising from each component separately. The potential of a uniform field <£ along the #-axis (the a-axis of the ellip- soid) is, in ellipsoidal co-ordinates, <f>o = - ®x = - (£V[(£ + «% + <**){£> + « 2 )/(* 2 - « 2 )(^ 2 - a 2 )]. (4.21) We write the field potential outside the ellipsoid as <f> = <f>o +</>', where <j> gives the required perturbation of the external field by the ellipsoid, and seek <J>' in the form *' = <hF(i). (4.22) In this function the factors depending on 77 and £ are the same as in ^0 ; this enables us to satisfy the boundary condition at £ = for arbitrary 17, £ (i.e. on the surface of the ellipsoid). Substituting (4.22) in Laplace's equation (4.6), we obtain for F(g) the equation d*F dF d a? + itvwwn - °- One solution of this equation is F = constant, and the other is m = ^ J g (£ + <> 2 Wi (4.23) The upper limit of integration is taken so that <f>' -> for g -> 00. The integral is an elliptic integral of the second kind. We must have <f> =, constant on the surface of the ellipsoid. For this condi- tion to be satisfied with £ = and arbitrary 77, £, the constant value of <f> must be zero. Determining the coefficient A in F(g) so that F(0) = —1, we obtain the following final expression for the field potential : *-4-fc^/jfrdy- (4 - 24) 1 Let us find the form of the potential <f>' at large distances r from the ellip- soid. For large r, the co-ordinate £ is large, and $ £ r 2 , as follows at once from equation (4.1). Hence r ds ^ r ds 2 J (s+a*)R s £ J ~sW = ^ 26 Electrostatics of Conductors §4 and the potential <f>' = (£ xVj4TTn {x) r z , where F = frrabc is the volume of the ellipsoid and n ix \ n ( v\ « fe) are denned by n (x) — \abc ds , . r ds - - «(») = i^c (* + a 2 )#/ 2 J(* + &2)#/ u (4.25) f ds n fe) = \abc . o The expression for <f>' is, as we should expect, the potential of an electric dipole : <£' = x^xj^, where the dipole moment of the ellipsoid is & x = <& x VI4irtf*\ (4.26) Analogous expressions give the dipole moment when the field G is along the y or z axis. The positive constants n&\ n^\ w (z) depend only on the shape of the ellipsoid, and not on its volume; they are called the depolarisation coefficients A If the co-ordinate axes do not necessarily coincide with those of the ellip- soid, formula (4.26) must be written in the tensor form WVym&t = <&. (4.27) The quantities n (x) , n^\ « fe) are the principal values of the symmetrical tensor nys of rank two. In the general case of arbitrary a, b, c, it follows from the definitions of n (z\ n (.y\ nfe) that n (x) < n (y) < M fe) if a > b > c . (4.28) Further, by adding the integrals for « te >, n^\ « fo) and using as the variable of integration u = R s 2 , we find r dw n (x) + n (y) + n (z) = l aoc ___ J U 3 ' 2 (a be) 1 whence n te> + „<*) + „<«) = 1. (4.29) The sum of the three depolarisation coefficients is thus unity; in tensor nota- tion, flu = 1. Since these coefficients are positive, none can exceed unity. For a sphere (a = b = c) it is evident from symmetry that n (x) = n (y) = w fe) = £. (4.30) For a cylinder with its axis in the ^-direction (a -> oo), we havet »te> = 0, nW = «fe> = i. (4.31) f Useful tables of these coefficients have been given by E. C. Stoner (Philosophical Magazine [7] 36, 803, 1945). . J These values for a sphere and a cylinder agree, of course, with those found in §3, Problems 1 and 2. §4 A conducting ellipsoid XI The elliptic integrals (4.25) can be expressed in terms of elementary func- tions if the ellipsoid is a spheroid. For a prolate spheroid {a > b = c) of eccentricity e = y^l — £ 2 /a 2 ), 1-e 2 / 1+e \ /log 2e\, nW = n<*> = £(1 -»<*>). w te) = 2*3 If the spheroid is nearly spherical (e <^ 1) we have approximately «to) = i-^ e 2 ) w (y) = w (z) = 1+^2. For an oblate spheroid (a = b > c) tfe) 1+e 2 (e-tan- 1 *;), n<- x) = nW = l{\-n^), where e = \Z(a 2 Jc 2 — 1). If e <^ 1, then (4.32) (4.33) (4.34) (4.35) PROBLEMS Problem 1 . Find the field of a charged conducting circular disc of radius a, expressing it in cylindrical co-ordinates. Find the distribution of charge on the disc. Solution. The charge distribution is obtained by taking the limit of formula (4.16) as c -*■ 0, z -*■ 0, with z\c — V(l — r 2 la 2 ) (where r 2 = x z +y 2 ), in accordance with (4.3). This gives 47ra 2 \ a 2 / The field potential is given in all space by formula (4.19), where we put c = and express f in terms of r and z by means of equation (4.1) with c = 0,u = £, a = b: <f> = - tan -1 - a Lr 2a 2 2 +z 2 -a 2 + V[0- 2 +z 2 -a 2 ) 2 +4a 2 * 2 ] ]• ff / Z2L 'A Fig. 9 Near the edge of the disc, we replace r and z by co-ordinates p and 6 such that z = p sin 0, r = a—p cos (Fig. 9; p <^a), obtaining in agreement with the general result derived in §3, Problem 3. 28 Electrostatics of Conductors §4 Problem 2. Determine the electric quadrupole moment of a charged ellipsoid. Solution. The quadrupole moment tensor of a charged conductor is defined as Due <= e(3xtxk— r*8uc), where e is the total charge, and the bar denotes an average such as XiXjc = - <J) XiXKO d/. It is evident that the axes of the ellipsoid are also the principal axes of the tensor Due- Using formula (4.16) for a, and for the element of surface of the ellipsoid the expression dxdy d/= dx dy I r* 2 y 2 z 2 l = zlc* N ti* 6* e* J' we obtain — r r zdxdy = Jc 2 ; = — f Andb J the integration over x and y covers twice the area of the cross-section of the ellipsoid by the xy-plane. Thus D xx = J e (2a 2 -& 2 -c 2 ), D yy = ie(26 2 -c 2 -a 2 ), Dzz = J«(2c 2 -a 2 ~& 2 ). Problem 3. Determine the distribution of charge on the surface of an uncharged con- ducting ellipsoid placed in a uniform external field. Solution. According to formula (1.9) we have = _jJL|"£f| = _T_L!f| by (4.5) the element of length along the normal to the surface of the ellipsoid is Aid£. Sub- stituting (4.24) and using the fact that "* = ihi ai-U-o = L2a 2 /iJ e -o (where v is a unit vector along the normal to the surface), we have a = QzvxfirmW when the external field is in the ^-direction. When the direction of the external field is arbitrary this becomes Air 4-irlnW n^ n<*> J Problem 4. The same as Problem 3, but for a plane circular disc of radius a lying parallel to the field, t Determine also the dipole moment of the disc. Solution. Let us regard the disc as the limit of a spheroid when the semiaxis c tends to zero. The depolarisation coefficient along this axis (the 2-axis) tends to 1, and those along the x and y axes tend to zero: n< z > = 1 —ncjla, n™ = «<"> = irc/Aa, by (4.34). The com- ponent v x of the unit vector along the normal to the surface of the spheroid tends to zero: _ x (x*+y 2 z 2 \"-* * c 2 __ xc( _ * 2 +y 2 \~* Hence the charge density is (£ v x (£p cos <f> \lt 70*) ~ 7r 2 V(a 2 -P 2 )' where p and <f> axe polar co-ordinates in the plane of the disc. The dipole moment of the disc is obtained from formula (4.26), and is & =■ 4a 3 ffi/3w. Thus it is proportional to a 3 , and not to the "volume" a 2 c of the disc. a = t The problem for a disc lying perpendicular to the field is trivial: the field remain uniform in all space, and charges a = ± (£/4w are induced on the two sides of the disc. §4 A conducting ellipsoid 29 Problem 5. Determine the field potential outside a conducting spheroid with its axis of symmetry parallel to a uniform external field. Solution. For a prolate spheroid (a > b = c, with the field ($S in the ^-direction) we find, on calculating the integral in formula (4.24), tanh-l VK* 2 ~b 2 )K£+a 2 )] - VK« 2 -*> 2 )/(£+a 2 )]| <t> = -<£*{l- tanh" 1 V(l -& 2 /a 2 ) - V(l -b 2 /a 2 ) J The co-ordinate £ is related to * and p = -\/{y 2 +z 2 ) by -j£_ + -*_ = ! i 2 +* a*+£ with < £ < oo in the space outside the ellipsoid. For an oblate spheroid (a = b > c) the field © is along the 2-axis. We must therefore re- place s+a 2 by $+c 2 and put ^o = —i&z in the integrals in (4.24). Then V[(a* -c 2 )/(g+c 2 )] -tan-* V[(a 2 -c 2 )/(£ +c 2 ) V(a 2 /c 2 -l)-tan-i V(a 2 /c 2 -l) where the co-ordinate £ is related to z and p = V(x 2 +y 2 ) by , « f V[(a 2 -c 2 )/(g+c 2 )]-tan-i V[(^-c 2 )/(|+c2) | * I V(a 2 /c 2 -l)-tan-i V(a 2 /c 2 -l) /' ' +^r-l. a 2 +£ c 2 +£ Problem 6. The same as Problem 5, but with the axis of symmetry perpendicular to the external field. Solution. For a prolate spheroid (with the field along the #-axis) Vtf +a 2 )IU+b 2 )-(a 2 -b 2 )-* tanh" 1 VK« 2 -&W +a 2 )}\ <l> = -<E*[l- a/6 2 -(a 2 -6 2 )-*tanh- 1 y/{\-b 2 la 2 ) For an oblate spheroid (with the field along the %-axis) ( a 2_ c 2)-» ten -i ^ [ ( a 2_ c 2)/(^ +c a ) ]_ x /(^ +c 2 )/( ^ +a 2 ) <£* 1- (a 2 -c 2 )-* tan- 1 y/{a 2 \c 2 - 1) -c/a 2 J Problem 7. A uniform field Qe in the sr-direction (in the half-space z < 0) is bounded by an earthed conducting plane at z = 0, containing a circular aperture. Determine the field and charge distribution on the plane. Solution. The xy-plane with a circular aperture of radius a and centre at the origin may be regarded as the limit of the hyperboloids of revolution of one sheet ,2 *2 p" z - — = 1, p 2 = x 2 +y 2 , F(0 - constant X J^^^r =constantX [-^ - *n-i-2-]; a 2 -\ v \ h| as |ij| -*■ 0. These hyperboloids are one of the families of co-ordinate surfaces in a system of oblate spheroidal co-ordinates with c — 0. The Cartesian co-ordinate z, according to (4.9), is given in term6 of £ and 17 by z = \/(£ h|)/a, and V£ must be taken with the positive and negative sign in the upper and lower half-space respectively. Let us seek a solution in the form <f> = — <&z F(£). For the function F(f) we obtain df ¥(!+*) "™" ~ L~V* " "" ~ V*J the constant of integration is put equal to zero in accordance with the condition <f> = for z -*■ +oo, i.e. V^ -*" +°o. The inverse tangent of a negative quantity must be taken as tan -1 (a/—V0 = w— tan -1 (a/\/£)» and not as —tan -1 (a/V£) since the potential would then be discontinuous at the aperture (£ = 0). The constant coefficient is chosen so that, for z -*■ — oo (i.e. for V£ -*• — oo and tan _1 (a/\/£) -»■ "■), 4> -*■ — ®*i and so we finally have On the conducting plane 17 = and the potential is zero, as it should be. 30 Electrostatics of Conductors §4 At large distances r = -y/O^ + p 2 ) from the aperture we have £ = r 2 , and the potential (in the upper half-plane) is i.e. we have a dipole field, the moment of the dipole being 2P = (£a 3 /377. The field decreases as 1/r 3 , and therefore the flux of the field through an infinitely remote surface (in the half-space z > 0) is zero. This means that all the lines of force passing through the aperture reach the upper side of the conducting plane. The distribution of charge on the conducting plane is given by r^l = - a 8<f> = + JLr tan -i_^- _ _£_1 _ l rafi a 8<f> (£ where the ^= signs refer to the upper and lower sides of the plane respectively. According to the formula n 2 Z 2 a 2 +£ | which relates £ to />, z, we have V£ == ±V(p 2 — <* 2 ) °n the plane z = 0. Thus the charge distribution on the lower side of the conducting plane is given by the formula ® / • -i a _l a \ a= ~^rA 7T - sm P + v( P 2 -a 2 ))- As p -»■ oo we have a = — (£/4ir, as we should expect. On the upper side = C / a . _ x a\ ° 47r2\V(p 2 -a 2 ) Sm p)' Problem 8. The same as Problem 7, but for a plane with a slit of width 26. Solution. The ay-plane with a slit along the x-axis may be regarded as the limit of the hyperbolic cylinders y 2 z 2 b 2 -H ~~M = as 1 17 1 -> 0. These hyperbolic cylinders are one of the families of co-ordinate surfaces in a system of ellipsoidal co-ordinates with a ->• 00, c -* 0. The Cartesian co-ordinate * = V«H)/6. As in Problem 7, we seek a solution in the form <f> = —(£zF(£), obtaining for the function F f d£ F = constant X Here the coefficient and the constant of integration are determined by the conditions that F = and 1 for z ->- +00 and —00 respectively (i.e. for V£ -»■ + 00 and —00), and the final result is ^l-tva+^o+vi] v\v\, lb where we now take Vf positive and the two signs =p correspond to the regions z > and z < 0. At large distances from the slit we have in the upper half -space £ ^ y 2 +z 2 = r 2 , and the potential is <f> S i&(£ V(\v\ £) = i&Wzfr 2 , i-e. the field of a two-dimensional dipole of moment i&b 2 per unit length of the slit (see the formula in §3, Problem 2). The distribution of charge on the conducting plane is given by sAv(y z -b 2 ) /" §5 The forces on a conductor 3 1 §5. The forces on a conductor In an electric field certain forces act on the surface of a conductor. These forces are easily calculated as follows. The momentum flux density in an electric field in a vacuum is given by the Maxwell stress tensor :t — vile = —(i-E 2 ^*; — EiE]c). The force on an element df of the surface of the body is just the "flux" of momentum through it from outside, and is therefore arad/k = o^n^d/ (the sign is changed because the normal vector n is outwards and not inwards). The quantity oacnic is thus the force T s per unit area of the surface. Since, at the surface of a conductor, the field E has no tangential component, we obtain F s = n£ 2 /87r, (5.1) or, introducing the surface charge density a, F s = 2ir(T 2 n = $<rE. We therefore conclude that a "negative pressure" acts on the surface of a conductor; it is directed along the outward normal to the surface, and its magnitude is equal to the energy density in the field. The total force F on the conductor is obtained by integrating the force (5.1) over the whole surface: F = | (tfy&r) df. ( 5 - 2 ) Usually, however, it is more convenient to calculate this quantity from the general laws of mechanics, by differentiating, the energy °tt. The force, in the direction of a co-ordinate q, acting on a conductor is — dW/dq, where the derivative signifies the rate of change of energy when the body is trans- lated in the ^-direction. The energy must be expressed in terms of the charges on the conductors (which give rise to the field), and the differentia- tion is performed with the charges constant. Denoting this by the suffix e, we write F q = -{d%ldq) e . (5.3) Similarly, the projection, on any axis, of the total moment of the forces on the conductor is K=-(d<%ldiP) e , (5.4) where if) is the angle of rotation of the body about that axis. f See The Classical Theory of Fields, §4-8, Addison- Wesley Press, Cambridge (Mass.), 1951 ; Pergamon Press, London, 1959. — cr^ is there denoted by T^p. In the present case we are applying this formula to a surface which does not precisely coincide with that of the body, but is some distance away, in order to exclude the effect of the field structure near the surface (see §1). 32 Electrostatics of Conductors §5 If, however, the energy is expressed as a function of the potentials of the conductors, and not of their charges, the calculation of the forces from the energy requires special consideration. The reason is that, to maintain constant the potential of a moving conductor, it is necessary to use other bodies. For example, the potential of a conductor can be kept constant by connecting it to another conductor of very large capacity, a "charge reser- voir". On receiving a charge e a , the conductor takes it from the reservoir, whose potential <f> a is unchanged on account of its large capacity, although its energy is reduced by e a j> a . When the whole system of conductors receives charges e a , the energy of the reservoirs connected to them changes by a total of —T,e a (f> a . Only the energy of the conductors, and not that of the reservoirs, appears in °tt. In this sense we can say that % pertains to a system which is not energetically closed. Thus, for a system of conductors whose potentials are kept constant, the part of the mechanical energy is played not by ^, but by #= W-^ecda- (5.5) Substituting (2.2), we find that °U and <% differ only in sign: % = - <%. (5.6) The force F q is obtained by differentiating $ with respect to q for constant potentials, i.e. F q = -{d%\h\ = W^?V (5.7) Thus the forces acting on a conductor can be obtained by differentiating % either for constant charges or for constant potentials, the only difference being that the derivative must be taken with the minus sign in the first case and with the plus sign in the second. The same result could be obtained more formally by starting from the differential identity d ^ = S <f> a de a - F q dq, (5.8) in which % is regarded as a function of the charges on the conductors and the co-ordinate q. This identity states that 8^jde a = <j> a and d%jdq= —F q . Using the variables <f> a instead of e a , we have d<# = -Xe a d<f> a -F q dq, (5.9) which gives (5.7). At the end of §2 we have discussed the energy of a conductor in a uniform external electric field. The total force on a conductor in a uniform field is, of course, zero. The expression for the energy (2.14) can, however, be used to determine the force acting on a conductor in a quasi-uniform field §5 The forces on a conductor 33 <£, i.e. a field which varies only slightly over the dimensions of the conduc- tor, In such a field the energy can still be calculated, to a first approxima- tion, from formula (2.14), and the force F is the gradient of this energy: F = -grad <% = |a ifc Fgrad (<&<&). (5.10) The total torque K is in general non-zero even in a uniform external field. By the general laws of mechanics K can be determined by considering an infinitesimal virtual rotation of the body. The change in energy in such a rotation is related to K by h°ll = — K-S<]>, Si|> being the angle of the rota- tion. A rotation through an angle S*J> in a uniform field is equivalent to a rotation of the field through an angle — SiJ> relative to the body. The change in the field is S<£ = — S<p x <£, and the change in energy is S^=(a^/a©).S<£= -Sty.&xdWldH. But d^jd(& = —&>, as we see from a comparison of formulae (2.13) and (2.14). Hence S^ = — ^X©-S<1>, whence K= ^x<£, (5.11) in accordance with the usual expression given by the theory of fields in a vacuum. If the total force and torque on a conductor are zero, the conductor remains at rest in the field, and effects involving the deformation of the body (called electrostriction) become important. The forces (5.1) on the surface of the conductor result in changes in its shape and volume. Because the force is an extending one, the volume of the body increases. A complete determina- tion of the deformation requires a solution of the equations of the theory of elasticity, with the given distribution of forces (5.1) on the surface of the body. If, however, we are interested only in, the change in volume, the problem can be solved very simply. To do so, we must bear in mind that, if the deformation is slight (as in fact is . true for electrostriction), the effect of the change of shape on the change of volume is of the second order of smallness. In the first approxima- tion, therefore, the change in volume can be regarded as the result of defor- mation without change in shape, i.e. as a volume expansion under the action of some effective excess pressure Ap which is uniformly distributed over the surface of the body and replaces the exact distribution given by (5.1). The relative change in volume is obtained by multiplying Ap by the coeffi- cient of uniform expansion of the substance. The pressure Ap is given, according to a well-known formula, by the derivative of the electric energy % of the body with respect to its volume: Ap = —d°U\dVA Let the deforming field be due to the charged conductor itself. Then the energy °U = %e 2 jC, and the pressure is Ap = —\e*dC~ x \dV. For a given t The quantity thus determined is the pressure exerted on the surface by the body itself; the pressure acting on the surface from outside is obtained by changing the sign. 34 Electrostatics of Conductors §5 shape, the capacity of the body (having the dimensions of length) is propor- tional to the linear dimension, i.e. to V 1/3 . Hence tAp = e*l6CV = e<f>/6V. (5.12) If an uncharged conductor is situated in a uniform external field ©, its energy is given by formula (2.14). The extending pressure is therefore A/> = £o«*(gi<g*. (5.13) PROBLEMS Problem 1. A small conductor of capacity c (equal in order of magnitude to its dimension) is at a distance r from the centre of a spherical conductor of large radius a (^> c). The distance r—a from the conductor to the surface of the sphere is supposed large compared with c, but not large compared with a. The two conductors are joined by a thin wire, so that they are at the same potential (f>. Determine the force of their mutual repulsion. Solution. Since the conductor c is small, we can suppose that its potential is the sum of the potential <f>a/r at a distance r from the centre of the large sphere and the potential e\c due to the charge e on the conductor itself. Hence <f> = <f>a/r+e/c, or e = c<f> (1 —a/r). The required force of interaction F is the Coulomb repulsion between the charge e on the con- ductor and the charge a<i> on the sphere : F = ^ H)- This expression is correct to within terms of higher order in c. Thus the small conductor is repelled from the sphere with a force which decreases as it approaches the surface. Problem 2. A charged conducting sphere is cut in half. Determine the force of repulsion between the hemispheres, t Solution. We imagine the hemispheres separated by an infinitely narrow slit, and deter- mine the force F on each of them by integrating over the surface the force (E 2 /8v) cos d, which is the projection of (5.1) on a direction perpendicular to the plane of separation of the hemispheres. In the slit E = 0, and on the outer surface E = e[a?, where a is the radius of the sphere and e the total charge on it. The result is F = e 2 /8a 2 . Problem 3. The same as Problem 2, but for an uncharged sphere in a uniform external field (H perpendicular to the plane of separation. Solution. As in Problem 2, except that the field on the surface of the sphere is E = 3 (£ cos (§3, Problem 1). The required force is F = 9a 2 (£ 2 /16. Problem 4. Determine the change in volume and in shape of a conducting sphere in a uniform external electric field. Solution. The change in volume AV/V = Ap/K, where K is the modulus of volume expansion of the material, and Ap is given by formula (5.13). For a sphere, otjfc = 8«a = 3&ijfc/4ir (§3, Problem 1), so that AV/V = 2<&j&-nK. As a result of the deformation, the sphere is changed into a prolate spheroid. To determine the eccentricity, we may regard the deformation as a uniform pure shear in the volume of the body, just as, to determine the change in the total volume, we regarded it as a uniform volume expansion. The condition of equilibrium for a deformed body may be formulated as requiring that the sum of the electrostatic and elastic energies should be a minimum. The former is, by (2.12) and (4.26), <% = 1_(£2 ~ I(g2 Srm - 8tt lOir R f In Problems 2 and 3 we assume that the hemispheres are at the same potential. §5 The farces on a conductor 35 where R is the original radius of the sphere, a and b the semiaxes of the spheroid, and n ^ J— 4 (a—b)/15R is the depolarisation coefficient (see (4.33).) Since the deformation is axially symmetrical about the direction of the field (the *-axis), only the components u xx and u yy = u zz of the strain tensor are non-zero. Since we are considering equilibrium with respect to a change in shape, we can regard the volume as unchanged, i.e. uu = 0. Hence the elastic energy may be writtenf ^el = i«** °HC V = K °XX — Oyy)(u X X — Uyy) V, where aue is the elastic stress tensor. We have a xx — °yy = 2p.(u X x —u yy ), where /* is the modu- lus of rigidity of the material, and u X x—u y y = (a—b)IR. Hence Making the sum <% eB + 'Wei a minimum, we have (a—b)[R — 9<E 2 /407r/i. Problem 5. Find the relation between frequency and wavelength for waves propagated on a charged plane surface of a liquid conductor (in a gravitational field). Obtain the condi- tion for this surface to be stable (Ya. I. Frenkel', 1935). Solution. Let the wave be propagated along the x-axis, with the sr-axis vertically upwards. The vertical displacement of points on the surface of the liquid is £ = ae*( fca; -«t). When the surface is at rest, the field above it is E z = E = 4ttcto, and its potential <f> = — 4iraoz, where <ro is the surface charge density. The potential of the field above the oscillating surface can be written as <f> = -~4iraoz+<f>i, with 0i = constant X e**^ - "^ e~ kz , <f>i being a small correc- tion which satisfies the equation A<f>i = and vanishes for z -> oo. On the surface itself, the potential must have a constant value, which we take to be zero, and so <£i = Artaot, for * = Q. According to (5.1), an additional negative pressure acts on the charged surface of the liquid ; this pressure is, as far as terms of the first order in <f>i, E 2 I&it ^ E z 2 I8it ^ 2iroo 2 +[kao<f>i]z~o =2irao 2 +4-iroo 2 k£. The constant term 2ttcto 2 is of no importance, since it can be included in the constant external pressure. The consideration of the hydrodynamical motion in the wave is entirely analogous to the theory of capillary waves J, differing only by the presence of the additional pressure mentioned above. At the surface of the liquid we have the boundary condition pg£+ p[dQ>l dt]i-o— ~a.d 2 Hdx 2 —\irao 2 kt, = 0, where a is the surface-tension coefficient, p the density of the liquid, and fl> its. velocity potential. <I> and £ are also related by dt/dt = [dQ>ldz]t-o. Sub- stituting in these two relations £ = ag*(**-<>>*) and O = Ae^"*'^ and eliminating a and A, we find the required relation between k and to ; a> 2 = k(gp-47T<ro 2 k+OLk 2 )lp. (1) If the surface of the liquid is to be stable, the frequency o> must be real for all values of k (since otherwise there would be complex <o with a positive imaginary part, and the factor e -ib>t w ould increase indefinitely). The condition for the right-hand side of (1) to be positive is (4ir<7o 2 ) 2 — 4gpa < 0, or ao 4 < gpa/47r 2 . This is the condition for stability. Problem 6. Find the condition of stability for a charged spherical drop (Rayleigh, 1882). Solution. The sum of the electrostatic and surface energies of the drop is ^ «= e 2 /2C + <*S, where a is the surface-tension coefficient of the liquid, C the capacity of the drop and S its surface area. Instability occurs (with increasing e) with respect to deformation of the sphere into a spheroid, and does so when <^ becomes a decreasing function of the eccentricity (for a given volume). The spherical shape always corresponds to an extremum of % ; the stability condition is therefore [d 2< %ld(a—b) 2 ] a =b > 0, where a and b are the semiaxes of the spheroid, and the differentiation is carried out with ab 2 = constant. Using the formula for the surface of a spheroid and (4.18) for its capacity, we find after a somewhat lengthy calculation e 2 < 16ira s a.. t See Theory of Elasticity, §4, Pergamon Press, London, 1959. % See Fluid Mechanics, §61, Pergamon Press, London, 1959. CHAPTER II ELECTROSTATICS OF DIELECTRICS §6. The electric field in dielectrics We shall now go on to consider a constant electric field in another class of substances, namely dielectrics. The fundamental property of dielectrics is that a constant current cannot flow in them. Hence the constant electric field need not be zero, as in conductors, and we have to derive the equations which describe this field. One equation is obtained by averaging equation (1.3), and is again curl E = 0. (6.1) A second equation is obtained by averaging the equation div e = Airp : div E = 4w/5. (6.2) Let us suppose that no charges are brought into the dielectric from out- side, which is the most usual and important case. Then the total charge in the volume of the dielectric is zero; even if it is placed in an electric field we have j pdV — 0. This integral equation, which must be valid for a body of any shape, means that the average charge density can be written as the divergence of a certain vector, which is usually denoted by — P: p = -divP, (6.3) while outside the body P = 0. For, on integrating over the volume bounded by a surface which encloses the body but nowhere enters it, we find jpdV = — JdivP dV = — <j>P«df = 0. P is called the dielectric polarisation, or simply the polarisation, of the body. A dielectric in which P differs from zero is said to be polarised. The vector P determines not only the volume charge density (6.3), but also the density a of the charges on the surface of the polarised dielectric. If we integrate formula (6.3) over an element of volume lying between two neighbouring unit areas, one on each side of the di- electric surface, we have, since P = on the outer area (cf. the derivation of formula (1.9)), o = Pn, (6.4) where P n is the component of the vector P along the outward normal to the surface. To see the physical significance of the quantity P itself, let us consider the total dipole moment of all the charges within the dielectric; unlike the 36 §6 The electric field in dielectrics 37 total charge, the total dipole moment need not be zero. By definition, it is the integral J" tpdV. Substituting p from (6.3) and again integrating over a volume which includes the whole body we have j rpdV = -j r div FdV = - j> r(df.P) + j (P-grad)r dV. The integral over the surface is zero, and in the second term we have (P-grad)r = P, so that jrpdV = JTdV. (6.5) Thus the polarisation vector is the dipole moment (or electric moment) per unit volume of the dielectric, t Substituting (6.3) in (6.2), we obtain the second equation of the electro- static field in the form div D = 0, (6.6) where we have introduced a quantity D defined by D = E + 4ttP, (6.7) called the electric induction.% The equation (6.6) has been derived by averaging the density of charges in the dielectric. If, however, charges not belonging to the dielectric are brought in from outside (we shall call these extraneous charges), then their density must be added to the right-hand side of equation (6.6) : divD = 47rp ex . (6.8) On the surface of separation between two different dielectrics, certain boundary conditions must be satisfied. One of these follows from the equa- tion curl E = 0. If the surface of separation is uniform as regards physical properties, || this condition requires the continuity of the tangential compor nent of the field: Ei* = E 2t ; (6.9) cf. the derivation of the condition (1.7). The second condition follows from the equation div D = 0, and requires the continuity of the normal compo- nent of the induction : D ln = D 2n - (6.10) t It should be noticed that the relation (6.3) inside the dielectric and the condition P = outside do not in themselves determine P uniquely; inside the dielectric we could add to P any vector of the form curl f. P can be completely determined only by establishing its connection with the dipole moment. X Sometimes the electric displacement, a term due to Maxwell, but one which is obsolete. || That is, as regards composition of the adjoining media, temperature, etc. If the dielectric is a crystal, the crystallographic direction of the surface must be constant, i.e. the surface must be a plane. 38 Electrostatics of Dielectrics §7 For a discontinuity in the normal component D n = D z would involve an infinity of the derivative dD z \dz, and therefore of divD. At a boundary between a dielectric and a conductor, E t = 0, and the condi- tion on the normal component is obtained from (6.8): E t = 0, D n = ±tto, (6.11) where a is the charge density on the surface of the conductor. §7. The dielectric permeability In order that equations (6.1) and (6.6) should form a complete set of equations determining the electrostatic field, they must be supplemented by a relation between the induction D and the field E. In the great majority of cases this relation may be supposed linear. It corresponds to the first terms in an expansion of D in powers of E, and its correctness is due to the smallness of the external electric fields in comparison with the internal molecular fields. The linear relation between D and E is especially simple in the most im- portant case, that of an isotropic dielectric. It is evident that, in an isotropic dielectric, the vectors D and E must be in the same direction. The linear relation between them is therefore a simple proportionality :t D = eE. (7.1) The coefficient e is the dielectric permeability or dielectric constant of the substance and is a function of its thermodynamic state. As well as the induction, the polarisation also is proportional to the field: P = kEe= ( € -1)E/4t7. (7.2) The quantity k is called the polarisation coefficient of the substance, or its dielectric susceptibility. Later (§14) we shall show that the dielectric per- meability always exceeds unity; the polarisability, accordingly, is always positive. The polarisability of a rarefied medium (a gas) may be regarded as proportional to its density. The boundary conditions (6.9) and (6.10) on the surface separating two isotropic dielectrics become E«l = E^2, ei-Enl = e2-E"«2. (7.3) Thus the normal component of the field is discontinuous, changing in inverse proportion to the dielectric permeability of the medium. t It should be mentioned, however, that this relation, which assumes that D and E vanish simultaneously, is, strictly speaking, valid only in dielectrics which are homogeneous as regards physical properties (composition, temperature, etc.). In inhomogeneous bodies D may be non-zero even when E = 0, and is determined by the gradients of thermodynamic quantities which vary through the body. The corresponding terms, however, are very small, and in practice are of no importance. We shall therefore use the relation (7.1) in what follows, even for inhomogeneous bodies. §7 The dielectric permeability 39 In a homogeneous dielectric, e = constant, and then it follows from div D = that div P = 0. By the definition (6.3) this means that the volume charge density in such a body is zero (but the surface density (6.4) is in general not zero). On the other hand, in an inhomogeneous dielectric we have a non-zero volume charge density €-1 1 €-1 1 p = -divP = -div D = D*grad = E- grade. 4n-e 4n- e 4n-e If we introduce the electric field potential by E = — grad <f>, then equa- tion (6.1) is automatically satisfied, and the equation divD= divcE = gives div (e grad <f>) = 0. (7.4) This equation becomes the ordinary Laplace's equation only in a homo- geneous dielectric medium. The boundary conditions (7.3) can be re- written as the following conditions on the potential: (7.5) eidfa/dn = €2d<f>2/dn; the continuity of the tangential derivatives of the potential is equivalent to the continuity of <£ itself. In a dielectric medium which is piecewise homogeneous, equation (7.4) reduces in each homogeneous region to Laplace's equation A<£ = 0, so that the dielectric permeability appears in the solution of the problem only through the conditions (7.5). These conditions, however, involve only the ratio of the dielectric permeabilities of two adjoining media. In particular, the solution of an electrostatic problem for a dielectric body of permeability €2, surrounded by a medium of permeability ei, is the same as for a body of permeability €2Jei, surrounded by a vacuum. Let us consider how the results obtained in Chapter I for the electrostatic field of conductors will be modified if these conductors are not in a vacuum but in a homogeneous and isotropic dielectric medium. In both cases the potential distribution satisfies the equation A<£ = 0, with the boundary condition that <£ is constant on the surface of the conductor, and the only difference is that, instead of E n = — d<f>/ dn = Ana, we have D n = - € d<f>/dn = 4t7(t, (7.6) giving the relation between the potential and the surface charge. Hence it is clear that the solution of the problem of the field of a charged conductor in a vacuum gives the solution of the same problem with a dielectric in place of the vacuum if we make the formal substitution <£ -> e<f>, e -> e or j> -> <f> y e -> e/e. For given charges on the conductors, the potential and the field are reduced by a factor e in comparison with their values in a vacuum. This reduction in the field can be explained as the result of a partial "screen- ing" of the charge on the conductor by the surface charges on the adjoining 4 40 Electrostatics of Dielectrics §7 polarised dielectric. If, on the other hand, the potentials of the conductors are maintained, then the field is unchanged but the charges are increased by a factor e. Finally, it may be noted that in electrostatics we may formally regard a conductor (uncharged) as a body of infinite dielectric permeability, in the sense that its effect on an external electric field is the same as that of a di- electric (of the same form) as e -> oo. For, since the boundary condition on the induction D is finite, D must remain finite in the body even for e ->■ oo. This means that E ->■ 0, in accordance with the properties of conductors. PROBLEMS Problem 1. Determine the field due to a point charge e at a distance h from a plane boun- dary separating two different dielectric media. Solution. Let O be the position of the charge e in medium 1, and O' its image in the plane of separation, situated in medium 2 (Fig. 10). We shall seek the field in medium 1 in the form of the field of two point charges, e and a fictitious charge e' at O' (cf. the method of images, §3): <f>i = e/eir+e'/eyr', where r and r' are the distances from O and O' respectively. In medium 2 we seek the field as that of a fictitious charge e" at O : fa = e"/ezr. On the boun- dary plane (r = r') the conditions (7.5) must hold, leading to the equations e—e' = e", (e+e')lei = e"lez, whence e' = e(ei— e2)/(ei+e2), e" = 2e2e/(ei+e2). (1) Fig. 10 For €2 -> oo we have e' — —e, <f>2 = 0, i.e. the result obtained in §3 for the field of a point charge near a conducting plane. The force acting on the charge e (the "image force") is ee' _ t e \ 2 < ~ (2A) 2 €i ~ \2h) Hi (ei-K 2 )' F > corresponds to repulsion. Problem 2. The same as Problem 1, but for an infinite charged straight wire parallel to a plane boundary surface at a distance h. Solution. As in Problem 1, except that the field potentials in the two media are <f>i = — (2e/ei) log r— (le'/ei) log r', <j>z — — (2e"/e2) logr, where e, e', e" are the charges per unit length of the wire and of its images, and r, r' are the distances in a plane perpendicular to the wire. The same expressions (1) are obtained for e', e" , and the force on unit length of the wire is F = 2ee'[2hei = e 2 (ei— €2)/Aei(ei+c2). §7 The dielectric permeability 41 Problem 3. Determine the field due to an infinite charged straight wire in a medium with dielectric constant ei, lying parallel to a cylinder of radius a and dielectric constant €2, at a distance b (> a) from its axis-t Solution. We seek the field in medium 1 as that produced in a homogeneous dielectric (with constant ei) by the actual wire (passing through O in Fig. 11), with charge e per unit length, and two fictitious wires with charges e' and —e' per unit length, passing through A and O' respectively. The point A is at a distance a 2 Jb from the axis of the cylinder. Then, for all points on the circumference, the distances r and r' from O and A are in a constant ratio r'jr = a/b, and so it is possible to satisfy the boundary conditions on this circumference. In medium 2 we seek the field as that produced in a homogeneous medium (with constant ea) by a fictitious charge e" on the wire passing through O. 00' --b AO' =a z /b Fig. 11 The boundary conditions on the surface of separation are conveniently formulated in terms of the potential <f> (E = — grad <f>) and the vector potential A (cf. §3), defined by D = curl A (in accordance with the equation div D = 0). In a two-dimensional problem, A is in the ar-direction (perpendicular to the plane of the figure). The conditions of con- tinuity for the tangential components of E and the normal component of D are equivalent to <f>i = fa, A\ — Az. For the field of a charged wire we have in polar co-ordinates r, 0: $ = — (2e/e) logr+ constant, A = 2e0+constant; cf. (3.18). Hence the boundary conditions are 2 2e" — (— e log r—e log r'+e' log a) = log r+constant, ei ea 2[e9+e'0'-e'(6+0')] = 2e"9, where the angles are as shown in Fig. 11, and we have used the fact that OO'B and BO' A are similar triangles. Hence ez(e-\-e') = cie", e—e'= e", and the expressions for e' and e" are again formulae (1) of Problem 1. The force acting on unit length of the charged wire is parallel to OO', and is 2ee'{ 1 1 \ F = eE = ( 1 = — ei \OA OO') ei( 2e 2 (€i-e 2 )a 2 i(ei+e 2 )6(fc2-a2)' F > corresponds to repulsion. Problem 4. The same as Problem 3, but for the case where the wire is inside a cylinder of dielectric permeability e2 (b < a). t The corresponding problem of a point charge near a dielectric sphere cannot be solved in closed form. 42 Electrostatics of Dielectrics §8 Solution. We seek the field in medium 2 as that due to the actual wire, of charge e per unit length (O in Fig. 12), and a fictitious wire of charge e' per unit length passing through A, which is now outside the cylinder. In medium 1 we seek the field as that of wires with charges e" and e—e" passing through O and O' respectively. By the same method as in the preceding problem we find e' = — e(ei— e^Kei+ez), e" = 2eiel(ei + e2). For e% > eithe wire is repelled from the surface of the cylinder by a force lee' 1 2e 2 (e 2 -€i)& F = e 2 OA e 2 (ei+« 2 )(a2-&2) Fig. 12 Problem 5. Show that the field potential 4>a(xb) at a point xb in an arbitrary inhomogeneous dielectric medium, due to a point charge e at Xa, is equal to the potential 4>b(ta) at xa due to the same charge at xb. Solution. The potentials 4>a{t) and <}>b{t) satisfy the equations div(egrad^) = — 47re8(r— xa), div(e grades) = — 4weS(r— xb)- Multiplying the first by <f>B and the latter by <f>A and subtracting, we have div (4>b e grad <I>a)— div (<}>a e grad </>b) = — 4ne8(x— r^)^(r)+4«8(r- XB)<f>A(r). Integration of this equation over all space gives the required relation : 4>a{tb) = <I>b(xa). §8. A dielectric ellipsoid The polarisation of a dielectric ellipsoid in a uniform external electric field has some unusual properties which render this example particularly interesting. Let us consider first a simple special case, that of a dielectric sphere in an external field ©. We denote its dielectric constant by € tf) , and that of the medium surrounding it by e (e) . We take the origin of spherical co-ordinates at the centre of the sphere, and the direction of © as the polar axis, and seek the field potential outside the sphere in the form <£ (e) = ©*r + ^4©'r/r 3 ; the first term is the potential of the external field imposed, and the second, which vanishes at infinity, gives the required change in potential due to the sphere (cf. §3, Problem 1, solution). Inside the sphere, we seek the field potential to the form <£ ( *> = — i?<£«r, the only function which satisfies Laplace's equation, remains finite at the centre of the sphere, and depends only on the constant vector <& (which is the only parameter of the problem). The constants A and B are determined by the boundary conditions on the surface of the sphere. It may be seen at once, however, that the field §8 A dielectric ellipsoid 43 in the sphere E tt) = Bf& is uniform and differs only in magnitude from the applied field ©. The boundary condition of continuity of the potential gives E«> = (£(1 — AIR 2 ), where R is the radius of the sphere, and the condition of continuity of the normal component of the induction gives D«> = efe>(&(l + 2ia//P). Eliminating A from these two equations, we obtain KD«> + 2e(«>E«>) = €<«>(£ (8.1) or, substituting D«> = €«>E (<) , E«> = 3e<e>(£/(2 e <a+e<«). (8.2) The problem of an infinite dielectric cylinder in an external field per- pendicular to its axis is solved in an entirely similar manner (cf. §3, Prob- lem 2). The field inside the cylinder, like that inside the sphere in the above example, is uniform. It satisfies the relation £(D«>+e<e>E«>) = €<*>©, (8.3) or E«> = 2efeHE/(€W +€<»). (8.4) The relations (8.1) and (8.3), in which the dielectric constant e W) of the sphere or cylinder does not appear explicitly, are particularly important because their validity does not depend on a linear relation between E and D within the body; they hold whatever the form of this relation (e.g. for anisotropic bodies). The analogous relations E» = © (8.5) or a cylinder in a longitudinal field and D® = € te>© (8.6) for a flat plate in a field perpendicular to it are similarly valid; these relations are evident at once from the boundary conditions. The property of causing a uniform field within itself on being placed in a uniform external field is found to pertain to any ellipsoid, whatever the ratio of the semiaxes a, b> c. The problem of the polarisation of a dielectric ellip- soid is solved by the use of ellipsoidal co-ordinates, in the same way as the corresponding problem for a conducting ellipsoid in §4. Let the external field be again in the ^-direction. The field potential out- side the ellipsoid may again be sought in the form (4.22): <f>' e = <hF(£)> with the function F (£) given by (4.23). Such a function cannot, however, appear in the field potential <fn inside the sphere, since it does not satisfy the condition that the field must be finite everywhere inside the ellipsoid. For let us consider the surface £ = — c 2 , which is an ellipse in the #y-plane, lying within the ellipsoid. For f -+ —c 2 , the integral (4.23) behaves as ^(g+c 2 ). 44 Electrostatics of Dielectrics §8 The field, i.e. the potential gradient, therefore behaves as l/\/(l+c 2 )> and becomes infinite at £ = — c 2 . Thus the only solution suitable for the field inside the ellipsoid is F(£) = constant, so that <f>t must be sought in the form fa = Bfa. We see that the potential fa differs only by a constant factor from the potential fa of the uniform field. In other words, the field inside the ellipsoid is also uniform. We shall not pause to write out the formulae for the field outside the ellipsoid, which are of little interest. The uniform field inside the ellipsoid can be found without actually writing out the boundary conditions, by using some results already known. Let us first suppose that the ellipsoid is in a vacuum (c te) = 1). Then there must be a linear relation between the vectors E tt) , D ft) and © (which are all in the ar-direction), of the form aE x +bD x = (£», where the coefficients a, b depend only on the shape of the ellipsoid, and not on its dielectric per- meability e (<) . The existence of such a relation follows from the form of the boundary conditions, as we saw above in the examples of the sphere and the cylinder. To determine a and b we notice that, in the trivial particular case € W) = 1, we have simply E = D = <£, and so a+b = 1. Another particular case for which the solution is known is that of a conducting ellipsoid. In a conductor E (i) = 0, and the induction D< f) , though it has no direct physical significance, may be regarded formally as being related to the total dipole moment of the ellipsoid by D = 4nP = ±rr&>jV. According to (4.26) we then have D x = (Sy» (aj) , i.e. b = »<*>, and soa= 1— « te) . Thus we conclude thatt (i - «<*>) m x + 1& m x = <s x . (8.7) Similar relations, but with other coefficients, hold for the fields in the y and z directions. Like the particular formulae (8.1) and (8.3), they are valid whatever the relation between E and D inside the ellipsoid. The field inside the ellipsoid, when © is in the ^-direction, is found from (8.7) by putting £>«>* = €«>£«>*: E% = Ck/[1 + (€«>- l)n<*>], (8.8) and the total dipole moment of the ellipsoid is g; = VP X = (c»-l)FE«y4*r = \abc{^-\)% x f[\ + {^-\)nM]. (8.9) If the field © has components along all three axes, then the field inside the ellipsoid is still uniform, but in general not parallel to ©. For an arbitrary choice of co-ordinate axes we can write the relation (8.7) in the general form £»! + ««(/>»*--£»*) = <&. (8-10) t This result can also be written El% = ®z — 4mtWP x . The quantity 4mt^P x is some- times called the depolarising field. A similar formula holds for a magnetised ellipsoid in a uniform external magnetic field (see §27). In this case «<*>, «<»>, n<*> are called demagnetisa- tion coefficients. §9 The dielectric permeability of a mixture 45 The transition to the case where the dielectric permeability of the medium differs from unity is effected by simply replacing e (,) by € W) /e (e) . Then formula (8.7) becomes (l-n^)^E% + n^m> x = <m x . (8.11) This formula can be applied, in particular, to the field inside an ellipsoidal cavity in an infinite dielectric medium. In this case e (<) = 1. PROBLEMS t Problem 1. Determine the torque on a spheroid in a uniform electric field. Solution. According to the general formula (16.13), the torque on an ellipsoid is K = & X ©, where 6* is the dipole moment of the ellipsoid. In a spheroid, the vector & is in a plane passing through the axis of symmetry and the direction of (J. The torque is per- pendicular to this plane, and a calculation of its magnitude from formulae (8.9) gives (*-l)2|l-3«|(E 2 Fsin2a K = 87r[ft€+ 1 — «][(1 — n)e+ 1 +n] ' where a is the angle between the direction of © and the axis of symmetry of the spheroid, and n is the depolarisation coefficient along the axis (so that the depolarisation coefficients in the directions perpendicular to the axis are $(1 —it)). The torque is directed so that it tends to turn the axis of symmetry of a prolate (n < \) or oblate (w > \) ellipsoid parallel or perpendicular to the field respectively. For a conducting ellipsoid (e -*■ oo) we have K = J 1 " 3 " 1 V<& sin 2a. 87r?i(l — n) Problem 2. A hollow dielectric sphere (of dielectric constant e and internal and external radii b and a) is in a uniform external field (£. Determine the field in the cavity. Solution. As above in the problem of a continuous sphere, we seek the field potentials in the vacuum outside the sphere (region 1) and in the cavity (region 3) in the forms <f>i = — (E cos 6 (r—A/r 2 ), <f>z = —B&r cos 0, and that in the dielectric (region 2) as ^2 = —CCS cos {r—Djr 3 ), where A, B, C, D are constants determined from the conditions of continuity of <f> and e d<f>fdr at the boundaries 1—2 and 2—3. Thus the field E 3 = Bd in the cavity is uniform, but the field E2 in the sphere is not. A calculation of the constant gives the result E 3 = 9e©/[(e+2)(2e+l)-2(e-l)2(6/a)3]. Problem 3. The same as Problem 2, but for a hollow cylinder in a uniform transverse field.} Solution. As in Problem 2, with the result E 3 = 4ee/[( € +l)2-(e-l)2(6/a)2]. §9. The dielectric permeability of a mixture If a substance is a finely dispersed mixture (an emulsion, powder mixture, etc.), we can consider the electric field averaged over volumes which are large compared with the scale of the inhomogeneities. The mixture is a homogeneous and isotropic medium with respect to such an average field, t In these three Problems the body is assumed to be in a vacuum. X In a longitudinal field the solution is clearly E3 = ffi. 46 Electrostatics of Dielectrics {9 and so may be characterised by an effective dielectric permeability, which we denote by e m ix. If E and D are the field and induction averaged in this way, then, by the definition of e m ix, T> = e mix E. (9.1) If all the particles in the mixture are isotropic, and the differences in their dielectric permeabilities are small in comparison with e itself, it is possible to calculate emix in a general form which is correct as far as terms of the second order in these differences. We write the local field as E = E + SE, and the local dielectric permeability as e + Se, where i = (l/V)jedV (9.2) is obtained by averaging over the volume. Then the mean induction is D = (e + S e )(E + SE) = e'E + SeSE, (9.3) since the mean values of Se and SE are zero by definition. In the zero-order approximation e m ix = e"; the first non-zero correction term will, of course, be of the second order in Se, as we see from (9.3). From the non-averaged equation div D = we have, as far as small terms of the first order, div[(e + Se)(E + SE)] = edivSE + E-gradSe = 0, or, substituting SE = — grad S<£, i /\8<f> = E-grad S e . Taking the gradient, we have ASE = -(l/e-)(E.grad)gradSe. (9.4) The averaging of the product SeSE in (9.3) is done in two stages. We first average over the volume of particles of a given kind, i.e. for a given Se. The value of SE thus averaged is easily obtained from equation (9.4): on account of the isotropy of the mixture as a whole, the operator 8 2 ldxj8xjc on the right-hand side of (9.4) becomes, after averaging, JSifcA, so that we have ASE = — (l/3e)EA8e, whence SE = -(l/3e")ESe. Multiplying by Se and effecting the final averaging over all components of the mixture, we obtain SeSE = — (l/3e)E(Se) 2 . Finally, substituting this expression in (9.3) and comparing with (9.1), we have the required result: emix = e--(l/3e")(Se)2; (9.5) This formula can be written in another manner if we put / (Se)2\ this is accurate to terms of the second order. Then emix* = el (9.6) §10 Thermodynamic relations for dielectrics in an electric field 47 Thus we can say that, in this approximation, the cube root of e is additive. PROBLEM Determine the dielectric permeability of an emulsion of low concentration but with an arbitrary difference between the dielectric permeabilities of the medium (ei) and the disperse phase (€2). Solution. In the integral y f (D-eiE) dV = D-eiE the integrand is zero except within particles of the emulsion. It is therefore proportional to the volume concentration c of the emulsion, and in calculating it we can assume that the par- ticles are in an external field which equals the mean field £. Assuming the particles spherical and using formula (8.2), we obtain for the proportionality coefficient between D and E €mix = «l+3cei(e2 — ei)/(e2+2ei). This formula is correct to terms of the first order in c. When ei and €2 are nearly equal it is the same (to the first order in c and the second in *%— €i) as the result given by formula (9.6) for small c. §10. Thermodynamic relations for dielectrics in an electric field The question of the change in thermodynamic properties owing to the presence of an electric field does not arise for conductors. Since there is no electric field inside a conductor, any change in its thermodynamic properties amounts simply to an increase in its total energy by the energy of the field which it produces in the surrounding space, t This quantity is quite inde- pendent of the thermodynamic state (and, in particular, of the temperature) of the body, and so does not affect the entropy, for example. On the other hand, an electric field penetrates into a dielectric and so has a great effect on its thermodynamic properties. To investigate this effect, let us first determine the work done on a thermally insulated dielectric when the field in it undergoes an infinitesimal change. The electric field in which the dielectric is placed must be imagined as due to various external charged conductors, and the change in the field can then be regarded as resulting from changes in the charges on these conductors.^ Let us suppose for simplicity that there is only one conductor, of charge e and potential <f>. The work which must be done to increase its charge by an infinitesimal amount he is SR = <f>8e; (10.1) this is the mechanical work done by the given field on a charge Se brought from infinity (where the field potential is zero) to the surface of the conductor, t We here neglect the energy of the attachment of the charge to the substance of the conductor ; this will be discussed in §22. % The final results which we shall obtain involve only the values of the field inside the dielectric, and therefore are independent of the origin of the field. For this reason there is no need for special discussion of the case where the field is produced, not by charged con- ductors, but (for instance) by extraneous charges placed in the dielectric itself or by pyro- electric polarisation of it (§13). 48 Electrostatics of Dielectrics §10 i.e. through a potential difference of <f>. We shall put 8R in a form which is expressed in terms of the field in the space filled with dielectric which surrounds the conductor. If D n is the component of the electric induction vector in the direction of the normal to the surface of the conductor (out of the dielectric and into the conductor), then the surface charge density on the conductor is —DuJAtt, so that Since the potential <f> is constant on the surface of the conductor, we can write 8R = <f>8e = I^SD-df = f div(<f>8D)dV. 4-7T J 4"7T J The last integral is taken over the whole volume outside the conductor. Since the varied field, like the original field, must satisfy the field equations, we have div 3D = 0, and so div (<£SD) = ^ div SD + SD»grad <f> = — E»SD. Thus the following important formula is obtained: 8R = J"(E.8D/4ir)dF. (10.2) It should be emphasised that the integration in (10.2) is over the whole field, including the vacuum if the dielectric does not occupy all space outside the conductor. The work done on a thermally insulated body is just the change in its energy at constant entropy. Hence the expression (10.2) must be included in the thermodynamic relation which gives the infinitesimal change in the total energy of the body; the latter contains also the energy of the electric field. Denoting the total energy by ^, we therefore have 8<% = T8#>+ — f E.SDdF, (10.3) AttJ where T is the temperature of the body and S? its entropy, t Accordingly we have for the total free energy % 3F = fy—TS? 8& = -#>8T+— (E-8DdV. (10.4) 4W Similar thermodynamic relations can be obtained for the quantities per- taining to unit volume of the body. Let U, S and p be the internal energy, t The body in general becomes inhomogeneous in an electric field, and so the volume (whose differential is usually included in the expression for 8<#) no longer characterises the state of the body. X This quantity is meaningful only when the temperature is constant throughout the body. §10 Thermodynamic relations for dielectrics in an electric field 49 entropy and mass of unit volume. It is well known that the ordinary thermo- dynamic relation (in the absence of a field) for the internal energy of unit volume is dU — TdS+^dp, where £ is the chemical potential of the sub- stance.! In the presence of a field in a dielectric, there must be added the integrand in (10.3): dU= TdS+Zdp + E-dDI4TT. (10.5) For the free energy per unit volume of the dielectric, F = U— TS, we therefore have dF= -Sdr+£dp + E.dD/4Tr. (10.6) These relations are the basis of the thermodynamics of dielectrics. We see that U and F are the thermodynamic potentials with respect to S, p, D and T, p, D respectively. In particular, we can obtain the field by dif- ferentiating these potentials with respect to the components of the vector D : E = MdU/3D) s , p = 4*(dFldD) T , p . (10.7) The free energy is more convenient in this respect, since it is to be differen- tiated at constant temperature, whereas the internal energy must be expressed in terms of the entropy, which is less easy. Together with U and F, it is convenient to introduce thermodynamic potentials in which the components of the vector E, instead of D, are the independent variables. Such are U = E/-E.D/4tt, F = F-E.D/4ir. (10.8) On differentiating these we have dt/= TdS+tdp-D-dE/4ir, dF= -SdT+£dp-D.dE/47r. (10.9) Hence, in particular, D = -47r(dUldE)s, p = -4*(dfldE)T, p . (10.10) It should be noticed that the relation between the thermodynamic quanti- ties with and without the tilde is exactly that which occurs in §5 for the energy of the electrostatic field of conductors in a vacuum. For the integral $ E»D dV can be transformed in an exactly similar manner to the one at the t See Statistical Physics, §24, Pergamon Press, London, 1958. Instead of the mass density we there use the number of particles N per unit volume, which is related to the density by p = Nm, where m is the mass of one particle. For this reason the chemical potentials as denned here and in Statistical Physics differ by a constant factor (the potential here being referred to unit mass, and there to one particle). We here denote the chemical potential by £ instead of the more usual letter ft. The use of the letter p for the mass density as well as the charge density cannot lead to any mis- understanding, because the two quantities never appear together. 50 Electrostatics of Dielectrics §10 beginning of §2, with the equation div D = inside the dielectric and the boundary condition D n = 4ttg on the surfaces of conductors : ij E .DdF=-ljgrad^Ddr = ^2/ <f>aDndf = ^- ( ian ) Hence we have for the internal energy, for example, fE-D W = #- I — — dV= Qt-Yfafito (10.12) in agreement with the definition (5.5). It is useful to derive also the formulae for infinitesimal changes in these quantities, expressed in terms of the charges and potentials of the conductors (the sources of the field). For example, the variation in the free energy (for a given temperature) is (&?> = SR = X<f>a8e a . (10.13) For the variation of IF we have (8&) T = (S^t-SSM, = - Xe a 8<f> a . (10.14) We can say that the quantities without the tilde are the thermodynamic potentials with respect to the charges on the conductors, while those with it are thermodynamic potentials with respect to their potentials. It is known from thermodynamics t that the various thermodynamic potentials have the property of being minima in a state of thermodynamic equilibrium, relative to various changes in the state of the body. In formu- lating these conditions of equilibrium in an electric field, it is necessary to state whether changes of state with constant charges on the conductors (the field sources) or those with constant potentials are being considered. For example, in equilibrium 2? and «# are minima with respect to changes in state occurring at constant temperature and (respectively) constant charges and potentials of the conductors (the same is true for °tt and % at constant entropy). If any processes (such as chemical reactions) which are not directly related to the electric field can occur in the body, the condition of equilibrium with respect to these processes is that F is a minimum for given density, tempera- ture and induction D, or that P is a minimum for constant density, tempera- ture and field E. Hitherto we have made no assumptions concerning the dependence of D on E, so that all the thermodynamic relations derived above are valid t See Statistical Physics, §15. §10 Thermodynamic relations for dielectrics in an electric field 51 whatever the nature of this dependence. Let us now apply them to an isotropic dielectric, where a linear relation D = eE holds. In this case integration of (10.5) and (10.6) gives U= U (S,p) + D^S^ y F = F (T, p ) + D2I8tt€, where Uq and Fq pertain to the dielectric in the absence of the field. Thus in this case the quantity D 2 l8ire = €E 2 J8tt = ED/87T is the change in the internal energy (for given entropy and density) or in the free energy (for given temperature and density), per unit volume of the dielectric medium, resulting from the presence of the field. The expressions for the potentials V and F are similarly er-tw,)-.*./*,. F = F (T,p)-€E2l$7T. K We see that the differences U—Uq and U—Uo in this case differ only in sign, as they did for an electric field in a vacuum (§5). In a dielectric medium, however, this simple result holds good only when there is a linear relation between D and E. We shall write out also, for future reference, formulae for the entropy density S and the chemical potential £, which follow from (10.15): /3F\ D 2 / 8e\ - * T >» + di>f),' (10 - 17) /dF\ E 2 /de \ \ dp / t,d 8tt\ dp / t These quantities, of course, differ from zero only inside the dielectric. The total free energy is obtained by integrating (10.15) over all space. By (10.11) we have ST-^o = jE.DdF/87r = ^e a <f> a - (10.19) This last expression is formally identical with the energy of the electrostatic field of conductors in a vacuum. The same result can be obtained directly by starting from the variation 8^ (10.13) for an infinitesimal change in the charges on the conductors. In the present case, when D and E are linearly related, all the field equations and their boundary conditions are also linear. Hence the potentials of the conductors must (as for the field in a vacuum) be linear functions of their charges, and integration of equation (10.13) gives (10.19). It should be emphasised that these arguments do not presuppose the di- electric to fill all space outside the conductors. If, however, this is so, we 52 Electrostatics of Dielectrics §11 can go further and use the results at the end of §7 to draw the following conclusion. For given charges on the conductors, the presence of the di- electric medium reduces by a factor e both the potentials of the conductors and the field energy, as compared with the values for a field in a vacuum. If, on the other hand, the potentials of the conductors are maintained con- stant, then their charges and the field energy are increased by a factor e. PROBLEM Determine the height h to which a liquid rises in a vertical plane condenser. Solution. For given potentials on the condenser plates, # must be a minimum. <# in- cludes the energy JpgA 2 of the liquid under gravity. From this condition we easily obtain h = (e-l)E*l8Trpg. §11. The total free energy of a dielectric The total free energy !F (or the total internal energy *%), as defined in §10, includes the energy of the external electric field which polarises the di- electric. It is also meaningful to consider the total free energy less the energy of the field which would be present in all space if the body were absent. We denote this field by <£. Then the total free energy in this sense is j(F-<S?/S7r)dV, (11.1) where F is the free energy density. Here we shall denote this quantity by the letter 3F> which in §10 signified J FdV. It should be emphasised that the difference between the two definitions of SF is a quantity independent of the thermodynamic state and properties of the dielectric, and hence it has no effect on the fundamental differential relations of thermodynamics pertain- ing to this quantity, t Let us calculate the change in & resulting from an infinitesimal change in the field which occurs at constant temperature and does not destroy the thermodynamic equilibrium of the medium. Since SF = E«8D/47r, we have SJ^ = /(E'SD— (£'S<g)dF/47r. This expression is identically equal to 8& = J(D-®).aedF/47r + + JE-(SD-8(£)dVI47T- J(D-E).S®dF/477. (11.2) In the first integral we write 8© = — grad 8<f> (where <f>o is the potential of the field ©) and integrate by parts: j grad8<MD-©)dF = <f S<£o(D-(E)-df- Js^ div(D-®)dr. t It may be noted that there would be no sense in subtracting E 2 j8v from F, because E is the field as modified by the presence of the dielectric, and so the difference F—E 2 j8ir could not be regarded as the free energy density of the dielectric as such. §11 The total free energy of a dielectric 53 It is easy to see that both the integrals on the right-hand side are zero. For the volume integral this follows at once from the equations div D = and div © = which the induction in the dielectric and the field in the vacuum must respectively satisfy. The surface integral is taken over the surfaces of the conductors which produce the field and over an infinitely distant surface. The latter of these is, as usual, zero, and for each of the conductors 8fo = constant, so that § 8<f>o(D— ©)-df = 8<f>o§(D— <£)-df. The field ©, by definition, is produced by the same sources as the field E and induction D (i.e. by the same conductors with given total charges e). Hence the two integrals § D n df and j (E»d/ are both equal to 4ttc, and their difference is zero. Similarly, we can see that the second term in (11.2) is also zero, by putting E = — grad <f> and using the same transformation. Finally, we have 8& = - j(T>-E)-8<£dV/47r = - j?>8<£dV. (11.3) It should be noticed that the integral in this expression need be taken only over the volume of the dielectric medium, since outside it P = 0. However, we must emphasise that the integrand P»S© cannot be inter- preted as the variation of the free energy density in the same way as was done with formulae (10.3), (10.4). First of all, this density must exist outside the body, which modifies the field in the surrounding space also. It is clear, moreover, that the energy density at any point in the body can depend only on the field actually present there, and not on the field which would be present if the body were removed. If the external field © is uniform, then 8& = -8®. JPdF = - ^.8©, (11.4) where $P is the total electric dipole moment of the body. Hence the thermo- dynamic identity for the free energy can be written in this case as d^ = -&>&T-0>-m. (11.5) The total electric moment of the body can therefore be obtained by dif- ferentiating the total free energy : & = -{d3F\W) T . (11.6) The latter formula can also be obtained directly from the general statistical formula where ffl is the Hamiltonian of the body as the system of its component particles, and A is any parameter characterising the external conditions in which the body is placed.! For a body in a uniform external field © ; the t See Statistical Physics, §§11, 15. 54 Electrostatics of Dielectrics §1 1 Hamiltonian contains a term — ©«^, where $ is the dipole moment opera- tor. Taking © as the parameter A, we obtain the required formula. If D and E are connected by the linear relation D = eE, we can similarly calculate explicitly not only the variation hSF but 3F itself. We have 3F-3F* = J(E.D-(£ 2 )dF/87r. This can be identically transformed into Jf-jFo = J(E + ®).(D-(£)dF/87r- J®.(D-E)dF/87r. The first term on the right is zero, as we see by putting E + ®= — grad(<£ + <£ ) and again using the same transformation. Hence we have ^-jFo(F,T)= -lJ©.Pdr. (11.7) In particular, in a uniform external field &-3?o{V,T) = -|©.^. (11.8) This last equation can also be obtained by direct integration of the rela- tion (11.3) if we notice that, since all the field equations are linear when D = eE, the electric moment &> must be a linear function of ©. The linear relation between the components of &> and © can be written &i = Fa!*®*, (11.9) as for conductors (§2). For a dielectric, however, the polarisability depends not only on the shape but also on the dielectric constant. The symmetry of the tensor a**, mentioned in §2, follows at once from the relation (11.6); it is sufficient to notice that the second derivative d 2 ^ j d^^i = — d&ijdt&k = — Yaw is independent of the order of differentiation. Formula (11.7) becomes still simpler in the important case where e is close to 1, i.e. the dielectric susceptibility k = (e— l)/4ir is small. In this case, in calculating the energy, we can neglect the modification of the field due to the presence of the body, putting P = kE ~ k®. Then jr_ jr = _!* J(£ 2 dF, (n.io) the integral being taken over the volume of the body. In a uniform field, the dipole moment &> = Vk(£, and the free energy is ^r_jr = -\ K V<&. (11.11) §12 Electrostriction of isotropic dielectrics 55 In the general case of an arbitrary relation between D and E, the simple formulae (11.7) and (11.8) do not hold. Here the formula *-J(*-S dr -J[*-!r-H d,r (1U2) may be useful in calculating ^\ its derivation is obvious after the above discussion. Here also the integrand in the latter integral is zero outside the body, so that the integration is taken only over the volume of the body. PROBLEM Derive the formula which replaces (11.7) when the body is not in a vacuum but in a medium of dielectric permeability e(*>. Solution. Using the same transformations as before, we find &-&0 = - — [ <g.(D-e« e >E) dF. §12. Electrostriction of isotropic dielectrics For a solid dielectric in an electric field the concept of pressure cannot be defined as for an isotropic body in the absence of a field, because the forces acting on a dielectric (which we shall determine in §§15, 16) vary over the body, and are anisotropic even if the body itself is isotropic. An exact determination of the deformation (electrostriction) of such a body involves the solution of a complex problem of the theory of elasticity. However, matters are much simpler if we are interested only in the change in the total volume of the body. As we saw in §5, the shape of the body may then be regarded as unchanged, i.e. the deformation may be regarded as a uniform volume compression or expansion. We shall neglect the dielectric properties of the external medium (the atmo- sphere, for instance) in which the body is situated, i.e. we suppose that e = 1. This medium thus serves merely to exert a uniform pressure on the surface of the body, which we shall denote by p. If 8F is the total free energy of the body, then we have the thermodynamic relation p = —(d^/dV)^ and accordingly the expression for the differential dJF contains a term — pdV. For example, in a uniform external field, (11.5) becomes d^= -SfdT-pdV-&>>d1&. We introduce the total thermodynamic potential of the body in accordance with the usual thermodynamic relation op = &+pV. (12.1) The differential of this quantity in a uniform external field is Ago = -&>dT+Vdp-0>-d®. (12.2) 56 Electrostatics of Dielectrics §12 The change in the thermodynamic quantities in an external electric field is usually a relatively small quantity. It is known t that a small change in the free energy (for given T and V) is equal to the small change in the thermo- dynamic potential (for given T and p). Hence, besides (11.8), we can write analogously op = ^o-|®-^ (12.3) for the thermodynamic potential of a body in a uniform external field. Here cpQ is the value for the body in the absence of the field and for given values of p and T, while 3F$ in (11.8) is the free energy in the absence of the field and for given values of V and T. Making explicit the dependence of the dipole moment on V and (£ accord- ing to (11.9), we can rewrite (12.3) as cp = epo(p, T)-W*nc®&k, (12.4) where the correction term must be expressed as a function of temperature and pressure by means of the equation of state for the body in the absence of the field. In particular, for a substance of small dielectric susceptibility this formula becomes simply gp = yodj>,T)-\KV<&; (12.5) cf. (11.11). The required change in volume V— Vq in the external field can now be obtained immediately by differentiating cp with respect to pressure for constant T and (£. For example, from (12.5) we have V-V = -^[d( K V)/dp] T . (12.6) This quantity may be either positive or negative (whereas, in electrostric- tion of conductors, the volume is always greater in the presence of the field). Similarly, we can calculate the amount of heat Q absorbed in a dielectric when an external electric field is isothermally applied (the external pressure being constant). J Differentiation of cp—cpQ with respect to temperature gives the change in the entropy of the body, and by multiplying this by T we obtain the required quantity of heat. For example, from (12.5) we obtain Q = ±&T[d( K V)ldT] p . (12.7) Positive values of Q correspond to absorption of heat. PROBLEMS Problem 1. Determine the change in volume and the electrocaloric effect for a dielectric ellipsoid in a uniform electric field parallel to one of its axes. t See Statistical Physics, §15. % If the body is thermally insulated, the application of the field results in a change of temperature AT = —Q/Cp, where C p is the specific heat at constant pressure. §12 Electrostriction of isotropic dielectrics 57 Solution. From formulae (12.3) and (8.9) we have V €-1 „ &> = &>o-- — Vfc 2 . on ne+l—n The relative change in volume is found to be V-Vo _ (£ 2 [ €-1 1 1 /3e\ I V~ ~ S^lne+1-nK ~ (ne+l—n)A~dp) T J' and the electrocaloric effect * 8tt lne + 1-n (ne+l-n) z \dT } P \ where 1/.K = —<MV)(dV I dp) T is the compressibility of the body, and a = (l/VXdV/dT)? the thermal expansion coefficient. In particular, for a plane disc in a field perpendicular to it, n = 1, so that F-Fo (S 2 r6-1 1 1 fde\ I P^~ ~~ 8^hr K ~ l?\dp) tY e .«[ii + iffll. * 8tt L e e 2 \ar/J For a similar disc (or any cylinder) in a longitudinal field, « = 0, and V-V (£ 2 f€-l /a e \ I 7V(£ 2 r , /^\1 Problem 2. Determine the difference between the heat capacity ^ of a plane disc in a field perpendicular to it, with a constant potential difference between its faces, and the heat capacity ^d at constant induction, the external pressure being maintained constant in each case, t Solution. According to the results of Problem 1, the entropy of the disc is The induction inside the disc is the same as the external field : D = (£. Hence, to calculate the heat capacity <&r>, we must differentiate Sf for constant (£. The potential difference between the faces of the disc is <f> = El = (£ //e, where / is its thickness. For a uniform com- pression or expansion of a body, I is proportional to Vi. Hence, to calculate the heat capacity #0, we must differentiate S? for constant (&Vi/e. The required difference is found to be Problem 3. Determine the electrocaloric effect in a homogeneous dielectric whose total volume is kept constant. Solution. Strictly speaking, when an external field is applied the density of the body changes (and ceases to be uniform), even if the total volume is kept constant. In calculating the change in the total entropy, however, we can ignore this and assume the density p constant at every point. J f ^ is the heat capacity of a disc between the plates of a plane condenser in circuit with a constant e.m.f. In an unconnected condenser with constant charges on the plates, the heat capacity of the disc is *& d- X The change in density Sp is of the second order with respect to the field (~i? 2 ), and the consequent change in the total entropy is of the fourth Order: the term in the change of total entropy which is linear in Sp is (dSoldp)f Sp dV, and the integral is zero because the total mass of the body is unaltered. 58 Electrostatics of Dielectrics §13 According to (10.17) the total entropy of the body is 1 / 8e ^^• T >+dw)J E3dr - where the integration is over the volume of the body. The amount of heat absorbed is *-=(£). J™ Problem 4. Determine the difference <$$ — <&d (see Problem 2) when the total volume of the disc is kept constant. Solution. When the volume, and therefore the thickness, of the disc are constant, dif- ferentiation for constant potential difference is equivalent to differentiation for constant field E. Using the formula of Problem 3 for the entropy we have TVE 2 / de \ 2 Problem 5. A condenser consists of two conducting surfaces at a distance h apart which is small compared with their dimensions ; the space between them is filled with a substance of dielectric permeability ei. A sphere of radius a <Z^h and dielectric permeability ez is placed in the condenser. Determine the change in capacity. Solution. Let the sphere be placed in the condenser in such a way that the potential difference <f> between the plates remains unchanged. The free energy for constant poten- tials of the conductors is 3?. In the absence of the sphere, & = — £Co<£ 2 , where Co is the original capacity of the condenser. Since the sphere is small, we may imagine it to be brought into a uniform field (£ = <f>lh, and the change in # is small. The small change in # at con- stant potentials is equal to the small change in & at constant charges on the sources of the field. Using the formula derived in §11, Problem, and (8.2), we have & = -iCo^ 2 -iaV«)(e(')- e ( e ))^ 2 /(2eW + e(*))/i 2 , whence the required capacity is C = Co+a»eM(e<«.-e<«>)/(2eM + «<«)A«. §13. Dielectric properties of crystals In 'an anisotropic dielectric medium (a crystal) the linear relation between the electric induction and the electric field is less simple, and does not reduce to a simple proportionality. The most general form of such a relation is Dt = D 0i + € ik E k , (13.1) where Do is a constant vector, and the quantities et k form a tensor of rank two, called the dielectric permeability tensor (or simply the dielectric tensor). The inhomogeneous term Do in (13.1) does not, however, appear for all crystals. The majority of the types of crystal symmetry do not admit this constant vector (see below), and we then have simply Di = nicEk- (13.2) The tensor e^ is symmetrical: Hk = € ki- (13.3) §13 Dielectric properties of crystals 59 In order to prove this, it is sufficient to use the thermodynamic relation (10.10) and to observe that the second derivative —4ird 2 FldE k dEi = dDijdEu = eoc is independent of the order of differentiation. For P itself we have (when (13.2) holds) the expression P = F -e ik EiE k IS7T. (13.4) The free energy F is F = F+EiDilbn- = Fo + e-iaDiDtl&ir. (13.5) Like every symmetrical tensor of rank two, the tensor e$ * can be brought to diagonal form by a suitable choice of the co-ordinate axes. In general, therefore, the tensor e is determined by three independent quantities, namely the three principal values e (1) , e (2) , e (3) . All these are necessarily greater than unity, just as e > 1 for an isotropic body (see §14). The number of different principal values of the tensor e* # may be less than three for certain symmetries of the crystal, t In crystals of the triclinic, monoclinic and rhombic systems, all three principal values are different; such crystals are said to be biaxial.% In crystals of the triclinic system, the directions of the principal axes of the tensor e^ are not uniquely related to any directions in the crystal. In those of the monoclinic system, one of the principal axes must coincide with the axis of symmetry of the second order or be perpendicular to the plane of symmetry of the crystal. In crystals of the rhombic system, all three princi- pal axes of the tensor e^ are crystallographically fixed. Next, in crystals of the tetragonal, rhombohedral and hexagonal systems, two of the three principal values are equal, so that there are only two inde- pendent quantities ; such crystals are said to be uniaxial. One of the principal axes coincides with the axis of crystal symmetry of the fourth, third or sixth order, but the directions of the other two principal axes can be chosen arbitrarily. || Finally, in crystals of the cubic system all three principal values of the tensor e* # are the same, and the directions of the principal axes are entirely arbitrary, ft This means that the tensor €<* is of the form eS^fc, i.e. it is deter- mined by a single scalar e. In other words, as regards their dielectric proper- ties, crystals of the cubic system are no different from isotropic bodies. t The fairly obvious symmetry properties of the tensor em that are given below can be very simply obtained by using a result of tensor algebra: to every symmetrical tensor of rank two there corresponds a tensor ellipsoid, the lengths of whose semiaxes are proportional to the principal values of the tensor. The symmetry of the ellipsoid corresponds to that of the crystal. X This name refers to the optical properties of the crystals; see §§78, 79. || In this case the tensor ellipsoid degenerates into a spheroid, completely symmetrical about the longitudinal axis. It should be emphasised that, as regards the physical properties of the crystal which are determined by a symmetrical tensor of rank two, the presence of an axis of symmetry of the third or higher order is equivalent to complete isotropy in the plane perpendicular to this axis. 1 1 The tensor ellipsoid here degenerates into a sphere. 60 Electrostatics of Dielectrics §13 Let us now examine the dielectric properties of crystals for which the constant term Do appears in (13.1). The presence of this term signifies that the dielectric is spontaneously polarised even in the absence of an external electric field. Such bodies are said to be pyroelectric. The magnitude of this spontaneous polarisation is, however, in practice always very small (in com- parison with the molecular fields). This is because large values of Do would lead to strong fields within the body, which is energetically unfavourable and therefore could not correspond to thermodynamic equilibrium. The small- ness of Do also ensures the legitimacy of an expansion of D in powers of E, of which (13.1) represents the first two terms. The thermodynamic quantities for a pyroelectric body are found by integrating the relation —fadF/BEt = Di = Doi + e ik E k , whence F = Fo-€ ik E i E k l8ir-E i D(Hl+*. (13.6) The free energy is F = F+EiDi/47T = F + € ik EiE k IS7T = Fo + e-h k (Di-Doi)(D k -Do k )IS7T. (13.7) It should be noted that the term in F linear in E% does not appear in F.f The total free energy of a pyroelectric can be calculated from formula (11.12) by substituting (13.7) and (13.1). If there is no external field, (& = 0, and we have simply F = J[F -(E.Do/87r)]dF. (13.8) It is remarkable that the free energy of a pyroelectric in the absence of an external field depends, like the field E, not only on the volume of the body but also on its shape. As has already been pointed out, the phenomenon of pyroelectricity is not possible for every crystal symmetry. Since, in any symmetry transforma- tion, all the properties of the crystal must remain unchanged, it is clear that the only crystals which can be pyroelectric are those in which there is a direction which is unchanged (and, in particular, not reversed) in all sym- metry transformations, and that this will be the direction of the constant vector Do. This condition is satisfied only by those symmetry groups which consist of a single axis together with planes of symmetry which pass through the axis. In particular, crystals having a centre of symmetry certainly cannot be t It should also be noted that in these formulae we neglect the piezoelectric effect, i.e. the effect of internal stresses on the electric properties of a body; see §17. The formulae given here are therefore, strictly speaking, applicable only when the fields are uniform throughout the body, and internal stresses do not arise. §13 Dielectric properties of crystals 61 pyroelectric. We may enumerate those out of the 32 crystal classes in which pyroelectricity occurs : triclinic system: C\ monoclinic system: C s , C2 rhombic system : C^ v tetragonal system: C4, C^ v rhombohedral system : C3, C$ v hexagonal system: C$, Cq v . There are, of course, no pyroelectric cubic crystals. In a crystal of class Ci the direction of the pyroelectric vector Do is not related to any direction fixed in the crystal ; in one of class C s , it must lie in the plane of symmetry. In all the remaining classes listed above the direction of Do is that of the axis of symmetry. It should be mentioned that, under ordinary conditions, pyroelectric crystals have zero total electric dipole moment, although their polarisation is not zero. The reason is that there is a non-zero field E inside a spon- taneously polarised dielectric. Since a body usually has a small but non-zero conductivity, the presence of a field gives rise to a current, which flows until the free charges formed on the surface of the body annihilate the field inside it. The same effect is produced by ions deposited on the surface from the air. Experimentally, pyroelectric properties are observed when a body is heated and a change in its spontaneous polarisation is detected. PROBLEMS Problem 1. Determine the field of a pyroelectric sphere in a vacuum. Solution. The field inside the sphere is uniform, and the field and induction are related by 2E = — D (as follows from (8.1) when © = 0, i.e. when there is no applied external field). Substituting in (13.1), we obtain the equation 2Ei+etkEk = — Dm- We take the co- ordinate axes to be the principal axes of the tensor ej*. Then this equation gives Ei = -Do*/(2+e<*>). The polarisation of the sphere is Pt = (A -Ei)/** = 3Do*/4tt(2 + €<«>). The field outside the sphere is that of an electric dipole of moment 3* = J*V. Problem 2. Determine the field of a point charge in a homogeneous anisotropic medium. Solution. The field of a point charge is given by the equation div D = 47r«8(r) (the charge being at the origin). In an anisotropic medium Dt = eucEk = —en d<l>ldxic; taking the co-ordinate axes x, y, z along the principal axes of the tensor €*&, we obtain for the poten- tial the equation eWdmdxZ + cMdmdyZ+eMdmdz 2 = -47re8(*) S(y) 8(z). By the introduction of new variables x' = x/vV*>, y' = y/V&K z' = z/Ve l * } , (D this becomes 32.A dU dU 4w — — H — H — = 8(*') S(y') 8(2'), t In Problems 2-5 the anisotropic dielectric is assumed not to be pyroelectric. 62 Electrostatics of Dielectrics §13 which formally differs from the equation for the field in a vacuum only in that e is replaced by e/V(e (,) « (l "e w )- Hence 4 = L = f r^l+-z! + .fir; V((i*wi) In tensor notation, independent of the system of co-ordinates chosen, we have <}> = elVdele'hkXiXk), where |e| is the determinant of the tensor cm. Problem 3. Determine the capacity of a conducting sphere, of radius a, in an anisotropic dielectric medium. Solution. By the transformation shown in Problem 2, the determination of the field of a sphere with charge e in an anisotropic medium reduces to the determination of the field in a vacuum due to a charge e' distributed over the surface of the ellipsoid zucx'ix'k = e^x' 2 + 4- € (v)^ / 2-j- e (z) 2r '2 = a 2 # Using formula (4.14) for the potential due to an ellipsoid, we find the required capacity to be given by ~C = 2V(« ( * ) « (, ' , « ( " ) ) J Lv "^/V "^/V "^>/J d ^' Problem 4. Determine the field in a flat anisotropic plate in a uniform external field C Solution. From the condition of continuity of the tangential component of the field it follows that E = H+An, where (£ is the uniform field outside the plate, n a unit vector normal to its surface, and A a constant. The constant is determined from the condition of continuity of the normal component of the induction, n-D = n»(fc, or mcvcEje = Tneu&ic J r +Aeatmnk = (£««*• Hence A = — {em— §ik)ni<&icl ei m nin m . Problem 5. Determine the torque on an anisotropic dielectric sphere, of radius a, in a uniform external field © in a vacuum. Solution. According to (8.2) we have for the field inside the sphere E x = 3©x/(e( a; )+2), and similarly for E y , E z . Here the axes of x, y, z are taken to be the principal axes of the tensor ei*. Hence the components of the dipole moment of the sphere are 4 e<*> — 1 The components of the torque on the sphere are Kz = 0?x(g) 2 = 3a 3 (E, <&y (€<*)-e«»))/(€(*)+2)(e(»)4-2), and similarly for K x , K y . Problem 6. An infinite anisotropic medium contains a spherical cavity of radius a. Express the field in the cavity in terms of the uniform field E^ far from the cavity. Solution. The transformation (1) of Problem 2 reduces the equation for the field potential in the medium to Laplace's equation for the field in a vacuum. The equation for the field in the cavity is transformed into that for the field in a medium with dielectric constants l/e (l \ 1/eM, l/e< 2 ). Moreover, the sphere is transformed into an ellipsoid with semiaxes a/-\A (ir) ! aly/dv), a/V e(e) ' Let nS x \ n<">, n<*> be the depolarisation coefficients of such an ellipsoid (given by formulae (4.25)). Applying formula (8.7) to the field of this ellipsoid, we obtain the relation V ' 8x' e<*> 8x' 8x' ' and similarly for the y and z directions. Returning to the original co-ordinates, we have d<f>ldx' = Ve {x) d<f>/dx = V^ x) E x , so that the field in the cavity is c (z) e (*)_ B (*)( e (*)_l) §14 The sign of the dielectric susceptibility 63 §14. The sign of the dielectric susceptibility To elucidate the way in which the thermodynamic quantities for a di- electric in a field depend on its dielectric constant, let us consider the formal problem of the change in the electric component of the total free energy of the body when e undergoes an infinitesimal change. For an isotropic (not necessarily homogeneous) body we have by (10.19) ^—^o = J(D 2 /87re)dF. When e changes, so does the induction, and the variation in the free energy is therefore fD-SD r D 2 rE-SD r E 2 h&r = dV- 8edV = dV- — StdV. J 4tt€ J S-rre 2 J 4tt J 8tt The first term in the last member is the same as (10.2), which gives the work done in an infinitesimal change in the field sources (i.e. charges on conduc- tors). In the present case, however, we are considering a change in the field but no change in the sources. This term therefore vanishes, leaving Sjr = - jS € (E2/8TT)dV. (14.1) From this formula there follows, first of all, an important result: any in- crease in the dielectric constant of the medium, even if in only a part of it (the sources of the field remaining unchanged), reduces the total free energy. In particular, we can say that the free energy is always reduced when un- charged conductors are brought into a dielectric medium, since these conductors may (in electrostatics) be regarded as bodies whose dielectric constant is infinite. This conclusion generalises the theorem (§2) that the energy of the electrostatic field in a vacuum is diminished when an uncharged conductor is placed in it. Formula (14.1) can also be used to prove the statement in §7 that the di- electric constant of any body exceeds unity, i.e. the dielectric susceptibility (c— l)/47r is positive. To show this, we must first show independently that the total change in the free energy of a dielectric when it is placed in an electric field is negative, t This can be done by the use of thermodynamic perturbation theory, the change in the free energy of the body being regarded as the result of a perturbation of its quantum energy levels by the electric field. According to this theory we havet *-*. = r,--22 E J»- Em «» -2*r( F ™- F ™ )2 - fl4 - 2) t The change proportional to the square of the field is meant. It may be recalled that, in pyroelectric bodies, the change in the free energy contains also a term linear in the field, which is of no interest here. X See Statistical Physics, §32, formulae (32.5), (32.6). The formulae given here differ from those in Statistical Physics only in form. 64 Electrostatics of Dielectrics §15 Here E n {0) are the unperturbed levels, F m «the matrix elements of the perturb- ing energy, and the bar denotes a statistical averaging with respect to the Gibbs distribution w n = exp {(^Q—En^kT). The term V nn in formula (14.2), which is linear in the field, is zero except in pyroelectric bodies. The quadratic change in the free energy, which is of interest here, is given by the remaining terms. It is evident from the form in which they are written here that they are negative. If we formally consider the change in the free energy as the result of a gradual change in the dielectric constant of the body from 1 to a given value €, it follows from formula (14.1) that ^—^o is negative only if e > 1. This completes the proof. In the same way we can prove the inequalities e W) > 1 for the principal values of the tensor e^ in an anisotropic dielectric medium. To do so, it is evidently sufficient to consider the energy of a field parallel to each of the three principal axes in turn. The total free energy is diminished, in particular, when any charge is brought up to a dielectric body from infinity (a process which may be regarded as an increase of e in a certain volume of the field round the charge). In order to conclude from this that any charge is attracted to a dielectric, we should, strictly speaking, prove also that F cannot attain a minimum for any finite distance between the charge and the body. We shall not pause here to prove this statement, especially as the presence of an attractive force between a charge and a dielectric may be regarded as a fairly evident consequence of the interaction between the charge and the dipole moment of the dielectric, which it polarises. We can deduce immediately from formula (14.1) the direction of motion of a dielectric body in an almost uniform electric field, i.e. one which may be regarded as uniform over the dimensions of the body. In this case E 2 is taken outside the integral, and the difference !F—SF§ is a negative quantity, proportional to E 2 . In order to take a position in which its free energy is a minimum, the body will therefore move in the direction of E increasing. §15. Electric forces in a fluid dielectric The problem of calculating the forces (called ponderotnotive forces) which act on a dielectric in an arbitrary non-uniform electric field is fairly compli- cated and requires separate consideration for fluids (liquids or gases) and for solids. We shall take first the simpler case, that of fluid dielectrics. We denote by f&V the force on a volume element dV, and call the vector f the force density. It is well known that the forces acting on any finite volume in a body can be reduced to forces applied to the surface of that volume, t This is a conse- quence of the law of conservation of momentum. The force acting on the t See Theory of Elasticity, §2, Pergamon Press, London, 1959. §15 Electric forces in a fluid dielectric 65 matter in a volume dV is the change in its momentum per unit time. This change must be equal to the amount of momentum entering the volume through its surface per unit time. If we denote the momentum flux tensor by — ewe, then (fidV= j>a ik df k , (15.1) where the integration on the right is over the surface of the volume V. The tensor anc is called the stress tensor. It is evident that ancdfk = criknkdf is the ith component of the force on a surface element d/ (n being a unit vector along the normal to the surface outwards from the volume under considera- tion). Similarly, the total torque acting on a given volume also reduces to a surface integral, by virtue of the law of conservation of angular momentum. This reduction is possible because of the symmetry of the stress tensor ( ffa . = om), which thus expresses the conservation law mentioned. On transforming the surface integral in (15.1) into a volume integral, we obtain J/idF= j (daa/ dxic)dV, whence, since the volume of integration is arbitrary, fi = dancjdxjc. (15- 2 ) This is a well-known formula giving the body forces in terms of the stress tensor. Let us now calculate the stress tensor. Any small region of the surface may be regarded as plane, and the properties of the body and the electric field near it as uniform. Hence, to simplify the derivation, we can with no loss of generality consider a plane-parallel layer of material (of thickness h and uniform composition, density and temperature) in an electric field which is uniform but whose direction is arbitrary, t This field may be imagined to be due to conducting planes, bearing appropriate charge distri- butions, applied to the surfaces of the layer. Following the general method for determining forces, we subject one of the conducting planes (the upper one, say) to a virtual translation over an infinitesimal distance £, whose direction is arbitrary and need not be that of the normal n. We shall suppose that the potential of the conductor remains unchanged at every point, and that the homogeneous deformation of the dielectric layer, resulting from the translation, is isothermal. A force — own* is exerted by the layer on unit area of the surface. In the virtual displacement this force does work — crfjfcWfclf. The work done in an isothermal deformation at constant potential is equal to the decrease in J FdV, i.e. in hF per unit surface area. Thus <*«&»* = K"F) = h8F+F8h. (15.3) f We thus ignore any terms in the stress tensor depending on the gradients of tempera- tore, field, etc. These terms, however, are vanishingly small in comparison with terms which do not contain derivatives, in the same way as any terms containing derivatives which might appear in the relation between D and E. 66 Electrostatics of Dielectrics §15 The thermodynamic quantities for the fluid depend (for given tempera- ture and field) only on its density; deformations which do not change the density (i.e. pure shears) do not affect the thermodynamic state. We can therefore write for an isothermal variation 8P in a fluid „ / dF\ / dP\ 8P = — .SE+I 8 P \ dE/T. \ dp /ET DSE / dP\ = -__+(_ 8 P . (15.4) 47T \ Op /E,T The change in the density of the layer is related to the change in its thick- ness by 8p = —pSh/h. The variation of the field is calculated as follows. At a given point in space (with radius vector r) there appears matter which was originally at r— u, where u is the particle displacement vector in the layer. Since, under the conditions stated (homogeneous deformation, and constant potential on the conducting planes), each particle carries its poten- tial with it, the change in the potential at a given point in space is 8<f> — <f>(r—u)—<f>(r) = — U'grad <f> = u«E, where E is the uniform field in the undeformed layer. Since the deformation is homogeneous, however, we have u = z\\h, (15.5) where z is the distance from the lower surface. Hence the variation of the field is SE = -n(E.§)/A. (15.6) Substituting the above expressions in (15.4) and using also the fact that &h = £ 2 = £»n, we obtain 1 dF oik&nic = — (n.D)(|.E)-5.np— -+§.ilP 4-7T Op dP. Jp~ Hence we have finally the following expression for the stress tensor: "« = [P-p(dPldp)E,T]8 ik + E i D k l4^. (15.7) (EiD k dP \ = \— A p-r-Oik + rdijc)^infc. \ 4it dp ) In isotropic media, which are those here considered, E and D are parallel. Hence EiDk = E^Di, and the tensor (15.7) is symmetrical, as it should be. If the linear relation D = eE holds, then P = Ffo,T)-eE*/&r; (15.8) see (10.16). Fq is the free energy per unit volume in the absence of the field. §15 Electric forces in a fluid dielectric 67 According to a well-known thermodynamic relation, the derivative of the free energy per unit mass with respect to the specific volume is the pressure : • a ( F °Y\ =F _ p ( d J°\ .d{ii P )\ P )\ T ° p \b p )t p = p ( Pf T) is the pressure which would be found in the medium in the absence of a field and for given values of p and T. Hence, substituting (15.8) in (15.7), we have E 2 r /de\ 1 eEtEjc cr ik = -MP»T)S 1k -—^-p^-J J 8 « + -^-- ( 15 - 9 ) In a vacuum, this expression becomes the familiar Maxwell stress tensor of the electric field :t or» = (EiE k -iE28 ik )l47T. The forces exerted on the surface of separation by two adjoining media must be equal and opposite: oi k n k = — or'^w*, where the quantities with and without the prime refer to the two media. The normal vectors n and n' are in opposite directions, so that o%»& = cr' ik n]c. (15.10) At the boundary of two isotropic media the condition of equality of the tangential forces is satisfied identically. For, substituting (15.7) in (15.10) and taking the tangential component, we obtain E«D» = E'tD' n . This equa- tion is satisfied by virtue of the boundary conditions of continuity on E t and D n . The condition of equality of the normal forces is, however, a non-trivial condition on the pressure difference between the two media. For example, let us consider a boundary between a liquid and the atmo- sphere (for which we can put € = 1). Denoting by a prime quantities pertaining to the atmosphere, and using formula (15.9) for aye, we have E 2 /8e\ 6 -po( P ,T) + -pl-) +-(E n *-m = -/>atm + -(^„ 2 -^ 2 ). 07T Using the boundary conditions Et = E' t , D n = eE n = D' n = E' n , we can rewrite this equation as P E 2 /de\ e-1 Po(R,T)-p & t m = P — - --— (e£ n 2 + Z^). (15.11) 07T \Op/T OTT This relation is to be taken as determining the density p of the liquid near its surface from the electric field in it. t See The Classical Theory of Fields, §4—8, Addison- Wesley Press, Cambridge (Mass.), 1951; Pergamon Press, London, 1959. 68 Electrostatics of Dielectrics §15 Let us now determine the body forces acting in a dielectric medium. Differentiating (15.9) in accordance with (15.2) gives 8 r E2 ( 8e \ i E2 8e l r i 8 2 8 i dxil Sit \dp/TJ S-rrdxi AttI 2 dxi dxjc J" On using the equation div D = 8D k /8x k — 0, the expression in the brackets in the last term can be reduced to dE k 8E t (dE k 8E t \ -eE k -—+D k —- = -D k t- — , OXi OXjc \ OXi OX k J which is zero, since curl E = 0. Thus we have f = -gradM* r) + -grad^2 /0 ^_jj --grade. (15.12) If the dielectric contains extraneous charges of density p e x, the force f contains a further term E div D/4tt, or, since div D = 47r/o e x, PexE; (15.13) however, it should not be supposed that this result is obvious (cf. §16, Problem 3). In a gas, as already mentioned in §7, we can assume the difference e — 1 to be proportional to the density. Then pde/dp — e— 1, and formula (15.12) takes the simpler form €-1 f = -grad/> + -r— grad£2. (15.14) Formula (15.12) is valid for media of both uniform and non-uniform composition. In the latter case e is a function not only of p and T but also of the concentration of the mixture, which varies through the medium. In a body of uniform composition, on the other hand, e is a function only of p and T, and grad e can be written as grade = (deldT) p gradT+(deldp) T gradp. Then (15.12) becomes f = -gradM* m£grad [*Qj ~(^) V^ T. (15.15) If the temperature also is constant through the body, the third term on the right is zero, and in the first term grad/>o can be replaced by p grad £o, in accordance with the thermodynamic identity for the chemical potential in the absence of a field, />d£o = dpo—SodT. Thus f = -pgradk (— ) 1. (15.16) L 877- \ dp! tj §16 Electric forces in solids 69 The expression in the brackets is just the chemical potential £ in an electric field (see (10.18)), and therefore f = — p grade. In particular, the condition of mechanical equilibrium f = is, for con- stant temperature, £ = t,Q-(E 2 l^)(d€Jd P ) T = constant, (15.17) in accordance with the thermodynamic condition of equilibrium, t This condition can usually be written still more simply. The change in density of the medium due to the field is proportional to E 2 . Hence, if the medium is of uniform density in the absence of the field, we can put p = constant in the last two terms in (15.15) when the field is present; an allowance for the change in p is beyond the accuracy of formulae which assume the linear relation D = eE. Then, equating to zero f from (15.15), we obtain the equilibrium condition at constant temperature in the form Po(p, T)-( P E 2 l87r)(deldp) T = constant, (15.18) which differs from (15.17) in that £ is replaced by po/p. §16. Electric forces in solids The dielectric properties of a solid body change not only when its density changes (as with liquids) but also under deformations (pure shears) which do not affect the density. Let us first consider bodies which are isotropic in the absence of the field. In general, the deformed body is no longer iso- tropic; in consequence, its dielectric properties also become anisotropic, and the scalar dielectric permeability e is replaced by the dielectric tensor The state of a slightly deformed body is described by the strain tensor 1 / dut dujA 2\dx]c dxi! where u(x,y,z) is the displacement vector for points in the body. Since these quantities are small, only the first-order terms in uac need be retained in the variation of the components e^. Accordingly, we represent the dielectric tensor of the deformed body as Hk = €<$ik + &iUik + atuifiiic. (16.1) Here e is the dielectric permeability of the undeformed body, and the other two terms, which contain the scalar constants «i, #2, form the most general tensor of rank two which can be constructed linearly from the components Uik- Let us now see where the derivation given in §15 must be modified. Since, in a solid body, P depends on all the components of the strain tensor, we must replace (15.4) by 8F = -D.SE/4tt + (dFldu ik )8u ik . For the virtual t See Statistical Physics, §25. 70 Electrostatics of Dielectrics §16 displacement considered, the vector u is given by formula (15.5), so that the strain tensor is u\ k = (tjin k +£ k ni)l2h. Substituting this in oF and using the symmetry of the tensor ui k , and therefore of the derivatives dF/duoc, we obtain 8F = -D.SEHw + itotlQdfldun. (16.2) It is now evident that we find, instead of (15.7), the following expression for the stress tensor :f oik = Fo ik + (dFldu ik ) TE +EiD k l4n. (16.3) Formula (16.3) is valid whatever the relation between D and E. For a body which is neither pyroelectric nor piezoelectric, so that Di = ei k E k , F is given by formula (13.4) and the required derivatives are dFjdunc = dFQlduiic—(aiEiE k +a2E 2 §ik)l%7T. We then put 6<* = £o$<* everywhere in (16.3) and obtain the following formula for the stress tensor: a ik = <rfl» tt + (2e - a^EiEjc/Srr - ( €0 + a 2 )E^ ik ^7t . (16.4) a (0 \ k is the stress tensor in the absence of an electric field, determined by the moduli of rigidity and compression according to the ordinary formulae of the theory of elasticity. Let us now make similar calculations for anisotropic solids.} The neces- sary modification of the above argument is as follows. When the layer undergoes a virtual deformation, its crystallographic axes are rotated, and their orientation relative to the electric field is therefore changed. On account of the anisotropy of the dielectric properties of the crystal, this leads to an additional change in F not shown in (16.2). To calculate this change we can equally well suppose that the crystal axes rotate through some angle S<|> relative to the field E, or that the field rotates through an angle — S<f> relative to the axes, and the latter approach is the more convenient. Thus the variation of the field (15.6) considered above must be augmented by the change in E on rotation through an angle — S<t>: SE= — n(E«^)/A— — §4>xE. The angle S<|> is related to the displacement vector u in the deformation by S<t> = \ curlu; this equation is easily obtained by noticing that, when the body rotates through an angle S<J>, its points are displaced by u = S<|>xr. Substituting u from (15.5), we find S<|> = curl z\\2h = nx£/2Z*, t The quantity P in this formula, and in all preceding formulae, is the free energy per unit volume. In the theory of elasticity, however, a somewhat different definition is usual : the thermodynamic quantities are referred to the amount of matter contained in unit volume of the undeformed body, which may after deformation occupy some other volume. It is easy to go from one definition to the other by expressing the relative volume change in the deformation in terms of the tensor mk ; on account of the presence of the derivative with respect to uoc in (16.3), this must be done with allowance for second-order terms. As a result, the first two terms on the right of (16.3) combine into one of the form dF/duuc, in accordance with the usual formula of elasticity theory. X We shall see in §17 that the phenomenon of electrostriction in crystals may, for some types of symmetry, differ markedly from that in isotropic bodies. Such crystals are said to be piezoelectric. Here, however, we discuss only electrostriction in non-piezoelectric bodies. §16 Electric forces in solids 71 and SE= -n(E.^)/A+Ex(nx^)/2A= -[n(E.^) + ?(n.E)]/2A. The first term in (16.2) becomes --D8E = — : [(n.D)(§.E) + (?.D)(n.E)] = -Uh& . \{EiD k + E k Di). Hence we see that the product EiD k in (16.3) must be replaced by the second factor in the last expression: dF 1 °ik = F8 ik + —- + —{EiD k + E k D t ). (16.5) CUilc 077 This expression is symmetrical in the suffixes i and k, as it should be. The expression (16.1) for the dielectric tensor, involving two scalar con- stants, must be replaced in the case of a dielectric crystal by Hk = c (0) ik + aiklmUim, (16.6) where Oikim is a constant tensor of rank four, symmetrical with respect to the pairs of suffixes t, k and /, m (but not with respect to an interchange of these pairs). The number of independent non-zero components of this tensor depends on the crystal class. We shall not pause to write out here the formula for the stress tensor (analogous to (16.4)) which is obtained by using (16.6). The formulae which we have obtained give the stresses inside a solid di- electric. They are not needed, however, if we wish to determine the total force F or the total torque K exerted on the body by the external field. Let us consider a body immersed in a fluid medium and kept at rest there. The total force on it is equal to the integral § ai k n k df, taken over the surface. Since the force ai k n k is continuous, it does not matter whether this integral is calculated from the values of ai k given by (16.4) or from formula (15.9), which relates to the medium surrounding the body. Let us suppose that this medium is in mechanical and thermal equilibrium. Then the calcula- tion is further simplified if we use the condition of equilibrium (15.18). From this condition, part of the stress tensor (15.9) is constant through the body, being a uniform compressing or expanding pressure and making no contribution to the total force F and torque K acting on the body. These can therefore be calculated by writing 0% as °ik = (eM(EiE k -±E28 ik ) (16.7) simply, where E is the field in the fluid and e its dielectric permeability; this expression differs only by a factor e from the Maxwell stress tensor of the electric field in a vacuum. Thus F = (e/47r)^[E(n.E)-i^ n]d/) (16>8) K = (e/477) <([rx E(n- E) -\E*r x n] d/. (16.9) 72 Electrostatics of Dielectrics §16 It may also be noted that, since the fluid is in equilibrium, we can take these integrals over any closed surface which surrounds the body in question (but, of course, does not enclose any of the charged bodies which are sources of the field). 4 The calculation of the total force on a dielectric in an electric field in a vacuum can also be approached in another way by expressing this force, not in terms of the actual field, but in terms of the field (£ which would be produced by the given sources in the absence of the dielectric; this is the "external field" in which the body is placed. Here it is assumed that the distribution of charges producing the field is unchanged when the body is brought in. This condition may not be fulfilled in practice — for example, if the charges are distributed over the surface of an extended conductor and the dielectric is brought to a finite distance from it. In a virtual translation of the body over an infinitesimal distance u, the total free energy of the body varies, according to ( 1 1 . 3), by 8$F = — J P • S(£d V, where 8© = (£(r + u)— (£(r) = (u«grad)(£ is the change in the field at any given point in the body. Since u = constant and curl © = 0, we have P.(u«grad)(£= P-grad(u.(g) = U'(P«grad)<£, so that 8& = — u- J"(P.grad)© dV. But 8!F = — u«F, and we therefore have for the required force t F = J (P.grad)(£dF. (16.10) Similarly, the total torque on the body can be determined. We shall not go through the calculation, but merely give the result: K = J"Px(&dK+J*rx(P.grad)©dF. (16.11) In an almost uniform field, which may be regarded as constant over the dimensions of the body, formula (16.10) gives to a first approximation F = (J PdF-grad)© = (^.grad)<£, (16.12) where £P is the total dipole moment of the polarised dielectric; this result, of course, could have been obtained by direct differentiation of SF from (11.8). In formula (16.11) we neglect the second term in the first approxi- mation and reach the natural conclusion that K = ^x<£. (16.13) f It should be emphasised, however, that the integrand in (16.10) cannot be interpreted as the force density. The reason is that the local forces in the dielectric arise not only from the field © but also from the internal fields which, by Newton's third law, contribute nothing to the total force, though they modify the distribution of forces over the volume of the body. §17 Piezoelectrics 73 PROBLEMS Problem 1 . A dielectric sphere of radius a in a uniform external field © is cut in half by a plane perpendicular to the field. Determine the force of attraction between the hemispheres. Solution. We imagine the hemispheres separated by an infinitely narrow slit and deter- mine the force from formula (16.8) with e = 1, integrating over the surface of a hemisphere ; E is the field in the vacuum near the surface. According to (8.2) the field EW inside the sphere is uniform and equal to 3©/(2+e), where e is the dielectric constant of the sphere. The field in the slit is perpendicular to the surface and is E = D<*> = 3e(fe/(2+e). On the outer surface of the sphere we have E r = DW r = -^- ® cos 6, Ee = E(% = — (£ sin 6, 2+e e+2 where 6 is the angle between the radius vector and the direction of (£. A calculation of the integral gives an attractive force f F = 9(e-l)2 a z (£ 2 /16(€+2) 2 . Problem 2. Determine the change in shape of a dielectric sphere in a uniform external electric field. Solution. As in §5, Problem 4. In determining the change in shape, we assume the volume of the sphere to be unchanged.}: The elastic part of the free energy is given by the same expression as in §5, Problem 4. The electric part is given by V €<*>— 1 -i^.®= (£2, * 8tt1 +«(e<*> -1) ' and the dielectric permeability in the ac-direction is, by (16.1), €<*> = eo+aiUxx = eo+ +%ai(u X x— u yy ) = co+§ai(a— b)jR. From the condition that the total free energy is a minimum we find a-b _ 9& (eo-l)2+5ai R ~ 4077/1 (e +2) 2 " For e<> -*■ <x> this tends to the value for a conducting sphere. Problem 3. Determine the body forces in an isotropic solid dielectric, assumed homoge- neous, when extraneous charges are present in it. Solution. Assuming eo, ai, az constant and using the equations curl E = 0, div D = co div E = 4Tp ex , we have from (16.4) /< = da ik _ daOhk 1 ., . . 8E 2 Sxte dxjc 1 „ v 8E* t ai\ §17. Piezoelectrics The internal stresses which occur in an isotropic dielectric in an electric field are proportional to the square of the field. The effect is similar in crystals belonging to some of the crystal classes. For certain types of symmetry, however, the electrostriction properties of the crystals are quite different. The internal stresses in these piezoelectric bodies resulting from t It is by chance that, in the limit e -> oo, this expression tends to the result obtained in §5, Problem 3, for a conducting sphere (indeed, the forces are in opposite directions). The two cases are evidently not physically equivalent, because there is no field in the slit between two Conducting hemispheres at the same potential, whereas in this problem there is a field in the slit. X The change in volume is determined in §12, Problem 1. 74 Electrostatics of Dielectrics §17 an electric field are proportional to the field itself. The converse effect also occurs : the deformation of a piezoelectric is accompanied by the appearance in it of a field proportional to the deformation. Since in a piezoelectric only the principal (linear) effect is of interest, we can neglect the terms quadratic in the field in the general formula (16.5). Then aac = F8ik+(dFlduijc) T #. In this section we shall use the thermo- dynamic quantities referred to the matter in unit volume of the undeformed body (see the first footnote to §16). Taking F in this sense, we have simply croc = (SFlduiJc) T>E . (17.1) Accordingly, the thermodynamic relation for the differential dF is dF = -SdT+aikduiic-D. dE/4rr. (17.2) The following remark should be made concerning the last term. In the form given here, this term (taken from (10.9)) pertains, strictly speaking, to unit volume of the deformed body. By ignoring this fact, we commit an error which, in the case of a piezoelectric, is of a higher order of smallness than the remaining terms in (17.2). The independent variables in (17.2) include the components of the tensor tint. It is sometimes convenient to use instead the components am. To do so, we must introduce the thermodynamic potential, defined as 0> = F-u ik aijc. (17.3) For the differential of this quantity we have d$ = -SdT-u ik da ik -D'dEI47T. (17.4) It must be emphasised that the use of the thermodynamic potential O in electrodynamics in accordance with formulae (17.3) and (17.4) rests on the validity of (17.1) and so is possible only for piezoelectric bodies. Having thus defined the necessary thermodynamic quantities, let us now ascertain the piezoelectric properties of crystals. If o% and E k are taken as independent variables, the induction D must be regarded as a function of them, and an expansion of this function must include the linear terms in them. The linear terms in the expansion of the components of a vector in powers of the components of a tensor of rank two can be written, in the most general case, as 4myi t ja akh where the constants yijci form a tensor of rank three, and the factor Att is introduced for convenience. Since the tensor ajd is symmetrical, it is clear that the tensor y ik i may also be supposed to have the symmetry property 7i,kl = 7i,lk- (17-5) For clarity we separate the symmetrical suffixes from the remaining one by a comma. We call yijci the piezoelectric tensor. If it is known, the piezo- electric properties of the crystal are entirely determined. §17 Piezoelectrics 75 Adding the piezoelectric terms to the expression (13.1) for the electric induction in the crystal, we have Dt = Doi+eikEjc + ^Yi^icrjci. (17-6) Corresponding additional terms appear in the thermodynamic quantities. The thermodynamic potential of a non-piezoelectric crystal in the absence of a field is O = <S> = <S>o—2tMMm0ik<rim, where <X>o pertains to the undeformed body, and the second term is the ordinary elastic energy, determined by the elastic constant tensor (HkimA For a piezoelectric we have <P = ®0 — ilHklm<Tik<nm— HkEiEklSTT — EiDoil^TT — yijiEiajci' (17.7) The form of the last three terms is given by the fact that the derivatives of O with respect to E\ (for given temperature and internal stresses), found from the relation Di — —4^-dOjdEi, must accord with (17.6). Knowing <I>, we can obtain from (17.4) a formula giving the strain tensor in terms of the stresses aye and the field E: tHk = - (^0/3(7ffc)rE = imamoim + yijutEi. (17.8) It should be mentioned that to regard the quantities fiycim and cm for a piezoelectric as elastic constants and dielectric permeability is to some extent conventional. With the definitions used here, they give respectively the strains as functions of the elastic stresses for a given field, and the induction as a function of the field for given stresses. If, however, the deformation occurs with a given value of the induction, or we consider the induction as a function of the field for given strains, the elastic constants and the dielectric permeability will be represented by other quantities, which can be expressed as somewhat complex functions of the components of the tensors /i, e and y. The field in a piezoelectric body must be determined together with its deformation, leading to a problem in both electrostatics and elasticity theory. We must seek a simultaneous solution of the electrostatic equations div D = 0, curl E = 0, (17.9) with D given by (17.6), and the equations of elastic equilibrium da ik /dx fc = 0, (17.10) with the appropriate boundary conditions at the surface of the body and use of the relation (17.8) between aye and the strains. In general this problem is very complex. t The tensor iHkim determines the relation between stress and strain: 1Mk = — d® J don = IHklmOlm- In Theory of Elasticity, §10, the converse relation on = Xikimuim is used. It is evident that the symmetry properties of the tensor paim are exactly the same as those of Xikim. The free energy F contains the elastic energy with the plus sign: •Pel = ihklmUikUim. The thermodynamic potential is obtained from F by subtracting oikUik, and so ^el = -Pel — ooeUUe = — ^XikimUikUim = — ilMklmOikOi m . 76 Electrostatics of Dielectrics §17 The problem is much simplified for a body of ellipsoidal form with a free surface (i.e. one subject to no external mechanical forces). In this case (§8), the field inside the body is uniform; the deformation is therefore homogeneous, and the elastic stresses o% = 0. t Finally, let us consider which types of crystal symmetry allow the existence of piezoelectricity; in other words, what are the restrictions imposed on the components of the tensor yi ja by the symmetry conditions. In general, this tensor (which is symmetrical in the suffixes k and /) has 18 independent non- zero components, but in reality the number of independent components is usually much smaller. In all symmetry transformations of a given crystal, the components of the tensor yija must remain unaltered in value. Hence it follows at once that no piezoelectric body can have a centre of symmetry or, in particular, be isotropic. For, on reflection in the centre (i.e. change of sign of all three co- ordinates), the components of a tensor of rank three change sign. Of the 32 crystal classes, only 20 allow piezoelectricity. These comprise the ten enumerated in §13 as allowing pyroelectricity (all pyroelectrics are also piezoelectrics) and the ten following classes : rhombic system: D2 tetragonal system : D4, D^a, $4 rhombohedral system: D3 hexagonal system: D 6 , C 3 h, D 3 n cubic system: T, T&. The non-zero components of the piezoelectric tensor for each class are given in the following Problems. PROBLEMS Problem 1. Determine the non-zero components of the tensor yj,*j for non-pyroelectric crystal classes which allow piezoelectricity. Solution. The class Dz has three mutually perpendicular axes of symmetry of the second order, which we take as the axes of x, y and z. Rotations through 180° about these axes change the sign of two out of the three co-ordinates. Since the components yt.jti are trans^ formed as the products XiXiexi, the only non-zero components are those with three different suffixes: yx.yz, yz.xy, Yy.zx. (The other non-zero components are equal to these, since y i>kl = y J( ifc.) Accordingly, the piezoelectric part of the thermodynamic potential ist Opie = —2{yx,yzEx<ryz J ryy,xzEya X z-{-yz,xyEzOxy). (l) The class Z>2<j is obtained by adding to the axes of class D2 two planes of symmetry passing through one axis (the s-axis, say) and bisecting the angles between the other two. Reflection in one of these planes gives the transformation x -*■ y, y -> *, z -*■ z. Hence the components yi.jfcj which differ by interchange of x and y must be equal, so that only two out of the three coefficients in (1) are now independent: yz.xy, Yx,yz = Yv.xz. f To avoid misunderstanding it should be recalled that, if we calculate the components of the strain tensor mic by direct differentiation of the actual expression for O with respect to oik, the derivatives with respect to components aa with i ¥* k give twice the correspond- ing components uit; see Theory 0/ Elasticity, §10, Problem, footnote. §17 Piezoelectrics 77 The class T is obtained from the class D2 by adding four diagonal axes of symmetry of the third order, rotations about which effect a cyclic permutation of x, y, z, e.g. x -+ z, y -> x, z -> y. Hence all three coefficients in (1) are equal: yx.yz = yz.xy = Yy.zx- The same result is obtained for the cubic class Ta. The class D4 has one axis of symmetry of the fourth order (the z-axis, say) and four of the second order lying in the xy-plane. Here the symmetry elements of the class Dz are supple- mented by a rotation through 90° about the ar-axis, i.e. the transformation * -> y, y -*■ —x, z -> z. Consequently, one of the coefficients in (1) must be zero iyz.xy — —yz.yx — —yz,xy = 0), and the other two are equal, but opposite in sign: yx.yz = —yy.xz- The same result is obtained for the class De. The class 1S4 includes the transformations x -*■ y, y -*■ —x, z -*■ — z and x -> — x, y -> — y, z -> z. The non-zero components are yz.xy, Vx.yz = yy.xz, yz.xx = —Yz.yy, yx.zx = —yy.zy. One of these can be made to vanish by a suitable choice of the * and y axes. The class D3 has one axis of symmetry of the third order (the sr-axis, say), and three of the second order lying in the xy-plane ; let one of these be the *-axis. To find the restrictions imposed by the presence of a third-order axis, we make a formal transformation by introducing the complex "co-ordinates" £ = x+iy, 17 = x—ty; the co-ordinate z remains unchanged. We must also transform the tensor yi.jti to these new co-ordinates, in which the suffixes take the values g, 17, z. In a rotation through 120° about the .z-axis these co-ordinates undergo the transformation f -*■ fe 2 "" 3 , i] -*■ ije -2 "" 3 , z -*■ z. The only components of the tensor yi,ici which remain unchanged and so may be different from zero are yz.rf, Yy.zg, Y£,tn> Y£&> Y-n.im and yz.zz- A rotation through 180° about the x-axis gives the transformation x -*■ x, y -*■ —y, z -> — z, or £ -*■ 17, 7) -»■ £, z -> — z; yz, v g and Yz.zt change sign and so must be zero, while the remaining components listed above are mutually transformed in pairs, giving y VtS g = —ys.zj,, y{,& = y^,^. In order to write an expression for <f> p i e , we must form the sum —yt.iciEiojei, in which the suffixes take the values £, 17, z: #pie = — 2y„«5(£i,<7 z5 — Ezozr,)— 75.55(^5^5+^)0^?). Here the components Ei and o-j* in the co-ordinates £, 17, z must also be expressed in terms of those in the original co-ordinates x, y, z. This is easily done by using the fact that the com- ponents of a tensor are transformed as the products of the corresponding co-ordinates. Hence, for example, from I s = x 2 —y 2 +2ixy, we have o^ = o X x— oyy+2io X y. The result is ^pie = 2a(Ey<Xzx — E x o t y)-{-b\2Eya X y— E x (oxx— o*yy)]> (2) where a = 2iy v ,z( and b = 2yg.(( are real constants. The relations between the components yi,jw in the co-ordinates *, y, z are, as we see from (2), f Yy.zx = — Yx.zy — a, yy,xy = — Vx.xx = Yx.yy ^ b. The class Dzn is obtained from the class D3 by adding a plane of symmetry (the «y-plane) perpendicular to the axis of the third order. Reflection in this plane changes the sign of z, and so y v , Z f = 0, so that only the term with the coefficient b remains in (2). The class Czn has an axis of the third order and a plane of symmetry perpendicular to it. Reflection in this plane changes the sign of z, and so all components yt.ki whose suffixes contain z an odd number of times must be zero. Taking into account also the restrictions derived above which are imposed by the third-order axis of symmetry, we find that only the two components y Vlim and y^.ff are not zero. These quantities must be complex conjugates in order that O should be real. Putting 2y v , rrri = a+ib, 2y£,g = a—ib, we find Ople= a[2EyO X y— Exioxx — <ryv)]+b[2ExOxy+Ey(oxx — o yy )]. (3) Either a orb can be made to vanish by a suitable choice of the x and y axes. Problem 2. The same as Problem 1, but for the crystal classes which allow pyroelectricity. f In non-orthogonal co-ordinates such as £, 17, z the covariant and contravariant compo- nents of tensors must be distinguished. This should have been done in returning to the original co-ordinates x, y, z. We avoid this necessity, however, by obtaining the required relations between the components yi,*i in the co-ordinates x, y, z directly from the form of the scalar combination (2). 78 Electrostatics of Dielectrics §17 Solution. Let the #-axis be the axis of symmetry of the second, third, fourth or sixth order, or in the class C s be perpendicular to the plane of symmetry. In the classes Cnv the xsr-plane is a plane of symmetry. By a suitable choice of axes three more components can be made zero in the class d, and one component in the classes C s , Cn- We give below for each class all the components yi.ki which are not zero. Class C\: all yi.ki. C s : all those in which the suffix z appears twice or not at all. Cjjwl Yz.xx, Yz.yy, Yz.zz, Yx.xz, Yy.yz. Ct.: the same, together with yx.yz, Yy,xz, Yz.xy- Civ- Yz.xx = Yz.yy, Yz.zz, Yx.xz = Yy.yz. Ca'. the same, together with yx.yz = —yy.xz. Csv- Yz.zz, yx.xz = yy.yz, yx.xx = — Yx.yy = — Yv.xy, Yz.xx — Yz.yy. Cs: the same, together with yx.yz = —Yy.zx, Yy.xx = —yy.yy = yx.xy. Cov'' Yz.zz, yx.xz = Yy.yz, Yz.xx = Yz.yy C&: the same, together with yx.yz — —yy.zx. Problem 3. Determine Young's modulus (the coefficient of proportionality between the extending stress and the relative extension) for a flat slab of a non-pyroelectric piezoelectric in the following cases : (a) where the slab is stretched by the plates of a short-circuited condenser, (b) where it is stretched by those of an uncharged condenser, (c) where it is stretched parallel to its plane with no external field. Solution, (a) In this case the field E inside the slab is zero. The only non-zero component of the tensor aw is the extending stress a zz (the ar-axis being perpendicular to the slab).f From (17.8) we have u Z z = pzzzzOzz, whence Young's modulus is E = l//x ZZ2Z . (b) In this case we have in the slab E x = E v = 0, D z = 0. From (17.6) and (17.8) we have Dz = e Z zEz+^Yz,zzCFzz = 0, u zz = pzzzzOzz+Yz.zzEz. Eliminating Ez, we obtain 1/2? = {J.zzzz—4-nyz,zz 2 lezz. (c) In this case also, E x = E y — 0, Dz = 0, but the extension is along the *-axis, say. Here we have Dz = e zz Ez-\-^yz,xxo X x = 0, u X x = pxxxxOxx+Yz.xxEz. Eliminating Ez, we obtain 1/E = iixxxx—^nyz.xx^hzz. Problem 4. Obtain an equation for the velocity of sound in a piezoelectric medium. Solution. In this problem it is more convenient to use iwc as the independent variables, ns tead of one. We write F in the form „ 1 1 F = Fo+^Xikim tine mm — — em EiEh— — EiDoi+Pt.ki Eiujci, 8ir Artt where fii.kl = — Afcifc'I' Yi.le'l', whence oik = dF/diUk = X{klmWm + fil.ikEi. The equations of motion from the theory of elasticity are doik duim dEi Hi — — = Aiklm— VPl.ik- — , oxk oXk oxk where u is the displacement vector, related to utk by 1 / 8m 8uk\ The equation div D = gives 1 / dm duk\ ~ 2\8xk dxj' 8Ek 8uu _ OXi OXi and the field can be expressed in terms of the field potential: Ei = —d<j>/dxi, which takes into account the equation curl E = 0. t It is not assumed to coincide with any particular crystallographic direction. §18 Thermodynamic inequalities 79 In a plane sound wave, u and 4> are proportional to exp[i(k.-r— wt)], and we find from the above equations that U) 2 m = XiicimkkkiUm—pl.ikkickit, eikkikjc<f>+4iTfii,jcikikjcUl = 0. Eliminating <f>, we can write the condition of compatibility of the resulting equations for m as \co 2 8ik — Xmmkikm— ^M.Pl,mikik m )(Pp,g]ckpkq)le r tk r kt\ = 0. For any given direction of the wave vector k, this equation determines three phase velocities of sound tojk, which are in general different. A characteristic property of a piezoelectric medium is the involved relation between the velocity and direction of the wave. §18. Thermodynamic inequalities According to the formulae of §10, the total free energy can be written as the integral &=JF(T,p,-D)dV, (18.1) taken over all space. We shall suppose that the function D(x, y, z) which appears in the integrand satisfies only the equation div D = (18.2) inside a dielectric and the condition D- df = lire (18.3) on the surface of a conductor which carries a given charge. These equations establish the relation between the field and its sources. Otherwise we regard the function D(#, y,z) as arbitrary, and in particular we do not require it to satisfy the second field equation curlE = (where E = fadF/dD) or the boundary condition <f) = constant on the surface of a conductor. We shall show that these equations can then be obtained from the condition that the integral (18.1) is a minimum with respect to changes in the function D(x,y, z) which satisfy equations (18.2) and (18.3). It should be emphasised that the possibility of this derivation is not a priori evident, since the field distributions which come into consideration in determining the minimum of the integral (18.1) do not necessarily correspond to physically possible states (because they do not satisfy all the field equations), whereas, in the thermo- dynamic condition that the free energy is a minimum, only the various physically possible states are considered. The problem of finding the minimum of the integral (18.1) with the subsidiary conditions (18.2) and (18.3) is solved by Lagrange's method of multipliers. We multiply the variation of the condition (18.2) by some as yet undetermined function — <£/4-7r of the co-ordinates, and that of the 80 Electrostatics of Dielectrics §18 condition (18.3) by some undetermined constant <£o/4-n-, and then equate to zero the sum of variations (8FdV (<f>div8DdV+ — (j>SD.df = 0. In the first term we write t 8F = (dF/dD) TfP >8I> = E-SD/477, and the second can be integrated by parts: j* <£ divSD dV = j$SD»df— — J SD-gr ad <f> dV. The result is J(E + grad<£).SDdF+<j# -<£)SD.df = 0. Hence we conclude that, throughout the volume, we must have E = — grad <j> (and so curl E = 0), and on the surface of a conductor <f> = <f>o = constant. These are the correct equations for the field, and the Lagrangian multiplier <f> is its potential. Similarly it can be shown that the equations for the electric induction are obtained from the condition that the integral #= J F (T, />, E)dF is a mini- mum, in which the function E(x,y, z) is varied with the subsidiary conditions E = —grad <f> and <f> = constant on the surface of a conductor. For 8# = j(dF/dE)-8EdV=jl>-griidS<f>dVl4iT = £ 8<l> D- df/4n— J8cf> div D dV^ = 0. The first integral is zero because 8<f> = on the surface, and from the second we find the required equation div D = 0, since S<£ is arbitrary in the volume. If the body is not in an external electric field (in particular, if there are no charged conductors), it may be possible to formulate the condition of thermo- dynamic equilibrium as the condition that the total free energy (18.1) has an absolute (unconditional) minimum. This amounts to the condition that the free energy density F is a minimum as a function of the independent variable D: dFjdD = E/47T = 0, i.e. the field must be zero in all space. If it is pos- sible to find a distribution of the induction such that div D = 0, this state will correspond to thermodynamic equilibrium. J t The free energy is the minimum for a given temperature. The variation is with respect to two independent quantities D and p. Here we are interested only in the result of varying with respect to D. The variation of the integral (18.1) with respect to density (with the subsidiary condition of constant mass, i.e. constant J> dV) gives one of the usual conditions of thermal equilibrium, namely the constancy of the chemical potential £. t Here we are considering bodies in which D need not be zero even if E = (see §19). Otherwise we have simply the trivial result E = D = in all space. §18 Thermodynamic inequalities 81 Equating to zero the first variation of the free energy, we find necessary but not sufficient conditions for this energy to be a minimum. The calculation of the sufficient conditions requires a discussion of the second variation. These conditions take the form of certain inequalities (called thermodynamic inequalities) and are the conditions which ensure the stability of the state of the body.t When there is a linear relation between D and E, the situation is much simplified, and the thermodynamic inequality of interest here (relating to the dielectric properties of the body) becomes evident. The total free energy is F Q + J(D 2 /87re)dF. It is clear that this can have a minimum only if c > 0, since otherwise the integral could be made to take any large negative value by making D 2 large enough. Thus in this case nothing new is learnt, since we know already that the dielectric permeability must in fact be not only positive but greater than unity (see §14). In the general case of an arbitrary relation between D and E, however, it is necessary to consider the second variation of the integral (18.1), and to vary simultaneously both D and p (leaving only the temperature constant). In an isotropic body, F(T, p, D) depends only on the magnitude of the vector D, but its three components vary independently. We take the direction of the vector D before variation as the s-axis. Then the change in the magni- tude of D is given in terms of the changes in its components, as far as the second-order terms, by 8D = 8D z + (8D x fl2D + (8D y fl2D. The first and second variations of the integral (18.1) are both contained in the expression n dF dF 1 d 2 F d*F 1 d*F \ r J _SD + — -8p + - — -(8DY + 8D8 P + (5/. 2 dF. J \ dD fy P 2 8D* K } dDdp H iJp* F) ) Substituting 8D and collecting the second-order terms, we find the second variation /■ ±^[ { 8D x f + (8D y ndV+ nl d 2 F d*F 1 d*F \ ♦Jhs^W^W^K (18 - 4) These two terms are independent. The first is positive if (\jD)dFjdD > 0. But BF/dD = E/4tt, so that the derivative dFjdD is positive or negative according as the vectors D and E are in the same or opposite directions. Thus these vectors must be in the same direction. The conditions for the second term in (18.4) to be positive are d^F/dp* > 0, (18.5) ^^_(^ 2 >0 . (18.6) t See Statistical Physics, §21. 82 Electrostatics of Dielectrics §18 Since dF/dp = £, dFjdD = Ej\ir, the first of these gives (dydp) D , T > 0, (18.7) and the second can be rewritten as a Jacobian : d(dF/ 3D, dF/dp) _ 1 8(E y Q 8(D,p) "Sa(A/>) Changing from the variables D, p to D, £, we have 8(E,0 d(E,Q 3(Z),0 (dE\ rib > 0. \dDlAdpJ D d(D,p) d(D,!Z)d(D,p) XdD/^dp) by (18.7), this gives (BEldD\, T > 0. (18.8) Thus we have derived the required thermodynamic inequalities. In the absence of a field, the inequality (18.7) becomes the usual condition that the isothermal compressibility is positive: (dp/8p)T > O.t The inequality (18.8) gives e > 0, since when E -> the induction D -> eE. Of the two inequalities (18.5), (18.6) the latter is the stronger; it may be violated while the first is not, whereas the reverse is impossible. The equation = 8*F d*F / d*F \ 2 _ d(E, t) ~dp^~d^~ \ dpdDj ~ d(D, P ) corresponds to what' is called the critical state.% This condition is more conveniently written in a different form by multiplying it by the non-zero factor 8(D, p)\d(E, p): 8(E, Qld(E, P ) = {dlld P ) Bt T = 0. (18.9) The determination of further conditions for the stability of the critical state of matter requires a study of the third and fourth variations ; we shall not pause to do this, but simply give the results: (dH/dp^E.T = 0, (18.10) (dK/dp3) E . T > 0, (18.11) in analogy with those found in the absence of an electric field. t It should be recalled that, in the absence of a field, £ is the thermodynamic potential of unit mass and, by the ordinary thermodynamic relations, its differential dC = dp/p - (Sip) dT, It t X See Statistical Physics, §80. so that (dt/dp)T = (l/p)(S/>/3/>)r. In the above derivation the second of the ordinary thermodynamic inequalities (that the specific heat is positive) is ignored. §19 Ferroelectrics 83 PROBLEM Determine the displacement of the critical point of a dielectric substance in an electric field. Solution. Substituting in (18.9) the expression for £ from (10.18), we find (d£o/3p)r — — (£ 2 /8w)(3 2 c/3p 2 )r = 0. For the chemical potential when E = we have (3£o/3p)r = (l/p)(d/>/3p)r (see the penultimate footnote to this section), where p = p{p, T) is the equation of state in the absence of the field. Thus (dpldp)r = (p£ 2 /8ir)(a 2 e/dp 2 ):r. When there is no field, the critical point is given by the equation (3p/3p)r = 0, and if it is stable we must also have (d 2 p/dp 2 )T = 0. Hence \dp/T SH> S*p d*p — ApH —AT ~ —AT, dp 2 r dpdT ~ dpdT where AT and Ap are the displacements of the critical temperature and density (assumed to be of the same order of smallness, which is confirmed by the result). The temperature displacement is therefore P E 2 / d 2 e\ 8ir \ dpt/Tl dpdT The displacement of the critical pressure is Ap = (dp/dT) fi AT. To determine the displace- ment Ap, equation (18.10) must be used in a similar manner. §19. Ferroelectrics The various crystalline modifications of a given substance may include some which are pyroelectric and some which are not. If the change from one to the other takes place by means of a second-order phase transition, then near the transition point the substance has a number of unusual proper- ties which distinguish it from ordinary pyroelectrics ; these are called ferro- electric properties. In an ordinary pyroelectric crystal, a change in the direction of the spon- taneous polarisation involves a considerable reconstruction of the crystal lattice. Even if the final result of this reconstruction is energetically favour- able, its realisation may still be impossible because it would require the surmounting of very high energy barriers. In a ferroelectric body, however, the situation is quite different because, near a second-order phase transition point (a Curie point), the arrangement of the atoms in the crystal lattice of the pyroelectric phase is only compara- tively little different from the arrangement in the non-pyroelectric lattice (and so the spontaneous polarisation also is small). For this reason the change in direction of the spontaneous polarisation here requires only a relatively slight reconstruction of the lattice (a slight displacement of the atoms) and can occur quite easily. The actual nature of the ferroelectric properties of a body depends on its crystal symmetry. The direction of the spontaneous polarisation of the pyro- electric phase (which we shall call the ferroelectric axis) is determined by the structure of the non-pyroelectric phase beyond the Curie point. In some cases it is uniquely determined, in the sense that the ferroelectric axis can lie in only one, crystallographically determinate, direction; the direction of 84 Electrostatics of Dielectrics §19 the spontaneous polarisation is then determined apart from sign, since in the non-pyroelectric phase the two opposite directions parallel to the ferro- electric axis must be entirely equivalent (otherwise this form of the crystal would also be pyroelectric). In other cases, the symmetry of the rion- pyroelectric phase may be such as to allow spontaneous polarisation in any of several crystallographically equivalent directions, t The quantitative theory of ferroelectricity can be developed in terms of the general theory of second-order phase transitions ;$ this has been done by V. L. Ginzburg (1945). The basis of the following considerations will be the thermodynamic stability of states. From this point of view the transition is characterised by the fact that, on one side of it, a state with D = can be stable, but on the other side any such state is unstable, and so there must be a non-zero induc- tion even when the field E is zero. For definiteness, we shall suppose below that the pyroelectric phase (D ^ 0) corresponds to temperatures T < (where is the transition point), but it should be emphasised that this dis- position of the phases, though the more usual, is not obligatory, and the opposite case is also found in Nature. Since our prime interest is in the dielectric properties of the substance, we shall first suppose that there are no internal stresses in the body. To deter- mine the stability conditions, we can start from the condition that the total thermodynamic potential of the body is a minimum (for a given temperature and zero stresses). As we have seen in §18, this reduces to the condition that the second variation of the thermodynamic potential per unit volume <D should be positive. For a state in which the induction is almost zero, the second variation of O is simply <E>— <J>o = {\l%Tr)€~\]cDiDic. If we take the co-ordinate axes to be the principal axes of the tensor e**, then The state with D = satisfies the stability conditions (i.e. can correspond to a minimum of O) so long as all three coefficients l/e (<) are positive. Hence the pyroelectric phase can be formed only when one of these three coeffi- cients changes sign. The point at which the second-order phase transition takes place is determined by the vanishing of that coefficient. t An instance of the first type is sodium potassium tartrate, whose non-pyroelectric phase has a rhombic symmetry. The ferroelectric axis appears in it (at the Curie point) in a completely definite crystallographic direction (one of the second-order axes), and the lattice becomes monoclinic. An instance of the second type is barium titanate. Its non-pyroelectric modification has a cubic lattice, and any of the three cubic axes may become the ferroelectric axis. After the spontaneous polarisation has appeared at the Curie point, these three directions, of course, are no longer equivalent. The ferroelectric axis becomes the only fourth-order axis, and the lattice becomes tetragonal. X See Statistical Physics, Chapter XIV. The discussion here following, however, is not based on the usual formulation. §19 Ferroehctrics 85 The ferroelectric axis is then the one for which l/e (<) is zero. Here various cases can arise, depending on the symmetry of the non-pyroelectric phase. If this symmetry is such that e te) ^ e^ ^ e^, only one of the coefficients in (19.1) is zero, and the position of the ferroelectric axis is uniquely defined. If e te) = e ( 2/ } = efe> (for which the symmetry must be cubic), all three coeffi- cients vanish simultaneously, and the ferroelectric axis may be in one of several directions (see below). Finally, if the symmetry is such that e te) = eW ^ e fe) } either one or two of the coefficients in (19.1) will vanish at the transition point. Let us consider first the case where the position of the ferroelectric axis, which we take as the #-axis, is uniquely determined. The dielectric properties of the crystal in the x and y directions then exhibit no anomalies, and to investigate the properties in the s'-direction we need consider only those terms in the thermodynamic potential which contain D z . The expression (19.1) represents the leading terms in an expansion of <X> in powers of D. Since l/e fe) is small near the transition point, it is necessary to take into account the next term beyond the quadratic in the expansion in powers of D z . There can be no odd powers in this expansion, since they would change sign with D z (and so <D would change), whereas here the two direc- tions along the #-axis are equivalent. The next term after the quadratic therefore involves D z *: In order that the state with D z — should be stable at the point T — 0, it is clearly necessary that the coefficient B should be positive there, and so positive in the neighbourhood of that point. Near the transition point, l/e fe) can be expanded in powers of the difference T— 0; the first term in the expansion is of the form cc(T— 0), the coefficient a being positive (so that 1/efe) > for T > 0). Thus €<*> = l/a(T-0), (19.2) and the thermodynamic potential is a(T-0) B <D = <D + -^- L D f+ Dt A. (19.3) 07T 107T These formulae are sufficient for the calculation of all ferroelectric proper- ties of present interest near the transition point. First of all, from the formula E z = 47rd®ldD z we have E z = a(T-0)D z + 5D 2 3. (19.4) This is the fundamental relation giving the field as a function of the induction in a ferroelectric. For T > (in the non-pyroelectric phase), D z is zero for E z = 0. As E z increases (for a given value of T— 0), the induction at first increases linearly 86 Electrostatics of Dielectrics §19 (D z = E z Jol{T—%)), but for sufficiently large values of E z we have T> z = {E z jBy. The proportionality coefficient e fe) in the linear relation is the dielectric constant of the non-pyroelectric phase. For T -> it increases without limit in inverse proportion to T— 0, but the linear relation then ceases to be valid. For T < (in the pyroelectric phase), the value D z = cannot corres- pond to a stable state. For E z = the induction has a non-zero value, which by (19.4) is D z = D z0 = ± VW© - T)IB]. (19.5) Thus the spontaneous polarisation P z q = D z oj4^r of a ferroelectric decreases towards the Curie point as \/(0 — T). The "dielectric constant" of the pyroelectric phase may be defined as the value of the derivative dD z ldE z for E z = 0. From (19.4) we have 1 = [— a (0— T) + 3BD z 2 ]dD z ldE z ; substituting (19.5), we have dD z jdE z = l/2a(0 — T) for E z = 0. For sufficiently small E z , the relation between D z and E z becomes D z -D z0 = E z /2x(e-T). (19.6) A comparison of (19.2) and (19.6) shows that the "dielectric constant" of the pyroelectric phase is half its value in the non-pyroelectric phase at the same distance from the Curie point. Differentiating O (19.3) with respect to temperature, we can find the entropy S= — (d<&[dT)D = *Sb— aZ) 2 2 /87r. Here the fourth-order term can be omitted, since the quadratic term is not zero. In the pyroelectric phase with E z = we have also D z = 0, so that S = 5b- For the pyroelectric phase, substituting D z from (19.5), we find S = So—ol 2 (® — T)I8ttB. Hence the specific heat of this phase at the transition point itself is C v = TdS/dT = Cpo + o^Q/SttB, (19.7) where C v q is the specific heat of the non-pyroelectric phase at this point. Thus, if the transition of the ferroelectric from one phase to the other takes place with E z — 0, it is accompanied by a sudden change in the specific heat, as happens in ordinary second-order phase transitions. Moreover, C p > Cpo, i.e. the specific heat increases when pyroelectricity appears. Let us further investigate equation (19.4) in the pyroelectric phase (i.e. for T < 0). Figure 13 shows the approximate curve of the function D z (E z ) given by this equation. We see, first of all, that the part CC of the curve (shown dashed in Fig. 13) does not correspond to stable states which can occur in Nature: on CC we have dE z \dD z = Atrd^jdD^ < 0, whereas the condition that the second variation of the thermodynamic potential should be positive requires this derivative to be positive also. The ordinates of the points C and C are given by the equation 8E z /3D z = 0, and so we conclude that the possible values of \D z \ in the pyroelectric phase are bounded below by the condition D z 2 > a(0-T)/3£. (19.8) §19 Ferroelectrics 87 If we consider states of a ferroelectric with given values of E z , there is still an ambiguity in the value of D z , in the range of abscissae between C and C, and the question arises of the physical significance of the two values. We shall assume the ferroelectric to be a homogeneous flat slab, with the ferro- electric axis perpendicular to it, lying between the plates of a condenser, which are maintained at given potentials, i.e. which set up a given uniform field E = E z . For given potentials on the conductors, the condition of stability requires that the thermodynamic potential <I> = <J>— E»D/4tt be a minimum. In particular, for E = there are two states in which D z has opposite signs (the points A and A' in Fig. 13) but O (= O) is the same. These two states, therefore, are equally stable, i.e. they are two "phases" which can exist in contact. Fig. 13 Hence it is clear that the portions AC and A'C of the curve correspond to states which are metastable but not absolutely stable. It is easy to see directly that the values of O on AC and A'C are in fact greater than its values of A'B' and AB for the same value of E z . The ordinates of A and A' are given by formula (19.5). Thus the range of metastability is a(e-T)/3B < D z 2 < «(®-T)/B. (19.9) The existence of these two "phases" with E = is very important, since it means that a ferroelectric body can be divided into a number of separate regions or domains in which the polarisation is in opposite directions. On the surfaces separating these domains, the normal component of D and the tangential component of E must be continuous. The latter condition is satisfied identically, because E = 0. From the former condition it follows that the domain boundaries must be parallel to the #-axis. 7 88 Electrostatics of Dielectrics §19 The actual shapes and sizes of the domains are determined by the condi- tion that the total thermodynamic potential of the body should be a mini- mum. This subject has not yet been much studied for ferroelectrics. If we are not interested in the details of the structure, and consider por- tions of the body which are large compared with the domains, we can use the induction B averaged over such portions. Its component D z can evi- dently take values in the range between the ordinates of A and A' in Fig. 13, i.e. - VK® - T)/B] <D Z < VW© - T)JB]. (19.10) In other words, if D z in Fig. 13 is taken as the induction averaged in this way, the vertical segment AA' corresponds to the region of domain structure, and the thick curve BAA'B' gives all stable states of the body. A ferroelectric must, in particular, have a domain structure if it is not in an external electric field. For we have seen in §18 that the conditions of thermodynamic equilibrium in the absence of an external field reduce to the condition that <I> should be an absolute minimum as a function of D, with E = everywhere, t Let us consider ferroelectrics which belong (in the non-pyroelectric phase) to the cubic system. The cubic symmetry requires that e te) = e ( ^ ) = e te) = c, and admits two independent fourth-order invariants formed from the components of the vector D, which may, for example, be taken as D x *+D y 4 + +D z 4 and D x 2 D y 2 +D x 2 D z 2 +D y W z 2 . Hence the expansion of the thermo- dynamic potential is of the form <D = ® +oL(T-®)(D x 2 + Dy 2 + D z 2 )ISTT + B(D x *+D y *+D z *)ll(m + + C(D x 2 D y 2 + D X 2 D Z 2 + ZVZ> z 2)/8tt, (19.11) where we have again put 1/e = <x.(T—Q), and a, B, C are constants. It must be borne in mind, however, that cubic symmetry may admit also a third-order invariant DxD y D z ; this happens for the crystal classes T and T&, where there is no centre of symmetry. In these cases the state with D = certainly cannot satisfy the stability condition (that €> should be a minimum), and so no Curie point can exist. Hence the ferroelectric transi- tion can occur only in crystals of the classes O, T^, Oa of the cubic system, in accordance with the expansion (19.11). The sum of the fourth-order terms in (19.11) must be essentially positive. Hence we must have B > 0, C > -B. (19.12) The spontaneous polarisation of a ferroelectric in the absence of an external field is determined, as already stated, by the condition that <X> should t It should be emphasised that here we are speaking of complete thermodynamic equi- librium. This exists in ferroelectrics, but cannot do so in ordinary pyroelectrics, because of the difficulty, already mentioned, of reorienting the polarisation and so forming domains in them. §19 Ferroelectrics 89 be a minimum as a function of D. In particular, since the second-order term in (19.11) is independent of the direction of D, the direction of the spontaneous polarisation is determined by the condition that the fourth- order terms are a minimum for a given absolute value of D. Two cases are possible. If C > B, the minimum of <J> corresponds to D being along any one of the axes x, y, z, i.e. along any of the three edges of the cube (the crystallographic directions [001], [010], [100]). If, however, C < B, O takes its minimum values when D is along any one of the spatial diagonals of the cube (the crystallographic directions [111], [111], etc.) i.e. when D x 2 = D y 2 = D z 2 = %D 2 . In the former case the spontaneously polarised pyroelectric phase of the ferroelectric has tetragonal symmetry, and in the latter case it has rhombohedral symmetry. Let us consider in more detail, for example, the first case (C > B), and take as the #-axis the direction of the spontaneous polarisation below the Curie point. The magnitude of this polarisation is determined by the mini- mum of the expression — <x(@ — T)D 2 /S7t + BD^J\6it, whence Do 2 = *(@-T)/B. (19.13) The "dielectric permeability" in the ^-direction below the Curie point is, of course, different from that in the x and y directions. If the field E is small, then D x , D y and D z —Do are also small. Differentiating the expression (19.11) gives E g = 4nd^ldD z = -x(@-T)D z + BD z 2 ~ 2BD Q \D Z -D ), E x = 47rd®/dD x ss [CD 2 - a(0 - T)]D Z , whence D 8 -Do-EJ2*&-n (19U) D X = BE X ^(Q-T)(C-B). K ' } Above the Curie point the dielectric permeability of a cubic ferroelectric is the same in all directions : € = l/ a (r-0). (19.15) Finally, let us briefly consider the elastic properties of ferroelectrics. According to its crystallographic class, the non-pyroelectric phase of a ferro- electric may or may not be piezoelectric, t Here particular interest attaches to piezoelectric crystals whose symmetry admits a piezoelectric relation between the deformation and the polarisation in the direction of the ferro- electric axis. These include the classes D2, D%a and S4; in each case the induction D z in the direction of the ferroelectric axis appears in the piezo- electric part of the thermodynamic potential through a term$— h zxy D z o xy . t The non-pyroelectric phase of a ferroelectric is piezoelectric if it belongs to one of eight out of the ten classes listed at the end of §17: D2, Da, Z>2<j, 54, D3, De, Csh, Dzn. X Since we are using here the potential $>, and not $ as in §17, the piezoelectric tensor h,ki is not the same as the tensor yi,ia introduced previously, but their symmetry properties are, of course, identical. 90 Electrostatics of Dielectrics §19 In the elastic energy of these crystals, the component a xy appears in a term —ftxyxyVxy 2 - Thus the thermodynamic potential near the Curie point is <D = ® + x(T-T )D 1! ?IS7T + BD z *ll67T-\D z a X y-fx,a X y\ (19.16) where for brevity we have put X ZyXy = \ Pxyxy = A*. The terms involving the other components are of no interest, since they lead to no anomaly of the piezoelectric properties near the Curie point. Differentiating <I> with respect to D z and o X y, we find the field E z and the deformation u xy :\ E z = 47Td®ldD z = a(T- To)D z + BD^-47rXa xy , (19.17) U X y = \XD z -\r\LO x y. (19.18) In the non-pyroelectnc region when E is small we can neglect the term in D 2 3 in (19.17): E z = OL(T-To)D z -47T\o x y. Substituting D z from (19.18), we find A f 2ttA 2 I Uxy = Mf-n) Ez+ V + W~n)\ axy ' The coefficient of a xy in this formula represents the modulus of elasticity for deformations in which the field E z is kept constant, while [jl in formula (19.18) is the modulus for constant induction D z . Hence we can write jxCB) = / x«>) + 2 7r A2/a(T- T ), (19.19) where the superscripts indicate the nature of the deformation. We see that the two coefficients behave entirely differently near the Curie point : whereas fji {J)) is a finite constant, fi^ E) increases without limit as the Curie point is approached. In the pyroelectric region, formula (19.18) shows that the spontaneous polarisation results in a certain deformation of the body. If there are no internal stresses and the field E is zero, the deformation u xy is proportional to D z0 , i.e. by (19.5) it is proportional to <\/(@ — T). If the symmetry (cubic, for example) of the non-pyroelectric phase of a ferroelectric does not admit a piezoelectric effect linear in D, then the first non-vanishing terms in an expansion of the thermodynamic potential in powers of o-^; and D are quadratic in the components Df, i.e. they are of the form — ytklmDiDkVlm, ( 1 9.20) where yuam is a tensor of rank four, symmetrical with respect to the pairs of suffixes i, k and /, m. f See the first footnote to §17, Problem 1, concerning differentiation with respect to the components uac. §19 Ferroelectrics 91 Doubt might be cast on the legitimacy of using the expression (19.20) in the thermodynamic potential, on the grounds that, as stated in §17, this potential can be used only when quadratic effects are neglected. However, the ferroelectrics form an exception because, near the Curie point, the field £ is smallt compared with the induction D. The use of the thermodynamic potential involves the neglect of quantities of the order of EDinu (or, what is the same thing, EDai^) y whereas the expression (19.20) is of the order of D 2 aac. t This is seen, for instance, from formula (19.4): the first term on the right-hand side contains the small quantity T — 0, and the second term is of the third order in D. CHAPTER III CONSTANT CURRENT §20. The current density and the conductivity Let us now consider the steady motion of charges in conductors, i.e. con- stant electric currents. We shall denote by j the mean charge flux density or electric current density. \ In a constant current, the spatial distribution of j is independent of time, and satisfies the equation divj = 0, (20.1) which states that the mean total charge in any volume of the conductor remains constant. The electric field in the conductor in which a constant current flows is also constant, and therefore satisfies the equation curl E = 0, (20.2) i.e. it is a potential field. Equations (20.1) and (20.2) must be supplemented by an equation relating j and E. This equation depends on the properties of the conductor, but in the great majority of cases it may be supposed linear (Ohm's law). If the conductor is homogeneous and isotropic, the linear relation is a simple proportionality: j = <xE. (20.3) The coefficient a depends on the nature and state of the conductor; it is called the electrical conductivity. In a homogeneous conductor, a — constant and, substituting (20.3) in (20.1), we have divE = 0. In this case the electric field potential satisfies Laplace's equation : A<f> = 0. At a boundary between two conducting media, the normal component of the current density must, of course, be continuous. Moreover, by the general condition that the tangential field component is continuous (which follows from curlE = 0; cf. (1.7) and (6.9)), the ration/or must be continu- ous. Thus the boundary conditions on the current density are jnl=jn2, jtt/<71 = jl*2/<72, (20.4) or, as conditions on the field, <riE n i = o%E n 2y Efi = Et2- (20.5) f I n this chapter we ignore the magnetic field due to the current, and therefore the reaction of that field on the current. If this effect is to be taken into account, the definition of the current density must be refined, which we do in §29. 92 §20 The current density and the conductivity 93 At a boundary between a conductor and a non-conductor we have simply /» = 0, or E n = O.t An electric field in the presence of a current does mechanical work on the current-carrying particles moving in the conductor; the work done per unit time and volume is evidently equal to the scalar product j«E. This work is dissipated into heat in the conductor. Thus the quantity of heat evolved per unit time and volume in a homogeneous conductor is yE=aE*=p/o. (20.6) This is Joule's law.% The evolution of heat results in an increase in the entropy of the body. When an amount of heat dQ = j*E dV is evolved, the entropy of the volume element dV increases by dQ/T. The rate of change of the total entropy of the body is therefore dSTjdt = J (j • E/T) dV. (20.7) Since the entropy must increase, this derivative must be positive. Putting j = ctE, we see that the conductivity a must therefore be positive. In an anisotropic body (a single crystal), the directions of the vectors j and E are in general different, and the linear relation between them is ji = o ik E k , (20.8) where the quantities a^ form a tensor of rank two, the conductivity tensor ; which is symmetrical (see below). The following remark should be made here. The symmetry of the crystal would admit also an inhomogeneous term in the linear relation between j and E, giving j$ = oikEk+ji (0 \ with j (0) a constant vector. The presence of this term would mean that the conductor was "pyroelectric", there being a non-zero field in it when j = 0. In reality, however, this is impossible, because the entropy must increase: the term j (0) *E in the integrand in (20.7) could take either sign, and so dS^/dt could not be invariably positive. Just as, for an isotropic medium, dSf\dt > leads to a > 0, so for an anisotropic medium this condition means that the principal values of the tensor aik must be positive. The dependence of the number of independent components of the tensor am on the symmetry of the crystal is the same as for any symmetrical tensor of rank two (see §13): for biaxial crystals, all three principal values are differ- ent, for uniaxial crystals two are equal, and for cubic crystals all three are f It should be noticed that the equations curl £ = 0, div(aE) = and the boundary conditions (20.5) thereon are formally identical with the equations for the electrostatic field in a dielectric, the only difference being that c is replaced by a. This enables us to solve problems of the current distribution in an infinite conductor if the solutions of the corres- ponding electrostatic problems are known. When the conductor is bounded by a non- conductor this analogy does not serve, because in electrostatics there is no medium for which e = 0. X In Russian "Joule and Lenz's law". 94 Constant Current §20 equal, i.e. a cubic crystal behaves as an isotropic body as regards its con- ductivity. The symmetry of the conductivity tensor vik = am (20.9) is a consequence of the symmetry of the kinetic coefficients. This general principle, due to L. Onsager, may be conveniently formulated, for use here and in §§25, 26, as follows.! Let x\,X2, ... be some quantities which characterise the state of the body at every point. We define also the quantities X a = -dSJdxa, (20.10) where S is the entropy of unit volume of the body, and the derivative is taken at constant energy of the volume. In a state close to equilibrium, the quantities x a are close to their equilibrium values, and the X a are small. Processes will occur in the body which tend to bring it into equilibrium. The rates of change of the quantities x a at each point are usually functions only of the values of the x a (or X a ) at that point. Expanding these functions in powers of X a and taking only the linear terms, we have dx a /dt= -XyabXb. (20.11) Then we can assert that the coefficients y a b (the kinetic coefficients) are symmetrical with respect to the suffixes a and b: Yab — Yba- (20.12) In order to make practical use of this principle, it is necessary to choose the quantities x a (or their derivatives x a ) in some manner, and then to deter- mine the X a . This can usually be done very simply by means of the formula for the rate of change of the total entropy of the body = -jX Xa ^r dV ' (2(U3) d^ f^ „ dx a ~dt where the integration is extended over the whole volume of the body. When a current flows in a conductor, dS^jdt is given by (20.7). Compar- ing this with (20.13), we see that, if the components of the current density vector j are taken as the quantities x a , then the quantities X a will be the components of the vector — E/7 1 . A comparison of formulae (20.8) and (20.11) shows that the kinetic coefficients in this case are the components of the conductivity tensor, multiplied by T. Thus the symmetry of this tensor follows immediately from the general relation (20.12). f See Statistical Physics, §119, Pergamon Press, London, 1958; Fluid Mechanics, §58, Pergamon Press, London, 1959. §20 The current density and the conductivity 95 PROBLEMS Problem 1. A system of electrodes maintained at constant potentials <f> a is immersed in a conducting medium. A current J a flows from each electrode. Determine the total amount of Joule heat evolved in the medium per unit time. Solution. The required amount of heat Q is given by the integral 0=/j.EdF= -Jj.grad^dF= -/div(^j)dr, taken over the volume of the medium. We transform this into a surface integral, using the fact thatjB = at the outer boundary of the medium, while on the surfaces of the electrodes 4> = constant = <j> a . The result is Q = 2 <f> a Ja. Problem 2. Determine the potential distribution in a conducting sphere with a current / entering at a point O and leaving at the point O' diametrically opposite to O. O Solution. Near O and O' (Fig. 14) the potential must be of the forms 4> — J/lnaRi and <f> = —JIliraRz respectively, Ri and i?2 being the distances from O and O'. These func- tions satisfy Laplace's equation, and the integrals —or J grad ^«df over infinitesimal hemi- spheres about O and O' are equal to ±/. We seek the potential at an arbitrary point P in the sphere in the form 2n<ARi R2 where ^ is a solution of Laplace's equation having no poles in or on the sphere. It is evident from symmetry that tfi, like <f>, is a function of the spherical co-ordinates r and only. On the surface of the sphere (r = a) we must have d<f>[dr = 0. Differentiating, we find the boundary condition on ifi: 5+4 dtfi 1(1 _i) 2a\Ri Rj for r = a. If f{r, 6) is any solution of Laplace's equation, then the function / f(r, 6) dr is also a solution, f Comparing this with the above boundary condition, we see that the t This is easily seen either by direct calculation or from the fact that any solution f(r, 6) of Laplace's equation depending only on r and 9 can be written/ = 'Lc n r n P n (cos 6), where the c n are constants and the P n are Legendre polynomials. 96 Constant Current §21 condition is met by the solution r dr *-*J(e-s)t Substituting i?i,2 = \/(a 2 +r 2 ^2ar cos 0) and effecting the integration, we have finally J 1 1 11/ n a+r cos a— r cos 6\\ 9 = ~ — \Ti 77 + — sinh" 1 : — sinh -1 ; — - — I . 2iro\Ri Rz 2a\ r sin r sin /) Problem 3. Show that the current distribution in a conductor is such that the energy dissipated is a minimum. Solution. The minimum concerned is that of the intergal J j*E dV = J (j 2 /a) dV, with the subsidiary condition div j = (conservation of charge). Varying with respect to j the integral J[(j 2 /°') —2<j> div j]dV, where 2<f> is an undetermined Lagrangian multiplier, and equat- ing the result to zero, we obtain the equation j = — a grad </> or curl (j/w) = 0, which is the same as (20.2) and (20.3). §21. The Hall effect If a conductor is in an external magnetic field H, the relation between the current density and the electric field is again given by j± = ant Ejc, but the components of the conductivity tensor ouc are functions of H and, what is particularly important, they are no longer symmetrical with respect to the suffixes i and k. The symmetry of this tensor was proved in §20 from the symmetry of the kinetic coefficients. In a magnetic field, however, this principle must be formulated somewhat differently: when the suffixes are interchanged, the direction of the magnetic field must be reversed, t Hence we now have for the components or^fc(H) the relations cr«(H) = ow(-H). (21.1) The quantities o-ffr(H) and ct;m(H) are not equal. Like any tensor of rank two, 0% can be divided into symmetrical and anti- symmetrical parts, which we denote by sue and a\u : Vile = Ste + Uijc. (21.2) By definition *«(H) = s ki (H), a ik (H) = -a M (H), (21.3) and from (21.1) it follows that **(H) = jm(-H) = ^&(-H), a ik (H) = aM(-H) = -a«(-H). (21.4) Thus the components of the tensor st k are even functions of the magnetic field, and those of aa are odd functions. f See Statistical Physics, §119. §21 The Hall effect 97 Any antisymmetrical tensor a\ k of rank two corresponds to some axial vector, whose components are a x = a yz , a y = — a XZy a z = a xy . (21.5) In terms of this vector, the components of the product ai k E k can be written as those of the vector product Ex a: ji = a ik E k = s ik E k + (Ex a)*. (21 .6) The Joule heat generated by the passage of the current is given by the product j»E. Since the vectors Exa and E are perpendicular, their scalar product is zero identically, and so j.E = s ik EiE k , (21.7) i.e. the Joule heat is determined (for a given field E) only by the symmetrical part of the conductivity tensor. The external magnetic field may usually be supposed weak, and the compo- nents of the conductivity tensor accordingly expanded in powers of that field. Since the function a(H) is odd, the expansion of this vector will involve only odd powers. The first terms are linear in the field, i.e. they are of the form at = <x. ik H k . (21.8) The vectors a and H are both axial, and the constants a** therefore form an ordinary (polar) tensor. The expansion of the even functions ^&(H) will involve only even powers. The first term is the conductivity ao,ik in the absence of the field, and the next terms are quadratic in the field : Sik = <ro,ik + PiklmHiH m . (21.9) The tensor fii k i m is symmetrical with respect to i, k and /, m. Thus the principal effect of the magnetic field is linear in the field and is given by the term E X a; it is called the Hall effect. As we see, it gives rise to a current perpendicular to the electric field, whose magnitude is propor- tional to the magnetic field. It should be borne in mind, however, that, for an arbitrary anisotropic medium, the Hall current is not the only current perpendicular to E; the current Si k E k also has a component in such a direction. The Hall effect may be differently regarded if we use the inverse formulae which express E in terms of the current density : Ei = a^ikjic The inverse tensor ct -1 ^, like at k itself, can be resolved into a symmetrical part pi k and an antisymmetrical part which may be represented by an axial vector b: Ei = pikjk+(}xb)i. (21.10) The tensor pw and the vector b have the same properties as sac and a. In particular, in weak magnetic fields the vector b is linear in the field. In formu- la (21.10) the Hall effect is represented by the term j X b, i.e. by an electric 98 Constant Current §21 field perpendicular to the current and proportional to the magnetic field and to the current j. The above relations are much simplified if the conductor is isotropic. The vectors a and b must then be parallel to the magnetic field, by sym- metry. The only non-zero components of the tensor pug are p X x = Pyy and p zz , the field being in the ^-direction. Denoting these two quantities by p and p and taking the current to lie in the xs-plane, we have E* = P±Jx> Ey = —#*> Ez = Pijz- (21.11) Hence we see that, in an isotropic conductor, the Hall field is the only electric field which is perpendicular to both the current and the magnetic field. In weak magnetic fields, the vectors b and H are related (in an isotropic body) by b = -RH. (21.12) simply. The constant R (called HalVs constant) may be either positive or negative. The form of the terms quadratic in H in the relation between E and j, which enter through the tensor p^, is easily seen from the fact that the only vectors linear in j and quadratic in H which can be constructed from j and H are (j»H)H and H 2 j. Hence the general form of the relation between E and j in an isotropic body, as far as the terms quadratic in H, is E = P oj + #Hxj+i8i# 2 j+i82(j-H)H. (21.13) PROBLEM Express the components of the inverse tensor a -1 ** in terms of those of sue and a. Solution. The calculations are most simply effected by taking a system of co-ordinates in which the axes are the principal axes of the tensor sin ; the form of the results in an arbitrary co-ordinate system can easily be deduced from their form in this particular case. The deter- minant J crj is SxX O.Z — Oy \a\ = —a e Syy a x CLy ~~Gx Szz = SxxSyySzz + Sxxa X 2 + Syyay 2 + Sztaz 2 . In the general case we evidently have M = M+Siicaiak. From the minors of this determinant we find the components of the inverse tensor: C _1 X z = Pxx = (SyySzz + ax 2 )l\o\, o _1 X y — Pxy+bi = (axay—azSzz)l\o\, ... . The general expressions which give these for the particular system of co-ordinates chosen are Pile = {* -1 <*M+aia*}/M, bi = —saeajel\a\. This completes the solution. §22 The contact potential 99 §22. The contact potential In order to remove a charged particle through the surface of a conductor, work must be done. The work required for a thermodynamically reversible removal of the particle is called the work function. This quantity is always positive; this follows immediately from the fact that a point charge is at- tracted to any neutral body, and therefore to any conductor (see §14). It will be more convenient to refer this work to unit (positive) charge; the sign of the work function W thus defined is the same as that of the charge on the particle removed. The work function depends both on the nature of the conductor (and its thermodynamic state, i.e. its temperature and density) and on that of the charged particle. For example, the work function for a given metal is differ- ent for the removal of a conduction electron and for the removal of an ion from the surface. It must also be emphasised that the work function is characteristic of the surface of the conductor. It therefore depends, for instance, on the treatment of the surface and the "contamination" of it. If the conductor is a single crystal, then the work function is different for different faces. To ascertain the physical nature of the dependence of the work function on the properties of the surface, let us establish its relation to the electric structure of the surface layer. If p(x) is the charge density not averaged over physically infinitesimal segments of the ac-axis (perpendicular to the layer), we can write Poisson's equation in that layer as d 2 <£/d* 2 = — 4ny>. Let the conductor occupy the region x < 0. Then a first integration gives — —4tt \ p dx, dx _*L and a second integration (by parts) gives X X <£ — <£(— oo) = — Attx I p dx + 4tt xp dx. — oo —oo For x -> oo, the integral X I pdx — oo tends very rapidly to zero (since the surface of an uncharged conductor is electrically neutral). Hence 00 <j>( + oo) — <f>(~ oo) = 4-7T xp dx. 100 Constant Current §22 The integral on the right is the dipole moment of the charges near the surface of the body. These charges form a "double layer", in which charges of opposite sign are separated and the dipole moment is non-zero. The struc- ture of the double layer, of course, depends on the properties of the surface (its crystallographic direction, contamination, etc.). The difference in the work function for different surfaces of a given conductor is determined by the difference in the dipole moments. If two different conductors are placed in contact, an exchange of charged particles may occur between them. Charges pass from the body with the smaller work function to that with the greater until a potential difference between them is set up which prevents further movement of charge. This is called a contact potential. Fig. 15 Fig. 15 shows a cross-section of two conductors in contact (a and b) near their surfaces AO and OB. Let the potentials of these surfaces be <f> a and <f>i, respectively. Then the contact potential is <f> a i, = <f>b~<f>a- The quantita- tive relation between this potential and the work functions is given by the condition of thermodynamic equilibrium. Let us consider the work which must be done on a particle of charge e to remove it from the conductor a through the surface AO, transfer it to the surface OB, and finally carry it into the conductor b. In a state of thermodynamic equilibrium, this work must be zero.t The work done on the particle in the three stages mentioned is eW a , e(cf>b—(f>a), and —eWb respectively. Putting the sum of these equal to zero, we find the required relation : <f> ab =W b -W a . (22.1) Thus the contact potential of the neighbouring free surfaces of two conduc- tors in contact is equal to the difference in their work functions. The existence of the contact potential results in the appearance of an electric field in the space outside the conductors. It is easy to determine t Of course, in reality a particle can pass from one conductor to another only through their surface of contact, and not through the space adjoining them, but the work done is independent of the path. §23 The galvanic cell 101 this field near the line of contact of the surfaces. In a small region near this line (the point O in Fig. 15), the surfaces may be regarded as plane. The field potential outside the conductors satisfies the equation 1 8 l d<f>\ 1 8*6 A0 = r— + - = 0, r r 8r\ 8rl r* 86* where r and 9 are polar co-ordinates with origin at O; on AO and OB the potential takes given constant values. We are interested in the solution which contains the lowest power of r; this is the leading term in an expansion of the potential in powers of the small distance r. The solution concerned is <f> = constant x 9. Measuring the angle 9 from AO and arbitrarily taking the potential on AO as zero, we have <f> = 4> ab djoL, (22.2) where a is the angle AOB. Thus the equipotential lines in the plane of the diagram are straight lines diverging from O. The lines of force are arcs of circles centred at O. The field is 1 8<j> <f> a b 1 £=-- t|=-— -; ( 22 - 3 ) r 89 a. r it decreases inversely as the distance from O. As has been said above, "contact" potentials also exist between the various faces of a single crystal of metal. Hence an electric field of the kind just described must exist near the edges of the crystal, t If several metallic conductors (at equal temperatures) are connected together, the potential between the extreme conductors is, as we easily de- duce from formula (22.1), simply the difference of their work functions, as it is for two conductors in direct contact. In particular, if the metal at each end is the same, the contact potential between the ends is zero. This is evident, however, because if there were a potential difference between two like conductors, a current would flow when they were connected, in contra- diction to the second law of thermodynamics. §23. The galvanic cell The statement at the end of §22 ceases to be valid if the circuit includes conductors in which the current is carried by different means (e.g. metals and solutions of electrolytes). Because the work function of a conductor is different for different charged particles (electrons and ions), the total contact potential in the circuit is not zero even when the conductors at each end are similar. This total potential difference is called the electromotive force or e.m.f. in the circuit ; it is just the potential difference between the two like conductors before the circuit is closed. When the circuit is closed, a current flows in it ; this is the basis of the operation of what are called galvanic cells. f In reality, all such fields are usually compensated by the field of ions from the atmo- sphere which "adhere" to the surface of the crystal. 102 Constant Current §23 The energy which maintains the current in the circuit is supplied by chemical transformations occurring in the cell. When we go completely round any closed circuit the field potential must, of course, return to its original value, i.e. the total change in the potential must be zero. Let us consider, for example, a contour on the surface of the conductors. When we pass from one conductor to another, the potential has a discontinuity <f> a b- The potential drop across any conductor is RJ> where / is the total current flowing through it and R is its resistance. Hence the total change in the potential round the circuit is E<£ a &— 2/R. Putting this equal to zero and using the facts that/ is the same at every point in the circuit and H>(j> a b is the electromotive force $ , we find JXR = S, (23.1) so that the current in a circuit containing a galvanic cell is equal to the e.m.f. divided by the total resistance of all the conductors in the circuit (including, of course, the internal resistance of the cell itself). Although the e.m.f. of a galvanic cell can be expressed as a sum of contact potentials, it is very important to note that it is in reality a thermodynamic quantity, determined entirely by the states of the conductors and independent of the properties of the surfaces separating them. This is clear, because 8 is just the work per unit charge which must be done on a charged particle when it is carried reversibly along the closed circuit. To illustrate this, let us consider a galvanic cell consisting of two electrodes of metals A and B immersed in solutions of electrolytes AX and BX, X~ being any anion. Let £4 and £# be the chemical potentials of the metals A and B, and Iax and Cbx those of the electrolytes in solution.! If an elemen- tary charge e is carried along the closed circuit, an ion A + passes into solution from the electrode A and an ion B + passes out of solution to the electrode B, the change in the charges on the electrodes being compensated by the passage of an electron from A to B through the external circuit. The result is that the electrode A loses one neutral atom, the electrode B gains one, and in the electrolyte solution one molecule of BX is replaced by one of AX. Since the work done in a reversible process (at constant temperature and pressure) is equal to the change in the thermodynamic potential of the sys- tem, we have e*AB = (Cb-Cbz)-(U-Uz), (23.2) which expresses the e.m.f. of the cell in terms of the properties of the material of the electrodes and of the electrolyte solution. From (23.2) we can also draw the following conclusion. If the solution contains three electrolytes AX, BX, CX and three metallic electrodes A, B, C, then the e.m.f.s between each pair of them are related by &AB + &BC = &AC- (23.3) t In this section we use the ordinary chemical potentials, i.e. those defined with respect to one particle. §24 EUctrocapiUarity 103 Using the general formulae of thermodynamics, we can relate the e.m.f. of a galvanic cell to the heat evolved when a current flows, which of course is actually an irreversible phenomenon. Let Q be the amount of heat generated (both in the cell itself and in the external circuit) when the unit charge passes along the circuit; Q is just the heat of the reaction which occurs in the cell when a current flows. By a well-known formula of thermodynamics, t it is related to the work <f by The definition of the partial derivative with respect to temperature depends on the conditions under which the process occurs. For example, if the current flows at constant pressure (as usually happens), then the differentiation is effected at constant pressure. §24. Electrocapillarity The presence of charges on the boundary between two conducting media affects the surface tension there. This phenomenon is called electrocapillarity. In practice, the media concerned are both liquids; usually one is a liquid metal (mercury) and the other is a solution of an electrolyte. Let 0i, <f>2 be the potentials of the two conductors, and e\, e2 the charges at the surface of separation. These charges are equal in magnitude and opposite in sign, and thus form a double layer on the surface. The differential of the potential gjo of a system of two conductors at given temperature and pressure is, taking into account the surface of separation, dgb = a.dS-eid<f>i-e2d<f>2, (24.1) where the term ccdS is the work done in a reversible change dS in the area S of the surface of separation; a is the surface-tension coefficient. t The thermodynamic potential cp in (24.1) may be replaced by its "sur- face part" ^?s, since the volume part is constant for given temperature and pressure, and is therefore of no interest here. Putting e\ = —e2 = e and the potential difference <f>i—<f>2 = <f>, we can write (24.1) as dgb s = oidS-ed<f>. (24.2) Hence (d^s/dS)^ = a, (24.3) a being expressed as a function of <f>. Integrating, we find that gd s = <x.S. t See Statistical Physics, §89. X See Statistical Physics, §1 39. 104 Constant Current §25 Substitution in (24.2) gives d(a«S) = acLS— ed<f>, or Sda. = — ed(f>, whence a = -(d*ld<f>) p ,T, (24.4) where a = e/S is the charge per unit area of the surface. The relation (24.4), first derived by G. Lippmann and J. W. Gibbs, is the fundamental formula in the theory of electrocapillarity. In a state of equilibrium, the thermodynamic potential <^> must be a minimum for given values of the electric potentials on the conductors. Regarding it as a function of the surface charges e, we can write the necessary conditions for a minimum as dyb s /de = d^/de* > 0, (24.5) where the derivatives are taken at constant area S. To calculate these, we express gb s in terms of the thermodynamic potential cjo s = §p s (e) : &>s = cp s (e)-e\$\-e<$z = cp s {e)-e^>. (24.6) The vanishing of the first derivative gives = <f> = u, de de and then the condition for the second derivative to be positive becomes d^gos d 2 £fo s d(f> 1 d<f> de* de 2 de Sda or >0, da/84, > 0. (24.7) This result was to be expected, since the double layer on the surface may be regarded as a condenser of capacity de/d4>. Differentiating equation (24.4) with respect to <j> and using (24.7), we find that dV^ 2 < 0. (24.8) This means that the point where da./d4> = —a = is a maximum of a as a function of <£. §25. Thermoelectric phenomena The condition that there should be no current in a metal is that there is thermodynamic equilibrium with respect to the conduction electrons. This means not only that the temperature must be constant throughout the body, but also that the sum e<£ + £o should be constant, where Co is the chemical potential of the conduction electrons in the metal (for 4> — 0).t If the metal t See Statistical Physics, §25. Here we take 5 to be the chemical potential denned in the usual manner, viz. per unit particle (electron). §25 Thermoelectric phenomena 105 is not homogeneous, £o is not constant throughout the body even if the temperature is constant. Hence the constancy of the electric potential <f> in this case does not mean the absence of a current in the metal, although the field E = — grad <f> is zero. This makes the ordinary definition of <f> (as the average of the true potential) inconvenient, if we wish to take inhomogeneous conductors into consideration. It is natural to redefine the potential as <f> + Cole, and we shall write this henceforward as <f> simply, t In a homogeneous metal, the change amounts to the adding of an unimportant constant to the potential. Accordingly, the "field" E = — grad <f> (which we shall use henceforward) is the same as the true mean field only in a homogeneous metal, and in general the two differ by the gradient of some function of the state. With this definition, the current and field are both zero in a state of thermodynamic equilibrium with respect to the conduction electrons, and the relation between them is j = oE (or j\ = at *£*) even if the metal is not homogeneous. Let us now consider a non-uniformly heated metal, which cannot be in thermodynamic equilibrium (with respect to the electrons). Then the field E is not zero even if the current is zero. In general, when both the current density j and the temperature gradient grad T are not zero, the relation between these quantities and the field can be written E = j/cr + agradT. (25.1) Here a is the ordinary conductivity, and a is another quantity which is an electrical characteristic of the metal. Here we suppose for simplicity that the substance is isotropic (or of cubic symmetry), and therefore write the proportionality coefficients as scalars. The linear relation between E and grad T is, of course, merely the first term of an expansion, but it is sufficient in view of the smallness of the temperature gradients occurring in practice. The same formula (25.1), in the form j = a(E-agradT), (25.2) shows that a current can flow in a non-uniformly heated metal even if the field E is zero. As well as the electric current density j, we can consider the energy flux density q. First of all, this quantity contains an amount <j>j resulting simply from the fact that each charged particle (electron) carries with it an energy e<f>. The difference q— <f>j, however, does not depend on the potential, and can be generally written as a linear function of the gradients grad <£ = — E and grad T, similarly to formula (25.2) for the current density. We shall for the present write this as q-^j = jSE-ygradr. t This definition can also be formulated as follows : the new e<f> is the change in the free energy when one electron is isothermally brought into the metal. In other words, <f> = dF/dp, where F is the free energy of the metal and p the charge on the conduction electrons per unit volume. v dV. 106 Constant Current §25 The symmetry of the kinetic coefficients gives a relation between the coeffi- cient j8 and the coefficient a in (25.2). To derive this, we calculate the rate of change of the total entropy of the conductor. The amount of heat evolved per unit time and volume is — div q. Hence we can put dS? fdivq ~d7 = J Using the equation div j = 0, we have divq 1 1 E«j ~Y~ = y{ div (q-^i) +div ^ = ^- dlv (q-<£0— Y' The first term is integrated by parts, giving dy fE-i r(q-<f>\)-gradT -a-H AV - y i dv - (25 - 3 > This formula shows that, if we take as the quantities dx a /dt (see §20) the components of the vectors j and q— </>j, then the corresponding quantities X a are the components of the vectors — E/T and grad T/T 2 . Accordingly in the relations E grad T E grad T q-<f>j = §T—-yT* T2 , the coefficients <raT 2 and jST must be equal. Thus jS = axT, so that q— <£j = o-aTE— y grad T. Finally, expressing E in terms of j and grad T by (25.1), we have the result q = (<f> + aT)j - k grad T, (25.4) where k = y— To? a is simply the ordinary thermal conductivity, which gives the heat flux in the absence of an electric current. It should be pointed out that the condition that d«^/d* should be positive places no new restriction on the thermoelectric coefficients. Substituting (25.1) and (25.4) in (25.3), we obtain + ^V>0, (2,5) whence we find only that the coefficients of thermal and electrical conduc- tivity must be positive. In the above formulae it was tacitly assumed that an inhomogeneity of pressure (or density) at constant temperature cannot cause a field (or current) to appear in the conductor, and consequently no term in grad/> was in- cluded in (25.2) or (25.4). The existence of such terms would, in fact, contra- dict the law of the increase of entropy: the integrand in (25.5) would then "d7~ J \~iPr §25 Thermoelectric phenomena 107 contain terms in the products j«grad/> and grad T«grad/>, which could be of either sign, and so the integral could not be necessarily positive. The relations (25.1) and (25.4) indicate various thermoelectric effects. Let us consider the amount of heat — div q evolved per unit time and volume in the conductor. Taking the divergence of (25.4), we have £=-divq = div(/cgradT) + E.j+j-grad(aT), or, substituting (25.1), i 2 Q = div(*cgrad T) + - — Tj-grada. (25.6) a The first term on the right pertains to ordinary thermal conduction, and the second term, proportional to the square of the current, is the Joule heat. The term of interest here is the third, which gives the thermoelectric effects. Let us assume the conductor to be homogeneous. Then the change in a is due only to the temperature gradient, and grad a = (da/d T) grad T; if, as usually happens, the pressure is constant through the body, dccjdT must be taken as (da/ #7%. Thus the amount of heat evolved (called the Thomson effect) is pj.gradT, where p =- Tda/dT. (25.7) The coefficient p is called the Thomson coefficient. It should be noticed that this effect is proportional to the first power of the current, and not to the second power like the Joule heat. It therefore changes sign when the current is reversed. The coefficient p may be either positive or negative. If p > 0, the Thomson heat is positive (i.e. heat is emitted) when the current flows in the direction of increasing temperature, and heat is absorbed when it flows in the opposite direction ; if p < the reverse is true. Another effect, called the Peltier effect, occurs when a current passes through a junction of two different metals. At the surface of contact, the temperature, the potential and the normal components of the current density and energy flux density are all continuous. Denoting by the suffixes 1 and 2 the values of quantities for the two metals and equating the normal com- ponents of q (25.4) on the two sides, we have, since <f>, T and j x are con- tinuous, [- icdT/dx]l= -j x T(<x. 2 -<x.i), the #-axis being taken along the normal to the surface. If the positive direction of this axis is from metal 1 to metal 2, then the expression on the left-hand side of this equation is the amount of heat taken from the surface per unit time and area by thermal conduction. This heat loss is balanced by the evolution at the junction of an amount of heat given by the right-hand side of the equation. Thus the amount of heat generated per unit time and area is jn 12 , where U 12 = - T(* 2 - «i). (25.8) 108 Constant Current §25 The quantity II 12 is called the Peltier coefficient. Like the Thomson effect, the Peltier effect is proportional to the first power of the current, and changes sign when the direction of the current is reversed. The Peltier coefficient is additive: II 13 == II 12+ II 23, where the suffixes 1, 2, 3 refer to three different metals. A comparison of formulae (25.7) and (25.8) shows that the Thomson and Peltier coefficients are related by d /IIi2\ "-« " T «r(-rY (25 - 9) Next, let us consider an open circuit containing two junctions, the two end conductors being of the same metal (1 in Fig. 16). We suppose that the junctions b and c are at different temperatures T\ and T2, while the tempera- ture at each end (a and d) is the same. Then there is a potential difference called a thermoelectromotive force, which we denote by <fy, between the ends. Fig. 16 To calculate this force, we put in (25.1) j = and integrate the field E = a grad T along the circuit (taken to be the #-axis) : d dT f dI f g T = a dx = ad7\ J dx J The integrations from a to b and from c to d are over temperatures from T2 to . Ti in metal 1, and that from b to c is over temperatures from T\ to T2 in metal 2. Thus = J(a 2 -ai)dT. (25.10) Comparing this with (25.8), we see that the thermo-e.m.f. is related to the Peltier coefficient by <ot c ni2 = - J ~j=dT (25.11) T Formulae (25.9) and (25.11) are called Thomson's relations. To conclude this section, we shall give the formulae for the current and heat flux in an anisotropic conductor. These are derived from the symmetry §25 Thermoelectric phenomena 109 of the kinetic coefficients in exactly the same way as formulae (25.1) and (25.4), and the results are Ei = o-^jcjjc+cmcdTjdxjc, qi-<f>ji = TccMJk- KucdTJdxic. Here o~Hk is the tensor inverse to the conductivity tensor ct^, and the tensors ak and Kijg are symmetrical. The thermoelectric tensor a**, however, is in general not symmetrical. PROBLEM Find the relations between the coefficients of the various thermogalvanomagnetic effects, i.e., those which occur when a current flows in the simultaneous presence of an electric field, a magnetic field, and a temperature gradient. Solution. The discussion is entirely similar to that given above for thermoelectric effects. It is conveniently carried out in tensor form, so as to be applicable to both isotropic and anisotropic conductors. We write the electric current density j and the heat flux q as (i) where all the coefficients are functions of the magnetic field. The symmetry of the kinetic coefficients gives a,*(H) = a w (-H), <*«*(H) = </*<(-H), MH) = a«(-H). Expressing E and q— $ in terms of j and grad T from (1), we have qi—<h* = P«cjk—KikdT/dxk, where the tensors a -1 , a, (3, #c are certain functions of the tensors a, b, c, d, and have the fol- lowing symmetry properties resulting from (2) : o-MH) = a-i w (-H), k«*(H) = /c*«(-H), /3«(H) = 7a*,(-H). K } These are the required relations in their most general form. They generalise those found in §25 for the case where there is no magnetic field and in §21 for the case where there is no temperature gradient. For an isotropic conductor in a weak magnetic field we have, as far as the first-order terms inH, E = j/a+a grad T+i?Hxj+iVHxgrad T, (5) q-# = aTj-K grad T+iVTUXj+LHXgrad T. (6) Here a and k are the ordinary coefficients of electrical and thermal conductivity, a is the thermoelectric coefficient which appears in (25.1), R is the Hall coefficient, and N and L are new coefficients. The term iVHxgrad T may be regarded as representing the effect of the magnetic field on the thermo-e.m.f . (called the Nernst effect), and the term LH x grad T as representing the effect of this field on the thermal conduction (called the Leduc-Righi effect). At a boundary between media, the normal components of the vectors j and q are continu- ous, and therefore so is that of the vector — k grad r+aTj+JVTHxj +LHx grad T. The term JVTHxj gives the influence of the magnetic field on the Peltier effect (called the Ettingshausen effect). 110 Constant Current §26 The amount of heat evolved in the conductor per unit time and volume is Q = — div q. Here we must substitute q from (6) and replace — grad <£ = E in accordance with (5). If the conductor is homogeneous, then the quantities a, N, L, etc. are functions of tempera- ture alone, and so their gradients are proportional to grad T. In the calculation we neglect all quantities of the second order in H, and to the same approximation we can take curl (j/a) = curl E = 0. We also note that the external field H (arising from sources outside the conductor under consideration) is such that curlH = O.f Finally, divj = 0, as for any constant current. The result is *2 1 A Q = — +div(* grad TJ-Tj-grad oc+ — — -(aNT 2 )j xH-grad T. a oT di The last term gives the change in the Thomson effect resulting from the presence of the magnetic field. §26. Diffusion phenomena The presence of diffusion causes certain phenomena in electrolyte solu- tions which do not occur in solid conductors. We shall assume, for simplicity, that the temperature is the same everywhere in the solution, and so consider only pure diffusion phenomena, uncomplicated by thermoelectric effects. Instead of the pressure p and the concentration c, it is more convenient to take as independent variables the pressure and the chemical potential £. We here define £ as the derivative of the thermodynamic potential of unit mass of the solution with respect to its concentration c (at constant p and T) ; by the concentration we mean the ratio of the mass of electrolyte in a volume element to the total mass of fluid in the same volume. $ It may be recalled that the constancy of the chemical potential is (like that of the pressure and the temperature) one of the conditions of thermodynamic equilibrium. The definition of the electric field potential given in §25 has to be some- what modified in this case, since the current is now carried by the ions of the dissolved electrolyte, and not by the conduction electrons. A suitable definition is (cf. the second footnote to §25) <f> = {d^jdp) c , where O is the thermodynamic potential and p the sum of the ion charges in unit volume of the solution (after differentiating we put p = 0, of course, because the solution is electrically neutral). The derivative is taken at constant mass concentration, i.e. at a given sum of the masses of ions of both signs in unit volume. f This neglects the very weak effect on the evolution of heat resulting from the magnetic fields of the currents themselves. % The chemical potentials are usually defined as £i = 3<B/3mi, £2 = 3G>/3«2, where O is the thermodynamic potential of any mass of the solution, and ni, «2 the numbers of particles of solute and solvent in that mass of solution. If O is the thermodynamic potential of unit mass, then the numbers n\ and nz are related by nwn+ nxm* — 1 (where mi, mz are the masses of the two kinds of particle), and the concentration c = mm\. Hence we have ao _ ao a«i do dm __ & £2 dc dni dc dm dc mi mz where £ is the chemical potential as here defined. §26 Diffusion phenomena 111 When a gradient of the chemical potential is present, a term proportional to it is added to the expression for the current density: j = o(E-j8grad9, (26.1) in analogy with the added term in (25.2). We shall see below that, for a given gradient of the chemical potential (and of the temperature), j must be independent of the pressure gradient, and so no term in grad p appears in(26.1).t As well as the electric current, we have to consider the transport of the mass of the electrolyte which takes place at the same time. It must be borne in mind that the passage of a current through the solution may be accom- panied by a macroscopic motion of the fluid. The mass flux density of the electrolyte resulting from this motion is pew, where v is the velocity and p the density of the solution. The electrolyte is also transported by molecular diffusion. We denote the diffusion flux density by i, so that the total flux density is pev+i. The irreversible processes of diffusion cause a further increase in entropy ; the rate of change of the total entropy isj . JgJdr-j'-g^dr. (26.2) Like the electric current density, the diffusion flux may be written as a linear combination of E and grad £, or of j and grad £. Using the sym- metry of the kinetic coefficients, we can relate one of the coefficients in this combination to the coefficient jS in (26.1), in exactly the same way as we did for j and q— <£j in §25. The result is {dl\dc) Vt T The coefficient of grad £ is here expressed in terms of the ordinary diffusion coefficient.|| The inadmissibility in (26.1) and (26.3) of terms proportional to the pressure gradient follows, as in §25, from the law of the increase of entropy: such terms would make the derivative of the total entropy (26.2) a quantity of variable sign. Formulae (26.1) and (26.3) give all the diffusion phenomena in electrolytes, but we shall not pause here to examine them more closely. f It should be emphasised, however, that, for a given concentration gradient j does depend on the pressure gradient: grad £ = ( 3£/ 8c) p ,t grade + (d^dp) c , T gradp. X The derivation of the second term is given in Fluid Mechanics, §57. || For j = and constant pressure and temperature we have i = — pD grad c. 112 Constant Current §26 PROBLEM Two parallel plates of a metal A are immersed in a solution of an electrolyte AX. Find the current density as a function of the potential difference applied between the plates. Solution. When the current passes, metal is dissolved from one plate and deposited on the other. The solvent (water) remains at rest, and a mass flux of metal of density t pv =jmle occurs in the solution, where j is the electric current density, and m and e are the mass and charge of an ion A + . This flux is also given by pv — i + pvc, where t is as shown in (26.3) ; assuming the pressure constant throughout the liquid, J we have pz ^ = [*-7 (1 -4'' (1) where * is the co-ordinate in the direction of a line joining the electrodes. Since j = constant in the solution, this gives 7 _ f 8 P Ddc m }l ~ J j3-m(l-c)/ e ' K) c i where a, cz are the concentrations at the surfaces of the plates, and / is the distance between them. The potential difference 8 between the plates is most simply found from the total amount of energy Q dissipated per unit time and unit area of the plates, which must equal jS. By (26.1), (26.2) we have d^ r (P Hldc\ z \ and therefore, using (1), pDdc , f*a{ J o(j8-i»(l-c) e) J BcV e '\ (3) Formulae (2) and (3) implicitly solve the problem. If the current j is small, the concentration difference cz—ci is also small. Replacing the integrals by ca — ci times the integrands, we find the effective specific resistance of the solution : / 1 1 8l\ -T7 = - + a pD del e J The first term in (3) gives the potential drop (/ (j/o) dx) due to the passage of the current. The second term is the e.m.f. due to the concentration gradient in the solution (in a certain sense analogous to the thermo-e.m.f.). This latter expression is independent of the con- ditions of the particular one-dimensional problem considered, and is the general expression for the e.m.f. of a "concentration cell". t It may be recalled that the hydrodynamic velocity v in a solution is defined so that p is the momentum of unit volume of the liquid; see Fluid Mechanics, §57. Hence the fact that in this case only the dissolved metal is moving (relative to the electrodes) does not affect the calculation of pv. X The change in pressure due to the motion of the liquid gives only terms of a higher order of smallness. CHAPTER IV CONSTANT MAGNETIC FIELD §27. Constant magnetic field A constant magnetic field in matter satisfies two of Maxwell's equations, obtained by averaging the microscopic equations lde 4tt divh = 0, curlh = — — +— P \. (27.1) c ot c The mean magnetic field is usually called the magnetic induction and denoted byB: n = B. (27.2) Hence the result of averaging the first equation (27.1) is divB = 0. (27.3) In the second equation, the time derivative gives zero on averaging, since the mean field is supposed constant, and so we have curlB = (4*r/<0/»v.' (27.4) The mean value of the microscopic current density is in general not zero in either conductors or dielectrics. The only difference between these two classes is that in dielectrics we always have J^F.df=0, (27.5) where the integral is taken over the area of any cross-section of the body ; in conductors, this integral need not be zero. Let us suppose to begin with that there is no net current in the body if it is a conductor, i.e. that (27.5) holds. The vanishing of the integral in (27.5) for every cross-section of the body means that the vector pv can be written as the curl of another vector, usually denoted by cM : pv = ccurlM, (27.6) where M is zero outside the body; compare the similar discussion in §6. For, integrating over a surface bounded by a curve which encloses the body and nowhere enters it, we have Jpv«^lf = c JcurlM'df = c|M»dl = 0. 113 114 Constant Magnetic Field §27 The vector M is called the magnetisation of the body. Substituting it in (27.4), we find curlH = 0, (27.7) where the vector H and the magnetic induction B are related by B = H + 4ttM, (27.8) which is analogous to the relation between the electric field E and induction D. Although H is, by analogy with E, usually called the magnetic field, it must be remembered that the true mean field is really B and not H. To see the physical significance of the quantity M, let us consider the total magnetic moment due to all the charged particles moving in the body. By the definition of the magnetic moment, t this is jrxfivdVJ2c = $Jr xcurlMdF. Since pv = outside the body, the integral can be taken over any volume which includes the body. We transform the integral as follows : JrxcurlMdF = -jr x(Mxdf)- J(Mxgrad) xrdF. The integral over the surface outside the body is zero. In the second term we have (Mxgrad)xr = — M divr+M = — 2M. Thus we obtain (rxpfdV = jMdF. (27.9) We see that the magnetisation vector is the magnetic moment per unit volume.J The equations (27.3) and (27.7) must be supplemented by a relation be- tween H and B in order to complete the system of equations. For example, in non-ferromagnetic bodies in fairly weak magnetic fields, B and H are linearly related. In isotropic bodies, this linear relation becomes a simple proportionality : B = fjH. (27.10) The coefficient /x is called the magnetic permeability. We also have M = %H, where the coefficient x = G*-l)/4* (27.11) is called the magnetic susceptibility. 1 2c t See The Classical Theory of Fields, §5-9, Addison-Wesley Press, Cambridge (Mass.), 1951; Pergamon Press, London, 1959. X The quantity M is completely determined only when this relation is established. The relation (27.6) inside the body, and M = outside it, do not uniquely define M: the gradient of any scalar could be added to M inside the body without affecting (27.6) (cf. the similar remark in the first footnote to §6). §27 Constant magnetic field 115 Unlike the dielectric constant e, which always exceeds unity, the magnetic permeability may be either greater or less than unity. (It is, however, always positive, as we shall prove in §30. The reason for the differing behaviour of jLt and € is discussed in §31.) The magnetic susceptibility x mav corres- pondingly be either positive or negative. Another, quantitative, difference is that the magnetic susceptibility of the great majority of bodies is very small in comparison with the dielectric susceptibility. This difference arises because the magnetisation of a (non- ferromagnetic) body is a relativistic effect, of order v 2 /c 2 , where v is the velocity of the electrons in the atoms, t From the equations div B = 0, curl H =0 it follows (cf. §6) that at a boundary between two different media we must have B ln = B 2n , Hit = H*. (27.12) This system of equations and boundary conditions is formally identical with those for the electrostatic field in a dielectric in the absence of free charges, differing only in that E and D are replaced by H and B respectively. Since curlH = 0, we can put H = — grad^; the equations for the potential ifi are the same as those for the electrostatic potential. Thus the solutions of the various problems of electrostatics discussed in Chapter II can be im- mediately applied to problems with a constant magnetic field. In particular, the formulae derived in §8 for a dielectric ellipsoid in a uniform electric field hold also, with appropriate substitutions, for a magnetic ellipsoid in a uniform magnetic field. The tangential component of the magnetic induction, unlike its normal component, is discontinuous at a surface separating two media. The magni- tude of the discontinuity can be related to the current density on the surface. To do this, we integrate both sides of equation (27.4) over a small interval A/ crossing the surface along the normal. We then let A/ tend to zero ; the integral Jpv d/ may tend to some finite limit. The quantity g = J>d/ (27.13) may be called the surface current density; it gives the charge passing per unit time across unit length of a line in the surface. We take the direction of g at a given point on the surface as the jy-axis, and the direction of the normal from medium 1 to medium 2 as the #-axis. Then the integration of equation (27.4) gives r/dB x BB g \ 4ir = 4tt J \ 8z dx J c c Since B x is continuous, the derivative 8B x /dz is finite, and so its integral tends to zero with A/. The integral of BB z jdx gives the difference in the t The ratio vjc appears with H in the Hamiltonian of the interaction of the body with the magnetic field, and again in the magnetic moments of the atoms or molecules. 116 Constant Magnetic Field §28 values of B z on the two sides of the surface. Thus B^ z —B\ z = —fagfc. This can be written in vector form : 4rrg/c = n x(B 2 - Bi) = 4?rn x(M 2 -Mi), (27.14) where n is a unit vector along the normal into region 2; the last member of (27.14) is obtained by using the continuity of the tangential component of H. §28. Magnetic symmetry of crystals There is a profound difference between the electric properties of crystals and their magnetic properties, which results from a difference in the be- haviour of charges and currents with respect to a change in the sign of the time. The invariance of the equations of motion with respect to this change means that the formal substitution t -> —t, on being applied to any state of thermodynamic equilibrium of a body, must give some possible equilibrium state. There are then two possibilities : either the state obtained by changing the sign of t is the same as the original state, or it is not. In this section we denote by p(x, y y z) and j(x, y, z) the true (micro- scopic) charge and current densities at any given point in the crystal, averaged only over time, and not over "physically infinitesimal" volumes as in the macroscopic theory. These are the functions which determine the electric and magnetic structure of the crystal respectively. When t is replaced by —t, j changes sign. If the state of the body remains unchanged, it follows that j = — j, i.e. j = 0. Thus there is a reason why bodies can exist in which the function }(x, y, z) is identically zero. In such bodies, not only the current density but also the (time) average magnetic field and magnetic moment vanish at every point (we are speaking, of course, of states in the absence of an external magnetic field). Such bodies may be said to have no "magnetic structure", and indeed the great majority of bodies fall into this category. The charge density />, on the other hand, is unchanged when t -> —t. There is therefore no reason why this function should be identically zero. In other words, there are no crystals without "electric structure", and herein lies the essential difference, mentioned at the beginning of this section, between the electric and the magnetic properties of crystals. Let us now consider crystals for which the change from t to — t results in a change of state, so that j # 0. We shall say that such bodies have a magnetic structure. First of all, we note that, although j is not zero, there can be no total current in an equilibrium state of the body, i.e. the integral j j dV taken over an elementary cell must always be zero.t Otherwise the t It should be emphasised that the cell spoken of here is the true elementary cell, whose definition involves the magnetic structure of the crystal, and which may be different from the purely crystallographic cell, which relates only to the symmetry of the charge distribu- tion in the lattice. §28 Magnetic symmetry of crystals 117 current would produce a macroscopic magnetic field, and the crystal would have a magnetic energy per unit volume increasing rapidly with its dimen- sions. Since such a state is energetically unfavourable, it could not corres- pond to thermodynamic equilibrium. The currents j may, however, produce a non-zero macroscopic magnetic moment, i.e. the integral JrxjdF, again taken over an elementary cell, need not be zero. Accordingly, the bodies for which j ^ may be divided into two types: those in which the macroscopic magnetic moment is not zero, called ferromagnetics, and those in which it is zero, called antiferro- magnetics. The symmetry of the current distribution j can be conveniently regarded as the symmetry of the arrangement and orientation of the magnetic moments of the individual atoms in the crystal. If j = 0, all these moments are changing their orientation in the course of time in an entirely random manner, so that the mean value of each moment is zero. In a ferromagnetic, the atomic moments are oriented mainly in one direction, causing a non-zero total moment in each elementary cell. In an antiferromagnetic, the mean atomic moments are not zero, i.e. they are not randomly oriented, but they are so arranged as to balance one another in each cell. What are the possible symmetry groups of the current distribution ( x, y, z)} This symmetry contains, first of all, the usual rotations, reflections and translations, and so the possible symmetry groups of j always include the usual 230 crystallographic space symmetry groups. These, however, are by no means all. As has already been mentioned, the substitution t -> —t changes the sign of the vector j. For this reason a new symmetry element comes in, namely that resulting from the reversal of all currents ; we shall denote this transformation by R. If the current distribution itself has the symmetry R, it follows that j = — j, i.e. j = 0, and the body has no mag- netic structure. A non-zero function }(x, y, z) may, however, be symmetrical with respect to various combinations of R with the other symmetry elements (rotations, reflections and translations). Thus the problem of determining the possible types of symmetry of the current distribution (the magnetic space groups) amounts to the enumeration of all possible groups containing both the transformations of the ordinary space groups and the combinations of these with R. If the symmetry of the current distribution is given, the crystallographic symmetry of the particle distribution, which is also the symmetry of the function p(x, y, z), is determined. It is the symmetry of the space group which is obtained from the symmetry group of j by formally regarding the transformation R as the identity (as it is with respect to the function p). If only the macroscopic properties of the body are of interest, however, it is not necessary to know the complete symmetry group of the function j(#, y, z). These properties depend only on the direction in the crystal, and the translational symmetry of the lattice does not affect them. As regards crystallographic structure, the "symmetry of directions" is specified by the 118 Constant Magnetic Field §28 32 crystal classes. These are the symmetry groups consisting of rotations and reflections only, and are obtained from the space groups by regarding every translation as the identity, and the screw axes and glide planes as simple axes and planes of symmetry. As regards the magnetic properties, the macroscopic symmetry can be classified by groups (consisting of rotations, reflections and combinations of these with R) which may be called the mag- netic crystal classes. They are related to the magnetic space groups in the same way as the ordinary crystal classes to the ordinary space groups. They include, firstly, the usual 32 classes, and those classes augmented by the element R. These augmented classes are, in particular, the macroscopic symmetry groups for all bodies having no magnetic structure, but they occur also in bodies with magnetic structure. This happens if the magnetic space symmetry group of such bodies includes R only in combination with trans- lations, and not alone. There are also 58 classes in which R enters only in combination with rotations or reflections. Each of these becomes one of the ordinary crystal classes if R is replaced by the identity, t It should be noted that the occurrence of magnetic structure (ferro- magnetic or antiferromagnetic) always involves comparatively weak inter- actions, t Hence the crystal structure of a magnetic body is only a slight modification of that in the non-magnetic phase, which usually changes into the magnetic phase when the temperature is reduced. In this respect ferro- magnetics, in particular, differ from ordinary pyroelectrics, but are analogous to ferroelectrics. If the magnetic crystal class of a body is specified, its macroscopic mag- netic properties are qualitatively determined. The most important of these is the presence or absence of a macroscopic magnetic moment, i.e. of spon- taneous magnetisation in the absence of an external field. The magnetic moment M is a vector, behaving as an axial vector (the vector product of two polar vectors) under rotation and reflection, and changing sign under the operation R. The crystal will possess spontaneous magnetisation if it has one or more directions such that a vector M in that direction and having f These classes are isomorphous with those discovered by A. V. Shubnikov for the symmetry groups of polyhedra with faces of two colours (called by him groups of mixed polarity). The element R corresponds to the operation of changing the colour of each face. See A. V. Shubnikov, Symmetry and antisymmetry of finite figures (Simmetriya i anti- simmetriya konechnykh figur), Moscow, 1951. A direct derivation as symmetry groups for the magnetic properties of bodies is given by B. A. Tavger and V. M. Zaitsev, Zhurnal eksperimental'noi i teoreticheskoi fiziki 30, 564, 1956; Soviet Physics JETP 3, 430, 1956. The total number of magnetic space groups is 1651 ; they are derived (as Shubnikov groups) by N. V. Belov, N. N. Neronova and T. S. Smirnova, Trudy Instituta Kristallo- grafii 11, 33, 1955 ; A. M. Zamorzaev, Kristallografiya 2, 15, 1957; Soviet Physics: Crystallo- graphy 2, 10, 1958. % The exchange interaction between the magnetic moments of atoms usually results in the saturation of the valency bonds and the formation of non-magnetic structures. A mag- netic structure results only from the relatively weak exchange interactions between deep- lying d and / electrons of atoms of elements in the intermediate groups of Mendeleev's system. §29 The magnetic field of a constant current 119 the above-mentioned properties is invariant under all transformations belong- ing to the magnetic crystal class concerned. We must again emphasise the difference between these (macroscopic) properties and the corresponding ones in electrostatics. The latter are qualitatively determined by the ordinary crystal class. In particular, a body is pyroelectric if its crystal class admits the existence of a polar vector P (the polarisation). It would, however, be entirely wrong to base conclusions about the existence or otherwise of a macroscopic magnetic moment on the behaviour of the axial vector M with respect to the transformations of the non-magnetic crystal class of the body concerned. As an illustration, let us consider a tetragonal lattice of identical atoms, with magnetic moments parallel to the tetragonal axis.t The magnetic crystal class comprises the fourth-order axis C4 (z) , two second-order axes combined with jR {C^R and C2 (y) R), the plane of symmetry ofc (z) perpendicu- lar to the z-axis, and two vertical planes of symmetry combined with jR (o-v^R and cr^R). This group admits the existence of a vector M along the tetragonal axis. The crystallographic symmetry class is obtained by replacing R by unity, i.e. it is the class D$h. This class does not admit the existence of an axial vector M, since the components M x , M y , M z would change sign on reflection in the planes o- (z) , a te) , oW respectively. The properties of bodies with a spontaneous non-zero macroscopic magnetic moment (ferromagnetics) will be discussed in detail in Chapter V. In all other crystals, in fairly weak fields, the relation between B and H is linear: Bi = MkHjc, (28.1) with no inhomogeneous term. The magnetic permeability tensor fx^ is sym- metrical. This follows from thermodynamic relations which will be derived in §30, in exactly the same way as the symmetry of the tensor eijc (§13). We may also mention two further phenomena possible in principle. One is piezomagnetism, resulting from the existence of a linear relation between the magnetic field and the deformation of a body (analogously to piezo- electricity; see §17). The other results from a linear relation between the magnetic and electric fields in a substance, which would cause, for example, a magnetisation proportional to the electric field. % Both these phenomena can occur for certain magnetic crystal symmetry classes. || §29. The magnetic field of a constant current If a conductor carries a non-zero total current, the mean current density in it can be written as pv = c curl M+j. The first term, resulting from the f Such, for example, is the lattice of iron in its ferromagnetic phase. Crystallographically, it is a cubic lattice slightly distorted along one of the fourth-order axes. % Effects of this type but quadratic in the field must in principle exist even in isotropic bodies, but are negligible. || Examples of these are given by I. E. DzyaloshinskiI, Zhurnal iksperimentaVnol i teore- ticheskoi fiziki 33, 807, 1957; 37, 881, 1959 (Soviet Physics JETP 6 (33), 621, 1958; 10 (37), 628, 1960). 120 Constant Magnetic Field §29 magnetisation of the medium, makes no contribution to the total current, so that the net charge transfer through a cross-section of the body is given by the integral Jj-df of the second term. The quantity j is called the conduc- tion current density A The statements made in §20 apply to this current; in particular, the energy dissipated per unit time and volume is E«j. The distribution of the current j over the volume of the conductor is given by the equations of §20, which do not involve the magnetic field due to j itself, if we neglect the effect of this field on the conductivity of the body. Hence the magnetic field of the currents must be determined for a given current distribution. The equations satisfied by this field differ from those in §27 by the presence of a term 4ttJ/c on the right-hand side of (27.7): div B = 0, (29.1) curlH = 4vjjc. (29.2) The conduction current density j, which is proportional to the electric field, does not become infinite, and in particular is finite on a surface separating two media. Hence the term on the right of (29.2) does not affect the boun- dary condition that the tangential component of H is continuous. To solve equations (29.1), (29.2), it is convenient to use the vector potential A, defined by B = curl A, (29.3) so that equation (29.1) is satisfied identically. Equation (29.3) does not uniquely define the vector potential, to which the gradient of any scalar may be added without affecting (29.3). For this reason we can impose on A a further condition, which we take to be divA = 0. (29.4) The equation for A is obtained by substituting (29.3) in (29.2). If the linear relation B = juH holds we have curl /-curl a) = 4irj/c. (29.5) In this form the equation is valid for any medium, homogeneous or not. In a homogeneous medium, p = constant, and since curl curl A = grad div A— A A = — A A we find from (29.5) A A = -4ir/ij/c. (29.6) If we have two or more adjoining media of different magnetic permeability fi, the general equation (29.5) has the form (29.6) in each homogeneous t The quantity c curl M is sometimes called the molecular current density. This name, however, is not in complete accordance with the actual physical picture of motion of charges in a conductor. For example, in a metal the conduction electrons, as well as those moving in the atoms, contribute to the magnetization Jl. §29 The magnetic field of a constant current 121 medium, while at the interfaces the tangential component of the vector (l//i.) curl A must be continuous. Moreover, the tangential component of A itself must be continuous, since a discontinuity would mean that the induction B was infinite at the boundary. The field equations are simpler in the two-dimensional problem of finding the magnetic field in a medium infinite and homogeneous in one direction (which we take as the ^-direction), the currents which produce the field being everywhere in that direction, with the current density j z =j depend- ing only on si and y. We make the plausible assumption (to be confirmed by the result) that the vector potential of such a field is also in the ^-direction: A z — A(x, y). The condition (29.4) is then satisfied identically; the magnetic field is everywhere parallel to the ry-plane. We denote by k a unit vector in the ^-direction; then curl A = curl /4k = grad^4 xk, curll-curlAl = curl ( xk) = -kdiv- . Hence equation (29.5) becomes grad.4 4tt div-? = fay), (29.7) fJ, c i.e. we in fact obtain one equation for the one scalar quantity A(x, y). For a piecewise homogeneous medium, (29.7) becomes AA = -47r{jLJ(x,y)lc, (29.8) with the boundary condition that A and (l//u,) dA/dn are continuous at an interface, t The magnetic field is easily found if the current distribution is sym- metrical about the #-axis: j z =j(r) (where r is the distance from that axis). In this case the lines of magnetic force are evidently the circles r — constant. The magnitude of the field is found at once from the formula (fH-dl = — fj.df, (29.9) which is the integral form of (29.2). Thus H(r) = 2J(r)/cr, (29.10) where J(r) is the total current within the radius r. t It should be noticed that the two-dimensional problem with a constant magnetic field is equivalent to the two-dimensional electrostatic problem of determining the electric field due to extraneous charges of density />«(*, y) in a dielectric medium. The equation to be solved in the latter problem is div(cgrad^) = — 4irp e *, where j> is the field potential; this differs from (29.7) only in that A,j/c and p are replaced by <f>, p ex and 1/e respectively. The boundary conditions on A and <f> are the same. A difference occurs, however, on passing to E and B from <f> and A respectively. The vectors E = — grad <f> and B = curl A are the same in magnitude but in perpendicular directions at any given point. 122 Constant Magnetic Field §29 The reduction of the vector equation (29.5) to a single scalar equation is possible also if the current distribution is axially symmetrical and has in cylindrical co-ordinates r, <j), z the form j r =j z = 0, j$ = j(r,z). We seek the vector potential in the form A r = A z = 0, A$ = A(r, z). The components of the magnetic induction B = curl A are B r = — 8A\8z> B z — (llr)d(rA)jdr, B$ = 0, and the ^-component of equation (29.2) gives 8 /l 8A\ 8 1 1 d \ 4tt rHr + tHt^ = — j{r > z) - (29 - n) czXjjL cz J orX/jLT or J c The equations for the magnetic field of the currents can be solved in a general form in the important case where the magnetic properties of the medium may be neglected, i.e. where we can put ju. = 1. The vector poten- tial then satisfies in all space the equation AA = — 4vjjc with no conditions at the interfaces between different media (including the surface of the conductor on which the current flows). The solution of this equation which vanishes at infinity ist c) R dV, (29.12) where R is the distance from the volume element dV to the point at which A is to be calculated. In taking the curl of this equation, we must remember that the integrand j/R is to be differentiated with respect to the co-ordinates of this point, of which j is independent, so that curl QIR) = grad (1/12) X j = -R X j/#3, where the radius vector R is from dV to the point under consideration. Thus ixR dV. (29.13) B = H = lf If the conductor on which the current flows is sufficiently thin (a thin wire), and if we are interested only in the field in the surrounding space, the thickness of the wire may be neglected. In what follows we shall often dis- cuss such linear currents. The integration over the volume of the conductor is then replaced by an integration along its length: the formulae for linear currents are obtained from those for volume currents by making the substi- tution }dV ->Jdl, where / is tne tota ^ current in the conductor. For example, from formulae (29.12) and (29.13) we have J fdl /rdlxR /nni ^ A -ih H = l cf-^- (29 - l4) The latter formula is Biot and Savart's law. t See The Classical Theory of Fields, §5-8. §29 The magnetic field of a constant current 123 This simple formula for the magnetic field of a linear current does not depend on the assumption that fi = 1. Since we neglect the thickness of the conductor, no boundary conditions at its surface need be applied, and the magnetic properties of the conducting material are of no importance (it may even be ferromagnetic). The solution of equation (29.6) for the field in the medium surrounding the conductor is therefore A -7h? b = t)-r^> (2915) whatever the magnetic susceptibility of that medium. Thus the presence of the medium simply changes the magnetic induction by a factor /u. The field H = B/yM is unchanged. The problem of determining the magnetic field of linear currents can also be solved as a problem of potential theory. Since we neglect the volume of conductors, we are in fact determining the field in a region containing no currents except along certain line singularities. In the absence of currents, a constant magnetic field has a scalar potential, which in a homogeneous medium satisfies Laplace's equation. There is, however, an important difference between the magnetic field potential and the electrostatic poten- tial : the latter is always a one- valued function, because curl E = in all space (including charged regions) and so the change in the potential in going round any closed contour (i.e. the circulation of E round that contour) is zero. The circulation of the magnetic field round a contour enclosing a linear current is not zero, but ^nj\c. Hence the potential changes by this amount on each passage round a contour enclosing a linear current, i.e. it is a many-valued function. If the currents lie in a finite region of space (and fx = 1 everywhere), the vector potential of the magnetic field at a great distance from the conductors is A = J£xR/ J R 3 , (29.16) where Jt = jrxjdVI2c (29.17) is the total magnetic moment of the system, t For a linear current, this becomes M =jjrxdl/2c, and can be transformed into an integral over a surface bounded by the line of the current. The product df = \t X dl is equal in magnitude to the area f See The Classical Theory of Fields, §5-9. In the derivation there given, we use explicitly the idea of a current as the result of the motion of individual charged particles. Such a derivation is, of course, quite general, but formula (29.16) can also be obtained by macro- scopic arguments (see Problem 4). 124 Constant Magnetic Field §29 of the triangular surface element formed by the vectors r and dl. The vector Jdf is independent of the particular surface (bounded by the current) over which it is taken. Thus the magnetic moment of a closed linear current is M = jjdf/c. (29.18) In particular, for a plane closed linear current the magnetic moment is simply JS/c, where S is the area of the plane enclosed by the current. To conclude this section, we may briefly discuss the energy flux in a conductor. The energy dissipated as Joule heat in the conductor is derived from the energy of the electromagnetic field. In a steady state, the "equation of continuity" which expresses the law of conservation of energy is -divS = jE, (29.19) where S is the energy flux density, given in a conductor by S = cExH/4rr, (29.20) which is formally the same as the expression for the Poynting vector for the field in a vacuum. This is easily verified directly by calculating div S from the equations curlE = and (29.2), when we obtain (29.19). Formula (29.20) also follows independently from the obvious condition that the normal component of S must be continuous at the surface of a conductor, if we use the continuity of E* and H« and the validity of (29.20) in the vacuum outside the body. PROBLEMS t Problem 1. Determine the scalar potential of the magnetic field of a closed linear current. Solution. We transform the line integral into one over a surface bounded by the line, obtaining J r i B = curl A = — - (df'grad) grad — c J R (where we have used the fact that A(1/JR) = 0). Since B = —grad <f>, we have for the scalar potential ^-Jdf.grad-=--j— . The integral is, geometrically, the solid angle ii subtended by the closed contour at the point considered. The above-mentioned many-valuedness of the potential is seen from the fact that, as this point describes a closed path round the wire, the angle Q changes suddenly from 2n to — lit. Problem 2. Find the magnetic field of a linear current flowing in a circle of radius a. Solution. We take the origin of cylindrical co-ordinates r, <f>, z at the centre of the circle, with the angle <f> measured from the plane which passes through the ar-axis and the point at In Problems 1-4, fi ■■!. §29 The magnetic field of a constant current 125 which the field is calculated. The vector potential has only one component, A* — A{r, z), and by formula (29.14) we have A * = ~J J £ cos «f> dl R c J Via a cos <f> d<f> ■\/(a 2 +r 2 +z 2 — 2ar cos <f>) Putting 6 = K^— w )» we find A^^rJ^Kl-mK-E], where k 2 — 4arl[(a+r) 2 +z 2 ], and K and E are complete elliptic integrals of the first and second kinds : dd. The components of the induction are dA* J 2z a r = — crV[(a+r)*+z*] L (a-r)*+z* J' 1 a J 2 r a 2 —r 2 —z 2 1 r or c v[(a+r) a +« 2 ]L (a— r) 2 +z 2 1 Here we have used the easily verified formulae eK E K dE _ E-K dk ~ kil-k 2 ) k' dk~ k ' On the axis (r = 0) we have B T = 0, B t = 2ira 2 J/c(a 2 +z 2 ) 3 ' 2 , as can also be found by a straightforward calculation. Problem 3. Determine the magnetic field in a cylindrical hole in a cylindrical conductor of infinite length carrying a current uniformly distributed over its cross-section (Fig. 17). x,x' Fig. 17 126 Constant Magnetic Field §30 Solution. If there were no hole, the field in the cylinder would be given by H'x = —litjylc, H' y = 2-njxjc. The dimensions and axes are as shown in Fig. 17. If a current of density —j were to flow in the inner cylinder, it would produce a field H" x = 2njy'Jc, H" v = —l-njx'/c. The required field in the hole is obtained by superposing these two fields. Since x—x' = OO' = h, and y — y', we have H x = 0, H v = lirjhlc = 2A//(6 2 — a z )c, i.e. a uniform field in the y-direction. Problem 4. Derive from (29.12) the formula (29.16) for the vector potential of the field far from the currents. Solution. We write R = Ro— r, where Ro and r are the radius vectors from the origin (situated somewhere among the currents) to the point considered and to the volume element dV respectively. Expanding the integrand in powers of r and using the fact that J" j dV == 0, we have Ai = (RklcR 3 ) J" xkjt dV. The suffix to R is omitted. Integrating by parts the identity J XiXk div j dV = gives J (jtXk+jkXi) dV — 0. Hence we can write Ai = (Rkl2cR s )I(xkji-Xij k ) dV, which is (29.16). Problem 5. Determine the magnetic field produced by a linear current in a magnetically anisotropic medium (A. S. Viglin). Solution. In the anisotropic medium surrounding the conductor we have div B = mtBHkldxt = 0, (1) where /*(* is the magnetic permeability tensor of the medium. Instead of introducing the vector potential by B = curl A, we use another vector C defined by Hi = eikifUcmSCildXm, (2) where etki is the antisymmetrical unit tensor. Then equation (1) is again satisfied identically. We can also impose on the vector C thus defined the condition divCs BCi/Bxi = 0. (3) Substituting (2) in curl H = 4-irj/c, we obtain em dHi/dxk = —pkpd z Ci[dXkdx p = 4irjtlc (using the condition (3) and the fact that etkieimn = ^im^kn—^in^m). The equation thus obtained for C is the same in form as that for the electric field potential resulting from charges in an anisotropic medium (§13, Problem 2). The solution is jdF -;/■ V(MrtiW where |f*| is the determinant of the tensor ink, and R the radius vector from the point con- sidered to dV. For a linear current we have / X dl cVM J Vi^ikRiRk) §30. Thermodynamic relations in a magnetic field The thermodynamic relations for a magnetic substance in a magnetic field are, as we shall see, very similar to the corresponding relations for a dielectric in an electric field. Their derivation, however, is quite different from that given in §10. This difference is ultimately due to the fact that a magnetic field, unlike an electric field, does no work on charges moving in it (since the force acting on a charge is perpendicular to its velocity). Hence, to calculate the change in the energy of the medium when a magnetic field is applied, we must examine the electric fields induced by the change in the magnetic field and determine the work done by these fields on the currents which produce the magnetic field. §30 Thermodynamic relations in a magnetic field 127 Thus the equation which relates electric and variable magnetic fields must be used. This equation is 1 dB curlE= ; (30.1) c ot it follows immediately on averaging the microscopic equation (1.3). During a time 8t, the field E does work 8t $ }*EdV on the currents j. This quantity with the opposite sign is the work 8R "done on the field" by the external e.m.f. which maintains the currents. Substituting j = c curl H/47T, we have 8R=-8t~ fE.curlHdF 4ttJ = 8t—(diy(ExH)dV-8t—(H'CurlEdV. The first integral, on being transformed to an integral over an infinitely distant surface, is seen to be zero. In the second integral we substitute curlE from (30.1) and put SB = 8t dB[dt for the change in the magnetic induction, obtaining finally 8R = J*H.SBdF/47r. (30.2) This formula appears entirely analogous to the expression (10.2) for the work done in an infinitesimal change in the electric field. It must be pointed out, however, that the physical analogy between the two formulae is actually not complete, since H, unlike E, is not the mean value of the microscopic field. Having derived formula (30.2), we can write down all the thermodynamic relations for a magnetic substance in a magnetic field by analogy with those given in §10 for a dielectric in an electric field, simply replacing E and D by H and B respectively. We shall give some of these formulae here for purposes of reference. The differentials of the total free energy and the total internal energy are 8& = -^Sr+jH.8BdF/4ir, (30.3) 8% = T8y + jU'8BdV/^jT y and those of the corresponding quantities per unit volume are dF= -Sdr+£dp+H.dB/4ir, dU= TdS+£dp + H-dBl47r. ' ' 128 Constant Magnetic Field §30 We need also the thermodynamic potentials V = C/-H-B/4tt, F = F-H.B/47T, (30.5) for which dF = - SdT+£d/>-B.dH/47r, dfr= rdS+£d/>-B.dH/477. ( ' ' If the linear relation B = piH. holds, we can write the expressions for all these quantities in the form U = U (S, P ) + #78^, F = F (T, p) + &/**?, V = U (S,p)-p,H2IS7r, P = F (T,p)-tJiH2/STT. l The work 8R (or, what is the same thing, the change 8F at constant temperature) can be written in a different form, in terms of the current density and the vector potential of the magnetic field. For this purpose we put SB = curl SA and (SJ*> = _ fH-curlSAdP = fdiv(Hx8A)dF+— fsA.curlHdF. AttJ AttJ The first integral is again zero, and the second gives (h&) T = Jj.SAdF/c. (30.8) A similar transformation gives (&^) r = -J*A.8jdF/c. (30.9) It is useful to note that in macroscopic electrodynamics the currents (sources of the magnetic field) are mathematically analogues of the poten- tials, not of the charges (the sources of the electric field). This is seen by comparing formulae (30.8) and (30.9) with the corresponding results for an electric field: (8&) T =j<f>8 P dV, (&^) T = - fptydV (30.10) (see (10.13), (10.14)). We observe that the charges and potentials appear in these formulae in the opposite order to the currents and potentials in formu- lae (30.8), (30.9). On account of the complete formal correspondence between the thermo- dynamic relations (expressed in terms of field and induction) for electric and magnetic fields, the thermodynamic inequalities derived in §18 can also §31 The total free energy of a magnetic substance 129 be applied to magnetic fields. In particular, we have seen that it follows from these inequalities that e > 0. In the electric case this result was of no interest, because it was weaker than the inequality e > 1 which follows on other grounds. In the magnetic case, however, the corresponding inequality [j, > is very important, as it is the only restriction on the values which can be taken by the magnetic permeability. §31. The total free energy of a magnetic substance In §11 expressions have been derived for the total free energy $F of a dielectric in an electric field. One of the thermodynamic properties of this quantity is that the change in it gives the work done by the electric field on the body when the charges producing the field remain constant. In a mag- netic field a similar part is played by the free energy &> since for given currents producing the field the change in & is the work done on the body. The following derivation is entirely analogous to that given in §11. The "total" quantity & is defined as SF -J(' + S dr " (3U) where <?) is the magnetic field which would be produced by the given cur- rents in the absence of the magnetisable medium. The plus sign appears in the parenthesis (instead of the minus sign as in (11.1)) because the value of & for a magnetic field in a vacuum is - J(§ 2 /87r) dV (see (30.7)). The integration in (31.1) is taken over all space, including the volume occupied by the conductors in which flow the currents producing the field, t Let us calculate the change in & (for a given temperature and no depar- ture from thermodynamic equilibrium in the medium) corresponding to an infinitesimal change in the field. Since 8F = -B«SH/4tt, we have S#= -J(B-SH-|).8^)dr/47r = -J(H-^).S^dr/47r-|B.(SH-8^)dr/47r-J(B-H).^dF/47r. (31.2) Introducing the vector potential % of the field $), we can write in the first term (H-£).S£ = (H-£).curlS$l = div[8H.(H-£)] + $2l.curl(H-$). t In §11 we took the integration in (11.1) over all space except the volume occupied by the charged conductors producing the field. This was possible because there is no electric field in a conductor, charged or not. There is a magnetic field, however, inside the conduc- tors which carry the currents, and they cannot be excluded in calculating the total free energy. 130 Constant Magnetic Field §31 By definition, the fields H and $ are produced by the same currents j, the distribution of which over the volume of the conductors is (see §29) inde- pendent of the field which they produce, i.e. is independent of the presence or absence of magnetic substances in the surrounding medium. Hence curlH and curl£ are both equal to 47rj/c, and so curl(H— £) = 0. The integral of div[S$l«(H — .£))] is transformed into an integral over an infinitely distant surface, and so vanishes. Similarly, we see that the second term on the right of (31.2) is zero; thus S#= -J(B-H).S^dr/477 = -JM>S$dV. (31.3) The expression which we have obtained for S«^ is exactly similar to (11.3) for the electrostatic problem. In particular, in a uniform magnetic field ^ we have for d^ an expression analogous to (11.5): && = -SP&T-J(-&%, (31.4) where M is the total magnetic moment of the body. Without repeating the subsequent calculations, we shall write down the following formulae by analogy with those in §11. If the linear relation B = juH holds, we have #-Sr (V,T) = -J*$.MdF. (31.5) In particular, if the external field is homogeneous, then &-&<&y, T) = -%%'JZ. (31.6) In the general case of an arbitrary relation between B and H, & can be calculated from the formula #= \{ P+ ~t~~ iM '*) dV U H-B \ = Jr~"~&r~* M '*) dr - (3L7) In §11 we gave also the simpler formulae obtained when the dielectric susceptibility is small. The analogous case for the magnetic problem is especially important because, as mentioned above, the magnetic suscepti- bility of the majority of bodies is indeed small. In this case f-,P = -l x j&dV. (31.8) §32 The energy of a system of currents 131 We can also derive results for the magnetic field analogous to those obtained in §14. These concern the change in the thermodynamic quantities resulting from an infinitesimal change in the magnetic permeability fi, the field sources being assumed unchanged. It is clear from the foregoing that we must consider the change in «^, and not that in 3F as in §14. We shall not repeat the derivation, which is similar to that of (14.1), but merely give the result : S#= -J8(jLH2dV/87T. (31.9) In §14 we used this formula to deduce that the dielectric susceptibility of any substance is positive. In the magnetic case we cannot draw this conclu- sion, and the magnetic susceptibility may be of either sign. The reason for this marked difference is that the Hamiltonian of a system of charges moving in a magnetic field contains not only terms linear in the field (as in the electric case) but also quadratic terms. Hence, in determining the change in the free energy of the body in the magnetic field by means of perturbation theory as in (14.2), we have a contribution in the first approximation as well as the second. In such a case no general conclusion can be drawn concerning the sign of the variation. It is positive for paramagnetic bodies and negative for diamagnetic ones. In §14 we also drew conclusions concerning the direction of motion of bodies in an electric field. Similar conclusions follow from (31.9), but, since fi may be either greater or less than 1, there is no universal result. For example, in an almost uniform field paramagnetic bodies {p, > 1) move in the direction of H increasing, and diamagnetic bodies (ji < 1) in the opposite direction. §32. The energy of a system of currents Let us consider a system of conductors with currents flowing in them and assume that neither the conductors nor the medium surrounding them are ferromagnetic, so that B = fiK everywhere. According to §30, the total free energy of the system is given in terms of the magnetic field of the currents by & = JH-BdVj&n. (32.1) Here we omit the quantity «^o> which is a constant (at a given temperature) and is not related to the currents. The integration in (32.1) is taken over all space, both inside and outside the conductors. The same energy can also be expressed in terms of the currents by means of the integral & = JA-jdVI2c; (32.2) 132 Constant Magnetic Field §32 cf. the derivation of (30.8) from (30.2). Here the integration extends only over the conductors, because j = outside them. Since the field equations are linear, the magnetic field can be written as the sum of the fields resulting from each current alone with no current in the other conductors: H = SH«. Then the total free energy (32.1) is & = S^ aa + Z&ab, (32.3) a a>b v ' where &aa = jH a .B a dF/87r, & ab = jHa.BfrdF/477. (32.4) We have put & a b = ^ baj since IVB 6 = juHa'Hb = Hft.B , where [i is the magnetic permeability at any point. The quantity & aa may be called the free self-energy of the current in the ath conductor, and && the interaction energy of the ath. and bth. conductors. It should be borne in mind, however, that these names are strictly correct only if the magnetic properties of both the conductors and the medium are neglected. Otherwise the field, and therefore the energy, of each current depend on the position and magnetic permeability of the other conductors. The quantities (32.4) can also be expressed in terms of the currents j in each conductor, in accordance with formula (32.2) : &am = j)a-AadV a l2c, & ab = j} a .A b dV a /c = jj b 'AadV b /c. (32.5) The integral in ^ aa is here taken only over the volume of the ath conductor; iFab can be written as either of the two expressions, in which the integration is over the volume of the ath and Mi conductor respectively. When the distribution of the current density over the volume of the conductor is given, «^ ao depends only on the total current J a passing through a cross-section. Both the current density j and the field which it produces will be proportional to J a . Hence the integral BF^ is proportional to J a 2 , and we write it ^aa = Laaja 2 l2c*, (32.6) where L aa is called the self-inductance of the conductor. Similarly, the interaction energy of two currents is proportional to the product J a J b : &ab = Labjajb/c*. (32.7) The quantity Lab is called the mutual inductance of the conductors. Thus the total free energy of a system of currents is * - ^2 W^+^W*/* - ^22 W«ft- (32.8) a a>b a b §32 The energy of a system of currents 133 The condition that this quadratic form should be positive definite places certain restrictions on the values of the coefficients. In particular L ao > for all a, and LaaLbb > Lab 2 - The calculation of the energy of currents in the general case of arbitrary three-dimensional conductors requires a complete solution of the field equations, and is a difficult problem. It becomes simpler if the magnetic permeability of both the conductors and the surrounding medium can be taken as unity. It should be noted that the energy of the currents is then no longer dependent on the thermodynamic state (in particular, on the tem- perature) of the bodies, and hence the free energy in the above formulae may be referred to simply as the energy. For fi = 1 the vector field potential due to the currents j is given by formula (29.12). Hence the self-energy of the ath conductor is ,_LffJ* 2c* J J R ^=™)n &ViV '' (32 - 9) where both integrations are taken over the volume of the conductor con- sidered, and R is the distance between dF"and dV. Similarly, the mutual energy of two conductors is & ab = -J J^dF a dr & , (32.10) where dV a and dVb are volume elements in the two conductors. The mutual energy of two linear currents is particularly easy to calculate. In formula (32.10) we change from volume currents to linear ones by replac- ing jadJ^o and jbdVb by J a dla and Jbdh respectively, and we find that the mutual inductance is L & = <j><j>dlo*dl&/.R. In this approximation, there- fore, Lab depends only on the shape, size and relative position of the two currents, and not on the distribution of current over the cross-section of each wire. It must be emphasised that this simple formula can be obtained for linear currents without imposing the condition that fi — 1. In the approxi- mation where the thickness of the wires is neglected, their magnetic pro- perties have no effect on the field which they produce, and therefore no effect on their mutual energy. If the magnetic permeability jj, of the medium surrounding the wires is different from unity, the vector potential is, by (29.15), simply multiplied by fi, and therefore so is the magnetic induction. The mutual inductance is therefore multiplied by the same factor, so that L ab = nffdla-dh/R. (32.11) The self-inductance of linear conductors is much more difficult to calculate ; we shall discuss it in §33. The total energy of a system of linear currents can be written in still 134 Constant Magnetic Field §32 another form. To do this, we return to the integral (32.2), which for linear currents becomes - iZ>4 A-dla, (32.12) where A is the vector potential of the total field at the element dl« of the ath conductor. The main error in going from (32.2) to (32.12) arises from neglecting the change in the field (including the field of the current con- sidered) over the cross-section of the wire. Each of the contour integrals in (32.12) can be transformed into a surface integral: j A-dla = J curl A.d& = jB-dfc, i.e. it is the flux of the magnetic induction or magnetic flux through the circuit of the ath current. We denote this flux by . Then * = ^5>° a - (32,13) a Similarly, the free energy & of a linear current / in an external magnetic field, i.e. the energy without the self-energy of the field sources, can be expressed in terms of the magnetic flux. Evidently SF = JQIc (32.14) where <I> is the flux of the external field through the circuit of the current J. If the external field is uniform, and fx = 1 in the external medium, then O = #• Jdf. Introducing the magnetic moment of the current in accor- dance with (29.18), we have & = J£*Si). Knowing the energy of a system of currents as a function of their shape, size and relative position, we can determine the forces on the conductors by simply differentiating with respect to the appropriate co-ordinates. Here, however, the question arises which characteristics of the currents should be kept constant in the differentiation. It is most convenient to differentiate at constant current. In this case the free energy is represented by ^, and so the generalised force F q in the direction of a generalised co-ordinate q is F q = —{d^jdq)j t T- The suffixes show that the differentiation is effected at constant current and constant temperature. Since we omit the term independent of the currents in the free energy, & and & differ only in sign, and so id&\ _ td&\ 1 ^ T T BLai \ 1 ^-^ dLab \Sqh \8qh 2c^ JV ° dq here and henceforward the suffix T to the derivatives is omitted, for brevity. §32 The energy of a system of currents 135 In particular, the forces exerted on a conductor by its own magnetic field are given by the formula 1 8L where L is the self-inductance of the conductor. The nature of these forces can be seen as follows. For given current (and temperature), & tends to be a minimum. Since & = —LJ^jlc 2 , this means that the forces on the con- ductor will tend to increase its self-inductance. The latter, having the dimensions of length, must be proportional to the dimension of the conduc- tor. Thus the effect of the magnetic field is to increase the size of the conductor. For a current in an external magnetic field we havet & = -& = -Jl-%. (32.17) In all the above formulae for the energy it is assumed that there is a linear relation between the magnetic field and induction. In the general case where this relation is arbitrary, analogous differential relations can be set up. The change in the free energy resulting from an infinitesimal change in the field (at constant temperature) is, by (30.8), 8^ = jySAdV/c or, for a system of linear currents, 8jr = -2/a<|>8A.dl«. C a J Proceeding as in the derivation of (32.13) from (32.12), we have 8SF = -yj a 8<I> a . (32.18) c*-i a Similarly, we find from (30.9) &#= --]T<D«8/.. (32.19) a Thus we can say that, for a system of linear currents, & is the thermo- dynamic potential with respect to the magnetic fluxes, and & with respect to the currents, the two potentials being related by & = &--^Ja®a. (32.20) a t The factor J which appears in (31.6) is absent in (32.17) because the magnetic moment of the current in the latter equation is independent of the field, whereas the magnetic moment in (31.6) is itself due to the field. 136 Constant Magnetic Field §33 Whatever the magnetic properties of the substance, therefore, the thermo- dynamic relations J a jc = 8&/dQ> ay ^ a /c = -d&jBJa (32.21) hold. If these formulae are applied to the case where the field and induction are linearly related, so that !F is given by (32.8), we obtain 0> a = -^Labjb. (32.22) C b Thus the inductances are the coefficients of proportionality between the magnetic fluxes and the currents which produce the magnetic field. The product Labjbjc is the magnetic flux through the circuit of the current J a due to the current Jb(b # a), and Laajajc is that due to the current J a itself. §33. The self-inductance of linear conductors In calculating the self-inductance of a linear conductor its thickness cannot be entirely neglected as it was in calculating the mutual inductance of two conductors. If it were, we should obtain from (32.9) the self -inductance L = §§dhdl'lR, where both integrals are taken along the same circuit, and this integral is logarithmically divergent because of the contribution from small R. The exact value of the self-inductance of a conductor depends on the distribution of current in it, which may vary with the manner of excitation of the current, i.e. with the manner of application of the electromotive force. For a linear conductor, however, the self-inductance does not, to a fairly high accuracy, depend on the distribution of current over the cross-section, t Let us write the self-inductance as L = L e + Li, where L e and Li result from the magnetic field energy outside and inside the conductor respec- tively. For a linear conductor, the "external" part L e makes the main contribution to the self-inductance. This is because most of the magnetic energy of a closed linear circuit resides in the field at distances from the wire large compared with its thickness. For the energy per unit length of an infinite straight wire is (fi e l87T)jH*-2iTr4r = (^/frr) \{2J \cry-2-nr dr = (^7 2 /c 2 ) Jdr/r, where r is the distance from the axis of the wire and fx e the magnetic perme- ability of the external medium. This integral diverges logarithmically for large r. For a closed linear circuit, of course, this divergence disappears, because the integral is "cut off" at distances of the order of the dimension t More precisely, it is independent of the distribution of current provided that the current density varies appreciably only over distances comparable with the thickness a of the wire. If, however, the distribution is such that the current density varies appreciably over distances small compared with a (as happens, for particular reasons, in the skin effect and in super- conductors), then the self-inductance does depend on the distribution. §33 The self-inductance of linear conductors 137 of the circuit. We obtain an approximate value for the energy on multi- plying this integral by the total length / of the wire, and taking / as the upper limit and the radius a of the wire as the lower limit. The result is (pej 2 llc 2 ) log(lJa), and hence the self-inductance is L = 2fi e l log(//a). (33 1) This expression is said to be of logarithmic accuracy: its relative error is of the order of l/log(//a), and the ratio Ija is assumed to be so large that its logarithm is large, t A particular case of a linear conductor is a solenoid, which consists of a wire wound in a helix, with the turns very close together. Neglecting the thickness of the wire and the distance between the turns, we have simply a conducting cylindrical surface with a "surface" conduction current on it. The equation curl H = 47rj/c within the conductor is here replaced by the boundary condition. n x(H 2 -Hi) = 47rg/c, (33.2) where g is the surface current density, Hi and H 2 the fields on each side of the surface, and n the unit normal vector into medium 2; cf. the derivation of (27.14). If the solenoid is of infinite length, the magnetic field which it produces can be found very simply. The surface currents flow in circles, and their density £ = nj, where/ is the current in the wire and n the number of turns per unit length of the solenoid. The field outside the cylinder is zero; the field inside is uniform and along the axis of the cylinder, and is H = Avnjjc. For this field evidently satisfies the equations div H = 0, curl H = in all space outside the conducting surface, and also the boundary condition (33.2) at that surface. Accordingly, the field energy per unit length of the cylinder is fieHhr&IZTr = lnhiWii e p\c\ where b is the radius of the cylinder and fi e pertains to the material within the solenoid. Neglecting the end effects, we can apply this formula also to a solenoid whose length h is finite, but large compared with b. Then the self-inductance is L = WnWhpe = 27T/ji e nbl, (33.3) where / = lirbnh is the total length of the wire. The greater self-inductance of a solenoid as compared with that of a straight wire of equal length (cf. (33.1)) is, of course, due to the mutual induction between adjoining turns. t The assertion made above that the self- inductance is independent of the current distribution actually applies not only to the approximation (33.1) but also to the next approximation, in which terms not containing the large logarithm are included (or, what is the same thing, the argument of the logarithm includes a coefficient) ; see the Problems at the end of this section. 138 Constant Magnetic Field §33 PROBLEMS t Problem 1. Determine the self-inductance of a closed circuit of thin wire of circular cross- section. Solution. The magnetic field in the wire can be taken to be the same as that inside an infinite straight cylinder: H = 2Jr/ca 2 , where r is the distance from the axis of the wire and a its radius. Hence we find the internal part of the self-inductance : 2c2 *** ' WAV-Vm, (1) where / is the length of the wire. To calculate L e , we notice that the field outside a thin wire is independent of the distri- bution of current over its cross-section. In particular, the energy ^ e of the external magnetic field is unchanged if we assume that the current flows only on the surface of the wire. The field inside the wire is then zero, and 3F e may be calculated as the total energy from formula (32.2). On account of the assumed surface distribution of the current, the integral in this formula becomes a line integral along the axis of the wire, and so the external part of the self-inductance is 2c 2 T f *-jr-i;J«l~-'«. where the value of A in the integrand is taken at the surface of the wire. In obtaining this formula we also use the fact that, in the approximation used here, the field is constant over the perimeter of a cross-section. Having reduced the problem to that of calculating A for r = a, we now make a different assumption concerning the current distribution, namely that the whole current J flows along the axis of the wire. The field on the surface of the wire is, in the approximation considered, unchanged by this assumption (nor would it be changed for a straight wire of circular cross-section). Then, by formula (29.14), we have w~-fr#L where R is the distance from the element dl of the axis to a given point on the surface of the wire. We divide the integral into two parts, one for which R > A and the other for which R < A, where A is a distance small compared with the dimension of the circuit but large compared with the radius a of the wire.J In the integral where R > A, a may be neglected and R taken simply as the distance between two points on the circuit. The vector integral where R < A may be assumed to be along the tangent at the point considered. Denoting by t the unit vector in that direction, we have f f£| g( f dl , 2finh-HA/q) L J Rir-a J V(« 2 +/ 2 ) R<& -A. £ 2t log(2A/a). This expression can be written as the integral J dVR, A>«>*<* where R is again the distance between points on the circuit. Adding the two integrals for R > A and R < A, we obtain J f dl R>ia for which the arbitrary parameter A has disappeared, as it should. t In Problems 1-6 we put (i e = 1. X A similar procedure was used to calculate the capacity of a thin ring in §2, Problem 4. §33 The self-inductance of linear conductors 139 The final result is therefore -*J : The integration here extends over all pairs of points on the circuit whose distance apart exceeds \a. Problem 2. Determine the self-inductance of a thin wire ring (of radius 6) of circular cross- section (of radius a). Solution. The integrand in (2), Problem 1, depends only on the central angle 4> subtended by the chord R, and R = 26 sin \<f>, while dl'dl' = dldl' cos <f>. Hence it ' cos <f>'2nb'b d<f> — — : — - — = 4trb[— log tan i<f>o—2 cos £&>]• zo sin i9 The lower limit of integration is determined from 26 sin £p\> = ia, whence po £ «/26. Substituting this value and adding Li = irbpt, we have to the required accuracy L = 4w6tlog(86/a)-2+i/ti]. In particular, for /*« = 1 we obtain L = 47T6[log(86/a)-(7/4)]. Problem 3. Determine the extension of a ring of wire (with m = 1) under the action of the magnetic field of a current flowing in it. Solution. The internal stresses parallel and perpendicular to the axis are, by (32.16), given by 2 J 2 8L p 8L ita i a % = , 2irabo. = . 1 2c 2 d(2irb)' x 2c* da Substituting L from Problem 2, we have j* r, 8 * 3 i J 2 a,== -^^L log 7"4j' ai ""5P- Hence the required relative extension of the ring ist A6 1 , J 2 / 86 3 \ — -^..-a-O - 55«(««7-4+H- where E is Young's modulus and a Poisson's ratio for the wire. Problem 4. Determine the self-inductance per unit length of a system of two parallel straight wires (with fit = 1) having circular cross-sections of radii a and 6, with their axes a distance h apart, and carrying equal currents J in opposite directions (Fig. 18). Fig. 18 f See Theory of Elasticity, §5, Pergamon Press, London, 1959. 140 Constant Magnetic Field §33 Solution. The vector potential of the magnetic field of each current is parallel to the axes of the wires, and so the two vector potentials can be added algebraically. For the mag- netic field of wire 1, with a uniformly distributed current +J, we have in cylindrical co- ordinates -#-£) for r< a, A t = -(c-1-2 log^) for r> a, where C is an arbitrary constant; A z is continuous at the surface of the wire. The formulae for wire 2 are obtained by substituting b for a and changing the sign of/. Integration over the cross-section of wire 1 in formula (32.2) gives 2c 2 ira 2 &JM-H-»-t)}* S? J J I 1 - ? +Iog m r d * dri = 2^(2 +2 log ih 2c 2 7ra 2 The integration over the cross-section of wire 2 gives the same thing with a in place of b. The required self-inductance per unit length of the double wire is therefore L = l+21og(A 2 /a6). Problem 5. Determine the self-inductance of a toroidal solenoid. 2 Fig. 19 Solution. We regard the solenoid as a toroidal conducting surface carrying surface currents of density g = NJ/2irr, where N is the total number of turns and J the current; the co-ordinates and dimensions are as shown in Fig. 19. The magnetic field outside the solenoid is zero, and inside the solenoid Ht r = Hiz — 0, Hi<j, — INJfcr, where r, z, <f> are cylindrical co-ordinates ; for this solution satisfies the equations div H = 0, curl H = and the boundary condition (33.2). t The energy of the magnetic field in the solenoid is f (Hi"/8ir) dV = (N z J z lc*)§z dr/r, where the integration is taken along the perimeter of the cross-section, and is easily effected by putting z = a sin 0, r — b+a cos 6. The self-inductance is found to be L = 4*W"[&— -•(*• -«")]. Problem 6. Determine the end-effect correction of order l\h to the expression (33.3) with He = 1) for the self-inductance of a cylindrical solenoid. t It is valid also for an annular solenoid of any cross-section. §34 Forces in a magnetic field 141 Solution. The self-inductance is calculated as a double integral over the surface of the solenoid : 1 -M/ S ir** J 2 where g is the surface current density (g = nj). In cylindrical co-ordinates A h to cos 9 dp dsi dsra F (A-Ocos^d^dS V[C*a-*i) 2 +4* 2 sin 2 i<f q = 8w62«2 r r V(S 2 +46 2 sin 2 ^)' where <f> is the angle between the diametral planes through d/i and d/a, and £ = zz—zi. Effecting the integration with respect to £, we have for h ^> b L S 8tt62« 2 f [a log -t-t-tt -A+26 sin ipl cos <f> d& J V o sin +0 J o and finally L = 4i7 2 6 2 « 2 [A-8J/3w]. Problem 7. Determine the factor by which the self-inductance of a plane circuit changes when it is placed on the surface of a half-space of magnetic permeability /*,. The internal part of the self-inductance is neglected. Solution. It is evident from symmetry that, in the absence of the half-space, the magnetic field of the current is symmetrical about the plane of the circuit, and the lines of magnetic force cross that plane normally. Let this field be Ho. We can satisfy the field equations and the boundary conditions on the surface of the half-space by putting H = 2/n«Ho/(^«+l) in the vacuum and B = fi e H = 2/x«Ho/(/x e +l) in the medium: B n and H t are then continuous at the boundary, and the circulation of H along any line of force is equal to that of Ho. Hence we easily see that, when the medium is present, the total energy of the field, and therefore the self-inductance of the circuit, are multiplied by 2^«/(^«+l). §34. Forces in a magnetic field To determine the forces on matter in a magnetic field hardly any further calculations are necessary, on account of the complete analogy with electro- statics. The analogy is due mainly to the fact that the expressions for the thermodynamic quantities in a magnetic field differ from those for an electric field only in that E and D are replaced by H and B respectively. In calcu- lating the stress tensor in §15 we used the fact that the electric field satisfies the equation curl E = 0, and is therefore a potential field. The magnetic field satisfies the equation curlH = 477J/C, (34.1) which reduces to curl H = only in the absence of conduction currents. In calculating the stress tensor, however, we must always put j = 0. Since j involves the derivatives of the magnetic field, an allowance for the currents in calculating the stresses would amount to adding to the stress tensor aw 142 Constant Magnetic Field §34 the very small corrections due to the non-uniformity of the field; cf. the second footnote to §15. Thus all the formulae obtained in §§15 and 16 for the stress tensor can be applied immediately for a magnetic field. For example, in a fluid medium with B = [iH. we have crtk = -po(p,T)Sik- — \fi-pl— J \$ik+ . (34.2) From this the volume forces are calculated by the formula ft = da^ldx^. If the medium is a conductor carrying a current, the calculation differs from that in §15 in that the equation curl H = is replaced by (34.1). Differentiating (34.2) and using also the equation div B = div (/i*H) = 0, we find 1 r /du\ I W f = -gradp +— gradp^—J J ___ gra d^- - — grad H 2 + — (H • grad)H. 07T 47T By a well-known formula of vector analysis, (Hgrad)H = |grad#2_ H xcurlH = igrad^2 + 4 7 rj x H/c. Thus f = -grad/> + -!-grad [# 2 />(|^)J -|^grad,*4~j xH < 34 ' 3 ) The last term does not appear in the corresponding formula (15.12). It would, however, be incorrect to suppose that the presence of this term means that a force can be isolated in f which is due to the conduction current. The reason is that, by (34.1), the current j is inseparable from non-uniformity of the field, and another term in (34.3) also involves the space derivatives of the field. When the magnetic permeability of the medium is appreciably different from unity, all the terms in (34.3) are in general of the same order of magnitude. If, however, as usually happens, fi is close to 1, the last term in (34.3) gives the main contribution to the force when a conduction current is present, and the remaining terms form only a small correction. In calculating the forces we can put /i = 1, obtaining simply f=jxH/^. (34.4) The term — grad/>o is of no interest henceforward, and we omit it. For fi = 1 the properties of the substance have no effect on the magnetic pheno- mena, and the expression (34.4) for the force is equally valid for fluid and for §34 Forces in a magnetic field 143 solid conductors. The total force exerted by a magnetic field on a conduc- tor carrying a current is given by the integral F = J xHdV/c. (34.5) Formula (34.4) can, of course, be very easily obtained from the familiar expression for the Lorentz force. The macroscopic force on a body at rest in a magnetic field is just the averaged Lorentz force exerted on the charged particles in the body by the microscopic field h: f = pvxh/c. For p = 1 the field h is equal to the mean field H, and the mean value of pv is the conduction current density. When a conductor moves, the forces (34.4) do mechanical work on it. At first sight it might appear that this contradicts the result that the Lorentz forces do no work on moving charges. In reality, of course, there is no contradiction, since the work done by the Lorentz forces in a moving con- ductor includes not only the mechanical work but also the work done by the electromotive forces induced in the conductor during its motion. These two quantities of work are equal and opposite; see the second footnote to §49. In the expression (34.4) H is the true value of the magnetic field due both to external sources and to the currents themselves on which the force (34.4) acts. In calculating the total force from (34.5), however, we can take H to be simply the external field 4) in which the conductor carrying a current is placed. The field of the conductor itself cannot, by the law of conservation of momentum, contribute to the total force acting on the conductor. The calculation of the forces is particularly simple for a linear conductor. Its magnetic properties are of no significance, and, if fi = 1 in the surround- ing medium, the total force on the conductor is given by the line integral F=/<fdlx£/c. (34.6) This expression can be written as an integral over a surface bounded by the current circuit. Using Stokes' theorem, we replace dl by the operator dfx grad, obtaining 4>dlx# = /(dfx grad) x#. Now (dfxgrad)x£ = - dfdiv# + grad(df.#) = - df div£ + df x curl £ + (df- grad) #. But div ijy = 0, and in the space outside the currents curl ^ = also. Thus F=jj(df.grad)|>/ C . (34.7) In particular, in an almost uniform external field .£) can be taken outside 144 Constant Magnetic Field §35 the integral, together with the operator grad. With the magnetic moment of the current given by (29.18), we then have the obvious result F = (^.grad)£. (34.8) Since M in this formula is constant, we can also write F = grad(^.£), (34.9) in agreement with the expression (32.17) for the energy of the current. The torque acting on a current in an almost uniform field is easily seen to be given by the usual expression K = M x£. (34.10) PROBLEM Determine the force on a straight wire carrying a current J and parallel to an infinite circular cylinder with magnetic permeability /*, radius a and axis at a distance b from the wire. Solution. On account of the relation, mentioned in the second footnote to §29, between two-dimensional problems of electrostatics and magnetostatics, the field of the current is obtained from the result in §7, Problem 3, by changing the notation. The field in the space round the cylinder is the same as that produced in a vacuum by the current J and currents +7' and -J' through A and O' (Fig. 11, §7) respectively, where J' = 0*-l)7/0i+l). The field within the cylinder is the same as that due to a current J" = 27/0*+ 1) through O. The force per unit length of the conductor is 2777 1 1 \ 27 2 a 2 (/*-D 6(& 2 -a 2 )(/i+l)c 2 ' Similarly we find (see §7, Problem 4) that a linear conductor passing through a cylindrical hole in a magnetic medium is attracted to the nearest surface of the hole by a force F = 2J26(/x-l)/(a 2 -6 2 )(/i+l)c 2 . §35. Gyromagnetic phenomena The possibilities of magnetising (non-ferromagnetic) bodies without applying an external magnetic field are severely limited by the requirement of invariance with respect to a change in the sign of the time. The electric polarisation of many bodies can be achieved without an external electric field by, for example, deforming them if they are piezoelectrics. Piezomagnetism, however, if it occurs at all, is a very rare phenomenon (see the end of §28), and certainly cannot occur in bodies having no magnetic structure. Magnetisation without an external magnetic field generally involves setting the body in motion. A uniform translation, of course, is of no use, by Galileo's relativity principle. A uniform rotation, however, causes a mag- netisation which is linearly dependent on the angular velocity Cl (the Barnett effect) ; this relation between the vectors M and SI is possible because both §35 Gyromagnetic phenomena 145 change sign when the sign of the time is reversed. Since both are axial vectors, the relation can hold even in an isotropic body, where it reduces to a simple proportionality between M and St. There must also be an inverse effect: a freely suspended body, on being magnetised, begins to rotate (the Einstein-de Haas effect). There is a simple thermodynamic relation between the two effects; it can be derived as follows. As we know,t the thermodynamic potential with respect to the angular velocity (for given temperature and volume of the body) is the free energy &' of the body in a system of co-ordinates rotating with it. The angular momentum L of the body is L= -d&'/dSl. (35.1) The gyromagnetic phenomena are described by adding to the free energy a further term which is the first term, in an expansion in powers of £2 and of the magnetisation M at each point in the body, which contains both SI and M. This term is linear in both, i.e. it is ^'gyro = - jX ik CliM k dV = -XijcQ.i^Tc, (35.2) where A^ is a constant tensor, in general unsymmetrical. According to (35.1) and (35.2) the angular momentum acquired by the body as a result of magnetisation is related to its total magnetic moment by Lgyroj = \k^k- It is usual to replace A** by the inverse tensor, denned as go; = (2mcle)X- 1 iki where e and m are the electron charge and mass. The dimensionless quantities gtk are called gyromagnetic coefficients. Then #i = (e/2mc)gi k LgyTo,k' (35.3) The expression (35.2) also shows that, as regards its magnetic effect, the rotation of the body is equivalent to an external field §< = A^Q^ or & = (2mc/e)g-hA. (35.4) We thus have the possibility, in principle, of calculating the magnetisation caused by the rotation. For example, if the magnetic susceptibility xtk °f the body is small, the magnetic moment which it acquires is independent of its shape and is •^i = X<*$fc = {Imcje^ikg'hk&i- Formulae (35.3) and (35.4) represent respectively the Einstein-de Haas and Barnett effects. We see that both effects are determined by the same tensor gik> t See Statistical Physics, §26, Pergamon Press, London, 1958. CHAPTER V FERROMAGNETISM §36. Ferromagnetics near the Curie point There is a close analogy between the magnetic properties of ferromagnetics and the electric properties of ferroelectrics. Both exhibit spontaneous polarisation, magnetic or electric, in macroscopic volumes. In each case, this polarisation vanishes at a temperature corresponding to a second-order phase transition (the Curie point). There are also, however, important differences between ferromagnetic and ferroelectric phenomena, arising from the difference in the microscopic interaction forces which bring about the spontaneous polarisation. In ferro- electrics, the interaction between the molecules in the crystal lattice is essen- tially anisotropic, and consequently the spontaneous polarisation vector is fairly closely related to certain directions in the crystal. In ferromagnetics, on the other hand, the spontaneous magnetisation is due mainly to the exchange interaction of the atoms, which is quite independent of the direc- tion of the total magnetic moment relative to the lattice, t It is true that, together with the exchange interaction, there is also a direct magnetic inter- action between the magnetic moments of the atoms. This interaction, how- ever, is an effect of order v 2 jc 2 (v being the electron velocities), since the magnetic moments themselves contain a factor v/c. The effects of this order include also the interaction of the magnetic moments of the atoms with the electric field of the crystal lattice. All these interactions, which may be called relativistic by virtue of the factor 1/c 2 in them, are weak in comparison with the exchange interaction, so that they can result only in a comparatively slight dependence of the energy of the crystal on the direction of magnetisation.}: Consequently, the magnetisation of a ferromagnetic is a quantity which, in the first approximation (i.e. on the basis of the exchange interaction), is conserved. This fact endows with greater physical significance the thermo- dynamic theory given below, in which the magnetisation tyl is regarded as t The exchange interaction is a quantum effect resulting from the symmetry of the wave functions of the system with respect to interchanges of the particles. The interchange symmetry of the wave functions, and therefore the exchange interaction, depend only on the total spin of the system, and not on the direction of the spin ; see Quantum Mechanics, §60, Pergamon Press, London, 1958. The importance of the exchange interaction in ferro- magnetics was first pointed out by Ya. I. Frenkel', Ya. G. Dorfman and W. Heisenbero (1928). % The order of magnitude of the ratio of the relativistic and exchange interactions is given by the ratio U &niS0 IN@, where £/ a mso is the magnetic anisotropy energy per unit volume (see §37), N the number of atoms per unit volume, and © the temperature of the Curie point. This ratio is usually between 10 -4 and 10~ 5 . 146 §36 Ferromagnetics near the Curie point 147 an independent variable, the actual value of which (as a function of tempera- ture, field, etc.) is afterwards determined by the appropriate conditions of thermal equilibrium. We denote by <I>o the thermodynamic potential per unit volume of the substance when H = 0, regarded as a function of the independent variable M (and of the other thermodynamic variables). We shall neglect the relati- vistic interactions, i.e. take into account only the exchange interaction. Then Oo may be a function of the magnitude of M, but not of its direction. In order to find the thermodynamic quantities when H is not zero, we start from the relation SO/0H = -B/4ir = - (H + 4n-M)/47r. Integrating this for a given value of the independent variable M, and using the fact that <|> = <1> = Oo for H = 0, we obtain $ = Oo(M)-M.H-# 2 /87r. (36.1) Hence the potential <X> is $ = + H.B/4tt = 0>o + i/ 2 /87r = <&o+(B-477M) 2 /87r. (36.2) When the magnetic anisotropy of the ferromagnetic is neglected the direc- tions of the vectors M and H are, of course, the same and so the vectors in formulae (36.1) and (36.2) may be replaced by their magnitudes. Near the Curie point, the magnetisation M is small. Using the general theory of second-order phase transitions, t we expand <bo(M) as a series in powers of the small quantity M. The expansion of an isotropic function in powers of the vector quantity M can contain only even powers : $ = (Dqo + JaJlfa + \bM* -MH- H 2 /Stt, f 36.3) where Ooo, a, b are functions only of temperature (and pressure). The Curie point T — is given by the vanishing of the coefficient a: a > for T > and a < for T < ®.t Near the Curie point, the function a(T) can be expanded in powers of T-0, i.e. we can write a = a(r-0), (36.4) where a is a positive quantity independent of temperature. The coefficient b is positive near the Curie point and may be replaced by its value at that point. For H = the minimum thermodynamic potential above the Curie point, where a > 0, is given by M = 0, i.e. there is no spontaneous polarisation. Below the Curie point, the value of M is given by the condition aO/dM = [a(T-0) + 6M2]M = 0. <E> is a minimum when the expression in brackets is zero, i.e. when M= VH®-T)/b]. (36.5) t See Statistical Physics, Chapter XIV, Pergamon Press, London, 1958. X This relation of the phases occurs in all known ferromagnetics, although it is not thermo- dynamically necessary. 148 Ferromagnetism §36 Thus, as we approach the Curie point, the spontaneous magnetisation decreases as <\/(® — T). Like any second-order phase transition, the transition at the Curie point (with It = 0) is accompanied by a discontinuity in the specific heat. Neglect- ing higher powers of M, we have for the entropy S = -8$ldT = Soo-lM^dajdT = Soo-faM*. In the non-ferromagnetic phase M = and S = Soo, while in the ferro- magnetic phase Mis given by (36.5), so that S =Soo + * 2 (T-®)l2b. Hence the change in the specific heat C p = TdS/dT is AC P = a 2 0/26. (36.6) Now let H ^ 0. The condition dft/dM = which determines the magnetisation becomes x{T-<d)M+bM* = H. (36.7) We define the magnetic susceptibility as X = (dMidH) H ^. From (36.7) 8M — [a(T-0) + 36M2] = 1. Above the Curie point M = when H = 0, so that X = l/a(T-0), (36.8) i.e. we have paramagnetism with susceptibility inversely proportional to T— (the Curie-Weiss law). Below the Curie point M is given by formula (36.5) when H = 0, and we obtain x = l/2a(0-T). (36.9) It should be pointed out that this quantity is not the susceptibility in the ordinary sense of the word (i.e. the coefficient of proportionality between M and H), since M # even when H = O.t The susceptibility (36.9) can actually attain values of the order of unity only in the immediate neighbourhood of the Curie point. Except in this region, which is of little interest, we may suppose that the magnetisation M changes only very slightly with the magnetic field and may be regarded as a constant for any given temperature. In the following sections we shall assume this to be true. t Formulae (36.8) and (36.9) are quantitatively correct for x *£ 1 on ty in crystals of the cubic system. For uniaxial crystals the anisotropy energy (see §37) should be taken into account, which in this case is proportional to M 2 , and for very small M may even exceed the term \aM 2 in (36.3). §37 The magnetic anisotropy energy 149 This constitutes a further difference between ferromagnetics and ferro- electrics: for the latter, BPjBE is in general not small even near the Curie point. The reason again lies in the smallness of the magnetic moments of the atoms in comparison with the electric dipole moments of the molecules. §37. The magnetic anisotropy energy As already mentioned, the anisotropy of the magnetic properties of ferro- magnetics is due to the relativistic interactions between their atoms, and these interactions are comparatively weak. In the macroscopic theory, the aniso- tropy is described by the addition to the thermodynamic potential of the magnetic anisotropy energy, which depends on the direction of magnetisation. The calculation of the anisotropy energy from the microscopic theory would require the use of quantum perturbation theory, the energy of the perturba- tion being represented by the terms in the Hamiltonian of the crystal which pertain to the relativistic interactions. The general form of the desired expres- sions, however, can be deduced without such calculations, from simple argu- ments concerning symmetry. The Hamiltonian of the relativistic interactions contains terms of the first and second powers in the electron spin vector operators; these are respec- tively the spin-orbit and spin-spin interactions. When perturbation theory is applied, therefore, the anisotropy energy is obtained as a power series in the direction cosines of the magnetisation vector. Now the anisotropy energy t/aniso, like the potential <X> itself, is invariant with respect to a change in the sign of the time, while the magnetisation M changes sign under this transformation. Hence it follows that the anisotropy energy must be an even function of the direction cosines of the vector M, and so, in the first non-zero approximation of perturbation theory, we shall obtain an expression of the form E/aniso = IfalcMiMu, (37.1) where /5» is a dimensionless symmetrical tensor of rank two, whose compo- nents are functions of temperature. Near the Curie point, the expression (37.1) may also be regarded as the first term in an expansion of the aniso- tropy energy in powers of the vector M, which in this range of temperature is a small quantity (but we must emphasise that this interpretation of formula (37.1) is not valid for other ranges of temperature). Hence it follows that, as T -> ®, the quantities jS^ tend to finite non-zero values. In uniaxial and biaxial crystals, a symmetrical tensor of rank two has respectively two and three independent components. Here, however, it must also be borne in mind that there is one quadratic combination, namely M x 2 + M y 2 + M z 2 = M 2 , which is independent of the direction of M and so cannot appear in the anisotropy energy. Hence the expression (37.1) for uniaxial and biaxial crystals contains only one and two independent coeffi- cients respectively. 150 Ferromagnetism §37 For example, in uniaxial crystals the anisotropy energy can be written C/aniso = W 2 + M y *) = ^M 2 ^20, ( 37 . 2 ) where is the angle between M and the #-axis, taken to be along the princi- pal axis of symmetry of the crystal. If the constant j8 is positive, the aniso- tropy energy is least when the magnetisation is in the ^-direction, and the #-axis is said to be the direction of easy magnetisation. If, however, j8 < 0, the direction of easy magnetisation lies in the xy-plane, in which case it is natural to write the anisotropy energy as C/aniso = *|j8|M z 2, ( 37 . 3 ) which is equivalent to (37.2) but is such that C/aniso = again corresponds to the direction of easy magnetisation. t The expression (37.3) is isotropic in the ry-plane. Hence the direction of easy magnetisation is here determined by terms of higher order (see Problem 1). Let us examine the relation between the magnetisation of a uniaxial ferro- magnetic and the magnetic field in it, assuming for definiteness that jS > O.t It should be recalled that we suppose the magnitude of M to be independent of H, so that only rotations of M are considered. It is evident from symmetry that the vector M lies in a plane through the #-axis and the direction of H (if terms of higher order, anisotropic in the xy-plane, are neglected in the anisotropy energy). We take this as the ##-plane. The thermodynamic poten- tial, including the anisotropy energy, is [ j O = 0) (M)+i J 8M a; 2 -M.H-// 2 /87r = 0>o(M) + ±pM2 sin 2 - M(H X sin + H z cos 0) - # 2 /8tt. (37.4) The dependence of M on H is given by the equilibrium condition d<t>jdd = 0, whence j8Afsin0cos0 = H x cos9-H z sm9. (37.5) This is an algebraic equation of the fourth degree for £ = sin 0: (pM£-H x y{l-e) =HK\ in which the coefficients of odd powers of £ are not zero. This equation has either two or four real roots (all less than unity). Since all such roots corres- pond to extrema of O(0), it is clear that, in the first case, this function has one minimum and one maximum and, in the second case, two minima and two maxima. In other words, the number of possible directions of the t An example of a uniaxial ferromagnetic is hexagonal cobalt, for which )3 > below ~200 °C and j3 < above that temperature. At room temperature, j3 = 4-2. % This case will always be taken when uniaxial crystals are discussed. || In the following discussion we shall use the expression (37.2) for the anisotropy energy. It should be pointed out, however, that the expansion of which (37.2) is the first term is usually not rapidly convergent in practice. For a satisfactory quantitative description of the phenomena, therefore, the next (fourth-order) term should be included; for a hexagonal crystal this term is proportional to sin 4 0. §37 The magnetic anisotropy energy 151 magnetisation M for a given field H is one and two respectively. Jn the second case, one direction (corresponding to the lower minimum of O) is thermo- dynamically completely stable, while the other (corresponding to the higher minimum) is thermodynamically metastable. Either of the two cases can occur, depending on the values of H x and H z . When these two parameters vary continuously, one case passes into the other at the point where one maximum and one minimum coalesce. The curve of $(0) then has a point of inflection instead of an extremum, i.e. both d^jdd and d 2 <I>/d0 2 .are zero. Writing equation (37.5) in the form sin cos and differentiating with respect to 0, we have H x jsm 3 d = -# 2 /cos 3 0. Eliminating from these two equations gives HfV + Hfl* = (j8M)2/3. (37.6) In the HxH z -pfane equation (37.6) represents a closed curve of the kind shown in Fig. 20. It divides the plane into two parts, in one of which meta- stable states can exist, while in the other they cannot. It is evident without further investigation that the region where metastable states do not exist is that outside the curve, because f or H -> oo only one direction of M can be stable, namely that of the field H. Fig. 20 The existence of metastable states means that what is called hysteresis can occur; this is an irreversible change of state in a ferromagnetic body when the external magnetic field is varied. The curve shown in Fig. 20 is therefore the "absolute limit" of hysteresis; this phenomenon cannot occur for fields outside the curve, t t The whole of the discussion in this chapter concerns only thermodynamic equilibrium states in ferromagnetics and therefore reversible processes in them. In particular, we entirely ignore the mechanism of hysteresis phenomena; these may arise from defects in the crystal, internal stresses, a polycrystalline state, and so on. ii 152 Ferromagnetism §37 States in which the field H is perpendicular to the direction of easy mag- netisation (H x = H, H z = 0) require special consideration. The thermo- dynamic potential is H 2 <D = <d +tfM*&m*e-HMsmO. (37.7) StT If H > j8M, O has only one minimum, at 9 = \n, i.e. the magnetisation is parallel to the field. If, however, H < j8M, then <I> has a minimum when M x = Msin0 = H/p, (37.8) to which there correspond two possible positions of the vector M (at angles 6 and tt — 0), symmetrical about the x-axis. Thus in this case there are two equilibrium states, which have the same value of <J> and are therefore equally stable. This result is very important, since it means that two "phases" can exist in contact in which the field H is the same but the magnetisation M (and therefore the induction B) is different. Thus a new possibility appears for reducing the total thermodynamic potential of the body: its volume may be divided into separate regions, in each of which the magnetisation has one of its two possible directions. These regions are called regions of spontaneous magnetisation or domains. The actual determination of the thermodynamic equilibrium structure of a ferromagnetic requires a consideration of the shape and size of the body as a whole. We shall return to this problem in §39. Let us consider a portion of the body which is small compared with the total volume but large compared with the domains. The field H x can be regarded as constant in this portion; we denote by M and B the values of M and B averaged over its volume. As well as H Xi the transverse component M x = H x jfi of the magnetisation is constant. The longitudinal component M z , however, has opposite signs in different domains, so that its mean value certainly cannot exceed \M Z \. Since H z = everywhere, the mean induc- tion is therefore ■ = M 1 + ?)' * * ^Ji^-f)- (37 - 9) These formulae give the range of values of the mean induction correspond- ing to the domain structure of a uniaxial ferromagnetic. Let us now consider ferromagnetic crystals of the cubic system. Their properties are markedly different from those of uniaxial and biaxial crystals. The reason is that the only quadratic combination which is invariant with respect to the cubic symmetry transformations and which can be formed from the components of the vector M is the sum M x 2 + M y 2 + M z 2 , which is independent of the direction of M. Hence the first non-vanishing term in the expansion of the anisotropy energy for a cubic crystal is the fourth-order §37 The magnetic anisotropy energy 153 term, not the second-order one. For this reason, the magnetic anisotropy effects in cubic crystals are in general less strong than in uniaxial and biaxial crystals. Cubic symmetry admits the following two quartic invariants formed from the components of the vector M: M x 2 M y 2 + M X 2 M Z 2 + M y 2 M z 2 and KMaP + My^ + Mz*). These invariants, however, are not independent, because their sum is the quantity \{M X 2 + M y 2 + M z 2 ) 2 , which is independent of the direction of M. Hence the anisotropy energy of a cubic ferromagnetic includes (in the approximation consideredt) only one constant, and may be written C/aniso = P(M x 2 M y 2 + M x 2 M z 2 + M y 2 M z 2 ), (37.10) or, equivalently, t/aniso = -IRMJ + MJ + MJ). (37.11) If j3 > (as, for example, in iron), the anisotropy energy has equal minimum values for three positions of the vector M, namely parallel to the edges of the cube (the x, y and z axes or, in crystallographic notation, [100], [010], [001]). Thus, in this case, the crystal has three equivalent axes of easy magnetisa- tion. If, on the other hand, £ < (as, for example, in nickel), then the aniso- tropy energy has minima when M x 2 = M y 2 = M z 2 = \M 2 , i.e. when the vector M is parallel to one of the four spatial diagonals of the cube [111], [Til], etc. These are then the directions of easy magnetisation. It should be noticed that, strictly speaking, a ferromagnetic cubic crystal, when spontaneously magnetised along one of the directions of easy mag- netisation, ceases to possess cubic symmetry, and so there is a displacement of the atoms, i.e. a distortion of the crystal lattice. Such a crystal, when magnetised parallel to an edge of the cube, becomes slightly tetragonal, while one magnetised parallel to a spatial diagonal becomes rhombohedral. In this respect cubic crystals differ from uniaxial crystals with the direction of easy magnetisation along the principal axis of symmetry, where a mag- netisation in this direction evidently does not change the symmetry of the crystal. The relation between M and H for a cubic crystal can in principle be investigated in the same way as was done above for a uniaxial crystal. How- ever, we shall not pause to discuss this, because the equations are more complex, and explicit analytical formulae cannot be obtained. PROBLEMS Problem 1. Find the terms of the next order (after the second) in the expansion of Lr anl80 for a uniaxial crystal, which give rise to anisotropy in the *y-plane. f The next approximation involves terms of the sixth order. In calculating the number of independent sextic invariants, we must exclude both M 6 , which is independent of the direction of M, and expressions which differ from the quartic invariants by a factor M 2 . This leaves only one invariant, which may be taken as Mz 2 M y 2 Mz z . 154 Ferromagnetism §37 Solution. The problem reduces to finding the independent combinations of lowest (even) order, formed from the components of the vector M, which are invariant with respect to the symmetry transformations of the crystal concerned and which contain Mx and My otherwise than in the form M x 2 +M y 2 . For tetragonal symmetry there is one such combina- tion, which may be taken as M x 2 M y 2 \ the combination i(M x 4 +M y A ) gives together with M x 2 M y 2 the sum l(M x 2 +M y 2 ) 2 , and is therefore not independent. For hexagonal symmetry, the anisotropy in the xy-plane appears only in the sixth-order terms ; the invariant combination of this order may be taken as —[(M X + iMy)«-(M X -iMy)G] = 2M X My(M X *-—M X Wy 2 + MyA. 6i \ 3 / Rhombohedral symmetry admits this sixth-order term and also one independent quartic combination, for example iMz[(Mx+iMy) 3 +(Mx-iMy)*] = MxMz(M x 2 -3My 2 ). The determination of the direction of easy magnetisation in the xy-plane requires a considera- tion of both these terms, since M z is small. Problem 2. A uniaxial ferromagnetic crystal is in the shape of a spheroid, the axis of easy magnetisation being the axis of revolution, and is placed in an external magnetic field $f. Determine the range of values of $) for which the body has a domain structure. Solution. According to the general properties of an ellipsoid in a uniform external field (§8), the induction B and field S ( = H) averaged over the domain structure are related to .ji) by nS z +(l -n)Hz = §> z , i(l -n)B x +Ul +n)H x = &r, where n is the demagnetisation coefficient in the direction of the axis of revolution (taken as the 2-axis). Putting H z = and using formulae (37.9), we obtain H x — 1+27t(1-m)/j8' Elimination of H x gives the required inequality a.-fe«-V("-^- s-° + „ „y ,. < w (47m) 2 [j8+2tt(1-«)]2 for the range in which there is a domain structure. Problem 3. Determine the magnetisation averaged over the crystallites (which have uniaxial symmetry) for a polycrystalline body in a strong magnetic field {H ^> AttM). Solution. In a particular crystallite, let 6 and ^ be the angles between the direction of easy magnetisation and, respectively, M and H. It is evident that, in a strong field, M and H will be in almost the same direction, i.e. the angle •& = 0—ift is small. Putting in (37.4) M*H = MH cos (d—tfi) and equating to zero the derivative d^jdd, we have & ^ sin •& = — (PM/H) sin d cos 9. The average magnetisation is clearly parallel to H, and is M = M c~oTl = M{\ -IP) = m[\ - ^—— sin 2 cos 2 0). The bar denotes averaging over the crystallites. Assuming that all directions of the axis of easy magnetisation of the crystallites are equally probable, we have P 2 M 2 \ M "(*-^)- Thus the mean magnetisation approaches saturation in the manner M—M "-' 1 /H 2 . Problem 4. The same as Problem 3, but for the case where the crystallites have cubic symmetry. Solution. The conditions for a minimum of the expression -MMx 4 + My* + Mz 4 )-(HxMx+HyMy + HzMz), with the subsidiary condition M x 2 +My 2 +M z 2 = constant, are 2frM* 3 +.H'x = XM x ,2$My 3 + §38 Magnetostriction of ferromagnetics 155 +H y = XM V , 2$Mz s +H e = AM:, where A is an undetermined Lagrangian multiplier. For large H, we therefore have M x S* -H x + — 2pH**+ ... , etc.; A A* adding the squares of the three equations, we obtain M 2 = H 2 /X 2 , i.e. A ^ H/M. The angle & between M and H is found from •& 2 ^ sin 2 £ = M 2 H 2 4|3 2 M« H 10 J^H x 2 H y 2 (H x 2 -H y 2 )\ where the summation is over cyclic permutations of the suffixes x, y, z. Averaging this expression over the orientations of the crystallites is equivalent to averaging over directions of the vector H. The latter averaging is effected by integrating over the angles which specify the direction of H, and the result isf / 8j8 2 M 6 \ §38. Magnetostriction of ferromagnetics A change in the magnetisation of a ferromagnetic in a magnetic field causes a deformation in it; this phenomenon is called magnetostriction, and may be due to either exchange interactions or relativistic interactions in the body. Since the exchange energy depends only on the magnitude of the magnetisation, its value can change only when this magnitude changes in the magnetic field. Although the latter change is, in general, very small, the exchange energy is large compared with the anisotropy energy. Hence the magnetostriction effects from each type of interaction may be of comparable magnitude. This happens, for instance, in uniaxial crystals. Marked deformations resulting from a change in the direction of M occur in fields H ~ $M\ the change in the magnitude M is considerable when H ^ 4ttM. These two values of H are almost the same, and so it is in general necessary to take account of both effects in discussing the magnetostriction of uniaxial ferro- magnetics. We shall not pause here to derive the formulae, which are fairly complex. In cubic crystals the situation is different, because the anisotropy energy is of the fourth order and therefore relatively small. A considerable mag- netostriction, due to the change in the direction of M, occurs even in com- paratively weak fields, where the change in the magnitude M may be entirely neglected. Let us consider these effects. f For a cubic crystal there is also a range of fields in which MH is large compared with the anisotropy energy but small compared with 4ttM 2 . The formula derived here is then invalid, because in deriving it we have neglected the fields in the body resulting from the differing directions of magnetisation in different crystallites. A more exact investigation for this case gives the same \\H 2 law but with a different coefficient. We shall not discuss this problem in more detail, because the results, for some reason not yet understood, disagree with those of experiment. 156 Ferromagnetism §38 The change in the relativistic interaction energy in the deformed body is described by the inclusion in the thermodynamic potential <E> of magneto- elastic terms depending on the components of the elasticity stress tensor a^ and the direction of the vector M (N. S. Akulov, 1928). The first such terms which do not vanish are linear in aye, and quadratic in the direction cosines of M because of the symmetry with respect to a change in the sign of the time. In general, therefore, the magnetoelastic energy is given by an expres- sion of the form C/ m _ei = —\iklm0ikMiM m , (38.1) where h iklm is a tensor of rank four, symmetrical with respect to the pairs of suffixes i,k and l,m (but not with respect to interchange of the two pairs). Near the Curie point, where the expansion in powers of the direction cosines of the vector M is equivalent to one in powers of its components, the quanti- ties \icim tend to constants. In calculating the number of independent components of the tensor X-tkim it must be borne in mind that the terms in (38.1) which involve the compo- nents of M in the form M x 2 + M y 2 + M z 2 are independent of the direction of M, and so may be omitted from the magnetoelastic energy, t Thus we find that, in a cubic crystal, the magnetoelastic energy contains two independent coefficients ; we shall write it as C/m-el = ~ Xl((TxxM x 2 + OyyMy 2 + cr zz M z 2 ) - - 2\{o X yM x My + O xz M x M z + Gy Z MyM z ). (38.2) The strain tensor is obtained by differentiating 4> with respect to the various components a«: m» = — d^jdatk, where $ includes also the ordinary elastic energy (with reversed sign; see the first footnote to §17). For a cubic crystal, the latter energy involves three independent elastic coefficients, and is of the form Uel = \ki{(s xx 2 + a-yy 2 + cr zz 2 ) + k^{a xx o yy + a xx a zz + a yy a zz ) + + k 3 (a X y 2 + XZ 2 + Oy Z 2 \ (38.3) The strain tensor is% U XX = klO xx + k 2 (<Tyy + V ZZ ) + X\M X 2 , u X y = hza X y-\-\M x M y ^ and similarly for the other components. These formulae give all the magnetostriction effects in the range of fields considered. In particular, if there are no internal stresses the change in the deformation resulting from a change in the direction of magnetisation is t There is consequently some arbitrariness in the choice of the Xikim, which simply reflects the arbitrariness involved in choosing the direction of M for which (applied mech- anical forces being absent) we regard the crystal as undeformed. t In differentiating o the second footnote to §17 should be recalled. §38 Magnetostriction of ferromagnetics 157 given by u xx = M** 2 , u xy = \MxM y , etc. It should be recalled that the magnitude of the deformation itself is to some extent arbitrary, because the direction of M for which the deformation is supposed zero is arbitrarily chosen. Let us now consider magnetostriction in fields so strong (H p 4ttM) that the anisotropy energy is unimportant and there is no domain structure, so that the directions of M and H may be assumed to coincide. Since the anisotropy energy is neglected, the particular symmetry of the crystal is of no importance, and the formulae given below are valid for any ferromagnetic. Let the body be placed in a uniform external magnetic field |>. Its total thermodynamic potential go ist gb = -M.% = -MV§, (38.5) where Jt = MV is the total magnetic moment of a body uniformly mag- netised in the direction of the field; we omit the term goo which is unrelated to the magnetic field. The strain tensor averaged over the volume of the body is u ik = -{\\V)dgb\doi k , whence * ik = * W (38.6) Thus the deformation is determined by the dependence of the magnetisation on the internal stresses. For cubic symmetry, any symmetrical tensor of rank two characterising the properties of the crystal reduces to a scalar multiple of S«. This is true, in particular, of the tensor c\MV)lda ik , so that the magnetostriction deforma- tion amounts in this case to a uniform compression or extension. If we are interested only in the change W in the total volume of the body, we can obtain it by simply differentiating go with respect to the pressure : W = dgbjdp = -%d{MV)ldp, (38.7) where p is to be regarded as a uniform pressure applied to the surface of the body. PROBLEM Determine the change in volume in magnetostriction of a ferromagnetic ellipsoid in an external field $ ~ 4wM parallel to one of its axes. The ferromagnetic is assumed to be a cubic crystal.^ Solution. When the anisotropy energy is neglected, the range for which the domain structure exists is given by B < AttM when H = 0. The bar denotes averaging over the t Here the definition of &> is that given in §12, which is applicable except when the deformation of the body is appreciably inhomogeneous. % In a uniaxial ferromagnetic with § ~ 4wJVf the anisotropy energy would have to be taken into account, but this is not necessary in a cubic crystal. 158 Ferromagnetism §39 volume of the body; cf. §37. In an ellipsoid nB+(\ —n)H = § ; putting H = 0, we find that the domain structure exists when |) < 4imM. Since nB = AmiM = £), the mean magnetisa- tion is M = §/47m. Hence the thermodynamic potential is &> = -F fMd£= -&VISim. (1) o If § > 47mM, the ellipsoid is magnetised entirely in the direction of the field, and M = M . Then & = - M$>V + lirMWn. (2) The expressions (1) and (2) are the same for £) = 4irMn. The required change in volume is obtained by differentiating gp with respect to pressure: 8V = - -^ for £ < 4tthM, 87m 3p SF = -$-^ +27m-^ ^ for § > 4-rmM. dp dp For § > 47mAf we obtain (38.7). §39. The domain structure of ferromagnetics As already mentioned in §37, there is a wide range of states in which a ferromagnetic must have what is called a domain structure, i.e. it must consist of various regions in which the directions of magnetisation are different, t This is true, in particular, of a ferromagnetic body which is not in an external magnetic field. Some conclusions concerning the shape of the surfaces separating the domains may be obtained directly from the boundary conditions on the magnetic field. Since the field H is the same in adjoining domains, the condition of continuity of the normal induction B n reduces to the con- tinuity of M n . In uniaxial crystals, the sign of M z is different in different domains, but M x and M y are the same. Under these conditions the con- tinuity of M n means that the surface of separation must be parallel to the #-axis, i.e. to the direction of easy magnetisation. Let us first examine the properties of the bounding surfaces as such, leaving aside the actual shape of the domains. These "surfaces" are in reality fairly narrow transition layers in which the direction of the magnetisation varies continuously between its directions in the two adjoining domains. The "width" of such a layer and the manner in which M varies within it are given by the conditions of thermodynamic equilibrium. The additional energy due to the non-uniformity of the magnetisation must be taken into account. The largest contribution to this "non-uniformity energy" is given by the exchange interaction. Macroscopically, this energy can be expressed t The concept of domains was first put forward by P. Weiss (1907). The thermodynamic theory of domains was given by L. D. Landau and E. M. Lifshitz (1935). §39 The domain structure of ferromagnetics 159 in terms of the space derivatives of M, which can be done in a general form if the gradient of the direction of M is supposed relatively small, i.e. if the change in the direction of the magnetic moments occurs over distances large compared with the distances between the atoms. In the present case, this condition is evidently fulfilled, because a considerable difference in the directions of the magnetic moments of adjoining atoms would lead to a very large increase in the exchange energy, and is therefore thermodynamically unfavourable. We denote the "non-uniformity energy" by C/non-u- The greatest terms in its expansion in powers of the various derivatives of the components of M are those quadratic in the first derivatives; there can be no linear terms, on account of the symmetry with respect to a change in the sign of the time. Next, because it originates from exchange forces, C/non-u cannot depend on the absolute direction of M at a given point in the crystal. The most general expression satisfying these conditions is , m i m i mn Unon-u = i^ik— ~ — ' \^- L ) OXi CX]c where aa is a symmetrical tensor. This quadratic form (in the derivatives) must, furthermore, be positive definite. In a uniaxial crystal, the tensor a* fc has two independent components, and the non-uniformity energy is of the form c/non-u^ y +yj+H^)' (39 - 2) ai and a 2 being positive. In a cubic crystal we have oci = <X2. The following remark should be made concerning (39.1). A thermo- dynamic meaning attaches not to Unon-u itself, but only to its integral over the volume of the body. It is therefore not necessary to include in Unon-u the terms containing products of the components of M and their second derivatives with respect to the co-ordinates, even though such terms are formally of the same order of magnitude as those in (39.1). The reason is that, on being integrated over the volume, they become products of first derivatives, i.e. they are included in (39.1).t As an example, let us consider the boundary between domains in a uniaxial crystal, assuming that the vector M is parallel or antiparallel to the direction of easy magnetisation (the .sr-axis). This is true, for example, in the absence of an external magnetic field. The structure of the transition layer is determined by the condition that its total free energy should be a minimum.J Here the exchange energy t The symmetry of the crystal may admit terms containing products of the first deriva- tives dMildxi and the components Mi. Such terms, on integration over the volume, would give expressions depending only on the properties of the surface of the body. X Here it is more correct to speak of the total free energy, and not of the total thermo- dynamic potential, because the deformation in the layer may be by no means homogeneous. 160 Ferromagnetism §39 tends to increase the thickness of the layer (i.e. to make the direction of M vary less rapidly). The anisotropy energy has the opposite effect, because any deviation of M from the direction of easy magnetisation increases this energy. We take the #-axis perpendicular to the plane of the layer ; the direction of M depends only on x. The rotation of the vector M across the layer must take place in the yz-pte.ne, i.e. M x = everywhere. This is seen as follows. The non-uniformity and anisotropy energies are independent of the plane in which the rotation of the magnetisation takes place. The presence of a non-zero component M x would necessarily result in a magnetic field which was thermodynamically unfavourable, because of the additional magnetic energy. For M x = in the domains; if M x # in the transition layer, then divM = dM x \dx ^ 0; since divB = div H + Att div M =0, this implies that div H # and therefore that H # 0. Let be the angle between M and the #-axis. Then the components of M are M x = 0, M y = Msin0, M z = Mcos0. The sum of the non- uniformity and anisotropy energies is given by the integral oo oo }[i«iW+ M z' 2 ) + ii^V] d* = W 2 f(*iO' 2 + P sin 2 0) d* f (39.3) —oo —oo where the prime denotes differentiation with respect to x. The remaining terms in the free energy are independent of the structure of the layer, and so can be omitted here. To determine the function 6(x) which makes this integral a minimum, we write down the corresponding Euler's equation ai0" -j8 sin cos = 0, of which the first integral is 0' 2 -(j8/oci) sin 2 = constant. Assuming the thickness of the transition layer small compared with that of the domains themselves, we can write the boundary conditions on this equation as = for x = — oo, = tx for x = + oo, (39 4) 0' = for x = ±oo (i.e. for = or ir). v " ' These state that adjoining domains are magnetised in opposite directions. Then the constant is zero and, integrating the equation 0' 2 = (]8/ai) sin 2 0, we obtain cos0 = -tanhfcvWai)], (39.5) which gives the manner of variation of the direction of magnetisation in the transition layer. The "thickness" of this layer is 8 ~ V( a i//0* Substituting (39.5) in (39.3), we have oc dx cosh 2 [x-\/(j3/(x.i)] §39 The domain structure of ferromagnetics 161 or, effecting the integration, 2MV(aij8). (39.6) If we regard the boundary between domains as a geometrical surface, then (39.6) is the "surface tension" which must be ascribed to this surface in order to take account of the energy needed to create the boundary. The shape and size of the domains in thermodynamic equilibrium are given by the condition that the total thermodynamic potential should be a minimum. They depend considerably on the actual shape and size of the body. In the simplest case, that of a ferromagnetic in the form of a flat plate, the domains may in principle form either parallel layers, or "filaments" across the body. In what follows we shall, for definiteness, speak of layers.! The formation of an entire new boundary between domains results in an increase in the total "surface tension" energy. This energy consequently tends to reduce the number of domains, i.e. to increase their thickness. The excess energy near the outer surface of the body has the opposite effect. In the body the magnetic field H = 0, and the anisotropy energy is also zero, because the vector M is in a direction of easy magnetisation. Near the surface, however, this is not so. In the limiting case where the coefficient j8 in the anisotropy energy is large, the layers must emerge at the surface with no change in the direction of M (Fig. 21a, where for definiteness we suppose that the surface is per- pendicular to the direction of easy magnetisation). Near the surface there is a magnetic field which penetrates into the surrounding space, and into the body, to distances of the order of the layer thickness a. (o) t Fig. 21 In the opposite case of small j8, a more favourable disposition is that where there is no magnetic field, and M deviates from the direction of easy mag- netisation. For H = we must have everywhere div B = 4tt div M = 0, and M n must be continuous at all domain boundaries and at the free surface. f The layered structure of domains seems to be the more usual. 162 Ferromagnetism §39 This is achieved by the setting up of "domains of closure" of triangular cross-section (Fig. 21b), in which the magnetisation is parallel to the surface of the body. The total volume of these regions, and therefore the aniso- tropy energy in them, are proportional to the layer thickness a. Thus in all cases the emergence of the domains at the surface of the body results in an excess energy which is the greater, the greater the thickness of the domains. This effect therefore tends to reduce the domain thickness. The actual thickness of the domains is determined by the equilibrium of the two oppositely acting effects. Let us suppose, for example, that the domains (in a plate) have the form of plane layers of constant thickness. The number of domains is proportional to \ja, while the surface-tension energy at the surfaces separating them is proportional to their total area, i.e. to L]a, where L is the total dimension of the body in the direction of the domains, i.e. the thickness of the plate. The energy of the emergence of the domains at the surface of the plate is proportional to a. The sum of these two energies has, as a function of a, a minimum when a has a value propor- tional to -\/L. Thus the thickness of the domains increases with the dimension of the body, but the quantitative law a ~ -y/L of this increase is based on the assumption that the domains are of constant thickness, and clearly cannot be valid for all values of L. The reason is that the thickness of the domains at the surface of the body cannot exceed some limiting value ajc which depends on the properties of the ferromagnetic substance but not on the shape and size of the body. The value of a^ is determined by the point at which, as a increases, the "splitting" of the domain near the surface to a depth ~ a becomes thermodynamically favourable. Such a point must necessarily be reached, since the energy of the emergence of one domain increases as a 2 , whereas the excess surface-tension energy resulting from the splitting of the domain increases only as a. Thus we conclude that, as the size of the body, and therefore the domain thickness, increase, a progressive "branching" of the domains occurs as they approach the surface of the body (E. M. Lifshitz, 1948). We shall not pause to investigate further the various possibilities, which have not yet been clearly ascertained, t As the dimensions of the body decrease, the formation of any domains at all ultimately becomes thermodynamically unfavourable, so that sufficiently small ferromagnetic particles are uniformly magnetised single domains. The criterion giving their dimension L is obtained by comparing the magnetic energy of a uniformly magnetised particle with the non-uniformity energy which would result if there were considerable non-uniformity in the distri- bution of the magnetisation over its volume. The former energy is of the f See S. V. Vonsovskii and Ya. S. Shur, Ferromagnetism (Ferromagnetizm), Moscow, 1948; C. Kittel, Reviews of Modern Physics 21, 541, 1949; E. M. Lifshitz, Zhurnal tksperi- mental'noi i teoreticheskoi fiziki 15, 97, 1945. §39 The domain structure of ferromagnetics 163 order M 2 V, and the latter of the order of oM 2 F/IA The condition for a single domain to be formed is therefore L 2 ^ a. (39.7) The thermodynamic potential of a uniformly magnetised particle in the absence of an external field is found by putting # = in the formula ^ = J[^ + ^-^' M ] dV (cf. 31.7)) and substituting for $ the sum of the expression (36.1) and the anisotropy energy C/ a niso: & = FC/amso-iM.jHdF. (39.8) The unimportant constant gi»o is omitted. Since M and H are linearly related, the second term is quadratic in the components of M: go = VUtniBo + WauMtM** ( 39 ' 9 ) where the symmetrical tensor a ik depends only on the shape of the particle. If the particle is ellipsoidal, for example, H is constant in it, and (when £ = 0) is related to M by H t + n ik (B k -H k ) = Hi + 47rn ik M k = (cf. (8.10)). In this case, therefore, the components aw are given in terms of those of the demagnetisation coefficient tensor by a% k = 4irnui. The direction of magnetisation of the particle in an external magnetic field £ is given by the condition that go, which now includes a term - V& • M, should be a minimum. For a cubic crystal we can put simply 0b = \Va ik MiM k - r$.M, (39.10) neglecting the anisotropy energy. In uniaxial (and in biaxial) ferromagnetics, however, the anisotropy energy is a quantity of the same order as the remain- ing terms. Writing this energy in the form (37.1), we have & = W(^ + MMiM k - VfrM. (39.11) In this form the problem is mathematically identical with the one in §37 concerning the dependence of the local magnetisation M on the local field H, the only difference being that H is replaced by |>, and p ik by a ik or PROBLEMS Problem 1. Determine the "surface-tension" coefficient at a boundary between domains in a cubic crystal, if the surface of separation makes an angle x with the plane (100) (the ys-plane) and the domains are magnetised in the direction [001] of easy magnetisation (the 2-axis). Solution. As well as the crystallographic co-ordinates x, y, z we use co-ordinates *', v', z'\ the z and z' axes coincide, and the yz and y'z' planes are at an angle x- The necessity 164 Ferromagnetism §39 of having no considerable magnetic field tends (as in a uniaxial crystal) to keep the vector M in the y'z'-plane in the transition layer. The presence of magnetic anisotropy in the x'y'- plane, however, causes M to depart slightly from the y'z'-plzne. Since the anisotropy energy in a cubic crystal is small, the component M x ' is also small and can be neglected with suffi- cient accuracy. Then M x ' = 0, My' = M sin 8, Mz = M cos 8, where 8 is the angle between M and the z-axis, or M x = M sin 8 sin x, My = M sin 8 cos x, M z = M cos 8. For the sum of the non-uniformity and anisotropy energies in the transition layer we find j {izM 2 ^-) +#W 4 (sin 2 cos 2 0+J sin 4 sin 2 2x)} d*'. (1) -eo Minimising this integral with the same boundary conditions (39.4) gives 2cot0 sinh *V(2j3M2/a) = - , n . (2) sin 2x Substituting in (1) and effecting the integration, we obtain the required surface tension: MV(2ai8){ 1+ 2V(4 i =S^2^ COSh " 1 i^)- (3) Formula (3) is valid for any angle x- Equation (2) for the structure of the transition layer becomes invalid, however, when x = or &*• I n tn i s case a finite width of the transition layer is obtained only when the magnetostriction in it is taken into account. Problem 2. Determine the energy of the magnetic field near the surface of a ferromagnetic at which plane-parallel domains perpendicular to the surface emerge without change in the direction of magnetisation (Fig. 21a). Solution. The problem of determining the magnetic field near such a surface is equiva- lent to the electrostatic problem of the field due to a plane divided into strips charged alter- nately positively and negatively with surface charge density or = ±M. Let the surface of the body be the plane z = 0, and let the jc-axis be perpendicular to the plane of the domains. The "surface charge density" o{x) is a periodic function with period 2a (a being the width of the domains), and its value in a typical period is a = —M for — a < x < 0, a = +M for < x < a. Its expansion in Fourier series is E(2n-\-l)irx c n sin , c n = 4M/(2n+l)7r. a n-0 The field potential satisfies Laplace's equation we seek ^ as a series — -H - = 0; 8x z 8z 2 #c, z )=Y,b n sin (2n+1)7r * eTdn+Dw/. where the two signs in the exponent relate to the half-spaces z > and z < 0. The coeffi- cients b n are given by the boundary condition — [8<f>/ dz] z -o++[d(f>l dz] t ~o- = 4ito, whence b n — 2ac n l(2n+l). §40 The antiferromagnetic Curie point 165 The required field energy can be calculated as the integral J / 0$ d/ over the "charged surface". The energy per unit area is a 00 [<r^1«»o dx = - >J c n bn 8aM 2 A 1 - 2 2.(2« + l)3- The value of the sum is 1 -052, and so the energy is 0-852 aM 2 . §40. The antiferromagnetic Curie point The passage of a body from an antiferromagnetic to a paramagnetic state usually takes place by a second-order phase transition, as in ferromagnetics. Since there is no spontaneous magnetisation in either the antiferromagnetic or the paramagnetic state, the change in the macroscopic magnetic properties of the substance as it passes through the antiferromagnetic Curie point affects only its magnetic susceptibility. In accordance with the general properties of second-order transitions, the components of the tensor jutk are continuous at the transition point, but their first derivatives with respect to the tempera- ture are discontinuous. The general theory of second-order phase transitions must be used for a quantitative investigation of antiferromagnetic transitions. The parameters in terms of which the thermodynamic potential must be expanded near the transition point are here some linear combinations (depending on the par- ticular magnetic symmetry of the lattice) of the mean magnetic moments mi, m 2 , ... at the various points of the elementary cell. As the transition point is approached, all these parameters tend, as usual, to zero as V(® ~ T )- The thermodynamic potential of an antiferromagnetic may involve terms of various types, resulting both from the exchange interaction of the magnetic moments and from their relativistic interaction; cf. the beginning of §36. The former type contain combinations of the moments mi, m2, ... depend- ing only on their relative orientation, and not on their orientation with respect to the crystal lattice. The relativistic terms, however, depend on the directions of the moments in the crystal, i.e. they lead to magnetic anisotropy of the crystal. As in ferromagnetics, the strong exchange interaction is the principal effect which causes an ordered arrangement of magnetic moments in an anti- ferromagnetic. The relativistic interactions cause the crystallographic anisotropy of its magnetic properties. There are certain types of magnetic symmetry which admit ferro- magnetism, yet have exchange interactions which do not alone result in ferro- magnetism. In such cases the spontaneous magnetisation is due only to the relativistic interactions, and is therefore very small. Such a body is anti- ferromagnetic, but the disposition of the magnetic moments deviates some- what from that of a pure antiferromagnetic, in such a way that the magnetic 166 Ferromagnetism §40 moments in a certain direction do not completely balance (I. E. Dzyalo- shinskii, 1957t). The ratio of the "ferromagnetic moment" to the value which it would have for a pure ferromagnetic is of the same order as the ratio of the relativistic and exchange energy densities (~ 10~ 3 to 10 -5 ). In sufficiently strong magnetic fields, the antiferromagnetic structure of the crystal must be thermodynamically unstable, and the orientation of all moments in the direction of the field becomes energetically favourable. This change in orientation usually involves a change (reduction) in the elementary cell of the magnetic structure of the lattice, and, like any change in the sym- metry properties, can occur only at a definite phase-transition point, which in most cases is a second-order- transition point. The "critical field" Her which destroys the antiferromagnetism is a function of temperature which vanishes for T = 0, being the transition point in the absence of the field. Thus the region of existence of the antiferromagnetic phase in the T/f-plane is bounded by a certain curve. f Zhumal eksperimental'nol i teoreticheskoi fiziki 32, 1547, 1957; Soviet Physics J ETP 5, 1259, 1957. CHAPTER VI SUPERCONDUCTIVITY §41. The magnetic properties of superconductors At temperatures close to absolute zero many metals enter a peculiar state whose most striking property, discovered by Kamerlingh Onnes in 1911, is what is called superconductivity, i.e. the complete absence of electric resistance to a constant current. Superconductivity first occurs at a definite temperature for each metal, called the superconductivity transition point. This absence of electric resistance, however, is not the most fundamental property of a superconductor. The transition involves profound changes in the magnetic properties of the metal and, as we shall see, the change in its electric properties is a necessary consequence. The magnetic properties of a superconducting metal can be described as follows. The magnetic field does not penetrate into the superconductor; since the mean magnetic field in the medium is, by definition, the magnetic induction B, we can say that throughout a superconductor B = (41.1) (W. Meissner and R. Ochsenfeld, 1933). This property holds whatever the conditions under which the transition to the superconducting state occurs. For example, if the metal is cooled in a magnetic field, then at the transition point the lines of magnetic force cease to enter the body.t However, it should be mentioned that the equation B = is not valid in a thin surface layer. It is found by experiment that the magnetic field penetrates into a superconductor to a depth large compared with the distances between the atoms, and usually of the order of 10 -5 cm, but depending on the metal concerned and on the temperature. For the same reason, the equation B = does not hold at all in thin films of metal or colloidal par- ticles whose thickness or dimension is of the order of the "penetration depth". In what follows, we shall consider only thick superconductors, and neglect the penetration of the magnetic field into a thin surface layer. t It should be mentioned that only "pure" superconductors, i.e. metallic elements and chemical compounds containing them in certain proportions, exhibit the above properties. We shall discuss only substances of these kinds. In superconducting alloys, the Meissner effect is not complete, and the magnetic field may penetrate into the superconductor, although there is still no electric resistance. The proof below that the vanishing of B implies zero resistance must therefore be taken as showing that this equation is a sufficient, but not necessary, condition for the resistance to be zero. 12 167 168 Superconductivity §41 As we know, the normal component of the induction must be continuous at any boundary between two media ; this condition follows from the equation div B = 0, which is universally valid. Since B = in a superconductor, the normal component of the external field must be zero on the surface, i.e. the field outside a superconductor must be everywhere tangential to its surface, the lines of magnetic force having the surface as their envelope. Using this result, we can easily find the forces acting on a superconductor in a magnetic field. As in §5 for an ordinary conductor in an electric field, we calculate the force per unit surface area as <Jiknjc, where o^ = {HiHjc — — %H 2 8ik)j47r is the Maxwell stress tensor for a magnetic field in a vacuum. Since in the present case n«Hg =0, where H e is the field just outside the body, we find F s = -H e 2 nlS7T, (41.2) i.e. the surface is subject to a compression, of magnitude equal to the field energy density. According to equation (27.4) CurlB = Arrpvlc, (41.3) and from the equation B = it follows that the mean current density is also zero everywhere inside the superconductor. That is, no macroscopic volume currents can flow in a superconductor. It should be emphasised that in a superconductor the conduction current cannot meaningfully be isolated from ~pv as it can in an ordinary conductor. For the same reason the mag- netisation M, and therefore H, have no physical significance here. Thus any electric current which flows in a superconductor must be a surface current. The surface current density g is given, according to (27.14), by the discontinuity in the tangential component of the induction at the boundary of the body. Since B = inside the superconductor, and B = H outside it, we have g = cnxH e /47T. (41.4) The presence of surface currents is not peculiar to superconductors. Similar currents can occur in any magnetised body, and their density is g= cnx(H e — B)/4-7r. Since the tangential component of H = B//* is con- tinuous on the surface of a normal (not superconducting) body, we have nxH« = nxB//*, and so the expression for g can be written c 1 — u. g = -nxB— ^ (41.5) 477 fl A fundamental difference between superconductors and other bodies, however, appears when we consider the total current through a cross-section of the body. In a non-superconductor the surface currents always balance, and the total current is zero. This is seen from the condition (41.5) which re- lates the current density g to the magnetic induction inside the body, and so to §42 The superconductivity current 169 the current g at every point on the surface. In superconductors, however, the condition (41.5) has no meaning. For the transition from the ordinary state (with magnetic permeability jh) to the superconducting state corres- ponds formally to the limit B -> and fi -> 0. The right-hand side of (41.5) then becomes indeterminatej and there is no condition which restricts the possible values of the current. Thus we have the important result that the currents flowing on the surface of a superconductor may amount to a non-zero total current. Of course, this can occur only in a multiply-connected body (a ring, for example), or in a simply-connected superconductor forming part of a closed circuit which includes also a source of the electromotive force needed to maintain the currents in the parts of the circuit which are not superconducting. It is very important to note that a steady flow of current on a super- conductor is possible even if no electric field is present. This means that no dissipation of energy occurs, whose replacement would involve the doing of work by an external field. This property of a superconductor may also be described by saying that it has no electric resistance, a result which is thus a necessary consequence of its magnetic properties. §42. The superconductivity current Let us consider in more detail some properties of superconductors which depend on their shape. If a superconductor is a simply-connected body, then no steady distribu- tion of surface currents on it can exist in the absence of an external magnetic field. This can be seen as follows. The surface currents would produce in the surrounding space a constant magnetic field vanishing at infinity. Like any constant magnetic field in a vacuum, this field would have a potential <j>, and by the boundary conditions on the superconductor the normal deriva- tive d<f>/dn would vanish at the surface. We know from potential theory, however, that if d(f>Jdn = on the surface of a simply-connected body and at infinity, then <f> is a constant in all space outside the body. Thus a mag- netic field of this kind cannot exist, and therefore neither can the assumed surface currents. An external magnetic field, on the other hand, causes currents to flow on the surface of a simply-connected superconductor, and these currents can be observed through the appearance of a magnetic moment of the whole body. This "magnetisation" is easily calculated for an ellipsoidal superconductor, t Let £ be the external field, parallel to one of the principal axes of the ellipsoid. The relation (l-w)H+«B = |> holds for the magnetic field H inside a non-superconducting ellipsoid, n being the demagnetisation coeffi- cient for the axis in question (see (8.7)). In a superconductor there is no t In the present section we always assume that the magnetic field does not exceed the value at which superconductivity ceases (see §43). 170 Superconductivity §42 "field" H, as we have already shown, and so the magnetisation M = (B— H)/47r also lacks its usual significance. Nevertheless, it is here convenient to introduce H and M as formal auxiliary quantities in the calculation of the total magnetic moment M = M.V (V being the volume of the ellipsoid), which retains its usual meaning. Putting B = in the superconducting ellipsoid, we find H = $/(!-«)> (42.1) and M = - FH/4tt = - F#/4tt(1 -«). (42.2) In particular, for a long cylinder in a longitudinal field n = 0, so that H = 4) and M = — V$y\4mA These values of M are the same as would be found if the body had a diamagnetic volume susceptibility of — 1/4-7T. The magnetic field H e just outside the ellipsoid is everywhere tangential to it, and so its magnitude can be determined at once from the condition that the tangential component of H is continuous. Within the ellipsoid H = jj)/(l— n); taking the tangential component, we have (l-n)H e = £sin0, (42.3) where 6 is the angle between the direction of the external field 4) and the normal to the surface at the point considered. The greatest value of H e occurs on the equator of the ellipsoid, and is £>/(l — n). It may be pointed out once more that there is no fundamental difference between the currents which cause the "magnetisation" of a superconductor and those which produce the total current in it: their physical nature is the same. This important fact makes possible, in particular, an immediate determination of the gyromagnetic coefficients for any superconductor. The momentum density of the electrons which form the "magnetising" currents differs from the current density only by a factor mje, e and m being the charge and mass of the electron. From the definition of the gyro- magnetic coefficients (see (35.3)) it follows at once that for a superconductor gik = &ik> Let us now consider multiply-connected superconductors. Their proper- ties are very different from those of simply-connected ones, mainly because it is no longer true that a steady distribution of surface currents is impossible in the absence of an external magnetic field. Moreover, the surface currents need not balance out, and may result in a non-zero total superconductivity current on the body, even if no external e.m.f. is applied. Let us consider a doubly-connected body (i.e. a ring), with no external magnetic field. We shall show that the state of such a body is entirely deter- mined if the total current J on it is given. The problem of determining the field of the ring can again be solved as a problem of potential theory, but the t These relations for a cylinder follow immediately from the continuity condition on H, and are therefore valid for a cylinder of any cross-section, circular or otherwise. §42 The superconductivity current 171 potential <f> is now a many-valued function, which changes by \ttJ\c when we go round any closed path interlinked with the ring (cf. §29). In order to state the problem in mathematically precise terms, we must draw some open surface which spans the ring. Then the problem is to solve Laplace's equation with the boundary conditions Bj>jdn = on the surface of the ring, <f> = at infinity, and fe-fa = ^wjjc on the chosen surface, where <f>i and ^2 are the values of the potential on the two sides of that surface. Such a problem is known from potential theory to have a unique solution, which does not depend on the form of the chosen surface. From the field near the surface of the ring, we can in turn uniquely determine the surface current distribution. The self-inductance of a superconducting ring is entirely determinate together with the current distribution. Here there is a marked difference from ordinary conductors, where the current distribution, and therefore the precise value of the self-inductance, depend on the manner of excitation of the current (§33). t In §32 we introduced the concept of the magnetic flux O through a linear conductor circuit, and showed that <E> = LJjc, where L is the self-inductance of the conducting circuit. For a superconducting ring, the magnetic flux is meaningful for any thickness, not necessarily small, of the ring. For, since the magnetic field is tangential, the magnetic flux through any part of the . surface of the ring is zero ; the magnetic flux through every surface spanning the ring is therefore the same. Moreover, the formula O = LJJc (42.4) remains valid, the self-inductance L being again defined in terms of the total energy of the magnetic field of the current. The total energy of the magnetic field of the superconductor is given by the integral J (H 2 l8ir)dV, taken over all space outside the body. Again spanning the ring by a surface C, we can use the field potential and write JH 2 dVj8ir= -JH.grad<f>dV/STT = J^divHdP787r-^tf»^d//8ir. The first term is zero, because div H = 0. The surface integral is taken over an infinitely remote surface, the surface of the ring, and the two sides t The self-inductance of a superconducting ring of radius b, made of wire whose cross- section is a circle of small radius a, is the same as the external part of the inductance of a non-superconducting ring, namely L = 4irb[\og (8b /a) — 2] ; see §33, Problem 2. The exact solution of the problem of a current in a superconducting circular ring was first given by V. A. Fok, Physikalische Zeitschrift der Sowjetunion 1, 215, 1932. 172 Superconductivity , §42 of the surface C. The first two of these give zero, so that jWdV/Zv = j>H n (cl>2-<f>i)dflS7T c = (J/2c)JH n df = J<l>l2c, where <I> is the magnetic flux through the surface C. Comparing this with the definition of the self-inductance, we have /3>/2c = LJ 2 /2c 2 , which gives (42.4). • If the ring is in an external magnetic field, the total magnetic flux O is composed of the flux LJjc and the flux <I> e of the external field. A very impor- tant property of a superconducting ring is that, even if the external field and the current vary, the magnetic flux through the ring remains constant : ■ LJ/c+<& e = Oo, a constant. (42.5) This follows immediately from the integral form of Maxwell's equation in the space outside the body: i a <j)H.df = - (fiE.dl. c 8t J J If the integration on the left-hand side is taken over a surface C which spans the ring, the contour of integration on the right-hand side is a line on the surface of the ring. On the surface of a superconductor, the tangential component of E is zero (since E = inside a superconductor and E* is continuous on the surface). Hence the left-hand side is zero, and therefore dO>/d* = 0. The relation (42.5) gives the variation of the current in the ring when the external field changes. For example, if the ring is made superconducting in an external field of flux Oo> which is then removed, a steady current J = cOo/L flows in the ring. The constancy of the magnetic flux through a superconducting ring holds not only when the external field changes but also when the shape of the ring or its position in space is altered, t An intuitive statement of this result is that the lines of force can never intersect the surface of the superconductor, and so cannot escape from the aperture of the ring. The above results can be immediately generalised to the case of multiply- connected superconducting bodies, including sets of rings. The state of an w-ply connected system in the absence of an external field is completely t This statement follows at once from the relation between the induced e.m.f. and the change in the magnetic flux through the circuit when it is moved (§49). §43 The critical field 173 determined by the « — 1 total currents J a . The relation (42.5) becomes the system of equations ZLabJl>+®e,a= <*0*. (42-6) 6 These equations hold, not only for any external field, but also for any change in shape or relative position. PROBLEM Determine the magnetic moment of a superconducting disc in an external magnetic field perpendicular to its plane, f Solution. The problem of a superconductor in a constant magnetic field is identical with the electrostatic problem of a dielectric of permeability e = 0. Regarding the disc as the limit of a spheroid as c -> (cf. §4, Problem 4), and using (8.9), we find with appropriate change of notation (the field £ being along the s-axis) M = —2a s £l3n. §43. The critical field A cylindrical superconductor in a longitudinal magnetic field has an addi- tional magnetic energy -\§*M = ^W/Stt. 'For a non-superconducting cylinder, on the other hand, the total energy would be almost unchanged when the external field was applied (we shall neglect the slight diamagnetism or paramagnetism of a non-superconducting metal, i.e. take fi = 1). Thus it is clear that, in sufficiently strong magnetic fields, the superconducting state must be thermodynamically less favourable than the normal state, and so the superconductivity must be destroyed. The value of the longitudinal magnetic field at which the superconductivity of a cylindrical body is destroyed depends on the metal concerned and on the temperature (and pressure). This value is called the critical field Her, and is one of the most important characteristics of a superconductor.! When the critical field is reached, the superconductivity is destroyed throughout the cylinder, because of the uniformity of the field over the surface. In bodies of other shapes, however, the destruction of superconduc- tivity is a more complex process, in which the volume occupied by matter in the normal state gradually extends as £ increases over some range (§44). Thus, at any temperature below the transition point, the metal can exist in either the superconducting or the normal state, denoted by the suffixes s and n respectively. We denote by ^so(V,T) and ^ n {V,T) the total free energies of the superconducting and normal body in the absence of an external f We consider this problem principally with a view to using the result elsewhere (see §75, Problem 2). For a superconducting disc the magnetic fields must in reality be very weak, since its superconductivity is very easily destroyed (see §43). % There is a sharp transition between the superconducting and normal states only in "pure" superconductors (see the footnote to §41), which are the only ones considered here. In alloys, the destruction of superconductivity and the penetration of the magnetic field occur gradually over a fairly wide range of fields, so that there is no critical field in the sense here defined. 174 Superconductivity §43 magnetic field; these quantities depend on the substance concerned and on the volume, but not on the shape, of the body. The free energy in the normal state does not change when the external field is applied, and so we omit the suffix in «^»o. In the superconducting state, however, the magnetic field considerably affects the free energy. For a superconducting cylinder, with given V and T, the free energy in a longitudinal external field § is & s = & s0 (V, T) + &VI8n. (43.1) From this we can derive all the other thermodynamic quantities. Differen- tiating (43.1) with respect to the volume, we find the pressure on the body: p = rtV,T)-&l*n t (43.2) whereto (V> T) is the pressure (for given Fand T) in the absence of the field. The equation (43.2) gives the relation between^, V and T, i.e. it is the equa- tion of state for a superconducting cylinder in an external magnetic field. We see that the volume V(p, T) in the presence of the magnetic field is the same as the volume with no magnetic field but a pressure p+gpj&n: This result accords, of course, with formula (41.2) for the force on the surface of a superconductor in a magnetic field. The thermodynamic potential t of the superconducting cylinder is cfo s = SF s +pV = ^soiV, T)+poV, the volume V being expressed in terms of p and T by (43.2). Hence we can write £P S {p, T) = 0°*(p + ^ T )> (43.3) where ^o s o(/>, T) is the thermodynamic potential in the absence of the field. Differentiating this equation with respect to T and to p, we obtain analogous relations for the entropy and the volume : ^s{p,T) = ^ sQ (p^T^ (43.4) V s (p,T)= Vm^^t}. (43.5) We can now write down the condition which determines the critical field. The transition of the cylinder from the superconducting to the normal state occurs when cp n becomes less than cp s (for given p and T). At the transition point we have §p s = cp n t i-e. SPsQ (p+^ r) = Wf. n ( 43 - 6 ) This is an exact thermodynamic relation.t The change in the thermodynamic t Here defined as in §12. % We give here calculations more accurate than is usually necessary, so as to exhibit more clearly the interrelation between the various thermodynamic quantities. §43 The critical field 175 potential in the magnetic field is usually a small correction to cpso(p, T). We can then expand the left-hand side of equation (43.6) in series, taking the first two terms: SPso(p, T) + ^V s0 (p, T) = gpfa n ( 43 - 7 ) where V s o(p, T) = dcpso(p, T)\dp is the volume of the superconducting cylinder in the absence of the field. Thus, in this approximation, we can say that the thermodynamic potential per unit volume is greater by H C t 2 IStt in the normal state than its value in the superconducting state. We denote by Tct = Tcr(p) the transition temperature in the absence of the magnetic field. Experiment shows that the transition concerned is a second-order phase transition. Hence, in particular, Hct(T) must tend continuously to zero at T = Tct. We know from the general theory of second-order phase transitions t that the change in the thermodynamic potential near the transition point is proportional to the square of T- T CT - We can therefore deduce from (43.7) that the critical field in this temperature range varies as the temperature difference T— Tct'. H CT = constant x (T cr - T). (43.8) Differentiating both sides of equation (43.6) with respect to temperature (for given pressure), remembering that Her is a function of T, and using (43.4), (43.5), we have *-*-:*]*(£)■ (43 - 9) where all the quantities £f n , Sf s , V s are for the point of transition between the two states of the body (i.e. for H = Her). Multiplying by T, we obtain the heat of the transition : „.„,._„. _!«^ ,,,., When the transition occurs at T = Tct (i.e. in the absence of the magnetic field), the quantity Q vanishes with #cr, in accordance with the fact that we have a second-order phase transition. A transition at T < Tct (in a magnetic field) involves absorption or evolution of heat, i.e. it is a first-order phase transition. Experiment shows that Hct increases monotonically with decreasing temperature throughout the range from Tct to zero. Hence the derivative dHci/dT is always negative, and we see from (43.10) that Q > 0, i.e. heat is absorbed in the (isothermal) transition from the superconducting to the normal state. f See Statistical Physics. §135, Pergamon Press, London, 1958. 176 Superconductivity As T -> 0, the entropy of the whole body must vanish, by Nernst's theorem. Hence it follows from (43.9) that dHcrjdT = for T = 0, i.e. the curve of Hct{T) intersects the i/cr-axis at right angles. We may differentiate the difference £f n — Sf s (43.9) again with respect to temperature, and again use equations (43.4), (43.5). Since also (dS^jdpJT = - ( 8 V/8 T) p , the result is d^n 8& s _ 3* (Hcx 2 x J Vg d (Hcx 2^ — — V S 8T 8T 3T2\ 8 I 8tt / 8T 8T\ 8tt / 8V S Y d ///cr 2 \l 2 Multiplying both sides of this equation by T, we obtain the difference of the specific heats (at constant pressure) of the two phases. The terms involving the thermal-expansion coefficient and the compressibility are usually very small in comparison with the remaining terms ; neglecting them, we have V S T 8 2 H CT V s T/8H CT \z . *._*._ _ fl(X _ + _(_JL). (4 3,2) This formula could also be obtained by direct differentiation of the approxi- mate relation (43.7). In this approximation the difference between V 8 and V s o, and between ^ s and ^o* may be neglected. For T = Tcr, the first term in (43.12) is zero, and we obtain the following formula, which relates the change in specific heat in the second-order phase transition (in the absence of an external magnetic field) to the temperature dependence of H C t : (A. J. Rutgers, 1933). Hence we see, in particular, that in this case #* > *^n. As the temperature falls, i.e. when the superconductivity is destroyed by the magnetic field, the difference *^ s — ^ n changes sign, because the difference Sf n — Sf s is zero for T = and for T = Tcr, and must have a maximum in between. We can similarly discuss effects related to the change in volume in the transition. To do so, we differentiate equation (43.6) with respect to pressure (for given temperature), Her being a function of p. This gives 8 1 H^\ or V n -Vs = ^-^—^, (43.14) 4tt 8p §43 The critical field Ml which determines the change in volume at the transition point, t For T = Tcr this difference is zero, like the entropy difference. The transition at temperatures T < Tcr, however, is accompanied by a change in volume, which may be of either sign, depending on the sign of the derivative (0Hcr/0p)i. For T = Tcr there is no change in volume, but the compres- sibility is discontinuous; the discontinuity is easily found by differentiating equation (43.14). It may be noted that, if we substitute in (43.14) \ dp ) T ~ \dT ) P \ dp ) Hl (obtained by differentiating the equation Hct(j>, T) = constant), we obtain the Clapeyron-Clausius equation t^t) = Q , (43.15) \dTJ H „ T(V n -V s ) where the derivative (dp/dT)H CT defines the change in pressure needed to keep the applied external field critical when the temperature changes. The physical significance of the critical field H CT is much wider than would appear from its definition in terms of the behaviour of a superconducting cylinder. The equation H = H C r is a condition of equilibrium which must be fulfilled at every point of a surface separating normal and superconduct- ing phases in the same body. This is evident from the following simple arguments. If a cylinder is in a longitudinal magnetic field H C t, then both the boundary conditions on the magnetic field and the conditions of thermo- dynamic stability are satisfied for all states in which an interior cylindrical part is in the superconducting state and the rest of the body is in the normal state, and the field at the boundary between these parts is Hei. Thus the surface of separation, on which H = Hot, is in "neutral equilibrium" with respect to its location. This is a characteristic property of phase equilibrium. In a variable magnetic field, the boundary between the superconducting and normal phases changes its position. The kinetics of this process is very complex, and its discussion requires a simultaneous solution of the equations of electrodynamics and of thermal conduction, taking into account the heat evolved in the phase transition. We shall not pause to carry out this investi- gation,t but merely give the boundary condition which must be satisfied at the moving boundary between the normal and superconducting phases. To derive this condition we take a co-ordinate system K' moving with the velocity v of the boundary between the phases. By the formulae for trans- formation of fields, the electric field E' in the system K' is related to the fields E and B in a fixed system K by E' = E+vxB/c; see (49.1). Since the t This difference must of course be distinguished from the change in volume (magneto- striction) of the superconductor when the field changes from zero to H CT . This can be foun from (43.5): V,(p, T) - V s0 (P, T) S (H„*l8nXdV.I dp) T . n _ . , , „ t It has been completed by I. M. Lifshitz, Zhurnal experimental not i teoreticheskoi fiziki 20, 834, 1950; Doklady Akademii Nauk SSSR 90, 363, 1953. 178 Superconductivity §44 boundary is at rest in the system K\ the usual condition of continuity of the tangential component of E' holds, i.e. nxE' = nxE-wB/c must be con- tinuous, where n is a unit vector normal to the surface, in the direction of the velocity v. In the superconducting phase E = B = 0, and in the normal phase B = Her at the boundary. We therefore find that a tangential electric field appears on the moving boundary, its direction being perpendicular to that of the magnetic field and its magnitude being E = vH CT /c. (43.16) §44. The intermediate state If a superconducting body of any shape is in an external magnetic field £) which is gradually increased, a stage is finally reached where the field at some point on the surface of the body becomes equal to the critical field Hot, but § itself is still less than Hct. For example, on the surface of an ellipsoid placed in a field £> parallel to one of its axes, the greatest value of the field occurs on the equator (see (42.3)), and is equal to Her when § = #cr(l-«). When <?) increases further, the body cannot remain entirely in the super- conducting state. Nor can it pass entirely into the normal state, because then the field would become .§ everywhere. Hence the superconductivity must be lost only in part. (b) Fig. 22 At first sight one might imagine that this process occurs as follows. As § increases, the superconductivity is lost in a gradually increasing part of the body, while a gradually decreasing part remains superconducting, and the whole body becomes normal when § = Her- It is easy to see, however, that such states of the body are thermodynamically unstable. On the surface separating the superconducting and normal phases the magnetic field is, as we know, tangential to the surface, and its magnitude is Her- That is, the lines of force are on the surface. If the boundary is convex to the normal phase, the equipotential surfaces of the field, being at right angles to the lines of force, will diverge into the normal region, as shown by dashed lines in Fig. 22a. The field decreases, however, in the direction in which the equi- potential surfaces diverge, so that we should have H < H C i in the shaded region, contrary to the supposition that this region is in the normal state. §44 The intermediate state 179 If, on the other hand, the boundary of the superconducting phase is concave, then the lines of force on that boundary must have a bend on the free surface of the superconducting region, to which the field is tangential (at the point O, in Fig. 22b). At a bend in a line of force, however, the field becomes infinite, which again contradicts the boundary conditions at the surface of the superconductor. The above arguments represent essentially another form of the situation which leads to the domain structure of ferroelectrics and ferromagnetics. Here also the conditions of thermodynamic stability have the result that, if the magnetic field reaches the value Her at even one point on the surface, the body is divided into numerous parallel alternating thin layers of normal and superconducting matter (L. Landau, 1937). This state of the supercon- ductor is called the intermediate state. As <?> increases, the total volume of the normal layers increases, and when £ = #cr the body becomes entirely normal. It should be emphasised that a body of arbitrary shape need not be entirely in the intermediate state/There may also be regions in the purely super- conducting and purely normal states; these must be separated by the region which is in the intermediate state. A simpler case is the ellipsoid already con- sidered. In a field parallel to the axis the intermediate state occurs in the range H CT (l-n) <$>< H CT , (44.1) and the whole volume of the ellipsoid is in this state, t The shape and size of the normal and superconducting layers in the inter- mediate state are determined by the conditions of thermodynamic equili- brium of the body as a whole, in the same manner as the shape of the domains in a ferromagnetic (§39). As there, the thickness of the layers is determined by two oppositely acting factors. The "surface tension" at the boundaries of the normal and superconducting phases tends to reduce the number of layers, i.e. to increase their thickness. The "energy of emergence' * of the layers at the free surface of the body has the opposite tendency. The layer thickness increases with the size of the body, and consequently (for the same reasons as in ferromagnetic domains) they must eventually branch near the surface.^ The intermediate state can also be described in an averaged manner if the thickness of the regions under consideration is large compared with the layer thickness (R. E. Peierls, and F. London, 1936). In this description it is t For a sphere (for example), n = J, and the intermediate state exists in the range S-Hcr < £ < H CT . For a cylinder in a transverse field, n = \, and the corresponding range is iflcr < § < #cr- For a cylinder in a longitudinal field, n = 0; there is no intermediate state, and the superconductivity is totally destroyed at £ = Her- Finally, for a flat plate in a transverse field n = 1, and it is in the intermediate state for any field £ < H cr . % The thickness of unbranched layers is calculated in Problem 2. A discussion of a model with multiple branching has been given by L. Landau, Zhurnal experimental' not i teoreti- cheskoi fiziki 13, 377, 1943 ; Journal of Physics 7, 99, 1943. The interrelation between the two models is considered by E. M. LlFSHlTZ and Yu. V. Sharvin, Doklady Akademii Nauk SSSR 79, 783, 1951. In certain conditions, when the external field is near zero or H cr , a "filamentary structure may be thermodynamically more favourable than the layered structure ; see E. R. Andrew, Proceedings of the Royal Society A194, 98, 1948. 180 Superconductivity §44 assumed that there is inside the body a magnetic induction B which varies from zero in the purely superconducting state to H CT in the purely normal state. If we ascribe a non-zero induction to the matter in the intermediate state, we must also ascribe to it a definite magnetic " field " fl. To deter- mine the. relation between these quantities, we must consider the true structure of the intermediate state. The magnetic field in a normal layer at its boundary with a superconduct- ing layer is Her, and by virtue of the assumed smallness of the layer thick- ness we can suppose that the field has this value everywhere in the normal layers. In the superconducting layers B = 0. Hence, averaging the magnetic field over a volume large compared with the layer thickness, we find that the mean induction B = x n HcT, where x n is the fraction of the volume that is in the normal state. Next, we determine the thermodynamic potential per unit volume of the body, taking as zero the value for the purely superconduct- ing state. In the absence of a magnetic field, unit volume of the normal phase has an excess thermodynamic potential Hcr 2 /87r.t When a magnetic field is present, a further Hqx 2 ^tt is added as magnetic energy, giving alto- gether Hcr 2 /47r. The mean thermodynamic potential per unit volume in the intermediate state is therefore O = XnHo^/^T = H CI S/47T. (44.2) The relation between S and fl is obtained from the general thermo- dynamic relation H = 47rd<I>/dB. In the present case we find that fl is parallel to B and its magnitude is H = # cr , (44.3) i.e. it is independent of the induction. A Fig. 23 If the relation between B and 3 is shown graphically (Fig. 23), then the segment OA of the axis of abscissae corresponds to the superconducting state, and the line BC (B = S) to the normal state. The vertical line AB (S = Her) corresponds to the intermediate state. Let n be a unit vector in the direction of the lines of force of the averaged magnetic field. Putting fl = HcvTi and substituting in the equation t Here we neglect all magnetostriction effects. Instead of the change in the thermo- dynamic potential we could therefore speak of the (equal) change in the free energy. §44 The intermediate state 181 curl fl = (which holds in the absence of a volume current), we find that curln = 0. Since n 2 = 1, we have gradn 2 = 2(n-grad)n + 2nx curln = 0, and therefore (n»grad)n = 0. This means that the direction of the vector n is constant. Thus the lines of force of the mean field are straight lines. Let us apply these results to an ellipsoid in the intermediate state. For a uniform field inside the ellipsoid, the relation {\-n)3+nB = <?) holds, whatever the relation between B and H. Putting ff = Her, we haVe B = $--—H m . (44-4) n n Thus the mean induction in the ellipsoid varies linearly with the external field, from zero when £ = (1 -n)#cr to Her when £ = Her. We may also write down an expression for the total thermodynamic potential go of an ellipsoid in the intermediate state. To do so, we start from the general formula -J[-" 2: s a ]«' (cf. (31.7)), which is also valid whatever the relation between B and H. Substituting 0>, H and B from (44.2)-(44.4), we obtain ^ = IU r 2-V r -$)2l, (44.5) 877 L n J V being the volume of the ellipsoid; cjhi is taken to be zero in the purely superconducting state of the ellipsoid, in the absence of a magnetic field. For a superconducting ellipsoid in an external field £ we have gb s = - \M-^ = T£ 2 /8tt(1 -«), in accordance with (31.6) and (42.2). These two equations give the same result for <?> = Hcr(l -n), as they should. Finally, it should be emphasised that the "averaged" description of the intermediate state given here is in reality not very accurate, because of the comparatively large thickness of the layers. For the same reason, this descrip- tion fails to reproduce certain phenomena related to the properties of the layer structure. These include the fact that the transition from the super- conducting to the intermediate state actually occurs only when £ slightly exceeds (1 -n)H CT . The reason for this "delay" is as follows. The passage into the intermediate state occurs when that state becomes thermodynami- cally stable, i.e. when gb t < cp s . The layered structure, however, has not only the "volume" energy (44.5) allotted to it in the "averaged" description but also additional energy resulting from the existence of the boundaries between the layers and their change in shape near the surface of the body. This results in some displacement of the transition point towards stronger fields.t t See the references in the second footnote to this section. 182 Superconductivity §44 PROBLEMS Problem 1. Determine the specific heat of an ellipsoid in the intermediate state. Solution. The entropy and thence the specific heat, are found by differentiating the thermodynamic potential (44.5) with respect to temperature. Neglecting the terms contain- ing the thermal-expansion coefficient, we obtain VT the prime denoting differentiation with respect to T; <# a is the specific heat of the body in the superconducting state, whose slight dependence on § we here neglect. Hence it follows that, as $ varies (at constant temperature), the specific heat changes discontinuously at the point £ = (1 —n)H CI from <tf s to 4-TTtl and thereafter varies linearly with §, reaching the value VT VT VT V, - —(Hcr'Z+HcrHcr") + ~ Her' 2 = V» + —Her' 2 for <?) = H cr , whence it falls discontinuously to <g n . Problem 2. Determine the shape and size of the normal and superconducting layers in a flat plate in the intermediate state in an external magnetic field § perpendicular to the plate; the layers are assumed unbranched (L. Landau, 1937). Solution. The normal and superconducting regions are layers parallel to the field, except near the surface of the plate. The lines of magnetic force (shown dashed in Fig. 24) pass only through the normal layers, and the boundaries of the superconducting layers are also lines of force, since B n = there. Since also H = H CT on the boundary between the normal and superconducting phases, the conditions at the boundaries of a superconducting layer are on BC H x = 0, on BA and CD HJ+Hf = H„*, (1) the co-ordinate axes being taken as shown in Fig. 24. Far from the plate, the field H must be the same as the external field |), i.e. for x -> — oo H x = §, H y = 0. (2) We use the scalar and vector potentials : H x = —d</>/8x = dA\dy,H y = —d<f>]dy = —dAjdx and the complex potential to = <$>—iA (cf. §3, (3)). On a line of force A = constant. We put A — on the line of force which reaches O and then branches into OCD and OB A, forming the boundary of one superconducting layer. The difference between the values of A at the boundaries of two successive superconducting layers is equal to the magnetic flux across the segment a = a t +a n , namely $a. Hence the value of A at the boundary of any superconducting layer is an integral multiple of §a. Using also the "complex field" -q = H x —iH y = —dw/dz, z = x+iy, we can write the conditions (1) as on BC re t] = 0, o: We introduce a new variable on BA and CD |i?| = H ct . (3) £ = exp( —l-nw/^d) — 1 (4) and regard i? as a function of £. £ is real on all boundary lines of force and on their continua- tions beyond the plate : £ = exp( — lirfl&a) — 1 . Since <f> is determined apart from a constant, its value at any one point can be chosen arbitrarily. Let <f> — at O. Then £ = there also. On the limiting line of force considered, §44 The intermediate state 183 far from the plate, £ = — 1 (since for * -> - oo we have <j> -*- -%x -> + oo). The value of £ at B or C, where the line of force enters the plate, is £o, say. On CD and BA, £ varies from Jo to oo. Then the conditions (1) and (3) can be written V = S, (5) for £ = -1 for < £ < Co re t\ = 0, for £o < £ H= H<„. The function tj(£) must, furthermore, be everywhere finite. D S On (6) Fig. 24 The conditions (6) are satisfied by the function For real negative £ the two roots are real, and are taken with the signs shown. For < £ < Co both are imaginary, and we take (7) -^MVf-Vd- 1 )]- with the minus and plus signs on OC and OB respectively. For £ > £o £o\_. /&>1 ,=MVHWt]> with the minus and plus signs on CD and BA respectively. The value of £o is found from the condition (5), and is l /l \ a (8) *-&-)'■ where h = §/H cr . 13 184 Superconductivity §44 The shape of the layer, i.e. the shape of the limiting line of force, is obtained by integrating the relation dz = — dw/17 over real £: dw ah r d£ Jaw _ ah f T) lit J v(Z+V Substituting 17(C), taking real and imaginary parts, and choosing appropriately the constants of integration, we obtain the following parametric equations of the line CD: =fh h -v|-v( &+ i,^v§±i;], 00 v ah r /Co d£ ah I where Y = %a s is the value of y for x -> oo ; see Fig. 24. The period a of the layered structure is related to the thicknesses a s and a n of the super- conducting and normal layers by a = a s +a n , a§ = a n H cr . The latter equation follows from the continuity of the magnetic flux, which passes entirely through normal layers. Hence a s = a(l —h), a n = ah. The period a is determined by the condition that the total thermodynamic potential of the plate is a minimum. The existence of "surface tension" at the boundaries between the normal and superconducting phases gives a term goi = 2/A • if C r 2 /8ra in the thermodynamic poten- tial per unit area of the surface of the plate. Here I is the thickness of the plate, and the surface- tension coefficient is written as A • H C t 2 I8t, where A has the dimensions of length. In calculat- ing this part of the energy we can, of course, neglect the curvature of the layers near the surface of the plate. The "energy of emergence" of the layers at the surface of the plate can be written as the sum of two parts. First, the increase in the volume of the normal layers as compared with the volume they would occupy if they were everywhere plane-parallel gives an additional energy GO He 4 f/v ^ Hcr SP% = - ( Y— y) dx— — , a J 8ir where the factor 4 takes into account the presence of four angles (such as B and C in Fig. 24) on the two sides of each of the 1/a superconducting layers. Second, the emergence of the layers at the surface of the plate changes the energy of the system in the external field, i.e. the energy —\M • ^. The magnetic moment of the plate is due to currents on the surfaces of the superconducting layers. When the tangential component of the induction changes discontinuously from H to zero, the surface current density is g — ±cH/4ir. Hence the magnetic moment per unit length in the sr-direction and per boun- dary surface of the superconducting layer is f H — —y ds, ds = \/(dx 2 +dy 2 ). J 4ir OCD If the layer did not emerge at the surface, there would be no segment OC, and on CD we should have y = Y. Hence the excess magnetic moment for each of the four angles is J Air J Air §44 The intermediate state 185 Accordingly, the excess energy is OO H OCD = ^\h<z j (- y d*+y ds) + J H„ dy]. The coordinates x and y, expressed in terms of £, are proportional to a. Hence all the integrals in fi»2+0°3 are proportional to a 2 , and this part of the thermodynamic potential is therefore proportional to a. The sum &>i+&>2+&>s is therefore of the formf #cr 2 r/A " sas '4rLT +<,r( * ) J- The condition that this is a minimum gives a = -\/\lNfW\- It should be noted that, in normal layers near the surface of the plate, the magnetic field may be considerably less than H CT , i.e. there is a situation corresponding to that shown in Fig. 22a. In this case the unfavourable thermodynamic state is made possible by the surface- tension energy, which prevents further reduction in the layer thickness. t The integrals in &°% and £Pz cannot be expressed in terms of elementary functions. The function /(A) has been tabulated by E. M. Lifshitz and Yu. V. Sharvin, loc. cit. CHAPTER VII QUASI-STATIC ELECTROMAGNETIC FIELD §45. Eddy currents So far we have discussed only constant electric and magnetic fields, and have used Maxwell's equation 10B curlE= (45.1) c 8t only as a step in deriving the expression for the energy of a magnetic field (§30). The nature of the variable electromagnetic fields in matter depends greatly on the kind of matter concerned and on the order of magnitude of the fre- quency of the field. In the present section we shall consider the phenomena which occur in extended conductors placed in a variable external magnetic field. We shall assume that the rate of change of the field is not too large, and therefore satisfies various conditions which will be derived below. Electromagnetic fields and currents which satisfy these conditions are said to be quasi-static. We shall first of all suppose that the wavelength A ~ cjm which corresponds (in the vacuum or dielectric surrounding the conductor) to the field frequency to is large compared with the dimension / of the body: a> <^ cjl. Then the magnetic field distribution outside the conductor at any instant can be described by the equations of a static field : div B = 0, curlH = 0, (45.2) all effects due to the finite velocity of propagation of electromagnetic dis- turbances being neglected. Of course, this neglect is permissible only at distances from the body which are small compared with A ; these are the only distances which need be considered in determining the field inside the body. The complete system of field equations inside the conductor consists of (45.1) together witht divB = 0, (45.3) curlH = 4ttoE/c. (45.4) f In an anisotropic body, o-E on the right-hand side of (45.4) must be replaced by the vector oucEic. 186 §45 Eddy currents 187 The second of these equations has been derived, strictly speaking, only for constant currents and magnetic fields. It is therefore necessary to specify conditions under which this equation can reliably be used for variable fields. In equation (45.4) the current has been written in terms of the electric field in accordance with the relation j = ctE with constant a, which holds for a steady state. This relation remains valid if the period of the field is large compared with the characteristic times of microscopic conduction. That is, the field frequency must be small compared with the reciprocal mean free time of the electrons in the conductor. For typical metals at room tempera- ture, the limiting frequencies given by this condition lie in the infra-red region of the spectrum, t There is another condition which restricts the applicability of the equations in this case. Being macroscopic equations, they presuppose that the electron mean free path is small compared with the distances over which the field changes appreciably. We shall return to this condition later. In equations (45.1) and (45.4), E is the induced electric field resulting from the variation of the magnetic field. When H is known, the field E can be immediately determined by equation (45.4). The equation for H is obtained by eliminating E from (45.1) and (45.4): 4tt 8B curlH = -curl . (45.5) c 2 dt o In a homogeneous medium of constant conductivity a and constant mag- netic permeability n, the factor \\a can be taken in front of the curl operator, and by (45.3) we have div B = /u div H = 0. Hence curl curl H = - AH, and we obtain the equation AH - -trir- (45 - 6) With the equation div H =0 this suffices to determine the magnetic field. It may be noted that equation (45.6) is a heat-conduction equation, the thermometric conductivity x being represented by c 2 /47r^cr. The boundary conditions on the magnetic field at the surface of a con- ductor are evident from the form of the equations, and are as before B nl = B n2 , H a = H, 2 . (45.7) t For poor conductors (e.g. semiconductors), equation (45.4) is valid only if a further condition, which may be more stringent, is satisfied. For such bodies it may be possible to define both a conductivity and a dielectric constant. Then a teim — (e/c) SEjdt is added to the right-hand side of (45.4), and the condition for this term to be small in comparison with AnaEjc is a/a>^ e. In good conductors (e.g. metals), on the other hand, o/(o^> 1 throughout the frequency range in which the conductivity can be regarded as constant (see also the sixth footnote to this section). 188 Quasi-static Electromagnetic Field §45 The expression on the right-hand side of equation (45.4), being bounded, does not affect the second of (45.7). For /t =1 we can put simply t Hi = H 2 . (45.8) The continuity of Ht implies that of (curl H) n and therefore, by (45.4), that of (orE) ra . Outside the conductor, a = 0, and we therefore conclude that on the surface E n j = 0, where the suffix / denotes the field inside the conductor. Since E n is zero, so is j n = oE n . Thus the system of equations under consideration necessarily implies the vanishing of the normal com- ponent of the current density on the surface of the conductor. In other words, in this approximation a variable magnetic field cannot cause the appearance of free charges on the surface of the conductor. The boundary condition (45.8) is insufficient for a complete formulation of the problem if the conductor is composite and its parts have different con- ductivities. At the interfaces between the parts we must use both the continuity of H and that of E<; the latter implies the condition (curlH)n/oi = (curlH), 2 /cT2 (45.9) on the magnetic field. Having established the basic equations, let us now examine the nature of the variable fields which they describe. Suppose that a conductor is placed in an external magnetic field which is suddenly removed. The field in and around the conductor does not vanish immediately ; the manner of its decay with time is given by equation (45.6). To solve a problem of this kind, we use the following procedure. We seek solutions of equation (45.6) which have the form H = H m (x, y, z)e~ ymt , where y m is a constant. The equation for the function H m (#, y, z) is then (c 2 /W)AH m = -y m H m . (45.10) For a conductor of given shape, this equation has non-zero solutions (satisfy- ing the necessary boundary conditions) only for certain y m , the eigenvalues of (45.10), all of which are real and positive. J The corresponding functions f For ordinary diamagnetic and paramagnetic bodies, /* is very nearly 1, and the inclusion of jit in the following formulae would be a pointless refinement. Values of /u. differing consid- erably from 1 occur in ferromagnetic metals, whose magnetic properties (in sufficiently weak fields) can be described in terms of a large constant permeability. For quite moderate frequen- cies, however, such substances exhibit a dispersion of /u. (i.e. a dependence of fi on the frequency ou), together with a decrease of fi almost to 1. We shall therefore put p = 1 in the present chapter. X This is easily seen as follows. So as to avoid having to take account of the boundary conditions at the surface of the body, we start from equation (45.5) and suppose a to vanish continuously outside the body. Multiplying both sides of the equation - 47ry m H m /c 2 - - curl [(1/a) curl H m ] by H m * and integrating over all space, we have £y» j \H m \*dV = jH OT *.curl CUrl g Hm dF= j- g IcurlHjW, whence it is evident that the y m are real and positive. §45 Eddy currents 189 Hm(x, y, z) form a complete set of orthogonal vector functions. Let the field distribution at the initial instant be H (tf, y, z). On expanding this in terms of the functions H m : we obtain the solution of the problem : H(x,y, z,t) = X c m e-ymtH m (x,y, z) (45.1 1) m gives the manner of decay of the field with time. The rate of decay is determined principally by the term in the sum for which y m is least ; let this be yi . The "decay time" of the field may be defined as t = 1/yx. The order of magnitude of t is evident from equation (45.10). Since AH ~ H// 2 , where / is the dimension of the conductor, we have T - AlTol^C*. (45.12) Another type of problem concerns the behaviour of a conductor in an external magnetic field which varies with frequency o>. The magnetic field penetrates into the conductor and induces in it a variable electric field, which in turn causes currents to appear; these are called eddy currents A A general idea of the way in which the field penetrates into the conductor can be obtained from the analogy already mentioned between equation (45.6) and the equation of thermal conduction. It is known from the theory of thermal conduction that a quantity which satisfies such an equation is "propagated" through a distance ~ V(x0 in time *• We can therefore immediately conclude that the magnetic field penetrates into the conductor to a distance 8, given in order of magnitude by 8 ~ ^(c 2 jaai). The same is true, of course, of the induced electric field and currents. In a variable field of frequency co, all quantities depend on the time through a factor e~ i(0t . Equation (45.6) then becomes AH= -47rt<rcoH/c 2 . (45.13) Let us consider two limiting cases. If the penetration depth S is large com- pared with the dimension of the body (low frequencies), we can put the right- hand side of (45.13) equal to zero as a first approximation. Then the magnetic field distribution at any instant will be the same as it would be in a steady state with the same external field. Let this solution be Hst; it is independent of the frequency (or rather involves the frequency only in the time factor e -i">ty The induced electric field appears only in the next approximation, being absent in the steady state. This corresponds to the fact that curl Hst = 0, and so the value of Est obtained from (45.4) is zero. To calculate E, t In Russian "Foucault currents". 1 90 Quasi-static Electromagnetic Field §45 therefore, we must use equation (45.1), according to which curlE = icoUst/c. (45.14) This equation, together with div E = (which follows from (45.4) when a is constant in the body), entirely determines the electric field distribution. It is seen to be proportional to the frequency co. The opposite limiting case is that where 8 <^ / (high frequencies). The condition for the macroscopic field equations to be applicable, mentioned at the beginning of this section, requires that 8 should still be large compared with the mean free path of the conduction electrons, t When 8 <^ I the magnetic field penetrates only into a thin surface layer of the conductor. In calculating the field outside the conductor we can neglect the thickness of this layer, i.e. assume that the magnetic field does not penetrate into the conductor at all. In this sense a conductor in a high- frequency magnetic field behaves like a superconductor in a constant field, and the field outside it must be calculated by solving the corresponding steady-state problem for a superconductor of the same shape. The true field distribution in the surface layer of the conductor can be investigated in a general manner by regarding small regions of the surface as plane. It is necessary to solve equation (45.13) for a conducting medium bounded by a plane surface, outside which the field has a given value Hoe~ i(ot , say. This vector is obtained as shown above, by solving the prob- lem for a semi-infinite medium, and is parallel to the surface of the conductor. The boundary condition (45.8) shows that the magnetic field in the conductor is also Ho£ - * w * at the surface. We take the surface of the conductor as the ary-plane, the conducting medium being in z > 0. Since the conditions of the problem are inde- pendent of x and y, the required field H depends only on the z co-ordinate (and on the time). We therefore have divH = dH z jdz = 0, and since H z = at the boundary it must be zero everywhere. By (45.13), the equation for H is d 2 H/a* 2 + A 2 H =0, where k = V(4Waw/c 2 ) = (l+OVC 2 ™™)/*- The solution of this equation which vanishes far from the surface is e ikz . Using the boundary condition at z = 0, we obtain H = Hoe-* /s eM s -M (45.15) where the penetration depth 8 is 8= cI^(2tto(o) and k = (l + i)/8. (45.16) The electric field is now determined by means of equation (45.4). If n is a unit vector in the ^-direction, we have E = V(W8^)(1 -OH x n. (45.17) Thus E ~ H8/X. f This condition is, in fact, the first to be violated in metals as the frequency increases. The condition a> <^ 1 /t, where r is the mean free time, may, however, be the more stringent for semiconductors of low conductivity. §45 Eddy currents 191 If the field H e-* w ' is "linearly polarised", then H can be made real by a suitable choice of the origin of time. We then take the direction of Ho as the y-axis. Taking the real part in (45.16) and (45.17), we have H = H y =H e-*< s cos 6-4 E = E X = H Q y/{uf4no)e-*i'ca&£-wt--^. (45.18) The eddy current density j = oE has the same distribution as E. The presence of eddy currents implies a dissipation of. the field energy, which appears as Joule heat. The time average energy Q dissipated in the conductor per unit time is Q = jyEdV = J <rE 2 dV. It can also be calculated as the mean field energy entering the conductor per unit time : Q = <J&.df = (c/4*r)<fExH-df, (45.19) the integral being taken over the surface of the conductor, t We have already seen that, in the limiting case 8 > /, the amplitude of the magnetic field inside the conductor is independent of the frequency, while that of the electric field is proportional to u>. The energy dissipation Q at low frequencies is therefore proportional to to 2 . When S < /, on the other hand, the magnetic and electric fields on the surface of the conductor are given by formulae (45.15) and (45.17) with z = 0. The Poynting vector is normal to the surface, and its mean value is S = (c/167r)\/(ci>/27ra)|Ho| 2 , the variation of H over the surface being given by the solution of the prob- lem of the static field outside a superconductor of the same shape (cf. above). The energy dissipation is »-is7^ W * (45 - 20) Thus at high frequencies it is proportional to \/co. The energy dissipation can also be expressed in terms of the total mag- netic moment Jt acquired by the conductor in the magnetic field. In a periodic field, the magnetic moment is likewise a periodic function of time, with the same frequency. According to formula (31.4), the rate of variation of the free energy is given by -Jt'dfrjdt, where £ is a uniform external t If any two quantities a(t) and b(t) are written in complex form (proportional to e~ i<0 t), the real parts must of course be taken before calculating their product. If, however, we are interested only in the time average value of the product, it may be calcula ted as % re ab*. The terms containing e ±2i ^* give zero on averaging, and so l(a+a*)(b+b*) = \(ab* + a*b). In particular, S can be calculated as the real part of the "complex Poynting vector": S = ie[^.*ExH*]. (45.19a) 192 Quasi-static Electromagnetic Field §45 field in which the conductor is placed. This expression does not imme- diately give the required energy dissipation, because the energy of the body changes not only on account of dissipation but also by the periodic move- ment of energy between the body and the surrounding field. If we average over time, however, the latter contribution vanishes, and the mean dissipa- tion of energy per unit time is Q = -Jt>d$>/dt. (45.21) If M and .£) are written in complex form, then dfy/dt = — icofy, and Q can be calculated as Q = -| repaid •$*) = \u> im{J(-b*). (45.22) The origin of the factor \ is explained in the last footnote. The components of the magnetic moment M are linear functions of the external field: J*i = Kott&t, (45.23) where the dimensionless coefficients a^(o>) depend on the shape of the body and on its orientation in the external field, but not on its volume V. In this formula we assume that M and |) are written in complex form, so that the cuijc are also in general complex. The tensor Voctk may be called the magnetic polarisability tensor for the body as a whole. This tensor is symmetrical:! a-ik = a-ki- (45.24) We can therefore write If also we write the complex quantities out as auk +i<*4k"> the energy dissipa- tion (45.22) becomes Q = *FW're(S<$**). (45.25) Thus the energy dissipation is determined by the imaginary part of the magnetic polarisability. We have already seen that Q is proportional to ofi for low frequencies, and to -y/co for high frequencies. We can therefore conclude that the quantities a^" in these two limiting cases are proportional to co and to 1/-\/oj respectively. Since they decrease both as co ->0 and co -> oo, they must have a maximum in between. The magnetic moment of a conductor in a variable magnetic field is due mainly to the conduction currents set up in the body; it is not zero even if fi = 1, when the moment in a constant field vanishes. The latter can be obtained from M{oy) by taking the limit as co -> 0. Hence it follows that the real part eta of the polarisability tends to a constant limit as co -> t See Statistical Physics, §124, Pergamon Press, London, 1958. §45 Eddy currents 193 (the limit being zero for fi = 1), corresponding to magnetisation in a constant field. In the limit w -> oo, when the magnetic field does not penetrate into the body, a {fc ' tends to a different constant limit, corresponding to the steady magnetisation of a superconductor of the same shape. PROBLEMS Problem 1. Determine the magnetic polarisability of an isotropic conducting sphere of radius a in a uniform periodic external field. Solution. The field H* inside the sphere satisfies the equations AHi+£ 2 H{ = 0, divHi = 0, where k = (l+i')/S. We write this field in the form H< = curl A, where A satisfies the equation AA+#>A = 0; since H is an axial vector, A is a polar vector. By symmetry, the only constant vector on which the required solution can depend is the ex- ternal field 4). We denote by/ the spherically symmetrical solution, finite for r = 0, of the scalar equation Af+k 2 f==0, namely /= (1/r) sin kr. Then the polar vector A, which satisfies the vector equation AA+ft 2 A = and depends linearly on the constant axial vector £), can be written as A = p curl (/£), where P is a constant. Thus we have Hi = p curl curl (/£>) = /3(y +* 2 /)£-/s(^ +* 2 /)(n-$)n, where n is a unit vector in the direction of r; the second derivative/ " has been eliminated by means of the equation A/+A 2 / =0- . The field H e outside the sphere satisfies the equations curl H« = 0, div H* = 0. We put He = — grad <£+|>; <f> satisfies the equation A<£ = and vanishes at infinity. Since <f> depends linearly on the constant vector £, we have <j> = — Va. £• grad (1/r), where V = 47ra 3 /3. Thus H, = Fagrad[($.grad)(l/r)]+$ Va It is evident that V<x£ is the magnetic moment of the sphere, so that Va is its magnetic polarisability (by symmetry, the tensor aij- reduces to a scalar aSa). On the surface of the sphere (r = a), all the components of H must be continuous. Equat- ing separately the components parallel and perpendicular to n, we obtain two equations to determine a and p. The polarisability per unit volume is found to be a = a'+ta" = — — 1 — - + — cot ak , 8?rL a 2 k 2 ak J 3[ 3 8 sinh (2a/ 8) -sin (2a/S) 1 a = ~8^L 1_ 2a cosh(2a/S)-cos(2a/8)J' 9S 2 r a sinh(2a/8)+sin(2a/S) a = — i['- \6ira 2 l 8 cosh(2a/8)-cos(2a/8) In the limit of low frequencies (8^> a), a .__J_(?) 4 _ 105ttW 20tAs; i For high frequencies (8 <^ a), An a 4 a 2 co 2 105 c 4 ' *ff<0 10c 2 ' lr 1 _i!l = _i.|'i__J£ 1 JttL 2aJ 8ttL 2aV(2woa>)J' 9 8 9c \6ira \6ira\f(2iTOOi)) 194 Quasi-static Electromagnetic Field §45 The limiting value Vol' = — $a s corresponds to the magnetic moment of a superconducting sphere; the corresponding value of a" could be found from formula (45.20), using the expression (42.3) for the field at the surface of a superconducting sphere. Problem 2. The same as Problem 1, but for a conducting cylinder (of radius a) in a uniform periodic magnetic field perpendicular to its axis. Solution. This problem is the "two-dimensional analogue" of Problem 1. In what follows all vector operations are two-dimensional operations in a plane perpendicular to the axis of the cylinder, and r is the radius vector in that plane. The field inside the cylinder is of the form Hi = curl curl (/£) (f , ,.,W J 2f ' = p\*- + k *f)$-fi(— +* 2 /)(n.|»n, where/ = Jo(kr) is the symmetrical solution of the two-dimensional equation A/+& 2 / = which is finite for r = 0. The field outside the cylinder is He = -2 Fa grad [(|>-grad) log r] + % 2 Vol = — i -[2(n.$)n-$)+$, where V = to 2 . The magnetic moment per unit length of the cylinder is Vctfy (see §3, Problem 2). From the condition H* = H e for r = a, as in Problem 1, we obtain .__±[ 1 _.lm*l>|. 2ttl kaJo(ka)i kaJo(ka)j using the relation Jo'{kr) = —kj\{kr). For 8 ^> a, expanding the Bessel functions in powers of ka, we have 24t7\8/ 8tAs/ 4< 6c 4 4c 2 For 8 <^.a, we use the asymptotic expressions for the Bessel functions, obtaining 2tt\ a) 2ir\ a\/(2iraa))/' 1 S c a. = 2tt a 2ira\/(2irow) Problem 3. The same as Problem 2, but for a magnetic field parallel to the axis of the cylinder. Solution. The magnetic field is everywhere parallel to the axis of the cylinder. Outside the cylinder we have H e = jr), and inside it H* =/.£), where/ is the symmetrical solu- tion of the two-dimensional equation /\J+k 2 f= which is 1 for r = a and finite for r = 0: Hi = $)Jo(kr)IJo(ka). The eddy currents in the cylinder are azimuthal (i.e. the only non-zero component isjj,), and are given in terms of the field H z = H by 4ir}/c = —dH/dr. The magnetic moment generated per unit length of the cylinder by the conduction currents is <Jt = ira 2 a.$ = (l/2c)J)VdF= — iJ(3H/3r)r 2 dr; it is parallel to the axis. Evaluating the integral, we have 1 I", 2 Mka)-] a. => 1— • 47TL kaJo(ka)Y Thus the longitudinal polarisability of the cylinder is half the transverse polarisability de- rived in Problem 2. Problem 4. Determine the least decay coefficient for the magnetic field in a conducting sphere. §46 The skin effect 195 Solution. The solutions of equations (45.10) for a sphere include functions of various symmetries. The most symmetrical solution is that which is defined by an arbitrary constant scalar. This solution is inapplicable, however, for the following reason: it would be spheri- cally symmetrical (H = HAj)) and would have to be H = constant/r in order to satisfy the equation divH = (l/r)3(rH)/3r = 0, which is valid both outside and inside the sphere; but this function is not finite at the centre of the sphere. The least value of y corresponds to one of the solutions defined by an arbitrary constant vector. The form of these solutions is evidently the same as has been found in Problem 1, the only difference being that the constant term in the field He must be omitted so as to have H = at infinity. The quantity k is now real (=V(4w<ry/c 2 )), and the vector |) is the arbitrary constant vector. From the boundary condition Hj = H« at r = a we obtain two equations, and on eliminating a and /? we find sin ka = 0. The smallest non-zero root of" this equation is ka = w, and so the smallest value of y is irc^/loa 2 . §46. The skin effect Let us consider the distribution of current density over the cross-section of a conductor in which a non-zero and variable total current is flowing. From the results of §45 we should expect that, as the frequency increases, the current will tend to be concentrated near the surface of the conductor. This phenomenon is called the skin effect. The exact solution of the problem of the skin effect depends, in general, not only on the shape of the conductor but also on the manner of excitation of the current in it, i.e. the nature of the variable external magnetic field which induces the current. An important particular case, however, is that where the current flows in a wire of thickness small compared with its length; here the current distribution is independent of the manner of excitation. In calculating the current distribution over the cross-section of a thin wire, the latter may be regarded as straight. The electric field is parallel to the axis of the wire, and the magnetic field vector H is in a plane perpendicu- lar to the axis. Let us consider a wire of circular cross-section. This is a particularly simple case, because the form of the field outside the wire is immediately obvious. By symmetry, E = constant over the surface of the wire (though the value of the constant varies with time). With this boundary condition, the only solution of the equations div E = 0, curl E = outside the wire is E = constant. Similarly, the magnetic field outside the wire must be the same as it would be outside a wire carrying a constant current equal to the instantaneous value of the variable current. Inside the wire, the electric field satisfies the equation AE = (4tt(t/c 2 )^E/3^ which is the same as equation (45.6) for H; it is obtained by eliminating H from (45.1) and (45.4), just as (45.6) was obtained by eliminating E. In cylindrical co-ordinates, with the #-axis along the axis of the wire, the only non-zero component of E is E z , which depends only on r. For a periodic field of frequency co we have ;*br) + * w - ' h '^r-T' (4<u) 196 Quasi-static Electromagnetic Field §46 where 8 is the penetration depth (45.16). The solution of this equation which remains finite at r = is E = E z = constant x/ (^) e "^> (46.2) where J is the Bessel function. The current density j = oE is similarly distributed. The magnetic field H± = H is found from the electric field by equation (45.1): ■ ' H icoHfjc = (curlE)^ = -dE z Jdr. (46.3) Since Jo(u) = -Ji(u), we obtain H = 11$= - constant x i^(47Tai/a))J 1 (kr)e- i<,)t , (46.4) the constant being the same as in (46.2); it is easily determined from the condition that H = lljca on the surface of the wire, a being the radius of the wire and / the total current in it. In the limiting case of low frequencies (a[8 ^ 1) we can take the first few terms of the expansions of the Bessel functions at every point in the cross- section : E z = constant x 1 — i{rj8f (r/S) 4 ] «-*•*, 2w [ 1 In H+ = constant x r 1 — i{rj8f (r/S)* , The amplitude of E, and therefore that of the current density, increase as 1 + (f/28) 4 with increasing distance r from the axis. In the opposite limiting case of high frequencies (a/8 > 1) we can use the asymptotic formula Jo[uV(%)] ~ «-¥!-««, (46.6) which is valid for large values of the argument, over most of the cross- section. Retaining only the rapidly varying exponential factor, we have E z = constant x e -(a-r>/V<a-rW-tf<w }2na (46 ' 7) H+ = constant x(l+i) / e -ia-r)/8 e i(a-r)/8-io>t. These formulae are, of course, the same as (45.15)-(45.17), which are valid near the surface of a conductor of any shape when the skin effect is strong. In the general case of a wire whose cross-section is not circular, the exact calculation of the skin effect is considerably more involved, since the fields inside and outside the wire must be determined simultaneously. Only in the limiting case of strong skin effect is the problem again simplified, because the field outside the wire may then be determined as the static field outside a superconductor of the same shape (§45). (46.5) >—i<i>t §47 The complex resistance 197 §47. The complex resistance If the frequency of the variable current is low, the instantaneous current J(t) in a linear circuit is determined by the instantaneous e.m.f. S: *(*) = Rftt), (47.1) where R is the resistance of the wire to a constant current. There is no reason, however, to expect a direct relation between the values of $ and / at the same instant for all frequencies. We can say only that the value of J(t) must be a linear function of the values of S'it) at all previous instants. This relation may be symbolically written as / = Z~ x ^ or, conversely, * = ZJ, (47.2) where Z is some linear operator, t If the functions £(t) and J(t) are expanded as Fourier integrals, then for each "monochromatic" component (depending on time through a factor *-*"*), the effect of the linear operator Z is simply multiplication by a quantity Z which depends on the frequency: $ = Z{w)J. (47.3) The function Z(co) is in general complex. It is called the complex resistance or impedance of the conductor. It is evident from a comparison of (47.3) and (47.1) that the ordinary resistance R is the zero-order term in an expansion of the function Z{w) in powers of w. To find the next term, we must take account both of R and of the self-inductance L of the conductor.} Let us consider a linear circuit containing a variable e.m.f. £(t). By the definition of «f, the work done per unit time by the electric field on the charges moving in the wire is $J. This work goes partly into Joule heat and partly to change the energy of the magnetic field of the current. By the definition of R and L, the Joule heat evolved in the wire per unit time is Rp, and the magnetic energy of the current is LJ 2 /2c 2 . The law of conserva- tion of energy therefore gives the equation d LP 1 dj or = */+i4 («•♦) f We shall not pause here to discuss the general properties of this operator, since they are entirely analogous to those of the operator e, which will be examined in detail in §§58 and 62. t Here, and in what follows, R and L denote the values for constant current. 198 Quasi-static Electromagnetic Field §47 In order to use the quadratic expressions &J and J 2 we must write g and J as real functions. Having derived the linear equation (47.4), how- ever, we can take complex monochromatic components: $ = $oe~ i<at , J = Joe~ i<ot . Then equation (47.4) gives the algebraic relation = (*-?*)j. whence Z = R-—a>L. (47.5) Taking the real part inj= $\Z, we have JW = /tnl 2T2,^ Ct *( < ° t -®> ^^ = ° )LIC2R ' (47 ' 6) y(R 2 +u> 2 L 2 /c 4; ) which determines the amplitude of the current and the phase difference between the current and the e.m.f. The real part of the expression (47.5) is the resistance R, which deter- mines the energy dissipation in the circuit. It is easy to see that, whatever the function Z{cS), a similar relation holds between re Z and the energy dissipation for a given current. On averaging with respect to time the power &J required to maintain the periodic current in the circuit, we obtain the part of this power which continually makes good the dissipative losses. The energy dissipation in the circuit per unit time is therefore Q = \ re {&J*\ where $ and J are expressed in complex form ; see the penultimate footnote to §45. Substituting $ = ZJ and denoting the real and imaginary parts of Z by Z' and Z" respectively :t Z = Z' + iZ", (47.7) we obtain Q = %Z'IJ\ 2 or, in terms of the real function J(t), Q = S'WJS (47.8) which gives the required relation. It may be noted that, since Q is necessarily positive, Z' is also positive : Z' > 0. '47.9) We may calculate Z{oS) for a wire of circular cross-section for any fre- quency,J i.e. without neglecting the skin effect. To do so, we again use the law of conservation of energy, but in a different form. We divide the power £J (where $ and / are real) into two parts, one being the change in the magnetic field energy outside the wire, and the other the total energy con- sumed inside the wire (both in changing the field and in evolution of t Sometimes called the resistance and reactance (in Russian : active and reactive resistances). X That is, any which satisfies the quasi-steady condition. §47 The complex resistance 199 heat). The second part can be calculated as the total energy flux entering the conductor through its surface per unit time. Thus we have J dt\2c*) 4tt c* J dt where L e is the external part of the self-inductance of the wire, E and H the electric and magnetic fields at its surface, a its radius, and / its length. The field H is related to the current / by H = IJjca. Hence, dividing the above equation by /, we have c* at This is a linear equation, and hence we can use complex quantities. Then i(x)L e <?=ZJ = r J+El, c 2 whence ico El ioi 2EI z '-7^ + J = -^ L ' + ^H- (47 - 10) For general frequencies, E and H are given by (46.2) and (46.4), and we have Z = *l* +i nJgg, (47.11) c 2 J x {ka) where R = l/irePo. When the skin effect is weak, we use the expansions (46.5) ; taking terms as far as (a/8) 4 and separating the real part, we find In the opposite case of a strong skin effect we use the expressions (46.7), obtaining Z' = Ra/28 = (lIcaWHlTTo), a* r 28 I co r le ] c 2 L a A c 2 l ay(2iTaa})\ It is seen from (47.11a) that we can put Z' = R if (7racoa 2 /c 2 ) 2 ^ 12. We also have Z"\Z' = wLjc 2 R = (77acoa 2 /c 2 ) 2 log (Ija), where L is given by (33.1). Comparing this with the inequality just given, we see that the range of frequencies in which the expression (47.5) can be used to take the self- inductance into account depends on the ratio l\a and is fairly narrow. In practice, however, the most important case is that in which the self- inductance of the circuit is due mainly to coils in it, whose self-inductance is large compared with that of an uncoiled wire (see §33). In such circuits 14 200 Quasi-static Electromagnetic Field §47 formula (47.5) (i.e. equation (47.4) with constant R and L) can be used over a fairly wide range of frequencies. Let us consider a circuit in a variable external magnetic field H e , which may be generated in any manner. We denote by E e the electric field which would be induced by the variable field H e in the absence of conductors. Both H c and E e vary only very slightly over the thickness of a thin wire (unlike the field of the currents in the wire). We can therefore discuss the circula- tion of E e round the current circuit without specifying the exact position of the contour of integration in the wire. This circulation is just the e.m.f. $ induced in the circuit by the variable external magnetic field. By the integral form of Maxwell's equation we have r 1 8 r 1 d<D e ^E,dl= ---J H-df----^ (47.13) where Q> e is the flux of the external field through the circuit. Substituting this expression in equation (47.4), we obtain 1 dj 1 dO e RJ+—L^ = i (47.14) J c 2 dt c dt v ' Taking the self-inductance term to the right-hand side, we have 1 dd> e LdJ 1 dO RJ= - c dt c 2 dt c dt where <I> = ^ e + LJ/c is the total magnetic flux from the external magnetic field and the field of the current. In this form the equation gives Ohm's law for the whole circuit, i.e. the equality of RJ to the total e.m.f. in the circuit. The formulation of equation (47.14) as expressing Ohm's law makes pos- sible a generalisation of it to the case where the shape of the circuit also varies with time. The self-inductance L is then a function of time, and (47.14) becomes Id 1 dO>e RJ= —z-tALJ)— — ^ ( 47 - 15 ) c l dt c dt In deriving this from the law of conservation of energy we should have to take into account also the work done in deforming the conductor. If there are several circuits in proximity, carrying currents J a , then for each of them <fr e in equation (47.14) is the sum of the magnetic fluxes due to all the other circuits (and to the external field, if any). The magnetic flux through the ath. circuit due to the current Ji, is Labjbjc, where L a b is the mutual inductance of the two circuits. We therefore have the following set of equations for the variable currents in the circuits : RaJa + -2Lal>4- = ^ ( 47 - 16 ) c iZ —> dt b §47 The complex resistance 201 The sum over b includes the self-inductance term (b = a), and <o a is the e.m.f. produced in the ath circuit by sources external to the system of currents considered. For periodic currents of a single frequency, the system of differential equations (47.16) becomes a set of algebraic equations: XZ ab J b = *«, (47.17) where the quantities lOi Zab = $abRa ~L a b (47.18) form the impedance matrix. Like (47.5), the expressions (47.18) represent the first terms in an expansion of the functions Z a &(o>) in powers of the frequency. It should be noted that, in this approximation, the circuits have no mutual effect on the real parts of their impedances. Such an effect arises because the magnetic field of the variable current in one conductor generates eddy currents, and therefore an additional dissipation of energy, in the other conductor. For linear conductors this effect is negligible, but it may become important if extended conductors are located near them. Finally, let us consider how the equations of variable currents in linear circuits obtained in this section are related to the general equations of a variable magnetic field in arbitrary conductors. We shall take the simple example of the current set up in a circuit when a constant e.m.f. Sq is removed at time t = 0. From equation (47.4) we havet J = Sq\R for t < 0, / = (<?olR)e-c 2 ™i< for t > 0. (47.19) We see that, after the removal of the e.m.f., the current decays exponentially with time, the decrement being y = c 2 R/L. (47.20) If the problem is exactly formulated, this y is the smallest of the y m obtained by solving the exact equation (45.10) for the conductor in question. Among the y m for a linear conductor there is one, the smallest, which is less than the others by a factor of the order of log (Ija), and this is (47.20). f Strictly speaking, these formulae are invalid for very small t, when the high-frequency terms in the Fourier expansions of the functions are important and so equation (47.4) cannot be used. During this short interval of time, however, the current J cannot change signifi- cantly, and so formula (47.19) gives the current at subsequent times with sufficient accuracy. 202 Quasi-static Electromagnetic Field §48 §48. Capacity in a quasi-steady current circuit A variable current, unlike a constant one, can flow in an open circuit as well as in a closed one. Let us consider a linear circuit whose ends are con- nected to the plates of a condenser, which are at a small distance apart. When a variable current flows in the circuit, the condenser plates will be periodically charged and discharged, thereby acting as sources and sinks of current in the open circuit. Since the distance between the condenser plates is small, the magnetic energy of the current can again be taken as LJ 2 /2c 2 , where L is the self- inductance of the closed circuit which would be obtained by joining the condenser plates by a short piece of wire. In applying the law of conserva- tion of energy, however, we must take into account not only the magnetic energy but also that of the electric field in the condenser. The latter energy is e 2 /2C, where C is the capacity of the condenser and + e(t) the charges on its plates. Proceeding as in the derivation of equation (47.4), we obtaint d LP d e 2 1 dj e de SJ = RP+ -+ = RP+—LJ— + . J J dt 2c 2 dt2C J c 2 J dt Cdt The current / is equal to the rate of decrease and increase of the charges on the two plates : J = dejdt. Dividing both sides of the equation by J and expressing J in terms of e, we have 1 d 2 e de e — L + R—+— = S. (48.1) c 2 dt 2 dt C v ; This is the required equation for a variable current in a circuit with a capacity. If $ is a periodic function of time having frequency o>, then equation (48.1) reduces to an algebraic relation between $ and the charge e, or between $ and the current/ = — icoe. We have, in fact, JZ = <f , where the impedance Z is defined by (oiL 1 \ \-i\ . \ c 2 coC Z = R-i\ — - — \. (48.2) Taking real parts in the relation J = S'/Z, we obtain Sc\ COS (cut — (t)) M " "Tf — 1l 1 VI + U 2 ~oZc) (cjjL 1 \ 1 tan(£ = I 1 — r \ c 2 ojCJ R (48.3) which give the current in a circuit to which an external e.m.f. $ = $0 cos cot is applied. t In the present section we neglect the skin effect. §48 Capacity in a quasi-steady current circuit 203 If S = 0, the current in the circuit consists of "free" electric oscillations. The (complex) frequency of these oscillations is given by Z = 0, whence Re* l\ c 2 {Rc 2 \ 2 l , AQA . ---•Wb-yj- (48 - 4) We may have either periodic oscillations damped with decrement Rc 2 \2h or an aperiodically damped discharge, depending on the sign of the radicand. In the limit as R -> we have undamped oscillations whose frequency is given by Thomson's formula: a> = cj^(LC). Equation (48.1) can be immediately generalised to a system of several inductively coupled circuits containing condensers. The current J a in the ath circuit is related to the charges ± e a on the corresponding condenser by Ja = de a jdt, and equation (48.1) is replaced by the set of equations 21 _ d 2 e b de a e a „ — L ab —— + Ra— + -pr = *•• ( 48 - 5 ) , c 2 dt 2 dt C a o For periodic (monochromatic) currents, these equations give the algebraic equations S^a&/6= *a, ( 48 - 6 ) o the matrix elements Z a b being given by the formulae 7 'ab = &ab{Ra + _L r )-^„,. (48.7) oiCJ c 2 The eigenfrequencies of the current system are given by the condition of compatibility of equations (48.6) when ff a = 0, i.e. by the condition for the determinant \Z a b\ to vanish: \Z ab \ = 0. (48.8) If the resistances R are not zero, all the "frequencies" have a non-zero ima- ginary part, and the electric oscillations are therefore damped. It should be noticed that equations (48.5) are formally identical with the mechanical equations of motion of a system with several degrees of freedom which executes small damped oscillations. The generalised co-ordinates are represented by the charges e a , and the generalised velocities by the currents J a = de a jdt. The "Lagrangian" of the system is ^ = Zw^^-Z^+Z 6 " *» < 48 - 9) a, b a a 204 Quasi-static Electromagnetic Field §48 The kinetic and potential energies of the mechanical system are represented by the magnetic and electric energies of the current system, and the quanti- ties $ a correspond to the externally applied forces which cause the forced oscillations of the system. The quantities R a appear in the dissipative function R = X \R a e a \ (48.10) Equations (48.5) are the analogues of Lagrange's equations d Z& dtf BR dt de' a de a de a (48.11) PROBLEMS Problem 1. Determine the eigenfrequencies of electric oscillations in two inductively coupled circuits containing self-inductances Li and Lz and capacities Ci and Cz, neglecting the resistances R\ and Rz. Solution. The required frequencies are determined from the condition \Z a b\ = Z11Z22 — Z12 2 = 0, where / CO 1 \ / o> 1 \ IOJ Zn = — i[ — Li — , Z22 = — i\— L2 — I, Zvi.= -Z.12. \C 2 toCl/ \C 2 C0C2/ c 2 Calculation gives L1C1+L2C2+ V[(^iCi-L 2 C 2 ) 2 +4CiC2Li2 2 ] C01.2 2 = C 2 2CiC2(LiL -L12 2 ) Both frequencies are purely real, owing to the fact that Ri and R2 have been neglected. As L12 -»■ 0, 001 and o>2 tend to cl^(Lid) and c/ VCL2C2). These are the frequencies for the two circuits separately. Problem 2. The same as Problem 1, but for a circuit consisting of a resistance R, a capacity C and an inductance L connected in parallel. Solution. The impedances of the three branches are Z\ = R, Z2 = ijoiC, Zs = —ioiLjc 2 , and the currents in them are such that _/i +.72+73 = 0, Z1J1 = Z2J2 = .Z3./3. Hence we have I/Z1+I/Z2+I/Z3 = 0, whence ™ = ~ 2RC ± V LLC ~ 4R 2 C 2 Y Problem 3. Discuss the propagation of electric oscillations in a circuit consisting of an infinite succession of identical meshes containing impedances as shown in Fig. 25. Find the range of frequencies which can be propagated in the circuit without damping. \ f The condition for the quasi-steady theory to be applicable to such a periodic circuit is that the dimension of one mesh should be small compared with the "wavelength" cjoi. §49 Motion of a conductor in a magnetic field 205 Solution. The current in mesh a is denoted by ta, as shown in Fig. 25. Kirchhoff's second law gives for this mesh Zii a +Z2(2i a — ta_i — t'a+i) = 0. This is a linear difference equation in the integral variable a, with constant coefficients. We seek the solution in the form ta = constant X q*, obtaining for the parameter q the equation g2 _( 2+ |) g+1 = . (1) Let —4 ^ Zi/Zt < 0, corresponding to values of a> 2 lying between c 2 /LiCi and c 2 (4/C2+l/Ci)/(4Z,2+I,i). Then equation (1) has two complex conjugate roots with moduli q\ = 1. This means that the current does not decrease from one mesh to the next, i.e. the electric oscillations are propagated in the circuit without being damped. Putting q = e m , where I is the length of one mesh and k is the "wave number" of the oscillations propagated in the circuit, we can calculate the velocity of propagation u from the general result u = douldk. Fig. 25 If, however, (o is outside the range mentioned, equation (1) has two real roots qi and 52, say; since qiqz = 1, one root (qi, say) is less than 1 in absolute magnitude, while q% is greater. It is easy to see that the propagation of undamped oscillations in the circuit is then impos- sible. To elucidate the reason for this, let us consider a circuit of large but finite length. An initial oscillatory impulse is given to one end of the circuit, the other end being closed in some manner. This closure corresponds mathematically to a certain boundary condition, by means of which we can determine the ratio of the coefficients c\ and c% in the general solution ci<7i - ( a fc" a) +C2<72 -(a k _a) , where a* is the "co-ordinate" of the end of the circuit. This ratio is of the order of unity. As a*— a increases, the second term in the solution rapidly becomes very small compared with the first term, because \qz\ > 1. Thus the solution is f a = ciqi~^k~ a '> everywhere except for a small part near the end of the circuit, and |t a | de- creases towards the end of the circuit. It should be emphasised that this damping does not involve dissipative absorption, because there is no resistance in the circuit; it can be imagined as being the result of reflection of the oscillatory impulse from each successive mesh of the circuit. §49. Motion of a conductor in a magnetic field Hitherto we have tacitly assumed that a conductor in an electromagnetic field is at rest in the frame of reference K in which E, H, etc. are defined. In particular, the relation j = aE between the current and the field is generally valid only for conductors at rest. To determine the corresponding relation in a moving conductor, we change from the frame K to another frame K! in which the conductor, or some part of it, is at rest at the instant considered. In this frame we have j = ctE', where E' is the electric field in K'. The well-known formula for the transformation of fields! gives E' in terms of the fields in K: E' = E + vxB/c, (49.1) f See The Classical Theory of Fields, §3-10, Addison-Wesley Press, Cambridge (Mass.) 1951 ; Pergamon Press, London, 1959. The microscopic values of the electric and magnetic fields are replaced by their averaged values e = E, fa. = B. 206 Quasi-static Electromagnetic Field §49 where v is the velocity of K' relative to K, i.e. in this case the velocity of the conductor, which we of course suppose small compared with the velocity of light. Thus we find j = a(E + vxB/c). (49.2) This gives the relation between the current and the field in moving con- ductors. The following remark should be made concerning its derivation. In going from one frame of reference to the other we have transformed the field but left the current j unaltered. The correct transformation of the current density gives only terms of a higher order of smallness if v <^ c. In formula (49.2) the second term, which appears as a result of the field transformation, is in general not small compared with the first term, despite the factor vjc. For example, if the electric field is due to electromagnetic induc- tion from a variable magnetic field, its order of magnitude contains a factor \\c as compared with the magnetic field. The energy dissipation in a conductor when a given current flows in it cannot, of course, depend on the motion of the conductor. The rate of evolution of Joule heat per unit volume in a moving conductor is therefore given in terms of the current density by the same expression pja as for a conductor at rest. The expression j«E, however, is replaced byt / 2 /cr = j.(E + vxB/<r). Thus, in a moving conductor, the sum E + vxB/c acts as an "effective" electric field producing the conduction current. Hence the e.m.f. acting in a closed linear circuit C is given by the integral £ = £(E + vxB/c).dl. (49.3) c This expression can be transformed as follows. According to Maxwell's equation, curl E = — (l/c)dB/cfr, and so <fE-dl = JcurlE-df = JVdf c s s or, denoting by <E> the magnetic flux through the surface S, which spans the circuit C, r l/8<!>\ cfE-dl = — t It is seen from this formula that the additional heat evolved in time St in a conductor moving in a magnetic field is 8* J j-v X B dV/c = - J uj X B dV/c, where u = vSt is the displacement in time St. This expression is equal and opposite to the work done on the conductor in time St by the volume forces f = j X B/c. This explains the apparent contradiction mentioned in §34. §49 Motion of a conductor in a magnetic field 207 The time derivative with the suffix v = denotes the rate of change of the magnetic flux due to the time variation of the magnetic field, the position of the contour C remaining unchanged. In the second term in (49.3), we put v = du/di, where du is an infinitesimal displacement of the circuit element d/. Then |vxB-dl = cfduxB-dl/d* = -j>B.df/df, c s where df = duxdl is an element of area on the "side" surface 5 between two infinitely close positions C and C" of the current circuit, which it occupies at times t and t + dt (Fig. 26). Since the total magnetic flux through any closed surface is zero, the flux through s must evidently equal the difference of the fluxes through surfaces spanning C and C". Thus <|>vXB«dl = -(£<!>/ d*)B=constant, c where the time derivative denotes the rate of change oi the magnetic flux due to the motion of the conductor in a constant field. Fig. 26 Adding the two terms, we have finally & = -(l/c)d®/dt, (49.4) where the time derivative now denotes the total rate of change of the magnetic flux through the moving circuit. Thus the expression (49.4), which is Faraday's law, is valid whatever the reason for the change in the magnetic flux, whether variation of the field itself (already discussed in §47, formual (47.13)) or motion of the conductor. In a constant magnetic field, the change in the flux is due entirely to the motion of the circuit. If the circuit moves in such a way that every point of it moves along a line of force, then the flux through the circuit does not vary. This is an obvious result of the fact that the magnetic flux through any closed surface is zero, and the flux through the "side" surface described by the moving circuit is in this case identically zero (since B n = on this surface). Thus we can say that, to induce an e.m.f., the conductor must certainly move so as to cross lines of magnetic force. 208 Quasi-static Electromagnetic Field §49 The electromagnetic field in a moving conductor is given by the equations curlE = -(l/c)dBldt t curlH = 4rrj/c = (4w<j/c)(E + vxB/0, div B = 0. Expressing E in terms of H by means of the second equation and substituting in the first, we obtain dB c* /curlH\ curl (v x B) = curl . (49.5) 8t 4tt \ a J In a homogeneous conductor with constant conductivity a and constant magnetic permeability ft, we have dU c* curl(vxH) = AH, divH = 0. (49.6) dt ^nafx These equations generalise those obtained in §45. It should be pointed out, however, that, if there is only one conductor moving as a whole (without change of shape) in an external magnetic field, then the solution of the problem is considerably simplified if we use a system of co-ordinates fixed in the conductor. In this system the conductor is at rest, and the external field varies with time in a given manner, so that we return to the eddy-current problems discussed in §45. This possibility does not depend on Galileo's (or on Einstein's) relativity principle, since the new system of co-ordinates is in general not inertial. The equivalence of the problems results from the above-mentioned fact that the electromagnetic induction is independent of the cause of the change in the magnetic flux. This equivalence can also be demonstrated mathematically. To do so, we expand the expression curl (vxB), using the facts that divB = and (for motion of the body as a whole) div v =0 (i.e. the body is "incompressible"). Then the left-hand side of equation (49.5) becomes dB/d* + (v.grad)B-(B.grad)v. (49.7) This sum is just the time derivative of B with respect to axes fixed in a rotating body. For the sum of the first two terms is the "substantial" time derivative dB/d*, which gives the rate of change of B at a point moving with velocity v. The third term takes into account the change in the direction of B relative to the body; it is zero for pure translation (v = constant) and equals — Six B for rotation (v =fixr, where SI is the angular velocity). To conclude this section, let us consider the phenomenon of unipolar induction, which occurs when a magnetised conductor rotates. If a stationary wire is connected to the rotating magnet by means of two sliding contacts A and B (Fig. 27) then a current flows in the wire. It is not difficult to calculate the e.m.f. which produces the current; the simplest procedure is to use a system of co-ordinates rotating with the magnet. If SI is the angular velocity §49 Motion of a conductor in a magnetic field 209 of rotation of the magnet, then in the new system the wire rotates with angular velocity -SI, while the magnet is at rest. Thus we have a conductor moving in a given constant magnetic field B due to a fixed magnet. We neglect the distortion of the field by the wire itself. According to formula (49.3), the e.m.f. between the ends of the wire is = - fvxBdl = — fBx(rxSi)«dl, ACB ACB (49.8) taken along the wire. This is the required solution. Fig. 27 PROBLEMS Problem 1. Determine the magnetic moment of a conducting sphere (with ja = 1) rotating uniformly in a uniform constant magnetic field, and the torque on the sphere. Solution. Let the external field have components <r>x, 0, § z in a fixed system of co- ordinates with the #-axis in the direction of the angular velocity vector SI. In a co-ordinate system £, -q, z which rotates with the sphere, the field components are §c = |)x cos ilt, § = -§ x sin at, $>z, or, in complex form, £? = $> x e~ int , £„ = -*$*« im , §>*■ Thus variable fields of frequency O act along the £ and r, axes, and the magnetic moment which they induce is Jl % = V re (<x£f;) = V&d*' cos Qf +<x" sin Clt), uTt, = V re («&,) = V§> x (-*' sin fi«+a" cos Clt), where Vol is the complex magnetic polarisability of the sphere, which has been determined in §45 Problem 1. Along the z-sxis, on the other hand, the magnetic field is constant, and therefore causes no magnetic moment (if /t = 1). The components of the magnetic moment in the fixed system of co-ordinates are Jl x = V«.'$ x , Jt v = VaTfe, -**= 0. Thus in this problem a' and a" give the components of the magnetic moment of the sphere respectively parallel and perpendicular to the plane of the vectors Si, and |). The torque on the sphere is K = M X |>. Its components relative to the fixed axes are K x = Va"& x £t, K y = -Fa'§x$ 2 , K. = -Va"$f. Problem 2. Determine the e.m.f. due to unipolar induction between the pole and the equator (Fig. 27) of a uniformly magnetised sphere rotating uniformly about the direction of magnetisation. Solution. When the sphere rotates about its direction of magnetisation, it generates a constant field, and, since no currents flow within the sphere, we find from (49.5) that curl (vxB) = 0. Hence the integral of vxB along the closed contour OACBO (Fig. 27) 210 Quasi-static Electromagnetic Field §50 is zero, and so the integration along ACB in formula (49.8) may be replaced by one along the path AOB, which lies inside the sphere. The integral along the segment AO of the axis of rotation is zero, since £2 and r are parallel ; the integral along the radius OB gives, since B and SI are parallel within the sphere, a Bo&rdr = B Oa 2 /2c, where a is the radius of the sphere and Bo the magnetic induction in it. In a uniformly magnetised sphere (in the absence of an external field) the induction is related to the mag- netisation by Bo+2H = (cf. (8.1)) and Bo—H = AitM, whence Bo = 8ttM/3. In terms of the total magnetic moment of the sphere we have finally & = CL^Ica. Problem 3. Determine the total charge which flows along a closed linear circuit when the magnetic flux through the circuit changes for any reason from one constant value ($i) to another (^2). Solution. The required total charge is the integral o Jdt, I where J{t) is the induction current in the circuit. Mathematically, this integral is the Fourier component of the function J(t) that has the frequency w = 0. It is therefore related to the corresponding component of the e.m.f. by 00 00 [Sdt = Z(0) jjdt; see (47.3). Putting Z(0) = R, where R is the resistance of the circuit to a constant current and & = — (1/c) d<D/d£, we have 00 §50. Excitation of currents by acceleration In discussing the motion of a conductor in §49 we have neglected possible effects of the acceleration, if any. The accelerated motion of a metal, how- ever, is equivalent to the action of additional inertia forces on the conduction electrons. If v is the acceleration of the conductor and m the mass of the electron, then the force on an electron is -mv. It affects the electron in the same way as an electric field mv/e, where — e is the charge on the electron. Thus the "effective" electric field on the conduction electrons in an acce- lerated metal is E' = E + mv/e. (50.1) The current density is accordingly j = a E f = <r{E + mv/e). (50.2) §50 Excitation of currents by acceleration 211 Expressing E in terms of E' from (50.1), we substitute in the equation curl E = —(\jc)dHldt (as usual, we put ju = 1). Then 1 8U m curlE' = + — curly. (50.3) c 8t e We write v as a sum v = u + SI x r, where u is the translational velocity and SI the angular velocity of rotation of the body. Differentiating with respect to time, we find the acceleration to be v =u + fllxv+ Slxr = u + flxu+ + fix(flxr) + Axr. The first two terms are independent of r, and there- fore give zero on differentiation with respect to the co-ordinates. The third term can be written as SI x (Six r) = — | grad (Slxr) 2 , and its curl is there- fore zero. Finally, curl (Slxr) — 2€l. Thus, substituting for v in equation (50.3), we have curlE' = -(l/c)aH/d* + 2m6/e or 1 dW curlE' = , (50.4) c dt where H' = rl-lmcSlje. (50.5) Since SI is independent of the co-ordinates, the equation curl H = 477-j/c is still valid if H is replaced by H' : curlH' =.4ir<rE'lc. (50.6) Eliminating E' from equations (50.4) and (50.6), we obtain for H' the equation AH' = (^a/c^dH'/dt, (50.7) which is the same as the equation for H in a conductor at rest. Outside the body, the field satisfies the equation AH = (the wavelength being supposed large compared with the dimension of the body), and H' satisfies the same equation. Finally, on the surface of the conductor H', like H, is continuous. The only difference is in the condition at infinity, where H tends to zero but H' tends to the limit —ImcSlje. Thus the problem of determining the variable magnetic field H near a non-uniformly rotating body is equivalent to that of determining the field H' near a body at rest in a uniform external magnetic field £ = -2mcSl/e. (50.8) The required field H e outside the conductor is obtained by subtracting |) from the solution H' of this latter problem, t t Misunderstanding may arise from the appearance of the angular velocity Si itself, and not its time derivative, in formula (50.8). We may therefore emphasise that the above dis- cussion, and therefore the significance here attached to the quantity (50.8), pertain only to non-uniform rotation. In particular, the field (50.8) is unrelated to the gyromagnetic effect (which appears even when the rotation is uniform, and is a small quantity here neglected). 212 Quasi-static Electromagnetic Field §50 The magnetic field thus produced, like any variable field, induces electric currents in the conductor itself. In a simply-connected body, these currents appear in the form of a magnetic moment. In a non-uniformly rotating ring, the effect appears as an e.m.f. — the Stewart-Tolman effect. PROBLEMS Problem 1. Determine the magnetic moment of a non-uniformly rotating sphere of radius a. The rate of rotation is assumed so small that the penetration depth 8 ^> a. Solution. The magnetic moment of the sphere in the field £>(t) (50.8) is M = Va.%, where a is an operator whose action on the Fourier components of the function $)(t) is given by the formulae of §45, Problem 1. For the components with frequencies a> such that S^>a we have M — y<x(a>).$ ~ — Amna 5 oioo£ll\5ce. This formula, when written M = (4irtna 5 o/15ce) dSi[dt, does not contain to explicitly, and is therefore valid also for the functions Jl and Si themselves, as well as their individual Fourier components (on the assumption that the Fourier expansion contains chiefly terms whose frequencies satisfy the above condition). Problem 2. Determine the total charge which flows along a thin circular ring when it ceases a uniform rotation about an axis perpendicular to its plane. Solution. In the formula obtained in §49, Problem 3, <£> must be taken as the flux of t he field $) (50.8). The total charge transferred when the angular velocity changes from Si r ,. , 2mc ^ ,„ maV n J eKc 2ire —00 where b is the radius of the ring and V its volume. Problem 3. Determine the current in a superconducting circular ring which ceases to rotate uniformly. Solution. From the condition that the total magnetic flux through the ring is constant (see (42.5)), we have 2mc 2 mc 2 b£l J = Qwfc 2 = eL 2e[log(8bla)-2] See the third footnote to §42 concerning the value of L. CHAPTER VIII MAGNETIC FLUID DYNAMICS §51. The equations of motion for a fluid in a magnetic field If a conducting fluid moves in a magnetic field, electric fields are induced in it and electric currents flow. The magnetic field exerts forces on these currents which may considerably modify the flow. Conversely, the currents them- selves modify the magnetic field. Thus we have a complex interaction between the magnetic and the fluid-dynamic phenomena, and the flow must be examined by combining the field equations with those of fluid dynamics. We shall use equations (49.6) as the field equations in a moving conduct- ing medium. The magnetic permeability of the media considered in magnetic fluid dynamics differs only slightly from unity, and the difference is unimpor- tant as regards the phenomena under discussion. We shall therefore take fi = 1 throughout the present chapter. The equations are then div H = 0, (51.1) m/dt = curl (v x H) + (c 2 /47r<r) AH. (51.2) By using these equations we assume that certain conditions are fulfilled. The period of variation of the field must be large compared with the mean free time of the conduction electrons. Then the relation between the current and the electric field involves the same conductivity a as for a constant current (see §45). t Here we assume that a is constant in the medium, and therefore, in particular, that the conductivity is independent of the magnetic field. For this to be so, the mean free path of the electrons must be small in comparison with the radius of curvature of their orbits in the magnetic field. That is, the mean free time must be small compared with the reciprocal of the electron Larmor frequency eHjmc. This condition may not hold if the medium is rarefied and the magnetic field is strong. The equations of fluid dynamics are the equation of continuity d P ldt+ div (px) = 0, (51.3) t In the second footnote to §45 the further condition ola>p> 1 was mentioned as being necessary for poor conductors. In good conductors this condition is always satisfied if the other conditions are. In the present case the frequency is represented by VjL, where L and V axe characteristic parameters of length and velocity which determine the properties of the flow. Thus we assume the condition oLjV ^>1 to hold. 213 214 Magnetic Fluid Dynamics §51 where p is the fluid density, and the Navier— Stokes equation dv 1 77 1 f — + (v^grad)v = grad/> + -Av + -(£ + \tj) grad diw + -, 8t p p P p where 77 and £ are the two coefficients of viscosity for the fluid, and f is the volume density of external (in this case, electromagnetic) forces. By formula (34.4) we have f = j x H/c = (curl H) x H/4tt. Thus the equation of motion of the fluid is — + (vgrad)v 11 1? 1 = grad/> H x curlH + - Av + -(£ + ^7) grad diw. (51.4) P 4tt P p p To these equations we must add the equation of state p=p( P ,T), (51.5) which relates the pressure, density and temperature of the fluid, and the equation of heat transfer. In ordinary fluid dynamics the latter ist ids \ dvf pT (— + vgrads = a'a-r— + div (k grad T). \ot / dxjc Here s is the entropy per unit mass of the fluid, and the left-hand side of the equation is the quantity of heat generated per unit time and volume in a moving fluid particle. The right-hand side is the energy dissipated per unit time and volume. The first term is due to viscosity ; a'ik is the viscous stress tensor : /8v t dv k 2 8vi\ = V — + -o ik —I + ibijc- \oxk oxi 5 oxi I The second term gives the dissipation due to thermal conduction, #c being the thermal conductivity. In a conducting fluid, a term giving the Joule heat must be added. The rate of evolution of this heat per unit volume is j 2 ja = (£ 2 /167r 2 <r)(curl H) 2 . The equation of heat transfer in magnetic fluid dynamics is therefore (ds \ dvi c 2 — + vgrads = a' tt — + div(*grad T) + — — (curlH) 2 . (51.6) Ot / 0Xk iOTT^a Equations (51.1)— (51.6) form a complete system of equations of magnetic fluid dynamics, on the assumptions stated at the beginning of this section. f See Fluid Mechanics, §49, Pergamon Press, London, 1959. §5 1 The equations of motion for a fluid in a magnetic field 215 Equations (51.4) and (51.6) can also be written in forms which express the laws of conservation of momentum and energy respectively. The Navier- Stokes equation of ordinary fluid dynamics can be written (using the equation of continuity) in the formt d{pvi)ldt = - dlliicldxic, (51.7) where Hoc is the momentum flux density tensor: U ik = pvi v k+ phk— a \ k . Equation (51.4) can be brought to the same form, but Uuc now contains an additional term. We have Hx curl H = igrad# 2 -(H-grad)H. Thus n ik = pvm + p8 ik - a' ik - (HiH k - W 2 8ik)l^r. (51.8) The added term is the Maxwell stress tensor of the magnetic field, as it should be. The equation of heat transfer can be transformed (using the other equa- tions of fluid dynamics) into an equation of conservation of energy. In ordinary fluid dynamics we have d{\pv 2 + pe)jdt = — divq, where q is the energy flux density: q = pv(|© 2 + w) - v«o' - Kgrad T; € and w = €+pjp are respectively the internal energy and heat function per unit mass of fluid. When a magnetic field is present in the conducting medium, the energy density includes also the magnetic energy # 2 /8tt, and the energy flux density includes also the Poynting vector cE x H/4tt. Express- ing E in the latter in terms of H we obtain q = p V (|^ 2 + w) + — H X (v XH) - 4n- c H X curlH - v-o' - /cgrad T, (51.9) 167T 2 <7 and the equation of conservation of energy is d / H 2 \ (51.10) It is not difficult to verify by direct calculation that equations (51.6) and (51.10) are equivalent. The equations are somewhat simplified if the moving fluid can be sup- posed incompressible. The equation of continuity (51.3) then reduces to div v = 0, while in equation (51.4) the last term is zero. For reference, we shall write out here the complete system of equations for an incompressible fluid (in equations (51.2) and (51.4) we have transformed the terms t See Fluid Mechanics, §15. IS 216 Magnetic Fluid Dynamics §51 curl(vxH) and HxcurlH respectively by the appropriate formulae of vector analysis) : divH = 0, divv = 0, (51.11) mfit + (vgrad)H = (Hgrad) v + (c 2 /4rra) AH, (51.12) Sv — + (v-grad)v 1 / H 2 \ 1 = --grad U + _-)+__ (H-grad)H + ^Av, (51.13) p \ 07T / *riTp where v = rj/p is the kinematic viscosity. Equation (51.6) is not needed in solving the problem of incompressible flow unless we are interested in the temperature distribution and its effect on the flow. Let us return to the general equation (51.2). In the limiting case of very high conductivity it becomes dH/dt = curl(v x H), (51.14) an equation which has a very important physical interpretation. We expand the right-hand side, using the fact that div H = : dH/dt = (Hgrad) v - (vgrad)H - H divv. Substituting from the equation of continuity (51.3) 1 dp v«grad/o divv = , p 8t p we obtain after a simple rearrangement of terms id \H /H \ W + v,grad J7 = l7 ,grad ) v ' The left-hand side is the "substantial" derivative, which gives the rate of change of H/p for a given fluid particle as it moves about. Denoting this derivative by d/d£, we have d /H \ -(H/ P )= (—gradj*;. (51.15) Let us now consider some "fluid line", i.e. a line which moves with the fluid particles composing it. Let SI be an element of length of this line ; we shall determine how SI varies with time. If v is the fluid velocity at one end of the element SI, then the fluid velocity at the other end is v + (Sl»grad)v. During a time interval dt> the length of SI therefore changes by d£(Sl»grad)v, i.e. d(Sl)/d* = (Sl»grad)v. We see that the rates of change of the vectors SI and H/p are given by identical formulae. Hence it follows that, if these vectors are initially in the same direction, they will remain parallel, and their lengths will remain in the same ratio. In other words, if two infinitely close §5 1 The equations of motion for a fluid in a magnetic field 217 fluid particles are on the same line of force at any time, then they will always be on that line of force, and the value of H\p will be proportional to the dis- tance between the particles. Passing now from particles at an infinitesimal distance apart to those at any distance apart, we conclude that every line of force moves with the fluid particles which lie on it. We can picture this by saying that (in the limit a ->• oo which we are considering) the lines of magnetic force are "frozen" in the fluid and move with it. The quantity H\p varies at every point proportionally to the extension of the corresponding "fluid line". If the fluid may be supposed incompressible p = constant, and the field H varies as the extension of the lines of force. These results can be viewed in another way: as any closed fluid contour moves about in the course of time, it cuts no line of force, i.e. the "number" of lines of force passing through the contour remains unchanged. This means (cf. §49) that the flux of the magnetic field through any surface spanning the fluid contour does not vary with time. To the question of when in fact dissipative processes in the fluid may be neglected there is no general answer, since the necessary conditions depend greatly on the nature of the motion and are, for instance, completely different for steady and for non-steady flows. We shall not investigate the general problem here. PROBLEM Determine the velocity distribution in an incompressible viscous conducting fluid in steady flow between two parallel solid planes, when a uniform external magnetic field Ho is applied perpendicular to the planes (J. Hartmann, 1937). Solution. It is natural to assume that the fluid velocity is everywhere in the same direc- tion, which we take as that of the *-axis, and depends only on the co-ordinate z (whose direction is perpendicular to the planes). The same is true of the longitudinal field H x resulting from the motion. The pressure p, however, depends on * also, because there must be a constant pressure gradient in the direction of motion in order to maintain a steady flow. The equation div v = is satisfied identically, while from div H = it follows that H z = constant = Ho. The ar-component of equation (51.13) gives 07T where P(x) is a function of x only. The pressure gradient in the ^-direction is — dp/dx = —dP/dx = constant. The ^-components of equations (51.12) and (51.13) give dz 4wff dz* d 2 » Ho dff* dP n 1 = constant = — — . \3) dz 2 \it dz dx The boundary conditions for viscous flow are v = for z = ±a, where 2a is the distance between the solid planes, and the plane z = lies half-way between them. The magnetic field must satisfy the conditions H x = for z = ±a, since the magnetic field outside the fluid is just Ho, and the tangential magnetic field component is continuous at the boundary. 218 Magnetic Fluid Dynamics §52 The solution of equations (2) and (3) which satisfies these conditions is cosh (a/ A) —cosh (z/A) v = vo- cosh(a/A) — 1 tj 47r // ,(*/a)sinh(a/A)-sinh(s/A) H x = -VQr- V(°v) ... , (4) c cosh (a/ A) — 1 where A = (clHo)V(.vl a )- The constant vo is the fluid velocity on the median plane z = 0. Its relation to the pressure gradient is given by substituting (4) in (3). The fluid velocity averaged over the cross-section is If, dPaA/a A\ v = — - \ v dz — (com— 1. 2a J d# 17 \ A a / The effect of the magnetic field on the flow is characterised by the ratio a/A = (aHolc)V(°lv)' For a/A <^ 1 we have / z\ dP a 2 v = vo\ 1 r), v — , \ a 2 / dx 3i7 in accordance with the results of ordinary fluid dynamics. If aj A ^> 1, then dP ac w = 7 ;( ) (l_g-(a-|2l)/A) > dx HoV( or iy When the magnetic field increases, the velocity profile is flattened over the major part of the cross-section, and the mean velocity is reduced (for a given pressure gradient). §52. Hydromagnetic waves Let us consider the propagation of small disturbances in a homogeneous conducting medium in a uniform constant magnetic field Ho. We shall assume that the viscosity, thermal conductivity and electric resistance (l/o-) of the medium are so small that their effects, due to the dissipation of energy, on the propagation of perturbations may be neglected in a first approximation.! Then the perturbations will be propagated as undamped waves.t Omitting all dissipative terms, we can rewrite the fundamental equations (51.1)-(51.4) as divH = 0, (52.1) dH/dt = curl(vxH), (52.2) dpldt + 6iv(pv) = 0, (52.3) dv grad p 1 — + (v-grad) v = - + (curlH) X H. (52.4) Bt p 47T/3 f It should be noted that, by putting l/o = 0, we extend the range of frequencies in which the equations are applicable: the conditions that a should exhibit no dispersion and should be independent of the magnetic field are now irrelevant. X The condition for this approximation to be valid is that the wave damping coefficient (calculated in the Problem at the end of this section) should be small. §52 Hydromagnetic waves 219 Equation (51.6) reduces to the equation of conservation of entropy (the condition for adiabatic flow). If the unperturbed medium is homogeneous, then this condition means that s = constant in the perturbed medium also, i.e. the flow is isentropic. We write H = H +h, p = po + p', p=po+p', (52.5) where the suffix denotes the constant equilibrium value, and h, p and p' are the small variations in the wave. The velocity v, which is zero in equili- brium, is a small quantity of the same order. Since the flow is isentropic, the changes in pressure and density are related by p' = {dpfdp) s p. But {dpjdp) s is the square of the velocity of sound, which we denote by u : p' = UQ 2 p ' m Neglecting terms of higher order than the first in equations (52.1)-(52.4), we obtain the linear equations divh = 0, dh/dt = curl(v X H), \ 0p7& + /»divv = 0, (52.6) dv/dt = - (m 2 /p) grad p'-(Hx curl h)/4ir/>. ' Here and in what follows we omit, for brevity, the suffix zero to the equili- brium values. For a perturbation periodic in time, the first of these equations follows from the second and can be omitted. We shall seek solutions of these equations which are proportional to exp [t(k-r— co*)], i.e. which describe the propagation of plane waves with wave vector k and frequency oo. The system of equations (52.6) then gives the algebraic equations - o»h = k x (v x H), cop = pk.v, -a>\ + (u 2 lp)p'k = - H x (k x hW. The first of these shows that the vector h is perpendicular to the wave vector k, which we shall take to be along the #-axis, with the plane of k and H as the xy-plane. We also introduce the phase velocity of the wave, u = o)/k. Eliminating p from the third equation by means of the second equation, and rewriting the result in components, we have uh z = - v z H x , uv z = - H x h z /4irp, (52.7) Uky = V X Hy - VyH X , UVy = - H X hy\^p, I U ° 2 \ TJU,^ (52 ' 8) Vx\u 1 = Hyhyj^np. We have here separated the equations into two groups, the first involving only h z and v z and the second only hy, v x and v y . It therefore follows that perturbations of the two groups of variables are propagated independently. The density, and therefore the pressure, belong to the second group, since p = pvxfu. (52.9) 220 Magnetic Fluid Dynamics §52 The compatibility condition for the two equations (52.7) is u = m = H x /^/(4n P ). (52.10) In these waves the component h z of the magnetic field which is perpendicular to the directions of propagation and of the constant field H oscillates, and with it the velocity v z , which is related to h z by v z = -h z /V(^r P ). (52.11) The relation between to and k (the dispersion relation, as it is called) given by (52.10) involves the direction of the wave vector: a> = H.k/V(4ir/>). The physical velocity of propagation of the waves is called the group velocity and is given by the derivative dco/dk. In the present case we have dajjdk = Hl-\/(4iTp), which does not involve the direction of k. The direction of propagation of the wave, in the sense of the direction of its group velocity, is the direction of H. Let us now consider waves described by equations (52.8). Equating to zero the determinant of these equations, we obtain (m 2 — Mo 2 ) I u 2 — HJ\ = u 2 Hy 2 \Ttpl Airp The roots of this quartic equation for u aret If // „ H 2 H xUo 11 1/ H* H xUo \ 47T/J \/( 7r / ) ) ± y(" + S-^)i- (5zi2) Thus we obtain two more types of wave. In these waves the quantities h y , v x and v y (and the density />') oscillate. The vectors h and v are in the plane of H and k. In the limiting case where H 2 < 47rpuo 2 we have u% £ wo, and it follows from equations (52.8) that v y <^ v x . In other words, in the limit waves of this type become ordinary sound waves propagated with velocity uq. The weak transverse field in the wave is related to v x by h y ^ v x H y /uo. In the same limiting case, us is the same as u\ to a first approximation, and "Vx = 0, v y ^ —h y j^/(ATrp) as in a wave of the first type, but with the vectors v and h parallel to the plane of k and H instead of perpendicular to it. We see also that in an incompressible fluid (corresponding formally to the limit mo -> oo) only one type of wave occurs, with two independent direc- tions of polarisation. The dispersion relation for these waves is given by t The roots of the quartic equation x*+ px 2 + q = can be written x= ± UV(- p + 2Vq) ± V(~ p- 2Vq)}- §52 Hydromagnetic waves 221 formula (52.10); the vectors v and h are perpendicular to k and are related by v = - h/V(4ir/>). < 52 - 13 ) Such waves were first discussed by H. Alfven (1942). t There is a simple interpretation of the result that, in a longitudinal mag- netic field, transverse displacements of the fluid are propagated in the form of waves. We have seen at the end of §51 that the lines of magnetic force behave like fluid lines when a -> oo. The transverse displacement of the fluid particles results in a curvature of these lines, and therefore in their stretching and, at some points, in their compression. The forces in a mag- netic field (expressed by the Maxwell stress tensor) are such as would occur if the lines of magnetic force tended to contract and also to repel one another.* Hence a curvature of the lines results in "quasi-elastic" forces which tend to straighten them, leading to further oscillations. It is interesting that, in an incompressible fluid, the plane hydromagnetic wave given by formulae (52.10) and (52.13) is in fact an exact solution of the equations, valid for any transverse field h (not necessarily small). (This state- ment does not apply, however, to a superposition of several plane waves propagated in different directions.) For, let us return to the exact equations (52.1)-(52.4). In an incompressible fluid, equation (52.3) becomes div v = 0. If we seek a solution in which all quantities depend on only one co-ordinate 9c and the time t , we find from this equation that v x = constant, and by taking another system of co-ordinates moving uniformly in the ^-direction we can put v x = 0. From the equation div H = it follows that H x = constant. Denoting the transverse components of H by h, we obtain from equations (52.2) and (52.4) (with v x = 0) dh/dt = H x d\\dx, dvjdt = (Hxfapflhl dx, i.e. the exact equations necessarily reduce to the linear equations for a plane wave with the phase velocity (52.10), v and h being related by (52.13). The x-component of equation (52.4) is i* + _L h 3.o, p dx 47T/> dx whence p + A 2 /8tt = constant, (52.14) which gives the manner of variation of pressure in the wave. Let us return to formulae (52.8) and (52.12), and consider the opposite limiting case, where H 2 > 4tt/)Mo 2 - We then have, in the first approxima- tion, u 2 = HI^/(4ttp). Since this expression is independent of k, the group velocity is of magnitude ui and its direction is that of k. In this wave the t They are sometimes called hydromagnetic waves. In the general case, where the magnetic fields are not small, the waves cannot be divided into hydromagnetic waves and ordinary soundwaves. .... „ ,-. ox X For, let a line of force be along the .sr-axis. Then the longitudinal stress ll z « (51.8) contains a negative term — H 2 /8tt, and the transverse stresses n** andllyj, contain a positive term H 2 IStt. 222 Magnetic Fluid Dynamics §5 vector v is perpendicular to H (Fig. 28), and its magnitude is given in terms of h = hy by v = h\^{^rrp). For us we have in this limiting case us = uoHx/H. The group velocity is daijdk = uqRJH. The vector v in this case is antiparallel to H, and its magnitude is given by v = hH 2 /4TTpuoH y . When the relation between H 2 and puo 2 is arbitrary, both «2 and us depend on the direction of the wave vector. When the angle between k and H increases, «2 increases monotonically and us decreases monotonically. It is easy to see that the inequalities us <: U\ < «2, "2 > uq, us < uo (52.15) always hold. If k is parallel to H (H y = 0, H x = H), u% and us are respec- tively equal to the greater and the smaller of uq and u\ — Hj-\/(AiTp). If k is perpendicular to H (H x = 0, H y = H), then H 2 "2 V \ ° 477/>/ (52.16) while u± and us are zero, i.e. only one type of wave exists. Fig. 28 In this last case it is possible to find exact solutions of the equations of magnetic fluid dynamics for a plane wave, without assuming its amplitude to be small (S. A. Kaplan and K. P. Stanyukovich, 1954). When H x = 0, H y = H, equation (52.1) is satisfied identically, and equations (52.2)-(52.4) give dHJdt + d{v x H)jdx = 0, (52.17) dp/dt + d(v xP )ldx = 0, (52.18) 1 8H 2 1 dp p 8x dv x dv x h V x 1 8t 8x Snp 8x (52.19) From the first two of these equations it is easily seen that the ratio Hjp = b satisfies the equation 8bj8t + v x 8bj8x = or db/dt =0, where the total derivative signifies the rate of change in a given fluid particle as it moves §52 Hydromagnetic waves 223 about. Hence, if the fluid is homogeneous at some initial instant, so that b is constant, then at all subsequent instants we havet H/ P = b = constant. (52.20) Substituting in the third equation H - pb, we obtain d ^ + J^=- l -% + b lA (52.21) 8t dx P dxV 87/ / Thus the magnetic field has been eliminated from the equations, and the problem reduces to the solution of equations (52.18) and (52.21). These equations differ from those for one-dimensional motion in ordinary fluid dynamics only by a change in the equation of state of the gas: the true pressure p = p(p) (for given entropy s) must be replaced by p*(p) = p(p) + + 6 2 /o 2 / 87T - Tnis fact enables us to apply the results of ordinary fluid dyna- mics to this case of magnetic fluid flow. In particular, the formulae giving the exact solution for one-dimensional travelling waves (Riemann's solution)}: can be applied, the velocity of sound being represented by -mi-ji^i') -a in accordance with formula (52.16). PROBLEM Determine the absorption coefficient (assumed small) for a hydromagnetic wave in an incompressible fluid. Solution. The absorption coefficient for a wave is defined as y — Q/2q, where Q is the (time) average energy dissipated per unit time and volume, and q is the mean energy flux density in the wave. The amplitude of the wave decreases as e-v* during its propagation. Q is given by the right-hand side of equation (51.6); in an incompressible fluid we have for a wave propagated in the ^-direction (and so v x = 0) Q = i,(dvldx) z +(c 2 ll67T2o)(8hldx)K In the energy flux density (51.9), we can omit the small dissipative terms, leaving q x = — Hxh.v/477. Using formulae (52.10) and (52.13), we have the result j:Lft + ±\ r 2«i3\ P 4W t In accordance with the general results (§51) concerning the relation between Hip and "fluid" lines of force, if we take into account the invariability of the length of these lines with time in the present case. % See Fluid Mechanics, §94. 224 Magnetic Fluid Dynamics §53 §53. Tangential and rotational discontinuities The equations of motion for an "ideal" magnetic fluid (having zero vis- cosity, thermal conductivity and electric resistance) admit discontinuous flows as in ordinary fluid dynamics. To elucidate the conditions which must be satisfied on a surface of discontinuity, let us consider an element of the surface and use a system of co-ordinates in which it is at rest.t First of all, the mass flux must be continuous at a surface of discontinuity : the mass of fluid entering from one side must be equal to the mass leaving on the other side. Thus pivi n = p2V2n> where the suffixes 1 and 2 refer to the two sides of the discontinuity, and the suffix n denotes the component of a vector normal to the surface. In what follows we shall denote the difference between the values of any quantity on the two sides of the surface of dis- continuity by enclosing it in square brackets. Thus [/>#«] = 0. Next, the energy flux must be continuous. Using the expression (51.9) and omitting the dissipative terms, we obtain [qn] = M^ 2 + «0 + VnH^Tr - i7 n v.H/47r] = 0. The momentum flux must also be continuous. This condition means that [n^»*] = 0, where 11^ is the momentum flux density tensor, and n is a unit vector normal to the surface. Using (51.8), we therefore have [p + pv n * + {H t * - H n *)/Sir] = 0, [pv n v t - HnHtl^rr] = 0, where the suffix t denotes the component tangential to the surface. Finally, the normal component of the magnetic field and the tangential component of the electric field must be continuous. If the conductivity of the medium is infinite, the induced electric field is given by E = — vxH/c, and the condition [E*] = leads to [H n vt— H#>»] = 0. In what follows it is more convenient to use the specific volume of the fluid {V = Up) in place of its density. The mass flux density through the discontinuity is denoted by j = pv n = v n \V. Since j and H n are continuous, we can write the remaining boundary condi- tions in the following form: j[w + \]W* + W + VU^4tt] = tf„[H r v,]/477, (53.1) lp] +P[V] + [H t 2]/87r = 0, (53.2) ;[v,] = H n \H t ]l47T, (53.3) H n [v t ] = j[VH t ]. (53.4) This is the fundamental system of equations of discontinuities in magnetic fluid dynamics. t This condition fixes only the velocity of the co-ordinate system in the direction norma to the surface. Any constant vector may be added to its tangential velocity. §53 Tangential and rotational discontinuities 225 In ordinary fluid dynamics, discontinuities of two entirely different kinds are possible: shock waves and tangential discontinuities. t Mathematically, the two types occur because some of the boundary conditions can be written as the vanishing of a product of two factors, and the two different solutions are obtained by equating the factors to zero in turn. This feature is not present in magnetic fluid dynamics, and it might therefore be supposed that only one type of discontinuity occurs. In reality, however, it is found that essentially different types of discontinuity again occur (F. de Hoffmann and E. Teller, 1950). Let us consider, first of all, discontinuities for which j = 0. This means that vm = V2n = 0, i.e. the fluid moves parallel to the surface of discon- tinuity. If H n ¥= 0, we see from equations (53.1)-(53.4) that the velocity, pressure and magnetic field must be continuous. The density (and therefore the entropy, temperature, etc.) may have any discontinuity. Such a surface may be called a contact discontinuity, and is simply the boundary between two media at rest which have different densities and temperatures. If both; and H n are zero, then three of the four equations (53.1)-(53.4) are satisfied identically, and therefore this is clearly a special case. We thus find a type of discontinuity which may be called a tangential discontinuity, as in ordinary fluid dynamics. At such a discontinuity the velocity and the magnetic field are tangential and can have any discontinuity in both magni- tude and direction: j = 0, H n = 0, [v,] # 0, \H t ] # 0. (53.5) The density discontinuity also can take any value, but the pressure dis- continuity is related to that of H t by equation (53.2): [V]*0, [/> + ^]=°- ( 53 - 6 ) The discontinuities of the other thermodynamic quantities (entropy, tempera- ture, etc.) are related to those of V and p by the equation of state. Another type of discontinuity is one in which the fluid density is con- tinuous. Since the flux; = v n jV is continuous, the normal velocity compo- nent is therefore continuous also : y^o, [V] = 0, [v n ] = 0. (53.7) On the right-hand side of equation (53.4) we can take V outside the brackets and divide this equation by equation (53.3), obtaining j = H n [V(^rV) (53.8) and [v] = ViVI^Wtl (53.9) t See Fluid Mechanics, §81. 226 Magnetic Fluid Dynamics §53 In equation (53.1) we put w = e+pV; since V is continuous, this equation can be rewritten as H n being replaced in accordance with (53.8). The second term is zero by (53.2) and the third term is zero by (53.9), so that we find [e] = 0, i.e. the internal energy also is continuous. Every other thermodynamic quantity is determined if e and V are given. Hence all the other thermodynamic quanti- ties, including the pressure, are continuous. It then follows from (53.2) that H* 2 is continuous, i.e. [p] = 0, [Ht\ = 0. (53.10) The fact that Ht and H n are both continuous means that the magnitude of H itself and its angle to the surface are likewise continuous. Formulae (53.7)— (53.10) give all the properties of the discontinuities under consideration. The thermodynamic quantities are continuous, but the mag- netic field is turned through an angle about the normal, its magnitude remaining unchanged. The vector Hj, and therefore (by (53.9)) the tan- gential velocity component, are discontinuous, but the normal velocity component v n =jV is continuous, and its value is *» = HnV(VM = Hn/Vi^p)- ( 5 3.H) We shall call these rotational discontinuities. It is useful to note that, by a suitable choice of the co-ordinate system, we can always ensure that the fluid velocity is parallel to the field on each side of a rotational discontinuity. To achieve this, we use a co-ordinate system moving with velocity vu - Hta V( VjAir) = v^t - ti2tV( VJAtt) . (Compare the first footnote to this section.) In the new system the ratio of each component of v to the corresponding component of H on either side of the discontinuity is V(VM> i-c vi = HiV(J74tt), v 2 = H 2 V(JW. (53.12) Thus in this system of co-ordinates the velocity is rotated with the magnetic field, its magnitude and angle to the normal remaining unchanged. The velocity v n is also minus the velocity of propagation of the discon- tinuity relative to the fluid. This is equal to the phase velocity u\ of one of the three types of hydromagnetic wave (§52). The occurrence of this equality for all rotational discontinuities is to some extent accidental, but when the discontinuities of the various quantities are small the equality must hold. For such a discontinuity is a weak perturbation, in which the velocity v and the magnetic field H receive small increments perpendicular to the plane through H and the normal n. This perturbation is of the type whose phase velocity is u\. The physical velocity of propagation of the front of a small perturbation is the normal component of the group velocity, i.e. its compo- §53 Tangential and rotational discontinuities 227 nent in the direction of the vector k. Since the relation between w and k is linear, we have k'dio/dk = co, and so this component is the same as the phase velocity oijk — u\. Although tangential and rotational discontinuities form two different types, there are also discontinuities having the properties of both. These discontinuities are such that v and H are tangential in direction and con- tinuous in magnitude. In ordinary fluid dynamics, tangential discontinuities are always unstable with respect to infinitesimal perturbations, and so are rapidly broadened into turbulent regions. A magnetic field, however, has a stabilising effect on the motion of a conducting fluid, and in this case tangential discontinuities may be stable. This result is a natural consequence of the fact that a perturbation involving fluid displacements transverse to the field leads to a stretching of the lines of magnetic force "frozen" in it, and therefore to the appearance of forces which tend to restore the unperturbed flow. An investigation of such discontinuities in an incompressible fluid by S. I. Syrovatskii (1953) has given the following two inequalities, which must both be satisfied if the discontinuity is stable: Hf + #2 2 > 2*p*2, (Hi x H 2 )2 > 2np{(Hi x v)2 + (H 2 x v)2}, where v = V2-V1 is the discontinuity of the velocity; see Problem l.t In reality, however, the existence of a small but finite viscosity and electric resistance in the fluid means that such tangential discontinuities cannot exist indefinitely, even if the conditions (53.13) are fulfilled. Although no turbu- lence occurs, the sharp discontinuity is replaced by a gradually widening transitional region, in which the velocity and the magnetic field change smoothly from one value to another. This is easily seen from the equations of motion (51.12) and (51.13) if the dissipative terms are retained. We take the ar-axis in the direction of the normal to the discontinuity. Assuming all quantities to depend on x (and possibly on the time), we can write the trans- verse components of these equations as 8H i /to = (<*l4**)3*H t ld**, dvt/dt = vd 2 vtldx 2 , the fluid being supposed incompressible. If we assume steady flow, the left-hand sides of equations (53.14) are zero, and the only solution which remains finite as * -> ± 00 is H t = constant, v t = constant, which contra- dicts the assumption that these quantities undergo a change at the discon- tinuity. Thus a tangential discontinuity cannot have a constant width such as is found for (e.g.) a weak shock wave. Equations (53.14) are heat-conduction t If the densities of the incompressible fluids on the two sides of the discontinuity are different, then p in these inequalities must be replaced by 2pip2/(pi + P2). 228 Magnetic Fluid Dynamics §53 equations. As we know from the theory of thermal conduction, a discon- tinuity in a quantity satisfying such an equation is gradually smoothed out into a transitional region, whose width increases as the square root of the time. Since the coefficients in the two equations (53.14) are different, the widths 8 V and ojy of the transitional regions for the velocity and the magnetic field are also different: *v ~ VW, *h = vW<0- (53.15) Rotational discontinuities in an incompressible fluid are stable with respect to infinitesimal perturbations, whatever the strength of the magnetic field (S. I. Syrovatskii, 1953). Like tangential discontinuities, however, they cannot have constant widths, but are gradually smoothed out by the viscosity and electric resistance of the fluid (see Problem 2). PROBLEMS Problem 1. Derive the condition for the stability of a tangential discontinuity in an incompressible perfectly conducting non-viscous fluid in a magnetic field (S. I. Syrovatskii). Solution, f We write v = vo+v', p = po+p', H = Ho+H', where vo, po and Ho are the constant (on each side of the discontinuity) unperturbed values, and v', p' and H' are small perturbations. Substituting in equations (51.11)— (51.13), we have for an ideal fluid div u' = 0, div v' = 0, (1) du'/dt = (u'grad)v'— (vgrad)u' (2) 8v' 1 f-(v«grad)v' = grad^'— u x curl u' dt p 1 = - - grad (p'+pw u') + (u • grad)u', (3) P where for brevity we have omitted the suffix and put u = H/y^wp). We take the diver- gence of equation (3) and use (1), obtaining Ate'+pu-u') = 0. (4) Let * = be the plane of the discontinuity, to which the vectors v and u are parallel. In each of the half-spaces x > and x < we seek all quantities v', u', p' in a form pro- portional to exp{i(k'r—<ot)+Kx}, where k is a vector in the yz-plsaie. From equation (4) we find that k 2 — k 2 = 0, so that we must put k — k for x < and * = — k for * > 0. We eliminate v' x from the ^-components of equations (2) and (3), obtaining^ p'+pu>u' = -«V^— {(«-k-v)*-(k.u)*}. (5) K'UK Let $ = £(y, z, t) be the displacement of the surface of discontinuity in the ^-direction due to the perturbation. The conditions (53.5) and (53.6) must hold on the displaced surface : [p+ P (u+u') 2 ] £ [p'+pu-ul = 0, \ uni+u'm £ u'xi— ui«grad £ = 0, > (6) Mn2+w'n2 = u' X 2— U2«grad £ = 0; I t Cf. Fluid Mechanics, §30. X The case where the expression in braces vanishes is of no interest, since a> is then real, whereas instability can occur only for complex to. §54 Shock waves 229 the condition of zero mass flux through the surface is satisfied automatically. Putting £ = constant Xexp{t(k»r—o>f)} and eliminating £, u x \ and u x z from the three equations (6), we obtain an equation giving the possible values of a»: (a,-k-vi)2+(<o-k-v a ) 2 = (k-ui) 2 +(k-u a ) 2 . This quadratic equation has no complex root if 2(k.ui) 2 +2(k-ua) 2 -{k-(v 2 -vi)} 2 > 0, or {2uiiUllc + 2ll2iUZk— {V2i— Vli)(V2k— Vlk))kikk > 0. This quadratic form is positive-definite if the trace and determinant of the tensor of rank two in the braces are both positive, and hence we obtain the conditions (53.13). Problem 2. Find the manner of widening of a rotational discontinuity with time. Solution. Assuming all quantities to depend only on the co-ordinate * (and on the time), we find from the equations div v = and div H = that v x = constant and H x = constant. Let the co-ordinate system be such that the values of v and H on each side of the discon- tinuity (outside the transitional layer) are related by (53.12). Then v x = u x , where u has the same meaning as in Problem 1. For the transverse components u* and \t we have from equations (51.12) and (51.13) 3u t du t dv t c 2 a^t Vu x = ux— h — — , 8t dx dx Aira dx 2 dvt 3vt 3ut 3 2 v t \-U X = Ms— \-V . dt dx dx dx 2 Since the difference Vt— u* tends to zero for x ->■ ±oo, because of the relations (53.12), this difference must be small in the transitional layer in comparison with the sum Vt+u*. Adding the equations (1), we can therefore neglect a term in Vt— Ut, obtaining a 1/ c 2 \ a 2 ■^ Vt+Ut) ^2(w + fe (Vt+Ut) - From this we see that the width of the discontinuity varies in a manner given by +M. V(( 4ira §54. Shock waves Let us now consider the type of discontinuity in which ; * 0, [F] # 0. (54.1) Such discontinuities are called shock waves, as in ordinary fluid dynamics. They are characterised by a discontinuity of density and by the fact that the gas moves through them (v n \ and v n 2 being non-zero). The normal com- ponent of the magnetic field may or may not be zero. On comparing equations (53.3) and (53.4) we see that, when H n i= 0, the vectors H« 2 -H«i and FaEfo- FiHa are parallel to the same vector v 2 «- v Ut and therefore to each other. Hence it follows that H«i and H«2 are parallel, i.e. the vectors Hi, H 2 and the normal to the surface are coplanar, unlike what happens (in general) in tangential and rotational discontinuities. This result holds also when H n = ; in this case, which we shall discuss later, it follows from (53.4) that VJlti = FssH^. 230 Magnetic Fluid Dynamics §54 The velocity discontinuity v$i — Vt2 lies in the same plane as Hi and H2. We can evidently, without loss of generality, assume that the vectors vi and V2 themselves lie in this plane, so that the motion in the shock wave is two- dimensional. Furthermore, it is easy to see that, if H n ^ 0, a suitable trans- formation of the co-ordinates will always ensure that the vectors v and H are parallel on each side of the discontinuity. To achieve this, we use a co- ordinate system which moves with velocity vt — (v n lH n )H.t = Vt — (jVjH v )'H.t (the value of this expression is the same on each side of the discontinuity, by (53.4)). In the following formulae, however, the choice of this particular co-ordinate system is not implied. Let us derive the relation for shock waves in magnetic gas dynamics which corresponds to the shock adiabatic (Hugoniot adiabatic) in ordinary gas dynamics. Eliminating \yi\ from (53.3) and (53.4) we have P[VH t ] = H n *[Ht]l4ir; (54.2) here we have replaced H$ by Ht, since H^i and H^ are parallel. In order to eliminate [v*] from equation (53.1), we rewrite that equation as + [ra?]/4ir - H n *[jty]l32n*j* = 0. The third term is zero by equation (53.3) and so v< does not appear. In the last term we substitute p from (54.2) and in the second term from (53.2), p = {p2-pi + (flia 8 - Ha*)l&r}l(Vi - V 2 ). (54.3) A simple calculation then gives €2 - «1 + \{p2 + pl)(V 2 ~Vi) + + (Vi - FiX^fc - H tl fl\(m = 0. (54.4) This is the equation of the shock adiabatic in magnetic gas dynamics. It differs from the ordinary equation by the presence of the third term. We may also write out again equation (53.3), which gives the discontinuity of vt in terms of that of Ht : v t 2 - v tl = H n (H t2 - H tl )l4TTJ. (54.5) Equations (54.2)-(54.5) form a complete system of equations of shock waves. As the discontinuities of all quantities tend to zero, the velocity of propaga- tion of the shock wave must tend to its value for small perturbations. In ordinary gas dynamics this means that the velocity of a weak shock wave tends to the velocity of sound. In magnetic gas dynamics, however, there are two different velocities 112 and M3 with which weak shock waves can be propagated, t f The velocity mi is, as mentioned in §53, the velocity of propagation of perturbations corresponding to rotational discontinuities. §54 Shock waves 231 Let us consider weak shock waves in more detail, and ascertain in which direction the various quantities change in them. Expanding equation (54.4) in powers of the discontinuities of pressure and entropy, we obtaint l07r\ dp I s When the gas passes through the shock wave, its entropy can only increase : s 2 > si. By an inequality of thermodynamics, we have (dV/dp) s < 0, and the derivative (dWldp 2 ) s is in fact positive for all the substances in question here. Hence we see from (54.6) that the inequality s 2 > *i implies that p 2 > pi, and therefore V 2 < V\. Thus we have a compression wave, as in ordinary gas dynamics. This result, which we have proved for weak shock waves, seems to hold for shock waves of any intensity. For weak shock waves we can also derive certain results concerning the direction of variation of the magnetic field. The changes in the various quantities when the state of the gas undergoes a slight perturbation are related by formulae (52.8) and (52.9). The changes 8p = p 2 -pi and 8(H t 2 ) = H t2 2 -H t i 2 are such that 8(H t 2 ) = Stt(u 2 - u Q 2 )8p. Since u 2 > « and« 3 < «o (see (52.15)), and from the above we necessarily have 8p > 0, we see that the quantities H t 2 , and therefore H 2 = H t 2 + H n 2 , vary in opposite directions in the two kinds of weak shock wave. The magnetic field is increased in a shock moving with velocity ~ u 2 , but it is reduced in one moving with velocity ~ Ms- Let us now consider shock waves in weak magnetic fields, i.e. assume that H 2 ^ pu 2 on either side of the discontinuity. No restriction is placed on the discontinuity of any quantity; in particular, the discontinuity in the magnetic field may be comparable with the magnitude of that field. There are again two possibilities. If the discontinuities of density and pressure are not small, we can neglect, in a first approximation, the last term in equation (54.4) and the magnetic field in formula (54.3). We thereby return to the formulae of ordinary fluid dynamics. Thus the relation between the discontinuities of the various thermodynamic quantities, and the rate of propagation of the shock, will be the same as for ordinary shock waves. The change in the magnetic field can be found from the relation (54.2). Since the right-hand side of this equation is of the third order of smallness with respect to the field, the same must be true of the left-hand side. As a first ap- proximation we can put [VH t ] = V 2 H t2 - V\H t \ £ 0, whence H t2 \H t \ = Vi/V 2 = p 2 jpi. Since in an ordinary shock wave we always have V\ > V 2 , we see that the magnetic field is strengthened in a shock of this type. t See Fluid Mechanics, §83. 16 232 Magnetic Fluid Dynamics §54 Equations (54.2)-(54.4) admit also another type of solution. The assump- tion that the field is small is also compatible with equation (54.2) for a wave in which V\ % V% and^ 2 is the second-order quantity P = HffaV, (54.7) where V is the common value of Vi and V 2 . It is seen from equation (54.3) that if we put V± = V2, we must to the same approximation put P2-P1 = - (H t2 2 - Ha*)l&r. (54.8) The continuity of the density means that a shock wave of this type can be regarded as a discontinuity in an incompressible fluid. The vector H t (and therefore y t ) has a discontinuity in magnitude but not in direction, and the discontinuity of pressure is given in terms of that of the magnetic field by formula (54.8) when the density is continuous. The rate of propagation of the discontinuity is v n2 = v nl =jV = H n y/{V\^Tr). This is a natural result, and the necessity for the existence of such discontinuities could have been foreseen. We saw in §52 that, in an incompressible fluid, there is only one velocity of propagation of small perturbations of the magnetic field, namely Hl\^(4iTp). Hence the fronts of small perturbations move with velocity u\ = H n l<s/(4TTp), whether the change SH in the field is parallel or perpendicu- lar to the plane of H and n. The latter case corresponds to weak rotational discontinuities (already discussed in §53) and the former, when the dis- continuities are small, is the type just considered. To ascertain the direction of variation of the magnetic field strength in such discontinuities, we return to equation (54.4), which has not yet been used, and rewrite it in the form (54.6), in whose derivation the discontinuity in the magnetic field was not assumed small compared with that field itself. Substi- tuting p 2 ~pi from (54.8), we find that the second term on the right of (54.6) is of the fourth order in the field, whereas the first term is of the sixth order and may be omitted. It follows at once from the condition s 2 > *i that Ht2 < Ha, i.e. that the magnetic field is weakened in such a discontinuity. Returning now to shock waves of any intensity in magnetic fields of any strength, we may consider two particular cases. Let the magnetic field in medium 1 be perpendicular to the shock wave front, i.e. H«i = 0. Then equa- tion (54.2) becomes pV 2 H t 2 = Hr?H t 2\^n- Hence it follows that either H12 = 0, or;' 2 = H n 2 l47rV2 with no restriction on H t 2- In the former case the magnetic field remains perpendicular to the surface of the discontinuity, and does not affect the properties of the shock wave, since it does not appear in the equations. In the second alternative we have a shock wave in which the field changes direction, propagated with velocity v n2 = jV 2 = H n /\/(47rp2) relative to the gas behind it. Another particular case is a shock wave parallel to the field on either side of it (H n = 0).t From (54.5) we then have v t2 = v t i, i.e. the tangential t For H n = there is only one type of shock wave, in accordance with the fact that m is zero. The shock waves corresponding to us become weak tangential discontinuities at rest relative to the fluid. §54 Shock waves 233 velocity component is continuous. By a suitable choice of co-ordinates therefore, we can always ensure that v t = on either side of the discontinuity, i.e. the gas moves perpendicularly to the discontinuity, and we shall hence- forth assume this. From equation (54.2) we have V2H2 = Pi-Hi- This rela- tion shows that equations (54.3) and (54.4) can be written j2 =(p 2 *-p 1 *)l(V 1 -V 2 ) i 6 2 *-ei* + i(/)2*+/>i*)(^2-Fi) =0, which differ from the ordinary equations for shock waves in the absence of a magnetic field only by a change in the equation of state: the true equa- tion of state p = p(V,s) must be replaced by p* =p*(V,s), where p* =p + b 2 ISiTV 2 , and b denotes the constant product HV. Accordingly e* must be defined so as to satisfy the thermodynamic relation ( dt* / d V) s = -p* , whence e* = e + b 2 /87rV. It has been shown in §53 that there are discontinuities which exhibit the properties of both tangential and rotational discontinuities. The discon- tinuities discussed here are related in this way to shock waves also. The transition between shock waves and rotational discontinuities is formed by a discontinuity in which there is no change in density and the only change in the magnetic field is that H t is reversed. The transition between shock waves and tangential discontinuities is formed by discontinuities in which v n = 0, H n = 0, and H* has any discontinuity in magnitude but none in direction. We may summarise as follows the discontinuities discussed in §§53-4: (1) Contact discontinuities: j = 0, KJ = 0, [V] * 0, \p] = 0, H n # 0, [H,] = 0. (2) Tangential discontinuities : j = 0, H ^0, [V] * 0, \p + ^J = 0, H n = 0, [H«] # 0. (3) Rotational discontinuities : j # 0, [x t ] * 0, [V] = 0, [/>] = 0, H n # 0, Ht changes direction but not magnitude. (4) Shock waves: j ^0, [V] ^ 0, Hi, H 2 and n coplanar. The following diagram shows the possible transitional cases: 234 Magnetic Fluid Dynamics §55 §55. The spontaneous magnetic field in turbulent motion of a con- ducting fluid Turbulent motion of a conducting fluid has the remarkable property that it may lead to spontaneous magnetic fields which are quite strong. There are always small perturbations in a conducting fluid, resulting from causes extraneous to the fluid motion itself, t and accompanied by very weak electric and magnetic fields. The question is whether these perturbations are, on the average, amplified or damped by the turbulent motion in the course of time. The following arguments show that either may occur, depending on the properties of the fluid itself. % The manner of variation with time of magnetic field perturbations, once they have arisen, is determined by two physical agencies. The dissipation of magnetic energy, which is converted into the Joule heat of the induced currents, tends to diminish the field. The magnetic field tends to increase, on the other hand, by the purely magnetic effect of the "stretching" of the lines of force. We have shown at the end of §51 that, when a fluid of sufficiently high conductivity is in motion, the lines of magnetic force move as fluid lines, and the magnetic field varies proportionally to the stretching at each point on each line of force. In turbulent motion any two neighbour- ing particles move apart, on the average, in the course of time. As a result, the lines of force are stretched and the magnetic field is strengthened. We shall show that in certain conditions these two opposite tendencies may balance, and this will provide a criterion distinguishing the cases where the magnetic field perturbations increase from those where they are damped. While the magnetic field resulting from the motion remains weak its reciprocal effect on the motion can be neglected. That is, we may consider ordinary fluid turbulence as providing a given "background" on which the magnetic perturbations develop. We assume a steady turbulent velocity distribution, the word "steady" being used in the sense usual in turbulence theory, i.e. referring to the average values of the motion. || Mathematically, we neglect the terms quadratic in the field in the equation of motion (51.13), returning to the ordinary Navier-Stokes equation: d-v/dt + (vgrad)v = - grad(p//>) + vAv (the fluid being supposed incompressible). If we use the formula (vgrad)v = \ grad v 2 — v x curl v and take the curl of the above equation, we obtain dStfdt = curl(v x SI) + v&Sl, (55.1) where we have put for brevity SI = | curl v. t For example, the magnetomechanical effect in rotating parts of a fluid, or even thermal fluctuations. X The results in §55 are due to G. K. Batchelor (1950). || The averaging is over times which are of the order of the periods of the corresponding turbulent fluctuations, but are, of course, small compared with the total time during which the system is observed. §55 Spontaneous magnetic field in turbulent motion of conducting fluid 235 Let us compare this equation with (51.2): dU/dt = curl(v x H) + (cS/W) AH, (55.2) which (for a given velocity distribution) determines the time variation of the magnetic field. We see that SI and H satisfy equations of the same form, which become identical if v = c^JAttg. In this case, therefore, there is a solution of equation (55.2) for which H = constant x SI. (55.3) Thus, if v = C2/W, (55.4) a steady magnetic field (in the same sense of the word "steady") can exist. This field, on the average, neither increases nor decreases, whatever the value of the constant coefficient in (55.3). We may say that there is neutral equili- brium, in which the two factors, mentioned above as determining the magnetic field, are exactly balanced. Hence, in turn, it is evident that, if the conductivity of the fluid exceeds c^j^ttv, the dissipative loss of electromagnetic energy will be insufficient to compensate the increase of the magnetic field by the stretching of the lines of force. Thus we obtain the inequality 4-m/a/c 2 > 1 (55.5) as the condition for the spontaneous appearance of magnetic fields by the growth of small magnetic perturbations, t We can say that this is the condition for turbulent motion to be unstable with respect to infinitesimal magnetic perturbations. It is noteworthy that the criterion can be established quantitatively, and not merely in orders of magnitude.}: The condition (55.5) as a criterion of the behaviour of the field is valid so long as the neglect of the reciprocal effect of the magnetic field on the flow, on which the derivation of (55.5) is based, holds good. The field will increase until some steady state, in which the reciprocal effect of the field cannot be neglected, is set up. Although, strictly speaking, the fluid-mechanical properties of the turbulence in this state are not those given a priori, the qualitative distribution and the order of magnitude of the resulting magnetic field can be determined as if they were. t The condition (55.5) is very stringent. For example, in mercury (a^l0 16 sec 1 , v = 1 -2 X 10- 3 cm 2 /sec), the quantity on the left of (55.5) is only 1 -5 X 10~ 7 . Since a and v increase with the mean free paths of the corresponding carriers of charge and mass, the condition (55.5) may be fulfilled, for example, in the Sun's chromosphere and corona, and in the ionised interstellar gas. % It should be mentioned that the foregoing arguments, however convincing, are not entirely conclusive. For example, Ya. B. Zel'dovich has shown (Zhurnal iksperimental'noi i teoreticheskoi fiziUZl, 154, 1956; Soviet Physics JETP 4, 460, 1957) that they are invalid in a hypothetical case of "two-dimensional" turbulence. 236 Magnetic Fluid Dynamics §55 It is easy to see that the magnetic field distribution must be similar to the turbulent distribution of SI. For SI may be regarded as the angular velocity of the fluid at any given point. Since the lines of magnetic force move with the fluid, the vector H rotates with the same angular velocity. Hence, if at any two points of a turbulent flow the instantaneous values of SI are uncorre- cted, the vectors H at those points will rotate in an uncorrelated manner, and their relative direction will vary randomly with time. In this connection we may refer to some purely fluid-mechanical properties of turbulence, t Turbulent flow may be regarded as a superposition of turbu- lent eddies of various sizes, from the largest / (the "external scale" of the turbulence) to the smallest Ao (the "internal scale"). The former is equal to a characteristic length which gives the size of the region in which the turbulent flow occurs. The quantity Ao gives, in order of magnitude, the distances at which viscosity, and the energy dissipation which it entails, become important; it can be expressed in terms of / and the Reynolds number R ~ uljv of the turbulent flow as a whole (u being of the order of the change in the mean velocity over a distance /), or in terms of the energy e dissipated in unit mass of the fluid in unit time : A - (v3/e)i - IIRK (55.6) The correlation between the velocities vi and V2 at two points 1 and 2 at a distance A apart is determined mainly by the eddies of size A. According to Kolmogorov and Obukhov's law, we have, for distances A > Ao, AvtAvje ~ A 2/3 , where Av = V2 — vi. At distances A < Ao, on the other hand, AviAvjc ~ A 2 . From this we can easily find the correlation of angular veloci- ties. Since the components of Sli and SI2 are expressed in terms of the derivatives of vi and V2, we find, by differentiating AvtAvje once with respect to the co-ordinates of point 1 and once with respect to those of point 2, SluCkk ~ A" 4 / 3 for A > A , 0.uQ.2k ~ constant for A <^ Ao. These formulae show that an appreciable correlation between the angular velocities exists only at distances up to those of the order of Ao, falling off rapidly at greater distances. From the above discussion, the distribution of the steady spontaneous magnetic field must be similar. The distribution is correlated only over regions of dimension ~ Ao. At greater distances the relative direction of the vectors H is practically random. The order of magnitude of the magnetic field can now be easily deter- mined by estimating the terms in the complete equation of motion dx/dt + (vgrad)v = - grad (/>//>) + v/\v - (1/4tt/j)H x curlH. t See Fluid Mechanics, §§31-33. §55 Spontaneous magnetic field in turbulent motion of conducting fluid 237 Since the vector H changes its direction completely over distances ~ Ao, the order of magnitude of the last term on the right-hand side is H 2 \A7rpXo. Let us now estimate the term (v»grad)v. For eddies of size A it is of the order of v^/X, where vx is the change in the velocity over a distance A. According to the formulae of turbulence theory we have v x ~ w(A//)* for A > A , v x ~ m(A//)VR for A < Ao. Hence the ratio t^ 2 /A~ A _1/3 for A > Ao and ~ A for A < Ao- Its greatest value is therefore reached when A ~ Ao. Thus (v»grad)v ~ v^/Xo. Finally, if the two terms are comparable in magnitude, we have H 2 „ 4tt P v X0 \ (55.9) According to (55.6) and (55.8), vxq ~ «R~ 1/4 ~ (ev) 1/4 . Hence we can also write H 2 ~ 4irpU 2 /^R „ 4tt P V(^)- (55.10) These formulae give the order of magnitude of the spontaneous magnetic field. It is of interest to compare the energy of this field with the kinetic energy of the turbulent flow. The latter energy resides mainly in the largest eddies (of size ~ /), and its order of magnitude is pu 2 . The mag- netic energy resides mainly in the "magnetic eddies", which are of small size (~ Ao). By (55.9), it is comparable with the kinetic energy of the turbulent eddies of this same size, but, by (55.10), it is small in comparison with the total kinetic energy. A more exact mathematical formulation of these state- ments can be attained by expanding the spatial distribution of velocity and magnetic field as Fourier integrals. The kinetic energy then resides mainly in the components with small wave numbers (k ~ 1//), while the magnetic energy is mainly in those with large wave numbers (k ~ 1/Ao). Turbulent flow results in a continuous transfer of energy from large eddies to small ones, with almost no viscous dissipation. This "energy flux" is dissipated only in the eddies of size Ao. In the absence of a magnetic field, the dissipation is due entirely to the viscosity of the fluid, but in the turbu- lence here considered the energy in the eddies of size Ao is partly dissipated by viscosity, partly converted into the energy of the magnetic field and only then dissipated as Joule heat. Let us estimate the time required to establish the steady state. For this purpose we return to equation (55.2). The two terms on the right-hand side are in order of magnitude respectively Hv\JXq = HvxqXo/Xo 2 ~ Hv/Xq 2 and c 2 H/4it0Xq 2 . Since we know precisely the condition (55.4) for the occur- rence of neutral equilibrium, we also know the exact relation between the coefficients in these two terms, and can write 8H / c 2 \H dt \ 4W Ao 2 238 Magnetic Fluid Dynamics §55 Hence we see that small perturbations increase with time according to the exponential function Ht -£)£)• (55 - n) If 4ttov/c 2 > 1 we have simply exp(v*/A 2 ). The time r during which an initial small perturbation ~ Hq develops into the steady field H (55.10) is then, in order of magnitude, Ao 2 , H 2 /v\* p(ev)i -v log w^(;) log w- (55 - 12) The random variation of the magnetic field with time in turbulent flow means that the (time) average value of H is zero. In other words, we can say that, in the case considered here (i.e. when a spontaneous field is possible), a non-zero mean field is incompatible with turbulence. The result must be that, when a moderate external magnetic field is applied to a fluid in turbu- lent motion (in a finite volume), the latter will behave like a superconductor. A strong field (H 2 > pu 2 ) must necessarily penetrate into the fluid and will suppress the turbulence. CHAPTER IX THE ELECTROMAGNETIC WAVE EQUATIONS §56. The field equations in a dielectric in the absence of dispersion In §45 we gave the equations for a variable electromagnetic field in a metal : curlH = 4t7(7E/c, curlE= - (I /c) dB/dt, (56.1) which hold when the field changes sufficiently slowly: the frequencies of the field must be such that the dependence of j on E (and of B on H, if needed) is that corresponding to the static case, f We shall now examine the corresponding problem for a variable electro- magnetic field in a dielectric, and shall formulate equations valid for fre- quencies such that the relations between D and E, and B and H, are the same as when the fields are constant. If, as usually happens, these relations are simple proportionalities, this means that we can put D = eE, B = fxH, (56.2) with the static values of e and fi. These relations are not valid (or, as we say, e and fj, exhibit dispersion) at frequencies comparable with the eigenfrequencies of the molecular or electronic vibrations which lead to the electric or magnetic polarisation of the matter. The order of magnitude of such frequencies depends on the substance concerned, and varies widely. It may also be entirely different for electric and for magnetic phenomena. J The equations div B = 0, (56.3) curlE= -(1/c) dB/dt (56.4) are obtained immediately by replacing e and h in the exact microscopic Maxwell's equations by their averaged values E and B, and therefore are always valid. The equation divD = (56.5) is obtained (§6) by averaging the exact microscopic equation div e = 47r/>, f The condition I <^ A does not relate to the validity of equations (56.1) as they stand. In the problems discussed in Chapter VII this condition was necessary in order to justify the neglect of retardation effects in the field outside the conductor. % In diamond, for example, the electric polarisation is due to the electrons, and the dispersion of e begins only in the ultra-violet. In a polar liquid such as water, the polarisation is due to the orientation of molecules with permanent dipole moments, and the dispersion of e appears at frequencies a <~ 10 11 , i.e. in the centimetre wavelength range. The dispersion of ix in ferromagnetics may begin at even lower frequencies. 239 240 The Electromagnetic Wave Equations §56 using only the fact that the total charge on the body is zero. This result is evidently independent of the assumption made in §6 that the field is static, and equation (56.5) is therefore valid in variable fields also. A further equation is to be obtained by averaging the exact equation lde 4tt curlh = 1 pv. (56.6) c dt c A direct averaging gives 1 dE 4tt_ curl B = + — pv. (56.7) c dt c When the macroscopic field depends on time, the establishment of the rela- tion between the mean value jov and the other quantities is fairly difficult. It is simpler to effect the averaging in the following more formal way. Let us assume for the moment that extraneous charges of volume density pex are placed in the dielectric. The motion of these charges causes an "extraneous current" j ex , and the conservation of charge is expressed by an equation of continuity : dpex/dt + divjex = 0. Instead of equation (56.5) we have divD = 4ir/oex; see (6.8). Differentiat- ing this equation with respect to time and using the equation of continuity, we obtain d(divD)/dt = 4irdpex/dt — -4rr divjex, or /8D \ divl — - + 47rjexl = 0. Hence it follows that the vector in parentheses can be written as the curl of another vector, which we denote by cH. Thus 4ir 1 3D curlH = — j ex + — — • (56.8) c c dt Outside the body this must be the same as the exact Maxwell's equation for the field in a vacuum, and therefore H is the magnetic field. Inside the body, in the static case, the current j ex is related to the magnetic field by the equation curl H = 47rj e x/c, where H is the quantity introduced in §27 and related in a definite manner to the mean field B. Hence it follows that, in the limit of zero frequency, the vector H in equation (56.8) is the static quantity H(B), and our present assumption that the field varies "slowly" means that the same relation H(B) holds between these variable fields. Thus H is a definite quantity, so that we can drop the auxiliary quantity jex and obtain the final equation curlH = (1/c) dD/dt. (56.9) §56 The field equations in a dielectric in the absence of dispersion 241 This equation replaces in dielectrics the first equation (56.1) for the field in metals. It might be supposed that the term in 8E\8t ought to be included when this equation is used for variable fields in metals also, giving *** e BE curlH = —aE + -—. (56.10) c c 8t In good conductors such as the true metals, however, the introduction of this term is pointless. The two terms on the right-hand side of (56.10) are essentially the first two terms in an expansion in powers of the field fre- quency. Since this frequency is assumed small, the second term must repre- sent at most a small correction. In actual fact, in metals the corrections for the effect of the spatial non-uniformity of the field become important sooner than the frequency correction (see the sixth footnote to §45). There are, however, substances, namely poor conductors, for which equation (56.10) may be meaningful. For such reasons as the small number of conduction electrons in semiconductors, or the small mobility of the ions in electrolyte solutions, these substances exhibit anomalously low conduc- tivity, and hence the second term on the right of equation (56.10) may be comparable with, or even exceed, the first term at frequencies for which a and e may still be regarded as constants. In a field of a single frequency to, the ratio of the second term to the first is co>/47ra. If this ratio is small, the body behaves as an ordinary conductor of conductivity a. At frequencies o) > Arrafe, it behaves as a dielectric with dielectric constant e. In a homogeneous medium with constant «• and /x, equations (56.3)— (56.5) and (56.9) become divE = 0, divH=0, (56.11) u8H e8E curlE = - - — , curlH = . (56.12) c Bt c 8t Eliminating E in the usual manner, we obtain e 8 €fx sm curl curl H = curlE = , c8t c 2 8t 2 and, since curl curl H = grad divH— AH = —AH, we reach the wave equation eu8m AH-— = 0. C 2 8fi A similar equation for E can be obtained by eliminating H. We see that the velocity of propagation of electromagnetic waves in a homogeneous dielectric is c/VM- (56.13) 242 The Electromagnetic Wave Equations §56 The electromagnetic energy flux density in a dielectric is given by the same formula as in a metal : S = cEx H/4tt. (56.14) This is easily seen by calculating div S. Using equations (56.4) and (56.9), we obtain divS = — (H-curlE - E-curlH) 1 / 3D 8B\ 3U , 4 x = E + H = , (56.15) Att\ dt BtJ at ' in accordance with the expression dU = (E«dD + H«dB)/47r for the dif- ferential of the internal energy of a dielectric at given density and entropy. The general requirements of relativistic invariance have the result that the energy flux density must be the same, apart from a factor c 2 , as the space density of the field momentum, f which is therefore E x H/4ttc. (56.16) This expression must, in particular, be used in determining the forces on a dielectric in a variable electromagnetic field. The force f per unit volume may be calculated from the stress tensor ow'. ft = Soutjdxit. Here, however, it must be remembered that aw is the momentum flux density, which in- cludes the momentum of both the matter and the electromagnetic field. If f is taken as the force on the medium, the rate of change of the field momentum per unit volume must be subtracted : **_1(BXH)«_ 8xi 8t \ttc In a constant field the last term is zero, and so this question did not arise previously. Since the field varies "slowly", the stress tensor may be taken to have the same value as in a constant field. For instance, in a fluid dielectric, ow is given by the sum of the electric part (15.9) and the magnetic part (34.2). In differentiating these expressions with respect to the co-ordinates we must use the fact that the equations curl E = 0, curl H = for a constant field (in the absence of currents) are replaced by equations (56.12). The result is E 2 f /de\ E 2 1 H 2 f = - grad^o - ^S rade + S rad [p[y) ^J ~ §^ grad ^ + r /du\ H 2 l €ii - 1 d t This follows from the symmetry of the four-dimensional energy-momentum tensor; see The Classical Theory of Fields, §4-7, Addison- Wesley Press, Cambridge (Mass.), 1951; Pergamon Press, London, 1959. §57 The electrodynamics of moving dielectrics 243 §57. The electrodynamics of moving dielectrics The motion of a medium results in an interaction between the electric and magnetic fields. Such phenomena for conductors have been discussed in §49; we shall now discuss them for dielectrics. Here we are in practice concerned with the phenomena occurring in moving media when external electric or magnetic fields are present. It should be emphasised that they are in no way related to the appearance of fields as a result of the motion itself (§§35, 50). Our starting point in §49 was the formulae giving the transformation of the field when the frame of reference is changed. There it was sufficient to know the general formulae for the transformation of electric and magnetic fields in a vacuum, the averaging of which gives immediately the formulae for the transformation of E and B. In dielectrics the problem is considerably more complex, because the electromagnetic field is described by a greater number of quantities. In the motion of macroscopic bodies, the velocities involved must in practice be small compared with the velocity of light. To obtain the necessary approximate transformation formulae, however, it is simplest to use the exact relativistic formulae which hold for all velocities. In the electrodynamics of the field in a vacuum, the components of the electric and magnetic field vectors e and h are actually components of an antisymmetrical four- dimensional tensor (or "four-tensor") of rank two.f The same is true of E and B, which are the mean values of e and h. Thus there is a four-tensor Fac whose components are given byt Foe = B z — By -iE x Bx — lEy -B x ~iE z iE y iE z (57.1) -B z By iE x Using this tensor, the first two Maxwell's equations, div B = 0, curl E = - (1/c) dB/dt, (57.2) can be written in the four-dimensional form 8F ik dF kl dF u ~T~ + -J- + T~ = °- < 57 ' 3 ) OXi CXf OX]z This shows the relativistic invariance of the equations. The applicability of equations (57.2) to moving bodies is evident, since they are obtained directly from the exact microscopic Maxwell's equations by replacing e and h by their averaged values E and B. t See The Classical Theory of Fields, §§3-9, 4-1. % In the present section (but not in the Problems) the tensor suffixes take the values 1,2, 3, 4, corresponding to the four-dimensional co-ordinates x\ — x, xz = y, x% — z, Xi = ict. 244 The Electromagnetic Wave Equations §57 The second pair of Maxwell's equations divD = 0, curl H = (1/c) dDjdt (57.4) also retain their form in moving media. This is seen from the arguments given in §56, in which we used only general properties of bodies (e.g. that the total charge is zero), equally valid for moving bodies and bodies at rest. However, the relations between D and E, and B and H, need not be the same as in bodies at rest. Since they are valid for bodies both at rest and in motion, equations (57.4) must be unaltered by the Lorentz transformation. For a field in a vacuum, the vectors D and H are the same as E and B, and the relativis- tic invariance of the second pair of Maxwell's equations appears in the fact that they also can be written in four- dimensional form, using the same tensor Fac'. dFijcjdxjc = O.f Hence it is clear that, to ensure the relativistic invariance of equations (57.4), it is necessary that the components of the vectors D and H should be transformed as the components of a four-tensor exactly similar to Fi/c, which we denote by Hm : H z — Hy -iD x H z H x -iD y Hy — H x -iD z iD x iD y iD z Hik = Using this tensor, we can write equations (57.4) in the form dHacjdxic = 0. (57.5) (57.6) Having elucidated that the quantities E, D, H, B form four-dimensional tensors, we have also ascertained the law of their transformation from one frame of reference to another. However, we are interested rather in the relations between the quantities in a moving medium, which generalise the relations D = cE and B = juH valid in a medium at rest. We denote by m the velocity four- vector of the medium ; its components are related to the three-dimensional velocity v by «iA3 = ««r../«/(i - y - «• = */j(i - y ■ From this four-vector and the four-tensors Fuc and Ha we form combina- tions which become E and D in a medium at rest. These combinations are the four- vectors FacUjc and HocUjc', for v = their time components are t See The Classical Theory of Fields, §4—5. §57 The electrodynamics of moving dielectrics 245 zero and their space components are E and D respectively. The four- dimensional generalisation of the equation D = eE is therefore evidently f HucUjc = eFikUic. (57.7) Similarly, we see that the generalisation of B = /uH is the four-dimensional equation FocUi + F k iUi + Fuujc = n(H ik ui + H k m + H u u k ). (57.8) Returning from the four-dimensional to the three-dimensional notation, we derive from these two equations the vector relations! D + V x Ulc = e(E + v x B/c), (57 9) B + E X v/c = ju(H + D X v/c). V ' These formulae, first derived by H. Minkowski (1908), are exact in the sense that no assumption has yet been made concerning the magnitude of the velocity. If the ratio v/c is assumed small the equations can be solved for D and B as far as terms of the first order to give D = eE + (ep - l)v x H/c, (57.10) B = M H + (e/x - 1)E X v/c. (57.11) These formulae, together with Maxwell's equations (57.2) and (57.4), form the basis for the electrodynamics of dielectrics in motion. The boundary conditions on Maxwell's equations are also somewhat modified. From the equations div D = 0, div B = the continuity of the normal components of the inductions follows as before : D n i = D n 2, B n \ = B n 2. (57.12) The conditions on the tangential components of the fields are most simply obtained by changing from the fixed frame of reference K to another, K\ which moves with the surface element considered, whose velocity along the normal n we denote by v n . The usual conditions, namely that E't and H' t are continuous, hold in the frame K'. By the relativistic transformation formulae, 1 1 these are equivalent to the continuity of the tangential compo- nents of the vectors E + vxB/c and H-vxD/t. Taking the components perpendicular to n and using equations (57.12), we obtain the required boundary conditions : n X (Ea - E0 = v n (B 2 - Bitfc, n x (H 2 - Hi) = - v n (D 2 - Ih)lc. l ' j t It should be noted that, by writing down relations involving only the local value of the velocity, we neglect slight effects due to the possibility of a velocity gradient, such as gyro- magnetic effects (§35). X If either of the relations D = eE and B = /xH does not hold in the medium at rest, the corresponding relation (57.9) is replaced by a different functional relation between the vector sums on the two sides of the equation. || See The Classical Theory of Fields, §3-10. 246 The Electromagnetic Wave Equations §57 If we substitute here the expressions (57.10) and (57.11), and neglect terms of higher order in v/c, we obtain n x (E 2 - Ei) = vnfa - pifHtlc, n X (H 2 - Hi) = - v n (€ 2 - €i)E*/<r. ( ' ' In this approximation the values of H and E on the two sides of the surface need not be distinguished on the right-hand sides of equations (57.14). If the body moves so that its surface moves tangentially to itself (e.g. a solid of revolution rotating about its axis), then v n = 0. Only in this case do the boundary conditions (57.13) or (57.14) reduce to the usual condi- tions that Et and H^ are continuous. PROBLEMS Problem 1. A dielectric sphere rotates uniformly in a vacuum in a uniform constant magnetic field £. Determine the resulting electric field near the sphere. Solution. In calculating the resulting electric field, the magnetic field may be taken to be the same as for a sphere at rest, since an allowance for the reciprocal effect of the magnetic field variation would give corrections of a higher order of smallness. Within the sphere, the magnetic field has the uniform value H«) = 3.|>/(2+/x); cf. (8.2). Since the rotation is steady, the resulting electric field is constant and, like any constant electric field, has a potential: E = — grad <f>. Outside the sphere, the potential satisfies the equation A^ (e) = 0; inside the sphere, it satisfies A4> w = 2(e,x-l)£2.HW/ce, (1) where Si is the angular velocity. The latter equation is obtained from div D = by sub- stituting for D the expression (57.10) with v = S2Xr. The condition that the normal component of D is continuous at the surface of the sphere gives ~ e RrL= + ! ^^- H(i) -( a - n )( H(i) - n )] = -[-^r] • ( 2 ) Here a is the radius of the sphere and n a unit radial vector. From the symmetry of the sphere, the required electric field is determined by only two constant vectors, Si and .£). From the components of these vectors we can form a bilinear scalar $)-Si and a bilinear tensor §jOfc+§fc^i— i&tk$)'Si, the sum of whose diagonal terms is zero. Accordingly, we seek the field potential outside the sphere in the form am — *n ^ 2 l^\ *r> niTllc 6 dxidxjc\rJ 2 r 3 where Dm is a constant tensor (with Da — 0), the electric quadrupole moment tensor of the sphere. f No term of the form constant/r can appear in ft e \ since such a term would give a non-zero total electric flux through a surface surrounding the sphere, whereas the sphere is uncharged. The field potential inside the sphere is sought in the form 4>m = I~Damnt+ ^-fl •»«>(** -a"). (4) 2a* 3ce The first term is the solution of the homogeneous equation /\<j> = 0, and the coefficient is chosen so as to give continuity of the potential, and therefore of Et, at the surface of the sphere. Substituting (3) and (4) in (2), we obtain a* 3(e/*-l) ^ Dik = n ,; v J , [&Q*+6*Qi-S8 tt 3.fl]. (5) c (3+2e)(2 + /n) t See The Classical Theory of Fields, §5-6. §58 The dispersion of the dielectric permeability 247 Thus a quadrupole electric field is formed near the rotating sphere, and the quadrupole moment of the sphere is given by formula (5).f In particular, if the axis of rotation (the ar-axis) is parallel to the external field, A* has only the diagonal components a* 4(c/*— 1) , c (3+2e)(2+/i) Problem 2. A magnetised sphere rotates uniformly in a vacuum about its axis, which is parallel to the direction of magnetisation. Determine the resulting electric field near the sphere.J Solution. The magnetic field inside the sphere is uniform, and is expressed in terms of the constant magnetisation M by the equations B<*'+2H< < ) = (cf. (8.1)) and B(*)~H«> = 4ttM, whence B«> = 8*rM/3, H<*> = -4ttM/3. The second of formulae (57.9) does not hold in this case, because the formula B = /tH is not valid for a ferro- magnetic at rest; from the first of (57.9) we have, inside the sphere, D = eE+evxB/c— vxH/c = eE+4w(2e+l)vXM/3c. The potential of the resulting electric field outside the sphere satisfies the equation /\$>(e) = o, and that inside the sphere satisfies A<£ (<) = 8u<2e+l)MQ/3ce. The boundary condition that D n is continuous at the surface of the sphere gives L dr \ r -a 3c L dr J r =-o where 9 is the angle between the normal n and the direction of SI and M (the sr-axis). We seek $ (e) and $ (i) in the forms Dantmi Dzz *(•> = —^ = —(3 cos 2 0-l), r 2 4irC2e4-l') ^(i) = —Dz& cos 2 »-l)+ - n ; M Cl(r*-aZ). \aP 9ce From the boundary condition we obtain the following expressions for the electric quadrupole moment of the rotating sphere : 4(2e+l) D™ = — „ , n , n .a z &^t D X x — Dyy = — iDzz, 3c(2e+3) where *# is the total magnetic moment of the sphere. For a metal sphere we must take e -»■ oo, giving D zz = —\&J(cP\Zc. §58. The dispersion of the dielectric permeability Let us now go on to study the important subject of rapidly varying electro- magnetic fields, whose frequencies are not restricted to be small in comparison with the frequencies which characterise the establishment of the electric and magnetic polarisation of the substances concerned. An electromagnetic field variable in time must necessarily be variable in space also. For a frequency <a, the spatial periodicity is characterised by a t Similarly, a quadruple magnetic field occurs near a sphere rotating in a uniform electric field. The magnetic quadrupole moment is given by (5) if the sign is changed and c, /x, £ are replaced by fi, e, ($* respectively. X If the direction of magnetisation is not the same as that of the axis of rotation, the problem is considerably changed, since the sphere then emits electromagnetic waves. 17 248 The Electromagnetic Wave Equations §58 wavelength A ~ cjto. As the frequency increases, A eventually becomes comparable with the atomic dimensions a. The macroscopic description of the field is thereafter invalid. The question may arise whether there is any frequency range in which, on the one hand, dispersion phenomena are important but, on the other hand, the macroscopic formulation still holds good. It is easy to see that such a range must exist. The most rapid manner of establishment of the electric or magnetic polarisation in matter is the electronic mechanism. Its relaxation time is of the order of the atomic time a/v, where v is the velocity of the electrons in the atom. Since »<c, even the wavelength A ~ ac/v corres- ponding to these times is large compared with a. In what follows we shall assume the condition A > a to hold.f It must be borne in mind, however, that this condition may not be sufficient: for metals at low temperatures there is a range of frequencies in which the macroscopic theory is inapplicable, although the inequality cfto > a is satisfied (see §67). The formal theory given below is equally applicable to metals and to dielectrics. At frequencies corresponding to the motion of the electrons within the atoms (optical frequencies) and at higher frequencies, there is, indeed, not even a quantitative difference in the properties of metals and dielectrics. It is clear from the discussion in §56 that Maxwell's equations divD = 0, divB = 0, (58.1) curlE = - (l/*)0B/0*, curlH = (l/c)8DJdt (58.2) remain formally the same in arbitrary variable electromagnetic fields. These equations are, however, largely useless until the relations between the quantities D, B, E and H which appear in them have been established. At the high frequencies at present under consideration, these relations bear no resemblance to those which are valid in the static case and which we have used for variable fields in the absence of dispersion. First of all, the principal property of these relations, namely the depen- dence of D and B only on the values of E and H at the instant considered, no longer holds good. In the general case of an arbitrary variable field, the values of D and B at a given instant are not determined only by the values of E and H at that instant. On the contrary, they depend in general on the values of E(t) and H(t) at every previous instant. This expresses the fact that the establishment of the electric or magnetic polarisation of the matter cannot keep up with the change in the electromagnetic field. The frequencies at which dispersion phenomena first appear may be completely different for the electric and the magnetic properties of the substance. t The effects (called the natural optical activity) resulting from terms of the next order in the small ratio a\ A will be considered in §83. §58 The dispersion of the dielectric permeability 249 In the present section we shall refer to the dependence of D on E; the specific features of the dispersion of magnetic properties will be discussed in §60. The polarisation vector P has been introduced in §6 by means of the definition p = - div P, p being the true (microscopic) charge density. This equation expresses the electric neutrality of the body as a whole, and together with the condition P = outside the body it shows that the total electric moment of the body is j P dV. This derivation is evidently valid for variable as well as for constant fields. Thus in any variable field, even if dispersion is present, the vector P = (D-E)/4tt retains its physical significance: it is the electric moment per unit volume. In rapidly varying fields, the field strengths involved are in practice always fairly small. Hence the relation between D and E can always be taken to be linear, f The most general linear relation between D(*) and the values of the function E(t) at all previous instants can be written in the integral form 00 B(t) = E(t) + J7(r)E(* - r)dr. (58.3) It is convenient to separate the term E(f), for reasons which will become evident later. In equation (58.3)/(t) is a function of time and of the proper- ties of the medium. By analogy with the electrostatic formula D = eE, we write the relation (58.3) in the symbolic form D = eE, where £ is a linear integral operator whose effect is shown by (58.3). Any variable field can be resolved by a Fourier expansion into a series of components of a single frequency, in which all quantities depend on time through the factor e-* w *. For such fields the relation (58.3) between D and E becomes D = e(w)E, (58.4) where the function e( co) is defined as 00 e(co)= 1+ ffW'dT. (58.5) Thus, for periodic fields, we can regard the dielectric permeability (the coefficient of proportionality between D and E) as a function of the frequency as well as of the properties of the medium. The dependence of e on the frequency is called its dispersion law. f Here we assume that D depends linearly on E alone, and not on H. In a constant field, a linear dependence of D on H is excluded by the requirement of invariance with respect to a change in the sign of the time. In a variable field, this condition no longer applies, and a linear relation between D and H is possible if the substance possesses symmetry of various kinds. It is, however, a small effect of the order of a/A, and is indeed the effect mentioned in the last footnote. 250 The Electromagnetic Wave Equations §58 The function e(o>) is in general complex. We denote its real and imaginary parts by e' and e" : €(co) = e'(to) + ie"(to). (58.6) From the definition (58.5) we see at once that e (_ w ) = €*(a>). (58.7) Separating the real and imaginary parts, we have e'(- a) = e'(co), e"(- ft>) = - e"(co). (58.8) Thus e is an even function of the frequency, and e" is an odd function. For frequencies which are small compared with those at which the dis- persion is large, we can expand e(o>) as a power series in to. The expansion of the even function €'(<*>) includes only even powers, and that of the odd function e"(co) includes only odd powers. In the limit as to -> 0, the func- tion e(co) in dielectrics tends, of course, to the electrostatic dielectric constant, which we here denote by eo. In dielectrics, therefore, the expansion of e'(o)) begins with the constant term e , while that of e"(co) begins, in general, with a term in to. The function e(w) at low frequencies can also be discussed for metals, if it is defined in such a way that, in the limit o> -> 0, the equation curlH = (l/<:)flD/a* becomes the equation curlH = AttoEIc for a constant field in a conductor. Comparing the two equations, we see that for co -> we must have SDjdt -> 4ttoE. But, in a periodic field, dD/dt = —itoeE, and we thus obtain the following expression for e(a>) in the limit of low frequencies : e(co) = Airicr/co. (58.9) Thus the expansion of the function e(a>) in conductors begins with an imaginary term in ljco, which is expressed in terms of the ordinary conduc- tivity a for constant currents. f The next term in the expansion of e(to) is a real constant, although for metals this constant does not have the same electrostatic significance as it does for dielectrics.}: Moreover, this term of the expansion may again be devoid of significance if the effects of the spatial non-uniformity of the field of the electromagnetic wave appear before those of its periodicity in time. t The imaginary part of the function e{oi) is sometimes represented in the form (58.9) for all frequencies; this amounts to introducing a new function a(o>), which has no physical significance apart from its relationship to e"(w). % To avoid misunderstanding, we should point out a slight change in notation in com- parison with §56. In equation (56.10) for poor conductors, e(a>) is (4mo/a>) + e. §60 The dispersion of the magnetic permeability 25 1 In superconductors there is always considerable non-uniformity, resulting from the smallness of the "penetration depth" of the magnetic field. It is not yet clear whether the concept of the dielectric permeability e(<o) has any meaning for superconductors. §59. The dielectric permeability at very high frequencies In the limit as to -> oo, the function e(o>) tends to unity. This is evident from simple physical considerations: when the field changes sufficiently rapidly, the polarisation processes responsible for the difference between the field E and the induction D cannot occur at all. It is possible to establish the limiting form of the function e(o>) at high frequencies, which is valid for all bodies, whether metals or dielectrics. The field frequency is assumed large compared with the "frequencies" of the motion of all, or at least the majority, of the electrons in the atoms forming the body. When this condition holds, we can calculate the polarisation of the substance by regarding the electrons as free and neglecting their inter- action with one another and with the nuclei of the atoms. The velocities v of the motion of the electrons in the atoms are small compared with the velocity of light. Hence the distances vja> which they traverse during one period of the electromagnetic wave are small compared with the wavelength c/to. For this reason we can assume the wave field uniform in determining the velocity acquired by an electron in that field. The equation of motion is m dv'/dt = eE = eEo<r iw ', where e and m are the electron charge and mass, and v' is the additional velocity acquired by the electron in the wave field. Hence v' = ieEjmoi. The displacement r of the electron due to the field is given by f = v', and therefore r = -eE/ma> 2 . The polarisation P of the body is the dipole moment per unit volume. Summing over all electrons, we find P = Ser = -e 2 NE/ma> 2 , where N is the number of electrons in all the atoms in unit volume of the substance. By the definition of the electric induction, we have D = eE = E+4nP. We thus have the formula e(a>) = 1 - 4rriV<? 2 /mco 2 . (59.1) The range of frequencies over which this formula is applicable begins, in practice, at the far ultra-violet for light elements and at the X-ray region for heavier elements, f §60. The dispersion of the magnetic permeability Unlike the dielectric polarisability, the magnetic susceptibility ceases to have any physical meaning at relatively low frequencies. To take account of the deviation of fi(to) from unity would then be an unwarrantable refinement. t If e(<o) is to retain the significance which it has in Maxwell's equations, the frequency must also satisfy the condition o> < c\a. We shall see later (§97), however, that the expres- sion (59.1) can be allotted a certain physical significance even at higher frequencies. 252 The Electromagnetic Wave Equations §60 To show this, let us investigate to what extent the physical meaning of the quantity M = (B — H)/47r, as being the magnetic moment per unit volume, is maintained in a variable field. The magnetic moment of a body is, by definition, the integral — ( r XptdV. (60.1) The mean value of the microscopic current density is related to the mean field by equation (56.7): 4tt_ 1 BE curl B = — pv + --—. (60.2) c c ot Subtracting the equation curl H = (lJc)8D/dt, we obtain pv = ccurlM + 8P/8L (60.3) The integral (60.1) can, as shown in §27, be put in the form JM dV only if p~v = c curl M and M = outside the body. Thus the physical meaning of M, and therefore of the magnetic suscep- tibility, depends on the possibility of neglecting the term dT?/dt in (60.3). Let us see to what extent the conditions can be fulfilled which make this neglect permissible. For a given frequency, the most favourable conditions for measuring the susceptibility are those where the body is as small as possible (to increase the space derivatives in curl M) and the electric field is as weak as possible (to reduce P). The field of an electromagnetic wave does not satisfy the latter condition, because E ~ H. Let us therefore consider a variable field, say in a solenoid, with the body under investigation placed on the axis. The electric field is due only to induction by the variable magnetic field, and the order of magnitude of E inside the body can be obtained by estimating the terms in the equation curlE= -(l/c)dB/8t, whence E/l ~ toH/c or E ~ (wllc)H, where / is the dimension of the body. Putting c— 1 ~ 1, we have dPJdt ~ <oE ~ oj 2 IH/c. For the space derivatives of the magnetic moment M = #H we have |ccurlM| ~ cxH/l. If \dP/dt\ is small com- pared with \c curl M|, we must have J2 <^ X c*lufi. (60.4) It is evident that the concept of magnetic susceptibility can be meaningful only if this inequality allows dimensions of the body which are (at least) just macroscopic, i.e. if it is compatible with the inequality / > a, where a is the atomic dimension. This condition is certainly not fulfilled for the optical frequency range ; for such frequencies, the magnetic susceptibility is always ~ v^jc 2 , where v is the electron velocity in the atom;f but the optical f The relaxation times for any paramagnetic or ferromagnetic processes are certainly large in comparison with the optical periods. §61 The field energy in dispersive media 253 frequencies themselves are ~ v/a, and therefore the right-hand side of the inequality (60.4) is ~ a 2 . Thus there is certainly no meaning in using the magnetic susceptibility from optical frequencies onward, and in discussing such phenomena we must put /* = 1. To distinguish between B and H in this frequency range would be an over-refinement. Actually, the same is true for many phen- omena even at frequencies well below the optical range. §61. The field energy in dispersive media The formula S = cEx H/4tt (61.1) for the energy flux density remains valid in variable electromagnetic fields, even if dispersion is present. This is evident from the arguments given at the end of §29: on account of the continuity of the tangential components of E and H, formula (61.1) follows from the condition that the normal component of S is continuous at the boundary of the body and the validity of a similar formula in the vacuum outside the body. The rate of change of the energy in unit volume of the body is div S. Using Maxwell's equations, we can write this expression as 1 / dD „ 8B \ - divS = d E -ir +H -i7) ; < 6L2 > see (56.15). In a dielectric medium without dispersion, when € and /x are real constants, this quantity can be regarded as the rate of change of the electromagnetic energy U= ( € E2 + m H2)/8tt, (61.3) which has an exact thermodynamic significance: it is the difference between the internal energy per unit volume with and without the field, the density and entropy remaining unchanged. In the presence of dispersion, no such simple interpretation is possible. Moreover, in the general case of arbitrary dispersion, the electromagnetic energy cannot be rationally defined as a thermodynamic quantity. This is because the presence of dispersion in general signifies a dissipation of energy, i.e. a dispersive medium is also an absorbing medium. To determine this dissipation, let us consider an electromagnetic field of a single frequency. By averaging with respect to time the expression (61.2), we find the steady rate of change of the energy, and this is the mean quantity Q of heat evolved per unit time and volume. Since the expression (61.2) is quadratic in the fields, all quantities must be written in real form. If, as is convenient for a field of a single frequency, we take E and H to be complex, then in (61.2) we must substitute for E and SDJdt respectively £(E+E*) and £(— iweE+icoe^E*), and similarly for H 254 The Electromagnetic Wave Equations §61 and dB/dt. On averaging with respect to time, the products E«E and E*»E*, which contain factors e T2io)t , give zero, leaving Q = TirK 6 * - e ) E * E * + 0** - J") H ' H *] = ^( € "I E I 2 + /*'W)- J.07T 07T This expression can also be written Q = o>(e"E2 + ^"!P)/47r, (61.4) where E and H are the real fields, and the bar denotes an average with respect to time. This important formula shows that the absorption (dissipation) of energy is determined by the imaginary parts of e and /*. The two terms in (61.4) are called the electric and magnetic losses respectively. On account of the law of increase of entropy, the sign of these losses is determinate : the dis- sipation of energy is accompanied by the evolution of heat, i.e. Q > 0. It therefore follows from (61.4) that the imaginary parts of e and //, are always positive : e" > 0, p" > (61.5) for all substances and at all frequencies.! The signs of the real parts of € and p for a> ^ are subject to no physical restriction. Any non-steady process in an actual body is to some extent thermo- dynamically irreversible. The electric and magnetic losses in a variable electromagnetic field therefore always occur to some extent, however slight. That is, the functions e"(<o) and p"(<o) are not exactly zero for any frequency other than zero. We shall see in §62 that this statement is of fundamental importance, although it does not exclude the possibility of only very small losses in certain frequency ranges. Such ranges, in which e" and /x" are very small in comparison with * and p, are called transparency ranges. It is possible to neglect the absorption in these ranges and to introduce the concept of the internal energy of the body in the electromagnetic field, in the same sense as in a constant field. To determine this quantity, it is not sufficient to consider a field of only a single frequency, since the strict periodicity results in no steady accumulation of electromagnetic energy. Let us therefore consider a field whose components have frequencies in a narrow range about some mean value a>o. The field strengths can be written E = E (t)e-^ot, H = Ho(t)e-i»ot, (61.6) t Strictly speaking, this statement applies to bodies which, in the absence of the variable field, are in thermodynamic equilibrium; we assume this condition to hold. If the body is not in thermal equilibrium, then Q may in principle be negative. The second law of thermo- dynamics requires only a net increase in entropy as a result of the effects of the variable electromagnetic field and of the absence of thermodynamic equilibrium, the latter effect being independent of the presence of the field. A hypothetical example of such a body is one in which all the atoms have been excited artificially (i.e. otherwise than by spontaneous thermal excitation). §61 The field energy in dispersive media 255 where E (*) and Ho(0 are functions of time which vary only slowly in com- parison with the factor *-*»o'. The real parts of these expressions are to be substituted on the right-hand side of (61.2), and we then average with respect to time over the period 27r/o> , which is small compared with the time of variation of the factors Eo and Ho. The first term in (61.2), with E written in complex form, is i(E+E*)4(D + D*)/4tt, and similarly for the second term. The products E-D and E*.D* vanish when averaged over time, and can therefore be ignored, leaving 1 / 3D* ^ 3D \ E-— - + E*.— • (61-7) 16tt\ dt dt I We write the derivative 8D/dt as /E, where / is the operator d£/dt, and ascertain the effect of this operator on a function of the form (61.6). If Eo were a constant, we should have simply/E = /(w)E, where/(o>) = -*W(co). We expand the function Eo(f) as a series of Fourier components Eo a e _fa ', with constant Eo a . Since Eo(*) varies only slowly, this series will include only components with a <^ w . We can therefore put /E 0a e-*< w o + a > = /(a + a> )Eoa<H< ft, o + <x)t da>o Summing the Fourier components, we have d/(ajo) dEo . # fEo{t)e-i"ot = /(o*)E <H<V + i ^^ L ~^ e °' Omitting henceforward the suffix to o>, we thus obtain 3D d(a>e) dE . , ... m = - icoe(co)E + _l—i— «-•* (61.8) 3t do> dt Substituting this expression in (61.7) and neglecting the imaginary part of e(o>) gives 1 dHL, »Eo 8Eo*\ 1 d(««) d since E-E* = E «Eo*. Adding a similar expression involving the magnetic field, we conclude that the steady rate of change of the energy in unit volume is given by dU/dt, where O _ _L« E .E* + ^*Wl . (61.9) 167T L da> dco J 256 The Electromagnetic Wave Equations §62 In terms of the real fields E and H this expression can be written 1 rd(a»e) — d(a> / a) — ] V 1 rdfcue)— d(cou)—l = — -T-^ 2 + -—^HA. (61.10) o7rL dco da> J This is the required result: V is the mean value of the electromagnetic part of the internal energy per unit volume of a transparent medium. If there is no dispersion, e and p are constants, and (61.10) becomes the mean value of (61.3), as it should. If the external supply of electromagnetic energy to the body is cut off, the absorption which is always present (even though very small) ultimately converts the energy V entirely into heat. Since, by the law of increase of entropy, there must be evolution and not absorption of heat, we must have V > 0. It therefore follows, by (61.9), that the inequalities d(we)/dto > 0, d((t)fi)/dco > must hold. In reality, these conditions are necessarily ful- filled, by virtue of more stringent inequalities always satisfied by the functions e(w) and fi(to) in transparency ranges (see §64). f Considerable interest attaches to the determination of the (time) average stress tensor giving the forces on matter in a variable electromagnetic field. This problem is meaningful for both absorbing and non-absorbing media, whereas that concerning the internal energy can be proposed only if absorp- tion is neglected. The corresponding formulae, however, have not yet been derived. §62. The relation between the real and imaginary parts of e(a>) The function /(t) in (58.3) is finite for all values of t, including zero.t For dielectrics it tends to zero as r -*-oo. This simply expresses the fact that the value of D(*) at any instant cannot be appreciably affected by the values of E(*) at remote instants. The physical agency underlying the integral relation (58.3) consists in the processes of the establishment of the electric polarisation. Hence the range of values in which the function /(t) differs appreciably from zero is of the order of the relaxation time which characterises these processes. The above statements are true also of metals, the only difference being that the function /(t) — Atto, rather than/(r) itself, tends to zero as t -> oo. This difference arises because the passage of a steady conduction current, though it does not cause any actual change in the physical state of the metal, in our equations leads formally to the presence of an induction D such that f The sum of the inequalities (64.1) and (64.2) shows, in fact, that the derivative d(we)/do) always exceeds unity. X It was to ensure this that the term E(£) was separated in (58.3), since otherwise the function /(t) would have a delta-function singularity at t = 0. §62 The relation between the real and imaginary parts of c(o>) 257 (llc)8Djdt = ^naEjcoT t 00 D(f) = f 4tt<tE(t) dr = -W j E(t - t) dr. -00 We have defined the function e(oi) by CO e(a>) = 1 + je^f(r) dr. (62.1) It is possible to derive some very general relations concerning this function by using the methods of the theory of functions of a complex variable. To do so, we regard w as a complex variable (co = to'+ito"), and ascertain the properties of the function e(cu) in the upper half of the <o-plane. From the definition (62.1) and the above-mentioned properties of the function /(t), it follows that e(o>) is a one- valued regular function everywhere in the upper half-plane. For, when a>" > 0, the integrand in (62.1) includes the exponentially decreasing factor c~ w " T and, since the function /(t) is finite throughout the region of integration, the integral converges. The function e(w) has no singularity on the real axis (a/' = 0), except possibly at the origin (where, for metals, «(o>) has a simple pole).f It is useful to notice that the conclusion that e(w) is regular in the upper half-plane is, physically, a consequence of the causality principle. The integration in (58.3) is, on account of this principle, taken only over times previous to t, and the region of integration in formula (62.1) therefore extends from to oo rather than from - oo to oo. It is evident also from the definition (62.1) that € (_ w *) = € *(o>). (62.2) This generalises the relation (58.7) for real to. In particular, for purely imaginary w we have e(*V) = «*(««"), i.e. the function e(w) is real on the imaginary axis : ime = for to = iui" . (62.3) It should be emphasised that the property (62.2) merely expresses the fact that the operator relation D = eE must give real values of D for real E. If the function E(f) is given by the real expression E = Eo*-*"* + E V W * , (62.4) t In the lower half-plane, the definition (62.1) is invalid, since the integral diverges. Hence the function €(oj) can be defined in the lower half-plane only as the analytical continu- ation of formula (62.1) from the upper half-plane, and in general has singularities. The function e(co) has a physical as well as a mathematical significance in the upper half- plane : it gives the relation between D and E for fields whose amplitude increases as e . In the lower half-plane, this physical interpretation is not possible, if only because the presence of a field which is damped as e-l w "l* implies an infinite field f or t -> — oo. 258 The Electromagnetic Wave Equations §62 then, applying the operator £ to each term, we have D = €(co)Eoe- io,t + e(- o>*)Eo*«*°**, and the condition for this to be real is just (62.2). According to the results of §61, the imaginary part of e(a>) is positive for positive real co = co', i.e. on the right-hand half of the real axis. Since, by (62.2), ime(-w') = — im e(to'), the imaginary part of e(co) is negative on the left-hand half of this axis. Thus ime > for oo = a/ > 0. (62.5) At co = 0, im e changes sign, passing through zero for dielectrics and through infinity for metals. This is the only point on the real axis for which im e(co) can vanish. When <o tends to infinity in any manner in the upper half-plane, e(co) tends to unity. This has been shown in §59 for the case where co tends to infinity along the real axis. The general result is seen from formula (62. 1) : if co -» oo in such a way that co" -> oo, the integral in (62. 1) vanishes because of the factor e~ W ' T in the integrand, while if co" remains finite but \co'\ -» oo the integral vanishes because of the oscillating factor e ib)r . The above properties of the function e(co) are sufficient to prove the following theorem: the function e(tu) does not take real values at any finite point in the upper half-plane except on the imaginary axis, where it de- creases monotonically from eo > 1 (for dielectrics) or from + oo (for metals) at co = iO to 1 at to = too. Hence, in particular, it follows that the function e(co) has no zeros in the upper half-plane. We shall not pause to prove this theorem, because it is identical with a general theorem concerning the "generalised susceptibility" (and the prop- erties of e(co) enumerated above exhibit a similar analogy), f For the same reason, the function e(a>) satisfies the general relations between the real and imaginary parts of the generalised susceptibility. We shall repeat here the derivation of these relations, in order to emphasise certain differences between dielectrics and metals. Let us take some real value coq of co, and integrate the expression (e— l)/(co— coq) round the contour C shown in Fig. 29. This contour in- Fig. 29 t See Statistical Physics, §122, Pergamon Press, London, 1958. The generalised suscep- tibility a(co) used there corresponds to e(to) — 1, which vanishes as « -> oo. §62 The relation between the real and imaginary parts of e(to) 259 eludes the whole of the real axis, indented upwards at the point to = too > 0, and also at the point to = if the latter is (as in metals) a pole of the func- tion e(to), and is completed by a semicircle of infinite radius. At infinity c -> 1, and the function (e — l)/(to- too) therefore tends to zero more rapidly than 1/to. The integral dco (62.6) f J (a — coo c consequently converges; since c(to) is regular in the upper half-plane, and the point <o = a> has been excluded from the region of integration, the function (e — l)/(co — too) is analytic everywhere inside the contour C, and the integral is therefore zero. The integral along the semicircle at infinity is also zero. We pass round the point too along a semicircle whose radius p -> 0. The direction of integration is clockwise, and the contribution to the integral is — ^7r[e(too) — 1]. If the function e(to) pertains to a dielectric, the indentation at the origin is unnecessary, and we therefore have -p + w 00 lim j — dco + dco - zV[e(coo) - 1] = 0. P-+°\ J CO — coo J CO — coo ) -oo p + w The expression in the braces is the integral from — oo to oo, taken as a principal value. Thus we have 00 1 P f dco - H>(co ) - 1] = 0. (62.7) J CO — coo —oo Here the variable of integration <a takes only real values. We replace it by x, call the given real value to instead of coo, and write the function e(co) of the real variable to, as in §58, in the form e(to) = e'(to)+/c"(to). Taking the real and imaginary parts of (62.7), we obtain the following two formulae: 00 1 r e E 'H - l = -p - TT J X "(*) dx, (62.8) 1 r €'(*) - 1 6 "(o,) = — P\ — — dx % (62.9) TT J X— CO -oo first derived by H. A. Kramers and R. de L. Kronig (1927). It should be emphasised that the only important property of the function c(to) used in 260 The Electromagnetic Wave Equations §62 the proof is that it is regular in the upper half-plane, f Hence we can say that Kramers and Kronig's formulae, like this property of e(a>), are a direct consequence of the causality principle. Using the fact that e"(x) is an odd function, we can rewrite (62.8) as 1 f e"(x) 1 ? e"(x) e'(co) - 1 = -P \ — —dx + -P — — d* TT J X — CO TT J X + CO 2 r xe"(x) = -P ~Y^ dx - (62.10) TT J X 1 — CO 1 If a metal is concerned, the function e(o>) has a pole at the point to = 0, near which e = 47ria/co (58.9). The passage along a semicircle round this point gives a further real term —(47tct/coo)7t, which must be added to the left-hand side of equation (62.7). Thus formula (62.9) becomes 1 fV(#) -1 Ait a € "(o>) = - -P\ -Aj! d* + — , (62.11) 77 J X — CO CO -oo but (62.8) and (62.10) remain unchanged. A further remark is also necessary as regards metals. We have said at the end of §58 that there may be ranges of frequency for metals in which the function e(to) becomes physically meaningless on account of the spatial non-uniformity of the field. In the formulae given here, however, the integration must be taken over all fre- quencies. In such cases e(<o) must be taken, in the frequency ranges con- cerned, as the function obtained by solving the formal problem of the behaviour of the body in a fictitious uniform periodic electric field (and not in the necessarily non-uniform field of the electromagnetic wave). Formula (62.10) is of particular importance: it makes possible a calcula- tion of the function e'(co) if the function e"{<o) is known even approximately (for example, empirically) for a given body. It is important to note that, for any function e"(a>) satisfying the physically necessary condition e" > for to > 0, formula (62.10) gives a function e'(w) consistent with all physical requirements, i.e. one which is in principle possible (the sign and magnitude of e' are subject to no general physical restrictions). This makes it possible to use formula (62.10) even when the function ^"(co) is approximate. Formula (62.9), on the other hand, does not give a physically possible function €"(co) for an arbitrary choice of the function e'(o>), since the condi- tion that e"(a>) > is not necessarily fulfilled. t The property e -> 1 as a> -> oo is not important: if the limit e(oo) were other than unity, we should simply take e — c(co) in place of e — 1, with corresponding obvious changes in formulae (62.8), (62.9). §62 The relation between the real and imaginary parts of e(a>) 261 In dispersion theory the expression for e'(to) is customarily written in the form e>) _ 1 = _^ P f^Ld*, (62.12) o where e and m are the charge and mass of the electron, and /(to) da> is called the oscillator strength (or "number of dispersion electrons") in the frequency range dto. According to (62.10), this quantity is related to e"(a>) by m /H = TT7" e "H- (62 - 13) For metals, /(co) tends to a finite limit as to -> 0. For sufficiently large w, x 2 can be neglected in comparison with to 2 in the integrand in (62.10). Then dx. c'(co) - 1 = f Xe"(x) WOT J Q For the dielectric constant at high frequencies, on the other hand, formula (59.1) holds, and a comparison shows that 00 m 27r 2 e 2 o f co € "(o>)do> = f f (to) dot = iV, (62.14) where iV is the total number of electrons per unit volume. If € f (w) is regular at <o = 0, we can take the limit to -» in formula (62.10), obtaining e '(0)-l = - — ^d*. (62.15) o If the point to = is a singularity of e"( o>) (as in metals), the limit of the integral (62.10) as to -> is not what is obtained by simply deleting the term in to. To calculate the limit, we must first replace e"(x) in the integrand by e"(x)- / hro/x; the value of the integral is unchanged, because d# P = 0. J x 2 — to 2 262 The Electromagnetic Wave Equations §62 For a dielectric, formula (62.15) can be rewritten as 4ire*N €0 _ l = o>- 2 , (62.16) m where the bar denotes averaging with respect to the "number of oscillators": N J co * = — I — dco. The expression (62.16) may be useful in estimating co- The following formula f relates the values of e(co) on the upper half of the imaginary axis to those of e"{<*>) on the real axis: 2 F Xe"(x) </co)-l=- — ±Ldx. (62.17) IT J X 1 + CO 1 Integrating this relation over all co, we obtain 00 00 f[ C (/a>)-l]dco = fe"(cu)dco. (62.18) All the above results are applicable, apart from slight changes, to the magnetic permeability /*(«>). The differences are due principally to the fact that the function /x(a>) ceases to be physically meaningful at relatively low frequencies. Hence, for example, Kramers and Kronig's formula must be applied to /a(o>) as follows. We consider not an infinite but a finite range of co (from to coi), which extends only to frequencies where p is still meaning- ful but no longer variable, so that its imaginary part may be taken as zero ; let the real quantity ja(coi) be denoted by (i±. Then formula (62.10) must be written as w i 2 C xa"(x) /.'(«) - R = -P\ -f^d*. (62.19) IT J X L — (O z Unlike eo, the value /jlq of fj,(0) may be either less than or greater than unity. The variation of fj,(w) along the imaginary axis is again a monotonic decrease, from j^o to fj,i < fjbo- t See Statistical Physics, formula (122.19). §63 A plane wave of a single frequency 263 §63. A plane wave of a single frequency Maxwell's equations (58.2) for a wave of a single frequency are za>/z(cu)H = ccurlE, /o>e(cu)E = — ccurlH. (63.1) These equations as they stand are complete, since equations (58.1) follow from (63.1) and so do not require separate consideration. Assuming the medium homogeneous, and eliminating H from equations (63.1), we obtain the second-order equation AE + £/x(w 2 /c 2 )E = 0; (63.2) elimination of E gives a similar equation for H. Let us consider a plane electromagnetic wave propagated in an infinite homogeneous medium. In a plane wave in a vacuum, the space dependence of the field is given by a factor e^'', with a real wave vector k. In con- sidering wave propagation in matter, however, it is in general necessary to take k complex: k = k'+*k", where the vectors k' and k" are real. Taking E and H as proportional to ei^' r , and carrying out the differentia- tion with respect to the co-ordinates in equations (63.1), we obtain o>/xH = ck x E, o>eE = -ckxH. (63.3) Eliminating E and H from these two equations, we obtain for the square of the wave vector £2 = #2 _ £"2 + 2zk'-k" = €fx^lc\ (63.4) We see that k can be real only if e and /x are real and positive. Even then, however, k may still be complex if k'»k" = 0; we shall meet with such a case in discussing total reflection in §66. It must be borne in mind that, in the general case of complex k, the term "plane wave" is purely conventional. Putting e ik ' r = e^- '*e~W' r , we see that the planes perpendicular to the vector k' are planes of constant phase. The planes of constant amplitude, however, are those perpendicular to k", the direction in which the wave is damped. The surfaces on which the field itself is constant are in general not planes at all. Such waves are called inhomogeneous plane waves, in contradistinction to ordinary "homogeneous" plane waves. The general relation between the electric and magnetic field components is given by formulae (63.3). In particular, taking the scalar product of these formulae with k, we obtain k.E = 0, k.H = 0, (63.5) and, squaring either and using (63.4), E2 = filPje. (63.6) It must be remembered, however, that because all three vectors k, E and H are complex these formulae do not in general have the same evident signifi- cance as when the vectors are real. 264 The Electromagnetic Wave Equations §63 We shall not give the cumbersome relations valid in the general case, but consider only the most important particular cases. Especially simple results are obtained for a wave propagated without damping in a non-absorbing (transparent) homogeneous medium. The wave vector is real, and its magnitude is k = ■\Z(€fi)colc = ncojc, (63.7) where n = VC^) * s called the refractive index of the medium. The electric and magnetic fields are both in a plane perpendicular to the vector k (a pure transverse wave) ; they are mutually perpendicular, and are related by H = <v/(*//*)l X E » (63.8) where 1 is a unit vector in the direction of k. Hence it follows that eE 2 = fiH 2 , but this does not mean (as it would in the absence of dispersion) that the electric and magnetic energies in the wave are equal, since these energies are given by different expressions (namely, the two terms in formula (61.10)). The velocity u with which the wave is propagated in the medium is given by the familiar expression for the group velocity :f dcu c U = ~TT = A/ v . • (63.9) ak d(«ct>)/da> It is easy to verify that u = SJC, (63.10) in accordance with its significance as the velocity of transfer of energy in the wave packet; here V is the energy density given by formula (61.9), and S = f/-E-E* (63.11) is the mean value of the Poynting vector. In the absence of dispersion, when the refractive index is independent of frequency, the expression (63.9) becomes simply c/n; cf. (56.13). Next, let us consider a more general case, the propagation of an electro- magnetic wave in an absorbing medium, the wave vector having a definite direction (i.e. k' and k" being parallel). Then the wave is literally plane, since the surfaces of constant field in it are planes perpendicular to the direction of propagation (a homogeneous plane wave). In this case we can introduce the "length" k of the wave vector, given by k = kl (1 being a unit vector in the direction of k' and k"), and from (63.4) we have k = y^e/^co/c. The complex quantity V( € / x ) * s usually written in the form n+iic, with real n and k, so that k = -\/(€ix)wJc = (n + iKJw/c. (63.12) t When considerable absorption occurs, the group velocity cannot be used, since in an absorbing medium wave packets are not propagated but rapidly "ironed out". §63 A plane wave of a single frequency 265 The quantity n is called the refractive index of the medium, and k the absorption coefficient'^ the latter gives the rate of damping of the wave during its propagation. It should be emphasised, however, that the damping of the wave need not be due to true absorption: dissipation of energy occurs only when e and /x. are complex, but k is different from zero if «r and p are real and of opposite sign. We may express n and k in terms of the real and imaginary parts of the dielectric constant (taking fj, = 1). From the equation n 2 — k 2 + 2inK = e = e' + U" we have n 2 — k 2 = e', 2«k = e". Solving these equations for n and k, we havef n = VW + V(*' 2 + "**)]}, (63.13) In particular, for metals and in the frequency range where formula (58.9) is valid, the imaginary part of e is large compared with its real part, and is related to the conductivity by e" = faa/to; neglecting e' in comparison with e", we find that n and k are equal : n = K = ^(lira/to). (63.14) The relation between the fields E and H in this homogeneous plane wave is again given by formula (63.8), but e and y, are now complex. The formula again shows that the two fields and the direction of propagation are mutually perpendicular. If /* = 1, we write -y/e = <\/(n 2 +K 2 )exp[i tan -1 (*/«)], which shows that the magnetic field is -y/(n 2 +K 2 ) times the electric field in magnitude and tan _1 (i<r/«) from it in phase; in particular, when (63.14) holds, the phase difference is |-7r. PROBLEM At a given instant < = Oan electromagnetic perturbation occurs in some region of space. The perturbation is not maintained by external agencies, and is therefore damped in time. Find the damping decrement. Solution. We expand the initial perturbation as a Fourier integral with respect to the co-ordinates, and consider a component having a (real) wave vector k. The time dependence of this component is given, for sufficiently large t, by a factor e _ * w * with a complex "fre- quency" to, which is to be determined; the damping decrement is — im to. From the equations — tile = curl E = tkXE, f)/c = curl H = tk x H we have, eliminat- ing H, fi/c a =kx(kxE). (1) We take the direction of k as the x-axis. The "longitudinal" part of the perturbation there- fore satisfies D x — 0, whence D x = 0. t Since e" > 0, the signs of n and k must be the same, in accordance with the fact that the wave is damped in the direction of propagation. The choice of positive signs in (63.13) corresponds to a wave propagated in the positive ac-direction. 266 The Electromagnetic Wave Equations §64 The relation between D x and E x is of the form e Ex{t) = t-W x = J F(t-r)D x (r) dr; (2) —00 cf. §58. Since we have D x (r) = for t > 0, it follows that o Exit) = J Fit-r)Dxir) dr. (3) -co Hence we see that, for large t , the time dependence of Ex is given essentially by that of the function Fit). For a field of a single frequency, (2) gives 1 °° = f Fix)e iax dx, or, conversely, 00 1 f 1 2n- J €(a>) —00 To estimate this integral for large t , we displace the path of integration into the lower half- plane of a, where the integrand decreases rapidly. The singularities of the function l/e(co), i.e. the zeros and branch points of e(o>), must be excluded from the contour. The integral is then essentially proportional to e"* u o*, where a»o is the singularity nearest the real axis. This gives the solution for the longitudinal part of the perturbation. For the transverse components, we have from (1) Dy,zlc 2 +k z E y , t = 0. A similar analysis gives the result that the required "frequency" wo is in this case the zero or branch point of the function a> 2 e(a>)— c 2 A 2 which lies nearest the real axis. §64. Transparent media Let us apply the general formulae derived in §62 to media which absorb only slightly in a given range of frequencies, i.e. assuming that for these frequencies the imaginary part of the dielectric permeability may be neglected. In such a case there is no need to take the principal value in formula (62.10), since the point x = o> does not in practice lie in the region of integration. The integral can then be differentiated in the usual way with respect to the parameter o>, giving 00 de 4ct> f Xe '(x) dx. -vJ dcu it J (to 2 — x 2 ) 2 o Since the integrand is positive throughout the region of integration, we conclude that de(o>)/do> > 0, (64.1) i.e.* if absorption is absent the dielectric constant is a monotonically increasing function of the frequency. §64 Transparent media 267 Similarly, in the same frequency range we obtain another inequality, d 4o> p *V'(*) —[o>2( e -!)] = _- K) dx > 0, dco it J (x* — ix) z Y o or d e /do> > 2(1 - e)/o>. (64.2) If c < 1, this inequality is more stringent than (64.1). It may be noted that the inequalities (64. 1) and (64.2) (together with the corresponding ones for fi(o>)) ensure that the inequality u < c is satisfied by the velocity of propagation of waves. For example, if p = 1 we have n = y'e and, replacing e by n 2 in (64.1) and (64.2), d(no>)/da> > n, d(nco)/da> > 1/w. (64.3) Thus we obtain two inequalities for the velocity u (63.9): u < c/n and u < en, whence u < c whether n < 1 or n > 1. These inequalities also show that u > 0, i.e. the group velocity is in the same direction as the wave vector. This is quite natural, even if not logically necessary. Let us suppose that the weak absorption extends over a wide range of frequencies, from a>i to a>2 (> a>i), and consider frequencies a> such that a>i <^ a* <^ o)2. The region of integration in (62.10) divides into two parts, x < a>i and x > a>2. In the former region we can neglect x in comparison with a>, and in the latter region co in comparison with x, in the denominator of the integrand : w i 2 ¥ dx 2 C e(co) = 1 + - €"(*) X€"(x)dx, (64.4) It J X 7T6t> 2 J i.e. the function e(<o) in this range is of the form a — b/cn 2 , where a and b are positive constants. The constant b can be expressed in terms of the "number of dispersion electrons" N± responsible for the absorption in the range from to coi (cf. (62.14)): e(o>) = a — ATrN\e 2 jmco 2 . (64.5) From this expression it follows, in particular, that, when the region of weak absorption is sufficiently wide, the dielectric permeability in general passes through zero. In this connection it should be recalled that a literally "transparent" medium is one in which e(a>) is not only real but also positive; if e is negative, the wave is damped inside the medium, even though no true dissipation of energy occurs. For the frequency at which e = the induction D is zero identically, and Maxwell's equations admit a variable electric field satisfying the single equation curl E = 0, with zero magnetic field. In other words, longitudinal electric waves can occur. To determine their velocity of propagation, we 268 The Electromagnetic Wave Equations §64 must take into account the dispersion of the dielectric permeability not only in frequency, but also with respect to the wave vector. The value of m for which e = is also a function of the wave vector. If the medium is iso- tropic, the next term after the zero-order term in the expansion of the scalar function a>(k) for which e[<o(k)] = is proportional to k 2 : to = a> +|ak 2 . Hence the velocity of propagation is u = dcofdk = <xk, and is proportional to the wave vector itself. PROBLEM A plane electromagnetic wave with a sharply defined forward front is incident normally on the boundary of a half-space (x > 0) occupied by a transparent medium with /* = 1. Determine the structure of the front of the transmitted wave (A. Sommerfeld and L. Brillouin, 1914). Solution. Let the wave be incident on the boundary of the medium at time t — 0, so that at * = the field (E or H) of the incident wave is E = for t < 0, E ~ <r i( V for t > 0. Expanding this field as a Fourier integral with respect to time, we reduce the prob- lem to that of waves of various frequencies and infinite extent incident on the boundary. The amplitude of the Fourier component of frequency w is proportional to 00 j* g<(o)-wo)T dr. When a wave of frequency o> is incident, the transmitted wave is of the form a(a>) e~ iu>t + ia>nx,c f where the amplitude a(w) is a slowly varying function of frequency. Hence the wave field in the medium in the present problem is oo oo E ~ Jdoi a(a))e-* w '+* wna; / c f e*< w -<V T dr. —oo In the region near the wave front, the important values of a> in this integral are those close to o>o. Using a new variable £ = a>— o>o, we replace a(o>) by a(a>o), and expand the exponent in powers of f . Omitting unimportant constants and phase factors, we have 00 00 E ~ J j exp{*f (t-« + ^ -i^ 8 *^-} di dr, where u = «(a>o) is the velocity of propagation (63.9), and «' = [dM/dw] w _ 0)() . Effecting the integration over £, we easily bring E to the form oo E ~ fe* ir > dij, w = (x-ut)lV(2x\u'\), to the sign in the exponent depending on that of «'. The intensity distribution near the wave front is given by 00 I 2 / ~ J e*V 2 dy . This expression is of the same form as that which gives the intensity distribution near the edge of the shadow in Fresnel diffraction, f For to > the intensity decreases monotoni- cally with increasing w, but for w < it oscillates with decreasing amplitude about a constant value to which it tends as w -> — oo . J ♦ t See The Classical Theory of Fields, §7-8. % At large distances preceding the front here considered there are found "precursors" propagated with velocity c. These correspond to the high-frequency Fourier components, for which e -> 1 . CHAPTER X THE PROPAGATION OF ELECTROMAGNETIC WAVES §65. Geometrical optics The condition for geometrical optics f to be applicable is that the wave- length A should be small in comparison with the characteristic dimension / of the problem. The relation between geometrical and wave optics is that, for A <^ /, any quantity <f> which describes the wave field (i.e. any component of E or H) is given by a formula of the type <f> = aeW where the amplitude a is a slowly varying function of the co-ordinates and time, and the phase iff is a large quantity which is "almost linear" in the co-ordinates and the time; it is called the eikonal, and is of great importance in geometrical optics. The time derivative of «/r gives the frequency of the wave: difi/dt = - a», (65.1) and the space derivatives give the wave vector: grad«£ = k, (65.2) and consequently the direction of the ray through any point in space. For a steady wave of a single frequency, the frequency is a constant and the time dependence of the eikonal is given by a term — at. We then intro- duce a function fa (also called the eikonal), such that j/t = — cot + (oo/c)iffi(x,y,z). (65.3) Then 0i is a function of the co-ordinates only, and its gradient is gradi/ri = n, (65.4) where n is a vector such that k = conjc. (65.5) The magnitude of n is equal to the refractive index n of the medium. J Hence the equation for the eikonal in ray propagation in a medium of refrac- tive index n(x, y, z) (a given function of the co-ordinates) is *-»-(■£)'♦(■£)■♦(£)•-* <*> t See The Classical Theory of Fields, §7-1, Addison- Wesley Press, Cambridge (Mass.), 1951 ; Pergamon Press, London, 1959. X Only transparent media are considered in geometrical optics. 269 270 The Propagation of Electromagnetic Waves §65 The equation of ray propagation in a steady state can also be derived from Fermat's principle, according to which the integral /k«dl (or, equivalently, the integral ?/ri = Jn»dl = Jnd/) along the path of the ray between two given points A and B has a value less than for any other path between A and B. Equating to zero the variation of this integral, we have B S^i = j (Sndl + wSdZ) = 0. A Let Sr be a displacement of the ray path under the variation. Then Sn = Sr»grad«, S d/ = l«dSr, where 1 is a unit vector tangential to the ray. Substituting in S^i and integrating by parts in the second term (using the fact that Sr = at A and B), we have B B S^tjl = I Sr«gradwd/ + I «l«dSr = J( grad „_^)). 8rd/ = . Hence d(«l)/d/ = gradw. (65.7) Expanding the derivative and putting d«/d/ = l«grad«, we obtain dl 1 — = -[gradw - l(l.gradn)]. (65.8) dl n This is the equation giving the form of the rays. We know from differential geometry that the derivative dl/d/ along the ray is equal to N/2?, where N is the unit vector along the principal normal and 2? the radius of curvature. Taking the scalar product of both sides of (65.8) with N, and using the fact that N and 1 are perpendicular, we have 1 gradn - = N.5 ; (65.9) 2? n the rays are therefore bent in the direction of increasing refractive index. The velocity of propagation of rays in geometrical optics is in the direc- tion of 1, and is given by the derivative u = dco/dk. (65.10) This is also called the group velocity, the ratio w/k being called the phase velocity. It must be remembered, however, that the latter is not the velocity of physical propagation of any quantity. §65 Geometrical optics 271 It is easy to derive also the equation which gives the rate of change of the radiation intensity along a ray. The intensity J is the magnitude of the (time) average Poynting vector. This vector, like the group velocity, is in the direction of 1: § = 71. In a steady state, the mean field energy density is constant at any given point in space. The equation of conservation of energy is therefore div § = 0, or div(71) = 0. (65.11) This is the required equation. Finally, let us consider how the direction of polarisation of linearly polarised radiation varies along a ray (S. M. Rytov, 1938). As we know from differential geometry, a curve in space (in this case, the ray) is charac- terised at every point by the mutually perpendicular unit vectors along the tangent (1), the principal normal (N) and the binormal (b), which form the natural trihedral. Since the electromagnetic waves are transverse, the vectors E and H are always coplanar with N and b. Let the direction of E at some point on the ray be the same as that of N, i.e. let E lie in the osculating plane (that of N and 1). The deviation of the curve from the osculating plane over a length d/ is of the third order of smallness with respect to d/. We can therefore say that, over a length d/ of the ray, the vector E remains in the original osculating plane. The ospu- lating plane at the other end of d/ is inclined to the original one at an angle d<f> = dl/T, where T is the radius of torsion. This is therefore the angle turned through by the vector E relative to N in the normal plane. Thus, over a distance d/ along the ray, the direction of polarisation rotates in the normal plane, its angle to the principal normal varying in accordance with the equation d<f>/dl = ljT. (65.12) In particular, when the torsion is zero, i.e. the ray is a plane curve, the direction of the vector E in the normal plane is constant, as is in any case evident from symmetry. PROBLEM Determine the velocity of propagation of light in a medium moving relative to the observer. Solution. Let o> and k be the frequency and wave vector of the light wave in a fixed frame of reference K, and o>', k' the corresponding quantities in a frame K' moving with the medium at velocity v relative to K. In the first approximation with respect to vjc (the only one we shall consider), the motion perpendicular to k has no effect on the propagation of light, and so, without loss of generality, we can assume that v and k are in the same direction. In the frame K' the medium is at rest, and a/ and k' are therefore related by ck' = a)'n(w')- (1) According to the relativistic transformation formulae f we have, as far as terms of the first f See The Classical Theory of Fields, §6-4. 272 The Propagation of Electromagnetic Waves §66 order in vjc t to' = oi—kv, k' = k — cov/c 2 . Substituting these expressions in (1) and ex- panding the function n(w'), we obtain to the same accuracy ta vu> I ' d(«co)\ k = n— + — Hl-M— 1, c c 2 \ dw / where n = n(u>). The velocity of propagation (the group velocity) is therefore vnco duo u = uo+v\ 1 —I — (2) (3) where uo = c[d(wa>)/da>] -1 is the velocity of propagation in a medium at rest. The phase velocity is to c I 1 co dn\ — = -+v[l- — + — k n \ n? n M do/' The first two terms in (3) can also be obtained by simply applying the relativistic formula for the addition of velocities, and the third is a dispersion effect, first discussed by H. A. Lorentz. §66. Reflection and refraction of electromagnetic waves Let us consider the reflection and refraction of a plane electromagnetic wave (of a single frequency) at a plane boundary between two homogeneous media, f Medium 1, from which the wave is incident, is assumed trans- parent, but not (for the present) medium 2. Quantities pertaining to the incident and reflected waves will be distinguished by the suffixes and 1 respectively, and those for the refracted wave by the suffix 2 (Fig. 30). The direction of the normal from the boundary plane into medium 2 is taken as the sr-axis. Fig. 30 Since there is complete homogeneity in the ry-plane, the dependence of the solution of the field equations on x and y must be the same in all space. The components k x , k y of the wave vector must therefore be the same for all three waves. Consequently, the directions of propagation of the three waves lie in one plane, which we take as the a^-plane. t We take /tt = 1 in both media. §66 Reflection and refraction of electromagnetic waves 273 From the equations fax = fax = fax (66.1) we find k\ z = — ko z = — (a)jc)\/ei cos 0o, k 2z = vT(*>A0 2€ 2 - fax 2 ] = W C W(*2 ~ e i sin2 o ). (66.2) The vector ko is, by definition, real, and so is ki. The quantity k 2z , however, is complex in an absorbing medium, and the sign of the root must be taken so that im&2 2 > 0, the refracted wave being damped towards the interior of medium 2. If both media are transparent, equations (66.1) give the familiar laws of reflection and refraction: sin 09 I e± n\ 01 = 00, -7-^= /- = -• ( 66 - 3 ) sin 0o V «2 »2 To determine the amplitudes of the reflected and refracted waves, we must use the boundary conditions at the surface of separation (z = 0), and we shall consider separately the two cases where the electric field Eo is in the plane of incidence and perpendicular to that plane ; from the results we can obtain the solution for the general case, where Eo can be resolved into compo- nents in these two directions. Let us first suppose that Eo is perpendicular to the plane of incidence. It is evident from symmetry that the same will be true of the fields Ei and E2 in the reflected and refracted waves. The vector H is in the xsr-plane. The boundary conditions require f the continuity of E y = E and H x \ by (63.3) H x = -cfaEy/w. The field in medium 1 is the sum of the fields in the incident and reflected waves, so that we obtain the two equations E0 + E1 = E2, fa z (Eo — E\) = fa z E 2 . The exponential factors in E cancel because k x (and therefore to) is the same in all three waves. In what follows, E signifies the complex amplitude of a wave. The solution of the above equations gives FresneVs formulae'. faz- &2z _ V e i cos 0o - -v/( € 2 - € i sin 2 o ) hj\ = Eo = Eo, faz + faz V € l cos #0 + V( € 2 - € 1 sm2 #o) 2&oz „ 2-vAicos0o Eq = — — Eq. (66.4) faz + faz V € i cos ^o + V( € 2 - e i sin 2 6c) t The boundary conditions on the normal components of B and D give nothing new in the present problem, because the equations div B = 0, div D = are consequences of equations (63.1). 274 The Propagation of Electromagnetic Waves §66 If both media are transparent, these formulae become, by (66.3), sin(0 2 -0 o ) hl = • , n TTT*' ' sm(0 2 + O ) . . n (66.5) 2 cos do sin #2 E 2 = Eo. sin(0 2 + o ) The case where E lies in the plane of incidence can be discussed similarly. Here it is more convenient to carry out the calculations for the magnetic field, which is perpendicular to the plane of incidence. A further two Fresnel's formulae are obtained: (66.6) € 2 ko z - ei&2z u * 2 COS 0<> ~~ V( e l e 2 - ei 2 Sin 2 O ) „ tl\ = Hq = ; /zO, «2&0z + «l&2z e 2 COS ^o + \/( e l e 2 — ei 2 sin 2 0o) 2e 2 ^0z 2e 2 COS do ti 2 = Hq = .no* €2^oz + nk2z € 2 cos 6 + V( € i e 2 - n 2 sin 2 6 ) If both media are transparent, these formulae may be written tan(0 o -0 2 ) Ul = 77i ^~T-"0> tan(0 o + 2 ) sin 20n H 2 = H . sin (0 O + 2 ) cos (0 O - 6 2 ) The reflection coefficient R is defined as the ratio of the (time) average energy flux reflected from the surface to the incident flux. Each of these fluxes is given by the averaged ^-component of the Poynting vector (63.11) for the wave in question, A Aicos0 1 |Ei| 2 |Ei|2 (66.7) R = -vAicos0 o |Eo| 2 |Eo| s For normal incidence (0 = 0) the two modes of polarisation are equiva- lent, and the reflection coefficient is given by •\Ai — V € 2 R = v . *. . (66.8) V e i + V e 2 This formula is valid whether the reflecting medium is transparent or not. If we put <\/e 2 = n 2 + iK 2 , and if medium 1 is a vacuum (ei = 1), then (n 2 — l) 2 + «"2 2 R = — — . (66.9) («2 + I) 2 + *2 2 The remaining discussion assumes that both media are transparent. The following general remark should be made first of all. The boundary between two different media is in reality not a geometrical surface but a thin transition §66 Reflection and refraction of electromagnetic waves 27 S layer. The validity of the formulae (66.1) does not rest on any assumptions concerning the nature of this layer. The derivation of Fresnel's formulae, on the other hand, is based on the use of the boundary conditions, and assumes that the thickness 8 of the transition layer is small compared with the wavelength A. The thickness 8 is usually comparable with the distances between the atoms, which are always small compared with A if the macro- scopic description of the field is legitimate, and so the condition A > 8 is usually fulfilled. In the opposite limiting case the phenomenon of refraction is entirely different in character. For 8 > A, geometrical optics is valid (A being small compared with the dimensions of the inhomogeneities in the medium). In this case, therefore, the propagation of the wave can be re- garded as the propagation of rays which undergo refraction in the transition layer but are not reflected from it. The reflection coefficient, therefore, would be zero. Let us return now to Fresnel's formulae. In reflection from a transparent medium, the coefficients of proportionality between Ei, E2 and Eo in these formulae are real, f This means that the wave phase either remains unchanged or changes by it, depending on the sign of the coefficients. In particular, the phase of the refracted wave is always the same as that of the incident wave. The reflection, on the other hand, may be accompanied by a change in phase.J For example, with normal incidence the phase of the wave is unchanged if ei > e 2 , but if ei < e 2 the vectors Ei and Eo are in opposite directions, i.e. the wave phase changes by it. The reflection coefficients for oblique incidence are, by (66.5) and (66.7), _ sin^-«o) _ «*■»(*-«,) x sin2(0 2 + o ) tan2(0 2 + o ) v ; Here, and in what follows, the suffixes _j_ and || refer to the cases where the field E is respectively perpendicular and parallel to the plane of incidence. The expressions (66. 10) are unaltered when 2 and 0o are interchanged (but the phase of the reflected wave changes by it, as is seen from formulae (66. 5) and (66.7)). The reflection coefficient for a wave incident from medium 1 at an angle 0o is therefore equal to that for a wave incident from medium 2 at an angle 2 . An interesting case is the reflection of light incident at an angle 0o such that #o + #2 = h 7 (th e reflected and refracted rays being thus perpendicular). Let this angle be 6 V \ sin 6 P = sin {^n— 2 ) = cos 2 , and the law of refrac- tion (66.3) gives tan 02, = V( £ 2/*i). (66.11) f We ignore for the moment the possibility of total reflection (see below). X Reflection from an absorbing medium leads in general to the appearance of elliptical polarisation. The explicit expressions for the amplitude and phase relations between the three waves are then extremely involved ; they are given by J. A. Stratton, Electromagnetic Theory, Chapter IX, McGraw-Hill, New York, 1941. 276 The Propagation of Electromagnetic Waves §66 For 0o = Op we have tan(02 + 0o) = oo, and R n = 0. Hence, whatever the direction of polarisation of light incident at this angle, the reflected light will be polarised so that the electric field is perpendicular to the plane of incidence. The reflected light is polarised in this way even when the incident light is natural: no component with any other polarisation is reflected. The angle 6 P is called the angle of total polarisation or the Brewster angle. It should be noticed that, whereas natural light can be totally polarised by reflection, this effect cannot be produced by refraction, whatever the angle of incidence. The reflection and refraction of plane-polarised light always results in plane-polarised light, but the direction of polarisation is in general not the same as in the incident light. Let yo be the angle between the direction of Eo and the plane of incidence, and yi, y^ the corresponding angles for the reflected and refracted waves. Using formulae (66.5) and (66.7), we easily obtain the relations cos (0o — 02) tanyi = tanyo, cos(»„ + * 2 ) tan 72 = cos (0o — 02) tan yo. The angles yo, y\ and y2 are equal for all angles of incidence only in the obvious cases yo = and yo = \n\ they are also equal for normal incidence (00 = 02 = 0) and for grazing incidence (0o = %n, in which case there is no refracted wave). In all other cases the formulae (66.12) give (by virtue of the inequalities < 0o, 02 < fyr an d, as we shall assume, < yo < \n, < yi> 72 < t) the inequalities yi > yo, y2 < yo- Thus the direction of E is turned away from the plane of incidence on reflection, but towards it on refraction. A comparison of the two formulae (66.10) shows that, at all angles of incidence except 0o = or far, i?„ < R ± . Hence, for example, when the incident light is natural the reflected light is partly polarised, and the pre- dominant direction of the electric field is perpendicular to the plane of incidence. The refracted light is partly polarised, with the predominant direction of E lying in the plane of incidence. The quantities R n and R ± depend quite differently on the angle of incidence. The coefficient R ± increases monotonically with the angle 0o from the value (66.8) for 0o = 0. The coefficient J?„ takes the same value (66.8) for 0o = 0, but as 0o increases /?„ decreases to zero at 0o = dp before monotonically increasing. Here two distinct cases occur. If the reflection is from the "optically denser" medium, i.e. €2 > ei, then jR„ and R ± increase to the common value of unity at 0o = \tt (grazing incidence). If, on the other hand, the reflecting medium is "optically less dense" (*2 < ei), both coefficients become equal to unity for 0o = 6 r , where sin0 r = V( € 2/ € i) = «2/«i; (66.13) §66 Reflection and refraction of electromagnetic waves 277 r is called the angle of total reflection. When 0o = #r the angle of refraction 02 = far, i-e. the refracted wave is propagated along the surface separating the media. Reflection from an optically less dense medium at angles 0o > 0r requires special consideration. In this case k% z is purely imaginary (see (66.2)), i.e. the field is damped in medium 2. The damping of the wave without true absorption (i.e. dissipation of energy) signifies that the average energy flux from medium 1 into medium 2 is zero (by simple calculation it can easily be seen that the vector § giving the average energy flux in medium 2 is in the ^-direction). That is, all the energy incident on the boundary is reflected back into medium 1, so that the reflection coefficients are R x = J?,, = 1. This phenomenon is called total reflection.^ The equality of R x and R „ to unity can, of course, be obtained directly from FresnePs formulae (66.4) and (66.6). For 0o > Or the proportionality coefficients between Ei and Eo become complex quantities, of the form (a — ib)l(a+ib). The quantities R ± and /?„ are given by the squared moduli of these coefficients, which are equal to unity. The formulae give, besides the ratio of the magnitudes of the fields in the reflected and incident waves, the difference in their phases. For this purpose we write Ei x = e-^xEo^ Ei t = e~**".Ebr Then} tan|Sj_ = V( € i sin2 0o - € 2 )/\Ai cos ^ ' (00.14) tan|S„ = \/( € i 2 sin 2 O — n^l^2 cos0 o . Thus total reflection involves a change in the wave phase which is in general different for the field components parallel and perpendicular to 'the plane of incidence. Hence, on reflection of a wave polarised in a plane inclined to the plane of incidence, the reflected wave will be elliptically polarised. || The phase difference 8 = 8 X — 8 , is easily found to be such that cos0oV(eisin2 o -e 2 ) tan£S = — . (66.15) y €i sm 2 0o The difference is zero only for 0o = r or 0o = \n. PROBLEMS Problem 1. Find the manner in which the reflection coefficient approaches unity near the angle of total reflection. Solution. We put do — Or— 8, where S is a small quantity, and expand sin 0o and cos do in formulae (66.10) in powers of 8. The result is # X= 1_4V(28)( W 2-1)-*, R t = l-4V(2S)n2(M2-l)-*, where n 2 = eijez > 1. The derivatives dR/dS become infinite as 8 _ * when 8 -> 0. f It may be mentioned that the reflection coefficient is always equal to unity in reflection from a medium with e real and negative. In such a medium there is again no true absorption, but the wave cannot penetrate into it. X If (a - ib)l(a + ib) = e-«s, then tan £S = b/a. || See The Classical Theory of Fields, §6-5. 278 The Propagation of Electromagnetic Waves §66 Problem 2. Find the reflection coefficient for almost grazing incidence of light from a vacuum on the surface of a body for which e is almost unity. Solution. Formulae (66.10) give the same reflection coefficient: R ± £* R t S* foo- V(^o 2 +e-l)]V(e-l) 2 , where ^o = i»— 0o. Problem 3. Determine the reflection coefficient for a wave incident from a vacuum on a medium for which both e and /* are different from unity. Solution. Calculations entirely analogous to those given above furnish the result |/x cos do — V^M - sin 2 0o)| 2 R,= I/* cos 0o+V( 6 J* — -sin 2 0o)l c cos 0o+ \/( e /* — sin 2 #o)| 2 e cos 0o+ V( e M — sin 2 0o)l Problem 4. A plane-parallel layer (region 2) lies between a vacuum (region 1) and an arbitrary medium (region 3). Light polarised parallel or perpendicular to the plane of incidence falls on the layer from the vacuum. Express the reflection coefficient jR in terms of those for semi-infinite media of the substances in regions 2 and 3. Solution. We denote by Ao and Ax the amplitudes of the field (E or H, whichever is parallel to the layer) in the incident and reflected waves. The field in the layer consists of the refracted wave (amplitude A%) and the wave reflected from region 3 (amplitude At.'). The boundary condition between regions 1 and 2 gives A 2 = a(Ai-ri2Ao) (1) where a and rx% are constants. In reflection from a semi-infinite medium of the substance in region 2, Az is zero, and so from (1) we have rxz — Ax/Ao, i.e. ri2 is the amplitude of reflection in that case. Another equation is obtained from (1) by interchanging A\ and Ao and replacing A% by Ai, which corresponds simply to a reversal of the sr-component of the wave vector: A = a(Ao-ri2Ai). (2) In region 3 there is only the transmitted wave, whose amplitude A3 satisfies the conditions A 2 eW = aAz, Az'e-W = —arz%Az (3) analogous to (1), (2) with Ax = 0. The exponential factors take account of the change in the wave phase over the thickness h of the layer, with 4> = (cohlc)V(ez-sin 2 9 ). (4) Eliminating A3 from equations (3), we obtain Az'e-W = rzsAzeW, (5) where rza = — r32. From equations (1), (2) and (5) we find the amplitude of reflection from the layer: _ Ai _ me-^+m r ~ Ao ~ e-W+rwn ' (6) and the reflection coefficient R = \r\ 2 . The significance of r 2 3 is found from the fact that, f or Ji = 0, r must be the amplitude of reflection ri3 from a semi-infinite medium of the substance in region 3. Hence rw — (ri2— ri3)l(ri2ri3— 1). (7) Formulae (6) and (7) give the required solution. It should be emphasised that their deriva- tion involves no assumptions concerning the properties of regions 2 and 3, which may be either transparent or not. §67 The surface impedance of metals 279 If regions 2 and 3 are transparent, then tfi, r\% and r\% are all real, and ras is the amplitude of reflection at the boundary between semi-infinite media of the substances in regions 2 and 3. From (6) we have _ (n2+r23) 2 — 4ri2r23 sin 2 tfi (ri2r23+l) 2 — 4ri2r23 sin 2 ^ As t/t varies, R varies between the limits [(n.2+r23)/(n.2r23+l)] 2 and [(rt2— r23)/(n2r23 — l)] 2 . For normal incidence n.2 = (m — W2)/(«i+M2), and ris and r23 are given by similar relations. If «2 2 = «iW3, then riz = rzz, and jR may be zero for some value of the thickness of the layer. If region 3 is a vacuum, then ri3 = 0, r23 = — *12, and (6) gives ri2(«- 21 *-l) sinhi'0 r = ■ = . (9) e -2i<\i _ ri2 2 sjnh j-,-0 _|. l Q g ( — ri2)] If also region 2 is transparent, we have 4i?i2 sin 2 if) R (l-i?i 2 ) 2 +4i?i2sin 2 1 A The transmission coefficient D for the layer (between vacua) is 1 — R only if region 2 is transparent. Otherwise D must be calculated from equations (l)-(3), putting 732 =ria. The amplitude of transmission d is and the transmission coefficient £> = |rf| 2 . Problem 5. Determine the reflection and transmission coefficients for light incident normally on a slab with a very large complex dielectric permeability e. Solution. In this case ri2 = (1 — V e )l(^ + V«0 ~ — (1— 2/\/ e )» and formula (9) of Problem 4 gives r = —[1 — (2/V e ) coth #] _1 , ^ = coh^/e/c. If the slab is so thin that (oh/c <^ 1/Vl e l> then we can put r = — [l+Hc/eayh] -1 , and distinguish two cases: for l/|e| < whle < 1/VM, R = 1 — 4cc"/«A|e|a, for coA/c < l/|e|, ii = w 2 /i 2 |e| 2 /4c 2 . The transmission coefficient is, by formula (10), for oih\c ~ 1/VM, d = — 2/\/e sinh tip, for wA/c < 1/VM, rf = (1 —ietoh/lc)- 1 . Again two cases can be distinguished : for 1/| c| < toA/c < 1/VM, -D = 4c 2 /o) 2 A 2 |e| 2 , for a>h/c < l/|e|, D = 1 -e"o>A/c. §67. The surface impedance of metals The dielectric permeability of metals is, in magnitude, large compared with unity at low frequencies (as <o -> 0, it tends to infinity as 1/w). The "wavelength" S ~ c/a)^\e\ in metalsf is then small compared with the wavelength A ~ c/w in vacuo. If 8 (but not necessarily A) is also small compared with the radii of curvature of the metal surface, the problem of the reflection of arbitrary electromagnetic waves from the metal can be considerably simplified. t Large values of \/e(<u) are almost always complex. The electromagnetic field is damped inside the body, so that the "wavelength" in the body is also the depth of penetration of the field. If e(o>) is expressed in terms of the conductivity by (58.9), the quantity 8 is the same as the penetration depth used in §45. 19 280 The Propagation of Electromagnetic Waves §67 The smallness of 8 implies that the derivatives of the field components inside the metal along the normal to the surface are large compared with the tangential derivatives. The field inside the metal near the surface can therefore be regarded as the field of a plane wave, and hence the fields Ef and Hf are related by E* = vW«)H« * n, (67.1) where n is a unit vector along the inward normal to the surface. Since Ej and H$ are continuous, their values outside the metal near the surface must be related in the same way. As M. A. Leontovich (1948) has pointed out, the equation (67.1) may be used as a boundary condition in determining the field outside the metal. Thus the problem of determining the external electromagnetic field can be solved without considering the field inside the metal. The quantity ■\/(fJ>/e) is called the surface impedance^ of the metal, and we denote it by £ = £' + it," : I - Vfc/c). (67-2) In the frequency range where e can be expressed in terms of the ordinary conductivity of the metal, we have I = (1 - i)y/(otnl87ra). (67.3) The (time) average energy flux through the surface of the metal is § = (cl&r) re(Et x H t *) = <*'|H«|2n/&r. ( 67 - 4 ) This is the energy which enters the metal and is dissipated therein. Hence we see, in particular, that H > 0. (67.5) This inequality determines the sign of the root in (67.2). As the frequency increases, the depth of penetration S becomes of the same order as the mean free path / of the conduction electrons. J In this case the spatial non-uniformity of the field renders impossible a macroscopic description of it in terms of the dielectric permeability e, a fact first pointed out by H. London (1940). It is remarkable that the condition v/l > to (v being the velocity of the conduction electrons), which ensures the absence of dispersion of the conductivity and the equality of the latter to its value a for a constant field, remains valid. It is of importance to note that a boundary condition of the form E* = £H t x n (67.6) t This name is usually given to the quantity A-n^jc, but we find that convention less satisfactory. X The mean free path depends considerably on the temperature of the metal. In practice, the temperatures considered are usually very low, in the helium range, and the phenomena under consideration occur in the range of very short radio waves. §67 The surface impedance of metals 281 still holds at such frequencies. The field inside the metal near the surface can again be regarded as a plane wave, although it is no longer described by the usual macroscopic Maxwell's equations. In such a wave the fields E and H must be linearly related, and the only possible linear relation between the axial vector H and the polar vector E is (67.6). The coefficient £. in this formula is the only quantity characterising the metal which must be known in order to find the external electromagnetic field. When the frequency increases further (usually into the infra-red region), the macroscopic description of the field again becomes possible, and € is again meaningful. The reason is that, on absorbing a quantum ha>, a conduc- tion electron acquires a large amount of energy, and its mean free path is therefore reduced, the inequality / <^ 8 being consequently again fulfilled. The impedance £ is again inversely proportional to \/e. f In this frequency range the real part of e(o>) is negative, and its imaginary part is small. The inequality / <^ 8 is the condition for both e' and e" to be macroscopically significant. The macroscopic significance of the large quantity e' alone, however, can be ensured by the fulfilment of the less stringent condition v/a> <^ 8, where v is the velocity of the conduction electrons in the metal. If this condition holds, the spatial inhomogeneity of the field may be neglected in considering the motion of the electrons. The inequality £' > is always satisfied by the real part of the imped- ance. If formula (67.2) holds, we can also draw certain conclusions concerning the sign of £". For example, if the dispersion of e is more important than that of fi (i.e. if /x. may be taken as real), the condition e" > gives £'£" < and, since £' > 0, £" < 0. This is the most usual case. If the dispersion of £ is determined by that of fi, however, a similar argument shows that £" > 0. The concept of impedance can also be applied to superconductors. A characteristic property of superconductors is that the penetration depth 8 is small even in the static case (ai = 0). At fairly low frequencies the magnetic field distribution can be taken to be the same as the static distribution. To determine the electric field we use the equation curl E = iaJH/c, taking the sr-axis along the outward normal to the surface of the superconductor. Neglecting the tangential derivatives in comparison with the large #-deriva- tives, we have dE x /dz = icuHy/c, and similarly for E y . Integrating with respect to z through the body gives o E z {0) = -j H y dz, t It should be borne in mind, however, that equation (67.6) can be used as a boundary condition only while |e| is large (i.e. £ is small), and certainly does not hold at optical fre- quencies. We assume that \t ~ 1, and so small £ correspond to large |e|. If fi^> 1, the inequality 8 <^ A must be fulfilled if the boundary condition (67.6) is valid, and therefore we must have \/(fie)^> 1, so that £ = V(m/ £ ) may not be small. 282 The Propagation of Electromagnetic Waves §67 E x (0) being the value of E x for z = 0, i.e. at the surface of the body. We quantitatively define the penetration depth by the relation o j H v dz = 8H y (0). (67.7) -co Then £^(0) = ico8Hy(0)/c. Comparing this with the boundary condition (67.6), we find that the impedance of a superconductor (in the frequency range considered, which in practice extends to about the centimetre wave- length region) is given by £ = - ico8/c. (67.8) This expression is the first term in an expansion of £(a>) in powers of the frequency, and the expansion for superconductors thus begins with a term in w. The next term, which is in co 2 and real, is the first term in the expansion of£'. The impedance £(<o), regarded as a function of the complex variable co, has many properties analogous to those of the function e(co) (V. L. Ginzburg, 1954). The boundary condition, which for a wave of a single frequency has the form (67.6), must in general be taken as the operator relation E t = tVL t X n, (67.9) expressing the value of E^ at any instant in terms of the values of H^ at all previous instants (cf. §58). As in §62, it therefore follows that the function £(a>) is regular in the upper half-plane of co, including the real axis except for the point w = 0. The condition that E* is real when H^ is real gives £(— co*) = t*{oo). Finally, since the energy dissipation is determined by the real part of £(o>) (and not by the imaginary part as for e(o>)), it follows that t,'(oi) is positive, and does not vanish for any real w except w = 0. Arguments similar to those given in §62 then lead to the conclusion that re 1(a)) > throughout the upper half-plane. Hence, in particular, £(a>) has no zeros in the upper half-plane. The regularity of £(co) in the upper half-plane again leads to Kramers and Kronig's formulae. A particularly important formula is 1 f°£'(*)-l £"(o>) = -~P \ ^-^ dx. •n J x — co —oo Using the fact that l'(x) is even, we can also write 1 ??(x)-l , 1 Fl'(x)-1 £"(o,) = --P \ -1^ dx + -P — — dx JT J X — CO TT J X + CO §67 The surface impedance of metals 283 or n«) = — p\ -f^ d *- ( 67 - 10 ) 77 J X* — CO* The term — 1 in the numerator of the integrand may be omitted, since the principal value of the integral of l/(x 2 — to 2 ) is zero. The above statements concerning the function £(<w) are, of course, equally applicable to the reciprocal function l/£(<o); the operator t," 1 converts E$ into HiXn. In particular, (67.10) becomes 2co Ftt-Hx)]' K-H«)]" = p\ \^ dx - ( 67 - n ) 77 J X* — OJ* For small £ this formula may be more useful than (67.10). In the form (67.11), however, it is not applicable to superconductors, for which £ _1 , according to (67.8), has a pole at w = 0. A simple modification in the derivation, analogous to that which changes (62.9) into (62.11), gives 77 J X* — CO* COO To conclude this section we shall discuss, as an example of the use of the impedance, the reflection of a plane electromagnetic wave incident from a vacuum on the plane surface of a metal with surface impedance £. If the vector E is polarised perpendicular to the plane of incidence, the boundary condition (67.6) gives E + E\ = £(//o — Hi) cos do = £(Eb — E{) cos do, the notation being the same as in §66. Hence, since £ is small, we have E\JEq = — (1 — 2£ cos do), and the reflection coefficient is R ± = 1 - 4£' cos do. (67.13) If, on the other hand, Eo lies in the plane of incidence, the boundary condition in the form £H$ = nxE ( gives Z(H + H{) = (Eo - £i) cos O = (#o - #i) cos Oi whence the reflection coefficient is R* cos 6q — £ (67.14) cos do + £ For angles of incidence not close to |77 R, = l-4£'sec0 o . (67.15) 284 The Propagation of Electromagnetic Waves §68 If, on the other hand, <f>o = \n — 6q <^ 1, then 4*-Z i?„ = (67.16) fo + t This expression takes a minimum value (|£| — £')/(|£| + £') for <f>Q = |£|. Except for the special case (67.16), the reflection coefficient for a surface with small £ is close to unity. A surface with £ -> is "perfectly conducting" and also "perfectly reflecting". The boundary condition at such a surface is simply E* = 0, similarly to that for the electrostatic field at the surface of a conductor. In a variable field, however, the fulfilment of this condition necessarily implies that of a certain condition on the magnetic field : the equa- tions icoH/c — curl E and E t — on the surface imply that H n = there. Thus the normal component of the magnetic field must be zero on a perfectly conducting surface in a variable electromagnetic field. In this respect such a surface resembles the surface of a superconductor in a constant magnetic field. PROBLEM Determine the intensity of thermal radiation (of a given frequency) from a plane surface of small impedance. Solution. According to Kirchhoff 's law, the intensity dl of thermal radiation into an element of solid angle do from an arbitrary surface is related to the intensity dlo of radiation from the surface of a black body by dl = (1 —R) dlo, where R is the reflection coefficient for natural light incident on the surface concerned. Calculating R = $(R X +R t ) from formulae (67.13) and (67.14) and using the isotropy of radiation from a black surface (d/o = Io do/In), we have in Hot' J (1 + cog2 tf , ^ 0+ £ /2+ ,,) , cos 6 sin 8 dO. cos 2 0+2£'cos0+£' 2 +r 2 ) Effecting the integration and omitting terms of higher order in £, we find In particular, for a metal whose impedance is given by formula (67.3) (n = 1), we have §68. The propagation of waves in an inhomogeneous medium Let us consider the propagation of electromagnetic waves in a medium which is electrically inhomogeneous but isotropic, f In Maxwell's equations curlE = iaiH/c, curlH = —iecoE/c (we put everywhere p = 1), € is a f For a discussion of wave propagation in an anisotropic medium in a constant magnetic field see Ya. L. Al'pert, V. L. Ginzburg and E. L. Feinberg, The Propagation of Radio Waves (Rasprostranenie radiovoln), Moscow and Leningrad, 1953. §68 The propagation of waves in an inhomogeneous medium 285 function of the co-ordinates. Substituting for H from the first equation in the second, we obtain for E the equation AE + ( € o)2/c2)E - grad divE = 0. (68.1) Elimination of E gives for H the equation AH + (e^2/ c 2)H + (l/ e ) grad e x curlH = 0. (68.2) These equations are considerably simplified in the "one-dimensional" case, where € varies only in one direction in space. We take this direction as the #-axis, and consider a wave whose direction of propagation lies in the xsr-plane. In such a wave all quantities are independent of y, and the uniformity of the medium in the x- direction means that the dependence on x can be taken as being through a factor e iKX , with k a constant. For k = the field depends only on z, i.e. we have a wave passing normally through a layer of matter in which e = e(z). If #c # 0, the wave is said to pass obliquely. For k^O two independent cases of polarisation must be distinguished. In one, the vector E is perpendicular to the plane of propagation of the wave (i.e. it is in the j-direction), and the magnetic field H accordingly lies in that plane. Equation (68. 1) becomes 8 2 E /ecu 2 \ a? + hr.-"*)*- a (68 - 3) In the other case, the field H is in the ^/-direction, and E lies in the plane of propagation. Here it is more convenient to start from equation (68.2), which gives 8 (\dH\ lufi k\ We shall call these two types of wave E waves and H waves respectively. The equations can be solved in a general form in the important case where the conditions of propagation approximate to those of geometrical optics. In what follows we shall assume that the function e(z) is real, j In equation (68.3) the quantity 2njy/f t where /(#).= ek 2 — k 2 , plays the part of a "wavelength" in the -^-direction. The approximation of geometrical optics corresponds to the inequality iv/ < '■ (68 - 5) t Equation (68.3) bears a formal resemblance to Schrodinger's equation for one-dimen- sional motion of a particle in quantum mechanics, and the approximation of geometrical optics corresponds to the quasi-classical case. Here we shall give the final results ; their derivation may be found in Quantum Mechanics, Chapter VII, Pergamon Press, London, 1958. 286 The Propagation of Electromagnetic Waves §68 and the two independent solutions of equation (68.3) are of the form constant e ±iHfte. (68.6) The condition (68.5) is certainly not fulfilled near any point where/ = 0. Let -3" = be such a point, with / > for z < and / < for z > 0. At sufficiently great distances on either side of z = 0, the solution of equation (68.3) is of the form (68.6), but to establish the relation between the coeffi- cients in the solutions for z > and z < it is necessary to examine the exact solution of equation (68.3) near z = 0. In the neighbourhood of this point, f{z) can be expanded as a power series in z : f = —ccz. The solution of the equation d 2 E/dz 2 — cczE = which is finite for all z is E = (^/a 1 /6)(D(a^), (68.7) where 1 °° <J>(!) = cos (^w 3 + ug) du s/tt J u is the Airy function ; we everywhere omit the factor e~ ia>t+iKX in E. The asymptotic form of the solution of equation (68.3) for large \z\ is E = — cos I ^/fdz + In) for z < 0, (68.8) E = ~~exp^- JVl/|d*) for*>0, with the same coefficient A as in (68.7). The first of these expressions represents the stationary wave obtained by superposing the wave incident in the positive ^-direction and the wave reflected from the plane z = 0. The amplitudes of these waves are both equal to \A\f l > i.e. the reflection coeffi- cient is unity. Only an exponentially damped field penetrates into the region z > 0. As the reflection point is approached, the wave amplitude increases, as is shown by the factor /* in the denominators in (68.8). To determine the field in the immediate vicinity of that point, the expression (68.7) must be used. This function decreases monotonically into the region z > and oscillates in the region z < 0, the successive maxima of |2?| continually decreasing. The first and highest maximum is reached at a*# = — 1 -02, and its value is E = 0-949 A<x~ 1/Q . §68 The propagation of waves in an inhomogeneous medium 287 So far we have spoken of solutions for E waves. It is easy to see that, in the approximation of geometrical optics, entirely similar formulae are valid for H waves. If we substitute in equation (68.4) H = u^/e, the derivatives of e appear as products with u, but not with u'; neglecting therefore the terms containing these derivatives, which are small by (68.5), we obtain for the function u(z) the equation d 2 tt /€(X) \ d*2 \ C 2 ; which is of the same form as (68.3). Hence the formulae for H differ from (68.6)-(68.8) only by a factor y/c. A curious difference in the behaviour of the two types of wave occurs when an obliquely incident wave (k =£ 0) is reflected from a layer in which e(z) passes through zero. The reflection takes place from the plane on which f(z) = ek 2 —K 2 = 0, i.e. the wave "does not reach" the plane where € = 0. The E wave penetrates beyond the latter plane only as an exponentially damped field. When an H wave is reflected, however, there is superposed on a similar damped field a strong local field near the plane on which e = (see Problem l).f PROBLEMS Problem 1. Determine the electric field near the point where e = when an obliquely (k # 0) incident H wave is reflected. Solution. Let e = at the point z = 0. Near this point, we write e = az, and equation (68.4) takes the form d 2 H ldH az* z az According to the general theory of linear differential equations, one of the solutions of this equation, which we call H\(z), has no singularity at z = 0, and its expansion in powers of z begins with z 2 : 1 1 Hi(z) = z 2 + -k% 4 - — ak 2 z5+ ... . o 15 The other independent solution has a logarithmic singularity, and its expansion is 2 2k 2 a mz) = Hi(z) logKZ+ — - -j^**+ - • The field H(z) is made up of these two solutions, and therefore tends to a constant Ho, say, as z ->■ 0. The leading terms in the electric field components are i 8H ik 2 Ho E x = - — — ££ — log kz, ek oz ak „ i 8H k „ kHq ek dx ek akz and become infinite as z -»■ 0. In reality, of course, the absorption which must be present in the medium, even though slight (i.e. the fact that the imaginary part of c is not exactly t It should be noted that this point is, a singularity of equation (68.4), and the approxi- mation of geometrical optics is therefore invalid near it, even though /(ar) does not vanish and the condition (68.5) may hold. 288 The Propagation of Electromagnetic Waves §69 zero), means that the field attains large but not infinite values compared with the weak field in the adjoining regions. Problem 2. A "surface" H wave can be propagated along a plane boundary between two media whose dielectric permeabilities ei and — |c2| are of opposite signs. The wave is damped in both media. Determine the relation between the frequency and the wave number. Solution. We take the boundary surface as the acy-plane, the wave being propagated in the ^-direction and the field H being in the y-direction. Let the half-space z > contain the medium with the positive permeability ei, and the half-space z < that with the nega- tive permeability £2. We seek the field in the wave damped as z ->■ ± oo in the form Hi = Hoe***-* 12 , «i = V(£ 2 -«J 2 ei/c 2 ) for z > 0, H 2 = Hoe ikx+K **, *2 = V^+^M/c 2 ) for z < 0, where k, k\ and *2 are real. The boundary condition that H y — H is continuous is already satisfied, and the continuity condition on E x gives (1/ej.) BHi/dz = (l/f2) BHz/dz for z = 0, or /ci/ei = K2/\ez\. This equation can be satisfied if ei < |e2| (and if ei€2< 0, as has been assumed). The relation between k and a> is k 2 = a> 2 ei|e2|/c 2 (|e2|— ei). It is easily seen that "surface" E waves cannot be propagated. §69. The reciprocity principle The emission of electromagnetic waves (of a single frequency) from a source consisting of a thin wire in an arbitrary medium is described by the equations curlE = icoB/c, curlH = — ioiDjc + 4rrj ex jc, (69.1) where j ex is the density of periodic currents flowing in the wire which are extraneous to the medium. Let two different sources (of the same frequency) be placed in the medium ; we denote by the suffixes 1 and 2 the fields due to these sources separately. The medium may be inhomogeneous and anisotropic. The only assumption which we shall make concerning the properties of the medium is that the linear relations Di = e^Ejc, Bi = [amHic hold, the tensors e$& and /x^ being symmetrical. Under these conditions it is possible to derive a relation between the fields of the two sources and the extraneous currents in them. We take the scalar products of the two equations curl Ei = i&Bi, curl Hi = — ikDi + 477Jex,i/c with H2 and E2 respectively, and of the corres- ponding equations for E2 and H2 with —Hi and — Ei. Adding all four together, we obtain (H2 • curl Ei — Ei • curl H2) + (E2 • curl Hi — Hi • curl E2) = (/a)/c)(Bi.H 2 - H1.B2) + (/aVc)(Ei.D 2 - Di-E 2 ) + + (4vr/c)(jex,l • E 2 - jex,2 • Ei). But Bi»H2 = iHkHiicH2i = Hi«B2, and Ei«D2 = Di-E2, so that the first two terms on the right-hand side are zero. The left-hand side can be trans- formed by a formula of vector analysis, and the result is div[Ei X H 2 - E 2 X Hi] = (47r/c)(j ex ,l-E2 - jex,2-Ei). We integrate this equation over all space ; the integral on the left-hand side can be transformed into one over an infinitely remote surface, and is zero. §69 The reciprocity principle 289 Thus we have J j ex ,i-E 2 dFi = Jjex,2-EidF 2 . (69.2) The integrals are taken only over the volumes of sources 1 and 2 respec- tively, since the currents j ex ,i and j ex ,2 are zero elsewhere. Since the wires are thin, the effect of each on the field of the other may be neglected, and therefore Ei and E 2 in formula (69.2) are the fields due to each of the two sources at the position of the other. Formula (69.2) is the required relation; it is called the reciprocity theorem. If the dimensions of the sources are small compared with the wavelength and with the distance between them, this formula can be simplified. The field of each source varies only slightly over the dimensions of the other, and in (69.2) we can take Ei and E 2 outside the integrals and replace them by Ei(2) and E 2 (l), 1 and 2 signifying the positions of the two sources: E 2 (l).Jj eX) idFi = E^.Jjex^dJ^. The integral J jex dV is just the time derivative of the total dipole moment &> of the source. Since & = —iioiP, we have finally E 2 (l).^»i = Ei(2).^ 2 . (69.3) This form of the reciprocity theorem applies, of course, only to dipole emission. If the dipole moment of the source is zero, or very small, the approximation made in going from the general formula (69.2) to (69.3) is inadequate; see Problem 1. PROBLEMS Problem 1. Derive the reciprocity theorem for quadrupole emitters and for magnetic dipole emitters. Solution. If /jex dV = 0, the next terms in the expansion must be taken in the integrals (69.2): f. dEn f ji'Ea dVi ^ — — xtju dFi J OXje J = 4\~a*~~ ~dx~) J ( x * u+x v 1 *) dVl+ l/dEti dE 2 k\ f we omit the suffix ex for brevity. The quadrupole moment tensor and the magnetic moment tensor are defined by t)iic = -iuiDik = J[3(xyfc+»fc/i)-2S iifc r.j] dV, = 1 f 2c J M = — rxj dV. 2c J Using the equation curl E = i<a B/c and assuming that e = constant near the sources (and so div E = 0), we obtain ji-E 2 dV - - — (— - + —^)Di,i k +iu>B2(l)>Jli. 12\ dxic oxi 1 290 The Propagation of Electromagnetic Waves §70 Hence we see that for quadrupole emitters the reciprocity theorem is \ dxk dxi ) ' \ Sxjc dxi ) and for magnetic dipole emitters B 2 (l)-^i = Bi(2).JT 2 . Problem 2. Determine the intensity of emission from a dipole source immersed in a homogeneous isotropic medium as a function of the permeabilities e and n of the medium. Solution. By substituting E = VW^E', H = H', a> = co'/V^m), equations (69.1) are brought to the form curl E' = ioiU'/c, curlH' = — ia>'E'/c+4-njexlc, which do not in- volve e or ft. The solution of these equations for dipole emission gives a vector field potential in the wave region f A' = (l/ci?o)Jjex dV, where Rq is the distance from the source; the phase factors are omitted, since they do not affect the calculation of the intensity. Hence we see that, for given j e x, we can put A' = Ao, where the suffix signifies the value for the source field in a vacuum. The values of H' and E' are H' = ik'xA' = i'V(€/t)kxAo = \/( c /*)Ho, E' = H'. Hence H = V(*/*)Ho, E = fiEo and I = 7o/x 3/2 e 1/2 . This is the required solution. §70. Electromagnetic oscillations in hollow resonators Let us consider the electric field in a hollow evacuated resonator with perfectly conducting walls. The equations of the field (of a single frequency) in the vacuum are curl E = icMjc, curlH = - icoE/c. (70.1) The boundary conditions on the surface of a perfect conductor (i.e. one whose impedance ■£ = 0) are E t =0, H n = 0. (70.2) To solve the problem, it suffices to consider either E or H. For instance, eliminating H from equations (70.1), we find that E satisfies the wave equation AE + (co2/ c 2)E = 0, (70.3) together with the equation divE = 0, (70.4) which does not follow from (70. 3). Solving these equations with the boundary condition E$ = 0, we find the field E, and then H can be derived from the first of (70. 1). The boundary condition H n = is automatically satisfied. When the shape and size of the cavity are given, equations (70.3) and (70.4) have solutions only for certain values of <o, called the eigenfrequencies of the electromagnetic oscillations of the resonator concerned. J For £ = t See The Classical Theory of Fields, §9-2. X The formulae for a resonator filled with a non-absorbing dielectric for which e and /* differ from unity are obtained from those for an evacuated resonator by replacing co, E and H by (i)V(eft), \/eE and \ZfiHL respectively. This is seen from the fact that the transformation just given converts equations (70.1) into the correct Maxwell's equations for the medium: curl E = ia)(iH./c, curl H = — iioeE/c. In particular, the presence of the medium reduces each eigenfrequency by a factor \/(e[i). §70 Electromagnetic oscillations in hollow resonators 291 the electromagnetic field does not penetrate into the metal, and no loss occurs there. All the characteristic oscillations are therefore undamped, and all the eigerifrequencies are real. The latter are infinite in number, and the order of magnitude of the lowest eigenfrequency coi is c/l, where / is the linear dimension of the cavity. This follows immediately from dimensional considerations, since / is the only dimensional parameter characterising the problem if the shape of the resonator is given. The high eigenfrequencies (<d > c/l) lie very close together, and the number of them per unit range of (o is V<t) 2 l2ir 2 c 3 , which depends on the volume V of the resonator but not on its shape, f The (time) average values of the electric and magnetic field energies in the resonator are respectively |J(|E|2/8w) dV and $ J(|H| 2 /8tt) dV. We shall show that they are equal. Using the first equation (70.1), we write JH.H* dV = (c 2 /a) 2 )JcurlE.curlE* dV. The second integral can be integrated by parts : f curl E- curl E*dF = j> curlE*-df x E + J E- curl curl E*dF. Since Et — on the boundary of the volume considered, the surface integral is zero, leaving J|H|2dF = —A E.curlcurlE*dF = - (r2 (<*/«») J" E-AE*dF or, by (70.3), J|H| 2 dF= f\E\*dV. (70.5) This completes the proof, t Undamped oscillations in a resonator are obtained if the impedance of its walls is assumed to be zero. Let us now ascertain the effect on the eigen- frequencies if the impedance of the walls is small but not zero. The (time) average energy dissipated in the walls of the resonator in unit time can be calculated as the flux of energy into the walls from the electro- magnetic field in the cavity. Using the boundary condition (67.6) on the surface of a body with impedance £, we write the normal component of the energy flux density as S n = (cjSrr) re (E t X H t *) = c£'|Hj| 2 /87r, where £' is the real part of £. In this expression, which already contains the small factor £', we can as a first approximation take H to be the field obtained t See The Classical Theory of Fields, §6-9. % By E and H we always mean the fields corresponding to a particular eigenfrequency. It is not difficult to show that the fields corresponding to two different eigenfrequencies % and ob are orthogonal: JE„- E 6 *dF= J"H„-H 6 *dr = 0. 292 The Propagation of Electromagnetic Waves §70 by solving the problem with £ = 0. The total energy dissipated is given by the integral ^riHM/, (70.6) taken over the internal surface of the resonator. The field amplitude is damped in time with a decrement obtained by dividing (70.6) by twice the total energy of the field, namely £ J*(|E|2+ |H|2) dF/877 = J|H|2 dV/S7r. The damping decrement is determined by the imaginary part |co"| of the complex .frequency co = co' + za/'.f Writing the formula in the complex form co — coo = — \ic—, — ; , (70.7) ¥ J|H|2dF V ' co and wo being the frequencies with and without allowance for £, we can determine not only the damping decrement but also the change in the eigen- frequencies themselves. The latter is seen to be determined by the imaginary part of £. We have mentioned in §67 that usually £" < 0, and the eigen- frequencies are then reduced. In actual calculations, it may be more convenient to transform the volume integral in the denominator of (70.7) into one over the surface. The result isj J|H| 2 dF = £^(|H| 2 - |E|2)r.df. (70.8) PROBLEMS Problem 1. Determine the eigenfrequencies of a cuboidal resonator with perfectly con- ducting walls. Solution. We take the axes of x, y, z along three concurrent edges of the cuboid; let the lengths of these edges be ax, as, «3- The solutions of equations (70.3) and (70.4) which satisfy the boundary condition Et = are Ex = A\ cos k x x sin ky y sin k z z . e~ imt (1) t In radio engineering the quality of the resonator, defined as the ratio a>72|a>"|, is generally used instead of the damping decrement. % Since the vector H is tangential to the surface, we have identically |(H.H*)(r.df) = |(H-H*)(r.df) -|(H-r)(H*.df) -|(H*.r)(H-df). The integrals on the right are transformed by putting df -*■ dFgrad, and using (70.1) we obtain |(H.H*)(r-df) = t*fr-(H x E* - H* x E) dV + J*H-H* dV. Similarly, using the identity r x (E x df) = E(r-df) — (r«E)df = (by the boundary condition E* = 0), we have |(E.E*)(r.df) = -f(E.E*)(r-df) + |(E.r)(E*.df) + ^(E*.r)(E.df) = ikjr-CH. x E* - H* x E) dV - JE-E* dV. Subtracting and using (70.5), we obtain formula (70.8). §71 The propagation of electromagnetic waves in waveguides 293 and similarly for E y , E z , where k x = nin/ai, k y — 11217/02, k z = 11311/03 (2) («i, «2, «3 being positive integers). The constants Ai, A2, A3 are related by Aikx+Azky+Azkz = 0, (3) and the eigenfrequencies are to 2 = c 2 (k x 2 -\-k y 2 +k z 2 ). The magnetic field is calculated from (1): Hz = —(icl<o)(A3k y —A2k z ) sin k x x cos k y y cos kzz-e'^ 1 , and similarly for fly, fl z . If two or all of the numbers n\, m, m are zero, E = 0. Hence the lowest frequency corres- ponds to an oscillation in which one of these numbers is and the other two are 1 . Since the relation (3) holds, the solution (1) (with given non-zero «i, 712, m) involves only two independent arbitrary constants, i.e. each eigenfrequency is doubly degenerate. The frequencies for which one of n\, nz, nz is zero are not degenerate. Problem 2. Determine the frequencies of electric dipole and magnetic dipole oscillations in a spherical resonator of radius a. Solution. In a stationary spherical electric dipole wave, the fields E and H are of the formf (ctri fey \ /Sin KY \ b), H = -ike- iu>t curl I bj, where b is a constant vector and k = tojc. The boundary condition nxE = at r = a gives cot ka — (ka^—ka. The smallest root of this equation is ka = 2-74. The frequency to = 2*74 cja is the lowest eigenfrequency of a spherical resonator. In a stationary spherical magnetic dipole wave, we have (c«ri fcy \ /sin ky \ b], H = e~ iM curl curl I bl. The boundary condition on E gives the equation tan ka = ka, whose smallest root is ka = 4-49. §71. The propagation of electromagnetic waves in waveguides A waveguide is a hollow pipet of infinite length, i.e. a cavity infinite in one direction, whereas the resonators discussed in §70 are of finite volume. The characteristic oscillations in a resonator are stationary waves, but those in a waveguide are "stationary" only in the transverse directions; waves travelling in the direction along the pipe can be propagated. Let us consider a straight waveguide of any (simply-connected) cross- section uniform along its length. We shall first suppose that the walls of the waveguide are perfectly conducting, and take the s'-axis along the waveguide. In a travelling wave propagated in the ^-direction, all quantities depend on z through a factor exp (ik z z)> with k z 3. constant. The electromagnetic waves possible in such a waveguide can be divided into two types: in one, H z = 0, and in the other E z = (Rayleigh, 1897). t See The Classical Theory of Fields, §9-6. X The formulae below hold for an evacuated waveguide. Those for a waveguide filled with a non-absorbing dielectric are obtained by means of the transformation given in the first footnote to §70. 294 The Propagation of Electromagnetic Waves §71 The former type, in which the magnetic field is purely transverse, are called electric-type waves or E waves. The latter, in which the electric field is purely transverse, are called magnetic-type waves or H waves, f Let us first consider E waves. The x and y components of equations (70. 1) give dE z a) 8E Z o> — ik z E y = i— H x , - — — + ik z E x = i—Hy, oy c ox c CO CO ik z H y = i — E x ikzH x = — i — E y . Hence c ik z 8E ik z 8E Z 77 17 &X — i ■"!/ — » K* ox k*, oy ico dE z ico 8E Z IT * TT ■ * (71.1) ck 2 8y ck 2 8x where k 2 = (co 2 /c 2 ) — k z 2 . Thus, in an E wave, all the transverse compo- nents of E and H can be expressed in terms of the longitudinal component of the electric field. This component must be determined by solving the wave equation, which takes the two-dimensional form A2E z + k 2 E z = (71.2) (A2 being the two-dimensional Laplacian). The boundary conditions for this equation are that the tangential components of E should vanish on the walls of the waveguide, and can be satisfied by putting E z = on the circumference of the cross-section. (71.3) According to formulae (71.1), the two-dimensional vector whose components are E x , E y is proportional to the two-dimensional gradient of E z . When the condition (71.3) holds, therefore, the tangential component of E in the xy-plane is also zero. Similarly, in an H wave the transverse components of E and H can be expressed in terms of the longitudinal component of the magnetic field : ik z 8H Z ik z 8H Z TT TT x 2 8x ' k 2 8y ' ico 8H Z ico 8H Z E x = — r~ — > Ey — — CK 8y ck 2 8x t These types are also known as TM (transverse-magnetic) and TE (transverse-electric) waves. §71 The propagation of electromagnetic waves in waveguides 295 The longitudinal field H z is given by the solution of the equation A2#* + * 2 H Z = (71.5) with the boundary condition 8H z /dn = on the circumference of the cross-section. (71.6) According to formulae (71.4), this condition ensures that the normal compo- nent of H is zero. Thus the problem of determining the electromagnetic field in a waveguide reduces to that of finding solutions of the two-dimensional wave equation A2/+/C 2 / = 0, with the boundary condition / = or df /dn = on the circumference of the cross-section. For a given cross-section, such solutions exist only for certain definite eigenvalues of the parameter k 2 . For each eigenvalue k 2 we have the relation a? = c 2 (k z 2 + k 2 ) (71.7) between the frequency w and the wave number k z of the wave. The velocity of propagation of the wave along the waveguide is given by the derivative do) ck z c 2 k z u z = = = — . (71.8) 8k z V(kz 2 + x 2 ) *> For given k, this varies from to c when k z varies from to 00. The (time) average energy flux density along the waveguide is given by the ^-component of the Poynting vector. A simple calculation, using formulae (71.1), gives for an E wave S z = -^re(E x H*% = -^4| g rad 2 £ 2 | 2 . 57T 8ttk4 The total energy flux q is obtained by integrating S z over the cross-section of the waveguide. We have BE J|grad 2 £ z |2d/= fa*-^dl- JE z *A2E z df. The first integral is taken along the circumference of the cross-section, and is zero on account of the boundary condition E z = 0. In the second integral we replace A2-Ez by —k 2 E z > and the result is q = -—\\E t \*df. (71.9) The expression obtained for an H wave is the same with H z instead of E z . The electromagnetic energy density W (per unit length of the waveguide) may be calculated similarly. It is simpler, however, to derive W directly from q, since we must have q = Wu z . From (71.8) and (71.9), therefore, w = T^n[\ E #*f- ( 7U °) 296 The Propagation of Electromagnetic Waves §71 It follows from (71.7) that, for each type of wave (for a given value of k 2 ) there is a minimum possible frequency, namely ck. At lower frequencies the propagation of waves of the type concerned is not possible. There is a smallest eigenvalue /cmin, which is not zero (see below). We therefore con- clude that there is a frequency eo m in = c/c m in below which no waves can be propagated along the waveguide. The order of magnitude of a>min is c/a, where a is the transverse dimension of the pipe. This statement is valid, however, only for waveguides in which the cross- section is simply connected (as we have hitherto assumed). When the cross-section is multiply connected,! tne situation is quite different. In such waveguides not only the E and H waves described above but also another type of wave, whose frequency is subject to no restriction, can be propa- gated. Such waves (called principal waves) are characterised by the fact that k z = k (i.e. k = 0); the velocity of propagation is equal to the velocity of light c. We shall derive the chief properties of such waves, and shall see why such waves cannot occur when the cross-section of the waveguide is simply connected. All the field components in a principal wave satisfy the two-dimensional Laplace's equation, A2/ = 0- With the boundary condition / = 0, the only solution of this equation regular throughout the cross-section (whether or not multiply connected) is / = 0. Hence we have E z = in a principal wave. With the boundary condition df/dn = 0, a regular solution is / = constant. It is easy to see, however, that when / is H z the constant must be zero (by a "constant", of course, we mean a quantity independent of x and y, and depending on z and t through the factor exp (ik z z — iwt)). For, integrating the equation 8H X 8H V ioi divH = — - + — - + —H z = ox cy c over the cross-section, we obtain §H n dl+(icoJc) \H Z d/ = 0; since H n = on the circumference of the cross-section and H z is constant over its area, it follows that H z = 0. Thus a principal wave is purely transverse. For E z = H z = 0, the x and y components of equations (70. 1) give H x = — E y , H y = E x , (71.11) i.e. the fields E and H are perpendicular and equal in magnitude. They are determined by the equations 8E Z 8E y 8E y dE x divE = — + — - = 0, (curl E) z = — -- — ? = 0, dx dy ox cy with the boundary condition E< = 0. t For example, the space between two pipes one inside the other, or the space outside two parallel pipes. §71 The propagation of electromagnetic waves in waveguides 297 We see that the dependence of E, and therefore of H, on x and y is given by the solution of a two-dimensional electrostatic problem : E = — grad2 <f>, where the potential <f> satisfies the equation A2<£ = with the boundary condition <f> = constant. In a simply-connected region, this boundary con- dition means that <f> = constant (and so E = 0) is the only solution regular throughout the region. This shows that waves of this type cannot be propa- gated along a waveguide whose cross-section is simply connected. In a multiply-connected region, on the other hand, the constant in the boundary condition need not be the same on the various separate parts of the boundary, and so Laplace's equation has solutions which are not trivial. The electric- field distribution over the cross-section of the waveguide is the same as the two-dimensional electrostatic field between the plates of a condenser at a given potential difference. So far we have assumed the walls of the waveguide to be perfectly con- ducting, f If the walls have a small but finite impedance, losses occur and the wave is therefore damped as it is propagated along the waveguide. The damping coefficient can be calculated in the same way as for the damping in time of electromagnetic oscillations in a resonator (§70). The amount of energy dissipated in unit time per unit length of the walls of the waveguide is given by the integral (c/87r)£'<j>|H| 2 d/, taken along the circumference of the cross-section ; H is the magnetic field calculated on the assumption that £ = 0. Dividing this expression by twice the energy flux q along the waveguide, we obtain the required damping coefficient a. With this definition, a gives the rate of damping of the wave amplitude, which decreases along the waveguide as e~ az . Expressing all quantities in terms of E z or H z by means of formulae (71.1) or (71.4), we obtain the following formulae for the absorption coeffi- cients : for an E wave 2K*k z c t\E t \*6f ( ' ' and for an H wave a = auT Pw ' ( • 3) In an actual calculation it may be convenient to transform the surface integ- rals in the denominators into integrals along the circumference. The neces- sary formulae, whose derivation is similar to that of (70.8), are JWd/= ^(n.r)|grad 2 ^|2d/, JWd/= — j>(n.r){ K *\H z \2 - | gra d 2 # z |2}a7. (71.14) f In particular, this assumption is necessary for a rigorous separation of waves with Ez = and those with H z = 0. 298 The Propagation of Electromagnetic Waves §71 When k z -> 0, i.e. the frequency to ->ck, the expressions (71.12) and (71.13) become infinite, but they are then no longer applicable, because their derivation presupposes that k is small compared with k z . Formulae (71.12) and (71.13) are not valid for a principal wave (in a waveguide with a multiply-connected cross-section), in which E z , H z and k are all zero. In this case all the field components can be expressed in terms of the scalar potential <f>. Using the fact that the fields H and E = — grad2<£ in a principal wave are perpendicular and equal in magni- tude, we obtain the absorption coefficient g'flgradaflSd/ a = ; ; . 1/1. 15) 2J|grad 2 ^|2d/ The propagation of a principal wave along a waveguide can be relatively simply discussed when its absorption coefficient is not small (so that formula (71.15) is inapplicable) but the wavelength c/a> is large compared with the transverse dimension of the waveguide. As has been mentioned, the transverse electric field in a principal wave at any instant corresponds to the electrostatic field in a condenser formed by the walls of the waveguide carrying equal and opposite charges. Let these charges be ± e(z) per unit length. They are related to the currents ±J{z) flowing on the walls by the "equation of continuity" de/dt = — dj/dz, or, for a field of a single frequency, icoe = djjdz. Next, let C be the capacity per unit length of the waveguide. The "potential difference" <f>2~<f>i be- tween its walls is efC; differentiating this with respect to z, we obtain the e.m.f. which maintains the current on the walls. (When absorption is present, the field is not purely transverse.) Equating the e.m.f. to ZJ, where Z is the impedance per unit length, we have d dz (i) - *> or dz (Vi) +i " ZJ = °- (7L16) Substituting Z = R-ia)L/c 2 , where R and L are the resistance and self- inductance per unit length of the waveguide, we can return from the single- frequency current components to currents which are arbitrary functions of time. Assuming the capacity C to be constant along the waveguide, we arrive at the telegrapher's equation : 1 d*J BJ L d*J -L _ R.± ± = 0. (71.17) C dz* 8t c 2 dt* §72 The scattering of electromagnetic waves by small particles 299 If there is no resistance (R — 0), this equation reduces, as it should, to the wave equation with a velocity of wave propagation -\/(c 2 /LC) = c.\ PROBLEMS Problem 1 . Find the values of k for waves propagated in a waveguide whose cross-section is a rectangle of sides a and b. Find the damping coefficients. Solution. In E waves J E z = constant X sin kxx sin k y y, where k x = mir/a, k y = nzirjb, with mi and «2 positive integers. In H waves H z = constant X cos kxx cos k y y, and one of «i and M2 may be zero. In both types of wave k 2 = k x 2 +k y 2 = 7r 2 (m 2 /a 2 +«2 2 /6 2 ). The smallest value of k corresponds to an Hio wave (the suffixes show the values of «i and 712) and is K mln = -n\a (we assume that a > b). The damping coefficients are calculated from formulae (71.12) and (71.13) and are: for E waves a = 2£'co(k x 2 b+ky 2 a)lcic 2 kzab, for Hn x o waves * = —(a+—b), ck z ab \ k 2 /' and for H ni n 2 waves (m, m *£ 0) 2ckH'[ , k z 2 a = (okzob [«+6+ _±<fe? a +V*)]. Problem 2. The same as Problem 1, but for a waveguide whose cross-section is a circle of radius a. Solution. Solving the wave equation in polar co-ordinates r, <}>, we have for E waves E s = constant Xj„(/cr)^n^ with the condition J n {ta) = 0, which gives the value of k. In H waves the value of H t is given by the same formula, but k is determined by the conditioning fa) = 0. The smallest value of k occurs for the Hi wave, and is « mIn = 1 -84/a. The damping coefficient is calculated from formulae (71.12)-(71.14). For E waves it is a = to^'/cakz, and for H waves cX,' K T n 2 a> 2 1 tok z a L c 2 K 2 (a 2 K 2 —n 2 )l §72. The scattering of electromagnetic waves by small particles Let us consider the scattering of electromagnetic waves by macroscopic particles whose dimensions are small compared with the wavelength A ~ c/a> of the wave undergoing scattering (Rayleigh, 1871). When this condition holds, the electromagnetic field near the particle may be supposed uniform. Being in a uniform field periodic in time, each particle acquires definite electric and magnetic moments &> and M., whose dependence on time is given by factors of the form e _fw *. The scattered wave can be described as being the result of emission by these variable moments. At distances R from t The equation LC — 1 follows from the mathematical equivalence of the problems of determining 1/C and L for a given cross-section. The electric and magnetic fields between perfectly conducting surfaces are perpendicular and equal in magnitude (see (71.11)), and if this magnitude is given on the surfaces the charge density and the current density are respectively determined. Hence the coefficients of proportionality (1/C and L) between the field energy and the squared charge and current respectively are the same. X We everywhere omit the factor exp(ik z z — teat). 300 The Propagation of Electromagnetic Waves §72 the particle which are large compared with A (the wave region), the fields in the scattered wave are given byf H' = — {n x^ + n x (M x n)}, c*R l (72.1) E' = H'xn, where the unit vector n gives the direction of scattering, and the values of & and M at the time t-R/c must be taken. We denote the fields in the scattered wave by primed letters and those in the incident wave by unprimed letters. The (time) average intensity of radiation scattered into a solid angle do is d/ = |c|H'|2R 2 do/47r; dividing by the energy flux density in the incident wave c|H| 2 /8tt = c|E| 2 /87r, we obtain the effective scattering cross- section. The calculation of &> and Jl is particularly simple if the dimensions of the particle are small in comparison not only with A but also with the "wave- length" S corresponding to the frequency to in the material of the particle. In this case we can calculate the polarisability of the particle from the formulae for an external uniform static field, the only difference being, of course, that the values taken for e and /z. are those corresponding to the given frequency to, and not the static values. If, as usually happens, /a is close to unity, the magnetic dipole term in formula (72. 1) may be omitted. For a spherical particle of volume V we have (see (8.9)) ^ = FaE, a = 3(c - l)/4«(« + 2), (72.2) and the effective scattering cross-section is do- = (a>/cy\<x.\W 2 sin 2 6 do, (72.3) where is the angle between the scattering direction n and the direction of the electric field E in the linearly polarised incident wave. The total effective cross-section is a = 87r|a| 2 co4F 2 /3c4. (72.4) The frequency dependence of the effective cross-section is determined by the factor to 4 and by the polarisability. At frequencies so low that a shows no dispersion, the scattering is proportional to to 4 . It may be noted also that the effective cross-section is proportional to the square of the volume of the particle. If the incident wave is unpolarised (natural light) then the differential effective cross-section must be obtained by averaging (72.3) over all direc- tions of the vector E in a plane perpendicular to the direction of propagation of the incident wave (i.e. perpendicular to its wave vector k). Denoting by & t See The Classical Theory of Fields, §9-12. §72 The scattering of electromagnetic waves by small particles 301 and <f> the polar angle and the azimuth of the direction of n relative to k (<f> being measured from the plane of k and E), we have cos 6 = sin & cos <f> (Fig. 31), so that da = (co/c) 4 |a| 2 r 2 (l - sin 2 & cos 2 <f>) do. (72.5) On averaging over (f>, we obtain the following formula for the effective cross- section for scattering of an unpolarised wave : f do- = l(w/c)*\<x.\ 2 V 2 (l + cos 2 «•) do, (72.6) where & is the angle between the directions of incidence and scattering. A *-H Fig. 31 From formula (72.5) we can easily find the degree of depolarisation of the scattered light. To do so, we notice that, for a given direction of E, E' lies in the plane of E and n. The direction of the electric field E' in the scattered wave therefore lies in the plane of k and n (the plane of scattering) or perpen- dicular to that plane, according as the azimuth <f> of the vector E, measured from the plane of k and n, is or £n\ Let 7, and I x be the intensities of scattered radiation having these two polarisations. The degree of depolari- sation is defined as the ratio of the smaller to the larger of these quantities. By (72.5) we have IJI ± = cos 2 &. If the scattering particle has a large dielectric permeability, 8 ~ c/aVH < A. (72.7) The dimensions of the particle may then be small compared with A but not small compared with 8. In the first approximation with respect to 1/e, the electric moment of the particle may be calculated as simply the moment of a conductor (e -> oo) in a uniform constant external field. In calculating the magnetic moment, however, the induced currents in the particle are of t For future reference we may note the formula sin 2 8 — i(l + cos 2 £). 302 The Propagation of Electromagnetic Waves §72 importance, and the problem cannot be taken as static; instead, we must seek a solution of equation (63.2) (with fx = 1) : AH + € W 2H/c2 = (72.8) which becomes the field of the incident wave far from the particle. The magnetic and electric moments are of the same order of magnitude, and both terms in formula (72.1) must be retained. The angular distribution and amount of scattering are different from those discussed above (see Problem 2). PROBLEMS Problem 1. Linearly polarised light is scattered by randomly oriented small particles whose electric polarisability tensor has three different principal values. Determine the depolarisation coefficient for the scattered light. Solution. Neglecting, as above, the magnetic moment, we have from (72.1) E' = (to 2 /c 2 i?)(n x 0>) x n. The required depolarisation coefficient is given by the ratio of the principal values of the two-dimensional tensor I a g = E' a E'p*, where the bar denotes an averaging over orienta- tions of the scattering particle for a given direction of scattering n, and the suffixes a and P take two values in the plane perpendicular to n. f It is more convenient, however, to aver- age the three-dimensional tensor tPi&'k* and then project it on the plane perpendicular to n; these components of the tensor SP^k* are proportional to the corresponding compo- nents 7 a p. Substituting 0>i = cttkEik, we have W»* = «UXicm*EiEm*. In effecting the averaging we use the formula attain,* = A8ik8im+B(8ii8}em+ SirnSkl)' This is the most general tensor of rank four which is symmetrical in i, k and /, m and contains only scalar constants. These constants are determined from two equations obtained by contracting the tensor, firstly with respect to i, k and /, m, secondly with respect to i, / and k, m. They are A = 2 ' ai<|2 i ~ |gi * 12 = l{|« 1 |«+|a a |»+|«,|«+4rc(aia«*+ai«a*+ai«,*)}, B = 3 l a ^-1 a **l 2 = ^{|ai|2+|a 2 |2+|a3| 2 -re( ai a2* + aia 3 * + a 2 a3*)}, where ai, 0C2, a3 are the principal values of the tensor aj». In a linearly polarised wave, the field amplitude E<*> (we omit the time factor e -<0> <) can always be defined so as to be real. Then we have fe * = (A+B)EiE k +B8i k E*. (1) Let the 2-axis be in the direction of n, and the »sr-plane contain the directions of n and E; these axes are the principal axes of the tensor 7 a p. Taking the appropriate components of the tensor (1), we find the depolarisation coefficient I v /I x = Bj[(A+B) sin 2 6+B], where is the angle between E and n. Problem 2. Determine the effective cross-section for scattering by a sphere of radius a, for which e is large; it is assumed that A^> a~S. t See The Classical Theory of Fields, §6-7. §73 The absorption of electromagnetic waves by small particles 303 Solution. The problem of calculating the magnetic moment acquired by a sphere with given e (and n — 1) in a variable magnetic field H is the same as that solved in §45, Problem 1, except that k in the formulae derived there must be replaced by co-y/e/c. Thus M = —a 3 yH., where */< 3 3 \ Y = 2\ 1+ ka COtka --w)' The electric moment can be calculated, in the first approximation with respect to 1/e, as simply the moment of a conducting (e -> co) sphere in a uniform constant electric field: 0» = a 3 E. Taking into account the fact that E and H are perpendicular, we have after a simple calculation, using (72.1), the following formula for the effective scattering cross-section: da = (a 6 <o 4 /c 4 ){|y| 2 cos 2 ^+sin 2 <£-(y+y*) cos S-+cos 2 &(cos 2 <f>+\y\ 2 sin 2 <f>)} do, where <f> and •& are the angles shown in Fig. 31. In scattering of unpolarised light we have da = (a 6 a)4/c4){i[l + |y|2][l+ CO s 2 *]-(y+y*) cos &} do, and the degree of depolarisation of the scattered light is IJI X = |(y— cos ft)/(l — y cos &)| 2 . The total scattering cross-section is a = 8wa 6 o> 4 (l + |y| a )/3c*. In the limit ka -> co (i.e. when A ^> a ^> 8) we have y — \, corresponding to scattering by a perfectly reflecting sphere into which neither the electric nor the magnetic field penetrates. §73. The absorption of electromagnetic waves by small particles The scattering of electromagnetic waves by particles is accompanied by absorption. The effective absorption cross-section is given by the ratio of the mean energy Q dissipated in a particle per unit time to the incident energy flux density. To calculate Q we can use the formula Q = -&>.&-Ji-h, (73.1) where &> and M are the total electric and magnetic moments of the particle, and the external fields © and ^ are replaced by the fields E and H in the scattered wave; cf. (45.21). Using the complex representation of quantities, we can write (see the penultimate footnote to §45) Q = - * re(^.E* + ^f .ft*) = faV(ae" + *m")\E\*, where a 6 and ocm are the electric and magnetic polarisabilities of the particle. Dividing by the incident energy flux, we obtain a = 4™F(or e " + *m")lc. (73.2) Let us apply this formula to absorption by a sphere of radius a <^ A, assuming it non-magnetic (p = 1). The nature of the absorption depends considerably on the magnitude of the dielectric permeability. If c is small, then we have both a <^ A and a <^ S. In this case the magnetic polarisability may be neglected in comparison with the electric polarisability. With the latter given by (72.2), we have a = 127rcoa^"/c[(e' + 2)2 + ( e ")2]. (73.3) If, on the other hand, JeJ > 1, the electric part of the absorption becomes small, and the magnetic absorption may be important even if we still have 304 The Propagation of Electromagnetic Waves §74 8 > a. When this last condition holds (i.e. \ka\ <^ 1), the magnetic polarisability is ccm = (&z) 2 /407r = a 2 to 2 e/4(kTC 2 and the effective absorption cross-section is 1277coa 3 e' (7 = 7 1 o> 2 a 2 \ b + 9^)- (73 - 4) When e increases further, the electric part of the absorption becomes small compared with the magnetic part. In the limit S <^ a (i.e. \ka\ > 1, cotka -> — i) we have ccm = 9i/87rka = 9«V£/877o>a, where £ = l/\/ € is the surface impedance of the sphere. Hence a = 67ra2£". (73.5) It may be noticed that this formula could have been obtained more directly, without using the general expression for the magnetic polarisability a TO (o>) of the sphere. When £ is small, the energy dissipation Q can be calculated by "integrating" the mean Poynting vector (67.4) over the surface of the sphere, the distribution of the magnetic field over the surface being given by the solution (42.3) of the problem of a superconducting (£ = 0) sphere in a uniform magnetic field. Knowing the effective absorption cross-section of the sphere, we can immediately determine the intensity of the thermal radiation emitted from the sphere. According to KirchhofTs law, f the intensity 6.1 in a frequency range do> is given in terms of a(w) by d/ = 47rCG(a))eo((o) du>, where eo((t)) = #<o 3 /47r 3 c 3 [exp (hto/T)— 1] is the spectral density of black-body radiation per unit volume and unit solid angle. §74. Diffraction by a wedge The ordinary approximate theory of diffraction^ is based on the assump- tion that the deviations from geometrical optics are small. It is thereby assumed, firstly, that all dimensions are large compared with the wavelength; this applies both to dimensions of bodies (screens) or apertures and to distances of bodies from the points of emission and observation of the light. Secondly, only small angles of diffraction are considered, i.e. the distri- bution of light is examined only in directions close to the edge of the geo- metrical shadow. Under these conditions, the actual optical properties of the substances involved are of no importance ; all that matters is that they are opaque. If these conditions are not fulfilled, the solution of the diffraction problem requires an exact solution of the wave equation, taking into account the appropriate boundary conditions on the surfaces of the bodies, which depend on their properties. The finding of such solutions offers exceptional mathe- matical difficulties, and has been effected for only a small number of prob- lems. A simplifying assumption is usually made concerning the properties t See Statistical Physics, §60, Pergamon Press, London, 1958. J See The Classical Theory of Fields, §§7-7 to 7-9. §74 Diffraction by a wedge 305 of the body at which the diffraction occurs, namely that it is perfectly con- ducting, and therefore perfectly reflecting. The following remark may be made here. It might seem reasonable to solve the diffraction problem on the assumption that the surface of the body is "black", i.e. completely absorbs light incident on it. In reality, however, such an assumption concerning the body in stating the exact problem of diffraction would involve a contradiction. The reason is that, if the sub- stance of the body is strongly absorbing, the coefficient of reflection is not small but, on the contrary, almost unity (see §67)). Hence a reflection coefficient close to zero implies a weakly absorbing substance and a thickness of the body which is large compared with the wavelength. In the exact theory of diffraction, parts of the surface of the body at a distance from its edge of the order of the wavelength are necessarily of importance ; but the thickness of the body near its edge is always small, so that the assumption that it is "black" is certainly untenable. Considerable theoretical interest attaches to the exact solution (first obtained by A. Sommerfeld, 1894) of the problem of diffraction at the edge of a perfectly conducting wedge bounded by two intersecting semi-infinite planes. A complete exposition of the very complex mathematical theory, which involves the use of special devices, is beyond the scope of this book. Here we shall give, for reference, the final results, f We take the edge of the wedge as the sr-axis in a system of cylindrical co-ordinates r, <f>, z. The front surface (OA in Fig. 32) corresponds to Fig. 32 f A detailed account of the calculations is given by A. Sommerfeld, Optics, Academic Press, New York, 1954; P. Frank and R. von Mises, Differential and Integral Equations in Physics (Differential- und Integralgleichungen der Physik), part 2, Chapter XX, 2nd ed., Vieweg, Brunswick, 1935. Another method of solution, due to M. I. Kontorovich and N. N. Lebedev, is given by G. A. Grinberg, Selected Problems in the Mathematical Theory of Electric and Magnetic Phenomena (Izbrannye voprosy matematicheskol teorii elektricheskikh i magnitnykh yavlenvC), Chapter XXII, Moscow, 1948. A modified solution for diffraction of a cylindrical wave emitted by a line source parallel to the edge of the wedge has been given by H. S. Carslaw, Proceedings of the London Mathe- matical Society 30, 121, 1899. 306 The Propagation of Electromagnetic Waves §74 tj> = 0, and the rear surface (OB) to (f> = y, where 2ir—y is the angle of the wedge, the region outside it being < <f> < y. Let a plane wave of a single frequency and unit amplitude be incident in the r^-plane on the front surface at an angle ^o to the surface; by symmetry, it is sufficient to consider angles <£o < iy. We shall distinguish two independent modes of polarisation of the incident wave, and therefore of the diffracted wave also : the edge of the wedge (the #-axis) may be parallel to either E or H. The letter u will denote E z and H z respectively. The electromagnetic field is then given in all space by the formula (the time factor e~* wi being everywhere omitted) u{r, <f>) = v(r, <f>-<f>o)+ v(r, j> + <&>), (74.1) where the upper and lower signs correspond to the polarisations with E and H respectively in the ^-direction, and the function v(r, if/) is given by the complex integral 1 r d£ v(r,ili\ = — e-*frrcos£ (74.2) where k = cojc. The path of integration C in the £-plane consists of the two loops Ci and C% shown in Fig. 33. The ends of these loops are at infinity Fig. 33 in parts of the £-plane (shaded in Fig. 33) where im cos £ < 0, and so the factor e-**rcos£ tends to zero at infinity. The integrand in (74.2) has poles on the real £-axis at the points £ = -ifi + 2ny, where n is any integer. The integration may be taken along a path D = D1+D2 (Fig. 33) instead of C, adding to the integral the residues of the integrand at the poles, if any, in the range — it ^ £ ^ it. We write v as v(r,+) = vo(r,if J ) + v d (r,M, (74.3) where v& is the integral (74.2) taken along the path D, and vq is the contri- bution from the residues at these poles. Each pole gives rise to a term exp [ — ikr cos (ip — 2ny)] in £>o, which represents either the incident wave or §74 Diffraction by a wedge 307 one of the waves reflected from the surface of the wedge in accordance with the laws of geometrical optics. The function v& represents the diffractive distortion of the wave. The field at distances from the edge of the wedge large compared with the wavelength is of the greatest interest. When kr > 1, the asymptotic formula f 7T sin(7r 2 /y) timA jv v * r > *> = //o u^ +M < 2;/ / n\ ( 74 ' 4) y^(2irkr) COS (7r 2 /y) - COS (Triply) holds, provided that the angle «/r satisfies the condition [cos {rfljy) - cos (77^/y)]2 > 1/kr. (74.5) The dependence on r of the function va, and therefore of the field u d (r, <f>) = v d (r,<f>-<f>o) + v d (r,<f)+(f)o), is given by a factor eMr/<y/r, i.e. this field resembles a cylindrical wave emitted by the edge of the wedge. In the form given above, (74. l)-(74. 5) are valid for any angles y and fo. The more detailed discussion of these formulae will be effected on the assumption (for definiteness) that the angles <f>o and y are so related (y > 7r+(f>o) that, in geometrical optics, two boundaries are formed: the boundary Ob of the complete shadow (region III in Fig. 32), and the boun- dary Oa of the "shadow" of the wave reflected from the surface OA.% In regions I, II, III the function uo(r, <f>) = vo(r, <f> — <f>o) + vo(r, <f> + (f)o) has the following forms : Region I : hq = e~ ikr cos ^ ~ $o> + e~ ikr cos ^ + ^o), Region II: u = e - ikrco * &-*<>), ) ( 74 - 6 ) Region III: wo = 0. These expressions, which do not vanish as kr -> oo, describe the incident (region II) or incident and reflected (region I) waves, undistorted by dif- fraction. The diffractive distortion of the field is given by formula (74.4), but the condition (74.5) ceases to hold when «/r approaches tt and the dif- ference \ift — 7r\ is no longer large compared with \j^/(kr). The values <f> + <f>o = tt correspond to the geometrical boundaries of the shadow ; for <f> — <f>o = tt we have the boundary of the complete shadow, and for <j> + (f>Q = tt that of the shadow of the reflected wave. In the immediate neighbourhood of these values a different asymptotic expression must be used, which is valid if the inequality \rp — Tr\ <^ 1 holds. This condition, t The next terms in this asymptotic expansion have been given by W. Pauli, Physical Review 54, 924, 1938. % In Fig. 32, <f>o < \tt. If <£o > \t, the boundary Oa lies to the right of the direction of the incident wave. If y < 7T + <f>o, there is no region of complete shadow, and reflection (single or multiple) takes place from both sides of the wedge. 308 The Propagation of Electromagnetic Waves §75 together with kr > 1, ensures the validity of the usual approximate theory of Fresnel diffraction, f Accordingly we have near the boundary Ob of the complete shadow the asymptotic expression w i -i r V W V(2w)J ( 74 - 7 ) —oo w = - ((f> - (f> - ir)^Qkr). Similarly, near the boundary Oa of the "shadow" of the reflected wave w 1 -i r u(r, <f>) = e~ ikr cos W ~ $o> + e~ ikr cos ^ + 0o> e ir > 2 diy, — oo (74.8) V) = - (<f> + <f>o - ■n-)-V / (P0- In this approximation the diffraction pattern is independent of the angle of the wedge and of the direction of polarisation of the wave. The ranges of applicability of formulae (74.4) and (74.7), (74.8) partly overlap. For example, near the boundary of the complete shadow the com- mon range of applicability is given by i>\<f>-<h-ir\> i/V(H and in this range u{r,<f>) = u (r,cf>) + _-J_««*r + *r>_! , (74.9) yylTTkr) <f> — <po — tt with «o given by (74.6). This expression can be obtained from (74.7) by using the asymptotic formulae for the Fresnel integral with large |«j| : w f e^dr) = (1 + i)V(br) + e iu ?l2iw for to > 0, —00 w f e^dt] = e iw *!2iw for tv < 0. §75. Diffraction by a plane screen The exact formula (74.2) for diffraction by a wedge can be brought to a comparatively simple form in the particular case of diffraction by a half- t See The Classical Theory of Fields, §7-8. §75 Diffraction by a plane screen 309 plane (y = 2tt).\ The complex integral in (74.2) can be reduced to a Fresnel integral : v(r,tfi) = e -«fcrcos^ + iw) ^ 2 dry, V' 7r J — oo (75.1) zv = y/{lkr) COS |^r. This formula holds for any values of r and ip. For kr > 1 and angles |^t — it\ > lj\/(kr) the asymptotic expression tto(r, 0) = - ««*+* > \ — (75.2) 2 y \2jnkr) cos f^ (formula (74.4) with y = 2tt) holds.J Using formula (75.2), the solution of the problem of diffraction by a plane perfectly conducting screen of any shape can be obtained in closed form. The only assumptions are that the dimensions of the screen and the distance from it are large compared with the wavelength, and that the angles of diffraction are moderately large (this region overlaps the region of small angles in which the ordinary Fresnel-diffraction formulae are valid). The result is in the form of an integral along the edge of the screen, analogously to the expression of the diffraction field, in the ordinary approximate theory, || as an integral over a surface spanning the aperture in a screen. We shall not pause to give the calculations here. In the exact theory of diffraction by plane perfectly conducting screens, there is a theorem (due to L. I. Mandel'shtam and M. A. Leontovich) in some ways analogous to Babinet's theorem in the approximate theory. Let us consider a plane screen with an aperture of any shape, and take the plane of the screen as z = 0. Let an electromagnetic wave be incident from the side z < 0, and let Eo, Ho be the total fields in the incident wave and the wave which would be reflected from the screen if there were no aperture. We assume the field continued beyond the screen (z > 0). Since H z = 0, Ef = for z = (by the boundary conditions at a perfectly conducting surface), the values of Eo and Ho f or z > and z < are related by Eoz{x, y, z) = E 0z (x, y, - z), Eo*(*, y, z) = - Eo ( (x, y, - *), H 0z (x, y,z)= - H 0z (x, y, - z), Hot(*, y, z) = Ho*(* , y, - z). Next, let E' and H' be the fields which would occur if a flat plate corres- ponding to the aperture in size, shape and position, and having infinite f See the references quoted in the second footnote to §74. X Yu. V. Vandakurov (Zhurnal Sksperimental'noi i teoreticheskoi fiziki 26, 3, 1954) has obtained the exact solution of the three-dimensional problem of the diffraction by a half- plane of electromagnetic waves emitted from an arbitrarily oriented electric or magnetic dipole at a finite distance from the edge of the half-plane. || See The Classical Theory of Fields, §7-7. 310 The Propagation of Electromagnetic Waves §75 magnetic permeability, were placed in the field Eo, Ho. Then the solution of the diffraction problem for the aperture in the screen is given by E = i(Eo+E'), H = KHo + H') for * < 0, E = i(E - E'), H = |(Ho - H') for z > 0. K To show this, we notice that the fields E', H' have the same symmetry (expressed by formulae (75.3)) as the fields E , Ho. They therefore satisfy on the plane z = the conditions E' t = 0, H'z = outside the aperture, E'a = - E'j 2 , H' z i = - H' Z 2 on the aperture, the suffixes 1 and 2 corresponding to z -> ± . They also satisfy the further conditions E' z = 0, H't — on the aperture, since the boundary conditions on the surface of a body with [a = oo are obtained from those for a perfectly conducting body (e = oo) by inter- changing E and H. Hence it is clear that the fields (75.4) satisfy the necessary conditions E t = 0, H z = on the surface of the screen (z -> — ) outside the aperture, and are continuous on the aperture. Finally, since E', H' tend to Eo, Ho at infinity, the fields (75.4) tend to E , H as z -> -oo and to zero as z -» + oo. They therefore satisfy all the conditions of the problem. This proves the theorem. Thus the problem of diffraction by an aperture in a screen with e = oo is equivalent to a problem of diffraction by a complementary screen with /x = oo. PROBLEMS Problem 1. A plane wave of a single frequency is incident normally on a slit cut in a perfectly conducting screen, the width la of the slit being large compared with the wave- length. Determine the distribution of light intensity beyond the slit, at large distances from it and for large angles of diffraction. Solution. For a > A, the diffraction field beyond the slit can be regarded as a super- position of fields arising from independent diffraction at each of the two edges of the slit and determined by means of the asymptotic formula (75.2). When the distances AP = n and BP = n from the edges of the slit to the point of observation (Fig. 34) are large com- pared with a, we can put, in the factors e ikr i and e ikr *, r\ = r—a sin x, ^2 = r+a sin x, and elsewhere r\ = r% S r; the angles between the s-axis and AP, OP, BP can all be taken as the angle of diffraction x- The result is gHkr+in) t s [ n (& a s j n x ) cos (ka sin x) \ ~ V(2nkr)\ sin^x ~ cos ix > Hence the intensity of light diffracted into an angle dx is (relative to the total intensity of light incident on the slit) 1 ( [" sin (ka sin x) l 2 [ cos (ka sin x) I 2 ] d _ 47r£aU sinix J L cos ix J' _ feqfr sin(feasinx) -| 2 1 J d ~ Al kasinx J C ° SX+ [2*acosix] 2 l * §75 Diffraction by a plane screen 311 For small x this expression becomes the formula for Fraunhofer diffraction by the slit: d/ = 1 sin 2 kax ■nka y 2 d* Problem 2. A plane wave is incident on a perfectly conducting plane with a circular aperture whose radius a is small compared with the wavelength. Determine the intensity of diffracted light passing through the aperture (Rayleigh, 1897). Solution. As stated above, this problem is equivalent to that of diffraction by a circular disc with ft = co, and, since a <^ A, we have the case of scattering by a small particle. According to §72, in order to solve the latter problem it is necessary to determine the static electric and magnetic polarisabilities of the disc. The field Eo is perpendicular to the plane of the disc, and the boundary condition E' z = is formally identical with the condition in electrostatics at the boundary of a body with e = 0. The field Ho is parallel to the disc, and the boundary condition H't = corresponds to a magnetostatic problem with n = co. Hence the electric and magnetic moments of the disc are (see §4, Problem 4, and §42, Prob- lem) & — — 2a 3 Eo/37r, M = 4a 3 Ho/37r. In going to the problem of diffraction by an aper- ture we must, in accordance with formulae (75.4), divide these expressions by 2 and then substitute them in the scattering formula (72.1). Thus the intensity of radiation diffracted into a solid angle do is t d/ = 4tt 9tt 2 c 4 c to 4 a 6 {nXEo— 2nX(H Xn)} do {(n x Eo) 2 +4(n x H ) 2 +4n-H x Eo} do. 4ir 9n 2 c* The total diffracted intensity is obtained by integration over a hemisphere, and is c 4a> 4 a 6 4w 27ttc 4 The "effective diffraction cross-section" may be defined as the ratio of the intensity of dif- fracted radiation to the energy flux density in the incident wave cE 2 \4tt (letters without suffixes refer to the incident wave). Two modes of polarisation of the incident wave may be distinguished: (a) the vector E in the incident wave is perpendicular to the plane of incidence (the xz- plane), i.e. it is parallel to the plane of the screen (the ay-plane). The sum of the fields in the incident and reflected waves at the surface of the screen is Eo = 0, Hox = 2H cos a = 2E cos a t The factor e-" * is omitted; E and H are real. 21 312 The Propagation of Electromagnetic Waves §75 (a being the angle of incidence). Hence 16a 6 a> 4 da = cos 2 a (1 —sin 2 & cos 2 4>) do, 97Hc 4 where & is the angle between the direction of diffraction n and the normal to the screen (the z-axis), and <f> is the azimuth of the vector n with respect to the plane of incidence. The total cross-section is a = (64w 4 a 6 /277rc 4 ) cos 2 a. (b) the vector E lies in the plane of incidence. Then JEb = Eoz = — IE sin a, = Hoy = 2H — 2E. The differential effective cross-section is 16a 6 w 4 da = cos 2 &+sin 2 & (cos 2 ^+1 sin 2 a)— sin & sin a cos ^} do, 9?Hc 4 and the total cross-section is a = (64w 4 a 6 /277rc 4 )(l +i sin 2 a). For natural incident light a = (64a> 4 a 6 /27irc 4 )(l — | sin 2 a). CHAPTER XI ELECTROMAGNETIC WAVES IN ANISOTROPIC MEDIA §76. The dielectric permeability of crystals The properties of an anisotropic medium with respect to electromagnetic waves are denned by the tensors e^(w) and fiik(<*>), which give the relation between the inductions and the fields :f Di = €u{<o)Ek t Bi = ]ii]c{o>)H]c. In what follows we shall, for definiteness, consider the electric field and the tensor e^; all the results obtained are valid for the tensor fine also. As to -> 0, the em tend to their static values, which have been shown in §13 to be symmetrical with respect to i and k. The proof was thermo- dynamical, and therefore holds only for states of thermodynamic equili- brium. In a variable field, a substance is of course not in equilibrium, and the proof in §13 is consequently invalid. To ascertain the properties of the tensor e^ we must use the generalised principle of the symmetry of the kinetic coefficients. It is easy to see that the components of the tensor e^ come under the general definition of the quantities <x a & :J the rate of change of the energy in a variable electric field is given by the integral / 1 dD -E.-dF. (76.!) A comparison with SP (124.7) shows that, if the components of the vector E at each point are taken as the quantities x a , the corresponding quantities f a will be the components of D. (The suffix a takes a continuous series of values, denumerating both the components of the vectors and the points in the body.) The coefficients a a & are then the components of the tensor e -1 ^. The symmetry properties of e ik are, of course, identical with those of its inverse. It should be noted that the components of the polarisability tensor for the whole body, i.e. the coefficients in the equations ^ = V<x.ij&ic, also come under the general definition. For the rate of change of the energy of a body placed in a variable external field © is -^.d(£/d*. (76.2) t It should be recalled that these quantities refer to the variable fields in the wave; the possible presence of a constant induction (in a pyroelectric or ferromagnetic crystal) is irrelevant to this discussion. t See Statistical Physics, §124, Pergamon Press, London, 1958. Formulae in this book will be referred to by means of the prefix SP. 313 314 Electromagnetic Waves in Anisotropic Media §76 Hence we see that, if the x a are the three components of the vector ^, then the corresponding^ are those of the vector (£, so that the coefficients a a & are in this case Va.^. Thus we can use the generalised principle of the symmetry of the kinetic coefficients (SP (124.13)) to deduce that the tensor e^ is symmetrical: Uk = m- (76.3) Here it is assumed that the body is not in an external magnetic field, f Repeating for the anisotropic case the derivation of formula (61.4), we find that the electric losses are given by io) -(**** - m)EiE k *. (76.4) The condition that absorption is absent is e^* = e^ = e^, i.e. the e^ must be real, as in an isotropic medium. When absorption is absent, the internal electromagnetic energy per unit volume can be defined as shown in §61. The formula for an anisotropic medium corresponding to (61.9) is V = __(*>€«.)£«♦£*. (76.5) l07r dco In §67 we used the surface impedance £, in terms of which the boundary conditions at the surface of a metal can be formulated even if the dielectric permeability is no longer meaningful. At the surface of an anisotropic body the boundary condition corresponding to (67.6) is E a = UH x n)„ (76.6) where £, a p(a>) is a two-dimensional tensor on the surface of the body. It should be borne in mind that the value of this tensor depends, in general, on the crystallographic direction of the surface concerned. The energy flux into the body is (c/4tt)ExH«ii = (c/47r)E«Hxn = (c/47r)i? a (Hxn) a . (Here E and H are real.) Hence we see that if, in applying the principle of the symmetry of the kinetic coefficients, we take the components E a as the x a , then the corresponding f a will be — (Hxn) a , i.e. f a will be -(i/w)(Hxn) a (returning to the complex form). The coeffi- cients a.ab are therefore the same, apart from a factor, as the components £ a/? , and we conclude that U = U (76.7) in the absence of an external magnetic field. t The properties of the tensor eoc in the presence of an external magnetic field will be discussed in §82. §77 A plane wave in an anisotropic medium 315 PROBLEM Express the components of the tensor £ a p m terms of those of i? a 3 — e_1 ap> assuming that the latter exists and that the body is non-magnetic (mk = Sik)- Solution. In an anisotropic medium, the equation £ 2 = 1/e (67.2) becomes £ a y£yp = y^. In components this gives f £ll 2 +£l2£21 = 1711. £22 2 +£l2£21 = ^22, £l2(£ll+£22) = 1712, £2l(£l +£22) = 1?21. The solution of these equations is £l2 = 1712/1, £21 = W£> £11 = [1711 ± VCmviM— wm)]/^ £22 = [•>?22±'v / ( l ?ii l ?22— yiW2i)]l£, i 2 = 1711 + >?22± 2 \/( '71122 — '?12'?2l). The choice of signs is determined by the condition that the absorption of energy must be positive. §77. A plane wave in an anisotropic medium In studying the optics of anisotropic bodies (crystals) we shall take only the most important case, where the medium may be supposed non-magnetic and transparent in a given range of frequencies. Accordingly, the relation between the electric and magnetic fields and inductions is D t = e«E to B = H. (77.1) The components of the dielectric tensor e^ are all real, and its principal values are positive. Maxwell's equations for the field of a wave of a single frequency w are icoH. = c curlE, icoD = - c curlH. (77.2) In a plane wave propagated in a transparent medium all quantities are pro- portional to e ik ' r , with a real wave vector k. Effecting the differentiation with respect to the co-ordinates, we obtain coH/c - k x E, coD/c = - k x H. (77.3) Hence we see, first of all, that the three vectors k, D, H are mutually perpendicular. Moreover, H is perpendicular to E, and so the three vectors D, E, k, being all perpendicular to H, must be coplanar. Fig. 35 shows the relative position of all these vectors. With respect to the direction of the wave vector D and H are transverse, but E is not. The diagram shows also the direction of the energy flux S in the wave. It is given by the vector product ExH, i.e. it is perpendicular to both E and H. The direction of S is not the same as that of k, unlike what happens for an isotropic medium. t We do not assume £12 = £21, and thereby allow for the presence of an external magnetic field. 316 Electromagnetic Waves in Anisotropic Media §77 Clearly the vector S is coplanar with E, D and k, and the angle between S and k is equal to that between E and D. We can define a vector n by k = conic. (77 A) The magnitude of this vector in an anisotropic medium depends on its direction, whereas in an isotropic medium n = \/e depends only on the frequency. f Using (77.4), we can write the fundamental formulae (77.3) as H=nxE, D = - n x H. (77.5) £ O Fig. 35 The energy flux vector in a plane wave is S = cEx H/4tt = (c/47r){£ 2 n - (E.n)E}; (77.6) in this formula E and H are real. So far we have not used the relation (77. 1) which involves the constants e ik characterising the material. This relation, together with equations (77.5), determines the function w(k). Substituting the first equation (77.5) in the second, we have D = n X (E x n) = n 2 E - (n.E)n. (77.7) If we equate the components of this vector to e^is* in accordance with (77.1), we obtain three linear homogeneous equations for the three components of E: n 2 Ei-n(n]cE]c = €«£* or (n 2 8ijc - mnjc - € ik )E k = 0. (77.8) The compatibility condition for these equations is that the determinant of their coefficients should vanish: \n 2 8ik - ninic — c{*| = 0. (77.9) In practice, this determinant is conveniently evaluated by taking as the axes of x, y, z the principal axes of the tensor c^ (called the principal di- electric axes). Let the principal values of the tensor be e (a;) , e { y\ e (z) . f The magnitude n is still called the refractive index, although it no longer bears the same simple relation to the law of refraction as in isotropic bodies. §77 A plane wave in an anisotropic medium 317 Then a simple calculation gives n\<&n£ + c^V + € ( 2 ) Wz 2) _ [n x ^x)^y + € te)) + + n y ^y\eW + e<*>) + w z 2 e (z)( e ^) + €<y>)] + e te) e (J/) € fe) = 0. (77.10) The sixth-order terms cancel when the determinant is expanded; this is, of course, no accident and is due ultimately to the fact that the wave has two, not three, independent directions of polarisation. Equation (77.10), called Fresnel's equation, is one of the fundamental equations of crystal optics. It determines implicitly the dispersion relation, i.e. the frequency as a function of the wave vector. (It should be recalled that the principal values e W) are functions of frequency, and so are, in some cases (see §79), the directions of the principal axes of the tensor €*#.) For waves of a single frequency, however, to, and therefore all the € (<) , are usually given constants, and equation (77.10) then gives the magnitude of the wave vector as a function of its direction. When the direction of n is given, (77.10) is a quadratic equation, for w 2 , with real coefficients. Hence two dif- ferent magnitudes of the wave vector correspond, in general, to each direc- tion of n. Equation (77.10) (with constant coefficients c w) ) defines in the co-ordinates n x > n y , n z the "wave-vector surface", f In general this is a surface of the fourth order, whose properties will be discussed in detail in the following sections. Here we shall mention some general properties of this surface. We first introduce another quantity characterising the propagation of light in an anisotropic medium. The direction of the light rays (in geometrical optics) is given by the group velocity vector dw/dk. In an isotropic medium, the direction of this vector is always the same as that of the wave vector, but in an anisotropic medium the two do not in general coincide. The rays may be characterised by a vector s, whose direction is that of the group velocity, while its magnitude is given by n-s = 1. (77.11) We shall call s the ray vector. Its significance is as follows. Let us consider a beam of rays (of a single frequency) propagated in all directions from some point. The value of the eikonal (which is, apart from a factor to/c, the wave phase ; see §65) at any point is given by the integral Jn*dl taken along the ray. Using the vector s which determines the direc- tion of the ray, we can put if/ = Jn»dl = J(n«s/*) d/ = J" dlfs. In a homo- geneous medium, s is constant along the ray, so that ip = LJs, where L is the length of the ray segment concerned. Hence we see that, if a segment equal (or proportional) to s is taken along each ray from the centre, the resulting surface is such that the phase of the rays is the same at every point. This is called the ray surface. t A much less convenient concept called the "surface of normals" or "surface of indices" has often been used; it is obtained by taking a point at a distance \\n (instead of n) in each direction. 318 Electromagnetic Waves in Anisotropic Media §77 The wave-vector surface and the ray surface are in a certain dual relation- ship. Let the equation of the wave- vector surface be written f{k Xi k y , k z , o>) = 0. Then the components of the group velocity vector are do) dfjdki = - -^-— , (77.12) dki df/dco i.e. they are proportional to the derivatives dfjdki, or, what is the same thing (since the derivatives are taken for constant w), to the derivatives df/dni. The components of the ray vector, therefore, are also proportional to df\dn%.\ But the vector df/dn is normal to the surface / = 0. Thus we conclude that the direction of the ray vector of a wave with given n is that of the normal at the corresponding point of the wave- vector surface. It is easy to see that the reverse is also true : the normal to the ray surface gives the direction of the corresponding wave vectors. For the equation s«Sn = 0, where Sn is an arbitrary infinitesimal change in n (for given a>), i.e. the vector of an infinitesimal displacement on the surface, expresses the fact that s is perpendicular to the wave-vector surface. Differentiating (again for given co) the equation n«s = 1, we obtain n«Ss + s«Sn = 0, and therefore n«Ss = 0, which proves the above statement. This relation between the surfaces of n and s can be made more precise. Let no be the radius vector of a point on the wave-vector surface, and so the corresponding ray vector. The equation (in co-ordinates n x , %, n z ) of the tangent plane at this point is so'( n_n o) = 0, which states that so is perpendicular to any vector n — no in the plane. Since so and no are related by so* no = 1, we can write the equation as s -n = 1. (77.13) Hence it follows that l/j is the length of the perpendicular from the origin to the tangent plane to the wave- vector surface at the point no. Conversely, the length of the perpendicular from the origin to the tangent plane to the ray surface at a point so is l/«o- To ascertain the location of the ray vector relative to the field vectors in the wave, we notice that the group velocity is always in the same direction as the (time) average energy flux vector. For let us consider a wave packet, occupying a small region of space. When the packet moves, the energy concentrated in it must evidently move with it, and the direction of the f Differentiating the left-hand side of equation (77.10) with respect to m and determining from the condition n«s = 1 the proportionality coefficient between Si and df/dm, we obtain the following relations between the components of s and n: e (s)( € (j/) _j_ e (z)) _ 2e(*> Ws 2 — (e<*> + e (y) )Wj/ 2 — (e ( *> + e (z) )w 2 2 Sx = Hx 2e<*> e <!/> e <z) _ nx 2 € (s)( € (y) + e (z>) _ % 2 e (2/)( e (s) + € (z)) _ Mi 2 € ( Z )( € (z) + 6 <v))' (77.12a) and similarly for s v , s z . §77 A plane wave in an anisotropic medium 319 energy flux is therefore the same as the direction of the velocity of the packet, i.e. the group velocity, f Since the Poynting vector is perpendicular to H and E, the same is true of s: sH = 0, s-E = 0. (77.14) A direct calculation, using formulae (77.5), (77.11) and (77.14), gives H = s x D, E=-sxH. (77.15) For example, sxH = sx(nxE) = n(s«E)-E(n«s) = -E. If we compare formulae (77.15) and (77.5), we see that they differ by the interchange of E and D, n and s, e ik and e -1 ^ (77.16) (the relation n«s = 1 remaining valid, of course). The last of these pairs must be included in order that the relation (77. 1) between D and E should remain valid. Thus the following useful rule may be formulated: an equation valid for one set of quantities can be converted into one valid for another set by means of the interchanges (77.16). In particular, the application of this rule to (77.10) gives immediately an analogous equation for s : _ L% 2( e (y) + e (z)) + % 2( e te) + e (z)) + Sz 2( € (x) + e (2/))] +1 = 0. (77.17) This equation gives the form of the ray surface. Like the wave- vector sur- face, it is of the fourth order. When the direction of s is given, (77.17) is a quadratic equation for s 2 , which in general has two different real roots. Thus two rays with different wave vectors can be propagated in any direc- tion in the crystal. Let us now consider the polarisation of waves propagated in an aniso- tropic medium. Equations (77.8), from which Fresnel's equation has been derived, are unsuitable for this, because they involve the field E, whereas it is the induction D which is transverse (to the given n) in the wave. In order to take account immediately of the fact that D is transverse, we use for the time being a new co-ordinate system with one axis in the direction f It is easy to demonstrate mathematically that the group velocity is in the same direction" as the Poynting vector. Differentiating formulae (77.5) (for given co), we obtain SD = SH x n + H x Sn, SH = n x SE + Sn x E. We take the scalar product of the first equation with E and of the second with H, obtaining E-SD = H-SH + ExH-Sn, H-SH = D-SE + ExH-Sn. But D« SE = HkEichEi = E-SD, and so, adding the two equations, we have E X H* Sn = 0, i.e. the vector E X H is normal to the wave-vector surface. This is the required result. The result thus obtained relates to the instantaneous, as well as to the average, energy flux. In this proof, however, the symmetry of the tensor ejfc is vital. The result is therefore not valid in the above form for media in which eat is not symmetrical (gyrotropic media, §82). The statement is still valid, however, for the average value of the Poynting vector. 320 Electromagnetic Waves in Anisotropic Media §77 of the wave vector, and denote the two transverse axes by Greek suffixes, which take the values 1 and 2. The transverse components of equation (77.7) give D x = n 2 E a ; substituting E a = e-^D^, where e~\ fi is a component of the tensor inverse to e^, we have D a — n 2 e- 1 afi Dp = 0, or (^- € -i a ^ = 0. (77.18) The condition for the two equations (a = 1, 2) in the two unknowns Z)i, Z>2 to be compatible is that their determinant should be zero. This condi- tion is, of course, the same as FresnePs equation, which was written in the original co-ordinates x, y, z. We now see also, however, that the vectors D corresponding to the two values of n are along the principal axes of the sym- metrical two-dimensional tensor of rank two e -1 ay? . According to general theorems it follows that these two vectors are perpendicular. Thus, in the two waves with the wave vector in the same direction, the electric induction vectors are linearly polarised in two perpendicular planes. Equations (77.18) have a simple geometrical interpretation. Let us draw the tensor ellipsoid corresponding the tensor e -1 ^, returning to the principal dielectric axes, i.e. the surface X 1/ 2 ***«*- -JS + -& + -0-1- < 77 - 19 ) (Fig. 36). Let this ellipsoid be cut by a plane through its centre perpendicular to the given direction of n. The section is in general an ellipse ; the lengths of its axes determine the values of n, and their directions determine the directions of the oscillations, i.e. the vectors D. Fig. 36 From this construction (with, in general, e te) , c^, e^ different) we see at once, in particular, that, if the wave vector is in (say) the ^-direction, the directions of polarisation (D) will be the y and z directions. If the vector n lies in one of the co-ordinate planes, e.g. the ary-plane, one of the directions of polarisation is also in that plane, and the other is in the ^-direction. The polarisations of two waves with the ray vector in the same direction have entirely similar properties. Instead of the directions of the induction §78 Optical properties of uniaxial crystals 321 D, we must now consider those of the vector E, which is transverse to s, and equations (77. 1 8) are replaced by the analogous equations (^-^)^ = 0. (77.20) The geometrical construction is here based on the tensor ellipsoid mXiX k = e<*>* 2 + e<yy + e®Z 2 = 1, (77.21) corresponding to the tensor cm itself (called the Fresnel ellipsoid). It should be emphasised that plane waves propagated in an anisotropic medium are completely linearly polarised in certain planes. In this respect the optical properties of anisotropic media are very different from those of isotropic media. A plane wave propagated in an isotropic medium is in general elliptically polarised, and is linearly polarised only in particular cases. This important difference arises because the case of complete isotropy of the medium is in a sense one of degeneracy, in which a single wave vector corresponds to two directions of polarisation, whereas in an anisotropic media there are in general two different wave vectors (in the same direction). The two linearly polarised waves propagated with the same value of n combine to form one elliptically polarised wave. §78. Optical properties of uniaxial crystals The optical properties of a crystal depend primarily on the symmetry of its dielectric tensor e^. In this respect all crystals fall under three types: cubic, uniaxial and biaxial (see §13). In a crystal of the cubic system Hk = eSflb, i.e. the three principal values of the tensor are equal, and the directions of the principal axes are arbitrary. As regards their optical proper- ties, therefore, cubic crystals are no different from isotropic bodies. The uniaxial crystals include those of the rhombohedral, tetragonal and hexagonal systems. Here one of the principal axes of the tensor e^ coincides with the axis of symmetry of the third, fourth or sixth order respectively ; in optics, this axis is called the optical axis of the crystal, and in what follows we shall take it as the ^-axis, denoting the corresponding principal value of *ik by €,,. The directions of the other two principal axes, in a plane per- pendicular to the optical axis, are arbitrary, and the corresponding principal values, which we denote by e ± , are equal. If in Fresnel's equation (77.10) we put € te) = e ( i/> = e ± , e (2 > = e„, the left-hand side is a product of two quadratic factors : (w 2 - e ± )[ € ^n z 2 + e ± (n x 2 + V) ~ fi«i] = °- In other words, the quartic equation gives the two quadratic equations n 2 = e ±i (78.1) nl + n l± n l=i 322 Electromagnetic Waves in Anisotropic Media §78 Geometrically, this signifies that the wave- vector surface, which is in general of the fourth order, becomes two separate surfaces, a sphere and an ellipsoid. Fig. 37 shows a cross-section of these surfaces. Two cases are possible: if € x > e„, the sphere lies outside the ellipsoid, but if e x < e„ it lies inside. In the first case we speak of a negative uniaxial crystal, and in the second case of a positive one. The two surfaces touch at opposite poles on the n z - axis. The direction of the optical axis therefore corresponds to only one value of the wave vector. Fig. 37 The ray surface is exactly similar in form. By the rule (77.16), its equation is obtained from (78.1) and (78.2) by replacing n by s and e by 1/e: s* = l/ ej , (78.3) ^ 2 + e„(% 2 + % 2 ) = 1. (78.4) In a positive crystal the ellipsoid lies within the sphere, and in a negative one outside. Thus we see that two types of wave can be propagated in a uniaxial crystal. With respect to one type, called ordinary waves, the crystal behaves like an isotropic body of refractive index n = V € _l- The magnitude of the wave vector is wn/c whatever its direction, and the direction of the ray vector is that of n. In waves of the second type, called extraordinary waves, the magnitude of the wave vector depends on the angle 6 which it makes with the optical axis. By (78.2) 1 sin 2 cos 2 - = + • (78.5) n* e € ± The ray vector in an extraordinary wave is not in the same direction as the wave vector, but is coplanar with that vector and the optical axis, their com- mon plane being called the principal section for the given n. Let this be the zx-phne; the ratio of the derivatives of the left-hand side of (78.2) with respect to n z and n x gives the direction of the ray vector: s x \s z = ejix/e^ng. Thus the angle 8' between the ray vector and the optical axis and the angle 6 satisfy the simple relation tan0' = (€ x /e„)tan0. (78.6) §78 Optical properties of uniaxial crystals 323 The directions of n and 1 are the same only for waves propagated along or perpendicular to the optical axis. The problem of the directions of polarisation of the ordinary and extra- ordinary waves is very easily solved. It is sufficient to observe that the four vectors E, D, s and n are always coplanar. In the extraordinary wave s and n are not in the same direction, but lie in the same principal section. This wave is therefore polarised so that the vectors E and D lie in the same princi- pal section as s and n. The vectors D in the ordinary and extraordinary waves with the same direction of n (or E, with the same direction of s) are perpendicular. Hence the polarisation of the ordinary wave is such that E and D lie in a plane perpendicular to the principal section. An exception is formed by waves propagated in the direction of the optical axis. In this direction there is no difference between the ordinary and the extraordinary wave, and so their polarisations combine to give a wave which is, in general, elliptically polarised. The refraction of a plane wave incident on the surface of a crystal is dif- ferent from refraction at a boundary between two isotropic media. The laws of refraction and reflection are again obtained from the continuity of the component n^ of the wave vector which is tangential to the plane of separa- tion. The wave vectors of the refracted and reflected waves therefore lie in the plane of incidence. In a crystal, however, two different refracted waves are formed, a phenomenon known as double refraction. They correspond to the two possible values of the normal component n n which satisfy FresnePs equation for a given tangential component n^. It should also be remembered that the observed direction of propagation of the rays is determined not by the wave vector but by the ray vector s, whose direction is different from that of n and in general does not lie in the plane of incidence. In a uniaxial crystal, ordinary and extraordinary refracted waves are formed. The ordinary wave is entirely analogous to the refracted wave in isotropic bodies; in particular, its ray vector (which is in the same direction as its wave vector) lies in the plane of incidence. The ray vector of the extraordinary wave in general does not lie in the plane of incidence. PROBLEMS Problem 1 . Find the direction of the extraordinary ray when ligjit incident from a vacuum is incident on a surface of a uniaxial crystal which is perpendicular to its optical axis. Solution. In this case the refracted ray lies in the plane of incidence, which we take as the xsr-plane, with the s-axis normal to the surface. The ^-component of the wave vector n x = sin ft (ft being the angle of incidence) is continuous ; the component n z for the refracted wave is found from (78.2): ** = A /(ejL--^sin2^. The direction of the refracted ray is given by (78.6): Cx n x V e x sin ft tan ft' e, n 2 V[ e «( e « — sin 2 ft)] where ft' is the angle of refraction. 324 Electromagnetic Waves in Anisotropic Media §79 Problem 2. Find the direction of the extraordinary ray when light is incident normally on a surface of a uniaxial crystal at any angle to the optical axis. Solution. The refracted ray lies in the ars-plane, which passes through the normal to the surface (the #-axis) and the optical axis. Let a be the angle between these axes. The ray vector s, whose components are proportional to the derivatives of the left-hand side of equation (78.2) with respect to the corresponding components of n, is proportional to where 1 is a unit vector in the direction of the optical axis. In the present case the wave vector n is in the ^-direction, so that sin" 5 a cos" a s e 1 . Hence we find s x ( e i~ e x) sin 2a tan $' Sz € i + c x+( e i~~ e x) cos 2a §79. Biaxial crystals In biaxial crystals the three principal values of the tensor e^ are all dif- ferent. The crystals of the triclinic, monoclinic and rhombic systems are of this type. In those of the triclinic system, the position of the principal di- electric axes is unrelated to any specific crystallographic direction; in particular, it varies with frequency, as do all the components e^. In crystals of the monoclinic system, one of the principal dielectric axes is crystallo- graphically fixed ; it coincides with the second- order axis of symmetry, or is perpendicular to the plane of symmetry. The position of the other two principal axes depends on the frequency. Finally, in crystals of the rhombic system, the position of all three principal axes is fixed: they must coincide with the three mutually perpendicular second-order axes of symmetry. The study of the optical properties of biaxial crystals involves the con- sideration of Fresnel's equation (77.10) in its general form. We shall assume for definiteness that ete) < e (y) < €<*>. (79.1) To ascertain the form of the fourth-order surface defined by equation (77.10), let us begin by finding its intersections with the co-ordinate planes. Putting in equation (77.10) n z = 0, we find that the left-hand side is the product of two factors : ( W 2 _ € te))( e te) Wa .2 + € (y) ny 2 _ € (x) e (2/)) = 0. Hence we see that the section by the xy-plane consists of the circle «2 = € te) (79.2) and the ellipse n<p w« 2 — + — = 1, (79.3) € (y) € te) ' v ' §79 Biaxial crystals 325 and by the assumption (79.1) the ellipse lies inside the circle. Similarly we find that the sections by the yz and xz planes are also composed of an ellipse and a circle ; in the js-plane the ellipse lies outside the circle, and in the xs-plane they intersect. Thus the wave-vector surface intersects itself, and is as shown in Fig. 38, where one octant is drawn. Fig. 38 This surface has four singular points of self-intersection, one in each quadrant of the xs-plane. The singular points of a surface whose equation is /far, %> n z ) = are given by the vanishing of all three first derivatives of the function/. Differentiating the left-hand side of (77.10), we obtain the equations n x [&\&> + e (2) ) - e (a % 2 - (e^Wa; 2 + €<2% 2 + e^n^)] = 0, % [ € W( € (*> + € <z>) - e (J/) W 2 _ ( € U) Wa .2 + € (y) ny 2 + € (z) nz 2fl = (), L (79.4) w 2 [ e (z)( e te) + &)) _ e (%2 _ ( € (x) nx 2 + € (y) % 2 + € fe) Wz 2)] = 0; the equation (77.10) itself must, of course, be satisfied also. Since we know that the required directions of n lie in the #*-plane, we put % = 0, and the two remaining equations give immediately f n x 2 = € (z)( e (y) _ € te)) € (z) _ € (x) ' «z 2 = e te)( e (z) _ € <i/)) € (z) _ € (x) ' (79.5) The directions of these vectors n are inclined to the 0-axis at an angle /? such that i € (z)( € (y) _ e te)\ * - ± J ^ M J - (79-6) n x = + tani n z e te)( € (z> _ e (y)) t It is easy to see that the solution thus found is the only real solution of equations (79.4). If none of n x , n y , n t is zero, the three equations (79.4) are inconsistent: they then involve only two unknowns, namely rfi and e^n* 2 + ^n y 2 + e(^n z 2 . Un x or n z is zero the solutions are imaginary. 326 Electromagnetic Waves in Anisotropic Media §79 This formula determines lines in two directions in the tf.s'-plane, each of which passes through two opposite singular points and is at an angle j8 to the sr-axis. These lines are called the optical axes or binomials of the crystal ; one of them is shown dashed in Fig. 38. The directions of the optical axes are evidently the only ones for which the wave vector has only one magni- tude, f The properties of the ray surface are entirely similar. To derive the corres- ponding formulae, it is sufficient to replace n by s and e by 1/e. In particular, there are two optical ray axes or biradials, also lying in the xs-plane and at an angle y to the #-axis, where y e i.y) — e te) / e te) Since e (a! > < e< 3 >, y < £. The directions of corresponding vectors n and s are given by the general formulae (77. 12a). Their directions are the same only for waves propagated along one of the co-ordinate axes (i.e. the principal dielectric axes). If n lies in one of the co-ordinate planes, s lies in that plane also. This rule, however, is subject to an important exception for wave vectors in the direction of the optical axes. When the values of n given by (79.5) are substituted in formulae (77.1.2a), the components of s take the indeterminate form 0/0. The origin and mean- ing of this indeterminacy are quite evident from the following geometrical considerations. Near a singular point, the inner and outer parts of the wave- vector surface are cones with a common vertex. At the vertex, which is the singular point itself, the direction of the normal to the surface becomes in- determinate ; and the direction of s as given by formulae (77.12a) is just the direction of the normal. In fact the wave vector along the binormal corres- ponds to an infinity of ray vectors, whose directions occupy a certain conical surface, called the cone of internal conical refraction. To determine this cone of rays, we could investigate the directions of the normals near the singular point. It is more informative, however, to use a geometrical construction from the ray surface. Fig. 39 shows one quadrant of the intersection of the ray surface with the xs"-plane (continuous curves), and also the intersection of the wave-vector surface, on a different scale. The line OS is the biradial, and ON the bi- normal. Let n# be the wave vector corresponding to the point iV. It is easy to see that the singular point N on the wave-vector surface corresponds to a singular tangent plane to the ray surface. This plane is perpendicular to ON, and touches the ray surface not at one point but along a curve, which is found to be a circle. In Fig. 39 the trace of this plane is shown by ab. This follows at once from the geometrical correspondence between the wave- vector t In the tensor ellipsoid (77.19) the binormals are the directions perpendicular to the circular sections of the ellipsoid. An ellipsoid has two such sections. §79 Biaxial crystals 327 surface and the ray surface (§77): if the tangent plane is drawn at any point s of the ray surface, then the perpendicular from the origin to this plane is in the same direction as the wave vector n corresponding to s, and its length is 1/n. In our case there must be an infinity of vectors s corresponding to the single value n = n^; hence the points on the ray surface which repre- sent these vectors s must lie in one tangent plane, which is perpendicular to nzy. Thus in Fig. 39 the triangle Oab is the section of the cone of internal conical refraction by the xs-plane. Fig. 39 There is no especial difficulty in carrying out a quantitative calculation corresponding to this geometrical picture, but we shall not do so here, and give only the final formulae. The equations of the circle in which the cone of refraction cuts the ray surface are (< (z) Ax) w + + {SxVb (X \^ Z) ~ &>)] ~ S z V[e {z \* iy) ~ * te) )]} X e (z) _ € (y) J € (y) _ e (x) ' (-J- y € (y) — e (x> \ 5 C*> W e<*> ' - (79 ' 8) SxVb (z \e (y) ~ ^ x) )] + W[ ete) ( ete) - * {y) )] = VW Z) ~ e {x) \ (79.9) The first of these equations is the equation of the cone of refraction if s x , s y , s z are regarded as three independent variables. The second is the equa- tion of the tangent plane to the ray surface. In particular, for s y = equation (79.8) gives the two equations Sx j&\<&> - «te>) s x ltte\t&> - €<*>) S Z ~ A/ e (a;) ( e(z) - e(v) )' ~S~z ~ N e (z) (e fe) - e^>) ' which determine the directions of the extreme rays (respectively Oa and Ob 22 328 Electromagnetic Waves in Anisotropic Media §79 in Fig. 39) in the section by the .x^-plane. The former is along the binormal (cf. (79.6)), which is perpendicular to the tangent ab. Similar results hold for the wave vectors corresponding to a given ray vector. The vector s along the biradial corresponds to an infinity of wave vectors, whose directions occupy the cone of external conical refraction. In Fig. 39 the triangle Oa'b' is the section of this cone by the xs-plane. The corresponding formulae are again obtained by substituting n for s and 1/e for e in the formulae (79.8), (79.9), and are € (2/)( e (z) _ e (z)) % 2 + [ Wa V(e (z) - * (2/) ) ~ «2\/( e(2/) - e (x) )] X x [n z eW^/( € (z) - € (y>) - n z eU>^/(z{y) _ e (*))] = 0, «aV( e(2/) ~ * (aj) ) + «zV( ete) - * {y) ) = V[e (y K* {z) ~ ete) )]- In observations of the internal conical refraction f we can use a flat plate cut perpendicular to the binormal (Fig. 40). The surface of the plate is covered by a diaphragm of small aperture, which selects a narrow beam from a plane light wave (i.e. one whose wave vector is in a definite direction) inci- dent on the plate. The wave vector in the wave transmitted into the plate is in the direction of the binormal, and so the rays are on the cone of internal refraction. The wave vector in the wave leaving the other side of the plate is the same as in the incident wave, and so the rays are on a circular cylinder. Fig. 40 To observe the external conical refraction, the plate must be cut per- pendicular to the biradial, and both its surfaces must be covered by dia- phragms having small apertures in exactly opposite positions. When the plate is illuminated by a convergent beam (i.e. one containing rays with all possible values of n), the diaphragms admit to the plate rays with s along the biradial, and therefore with directions of n occupying the surface of the cone of external conical refraction. The light leaving the second aperture is therefore on a conical surface, although this does not exactly coincide with the cone of external refraction, on account of the refraction on leaving the plate. The laws of refraction at the surface of a biaxial crystal for an arbitrary direc- tion of incidence are extremely complex, and we shall not pause to discuss f We shall describe only the principle of the experiment. §80 Double refraction in an electric field 329 them here.f but only mention that, unlike what happens for a uniaxial crystal, both refracted waves are "extraordinary" and, in particular, the rays of neither lie in the plane of incidence. §80. Double refraction in an electric field An isotropic body becomes optically anisotropic when placed in a constant electric field. This anisotropy may be regarded as the result of a change in the dielectric constant due to the constant field. Although this change is relatively very slight, it is important here because it leads to a qualitative change in the optical properties of bodies. In this section we denote by E the constant electric field in the body,J and expand the dielectric tensor e^ in powers of E. In an isotropic body in the zero-order approximation, we have e^ = e (0) S^. There can be no terms in eik which are of the first order in the field, since in an isotropic body there is no constant vector with which a tensor of rank two linear in E could be constructed. The next terms in the expansion of e^ must therefore be quadratic in the field. From the components of the vector E we can form two symmetrical tensors of rank two, E 2 8m and EfEk. The former does not alter the symmetry of the tensor e^Snc, and the addition of it amounts to a small correction in the scalar constant e (0) , which evidently does not result in optical anisotropy and is therefore of no interest. Thus we arrive at the following form of the dielectric tensor as a function of the field : €« = «i* + x£i£*, (80.1) where a is a scalar constant. One of the principal axes of this tensor coincides with the direction of the electric field, and the corresponding principal value is * €„ = e«»+a£2. ( 8 0.2) The other two principal values are both equal to C _L = e<o>, (80.3) and the position of the corresponding principal axes in a plane perpendicular to the field is arbitrary. Thus an isotropic body in an electric field behaves optically as a uniaxial crystal (the Kerr effect). The change in optical symmetry in an electric field may occur in a crystal also (for example, an optically uniaxial crystal may become biaxial, and a cubic crystal may cease to be optically isotropic), and here the effect may be of the first order in the field. This linear effect corresponds to a dielectric tensor of the form € ik = eui {0) + at&iEi, where the coefficients <x. ik i form a tensor of rank three symmetrical in the suffixes i and k (a«i = a*«). The t A detailed account of the calculations may be found in the article by G. SziVESSY Handbuch der Physik, vol. XX, Chapter 11, Springer, Berlin, 1928. ' X Not to be confused with the variable field of the wave, which is usually very weak. 330 Electromagnetic Waves in Anisotropic Media §81 symmetry of this tensor is the same as that of the piezoelectric tensor. The effect in question therefore occurs in the twenty crystal classes which admit piezoelectricity. §81. Mechanical-optical effects Besides the Kerr effect discussed in §80, there are other ways in which the optical symmetry of a medium can be changed by external agencies. These include, first of all, the effect of elastic deformations on the optical properties of solids. In particular, such deformations may render an isotropic solid body optically anisotropic. Such phenomena are described by the inclusion in Hk{u>) of additional terms proportional to the components of the deforma- tion tensor. The corresponding formulae are exactly the same as (16.1) and (16.6) for the static dielectric permeability, except that the coefficients are now functions of frequency. In the deformation of an isotropic body, for example, we have eoc = e (0) S^ + aiUijc + a^uahtk. (81.1) The coefficients «i(a>) and a^ico) are called elastic-optical constants. Another case is the occurrence of optical anisotropy in a moving fluid. Here we do not refer to the relativistic effects described by the equations of §57; the effects to be considered are due to the presence of velocity gradients in the fluid. The corresponding general expression for the dielectric tensor is m . = Ma + J^ + ^) + J^.^\ (81 . 2) and represents the first terms in an expansion of e^ in powers of the deriva- tives of the velocity. In an incompressible fluid dvijdxi = div v = 0, and the last two terms in (81.2) give zero on contraction; e (0) is the dielectric permeability of the fluid at rest.f The second and third terms in (81.2) are respectively symmetrical and antisymmetrical in the suffixes i and k. For uniform rotation of the fluid we have v = Slxr, where £1 is the angu- lar velocity of rotation, and the symmetrical term is zero.J These phenomena are of practical importance only in such systems as suspensions and colloidal solutions of anisotropically shaped particles. f To avoid misunderstanding, it should be emphasised that the symmetry relations dis- cussed in Statistical Physics §124 (the generalised principle of symmetry of the kinetic coefficients) do not apply to the expression (81.2). These relations are derived on the assump- tion that the processes corresponding to the coefficients under consideration are the only cause of energy dissipation in the system. In the present case, however, besides the dissipation in the variable electromagnetic field in the wave, there is another mode of dissipation, which is unrelated to the field, namely the internal friction in the non-uniform fluid stream. t See §82 for the optical properties resulting from the antisymmetrical part of the tensor etfc. §82 Magnetic-optical effects 331 In this case the effect (called the Maxwell effect) is due primarily to the orienting of particles suspended in the fluid by the action of the velocity gradients. Since a uniform rotation cannot orient the particles, it follows that A2 <^ Ai, and we can write simply €ut = ^B fk + X 1 (—=- + -^\. (81.3) §82. Magnetic-optical effects In the presence of a constant magnetic field H, f the tensor e^ is no longer symmetrical. The generalised principle of symmetry of the kinetic coeffi- cients given by SP (124.14) requires that e«(H)-€«(-H). (82.1) The condition that absorption is absent requires that the tensor should be Hermitian : Hk = e&f*, (82.2) as is seen from (76.4), but not that it should be real. Equation (82.2) implies only that the real and imaginary parts of em must be respectively symmetrical and antisymmetrical : Hk = ejw\ Hk" = — ***"• (82.3) Using (82.1), we have efjt'(H) = e W '(H) = e ik \- H), €**"(H) = - €«"(H) = - €«"(- H), C ' j i.e. in a non-absorbing medium e^' is an even function of H, and €&" an odd function. The inverse tensor e -1 ^ evidently has the same symmetry properties, and is more convenient for use in the following calculations. To simplify the notation we shall writet e~Hk = ?)ik = rut' + irjik". (82.5) Any antisymmetrical tensor of rank two is equivalent (dual) to some axial vector; let the vector corresponding to the tensor 17^" be G. Using the anti- symmetrical unit tensor em, we can write the relation between the compo- nents 7]nc" and Gt as W = e ikiG h (82.6) t Not to be confused with the weak variable field of the electromagnetic wave. X Of course, ij**' and t\ik" are not the tensors inverse to euc' and eue". 332 Electromagnetic Waves in Anisotropic Media §82 or, in components, r) xy " = G z , rj zx " = G y , t] yz n = G x . The relation Ei = -qijcDjc between the electric field and induction becomes E t = {7) ik ' + ie m G t )D k = rjmDjc + «(D X G) t . (82.7) A medium in which the relation between E and D is of this form is said to be gyrotropic. f We may give a general discussion of the nature of waves propagated in an arbitrary gyrotropic medium, assumed anisotropic, with no restriction on the magnitude of the magnetic field. J We take the direction of the wave vector as the .sr-axis. Then equations (77.18) become \Vcl0 ~ -£«iA D e = Viae + i7 l*e" ~ -^Ke) D e = °> ( 82 - 8 ) where the suffixes a, jS take the values x, y. The directions of the x and y axes are taken along the principal axes of the two-dimensional tensor t]^ ; and we denote the corresponding principal values of this tensor by l/«oi 2 and l/«02 2 . Then the equations become (— - -)d x + iG z D y = 0, W nJ (82.9) / 1 1\ K } -iG z D x +i—---)Dy = 0. The condition that the determinant of these equations vanishes gives an equation quadratic in n 2 : \ n 2 «oi 2 / \n £ nmrl whose roots give the two values of n for a given direction of n:j| l.i(JL + _L) + I\H±.±)\gA. (82.11) n* 2\»oi 2 n 2 2 / ~ V L4\«oi 2 «02 2 / J f The gyration vector is the vector g in the opposite relation Dt = € ik f E k + i(E x g) f . (82.7a) The coefficients in (82.7) and (82.7a) are related as follows (cf. §21, Problem): r)ik = {WW- 1 * -gigk)lU\, ,„ _ . ^ / /l l (»2.7b) where |e| and |€'| are the determinants of the tensors eik and eik'. X The medium is again assumed non-magnetic with respect to the variable field of the electromagnetic wave, i.e. fiik(,o) = S^. This, however, does not exclude a constant field magnetising the medium (i.e. the static permeability may differ from unity). The properties derived for 6fjfc(a>) are equally applicable to the tensor fJ4k(<o) in a frequency range where the dispersion of the magnetic permeability is of importance. || When there is no field, G = and n = noi or no2. It should be remembered, however, that when the field is present noi and M02 in equation (82.10) are not in general the values of n f or H = 0, since not only G but also the components i)ik depend on the field. §82 Magnetic-optical effects 333 Substituting these values in equations (82.9), we find the corresponding ratios D p /D x : ^ = _wi(_L _J_U /ri/j__ ±\\<u]\ (8 2.i2) D x G z l2\«oi2 «02 2 / V L4Ui 2 «02 2 / II The purely imaginary value of the ratio D y /D x signifies that the waves are elliptically polarised, and the principal axes of the ellipses are the * and y axes. The product of the two values of the ratio is easily seen to be unity. Thus, if in one wave D y = ipD x , where the real quantity p is the ratio of the axes of the polarisation ellipse, then in the other wave D y — — iD x \p. This means that the polarisation ellipses of the two waves have the same axis ratio, but are 90° apart, and the directions of rotation are opposite (Fig. 41). f Fig. 41 The components Gi and rjut' are functions of the magnetic field. If, as usually happens, the magnetic field is fairly weak, we can expand in powers of the field. The vector G is zero in the absence of the field, and so for a weak field we can put Gt = focHjc, (82.13) where/ifc is a tensor of rank two, in general not symmetrical. This dependence is in accordance with the general rule (82.4) whereby, in a transparent medium, the components of the antisymmetrical tensor rjm" (and €*&") must be odd functions of H. The symmetrical components r)uc' are even functions of the magnetic field. The first correction terms (which do not appear in the absence of the field) in t\iu are therefore quadratic in the field.? In the general case of an arbitrarily directed wave vector, the magnetic field has little effect on the propagation of light in the crystal, causing only t If the vectors D in the two waves are denoted by Di and D2, these relations may be written Di-Dg* = DixDix* + Di y D2y* = 0. This is a general property of the eigenvectors on reduction to the principal axes of a Hermitian tensor (in this case, the tensor r}a&'). X When second-order quantities are neglected, formulae (82.7b) reduce to the simpler forms Vile = €~h Gt = — ei*'£*/ie'| (82.13a) 334 Electromagnetic Waves in Anisotropic Media §82 a slight ellipticity of the oscillations, with an axis ratio of the polarisation ellipse which is small (of the first order with respect to the field). The directions of the optical axes (and neighbouring directions) form an exception. The two values of n are equal in the absence of the field when the wave vector is along one of these axes. The roots of equation (82.10) then differ from these values by first-order quantities,! and the resulting effects are analogous to those in isotropic bodies, which we shall now con- sider. The magnetic-optical effect in isotropic bodies (and in crystals of the cubic system) is of particular interest on account of its nature and its com- paratively large magnitude. Neglecting second-order quantities, we have 77^' = e _1 S^, where e is the dielectric permeability of the isotropic medium in the absence of the magnetic field. The relation between D and E is E = -D + iD x G, (82.14) € or D = eE + iE x g; (82.15) in the same approximation, the vectors g and G are related by G = - g/e 2 . (82.16) The dependence of g (or G) on the external field reduces in an isotropic medium to simple proportionality: g=/H, (82.17) in which the scalar constant / may be either positive or negative. In equation (82.10) we now have «oi = «02 = «o = \A> tne refractive index in the absence of the field. Hence 1/n 2 = + G z + lfn 2 or, to the same accuracy, «+ 2 = wo 2 ±«o 4 £z= wo 2 +g z . • (82.18) Since the #-axis is in the direction of n, we can write this formula, to the same accuracy, in the vector form (n ± ^g) 2 = no*. (82.19) Hence we see that the wave- vector surface in this case consists of two spheres of radius no, whose centres are at distances ±g/2no from the origin in the direction of G. t It should be noticed that the two roots of (82.10) do not become equal. The geometrical significance of this is that the two parts of the wave-vector surface are separated. §82 Magnetic-optical effects 335 A different polarisation of the wave corresponds to each of the two values of n : we have D x = +iD y , (82.20) where the signs correspond to those in (82.18). The equality of the magni- tudes of D x and D y , and their phase difference of + \tt, signify a circular polarisation of the wave, with the direction of rotation of the vector D respec- tively anticlockwise and clockwise looking along the wave vector (or, to use the customary expressions, with right-hand and left-hand polarisation respectively). The difference between the refractive indices in the left-hand and right- hand polarised waves has the result that two circularly polarised refracted waves are formed at the surface of a gyrotropic body. This phenomenon is called double circular refraction. Let a linearly polarised plane wave be incident normally on a slab of thick- ness /. We take the direction of incidence as the #-axis, and that of the vector E ( = D) in the incident wave as the x-axis. The linear oscillation can be represented as the sum of two circular oscillations with opposite directions of rotation, which are then propagated through the slab with different wave vectors k ± = ojn ± /c. Arbitrarily taking the wave amplitude as unity, we have D x = i[exp (ik + z)+exp (ik-z)] t D y = %i[— exp (ik + z) + exp (ik-z)], or, putting k = %(k + + k-) and k = %(k + — k-), D x = l e ikz( e iK Z + e -iK Z } _ e ikz cos KZy D y = \ie ikz { - e iKZ + e~ iKZ ) = e ikz sin kz. When the wave leaves the slab we have D y /D z = tan kI = tan (la)g/2cno). Since this ratio is real, the wave remains linearly polarised, but the direc- tion of polarisation is changed (the Faraday effect). The angle through which the plane of polarisation is rotated is proportional to the path traversed by the wave; the angle per unit length in the direction of the wave vector is ( wg/2cno) cos 6, where 6 is the angle between n and g. It should be noticed that, when the direction of the magnetic field is given, the direction of rotation of the plane of polarisation (with respect to the direction of n) is reversed (left-hand becoming right-hand, and vice versa) when the sign of n is changed. If the ray traverses the same path twice in opposite directions, the total rotation of the plane of polarisation is there- fore double the value resulting from a single traversal. For 6 = \n (the wave vector perpendicular to the magnetic field), the effect linear in the field given by formulae (82.18) disappears, in accordance with the general rule stated above that only the component of g in the direc- tion of n affects the propagation of light. For angles 6 close to \n we must therefore take account of the terms proportional to the square of the field, and in particular these terms must be included in the tensor 77^'. By virtue of the axial symmetry about the direction of the field, two principal 336 Electromagnetic Waves in Anisotropic Media §82 values of the symmetrical tensor ii«/ are equal, as for a uniaxial crystal. We shall take the #-axis in the direction of the field, and denote by 77 , and 77 x the principal values of 77^' in the directions parallel and perpendicular to the magnetic field. The difference rj^—r]^ is proportional to H 2 . Let us consider the purely quadratic effect (called the Cotton-Mouton effect) which occurs when n and g are perpendicular. In equations (82.9) and (82.10) we have G z = 0, and l/«oi 2 > V w 02 2 are respectively 77 „, i] x . Thus in one wave we have 1/n 2 = 77 „ , D y = 0; this wave is linearly polarised, and the vector D is parallel to the #-axis. In the other wave l[n 2 = rj ±y D x = 0, i.e. D is parallel to the j-axis. Let linearly polarised light be inci- dent normally on a slab in a magnetic field parallel to its surface. The two components in the slab (with vectors D in the xz and yz planes) are propa- gated with different values of n. Consequently the light leaving the slab is elliptically polarised. PROBLEMS Problem 1. Determine the directions of the rays when a ray incident from a vacuum is refracted at the surface of an isotropic body in a magnetic field. Solution. The direction of the ray vector s is given by the normal to the wave-vector surface. Differentiating the left-hand side of equation (82.19) with respect to the compo- nents of the vector n, we find that s is proportional to n±g/2wo. The square of the latter expression is wo 2 , and so the unit vector in the direction of the ray is given by :_i/. ± JLA a) * «o\ 2«o / Let the angle of incidence be 9. The refracted rays do not in general lie in the plane of incidence, and their directions are given by the angle 6' to the normal to the surface and the azimuth ^' measured from the plane of incidence. We take the latter as the as-plane, with the ar-axis perpendicular to the surface. The components n x and n v of the wave vector are unaltered by refraction. In the incident ray they are n x = sin 0, n y = 0. Substituting these values in (1), we find the x and y components of the unit vector s/s, which give immediately the directions of the refracted rays : 1 1 sin 6' cos </>' = — sin 6 ± - — -g x , no 2m 1 sin 6' sin j>' — ± — — -gy. 2mo z When the angle of incidence is not small, the azimuth <f>' is small, and we can write <f>' = ±g v /2no sin 0, • a' sin e _ L 8* sinfl = ±-^-T- wo 2m £ For normal incidence (6 = 0) we take the xs-plane through the vector G; then ^' = 0, and 6' = sin 6' = ±gx/2no 2 . Although this formula does not involve g g , it is not valid if gz = 0, since the approximation linear in the field is inadequate when n and g are perpen- dicular. Problem 2. Determine the polarisation of the reflected light when a linearly polarised wave is incident normally from a vacuum on the surface of a body rendered anisotropic by a magnetic field. Solution. For normal incidence the direction of the wave vector is unaltered by the passage of the wave into the medium. In all three waves (incident, reflected and refracted) §83 Natural optical activity 337 the vectors H are therefore parallel to the surface (the ay-plane). The electric vector E in the incident and reflected waves is also parallel to the *-y-plane; in the refracted wave Ez t 6 0, but the relation between the x and y components of E and H is the same as in an isotropic body (H x = —nE y , H y = nE x ). If the polarisation of the incident wave is the same as that of one of the two types of wave which can be propagated in the anisotropic medium concerned, with the given direction of n, then there is only one refracted wave, which has this polarisation. The problem is then formally identical with that of reflection from an isotropic body, and the fields Ei and Eo in the reflected and incident waves are re- lated by Ei=(l-n)Eo/(l+«), (1) where n is the refractive index corresponding to this polarisation. The linear polarisation can be regarded as resulting from the superposition of two circular polarisations with opposite directions of rotation. If Eo in the incident field is in the re- direction, we put Eo = Eo + +Eo~, where Eo + x = iEo + y = \Eo, Eo~x = —iEo~y = $Eo. Using formula (1) for each wave, with n ± given by (82.18), we obtain Ei x = ±Eo\— + — ^Eo- ll+n+ 1 + n-J 1 1+mo E ly = ttEo\— — — £*iE tt Ll+«_ 1+n+J 1 — n- 1 — M+"| ^ g cos 6 1 + n+ J «o( 1 + wo) 2 ' where is the angle between the direction of the incidence and the vector g. Hence we see that the reflected wave is elliptically polarised, the major axis of the ellipse being in the ^-direction, and the ratio of the minor and major axes being (g cos 0)/«o(«o 2 — 1). Problem 3. Determine the limiting form of the frequency dependence of the gyration vector at high frequencies. Solution. The calculations are similar to those in §59, except that the electron equation of motion must include the Lorentz force due to the constant external magnetic field H: dv' m— — = eEoe-iM+ev'xHIc. dt If <o ^> eHlmc, this equation can be solved by successive approximations. As far as terms of the first order in H we have ic &^ v' = E — — E x H, mm m?co 2 c and the induction is then D = < w )E+ty(«)ExH, where e(a>) is given by (59.1) and/(a>) = —4irNe 3 /cm 2 a> 3 . §83. Natural optical activity The frequency dispersion of the dielectric (and magnetic) permeability results from the dependence of the macroscopic properties of matter on the time variation of the electromagnetic field. The dependence on its spatial variation has been ignored up to this point. The condition for this treatment to be valid is that the atomic dimension a should be small compared with the wavelength A (see §58). The inequality a <^ A is a necessary condition for the macroscopic theory to be applicable at all. When the quantities involving the small ratio a/A are entirely neglected, however, certain kinds of effect are overlooked which make their appearance when the next terms in a/A after the zero-order approximation are included. We shall now discuss these effects. 338 Electromagnetic Waves in Anisotropic Media §83 The expansion in powers of a/X corresponds, in the macroscopic theory, to an expansion of the induction D in powers of the spatial derivatives of the field E as well as of E itself. Taking only the first-order terms, we must include terms proportional to the first powers of the first-order derivatives. For a field of a single frequency u> we can write the expansion as Di = e ik «»E k + yiadEtldxh (83.1) where e^ (0) and yaa are functions of frequency. Before proceeding to investigate this expression, we should make the following remark. To the accuracy used here there is no physical significance in separating the mean value of the microscopic current density pv into the two parts BPJdt and c curl M. In the present theory, therefore, it is appro- priate to write Maxwell's equations as 10B curlE = , c dt (83.2) curl B = , c dt without introducing H as well as the mean microscopic magnetic field E = B. Instead, all terms resulting from the averaging of the microscopic currents are supposed included in the definition of D. The symmetry properties of the tensor yun in (83.1) are determined by applying the generalised principle of symmetry of the kinetic coefficients, as was done in §76 for the tensor e ik . We saw in §76 that, if the components of the vector E at each point in the body are taken as the quantities x a , then the corresponding f a will be the components of the vector D. The presence of the spatial derivatives in the relations (83.1), however, interferes with the direct application of the symmetry principle, which is best used as follows. Let x a and x' a be two different sets of values of the x a , and f a ,f' a the corres- ponding sets of values of the f a . By the symmetry (a a& = a a& ) of the coeffi- cients in the relations x a = Sa«&/&, x'a = 2<W'& 6 we have Vxaf'a = Vx f af a . (83.3) In the present case, this equation takes the form JE<D'i dV = JjE'iD* dV. Substituting (83.1) and using the known symmetry of €*>«, we obtain f ^'* JT r f v> dEk Ajr YiiclEi— — dV = J- yociEi—dV §83 Natural optical activity 339 or, integrating by parts on one side of the equation, f 8E' k r dE'i r dE ' k J OXl J OXi J OXl Since the functions E and E' are arbitrary, we therefore have the required symmetry property : Ym = — ym- (83.4) We shall also suppose that no absorption takes place in the medium. Let us ascertain what conditions are thereby imposed on the tensor yaa. The dissipation of energy in a periodic field is given by the (time) average value of the integral -(1/4tt) JE-(dD/&) dV. Here E and D are real; if we use the complex representation, the integral to be averaged can be written 1 r i 8D* 0D\ ioi r E + E* dV = (E.D* - E*.D)dF. 16tt J \ 8t 8tl 16ttJ k } Substituting(83. l)and using the fact that e (0) ^ is real in a transparent medium, we obtain 16tt) V 8E k * 8E k \ YiM*Ei— nuEi*-- — dV OXl OXl I 16ttJ \ dE k * dE t *\ YikfEi— — + y ik iE k -- — \dV oxi oxi l iu) r dE k * = - 77" I (y*w* + Ykil)Ei— — dV. l07T J OXl 8xi This expression is zero identically if yi k f = —y k u = yi k i. Thus we con- clude that, if absorption is absent, the tensor yiu must be real. For a plane wave, with wave vector k = <oti/c, we have 8E k /dxi = i<oE k ni/c, so that Di = €i k E k , where Hk = e (0) ta + icoytkini/c (83.5) is the dielectric permeability tensor, which now exhibits dispersion with respect to both frequency and wave vector, f Instead of the antisymmetrical tensor of rank two yiuni, we shall use the gyration vector g, which is dual to it. This vector is given by coyikim/c = e ik igi, (83.6) i.e. Hk = e m ik + iemgi, (83.7) f When a> -> the quantities yuci, which do not pertain to the expansion in powers of w, tend to constants. The imaginary part of cm therefore tends to zero as the first power of the frequency. 340 Electromagnetic Waves in Anisotropic Media §83 which is formally the same as the expression used in §82. The only difference is that in §82 the vector g depended only on the properties of the medium (and on the applied magnetic field), whereas here the gyration vector depends also on the wave vector of the field. According to (83.6) the components of this vector are linear functions of the components of n, i.e. gi = gikfik. (83.8) Substituting (83.8) in (83.6), we find wyucinifc = ei]e m g m inu or, since n is arbitrary, wynci\c = eocmgmi, (83.9) which gives the relation between the components of the tensor yaa of rank three and the pseudotensor guc of rank two. f The particular crystallographic symmetry of the body places certain restric- tions on the components of the tensor yua (or gut) and, in particular, may have the result that all the components are zero. For example, the tensor yua cannot exist in bodies having a centre of symmetry: when the sign of each co-ordinate is changed (inversion), all the components of a tensor of rank three (and of a pseudotensor of rank two) change sign, whereas by the sym- metry of the body they must remain unchanged by this transformation. Bodies in which the tensor gat is not zero are said to have natural optical activity. Thus the existence of optical activity certainly implies that the body has no centre of symmetry. Let us first consider the natural optical activity of isotropic bodies. If a liquid or gas consists of a substance having no stereoisomer, it is symmetrical not only with respect to any rotation but also with respect to reflection (inver- sion) about any point, and can have no optical activity. Such activity can occur only in fluids having two stereoisomeric forms, and the two forms must be present in different quantities. The fluid then has no centre of symmetry. In an isotropic body, and in crystals of the cubic system, the pseudotensor gik reduces to a pseudoscalar : gm=f8m; '(83.10) the tensor yua is given in terms of /by yua = cfeua/a). A pseudoscalar is a quantity which changes sign on inversion of the co-ordinates. The two stereoisomers are converted into one another by the operation of inversion, and so their values of /are the same with opposite signs. Thus, in an optically active isotropic body, the gyration vector g = /n, and the relation between the electric induction and field in the wave is given by D = ffi + pxn. (83.11) Since D^n = 0, it follows that E«n = 0. That is, in such a wave not only the induction D (as in any medium) but also the field E is transverse to the direction of n. t In components gxx = <*>Yyzx\c, g X y = o>Yyzy\c, gyx — toyzxxjc, etc. §83 Natural optical activity 341 The change in the refractive index n when allowance is made for the natural optical activity is a small quantity. In determining this change we can there- fore put n = no = \A (0) m tne small term Exg in (83.11). Then the prob- lem of calculating the difference n — no is formally identical with that con- sidered in §82 of the change in n due to the magnetic field, except that g has a different meaning and is always parallel to n (the #-axis in §82). By analogy with (82.18) we can therefore derive immediately the equation » ± 2 = «o 2 ± g = «o 2 ± fno. (83.12) These two values correspond (cf. (82.20)) to the following ratios of the two components of E (or D) : E z = ± iE y , (83.13) i.e. to waves which are left-hand and right-hand circularly polarised. It may also be noted that the magnitude of n is independent of its direction, and therefore the direction of n is the same as that of the ray vector s. Thus we see that the optical properties of a naturally active isotropic body resemble those of an inactive body in a magnetic field: it exhibits double circular refraction, and when a linearly polarised wave is propagated in it the plane of polarisation is rotated. The angle of rotation per unit path length of the ray is <nf\2c. The sign of the constant g, and therefore the direction of rotation, are opposite for the two stereoisomers, and we therefore speak of dextrorotatory and laevorotatory stereoisomers. Unlike the rotation of the plane of polarisation in a magnetic field, the magnitude and sign of the rotation in naturally active substances do not depend on the direction of propagation of the ray. Hence, if a linearly polarised ray traverses the same path in a naturally active medium twice in opposite directions, the plane of polarisation is unchanged. Let us now consider naturally active crystals. We shall not give here a systematic analysis of all possible cases of symmetry (see the Problem), but simply note that natural activity is impossible if a centre of symmetry is present, but possible if there is a plane of symmetry or a rotary-reflection axis. It should be emphasised that the conditions for the existence of natural activity in crystals are not the same as those which allow the existence of crystals in two mirror-image (enantiomorphic) forms; the latter conditions are more stringent, and require the absence of both a centre and a plane of symmetry. Thus a crystal can be optically active and yet be identical with its mirror image. In a naturally active crystal (uniaxial or biaxial), when light is propa- gated with an arbitrary direction of the wave vector, we have essentially ordinary double refraction of linearly polarised waves; the allowance for the activity would amount to replacing the strictly linear polarisation by an elliptical polarisation with an axis ratio of the first order of smallness. The only exception is formed by the directions of the optical axes, along 342 Electromagnetic Waves in Anisotropic Media §83 which, if the activity is neglected, the two roots of Fresnel's equation coin- cide. In these directions the phenomenon of natural activity of crystals is analogous to that of isotropic bodies : double circular refraction of the first order occurs, with a corresponding rotation of the plane of polarisation of linearly polarised waves. These phenomena rapidly disappear as the wave vector deviates from the direction of the optical axis. For a quantitative calculation of natural activity in crystals it is more convenient to use, not the expression giving D in terms of E, but the inverse, as in §82. As far as first-order quantities this is Ei = ^- 1 aD t + (D x G) h (83.14) where the vector G is related to the g previously used by Gf = — e (0) ^fc/|e (0) | ; see (82.13a). Owing to the formal correspondence between this expression and (82.7), the equations (82.9) and (82.10) are again valid. In these equations G z is the component of G in the direction of n. If we write G in the form Gt = G iJc n k , (83.15) in analogy with (83.8), the component is proportional to n-G = Gncimje. (83.16) This quadratic form determines the optical properties of a naturally active crystal. The tensor G^ itself need not be symmetrical, but if it is separated into symmetrical and antisymmetrical parts the latter does not appear in the form (83.16). Thus we conclude that the tensor Guc may be assumed symmetrical in discussing the optical properties of naturally active crystals. PROBLEM Find the restrictions imposed by crystal symmetry on the components of the tensor Solution. Under any rotation, the pseudotensor Guc behaves as a true tensor ; in parti- cular, the presence of an axis of symmetry of order higher than the second results, as for a true symmetrical tensor of rank two, in complete isotropy in a plane perpendicular to the axis. The behaviour of the pseudotensor Gac under reflection is determined by the fact that it is dual to a true tensor of rank three : under any reflection which changes the sign of a given component of a true tensor of rank two, the corresponding component of Gac remains unchanged, and vice versa. For example, on reflection in the ysr-plane the components Gxx, G yy , Gzz, G yz change sign, but G X y, Gxz do not. We give below the non-vanishing components of the tensor Gm for all crystal classes which allow natural activity. The sr-axis is taken along the axis of symmetry of the third, fourth or sixth order or (in the classes Cz, C% v ) along the only second-order axis of symmetry or (in the class C s ) perpendicular to the plane of symmetry. When three mutually perpendicu- lar axes of symmetry are present, they are the co-ordinate axes. Class C%: all. Class Cz: Gxx, Gyy, Gzz, G X y, the last of which may be made to vanish by a suitable choice of the x and y axes. Class C s : G X i, Gyz, one of which may be made to vanish by a suitable choice of the x and y axes. Class Czv' G X y (the xz and yz planes being planes of symmetry). Class Dz' Gxx, Gyy, Gzz. Classes Cs, C4, Ce, Da, D4, D6*. Gxx = G yy , Gzz- §83 Natural optical activity 343 Class S4: Gxx — —Gy y> G X y, one of which may be made to vanish by a suitable choice of the x and y axes. Class D2d- G X y (the * and y axes being in vertical planes of symmetry). Classes T, O: Gxx = G yy = G sz . It may be noted that, in uniaxial crystals of the classes S4 and D2&, the scalar (83.16) is zero if the vector n is in the sr-direction, since G zl = 0. This means that in these crystals there is no natural-activity effect in the direction of the optical axis. In a biaxial crystal of the class C% v the optical axes are in one of the planes of symmetry. For vectors n lying in the xz or yz plane the scalar (83.16) is again identically zero, so that here also there is no effect in the direction of the optical axes. The only crystal class which allows rotation of the plane of polarisation along the optical axis but not enantiomorphism is the monoclinic class C». 23 CHAPTER XII THE PASSAGE OF FAST PARTICLES THROUGH MATTER §84. Ionisation losses by fast particles in matter: the non-relativistic case A fast charged particle, in passing through matter, ionises the atoms and thereby loses energy, f In gases, the ionisation losses can be regarded as being due to collisions between the fast particle and individual atoms. In a solid or liquid medium, however, several atoms interact simultaneously with the particle. The effect of this on the energy loss by the particle can be macroscopically regarded as resulting from the dielectric polarisation of the medium by the charge. Let us first consider this effect for non-relativistic velocities of the particle. We shall see that the polarisation of the medium then has only a slight effect on the losses. The derivation of this result is of interest because the method can be extended to other cases. Let us first of all ascertain the conditions under which the phenomenon can be macroscopically considered. The spectral resolution of the field produced at a distance r from the path of a particle moving with velocity v consists chiefly of terms whose frequency is of the order vfr (the reciprocal of the "collision time"). The ionisation of an atom can be effected by field components of frequency a> ^ a>o, where a>o is some mean frequency cor- responding to the motion of the majority of the electrons in the atom. The particle therefore interacts simultaneously with many atoms if vjcoo is large compared with the distances between the atoms. In solids and liquids these distances are of the same order of magnitude as the dimension a of the atoms themselves. Thus we obtain the condition v > acoQ, i.e. the velocity of the ionising particle must be large compared with the velocities of the atomic electrons (or at least of the majority of them).t Let us now determine the field produced by a charged particle moving through matter. In the non-relativistic case it is sufficient to consider only the electric field, defined by the scalar potential <f>. This potential satisfies Poisson's equation £A<£ = - 47reS(r - vt), (84.1) f We speak, as is customary, of "ionisation losses", but these are, of course, understood to include losses due to the excitation of atoms to discrete energy levels. X The corresponding condition for the energy E of the particle is Ep> MI/m, where M is the mass of the particle, m that of the electron, and / some mean ionisation energy for the majority of the electrons in the atom. 344 §84 Ionization losses by fast particles in matter 345 in which the "dielectric constant" is written as an operator, and the expres- sion e8(r—vt) on the right-hand side is the density due to a point charge e moving with constant velocity v. f We expand <f> as a Fourier space integral : 00 <£ = f 0kexp(fk-r)dk. (84.2) —oo Taking the Laplacian of this equation, we have 00 /\,<f> = — I <f>kk 2 exp(fk«r)dk, —00 whence it is seen that the Fourier component of A<£ is (A^)k = —k 2 <f>^. Taking the Fourier component of equation (84.1) gives £(A<£)k = - -— f ±neh{r - v*) exp(- ik-r)dV e = exp ( — itv-k). Thus €^t = (e/2jr 2 k 2 )exp(-itv»k), and <£ k therefore depends on time through a factor exp ( — itv-k). The operator e acting on a function exp ( — iatt) multiplies it by «(to). Hence e fa = o 2M ,u ^ ex P(~ itv ' k )' 27T 2 « 2 €(k«V) The Fourier components of the field and of the potential are related by Ejj exp (ik-r) = -grad [«^exp (ik-r)] = -ik<f> k exp («k-r), or E k = -ik<f>^ Thus iek 27T 2 /J 2 e(k«v) The total field strength is obtained by inverting the Fourier transform: 00 E = J Ekexp(fk.r)dk. (84.4) —00 The energy loss by the moving particle is just the work done by the force cE exerted on the particle by the field which it produces. Taking the value of the field at the point occupied by the particle, namely t We assume that the particle moves in a straight line, and thereby neglect scattering, as is always permissible in problems of this type. If the charge on the particle is ze, then all the formulae pertaining to energy loss in this and the following sections should be multiplied by z z . 346 The Passage of Fast Particles Through Matter §84 r = vt, we obtain in the integrand in (84.4) a factor exp (itv-k) which cancels with the factor exp ( — itv>k) in the expression (84.3) for E^. Hence the force F is F=-_J_— dk. ie i ~2n 2 J k 2 e(k>v) — 00 It is evident that the direction of the force F is opposite to that of the velocity v; let the latter be the ^-direction. Putting k x v = a>,q = -\/(ky 2 + kz 2 ) and replacing d&^d&z by 2-nq dq, we can write the magnitude of F as 00 Qo A A * * (84.5) -tJJ (co)(q 2 v 2 + co 2 ) -oo o The choice of qo is discussed below. The following remark should be made concerning the integration with respect to o> in formula (84.5). As to -> oo the function e(co) -> 1, and the integral is logarithmically divergent. This happens because we ought to have subtracted from the field E the field which would be present if the particle were moving in a vacuum (i.e. if € = 1); this field evidently does not affect the energy lost by the particle in matter. If this subtraction were effected, 1/e in the integrand of (84.5) would be diminished by unity, and the integral would converge. The same result can be obtained by taking the integration from — R to +R and then letting R tend to infinity. Since the function e'(a>) is even, the real part of the integrand is an odd function of the frequency, and gives zero. The integral of the imaginary part of the integrand converges. In what follows we shall sometimes find it convenient to use the notation l/.e(a>) = 7j(a>) = rj' + it{\ (84.6) with -q'(w) and i/'(ai) respectively even and odd functions, and -q" = — e"/|c| 2 < 0. Formula (84.5) can be rewritten in the explicitly real form 7T J J (q 2 V 2 + a> 2 ) The energy loss per unit path length is the work done by the force over that distance, which is just F; it is called the stopping power of the substance with respect to the particle. According to the general rules of quantum mechanics, the Fourier com- ponent of the field whose wave vector is k transmits to the S-electron released in ionisation a momentum hk. For sufficiently large q ( > coo/v) we have k 2 = q 2 + to 2 /v 2 x q 2 , so that the momentum transferred is approximately /*q. A given value of q corresponds to collisions with impact parameter ~ 1/q. Hence the condition for the macroscopic treatment to be valid is l/q p a. Accordingly, we take as the upper limit of integration a value qo §84 Ionisation losses by fast particles in matter 247 such thaf wqJv <^ go <^ l/«. The quantity F(qo) is the energy loss of a fast particle with transfer of momentum not exceeding hqo to the atomic electron. Integrating with respect to q in (84.7), we obtain 2e 2 r Gov F(qo) = — HV'HI log— dco. (84.8) 77^ J CO This formula cannot be further transformed in a general manner, but it can be written in a more convenient form as follows. We first calculate the integral 00 00 co?/'(co) da> = — \l ' I (co/e) da>. —oo To do so, we notice that, if the integration is taken in the complex co-plane along a contour consisting of the real axis and a very large semicircle a in the upper half-plane, the integral is zero, since the integrand has no poles in the upper half-plane. For large values of to, the function e(o>) is given by formula (59.1): Aire^N <co) = 1 ~. (84.9) The integration along the large semicircle a can be carried out by using this formula, and the result isf f liriNe 2 C dco - cotj'Xw) dw = = 27rW* 2 /w. (84.10) J m J co a- We define a mean frequency of the motion of the atomic electrons by oo coi/'(co) log a) dco logcS = 00 J arq" '(co) dco oo f co|V'(co)l log co dco. (84.11) 277We 2 t This is the same as the value of the integral CO I <oe"(<o) dco o (see (62.14)), as it should be, since, as |a>| -*- oo, |e| -*■ 1 and 17" -> — e" 348 The Passage of Fast Particles Through Matter §84 Then formula (84.8) can be written • F(q ) = (47TNe*lmv*)log(qovla>). (84.12) The following remark should be made here. It might seem from the form of (84.7) or (84.11) that the main contribution to the ionisation losses (84.12) comes from frequencies at which there is considerable absorption. This is not so; these formulae may contain a considerable contribution from ranges in which e" is small. The reason is that in such ranges the function e(o>) « e'(a>) may pass through zero. It is seen from formula (84.5) that the zeros of e(a)) are poles of the integrand. In reality, of course, €"(<o) is not exactly zero, and so the zeros of e(a>) are not on the real axis but just below it. Hence, when the expression used for c(a>) is real and passes through zero, the contour must be indented upwards at the: pole of the integrand, and so a contribution to the integral occurs. For example, if the function e(to) is given by (64.5), the contribution to the retardation (84.12) from the poles ± a)\ (where e(a>i) = 0) is easily seen, by direct calculation from (84.7), to be (4nNe /l /mv 2 a 2 ) log (qiv/wi). In order to find the energy loss F(qi) with transfer of momentum not exceeding some value hqi > hqo, we must "join" formula (84.12) to that given by the quantum theory of collisions, corresponding to energy loss by collisions with single atoms. This can be done by using the fact that the ranges of applicability of the two formulae overlap. As we know from the theory of collisions, the energy loss with transfer of momentum in a range of hdq is dF= (47TNe*lmvZ)dqlq, (84.13) and this formula is applicable (in the non-relativistic case) for any value of q > (oo/v which is compatible with the laws of conservation of momentum and energy, provided that the energy transferred is small compared with the initial energy, of the fast particle, f The energy loss with all values of q between qo and q\ is accordingly (^irNe^lmv 2 ) log (qi/qo)> When this quantity is added to formula (84.12), qo is replaced by q\, so that F( qi ) = (^Ne^/mv 2 ) log(^/d>). (84.14) If a momentum hq\ large compared with the atomic momenta is given to an atomic electron, its energy is E\ = h 2 qi 2 /2m. Thus we can write F(£i) = {2TrNet\mv 2 )\og(2mv 2 E x \h 2 ib 2 ). (84.15) f See Quantum Mechanics, §121, Pergamon Press, London, 1958. The "effective retarda- tion" used there differs from Fbya factor N. Formula (84.13) applies to collisions with free electrons. Its range of applicability as hitherto determined (q ^> am/v), however, extends to values of q for which the atomic electrons cannot be regarded as free. The condition for this is q % wo/wo, where vo is the order of magnitude of the velocity of the majority of the atomic electrons ; the energy tfiq z l2m of the S-electron is then large compared with atomic energies. §85 Ionisation losses by fast particles : the relativistic case 349 This formula gives the energy loss of a fast particle (an electron, for example) by ionisation with a transfer of energy not exceeding E\. It differs from the usual formula derived from a microscopic discussion of collisions, neglecting interactions between atoms, f only by the definition of the "ionisa- tion energy", which is here represented by hw. The mean (with respect to the electrons) ionisation energy of an atom is usually almost independent of its interaction with other atoms, being determined mainly by the electrons of the inner shells, which are almost unaffected by that interaction. More- over, this quantity appears here only in a logarithm, and so the exact definition of it has even less effect on the magnitude of the energy loss. The maximum energy which can be transmitted to an atomic electron in its interaction with a fast heavy particle is 2mv 2 , and is small compared with the original energy of the heavy particle.^ Substituting this value for E\ in (84.15), we obtain the total ionisation losses of a heavy particle: F = (47rNe i lmv 2 ) \og(2mv 2 lhw). (84.16) This differs from the usual formula || only in the definition of the ionisation energy as hoi. §85. Ionisation losses by fast particles in matter: the relativistic case At velocities comparable with that of light, the effect of the polarisation of the medium on its stopping power with respect to a fast particle may become very important even in gases, f f To derive the appropriate formulae, we use a method analogous to that used in §84, but it is now necessary to begin from the complete Maxwell's equations. When extraneous charges are present with volume density p ex , and extraneous currents with density j ex , these equations arett 1 /YFT divH = 0, curlE = , (85.1) c dt iaiE Att div£E = 47rp ex , curlH = -— + — j ex . (85.2) c ot c In the present case the extraneous charge and current distribution are given by pex = eh{r - \t), jex = ev 8(r - vt). (85.3) t See Quantum Mechanics, formula (121.13). X When a heavy particle collides with an electron, the maximum transferable momentum Hqm&x is small compared with the momentum Mv of the heavy particle. The change in the energy of this particle is therefore v«/jq, and equating this to the electron energy we have H^/lm = fiv«q ^ hvq, whence hqmax. — 2mv, Ei,max = 2mv 2 . |j See Quantum Mechanics, formula (122.10). f t This effect was pointed out by E. Fermi (1940), who performed the calculation for the particular case of a gas whose atoms are regarded as harmonic oscillators. The general derivation given here is due to L. Landau. JJ We put /x(a>) = 1 , since matter does not exhibit magnetic properties at the frequencies important as regards ionisation losses. 350 The Passage of Fast Particles Through Matter §85 We introduce scalar and vector potentials, with the usual definitions : 1 BA H = curlA, E = grad<£, (85.4) c dt so that equations (85.1) are satisfied identically. The additional condition ldty divA + -=0 (85.5) c dt is imposed on the potentials A and <f>; this is a generalisation of the usual Lorentz condition in the theory of radiation. Then, substituting (85.4) in (85.2), we obtain the following equations for the potentials: £ d 2 A 4tt AA "T^i" = --*vS(r-vf), c l ct l c (85.6) We expand A and <f> as Fourier space integrals. Taking the Fourier com- ponents of equations (85.6), we have (cf. §84) £ 8 2 A k ev k 2 A* -\ = exp(- itV'k), / e 8 2 d> k \ e T Vt ' + ^l^) = 2^ exp( -' Yv - k) - Hence we see that A k and <f> k depend on time through a factor exp ( — itv*k). We again put to = k»v = k x v, and obtain e v A k = e~ iu>t , 2rr*c & - w 2 e(a>)/c 2 v ;/ (85.7) e 1 x _ e -i*>t m Y 2tt 2 6(co) & - a> 2 e(oi)/c 2 The Fourier component of the electric field is Ek = io*A k \c — ik<f> k . (85.8) From these formulae the force F = eE acting on the particle is found in the same way as in §84. f Using the same notation, we now have ie 2 a 2 (i-^) <0 * d * d<u (85.9) i'l**^-*)] t The magnetic force ev X H/e is seen by symmetry to be zero, and in any case is per- pendicular to the velocity of the particle and so does no work on it. §85 Ionisation losses by fast particles : the relativistic case 351 As c -> oo this formula tends, of course, to (84.5). Let us first carry out the integration with respect to frequency. In order to effect an integration in the complex o>-plane, we first ascertain the poles of the integrand in the upper half-plane. The function €(o>) has no singu- larity and no zero in this half-plane, and so the required poles can only be the zeros of the expression to*l -q 2 . U 2 W We shall show that, for any value of the positive real quantity q 2 , this expres- sion vanishes for only one value of to. The proof is as follows. Let We consider the integral 1 r df(to) dco 2m J dco f(to) - a! taken along a contour C consisting of the real axis and a large semicircle (Fig. 42). The function f(w) has no pole in the upper half-plane or on the real axisjf the integral in question therefore gives the number of zeros of the function /(o>)- a in the upper half-plane. To calculate its value, we write it as (85.10) 1 f d/ ^ lid J /— a Fig. 42 t For metals e(o>) has a pole at to — 0, but to 2 e always tends to zero with at. 352 The Passage of Fast Particles Through Matter §85 For o} = 0, / = 0. For positive real a> we have im/ > 0, and for negative real o> im/ < 0. At infinity / tends to -a> 2 [(l/s> 2 )-(l/c 2 )], and therefore / goes round a large circle when to goes round the large semicircle. Hence we see that the path of integration C" in the /-plane is of the kind shown in Fig. 42. Let a — q 2 be a positive real number, as in Fig. 42. Then, in going round C", the argument of the complex number/— a changes by 2tt, and the integral (85.10) is equal to unity. This completes the proof, f Furthermore, it is easy to see that this single root of the equation f(<o) — q 2 = lies on the imaginary a>-axis: for purely imaginary <o the function /(eu), like e(o>), is real and takes all values from to oo, including q 2 . Let us now return to the integral with respect to co in (85.9): (J--i), \ ev 2 c 2 / \c 2 V 2 ] This can be written as the difference between the integral along the contour C and that along the large semicircle. The latter is jdco/a) = iir, and the former is 2ni times the residue of the integrand at its only pole. Let a>(q) be the function defined by the equation a>*(— ) = q 2 . (85.11) \ c 2 v 2 l Then, since the residue of an expression f(z)/<f>(%) at a pole z = zq is f(zo)/<l>'(zo), the integral along C is f-L-i) J-i-i) \ €V 2 C 2 / \ eV 2 C 2 J r Vd 2 ~ v 2 ) J 2mi — - — = 2mi- d f J* 1\1 -d? 2 /d dco Collecting these expressions and substituting in (85.9), we have Qo F = e 2 ,(_L-I) \ ev 2 c 2 J q dq/dco + 1 qdq t If a is negative the argument of / — a changes by 4«- on going round C", so that the integral (85.10) is equal to 2, i.e. the function / (<a) + \a\ has two zeros in the upper half- plane. §85 Ionisation losses by fast particles: the relativistic case 353 or, replacing the integration with respect to q in the first term by one with respect to co, p = e 2 f [ 1 o> do> + \e 2 q$ «(0) UQo) 1 = — f [ lLdco + |eV + V 2 J L^w) J -K0) + ¥*(-, - \)[« 2 (<lo) - ^(0)]. (85.12) \ V 1 C l I. Large values of q correspond to large absolute values <o of the root of equa- tion (85.11). Using therefore the expression (84.9) for e(w), we find where we have put j8 = ^[\-v 2 Jc 2 ]. Substitution in (85.12) gives e* iV Tt 1 1 2nN* e 2 B 2 F= 6 - U--lLd«, -^(0); (85.13) v 2 J Le(co) J mc 2 2v 2 in the integral, only the leading term ivqojp need be retained in <o(qo). The integration in (85.13) is over purely imaginary values of a>. We use the real variable co" = to/i, with the lower limit £ = o>(0)/f, and again put 1/e = r) (84.6). The required integral is vqlB - J fo(lV)- l]co"dw". I The values of the function 77(0) on the imaginary axis can be expressed in terms of its imaginary part on the real axis: V (ia>")-1=- f- 77 J X X7)"(X) ax :2 + a/' 2 (cf. (62.17)). Hence the integral is (if we neglect x in comparison with vqo) 2 rf° %"(*)i«>"<w-d« _ 1 ? »y dx w J J *» + »"« ~ » J *™ ( " g W* 2 + « /32(* 2 + fO of 354 The Passage of Fast Particles Through Matter §85 We substitute this result in (85.13), and for simplicity put logQs J log («« + £*), (85.14) where the bar denotes an averaging with weight io\rj" (co)|, as in (84.11). Then inNe* q v 2ttN(A e 2 B 2 F{qo) = ^ logf- — + -tp. (85.15) Two cases must be considered in the further examination of this formula. Let us first suppose that the medium is a dielectric, and that the velocity of the particle satisfies the condition v* < c 2 /e , (85.16) where eo = e (0) is the electrostatic value of the dielectric permeability. On the imaginary axis the function e(a>) decreases monotonically from eo > 1 for co = to 1 for <a = zoo. The expression on the left-hand side of equa- tion (85.11) therefore increases monotonically from to go, and for q = (85.11) gives tu = 0. Thus we must put £ = in (85.15); then Q, becomes the mean atomic frequency d> (84. 1 1), and 4ttA^ 4 r Qov v 2 1 F(qo) = i-logfr-^" • (85-17) For v <^ c this formula becomes (84.12), as it should. The value of qo is such that qo <4 1/a, where a is the order of magnitude of the distances between the atoms (in solids and liquids equal to the dimen- sion of the atoms). In order to extend the formula to higher values of the transferred momentum and energy, it must be "joined" to the formulae of the ordinary theory of collisions, as in §84, but the joining must now be carried out in two stages. First, using formula (84.13), we enter the range of q corresponding to energy transfers large compared with atomic energies but not yet relativistic. Formula (85.17) is unchanged in form, but now involves the S-electron energy H 2 q 2 j2m. Calling this E± f we have 2irNe*[ 2mv 2 Ei v 2 l /f ^,^ F(Ei) =^h^~d- (85 - 18) We can now go on to the relativistic values of E\ by using a formula of relati- vistic collision theory, according to which the stopping power with energy transfer between E' and E' + dE' is (27rNe*/mv 2 ) dE'/E' (85.19) if E' is small compared with the maximum transfer -Ei >m ax compatible with the laws of conservation of momentum and energy for a collision between the fast particle concerned and a free electron. (In the non-relativistic case, this formula is the same as (84.13).) Since the integration of (85.19) §85 Ionisation losses by fast particles: the relativistic case 355 gives a term in log E\ it is clear that formula (85.18) is unchanged in form, and it is therefore valid for all E\ <^ iE^max. The maximum energy transfer to an electron from a heavy particle isf Ex max « 2mv 2 jp 2 . If £i >m ax is small compared with the total energy E of the fast particle (i.e. if ' E <4 M 2 c 2 \m), the differential expression for the energy lost by free electrons is mv 2 \E' 2mc 2 / for all E\ whatever the kind of heavy particle concerned. The energy loss additional to (85.18), with energy transfer from Ex to tfi.max (with E\ <^ .E^max) is then 2^/ ZW /PW\ = ^fl/w 2 ^ _ t_\ (8 5.20) mv 2 I 8 E x 2mc 2 ) mv 2 \ S j8*£i c*/ Adding this to (85.18), we find the total stopping power with respect to the heavy particle : F^^L^-t). (85.21) mv 2 \ pzkcb c 2 } Formulae (85.18) and (85.21) differ from those of the usual theory only in that the "ionisation energy" is hd>. Let us now turn to the second case, namely that where v* > c 2 le , (85.22) which, in particular, always holds for metals, where e = oo. The expression a> 2 ( € /c 2 -l/v 2 ) on the left-hand side of equation (85.11) then has two zeros on the imaginary w-axis, one at o> - and the other at a = i£, where £ is defined by «(#) = c 2 /v 2 . (85.23) In the range from to i£ the expression o> 2 (e/c 2 - 1/v 2 ) is negative, and for | <u | > I it takes all positive values from to oo. As q -> 0, therefore, the root of equation (85.11) in this case tends to £, which is the value to be substituted in (85.14) and (85.15). Two limiting cases may be considered. If | is small compared with the atomic frequencies w , then the last term in (85.15) may be neglected, and Q « cD. Thus we return to formula (85.17). The opposite limiting case, where £ > co , is of particular interest. Since, for large £, the function e(i£) tends to 1, it is evident from (85.23) that this case corresponds to ultra-relativistic velocities of the particle. Using formula (84.9) for e(to), we can write equation (85.23) as l + ^rrNe 2 /m£ 2 = c 2 /v 2 , whence £2 = 47rNe 2 v 2 /mc 2 p 2 « ^Ne 2 \m^ 2 . t See The Classical Theory of Fields, §2-5, Addison- Wesley Press, Cambridge (Mass.), 1951 ; Pergamon Press, London, 1959. 356 The Passage of Fast Particles Through Matter §85 As the velocity of the particle increases, the condition £ > o>o is ulti- mately fulfilled in any medium, i.e. whatever the electron density N (even in a gas). The velocity required is, however, the greater, the smaller N, i.e. the more rarefied the medium. From (85.14) we then have simply Q « £. Putting also v « c, we find that the last two terms in (85.15) cancel, leaving F(q ) = (2irNe*/mc2) log (m^q^/AvN^). Extending this formula, in the same manner as above, to large values of the momentum and energy transfer, we find the following expression for the energy loss of an ultra-relativistic particle with an energy transfer not exceeding E 1 (^ E lmax ): F(Ei) = (2wiVe 4 /»ic a )log(m2ca£ , i/27riVca* 2 ). (85.24) This result is considerably different from that obtained in the ordinary collision theory, which neglects the polarisation of the medium. According to that theory, in the ultra-relativistic range the stopping power F(E{) continues to increase (though only logarithmically) with the energy of the particle. The polarisation of the medium results in a screening of the charge, and the increase in the losses is thereby finally stopped; it tends to the constant value (independent of jS) given by formula (85.24). For heavy particles a formula can also be derived for the total stopping power with any energy transfer up to J5i f max (if the latter is small compared with the energy of the particle itself). Again using the expression (85.20), in which we can now put v = c, we find 27rAfc4 r nPc* 1 = ~lnc2~[ ° g 7rNe 2 h^ ~ } ( • ) We see that the total stopping power continues to increase with the velocity of the particle, owing to "close" collisions with a large energy transfer, for which the polarisation of the medium has no screening effect. This increase, however, is rather slower than that given by the theory when the polarisation is neglected. It may also be noted that the presence of the electron density iV in the argument of the logarithm in formulae (85.24) and (85.25) results in the following property of energy losses of ultra-relativistic particles : when such a particle passes through different substances containing the same number of electrons per unit surface area, the losses are smaller in media with larger N. Finally, we may point out that a measurement of the energy losses of fast particles in matter makes possible, in principle, the determination of the function e(i£j) for the substance concerned. It is easy to show that the exact expression for F for the case (85.22) is such that d(©2) 2c 2 ' v ' §86 Cherenkov radiation 357 where F is the quantity given by formula (85.18) or (85.21). F is measured; the derivative d( J F ^ 2 )/d(^ 2 ) contains only the known quantities N and v, and can be calculated. Thus, using (85.26), each value of £ can be related to a value of v, and the value of e(i£) can then be calculated from (85.23). §86. Cherenkov radiation A charged particle moving in a transparent medium emits, in certain cir- cumstances, an unusual type of radiation, first observed by P. A. Cherenkov and S. I. Vavilov, and theoretically interpreted by I. E. Tamm and I. M. Frank (1937). It must be emphasised that this radiation is entirely unrelated to the bremsstrahlung which is almost always emitted by a rapidly moving electron. The latter radiation is emitted by the moving electron itself when it collides with atoms. The Cherenkov effect, however, involves radiation emitted by the medium under the action of the field of the particle moving in it. The distinction between the two types of radiation appears with particular clarity when the particle has a very large mass : the bremsstrahlung disappears, but the Cherenkov radiation is unaffected. The wave vector and frequency of an electromagnetic wave propagated in a transparent medium are related by k = nw/c, where n = \/e is the refractive index, which is real.f We have seen that the frequency of the Fourier component of the field of a particle moving uniformly in the x- direction in a medium is related to the ^-component of the wave vector by a> = k x v. If this component is a freely propagated wave, these two relations must be consistent. Since k > k x , it follows that we must have v > cjn{w). (86.1) Thus radiation of frequency o> occurs if the velocity of the particle exceeds the phase velocity of waves of that frequency in the medium concerned. Let 6 be the angle between the direction of motion of the particle and the direction of emission. We have k x = k cos 6 = (weo/c) cos and, since k x = <o/v, we find that cos# = c]nv. (86.2) Thus a definite value of the angle 6 corresponds to radiation of a given fre- quency. That is, the radiation of each frequency is emitted forwards, and is distributed over the surface of a cone of vertical angle 20, where 6 is given by (86.2). The distributions of the radiation in angle and in frequency are thus related in a definite manner. f We again suppose the medium isotropic and non-magnetic. The Cherenkov radiation in an anisotropic medium has been discussed by V. L. Ginzburg, Zhurnal eksperimental'noi i teoreticheskot fiziki 10, 608, 1940; A. A. Kolomenskii, Doklady Akademii Nauk SSSR 86, 1097, 1952; M. I. Kaganov, Zhurnal tekhnicheskoi fiziki 23, 507, 1953. A review of various cases in the theory of Cherenkov radiation and an extensive biblio- graphy is given by B. M. BoLOTOvSKii, Uspekhi fizicheskikh nauk 67, 201, 1957. 358 The Passage of Fast Particles Through Matter §86 The emission of electromagnetic waves, if it occurs, involves a loss of energy by the moving particle. This loss forms part, through a small part, of the total losses calculated in §85. f In this sense the name "ionisation losses" is not quite accurate. We shall now find the corresponding part of the total losses, and thus determine the intensity of the Cherenkov radiation. According to (85.9), the energy loss in the frequency interval dto is /e 2 ^ /l 1 \ dF = - dco— > o> 77 ^ \c 2 eW qdq \c 2 v 2 / where the summation is over terms with at = ±|to|. We introduce as a new variable £ = q 2 \c 2 v 2 / Then dF= -dJ~yJ ) f 2tt^ U 2 eW J In integrating along the real |-axis we must pass round the singular point f = (for which q 2 +k x 2 = k 2 ) in some manner, which is determined by the fact that, although we suppose e(w) real (the medium being trans- parent), it actually has a small imaginary part, which is positive for w > and negative for to < 0. Accordingly, $ has a small negative or positive imaginary part, and the path of integration ought to pass below or above the real axis respectively. This means that, when the path of integration is displaced to the real axis, we must pass below or above the singular point respectively. This gives a contribution to dF, and the real parts cancel in the sum. Indenting the path of integration with infinitesimal semicircles, we find Jd|/| = 2/7 Thus the final formula is e 2 l c 2 \ dF = - l-- T Udto, (86.3) which gives the intensity of the radiation in a frequency interval dto. According to (86.2), this radiation is emitted in an angle interval c dn d0 = . dto. (86.4) vn 2 sin 6 dco f The bremsstrahlung is not included therein. Rg6 Cherenkov radiation 359 The total intensity of the radiation is obtained by integrating (86.3) over all frequencies for which the medium is transparent. It is easy to determine the polarisation of the Cherenkov radiation. As we see from (85.7) the vector potential of the radiation field is parallel to the velocity v. The magnetic field 1^ = ikx\ is therefore perpendicular to the plane containing v and the ray direction k. The electric field (in the "wave region") is perpendicular to the magnetic field, and therefore lies in that plane. In connection with our discussion of the radiation emitted by a particle moving in matter, we may mention another effect whose existence has been deduced by V. L. Ginzburg and I. M. Frank: a particle must emit radiation on passing from one medium to another. This "transition" radiation is in principle different from the Cherenkov radiation, in that it must occur for any velocity of the particle, not necessarily exceeding the phase velocity of light in the medium. It is also unrelated to the bremsstrahlung which also occurs when charged particles are incident on a surface separating two media. As with Cherenkov radiation, the distinction is particularly clear for a particle of infinite mass, for which the bremsstrahlung is zero but the transition radiation is not. f t A simple derivation of the formulae for the transition radiation is given by G. M. Garibyan, Zhurnal eksperimentaVnoi i teoreticheskoi fiziki 33, 1403, 1957; Soviet Physics JETP 6 (33), 1079, 1958. 24 CHAPTER XIII ELECTROMAGNETIC FLUCTUATIONS §87. Current fluctuations in linear circuits We may apply the general theory of fluctuations f to the interesting problem of current fluctuations in linear electric circuits, first considered by H. Nyquist (1928). The current fluctuations are free electrical oscillations in the conductor (i.e. they occur in the absence of any externally applied e.m.f.). In a closed linear circuit the oscillations of greatest interest are, of course, those in which a non-zero total current J flows in the conductor. In what follows we shall assume that the condition for a quasi-steady state holds : the dimen- sions of the circuit are small compared with the wavelength A ~ cjto. Then the total current J is the same at every point in the circuit, and is a function of time only. In order to find the spectral resolution of the current fluctuations, we take / as the quantity x which appears in the general formulae of SP §124. In order to ascertain the corresponding meaning of a, let us suppose that an external e.m.f. <f acts on the circuit. Then the rate of dissipation of energy in the circuit is Q = J $ . A comparison with SP (124.7) shows that/ = — <f, or, if in this linear relation we take / and & proportional to e- i<ot , $ = io>f. But the current and the e.m.f. in a linear circuit are related by $ = ZJ, where Z(<o) is the impedance of the circuit; see §47. Hence / = 6\Z = iwf/Z, whence we conclude that <x(a>) = ta>/Z(a>). Its imaginary part is a" = im (twJZ) = ojR/\Z\ 2 , where R(w) = re Z(a>). The formulae below do not depend on the particular nature of the phenomena which result in the dispersion of the circuit resistance. From SP (123.8) we now find for the required current fluctuations hco hco ■ ^ = 2tt|Z| 2 COt 2T' This formula can be written in another form by regarding the current fluctuation as the result of a "random" e.m.f. S m = Z(w)J 0) . This is given by tioi hixi ,„„ „ v 0^ = — -#( w )coth-— • (87-2) Lit Ll t See Statistical Physics, §123, Pergamon Press, London, 1958. Sections and formulae in this book will be referred to by means of the prefix SP. 360 §88 Electromagnetic field fluctuations 361 In the classical case (hw <4 T) we have (**). = TR{a>)l>*. (87.3) §88. Electromagnetic field fluctuations The electromagnetic quantities E, H, . . . which appear in macroscopic elec- trodynamics are obtained by an averaging process, which can be regarded as consisting of two operations. If we take, for clarity, the classical view, then we have the averaging over a physically infinitesimal volume, the particles in that volume being in fixed positions, followed by the averaging with respect to the motion of the particles. In considering electromagnetic fluc- tuations we are concerned with the oscillations in time of quantities averaged over physically infinitesimal volumes, and the quantities discussed below will be of this kind. It should be noted that, if we take the quantum view, we can consider the volume average of the operator of a quantity, but not that of the quantity itself, and the second stage in the averaging consists in determining the expectation value of this operator by the use of quantum probabilities. Strictly speaking, therefore, the quantities E, H, . . . mentioned below should be regarded as operators of quantum mechanics, but this does not affect the final results, and to simplify the formulae we shall regard E, H, . . . as classi- cal quantities. As a result of fluctuations in the position and motion of the charges in a body, spontaneous local electric and magnetic moments occur in it; let the values of these moments per unit volume be respectively K/4rr and L/47T. They are in a sense analogous to the spontaneous polarisation of pyroelec- trics and the spontaneous magnetisation of ferromagnetics, but of course differ in that they give zero on averaging. The relation between the induc- tion and the field for these electric and magnetic fluctuations is given by Di = etkEjc + Ku Bi = (LiicHjc + Li, (88.1) and their "Fourier components" are Di(o = e«fc(">)-Ek> + Kia,, Bia = IHki^Hjca + Liu. Maxwell's equations are (curlEJ* = (ia>/c)(fi ik H]ca, + L io} ), (88.3) (curlHJf = - (ia>lc)(e ik E km + Ku,). (88.4) We call K and L the extraneous fluctuating inductions, but this name is, of course, conventional and refers to the way in which these quantities are formally defined rather than to their physical nature. In order to use the general formulae derived in SP §124 we must establish the relations between the electromagnetic quantities under consideration and 362 Electromagnetic Fluctuations §88 the quantities x a , f a which appear in the general theory. This is done as follows. We suppose, in a purely formal manner, that the quantities K and L are not spontaneously arising moments but the result of an external action, namely the placing of certain extraneous electric charges and currents in the body, and calculate the consequent change in the energy of the body. To do this we observe that the equation of conservation of energy, in the form which follows from Maxwell's equations, is / 1 ( dD dB\ c • — »E + H \dV= (fcExH-df, M dt dt I 4tt ^ or, substituting from (88. 1), f 1 ( d d \ J U E % { * ikEk) + H *dP aHk) ) r 1 ff 1 dl.\ J)ExH.df E + H-— \dV. J 4vr J \ dt dt) c Hence we see that the change in energy due to the "external action" con- sidered is E 3 + H 3) dF . (88.5) at H) -=/( In SP §124 we considered a discrete series of fluctuating quantities x a , whereas here we have a continuous series (the values of the fields at every point in the body). We shall evade this unimportant difficulty in a purely formal manner, by dividing the volume of the body into small but finite portions AF and taking some mean values of the fields in each portion; the passage to infinitesimal portions will be made in the final formulae. Thus the integral in (88.5) is replaced by the sum 1 W_ dK __ SL 4^ f dK dL) r E + H-— AK, I dt dt taken over all the portions AV. Comparing this expression with SP (124.7), we see that, if the x a are taken to be the components of the vectors EAF/4tt, HAF/4tt in each portion AV, then the corresponding f a will be the components of the vectors K and L: ^^EAF/477, HAF/47T; The relations SP (124.11) f ao) = S <x.- 1 ab{o))x b(l)y (88.7) b §88 Electromagnetic field fluctuations 363 which give the relation between/ w and # w , correspond to Maxwell's equations (88.3), (88.4), and so we have K ib) = - e m E kb) + (*V/o>)(curlH w ) f , Liu = - WkHk» ~ (ic/coXcurlEJ,. The coefficients or\ b are found by comparing (88.8) with (88.7), using the definitions (88.6) ; the suffixes a and b denumerate both the components of the vectors E, H and the portions AV. The curl operators in (88.8) are to be regarded as difference operators, defined with respect to a discrete set of points (say the centres of the portions AV). The actual form of these operators is, however, of no importance, since it is here sufficient to note that the operators acting on H w and E w in (88.8) are purely imaginary and differ only in sign. This means that the relations a -1 ,* = (orha)* are satisfied by the coefficients a -1 ^ which relate the values of K and L at a given point to those of H and E respectively at various points. According to the general formula SP (124.12) it therefore follows at once that {K tl L K ) m = 0, (88.9) where the suffixes 1 and 2 signify that the quantities are taken at the points ri and r 2 respectively. Formula (88.9) is valid whether ri = r 2 or not. Next, from the first equation (88.8), using (88.6), we see that the coefficients ar^a which relate K io) and Ejc w are -e ik 4tt/AV if K w and E w refer to the same point in space, and zero otherwise. By SP (124.12) we therefore have (KaKn). = (n # r 2 ), (KtKjc^ = ih(ctt* - ^)-^r coth(hojj2T). Passing now to the limit AV -> 0, we can evidently write both these formulae together as (KaKn) m = ih{e ki * - €«) S(r 2 - n) coth (ha>/2T), (88.10) where ri and r 2 refer to any two points in the body. In what follows we shall assume that the body is not in an external magnetic field. Then e^ = e k i, and (88.10) can be written (KaKn) m = 2WS(r 2 - n) coth(feo>/2T). (88.11) In an entirely similar manner we may derive the formula (LaL M ). = lh m " S(r 2 - n) coth (hco/2T). (88.12) Thus the fluctuations of the "extraneous" inductions at two points in the body are correlated only in the limit when the two points coincide (r 2 -> ri). This limit, of course, must be taken in the macroscopic sense, and the above statement really means that the correlation extends only to distances 364 Electromagnetic Fluctuations §88 comparable with the dimension of the atoms. It is most important to observe that the correlation formulae for the extraneous inductions do not depend on the shape of the body ; in this sense the formulae are universally valid. Formulae (88.11) and (88.12) can be put in another form for fairly low frequencies (the quasi-static range), when the tensor e^ can be expressed in terms of the constant (frequency-independent) conductivity tensor ai k by *ik — 4-7rt(T{fc/a>. (88.13) We then introduce the quantity j = (l/47r)dK/*fr, or j w = - ioKJ4ir. (88.14) The significance of this quantity is seen from the resulting form of equation (88.4): (curlHJ« = {^jc){a ik E kb) +ju,). (88.15) From this we find that the total fluctuation of the current density is at k E k +ji, so that the vector j is the "extraneous" current which is not related to the electric field E. For frequencies at which (88.13) holds and not too low temperatures we have T > h<o, so that coth (hwjlT) « 2T/ha>. Formula (88.11) thus becomes GW«). = (TMa ik S(r 2 - n). (88.16) Formula (88.16) was derived, in another manner, by M. A. Leontovich and S. M. Rytov (1952), and formulae (88.11) and (88.12) by S. M. Rytov (1953). Together with equations (88.3) and (88.4), these equations in prin- ciple solve the problem of calculating the electromagnetic fluctuations in any body. The solution proceeds as follows. Regarding K w and L w as known functions of the co-ordinates, we solve equations (88.3), (88.4) for E w and H w , taking into account the appropriate boundary conditions: the tangential components of E w and H w are continuous at the surface of the body (outside the body, of course, K = L = 0, but E and H are not zero). We thus obtain E w and H w as linear functionals of K w and L w . Accordingly, any quantity quadratic (or bilinear) in E w and H w can be expressed in terms of quadratic functionals of K w and L w , and the mean values are calculated from formulae (88.11), (88.12); K w and L w do not appear in the final result. As an example, let us consider electromagnetic fluctuations in an infinite isotropic medium (S. M. Rytov, 1953). We assume the magnetic per- meability of the medium to be unity. Then p" = 0, and we must put L = also. Thus equations (88.3) and (88.4) become curlE w = io)UJc, curlH w = - /a>(eE w + KJ/c, (88.17) and (K a K k2 ) u = 2»c"a«8(i* - ri) coth(ha>l2T). (88.18) §88 Electromagnetic field fluctuations 365 We write K w as a spatial Fourier integral: K w (r) = J g w (p) exp(/p.r)dp. (88.19) —oo Then 00 gJP) = ^f\ K-M exp( ~ /p * r)dr ' —oo g/(P) = g-i-P)- Let us determine the correlation function for the components gjp). To do so, we write the product gtMgkAp') ^ a double integral: giMgkofip') 00 00 = 7^ f f ^ari)^^(r2)exp[-/(p.ri + p'.r 2 )]dridr 2 . (2tt) 6 J J —oo —oo Averaging by means of the formula K i<0 {ri)K kb ,(r 2 ) = (K a K k2 )J(co + a/), substituting (88.18) and effecting the integration over either n or r 2 , we obtain, on account of the factor S(r 2 -ri) in the integrand, giMg*o>(P') = 2fte"8(a> + a/) 3a; coth(ka>l2T) x (2*) or, finally, 00 exp [ - i(p + p') «r] dr (277)6 J FL ^ V) J giMgic^l = -r*"ZacK«> + ")S(P + P') coth(^co/2T). (88.20) 47T 5 Equations (88.17) may be solved by Fourier's method. As well as repre- senting K w as the integral (88.19), we put 00 E w = Ja(p)exp(/p-r)dp, —oo 00 H w = - J p X a exp (*p-r) dp. 366 Electromagnetic Fluctuations §88 Then the first equation (88.17) is satisfied, and substitution in the second equation gives px(pxa) = — A 2 (ea+g), whence a = [k*eg - (p-g)p]/<£ 2 - €#). Using this expression and formula (88.20), we obtain for the correlation of the Fourier components of the electric field he" hco atjpfajp') = 3(p + p')S(o> + to') coth — x &\e\* h ilc -p iP lc [k\*+e*)-p*] x . (88.21) Finally, the spatial correlation of the fluctuation of the electric field is obtained by inverting the Fourier transformation: Efa(ri)£*,*(ra) 00 00 = j / %(p)«^(p') exp |>'(p-ri + p'-r 2 )] dp dp'. —oo —oo One integration can be effected immediately, because of the delta function in (88.21). To carry out the second integration we must expand (88.21) in partial fractions, and then use the formulae oo J exp(»p.r) dp = 2 y- —oo p^exp(sp.r) = _ 2j7 , g2 ( e - Kr \ J p* + k* dxidxjc \ r J —oo The first of these is obtained by taking the Fourier component of the well- known relation e -KT ( A _ K 2) = _ 4^S( r ), (88.22) r and the second by differentiating the first. The result is h hut i k? (EnEtt^ = — coth-- — (e-^-e - e -*r<-e* )8ik + 47« 21 { r + — ?!_[l( e * c -fcrv- e _ ce -*rV-e*)l I (88.23) lei 2 dxidxjc Yr j) §89 Black-body radiation in a transparent medium 367 where r = |r 2 -ri|, and the root y/-c is taken ^^ ihe "S 11 for which reA /- e > 0. In particular, contracting with respect to the suffixes i and k and using the relation (88.22), we find (El .E 2 ) w = A cothgl^^rv- _ e -*rv- e *) + S(r)j. (88.24) We can similarly calculate the correlation of the various components H w , both among themselves and with the E w , but shall not pause to do so here. §89. Black-body radiation in a transparent medium The presence of the factors e" and /*" in formulae (88.11) and (88.12) emphasises the relation between electromagnetic fluctuations and absorption in a medium. If we take the limit as e" -» (with e > 0) in formulae (88.23) and (88.24), the result is not zero. This arises from a difference in the order of passage to two limits, those of infinite medium and zero e". Since, in an infinite medium, any non-zero value of e", no matter how small, causes absorption, the result obtained by passing to the limits in our order pertains to a transparent medium in which, as in any actual medium, there is in fact some absorption. For example, let us find the limiting form of formula (88.24). To do so, we note that, for small e", y/-e = V(- € '-*' e ") * -W € '( l + ¥*"/*), V~ € * = ^/(_ e ' + tV') &iy/€'{\-\U"le). The choice of signs is determined by the condition that the real part should be positive. In the limit e" -> 0, therefore, co 2 h sin comic . hw (Ei-Ea). = — coth— , 7TC 2 r 11 where n = -yA * s ^ refractive index. Since there is no delta-function term, this expression remains finite when ri = r 2 : (E2) w = (cu3^«/ttc3) coth(ha>l2T). (89.1) The spectral density of the electric field energy per unit volume is (cf. (61.10) and SP (118.6)) 1 d(« 2 co) -2(E2) W -1_^. 57T ClCU Substituting (89.1), we have ufihn d(w 2 co) hoj coth- 4tt 2 c3 do> IT 368 Electromagnetic Fluctuations §90 The mean square of the magnetic field can be calculated similarly. It is found that (H 2 ) w = e(E 2 ) w , and so the magnetic energy is 1 o) z hn z hco — 2(H 2 ) W = coth . We shall not give the detailed calculations here, since the final result which is obtained below is in any case obvious. Thus the total spectral density of the electromagnetic energy density in the fluctuation fields is co z h l d(» 2 a>) \ h (d^co) \ hat n h n z I coth dco J IT hco \ co 2 n 2 d (Hco \ coW d hhco H ) (nco). The first term in the parentheses relates to the zero-order oscillations of the field; the second term gives the energy of thermodynamic-equilibrium electromagnetic radiation in a transparent medium (i.e. the energy of black- body radiation) : hco co 2 n 2 d — (nco). (89.2) e h<o/T _ 1 ^2^3 dco This formula could also be obtained, without considering fluctuations, by an appropriate generalisation of Planck's formula for black-body radia- tion in a vacuum. According to this formula, the energy of black-body radia- tion per unit volume having wave-vector components in an interval dk x , dky, dk z is hco 2dkxdkydk z e*»l T - 1 (2^)3 * the factor 2 arises because of the two directions of polarisation. To obtain the spectral energy density, we must replace dk x dk y dk z by 4irA 2 dk and substitute k = cojc. To go from a vacuum to a transparent medium it is sufficient to put k = nco/c instead of k = to/c, i.e. k 2 dk = k 2 (dk/dco) dco = (afinZjc 3 ) d(nco)fdco, which gives formula (89.2). It should be noted that this formula remains valid even if p ^ 1, provided that n is interpreted as §90. Forces of molecular attraction between solid bodies The theory of electromagnetic fluctuations can be used to calculate the forces of interaction between any two macroscopic bodies whose surfaces are a very short distance apart (E. M. Lifshitz, 1954). In what follows we assume only that this distance is large compared with those between the atoms. In this case the problem can be treated macroscopically. §90 Forces of molecular attraction between solid bodies 369 We may consider the interaction between bodies as resulting from the fluctuations of the electromagnetic field which always occur in an absorbing medium and also outside it. If the space between the surfaces is a vacuum, this means of interaction is evidently the only one. Let us regard the interacting bodies as two media occupying half-spaces with plane parallel boundaries at a distance / apart. The fluctuations of the electromagnetic field in the two media and in the space between them can be found by solving equations (88.17)f with the appropriate boundary condi- tions (continuity of the tangential components of E w and HJ at the two surfaces. The solution is most conveniently effected by expanding the required functions (and the quantity K w ) as Fourier integrals with respect to the transverse co-ordinates y, z (the #-axis being normal to the surfaces) ; this gives a system of linear inhomogeneous ordinary differential equations to determine the fields as functions of x. Solving these equations, we obtain integral expressions for E w and H w , whose integrands contain the "external" fluctuation fields Ki w and K 2w in the two media. Actually, it is sufficient to obtain the explicit forms of E w and H w in the space between the media, since the mutual attraction force F w per unit area of either surface can be calculated as the ^-component of the Maxwell stress tensor, statistically averaged in accordance with formula (88.18). Since the calculations involve only the spectral components of the fields, the required total attraction force F must be obtained by integrating F w over all frequencies .% The calculations are somewhat laborious; we shall not go through them here, but give only the final result. The force is|| f T ha)l[(si+ p)(s2 + p) at , A pafi coth —J ; F {) ^ er*tP" /• - 1 + J J F 2T\Y{ Sl -p){s2-p) J + \(*i + *iP)^+<*P) e - 2ip „ l/e _ {\ - 1 ) dp d(x)> (9 o.!) L(s 1 -e 1 p)(s 2 -€2p) J ) where ei(<o), e 2 (to) are the dielectric permeabilities of the two media, and *i = #iH - 1 +P 2 l *2 = VM*>) - 1 +p*], (90.2) the signs of the roots being taken so that the imaginary parts of *i and $2 are positive, ff The paths of integration are shown in Fig. 43a. The integra- t The magnetic permeabilities of the two bodies are assumed to be unity. X The value of F M resulting from the calculation includes a term which diverges on integration with respect to <o. This term, however, is independent of I, and represents the pressure exerted on the surface by the black-body radiation in the vacuum. In an actual problem these forces act on all sides of a body and cancel out, so that the term in question does not relate to the mutual attraction under consideration, and must be omitted. || SeeE. M. Lifshitz, Zhurnal eksperimental'noi i teoretichesko! fiziki 29, 94, 1955; Soviet Physics JETP 2, 73, 1956. . 1 1 Since the imaginary part of the radicand (e") is positive, im s > implies re s > 0. 370 Electromagnetic Fluctuations §90 tion with respect to to is over real values from to oo ; that with respect to p is along the real axis from 1 to 0, and thence along the imaginary axis to «oo. If the temperature of the bodies may be taken as zero (see below), cotti(hco/2T) in (90.1) is replaced by unity. We shall begin by discussing formula (90. 1) for this particular case. (a) © ® (b) © ® (0 ® Fig. 43 Both the complex form of (90.1) and the appearance of the expression g-Zipai/c^ which oscillates on the real part of the path of integration with respect to p, are inconvenient. The latter fact, in particular, hampers the calculation of the integral for large values of /, when the oscillation becomes very rapid. This difficulty can be removed by appropriate changes in the paths of integration in the planes of the complex variables a> and/> : they must be displaced in such a way that the integration with respect to p is taken over only real values, and that with respect to a> over only imaginary ones (Fig. 43b). Then the exponent —lipwljc is always real. f The result is the following expression for the interaction force (when T= 0): F = 2ttW J J F \1(S1-P)(S2-P) J 1 (S1-P)(S2~P) if\ + (si + eip) (s 2 + € 2 p) L(*l - ev (*1 ~ cip) (S2 ~ €2p) e 2pUc -I ] 'jd/^. (90.3) f This transformation is permissible if there is some way of simultaneously displacing both paths without passing through a pole of the integrand. A detailed investigation, using the properties of the function e(a>) given in §62, shows that this is so. §90 Forces of molecular attraction between solid bodies 371 Here we have put a = % for imaginary co; ei and e 2 denote the real functions €i(/£) and € 2 (t£). The sign re has been omitted, since the expression (90.3) is evidently real. This formula makes possible, in principle, a calculation of the force F for any distance I if the functions e(*|) for the two bodies are known. These functions can be expressed in terms of the imaginary part of e(a>) for real o>, by formula (62.17). Thus we can say that the law of interaction of the bodies is entirely determined when the functions e"(w) in them are given. Let us consider the limiting case of distances / which are small compared with the wavelengths A of greatest importance in the absorption spectra of the bodies. The temperatures which occur in solids and liquids are always small compared with the important values of ho) ~ hwo (where a>o ~ 27rc/Xo). Hence we can assume that T = and use formula (90.3). On account of the exponentially increasing factor e 2 ^ l/c in the denomina- tors in the integrand, the main contribution to the integral with respect to p comes from values such that p£ljc ~ 1. Then p > 1, and hence we can put 5i « S2 « p in determining the leading terms. In this approximation the first term in square brackets in (90.3) is zero. The second term gives F = h ?? * 2 d*d| (9Q4) I6772/3 m&" where the new variable of integration x = 2pgl/c, and the lower limit of integration 2£ljc has been replaced in this approximation by zero. Formula (90.4) gives the force of attraction in the limiting case of small /. It is inversely proportional to the cube of the distance. The function e(*'£) — 1 decreases monotonically to zero with increasing £. Values of $ exceeding some go therefore make no important contribution to the integral ; the condi- tion for / to be small is / <^ c/|o- We shall show how the passage to the limit of the interaction between indi- vidual atoms is made in (90.4). To do so, we formally assume both media to be so rarefied that the differences ei- 1 and e%— 1 are almost zero, and(90.4) gives with sufficient accuracy F = 64t7 2 /3 00 00 j J *V-*(ei - l)(e 2 - l)dtf d| OD = 32^ J t^-™' 1 ^- 372 Electromagnetic Fluctuations §90 Expressing €(ii-) in terms of e"(a>) on the real axis by (62.17) we obtain 00 oo oo oo coia)2ei"(a>i)e 2 "(a> 2 ) a£ atuidco2 -Jill ("l 2 + | 2 )("2 2 + £ 2 ) oo oo 2 f f ei"(a)i)e 2 "(w2) acuiaa)2, -:// a>i + OJ2 and the force F is 00 00 16tt3/3 f f " N " (Ma V j^ (90.5) J J Ct»l + C02 The force of interaction between rarefied media may be regarded as the resultant of the interactions between pairs of molecules. Then the force (90.5) corresponds to an interaction of molecules with an energy which depends on the distance jR between them: 00 00 V = 3 JL- f f 1^M^l dwidw2 , (9 o. 6) where N is the number of atoms per unit volume. Formula (90.5) is obtained from this by integration over the two half-spaces separated by a gap of width /, followed by differentiation of the total energy with respect to /. Formula (90.6) is the same as that derived by F. London by applying the ordinary perturbation theory of quantum mechanics to the dipole interaction between atoms. In making the comparison, it should be borne in mind that e"(w) is related to the spectral density of "oscillator strengths" /(a>) by (62.13). The oscillator strengths are expressed, in the usual manner, in terms of the squared matrix elements of the dipole moment of the atom. Thus we see that the microscopic formula can be derived from the macro- scopic theory. Let us now consider the opposite limiting case, where the distance / is large compared with the wavelengths Ao which are of greatest importance in the absorption spectra of the bodies. The temperature will at first be sup- posed zero, as before. §90 Forces of molecular attraction between solid bodies 373 In the general formula (90.3) we again introduce as a new variable of integration x = 2p$lc, but leave p instead of £ as the second variable : F = Jl. f p*fr fr + *>fr + *W i"r+ 32tt2/4 J J pA L(*i - />) (*a - *) J o l r(*i + nP)(*2 + «?f)^_ n * L(*l - €lp) (S2 ~ Vp) J ' e = e(ixc/2pl), S = y/Wixcftpl) - 1 + /> 2 ]. On account of the factor e* in the denominators, the important values of x are - 1, and, since p > 1, the argument of e is almost zero (for large /) throughout the important range of values of the variables. We can there- fore replace ei and c 2 by their values for to = 0, i.e. the electrostatic dielectric permeabilities, which we denote by eio and € 20 . For metals, the function €(co) tends to infinity as <o -> 0, and so e = oo. Thus we have finally he r° r°V j T (sio + p)(s2o+p) gX _ J F = M J J p* \[{sio -P){S20-P) 6 J -1 + i + [-(no + *ioj>)(*2o + wP^A- 1 }^^ (9 o.7) L ($10 - n0^)(*20 - €20/>) J ) S10 = V(«10 - 1 + P 2 \ 5 20 = \/( e 20 ~ 1 + P 2 )' Here the force of attraction is inversely proportional to Z 4 . It is noteworthy that, in this limiting case, the force depends only on the electrostatic dielec- tric permeabilities of the two media. Let us consider some special cases. A particularly simple result is obtained when both media are metals. Putting in (90.7) eio = e 2 o = 00, we find fc [ F x* d P dx = fc^_ (90 gv 167r2/4j J /*(«*- 1) Z 4 240* 1 This force is independent of the kind of metal concerned (a property which ceases to hold at small distances, the interaction then depending on the values of €(/£) for all £ and not only for | = 0).t t Formula (90.8) had previously been derived in another manner by H. B. G. Casimir (1948). 374 Electromagnetic Fluctuations §90 For two media of the same dielectric (eio = €20 = eo), numerical integration of (90.7) gives he 7T 2 / eo — 1 \ 2 F = 1 P 240\ € + 1 r (90.9) where <£(eo) is a function shown graphically in Fig. 44. 06 0-6 w° 0-4 02 0-2 0-4 Fig. 44 0-6 0-8 Finally, we can make the transition in formula (90.7) to the case of inter- action between individual molecules. As previously, we assume the two media to be so rarefied that the differences eio — 1 and €20 — 1 are small. Retaining only the first non- vanishing term in an expansion of the integrand in (90.7) in powers of these differences, we obtain 00 00 he r f 1 - 2/> 2 + 2/> 4 F = X?e~*dx — d/>(eio - l)(e 20 - 1) or he 23 F = ( ei0 - l)( €20 - 1). This force corresponds to a molecular interaction with energy 23/*c (eio - l)(f20 - 1) 23hc U = 647r3#7 N^ 4ttR7 aia 2 , (90.10) (90.11) where ai and cx.2 are the static polarisabilities of the two molecules. This formula is the same aS that obtained by H. B. G. Casimir and D. Polder §90 Forces of molecular attraction between solid bodies 375 (1948), using quantum methods, for the attraction between two molecules at a large distance apart, when the delay in interaction becomes important. To obtain formulae which take account of the temperature we return to the initial expression (90. 1) and see how the transformation which for T = leads to (9.0.3) must be modified when T ^ 0. The function coth (hwjlT) has an infinite number of poles on the imaginary axis, at the points con = Hn = 1™Tn\K (90.12) where n is any integer. When the path of integration with respect to w is moved on to the imaginary axis, therefore, it must be indented by semicircles at these poles, and by a quarter-circle at a> = (Fig. 43c). This gives rise to contributions to the real part of the integral, equal to in {^iri for n = 0) times the residues of the integrand at the poles. The integration along the imaginary axis between the poles gives only imaginary quantities, which do not affect the real part. Thus we have 00 "* ^=0 J U (il. " P)(S2n - P) J + r(i. + i^X*. + ^P\mniic -\VW (90.13) Y{sin - *lnp){s2n — ^2np) J J % = V( e n - 1 + p% en = e(*fn). The prime indicates that the term with n = is halved. As T -> 0, the distances between the poles tend to zero, the summation over n can be re- placed by an integration with respect to £, and we return to formula (90.3), which does not involve T. Whereas, in the limiting case of small distances, the temperature can always be taken as zero in determining the interaction force, at large distances the effect of the temperature may be considerable. The characteristic tem- perature for a distance / is hcjl, and the condition for T to be negligible is, roughly, lT\hc <^ 1. At sufficiently low temperatures this condition is compatible with / > A , but at high temperatures the two conditions may be contradictory, and the limiting form (90.7) is then never applicable. Let us consider the limiting case of distances so large that IT J he > 1. Then only the first term in the sum in (90.13) need be retained. We cannot at once put n = 0, however, because an indeterminacy results: the factor i n z is zero, but the integral with respect to p diverges. This difficulty may be circumvented by replacing p by a new variable of integration x = 2p£ n l/c (the factor £ n 3 being thereby removed). Putting now n = we obtain F = 16ttP o 00 [4 ( " +lfa + 1) .-ll"V (90.14) J L(cio-l)(«ao-l) J 25 376 Electromagnetic Fluctuations §90 Thus, at sufficiently large distances, the force of interaction decreases less rapidly and returns to the l// 3 law, with a coefficient which depends on the temperature and on the static value of the dielectric permeability. The re- maining terms in the sum (90.13) all diminish exponentially when IT/hc is large. CHAPTER XIV SCATTERING OF ELECTROMAGNETIC WAVES §91. The general theory of scattering in isotropic media In the theory of propagation of electromagnetic waves in transparent media discussed in Chapters IX-XI, a phenomenon has been neglected which, though not prominent, is of fundamental importance : scattering. Scattering results in the appearance of scattered waves of small intensity, whose fre- quencies and directions are not those of the main wave. Scattering is ultimately due to the change in the motion of the charges in the medium under the influence of the field of the incident wave, resulting in the emission of the scattered waves. The microscopic mechanism of scattering must be investigated by quantum methods, but this investigation is not needed in developing the macroscopic theory described below. We shall therefore give only some brief remarks on the nature of the processes which cause the change in the wave frequency on scattering. The basic scattering process consists in the absorption of the original quantum ho> by the scattering system and the simultaneous emission by that system of another quantum hat'. The frequency to of the scattered quantum may be either less or greater than <o ; these two cases are called respectively Stokes scattering and anti-Stokes scattering. In the former case the system absorbs an amount of energy h((o — a/); in the latter case it emits h(<o' — <o) and makes a transition to a state of lower energy. In the simple case of a gas, for example, scattering takes place at individual molecules, and the change in frequency may be due either to a transition of the molecule to another energy level or to a change in the kinetic energy of its motion. Another kind of process occurs when the primary quantum hto remains unchanged but causes the scattering system to emit two quanta: one of energy h<o, with the same frequency and direction, and a "scattered" quan- tum hoi . The energy h(to+u>') is obtained from the scattering system. Processes of this type, however, are, under ordinary conditions, very rare in comparison with those of the first type, and are of little importance as regards the phenomenon of scattering, f Proceeding now to consider the macroscopic theory of scattering, we must first make precise the meaning of the averaging processes performed in that theory. As already mentioned at the beginning of §88, the averaging of quantities in macroscopic electrodynamics can be regarded as comprising f We shall see in §92 that this stimulated emission is unimportant at all temperatures T <^ H(a>+ <a). It may become significant for radio waves. 377 378 Scattering of Electromagnetic Waves §91 two operations, that of averaging over a physically infinitesimal volume with a given position of all the particles in it, followed by that of averaging the result with respect to the motion of the particles. In the theory of scatter- ing, however, this procedure is impossible, because the averaging with respect to the motion of the particles annuls the very phenomenon which is to be discussed. Thus (e.g.) the field and induction of the scattered wave which appear in the theory of scattering must be taken to be those resulting from the first averaging only. The single-frequency components of the fields in the scattered wave, taken in this sense, will be denoted in this section by E\ H', D' and B'. The fields in the incident wave will be denoted by the unprimed letters E, H. In the present chapter we always suppose the incident wave to be of a single frequency w. In the propagation of the scattered wave we have the relation D' = e(o/)E' between the electric induction and field (the scattering medium being assumed isotropic), but this relation does not reveal the phenomenon of scattering, i.e. the formation of the scattered wave from the incident wave. To describe this, additional small terms must be included in the expression for D'. In the first approximation, these terms must be linear in the field of the incident wave. The most general form of the relation is then. D'i = e'EU + a. ik E k + PaEjc*. (91.1) Here e denotes e(o/); on k and jS^ are tensors which characterise the scatter- ing properties of the medium. In general they are not symmetrical, and their components are functions both of the frequency to of the scattered wave and of the primary frequency w. f The last term in (91.1) pertains to the part of the scattering which results from processes of stimulated emission. All the terms on the right-hand side of equation (91.1) must correspond to the same frequency a> as D on the left-hand side. Since E* has the frequency — w, the frequency of the quanti- ties fiijc must be cj + oj' to make the frequency of the products Pi k E k * equal to o>' . But co + <o' is the frequency which characterises processes of stimulated emis- sion. Because this effect is small, as mentioned above, we can neglect the corresponding term in (91.1), and in what follows we shall write D'i = e'E'i + * ik E k . (91.2) Similar formulae give the relation between B' and H'. We shall, however, neglect the magnetic properties of the medium, which are usually of no importance as regards the scattering of light, and therefore put B' = H'. Maxwell's equations for the field in the scattered wave are curl E' = ito'H'/c, curl H' = — ico'D'/c. Eliminating H' from these equations, we f The fact that a and /? are tensors does not, of course, contradict the assumed isotropy of the medium. Only the fully averaged properties of the medium are isotropic; the local deviations from the average properties, which include the additional terms in (91.1), need not be isotropic. §91 The general theory of scattering in isotropic media 379 find curl curl E' = a>' 2 D'/c 2 . Substituting from (91.2) E' = D'/e'-a-E/e', where a«E denotes the vector whose components are a^&> and using the equation div D' = 0, we obtain for D' the equation AD' + &' 2 D' = - curl curl (a- E), (91.3) where k' = oi^/e'jc is the wave number of the scattered wave. For an exact formulation of the conditions under which equation (91.3) is to be solved, we divide the scattering medium into small regions (whose dimensions are still large compared with molecular distances). On account of the molecular nature of the scattering processes, their correlation at dif- ferent points in the medium (assumed non-crystalline) extends in general only to molecular distances, f Hence the scattered light from the various regions is non-coherent. We can therefore treat scattering from one region as if the light were not scattered at all in the remainder of the medium. In this way we calculate the field of the scattered wave at a large distance from the scattering region. Using a well-known approximation for the retarded potentials at a large distance from the source,* we can immediately derive the required solution of equation (91.3): D' = Icurlcurl ^^^ f oc-E exp(- zk'.r)dF. (91.4) 4-tt Ro J Here Ro is the radius vector from some point within the scattering volume (the integration being over that volume) to the point where the field is to be calculated; the vector k' is in the direction of Ro. The integral in (91.4) is independent of the co-ordinates of the point considered; retaining in the differentiation, as usual, only terms in l/i?o, we obtain D = - eXp(ik ' Ro) k'x[k'x fa.Eexp(-ik'.r)dF]. 47tRo j Since, at the point considered, the medium is regarded as not scattering, the relation between D' and E' there is given by D' = e'E' simply. In the field of the incident wave E we separate a factor periodic in space, putting E = Eoexp (zk«r). Then, with the notation G = J*<x.E exp(-*q.r)dF, (91.5) where q = k' — k, we have £ , _ _exp(,*'flo) k , x (k , x G) (91 6) \ttRqz t Exceptions may occur for particular cases of scattering, which will be discussed in §94. In such cases the dimensions of the scattering regions must be supposed large in comparison with the wavelength of the light. X See The Classical Theory of Fields, §9-2, Addison- Wesley Press, Cambridge (Mass.), 1951 ; Pergamon Press, London, 1959. 380 Scattering of Electromagnetic Waves §91 The vector E' is perpendicular to the direction k' of the scattered wave, and is given by the component of the vector G perpendicular to k'. Having thus determined the non-averaged field in the scattered wave, we can now investigate the intensity and polarisation of the scattered light. To do so, we form the tensor hk = E' t E' k *, (91.7) where the bar denotes the final averaging over the motion of the particles, which so far has not been carried out. The averaging of a quadratic expres- sion gives, of course, a result which is not zero. Since E' is perpendicular to k\ the tensor Im has non-zero components only in the plane perpendicular to k'. These components form a two-dimensional tensor 7 ay? in that plane (Greek suffixes take two values). The tensor I a/S is, by definition, Hermitian: I a p = I fi( *. It can be reduced to "principal axes", and the ratio of its two principal values gives the degree of depolarisation, while their sum is pro- portional to the total intensity, f The products E'iE'k* involve products of integrals Gi, which must also be averaged. Writing the product as a double integral, we have GiG k * = EoiEo m * j j ao.iafa.,2* exp [- *q.(n - r 2 )] dFi dF 2 . (91.8) The suffixes 1 and 2 indicate that the values of a are taken at two different points in space. In averaging the integrand it must be remembered that the correlation between the values of a at different points in the body extends in general only over molecular distances. After averaging, therefore, the integrand will be appreciably different from zero only for |r2 — ri| ~ a, where a is of the order of molecular distances. The exponent is ~ a/A, where A is the wavelength of the scattered wave ; but a/X <^ 1 if the macroscopic theory is applicable, and so we can replace the exponential factor by unity.J Next, the integration with respect to the co-ordinates ri and r 2 can be replaced by one with respect to |(ri + r 2 ) and r = ri - r 2 . Since the integrand depends, after averaging, on r only, we have G^*> = VEoiEom* / oni,^ km ,2*dV, (91.9) where V is the volume of the scattering region. It is evident a priori that the scattering must be proportional to V. It should be noted that the direction of the wave vector k in the incident wave appears neither in (91.9) nor, consequently, in the following formulae. f See Classical Theory of Fields, §6-7. The reduction of an Hermitian tensor to principal axes means putting it in the form hk = hmmki* + ^msnta*, where m, m are, in general, perpendicular complex "unit" vectors: m»nj* = 1, ri2»n2* = 1, ni»na* = 0. The prin- cipal values Ai, A2 of an Hermitian tensor are real. % This procedure requires further discussion in the case of Rayleigh scattering (§94). §91 The general theory of scattering in isotropic media 381 The integrals in (91.9) form a tensor of rank four, which depends only on the properties of the scattering medium. Since the medium is isotropic, the most general form of this tensor is f a«,ia fcm>2 * dV = \{a + c)8 a 8 km + \{a - c)h im hi + bo ik 8i m , (91.10) where a, b and c are scalar functions of a> and to. This tensor is automatically symmetrical with respect to an interchange of the suffixes i, / and k, m\ this interchange is equivalent to taking the complex conjugate, since the points 1 and 2 are equivalent; the tensor (91.10) is therefore real, and so are a, b } c. Substituting (91.10) in (91.9) we obtain G^* = V{\{a + c)E 0i E ok * + \{a - c)E Qi *E 01c + bE 0i Eoi*8i k }. (91.11) This expression could have been written down at once, since it is the most general Hermitian tensor of rank two which is quadratic in Eo and involves no other particular directions. This tensor is, of course, not transverse to k\ The required general form of the tensor/^ is obtained by "projecting" the tensor (91.11) on a plane perpendicular to k'; to do this, it is sufficient to take a co-ordinate system with one axis in the direction of k' and find the components of the tensor along the other two axes. Let us consider the scattering of a linearly polarised wave. The amplitude of the field E can be defined as a real quantity, f The components of the tensor I afi for the scattered light are therefore also real. This means that the scattered light is partially polarised, and can be divided into two independent (non-coherent) waves, each of which is linearly polarised. Since there are only two distinctive directions (those of Eo and k') on which the tensor I afi can depend, it is evident that one of these waves must be polarised with E' in the plane of E and k\ and the other with E' perpendicular to this plane. The intensities of the two scattered-light components will be denoted by Jiand h\ they are the principal values of the tensor J a/ff . For real E , the expression (91.11) becomes ~G&* = V{aE 0i Eo k + bE^hac). (91.12) We may note first of all that the scattering of linearly polarised light is deter- mined by two, not three, independent constants. To find h and h, we take the components of E in the two directions mentioned. The correspond- ing components of the tensor (91.12) give the result h-asitfO + b, h~b, (91.13) the coefficients of proportionality being the same ; 6 is the angle between Eo and the direction of scattering k'. The intensity of the scattered-light compo- nent whose electric field is polarised perpendicular to the plane of E and k' is independent of the direction of scattering. t See The Classical Theory of Fields, §§6-5, 6-7. We shall not consider here the scattering of elliptically polarised light, on account of the complexity of the formulae. 382 Scattering of Electromagnetic Waves §91 When natural light passes through a medium, the scattered light is par- tially polarised, and it is evident from symmetry that the two non-coherent components are linearly polarised, with their electric fields parallel and per- pendicular to the scattering plane (the plane of k and k'). Let the intensi- ties of these components be 7„ and 7 X respectively. To determine these, we average (91. 1 1) over all directions of the vector Eo in the plane perpendicu- lar to k. The averaging of the product EqiEq^ gives EoiEo k * = J|Eo| 2 (S^ - nm), (91.14) where n is a unit vector in the direction of k. This is a tensor of rank two which depends only on the direction of k, gives |Eo| 2 on contraction, and satisfies the condition ntEoiEok* = (n^Eo^ofc* = 0. Thus we have, when natural light is scattered, G^ = V\E \ 2 {ka(8 ik - mn k ) + b8 ik }. (91.15) Finally, taking the components of this tensor in the two directions of polarisa- tion, we obtain the required formulae : \a cos 2 & + b, I ± ~ \a + b, (91.16) where & is the scattering angle (i.e. that between k and k'). Let us return to formula (91.10), which relates the scalar quantities a, b and c to the tensor a^. Like any tensor of rank two, a** can be written, in general, as a sum of three independent parts : a-ik = l<x<>ik + Hk + dik, (91.17) where a = a^ is a scalar, syc a symmetrical tensor whose trace is zero (sac = s k i, Hi = 0) and am an antisymmetrical tensor. We substitute this in (91.10) and contract with respect to various pairs of suffixes, obtaining the three equations f 6a + 3b + Zc = Ja Wj iaM J 2*dF = Jaia 2 *dr, 3a + % = jaik,i«4k,2*dV = ijaia 2 * dV + Js ik ,iSik,2*dV + JW,i«M;,2* dV, 6a + 3b - 3c = \oi ik> i(x. k i t 2*dV = jjaia 2 * dV + js ik>1 Si kt 2* dV - ja ik> ia ik , 2 * dV. ► (91.18) t The integrals on the right-hand sides of these equations are positive, since each can be written as a square by a transformation inverse to that whereby (91.8) becomes (91.9). Expressing the three integrals in terms of a, b, c (i.e. solving equations (91.18) for these in- tegrals) we obtain the inequalities 2a + b + c > 0, 2b + c — a > 0, 2b + a — c > 0. From these, in particular, it follows that b > 0. §92 The principle of detailed balancing applied to scattering 383 The right-hand sides of these equations, and therefore their solutions for a, b, c, do not involve cross-products of a, s ijc and am. This means that scattering can always be regarded as a superposition of three types of process, which may be called scalar, symmetrical and antisymmetrical scattering. We shall discuss each of these in turn. Retaining only the first terms on the right of equations (91.18), we have a = c = -[^wFdV, 6 = 0. (91.19) It is seen from (91.13) that, in scalar scattering of polarised light, the scattered light is itself completely polarised, and its angular intensity distribution is given by I = (3/2) sin 2 0. (Here and henceforward the expressions for I are normalised so as to give unity on averaging over directions.) In scattering of natural light, however, the angular distribution of the total intensity and the degree of depolarisation of the scattered light are given, according to (91.16), by I = I ± + I^ = f(l + cos 2 &), IJI ± = cos 2 &; see the second footnote to §72. For symmetrical scattering, equations (91.18) give = -b = - -c = — sa,isa,2* dV. 3 5 30 J (91.20) In scattering of polarised light we have I = h + h = in>(6 + sin 2 0), hjh = 3/(3+ sin 2 0), and in scattering of natural light I = f^(14-sin 2 ^), IJI ± = l-£sin 2 &. Finally, for antisymmetrical scattering we obtain b = c = - a = - f aa,iaa,2*dV; (91.21) in scattering of polarised light / = f (1 + cos 2 0), hjh = cos 2 0, and in scatter- ing of natural light I = |(2+ sin 2 &), IJI t = 1/(1+ sin 2 &). §92. The principle of detailed balancing applied to scattering The general principle of detailed balancing f can be used to obtain a relation between the intensities in various scattering processes. Let dwi2 be the probability that a quantum %oi\ is scattered (on a path of unit length) and gives rise to a quantum /za> 2 in the solid angle element dor, let dw 2 i be the probability of the converse process, in which a quantum ha) 2 yields a quantum hw\ in the solid angle element doi. According to the principle of detailed balancing we have dw\i\h<^doi = dw2ijki 2 doi, where ki and k 2 are the wave numbers of the two quanta. Substituting k± 2 = eicoi 2 /c 2 , & 2 2 = €2( o2 2 Jc 2 (where €1 = e(o>i), e 2 = <o> 2 )), we obtain eicoi 2 do>i2/do2 = £20>2 2 dw>2i/doi. (92.1) t See Quantum Mechanics, §116, Pergamon Press, London, 1958. 384 Scattering of Electromagnetic Waves §92 Here it is assumed that the initial and final states of the scattering system correspond to discrete energy levels E\ and E 2 , related by E\ + h w\ = E 2 +hw 2 . This statement of the problem is not quite true to reality, since the energy levels of a macroscopic body are extremely closely spaced and can be regarded as quasi-continuous. Instead of the scattering probability dw±2 with an exactly determined fre- quency change, we must therefore use the probability of scattering into a frequency range da>2, i.e. of the body's entering a state whose energy lies in a range dE 2 = hda) 2 . Denoting this probability (again per unit path length) by dhi 2 , we have dhi 2 = dzo 12 dT 2 = dwi 2 (dr 2 /dE 2 )h doj 2 , where dr 2 is the number of quantum states of the body in the energy range dE 2 . Instead of (92. 1), we therefore have dl\ dh 12 dr 2 dA 2 i eio>i' s — = - — e 2 u)2r d£i do 2 da>2 dE 2 doida>i According to a well-known relation between the statistical weight of a macroscopic state of a body and its entropy Sf, the derivative dT/dE is essentially exp ST, so that (dTi/cLEi) :(dT 2 ldE 2 ) = exp (S^i - Sf 2 ). Since the relative change in the energy of the body resulting from the scattering of one quantum is negligible, the relative change in entropy is also small, and can be taken as ^i-^ 2 = {d^ldE){E x - E 2 ) = (E 1 -E 2 )/T = tya*- an)/T. Using this result, we can write the final expression of the principle of detailed balancing for scattering in the form d/h2 dh 2 \ e-^^eim 2 — = e-^2/T €2C02 2 . (92.2) do2 do) 2 doi dct>i The quantity dh, whose dimensions are cm -1 , is called the differential extinction coefficient for scattering of light. It can also be defined as follows : dh is the ratio of the number of quanta scattered in the direction do and the frequency range dw per unit time and volume to the incident photon flux density. By integrating dh over all directions and frequencies of the scat- tered light, we obtain the total extinction coefficient, which represents the damping decrement of the photon flux density as the light passes through the scattering medium. Let w 2 < <oi. The relation (92.2) connects the intensities (extinction coefficients) of Stokes (1 ->2) and anti-Stokes (2 -+ 1) scattering. We see that the latter is in general less than the former by approximately the factor e -h{o x -o 2 )iT % Thi s is a very general result, and corresponds to the fact that the transfer of energy from the body to the electromagnetic field reduces the probability of the process by a factor e~^ EIT , where A£ is the energy trans- ferred. In particular, the stimulated emission, in which the body gives up an energy ^(oii+oj 2 ) in each scattering process, is therefore usually very weak. The probability of such a process, when /*(oii+ u> 2 ) > T, contains the small factor e - h ^+ (a » )/T . §93 Scattering with small change of frequency 385 The general relation (92.2) is much simplified in the important case of scattering with a relatively small change in frequency. We shall denote o>i by co simply, and the small difference w^-wy by Aco(<^co), and put for brevity d/n 2 /do 2 dco 2 = I(a>, Aai). In the non-exponential factors e<f in (92.2) we can neglect the difference A to; these factors then cancel, leaving I(a>,Aco)e-WT = /(a, + Aco, - Aco>r*<" + ^' T . In the first argument of the function /(co+Aco, -Aco), which gives the initial frequency of the light, we can neglect Aco, i.e. refer the scattered intensity to a somewhat displaced frequency of the incident light. Then /(«, Aco) = /(co, - A«)e-*A-/r (92.3) In this approximation I on each side of the equation refers to the same frequency of the incident light. In other words, the relation (92.3) gives a simple relation between Stokes and anti- Stokes scattering of the same light with the same magnitude of the frequency change Aco. §93. Scattering with small change of frequency The theory given in §91 is entirely general, and is applicable to all cases of scattering in an isotropic medium, whatever the mechanism of scattering. Such a general discussion, of course, cannot proceed very far, and a further investigation of the phenomenon of scattering requires some restrictive assumptions. In most practical cases the scattering of light involves only a relatively small change in frequency, Aco = to' -co. The calculations given below pertain to this case. Besides the condition A to <^ co, we shall suppose that the relative change in the refractive index of the medium over the frequency range Aco is small. This condition means that the frequency <o must riot lie close to a range in which the scattering medium is also absorbing. If o) is in the optical range, the microscopic mechanism of scattering with small Aco may involve various kinds of motion of atoms and molecules (as opposed to the purely electronic motions which give rise to optical transi- tions), including intramolecular vibrations of atoms, rotations or vibrations of molecules, etc. Let q = q(t) denote the set of co-ordinates describing the motion which causes the scattering, f Since this motion is relatively slow, the macroscopic description of the motion can be regarded from a different standpoint by introducing the dielectric permeability tensor € ik (q), whose components at any instant depend only on the values of the co-ordinates q at that instant as parameters. This property follows from the assumed smallness of the relative change in e. The dielectric permeability thus defined pertains to the field averaged with respect to the electron motion for a given position of t For simplicity, we shall give a classical discussion. The results are actually still valid when quantum mechanics is used to describe the motion of the nuclei. 386 Scattering of Electromagnetic Waves §93 the nuclei. When the averaging of the field with respect to the motion of the nuclei is carried out, the dielectric permeability reduces to the scalar €(a>). Let the deviation of e^ from this value be Se^: ea(q) = At* + 8e ik (q). (93.1) The tensor e ik gives the relation between the field and the induction as functions of time. It should be emphasised that the incident wave is still assumed to have a single frequency a), but the field E' in the scattered wave is now regarded as a function of time, not resolved into single-frequency components. The total field consists of the field E in the incident wave and the field E' in the scattered wave. Thus Dt + D\ = e ik (Ek + E'jc). Cancelling Di = cEi and omitting the second-order term he^E'^ we obtain D'i = cE't + 8e ik (q)E k . (93.2) The relation (93.2) is of the same form as (91.2). There is a difference, however, in that with this approach it is clear that the tensor km = Sea is symmetrical. This follows at once from the general theorem concerning the symmetry of the dielectric permeability tensor. Furthermore, since this tensor is real for a transparent medium, the tensor 8e^ is also real. Since the tensor cum has no antisymmetrical part, there is no antisym- metrical scattering (§91) with small change in frequency. Let us calculate the total scattered intensity with all frequency changes A to <^ o>. This can easily be done as follows. In equation (91.3) for the field in the scattered wave we can replace k' by k = ofy/ejc (and take the value of a for a/ = a>) ; this equation does not then involve a/, i.e. it is the same for every component of the spectral resolution of the field. The equa- tion is therefore valid for the unresolved field in the scattered wave, which we shall denote by the same letter E'. Using the solution (91.6), we obtain A 4 — w 4 — lE'l 2 = |G| 2 sin2 = |G2sin 2 0, where 6 is the angle between k and G, and the bar denotes, as in §91, the final average with respect to the motion of the particles (i.e. with respect to the time dependence of q). We define the extinction coefficient h as the ratio of the total intensity of light scattered in all directions per unit volume of the scattering medium to the incident flux density :f |Gp h = Ljww- F|E|2J ' ' 6ttc*V |E|2 t This definition differs by a factor ai'lm from the general definition (in terms of the number of scattered quanta) given in §92. In the present case this factor may be taken as unity, and the two definitions are equivalent. §94 Rayleigh scattering in gases and liquids 387 As we have seen in §91, in calculating the mean value |G[ 2 we can replace the exponential factor in the integrand in G by unity, so that [Gp = EotEm? j Sen dV j SeikdV. The expression to be averaged is a tensor of rank two and, since the medium is isotropic, the result of the averaging is J 8e U dV j" Se lk dV = i8«( j Bem.dV) . Thus we have finally h = ^LU\8e lm dv) 2 , (93.3) or h = (o>4/1877c4)F(S^ m )r 2 , ( 93 - 4 ) where the suffix V denotes an averaging over the volume V. The mean value of the squared integral can be written as the mean value of a double integral, and is found to be proportional to the volume V (cf. §91). Hence the value of the extinction coefficient is independent of the scattering volume, as it should be, and also of the polarisation of the incident light. Formula (93.4) can be regarded in the following way. We can say formally that scattering would not occur in a completely homogeneous medium (i.e. one whose dielectric permeability is exactly constant). The scattering can be macroscopically described as resulting from inhomogeneities in the medium. The variation of these inhomogeneities with time, when resolved into spectral components, gives the change in frequency of the light when it is scattered. §94. Rayleigh scattering in gases and liquids Two types of scattering can be distinguished, depending on the change in frequency of the light: (1) combination scattering, which is the Raman- Landsberg-MandeVshtam effect and results in the appearance in the scattered light of lines whose frequency differs from that of the incident light, (2) Rayleigh scattering, in which the frequency is essentially unchanged. Combination scattering in gases results from a change, due to the incident light, in the vibrational, rotational or electronic state of the molecule, f Rayleigh scattering, on the other hand, does not involve a change in the internal state of the molecule. In the limiting case of a rarefied gas, when the mean free path / of the molecules is large compared with the wave- length A of the light, scattering takes place independently at each molecule, and can be discussed microscopically, using quantum mechanics. t Under ordinary observational conditions, electronic transitions are unimportant. 388 Scattering of Electromagnetic Waves §94 Here we shall discuss the opposite limiting case, where / < A, f and the Rayleigh scattering in gases can be divided into two parts. One part is due to irregularities in the orientation of the molecules (called fluctuations of anisotropy). The other part is scattering by fluctuations in the gas density. The orientation of the molecules is entirely changed by a few collisions, i.e. after a time of the order of the mean free time t. Hence the scattering by fluctuations of anisotropy results in the appearance of a relatively broad line with its peak at a/ = w and width ~ h/r. The scattering by fluctuations of density gives a much sharper line superposed on the other. As we shall see below, fluctuations of density in volumes ~ A 3 are of importance in the scattering of light with wavelength A. Since these volumes are large, the fluctuations in them occur comparatively slowly, and so the scattered line is narrow. In what follows we shall regard this sharp line as being undis- placed. The scattering by density fluctuations is scalar scattering (see the end of §91): since the density p is a scalar, so is the change in the dielectric perme- ability Se resulting from a change in p. The change in the dielectric permeability in fluctuations of anisotropy, on the other hand, is described by a symmetrical tensor Sew with zero trace. The latter property follows from the fact that the effect must vanish on averaging over all directions. Thus the scattering by anisotropy fluctuations is symmetrical scattering. In liquids the situation is less simple. Combination scattering can arise only from a change in the vibrational or electronic state of the molecule; rotational combination lines do not occur for scattering in liquids. The reason is that, because of the strong interaction between molecules in a liquid, they cannot rotate freely so as to acquire discrete rotational energy levels. The rotation of the molecules, therefore, like any motion in which their relative position changes, contributes in a liquid only to the relatively broad scattering line at <o' = w, which in this case may be regarded as the effect of Rayleigh scattering. The relaxation time of such motions depends on the viscosity of the liquid. The possibility of separating from the total Rayleigh scattering in a liquid a part due to thermodynamic fluctuations (of density or temperature) depends on the magnitudes of the various relaxation times. It is necessary that the relaxation times of all processes of establishment of equilibrium in the liquid should be small in comparison with the times characterising the fluctuations concerned. In this case a narrow "undisplaced" line and a broader one are observed. The undisplaced line corresponds to scalar scattering. The broader background, however, does not in general correspond, as it does in gases, to purely symmetrical scattering with no scalar part. The total intensity of the undisplaced line is easily calculated by means of t More precisely, the necessary condition is / <^ A sin i&, where & is the scattering angle. This is because the expression (94.4) which gives the scattered intensity involves the fre- quency only in the expression q = (2cd/c) sin i&. §94 Rayleigh scattering in gases and liquids 389 the general formula (93.4). For scalar scattering Be ik = Se8 ifc , and the extinction coefficient is therefore h . -?Lv&y. (94.D 677c 4 If 8 P and ST are the changes in density and temperature, then be = (ae/0/>)r8p + {dejdT) p hT. The fluctuations of density and temperature are statistically independent (EfSp = 0), and their mean squares are (MV = Tt/pCvV, (W = (TplV)(8pldp) T , where c v is the specific heat per unit mass. Thus we have finally This formula was first derived by A. Einstein (1910). For gases formula (94.2) becomes much simpler. The dielectric perme- ability of a gas (at optical frequencies) is almost independent of temperature, and hence the second term in the brackets can be neglected. The density dependence is that e- 1 is proportional to p, and hence p(de/dp) T « e - 1 « 2(w - 1), where n = V € is th e refractive index. Since, from the equation of state of a perfect gas, (l/p)(8pldp) T = 1/NT, where N is the number of particles in unit volume, we find that h = 2a>*(n - \flZTTC*N. (94.3) This formula was first derived by Rayleigh (1881). Let us now examine the fine structure of the undisplaced line. This requires a consideration of the time variation of the fluctuations. In this respect, thermodynamic fluctuations fall into two classes.t Adiabatic fluctua- tions of pressure in a fluid are propagated as undamped waves with the velocity of sound u\ we here neglect the absorption of sound, since it causes only a broadening of the line (see below). Fluctuations of entropy at constant pressure, however, are not propagated relative to the fluid, and are damped only gradually as a result of thermal conduction. The time variation of the intensity (not averaged with respect to time) is given by the squared modulus of the integral G(*) = J* §€(*). exp(- fq.r)dF.Eo, (94.4) t See Statistical Physics, §111, Pergamon Press, London, 1958. X See Fluid Mechanics, §79, Pergamon Press, London, 1959. 390 Scattering of Electromagnetic Waves §94 in which he is regarded as a function of time. In order to determine the shape of the scattering line, G(t) must be resolved into spectral components (i.e. Se(t) must be so resolved); the distribution of intensity as a function of Aco will then be given by the squared modulus of the component G Aw . However, the factor exp( — /q»r) in (94.4) cannot be replaced by unity, as we have done hitherto. The reason is that the quantity |G A J 2 depends markedly on the correlation of the time variation of the fluctuations at different points in space. This is clear when |G A J 2 is written as a double integral j j 8e(t)8e(f)exp[- /q-(r - r')] exp[*Aeo(* - t')]dVdV dtdt'. On account of the wave propagation of sound disturbances, the time variation of pressure fluctuation is correlated even at great distances. This fact was of no importance in determining the total intensity of the line, which is obtained by averaging the square |G(?)| 2 with respect to time; since, in this case, G(t) and G*(t) are taken at the same instant, it follows that only the correla- tion between the values of Sc at different points at the same instant is of importance, and this correlation extends only over short distances. Let us first consider the changes Se which result from pressure fluctuations. The quantity (94.4) is the Fourier space component of the fluctuation he whose wave vector is q; its time dependence is given by e-^ Aw , where Aw = ±qu. Since to « a/, we have q = |k' — k| = (2cu/c) sin-|&, where & is the angle between k and k'. If the corresponding value of Aw is denoted by Actio, then Ao>o = qu = ± (2cou/c) sin^&. (94.5) Thus the scattering by pressure fluctuations results in the appearance of a doublet (called the MandeV shtam-Brillouin doublet), the distance 2Atuo between whose components depends on the angle of scattering. The fluctuations of entropy have zero frequency, as stated above, and so scattering by them gives a central line with A to = 0. Let us determine the intensities of the doublet and the central line. The total intensity of the undisplaced line is given by formula (94.2), so that it is sufficient to determine, say, Jdoubiet/itotai (where /doublet is the combined intensity of the two components of the doublet, i.e. twice the intensity of each component f). Since the doublet lines are due to scattering by adiabatic pres- sure fluctuations, their intensity is given by the mean square (de/dp)s 2 (8p)v 2 - Using the formula for adiabatic pressure fluctuations and a simple trans- formation by means of the formula for the ratio of adiabatic and isothermal f The difference between the intensities of the two components is, according to formula (92.3), usually negligible, since /jAwo <C T. §94 Rayleigh scattering in gases and liquids 391 compressibilities, we obtain /d€\ 2 pT/dp\ /a € \a V \8p)s\dp)s Vc v \dp) T \dpJ s The adiabatic derivative {d€Jdp) s can be expressed in terms of more con- venient quantities by transforming it to the variables p and T: {d€ j dp ) s = {deldp) T + {Tlc vP *){dpldT) p {d € ldT) p . The required ratio of intensities is given by the ratio of (94.6) to the mean square total fluctuation (the expression in brackets in (94.2)). We shall not give the cumbersome general formula, but only the simpler form obtained when the temperature dependence of e is neglected : /*dout)let//*total = C v \c v ("4.7) (L. Landau and G. Placzek, 1933). To determine the shape of the lines, it is necessary to consider the dissipa- tive processes which result in the "decay" of the fluctuations. These processes cause a damping of the fluctuation amplitude as «-?', where y is a definite constant. If the "eigenfrequency" of the oscillations is Aa> , the total time dependence is given by e-W A «*>+y). The intensity distribution in the line is proportional to the squared moduli of the Fourier components of this factor, i.e. d/ = — dAc, (94.8) it (Aco - Ao; ) 2 + y 2 where 7 is the total intensity of the line. This is called the dispersion form of the line. The "width" is y. According to formulae derived in the theory of absorption of sound, f the damping coefficient for sound fluctuations with wave vector q is where 77, £ are the viscosity coefficients of the fluid and k its thermal conduc- tivity. Substituting q 2 = 2(<o/c) 2 (l-cos &), we obtain the following ex- pression for the width of the doublet components : y = -^(1 - cos *) [1 + £ + *(1 - 1)1 . (94.9) pc 2 L3 \c v Cp/ J t See Fluid Mechanics, §77. 26 392 Scattering of Electromagnetic Waves §94 The damping of isobaric fluctuations of entropy (and therefore of tempera- ture) is determined by the heat-conduction equation dTjdt = xAT, where x is the thermometric conductivity. For fluctuations with wave vector q (i.e. spatial variation as exp(*q»r)), we therefore have y = xq 2 = 2x(w 2 /<: 2 )(l - cos 9). (94.10) The shape of the central line is given by (94.8) with Awo= 0, the width y being (94.10). As already mentioned at the beginning of this section, the above theory is applicable to scattering in a liquid if all the relaxation times in it are small compared with those characterising the fluctuations. It should be borne in mind that, in any liquid, there are relaxation times of various orders of magnitude. The most rapid relaxation process, apparently, is the "decay" of elastic stresses in the liquid. The corresponding Maxzoellian relaxation time is r M ~ r)/G, where G is the modulus of rigidity, f The reorientation of the molecules, i.e. the "decay" of the anisotropy fluctuations, takes place less rapidly. The corresponding Debye relaxation time is r D ~ 7)a 3 /kT, where a is the dimension of the molecule; the difference between r M and r D is particularly large in liquids with large molecules. Finally, various other slow relaxation processes leading to the dispersion of sound are also possible (e.g. chemical reactions, slow transfer of energy to vibrational degrees of freedom of the molecule). The important processes as regards scattering are those for which 1/t is comparable with the frequency of the "sound" distur- bances which cause the scattering. There is as yet no complete survey of all the possible cases, and we shall not give one here, but merely mention that, when the viscosity of the liquid is sufficiently high, and so tm > 1/<Z M ~ c/cjdu sin^&, the liquid behaves as an amorphous solid with respect to the scattering of light. Finally, we may note an unusual type of scattering which occurs at the free surface of a liquid. The fluctuations have the result that this surface is no longer perfectly plane, and the consequent "roughness" causes a partial scattering of the light reflected from it (L. I. Mandel'shtam, 1913)4 PROBLEM Light is scattered in a gas whose molecules are linear, with polarisabilities a, and <x ± along and across the axis respectively. Determine the intensity resulting from the various types of scattering. Solution. The total intensity of scattered light (for given vibrational and electronic states of the molecules) includes the Rayleigh scattering and the rotational part of the com- bination scattering. Since the scattering takes place at the individual molecules of the gas, t See Theory of Elasticity, §31, Pergamon Press, London, 1959. t See L. I. Mandel'shtam, Annalen der Physik 41, 609, 1913, where a calculation is given for light scattered in the plane of incidence. §95 Critical opalescence 393 the total extinction coefficient is most simply obtained from formula (72.3), by multiplying by the number of particles per unit volume N and replacing the squared polarisability by Ja«2 = £(«. 2 + 2a x 2): A = ^ ai * + 20. (1) 9c* The undisplaced Rayleigh line is due to the scalar part of the polarisability, i.e. it is the same as if the polarisability tensor of the molecule were ianSi*. The same formula, (72.3), therefore gives Aundisp = *" («i+2a x ) 2 . (2) 27c* The difference Motai— Aundisp includes the "background" (scattering by anisotropy fluctua- tions) and the rotational combination scattering. In order to separate the former, we must first average the polarisability tensor of the molecule with respect to rotation about some particular axis (perpendicular to the axis of the molecule). The polarisability along the axis of rotation averaged in this way is evidently oc ± , and that along any direction in a plane perpendicular to the axis of rotation is l( a x+ a i)- In other words, a molecule rotating about a given axis is to be regarded as a particle for which the principal values of the polaris- ability tensor are a ± , K a x+ a i)> i( a x+ a i)- Using these, [we calculate the symmetrical tensor oc«r— $olu8uc, whose trace is zero, and then a procedure similar to the derivation of formulae (1) and (2) gives 8™*N (ax-«.) 2 ,,, Abackg - —^ £ • V) Finally, the intensity of the rotation combination scattering is obtained by subtracting (2) and (3) from (1): Zmo*N (tt x -a,) 2 Acombin — — — 2 * §95. Critical opalescence The isothermal compressibility (dp/dp)T increases without limit as the critical state is approached. The expression (94.2) for the total intensity due to scalar Rayleigh scattering therefore increases also. This indicates a marked increase in scattering near the critical point, called critical opalescence, f The formula (94.2) itself is, however, inapplicable, because the expressions for the thermodynamic fluctuations used in its derivation are no longer correct. The increase in intensity does not take place for all three components of the fine structure of the Rayleigh line, but only for the central component. According to (94.2) and (94.7), the intensity of the doublet is c p \dp/T\dp/T "doublet = 67TC 4 The thermodynamic formula Cp C<Q = T (dp/dT)/ p 2 {dp\dp) T t A similar phenomenon occurs for scattering in a solid near the critical point of a second- order phase transition. It has been discussed by V. L. Ginzburg, Doklady Akademii Nauk SSSR 105, 240, 1955. 394 Scattering of Electromagnetic Waves §95 gives near the critical point " doubiet = ^jm&WT - (95 - 1} As we shall see below, the factor exp( — /q»r) in (94.4) cannot be replaced by unity near the critical point, even in calculating the total scattered intensity. Let dh be the differential extinction coefficient, relating to scatter- ing into a given solid angle do (corresponding to a given value of q = k — k'). Considering, for definiteness, the scattering of unpolarised light, and using the result that the angular dependence (for scalar scattering) is given by the expression f(l +cos 2 -8-), we have dh = A 1 6ttc4 V J Seexp(— iq>r)dV 2 do' . f(l + cos 2 a-) . (95.2) 4?r Near the critical point, the density fluctuations increase but the tem- perature fluctuations remain finite. It is therefore sufficient to consider 8e — (de/dpJTSp, so that o> 4 /8e\2 1 I , 2 A ' .|(1 + cos 2 vJL. (95.3) 477 According to the theory of fluctuations, the mean square density fluctua- tion near the critical point can be expressed in terms of the coefficients a and b in the formula F - F = |a(o»2 + iftgrad op) 2 , (95.4) where F is the free energy per unit volume, f This formula gives the leading terms in an expansion of the change in the free energy in powers of 8p and of its gradient; the latter has to be taken into account because of the amplification of local inhomogeneities in the body near the critical point. The constant a is expressed in terms of the ordinary thermodynamic quantities byt a = (l/p)(dpl8p) T . (95.5) The mean square in (95.3) can be expressed in terms of a and b by |Spexp(-/q.r)dr = VT/(a + btf). (95.6) f See Statistical Physics, §116. % The derivative {dFjdp)T is the thermodynamic potential per unit mass, and the second derivative is therefore a = (8 2 F[8p 2 )t = (3$/3p)r = (l/p)(S/)/3p)2'. §96 Scattering in amorphous solids 395 Substituting in (95.3), we obtain the final result ih = _^(t\* 1 + C °f 9 do'. (95.7) p\dp/T & This formula was first derived by L. S. Ornstein and F. Zernike (1914). When the angle & is not small, the first term in the denominator may be neglected, and a? /0e\2 l + cos2& dA = — I do • (95.8) 647T 2 c%\dp/ T 1 -cos& The total intensity scattered in all directions is obtained by integrating (95.7) with respect to o. When (dp/8p) T = 0, i.e. at the critical point, the integral is logarithmically divergent for small angles. In reality, the integra- tion should be extended only to angles of the order of the diffraction angle ( ~ A/L, where L is the dimension of the body). The total intensity therefore depends logarithmically on the dimension of the scattering body. §96. Scattering in amorphous solids Rayleigh scattering in amorphous solids differs considerably from that in fluids. In an isotropic solid there are two velocities of propagation of sound, ui (longitudinal) and u t (transverse). The fine structure of the Rayleigh line therefore includes not one but two Mandel'shtam-Brillouin doublets. They are due to scattering by transverse and longitudinal "sound waves", and their distances from the centre of the line are respectively ±Ao>j, ±A(o t , where A^ = qui, A<*>t = qut. Since ui > ut, it follows that Awi > Aw*. The central component of the line is again due to fluctuations which are not propagated relative to the medium. In this case the main fluctuations of the latter type are those of structure. In an amorphous body, where the atoms are not arranged in an ordered manner, these fluctuations are comparatively large and vary only slowly with time (on account of the extreme slowness of the diffusion processes in a solid). Scattering by these fluctuations leads to a strong line whose width is almost zero. As regards polarisation and angular distribution, this line results from a superposition of scalar and symmetrical scattering. Next, let us consider the doublet components of the Rayleigh line in amorphous bodies. Here we cannot put exp( — *q-r) = 1 in the integral G, as we did for fluids, even in calculating the total intensity (and polarisation) of the scattered light ; moreover, the scattering cannot be classified according to dependence on angle as in §91. The reason is that, in a solid, the effect of any deformation (in this case, fluctuations) extends to considerable distances. Hence the fluctuations at different points in the body at the same instant are correlated even at distances large compared with 1/q. 396 Scattering of Electromagnetic Waves §96 The field in the scattered wave is w 2 exp(j&i? ) *---S&r in ' x < n ' xG >' (9U) where Gt = J* Se^ exp( - iq . r) d V . E ok , (96.2) and n' is a unit vector in the direction of scattering. The change in the dielectric permeability resulting from the deformation of an isotropic body is <W = aiunc + azuuSijc, (96.3) where ui k is the strain tensor (see (81.1)). Since the integral (96.2) isolates from Setjc the Fourier space component with wave vector q, ut k in (96.3) must be taken as the deformation in a sound wave with this wave vector. We therefore write the displacement vector as u = re{uoexp(/q.r)} = £[uoexp(/q-r) + uo*exp(- *q«r)], (96.4) whence the strain tensor is 1 idui 8ujc\ 2\dx k Bxil = re{fy(u iq k + woA#i)exp(zq.r)}, and the volume integral is j u ik exp( - iq • r) d V = liV{uQiq k + u 0k qi). (96.5) Let us first consider scattering by transverse "sound" waves. Since in a transverse wave u is perpendicular to q, and uu = 0, 8e ik = a\Ui k . Using (96.5), we therefore have G = i*rai{uo(q-Eo) + q(uo-E )}. (96.6) A transverse sound wave can have two independent directions of polari- sation: the vector u may be in the plane of k and k', or perpendicular to that plane. Since E is perpendicular to k, it is easy to see that in the first case the component of G in the plane perpendicular to k' is zero. Thus transverse sound waves "polarised" in the plane of k and k' do not scatter light. If the vector u is perpendicular to the plane of k and k', a simple calcu- lation, using (96.1) and (96.6), gives for the field in the scattered wave a) 2 exp (ikRo) .„ , „ E\ = F „ V . \axiVquo cos \* . E ±y ^ RoC (96.7) oj 2 exp (ikRo) . r „ E' = L± -.lanVquocosl&.Et. AttRoC 2 - §96 Scattering in amorphous solids 397 Here & is, as usual, the angle between k and k', and the suffixes || and J_ denote components in the plane of scattering and perpendicular to that plane. The coefficient of proportionality in these two formulae involves the same fluctuation mo. This means that no depolarisation occurs on scattering: linearly polarised light remains so (though it is polarised in a different plane). Since the coefficients in formulae (96.7) are exactly the same, the extinc- tion coefficient dh does not depend on the state of polarisation of the incident light, and is dn = iSH^\ FSpcosH^-do. (96.8) \ 167TC 2 / It remains to determine the mean square amplitude of the fluctuation uq. From the point of view of the general theory of thermodynamic fluctuations, the sound wave (96.4) may be regarded as a combination of two classical oscillators (waves propagated to the right and to the left), each having a mean kinetic energy %T. Since the frequency of the oscillations is here Aw = quu the m.?an kinetic energy is $Vpu 2 = \Vp{utqf\iio\ 2 . Equating this to 2 . %T, we have |^j2 = iTJVpuPq 2 . (96.9) Finally, substituting (96.9) in (96.8), we obtain dh = — cos*i&do. (96.10) The angular dependence of the scattering is totally different from that which occurs in fluids. Let us now consider scattering by longitudinal "sound" waves. In these waves u is parallel to q, and from (96.3) and (96.4) we find n x .„ / q(q-Eo) , v \ G = fyVuoqlai — + a 2 E [. A simple calculation gives for the field in the scattered wave to 2 exp (ikRo) co 2 exp (ikRo) E i = — a n o -hiVuoqtkai + (z a i + fl 2) cos &]E t . 'hrRoC 2 (96.11) In this case also there is no depolarisation on scattering. The angular dis- tribution and the extinction coefficient, however, depend on the state and direction of the polarisation of the incident light. We shall not pause to write out the relevant formulae, which are somewhat cumbersome. The calculations are wholly similar to those given above, and the expression for |mq| 2 differs only in that ut is replaced by ui in (96.9). CHAPTER XV DIFFRACTION OF X-RAYS IN CRYSTALS §97. The general theory of X-ray diffraction The phenomenon of X-ray diffraction in crystals occupies a special place in the electrodynamics of matter, since the wavelengths concerned are comparable with the distances between atoms. For this reason the usual macroscopic approach to matter as a continuous medium is entirely invalid, and we must begin by considering scattering by individual charged particles, and essentially by electrons ; the scattering by nuclei is unimportant, because of their much greater mass. The frequencies of the motion of electrons in the atom are of order wo ~ v/a, where v is their velocity and a the dimension of the atom. If A ~ a, then, since v <^ c, these frequencies are small compared with the X-ray frequency a> ~ cjX. This makes it possible to write the equation of motion of an electron in the field of the electromagnetic wave as mv' = eE, (97.1) i.e. the electrons may be regarded as free (see §59). From (97. 1) we find the additional velocity acquired by the electron under the action of the wave field: v' = ieE/ma). Let n(x, y, z) be the number density of electrons in a crystal, averaged over the quantum states of the electrons and over the statistical distribution of the thermal motion of the nuclei in the lattice. It should be emphasised that the usual macroscopic averaging over physically infinitesimal volume elements is not included, i.e. n(x, y, z) is the actual density of the "electron cloud" in the crystal lattice. The corresponding current density due to the wave field is : j' = en\' — ie 2 JiE/mco. (97.2) We substitute this current in the microscopic Maxwell's equations : curlE = iwH/c, (97.3) curlH = — icoE/c + 4-ny/c iw I ^ne 2 n --7 1 i/ 4ire 2 n\ -1 r )E. (97.4) We thereby take account of its reciprocal effect on the field, i.e. scattering. 398 §97 The general theory of X-ray diffraction 399 It is, of course, assumed that this effect is small, i.e. that the inequality 47re%/ma> 2 <^ 1 (97.5) holds. Putting D = cE, where 47re 2 » e = 1 -, (97.6) mm 1 in accordance with the usual definition of the induction, we reduce equation (97.4) to the usual form curl H = -ioiDjc. Thus, in this sense, the expres- sion (97.6) for the dielectric permeability (cf. (59.1)) can be used even for wavelengths A ~ a, though it must of course be remembered that the symbols E and D no longer retain their previous meanings : they now pertain to the field which has not been averaged over physically infinitesimal volumes, and e is accordingly a function of the co-ordinates. In the scattering of X-rays by heavy atoms it may happen that the condi- tion co > coq is fulfilled for the outer electron shells but not for the inner ones, where to < coo and so the inequality A > a holds. In this case the dielectric permeability can still be regarded as the coefficient of propor- tionality between D and E, but the formula corresponding to (97.6) gives only the contribution of the outer electrons. That of the inner electrons must in principle be calculated by averaging over the volume of their shells. Thus, if we put D = eE with e a function of the co-ordinates, all possible cases are allowed for. In what follows we shall, for definiteness, use the expression (97.6). In effecting the averaging of the electron density in (97.2) to obtain n(x, y, z) independent of time, we exclude a possible change of frequency on scattering. That is, we consider only strictly coherent scattering, with no change in frequency. Eliminating H from the two equations (97.3) and (97.4), we obtain curl curl E = ccFD/c 2 . Here we substitute E = T>+47re 2 nE/mco 2 and ex- pand the expression curl curl E, using the fact that div D = 0, as follows from (97.4). Then AD + u> 2 D/c 2 = curl curl (47re%E/wa> 2 ). (97.7) On the right-hand side of this equation, which already contains the small quantity 4r7re 2 njmco 2 , E must be taken as the given field of the incident wave. Let us find the solution of equation (97.7) in the region outside the scattering crystal and at large distances from it. f Since this equation is of the same form as equation (91.3), the required solution is obtained immediately by t In solving equation (91.3) it was not possible to consider the field outside the body, since the boundary conditions on the surface would have had to be taken into account (the quantity e' on the left-hand side being different inside and outside the body). The left-hand side of equation (97.7), however, is the same in all space. 400 Diffraction of X-rays in Crystals §97 analogy with (91.4) : ? 2 exp (ikRo) E = men 2 Rq k' X (k' X E ) f n exp(- *q.r)dF. (97.8) Here R is the distance from the origin, which is within the crystal, to the point considered; q = k' — k; k = k' = wfc; Eo is the amplitude of the incident wave. We put E instead of D on the left-hand side because the two are equal in the vacuum outside the crystal. To characterise the intensity of X-ray diffraction we use an effective cross- section or, defined as the ratio of the intensity diffracted into a solid angle do' to the energy flux density in the incident wave. By (97.8) we have da = ( 1 sin 2 nexp(-iq>r)dV do', (97.9) where 9 is the angle between Eo and k'. If the incident radiation is "natural" (not polarised), the factor sin 2 6 in this formula becomes |(l+cos 2 &), where & is the angle between k and k' (see the second footnote to §72) : 1/ e 2 \ 2 f da = -( (l + cos 2 &) nexp(-*q.r)dF 2\mc 2 J J do'. (97.10) In what follows we shall, for definiteness, consider this particular case. We see that the intensity of radiation diffracted in a given direction is essentially proportional to the squared modulus of the integral jnexp(-iq-r)dV, (97.11) i.e. the Fourier space component (with the appropriate value of q) of the electron density. As q .-> this integral becomes simply the electron density n averaged over a lattice cell. If n is replaced by n in equations (97.3) and (97.4), we obtain the usual macroscopic Maxwell's equations, with dielectric permeability e(a>) = \-ATte 2 n\ma> 2 . According to these equations, when X-rays pass through a crystal they are refracted according to the ordinary laws of refraction, with refractive index V € - Thus diffraction through small angles amounts to ordinary refraction, which is of no interest here. In what follows we shall always assume that q is appreciably different from zero. The electron density, like any function of position in a crystal lattice, can be expanded as a Fourier series : n = S n b exp (2mb • r), (97. 12) b where the summation is taken over all periods b of the reciprocal lattice, f t See Statistical Physics, §132, Pergamon Press, London, 1958. §97 The general theory of X-ray diffraction 401 When (97.12) is substituted in (97.11) and the result is integrated over the volume of the crystal, we obtain practically zero except for values of q close to some 2-nh. Between these values the intensity is negligible. We can therefore consider each diffraction maximum separately, putting n = «bexp(27rtb«r) with the appropriate value of b. Substitution in (97. 10) gives l/e 2 \ 2 da = - (1 + cos 2 $)» b 2 x 2\mc 2 / x I f exp [- t(k' - k - 27rb).r] dV do'. (97.13) The strongest maxima occur in directions for which the equation k' - k = 2db (97.14) (Laue's equation) is exactly satisfied, and are called principal maxima. For given b, however, a principal maximum does not occur for an arbitrary direction and frequency of the incident radiation. If the equation (97.14) is written as k' = k + 2?rb and squared, and we use the fact that k 2 = k' 2 , we have bk = - 7tb\ (97.15) This equation determines the values of the wave vector k for which principal maxima occur with the given value of b. Geometrically, equation (97.15) represents a plane in k-space perpendicular to the vector b at a distance irb from the origin. In particular, we see that k ^ irb. Since |k' - k| = 2k sin $&, it follows from (97. 14) that ksm%d- = 7rb (97.16) (Bragg and Vul'f's equation), which determines the angle of diffraction at the principal maximum. Any vector b of the reciprocal lattice determines a family of crystal planes represented by the equations r»b = constant integer. These planes are perpendicular to b, and the vectors k and k' corresponding to the condition (97.14) make equal angles of incidence and reflection with the planes (Fig. 45). For this reason, diffraction at a principal maximum is sometimes spoken of as "reflection" from the corresponding crystal planes. The total intensity of the diffraction "spot" near a maximum is obtained by integrating (97.13) over a solid angle about the direction of k\ Let us determine the intensity near a principal maximum. We denote by k'o the value of k' corresponding to Laue's equation for a given k: k'o = k + 27rb, and put also x = k' — k'o. Near the maximum, x is small; since k' and k'o 402 Diffraction of X-rays in Crystals §97 differ only in direction, x is perpendicular to k'o. The solid angle element can therefore be written do' = dK X dKy/k' 2 = d.K X di<ylk 2 , where the sr-axis is taken in the direction of k'o. Thus (97.17) 1 / e 2 ^2 ° ~ 2k 2 [mc* )2 (1 + cos 2 &)|« b | 2 j f dK x d Ky I f exp(- i*..r)dV\ Zirb /' N / \ / \ / \ / \ / \ / \ / \ / \ / \ / \ ^v JLr \5 %/ Fig. 45 In the volume integral we can effect the integration with respect to z, since exp( — /x»r) is independent of z: j exp(-iycr) dV = /Zexp(— zx»r)d/, where d/ = dx dy and Z = Z(x, y) is the length of the body in the direction of k'o. Finally, using a well-known formula in the theory of Fourier integrals : f \<t> K \*dK X d Ky = — - U 2 dxdy, (97.18) J \LttY j (2n) where <l>* -&vl«* y) exp(— ix*r)dxdy are the two-dimensional Fourier components, we obtain 27T 2 / e 2 \ 2 = ^(^)V + cos 2 &)|« b | 2 fZ 2 d/ k 2 \mc 2 ] J = —(—) sin 2 ^(l + cos 2 $)|" b | 2 ( Z 2 df. b 2 \mc 2 / J (97.19) The integral is of the order of Z, 4 , where L is the linear dimension of the body. Thus the total effective cross-section, and therefore the total intensity of the spot, are proportional to F 4/3 , where V is the volume of the body. The maximum intensity, however, follows a different law. For k' — k = 2rrb, §97 The general theory of X-ray diffraction 403 the integral in (97.13) is just V, and so da is proportional to V 2 : (—) = U—)\l + cos* &)\n h \*V*. (97.20) \do'/max 2\mc 2 / The sharpness of the maximum is shown by the fact that the maximum intensity is proportional to a higher power of V than the total intensity. The "width" of the peak is evidently proportional to V 4/3 fV 2 = V~ 2/3 . The theory given above is valid only if the diffraction effect is small. We now see that this requirement imposes a certain condition on the dimension of the crystal: a must be small compared with the geometrical cross-section of the body ( ~ L 2 ), whence <? 2 L — T |«b| <^ 1. (97.21) PROBLEMS Problem 1. Determine the intensity distribution in the diffraction spot round a principal maximum in diffraction by a crystal in the form of a cuboid of sides L x , L y , L z . Solution. As above, we use the vector X = k'— k'o, and take the axes of co-ordinates parallel to the sides of the cuboid, with the origin at its centre. The integral Jexp(— t'X«r) dV becomes a product of three integrals of the form *£* 2 exp(— Ik x x) dx — — sin \kxL x . -L* Thus / e 2 \ 2 1 da = 321 — -1 (1 + cos 2 &)|« b | 2 — - — - — - sin 2 \k x L x sin 2 \k v L v sin 2 \kzL z do'. XmC*/ K x i K V i Kz i K x "Ky'K Z The components of the vector x are not independent, being related by the condition x-k'o = 0. Problem 2. The same as Problem 1, but for diffraction by a spherical crystal of radius a. Solution. We again put x = k'— k'o, and take the sr-axis in the direction of x, with the origin at the centre of the sphere. Then a J exp(— i/<z) dV = j" 7r(a 2 — z 2 ) exp(— Ikz) dz —a = — r(sin Ka — ko cos ko). Thus / e 2 \ 2 1 da = Sir 2 \ — -) (1 + cos 2 *)|mJ 2 — (sin ko — ko cos ko) 2 do'. \mcv " k 6 Problem 3. Determine the total intensity of the diffraction spot round a subsidiary maximum. Solution. In this case the wave vector k of the incident wave does not satisfy the condi- tion (97.15). As shown above (97.15) is the equation of a plane perpendicular to the vector b. Let the small displacement of the terminus of the vector k from this plane be i?b, where i) <^ 1. That is, we put k = ko+i?b, where ko satisfies equation (97.15) (Fig. 46). 404 Diffraction of X-rays in Crystals §98 The maximum intensity in the spot occurs for a direction of k' for which the difference k'— (k+27rb) has its least magnitude (so that the integral in (97.13) has its maximum value). The magnitude of the difference of two vectors, one of which is arbitrary in direc- tion, has its least value when they are parallel. Hence, since k' — k, we have |k'-k-2db| m m = £-|k+2i7b| # s -(k+2db) 2 Since k is close to ko and we are considering the region near the maximum, k' ^ k+2wb and the denominator can be replaced by 2k. In the numerator, we expand the squared parenthesis and obtain -2k-2irb-(2irb) 2 = [-2ko-2»rb-(2wb) 2 ]-2 1? b-27rb = -4i7ij& 2 . Thus |k'-k-27rb|min ^ -2nr)b*lk. Next, we put 2itrjtP\ k' = (k+27rb)(l- -^-Wk, and take the sr-axis in the direction of k+27rb. This reduces the problem to the calculation of the integral (cf. the derivation of formula (97.19)) J $dK X d* y \j exp{2mr)b 2 /k-z-Wr} dV\ 2 ff, j If , .„ sin (-n^ZIk) I = J J d^d^J « P (-,x.r) ^^ d/| Finally, using formula (97.18), we obtain — Sirb) <1+C0,W)W, J sin 2 (7rr)b 2 Z/k) d/. (Trr)b 2 lk)* As i) -> this formula becomes (97.19). If 7n?6 2 Z/&> 1 (which is compatible with t\ < 1), the squared sine can be replaced by its mean value \, and we have / e 2 \ 2 l+cos 2 £ K\ 2 S, where S is the area of the "shadow", i.e. the projection of the body on the xy-plane. §98. The integral intensity The formulae derived in §97 give the diffracted intensity when a plane wave of a single frequency is incident on a crystal. Let us now consider some cases where these conditions are not fulfilled. §98 The integral intensity 405 First, let the incident wave be plane but not of a single frequency,! its spectral resolution including waves with wave vectors k whose directions are the same but whose magnitudes k = wjc are not. Let p(k) be the frequency distribution of the incident radiation intensity, normalised by the condition j P (k) dk=h The total intensity of the diffraction spot is determined by the effective cross-section, which is obtained by multiplying the expression (97.13) by p(k) and integrating with respect to d and k : a = 2 W/ l%|2 J J I J 6XP C ~ ^ " k " 2db) ' r] dV \ X x (1 + cos2&) P (£)do'd&. (98.1) We put temporarily K = k' — k — 2irb and write the squared modulus as a double integral: | Jexp(- JK.r)dF|2 = j Jexp[tK.(r 2 - ri)]dFidF 2 . Using instead of ri and r 2 the variables |(ri + r 2 ) and r = r 2 — riand integrat- ing with respect to the first gives | Jexp(iK«r) dV\ 2 = V Jexp(jK-r) dV. In the remaining integral we can effect the integration over all space, J and the result is | J exp (tK-r) dF|2 = (2tt)3F8(K). (98.2) Substituting this result in (98.1), we obtain / e 2 \ 2 , a = 4tt3 |« b \W{\ + cos 2 Sx>) x \mc 2 / ' x J J S(k' - k - 27rb)/)(A) do' d& ; (98.3) on account of the presence of the delta function, the factor 1 + cos 2 & in the integrand can be replaced by its value at & = &q, where &o is the angle between the k and k' which satisfy Laue's condition (denoted by ko and k' = k + 27rb). The integration with respect to d can be carried out by noticing that it is equivalent to an integration with respect to dk' = k'*dk'do' = ££'d(A'2)do\ f Corresponding to Laue's method in the X-ray analysis of crystals. % This is possible because we require only the total intensity of the diffraction spot, and not its width. 406 Diffraction of X-rays in Crystals §98 if an additional factor (2/k)S(k' 2 -k 2 ) is included in the integrand. Thus the integral in (98.3) becomes // 2 -8(k' - k - 27rb)S(£' 2 - &)p(k)dk'dk. k Effecting the integration with respect to k' by means of the first delta func- tion, we can replace k' 2 by (k + 2rrb) 2 in the second delta function, and the result is f -3(4,^2 + 4nh.k) P (k) dk = f S(b-k + irW)p{k) dk, so that a = 2tt4^—\ \n*\W{\ + cos 2 # ) f -o(b-k + 7rb 2 ) P (k)dk. (98.4) \mc 2 / J k Finally, we have to carry out the integration over k (the direction n = k/k being given). The argument of the delta function is zero for k = ko, and the integral is p(ko)/ko\b*n\ = p(ko)/\b'ko\ = p(ko)J7rb 2 . Thus a = 2tt(—) \m\W(l + cos 2 & )p(koW. (98.5) Let us now consider another case, where the incident wave is of a single frequency but its components have varying directions of k which differ by rotation about some axis;f let 1 be a unit vector along that axis, and «/rthe angle of rotation about it. Let p(ip) be the angular distribution of the incident radiation intensity, normalised by the condition The calculations leading to formula (98.4) are valid in this case also, except that the integration with p(k) dk must be replaced by one with p(+)d+: a ■ a = 2tt 2 (— ) \n h \W(l + cos 2 & ) f -S(b-k + nrb*)p{<p) dtp. (98.6) \mc 2 / J k We again denote by ko the value of k for which the argument of the delta function is zero, and measure \p from the plane of 1 and ko. For small «/», k = k + (lxk )^. Then the integral in (98.6) becomes I -S(b-1 x k ^)/#)d«£ = />(0)/*|b-l X ko| k = />(0)/& 2 |b.l x n | = p(0)sva*(l$f i )l'n z lfi\b'l X no|. t Corresponding to Bragg's method (the rotation method) in X-ray analysis. The rotation referred to is that of the crystal about 1, not that of the direction of k. §99 Diffuse thermal scattering of X-rays 407 Thus 2 / *2 \2 p(0) CT = » (— H sinHa (l + cos^o)«b 2 F |u ^ (98.7) b 2 \mc 2 ) |b*lxno| Finally, let us consider the diffraction of a plane wave, of a single fre- quency, from a body consisting of crystallites arranged at random, t Let k'o and bo be values of k' and b such that Laue's condition k'o = k+27rbo is satisfied. The directions of k'o and bo are not uniquely determined, since Laue's condition is, of course, still fulfilled when the triangle k, 27rbo, k'o is rotated about the direction of k. Thus the principal maximum corresponds to directions of k' occupying a conical surface of vertical angle 2&o- Instead of a diffraction "spot" we now have a "ring". The required total effective cross-section is determined by a formula which differs from (98.4) only in that the integration with p(k)dk is replaced by an averaging over the directions of b : / e 2 \2 /• 1 do b a = 2tt 2 V\ n b 2(l + cos2& ) -S(b • k + tt6 2 )— -, (98.8) \ mc 2 / J k 47T where do b is an element of solid angle about the direction of b. Denoting by a the angle between k and b, we can write the integral in (98.8) as s 1 27rrfcosa I 1 -8(bk cosa+7r6 2 ) = = sinH&o- k K ' 4tt 2bk 2 2b*ir 2 * Each of the three cases considered in this section corresponds to a particular method of averaging the diffraction pattern. The dependence of the total averaged diffraction intensity on the volume of the body reduces, as we should expect, to a simple proportionality. In the pattern which is not averaged, the intensity and its distribution over the spot depend more markedly on the volume. §99. Diffuse thermal scattering of X-rays In §§97 and 98 we have taken n(x, y, z) to be the time average electron density in the crystal: various density oscillations were thereby excluded, and consequently so was the corresponding (non-coherent) scattering of X-rays. One cause of non-coherent scattering is the thermal fluctuations of density. This scattering is "diffusely" distributed in all directions, but it is characterised by a relatively high intensity near directions corresponding to the sharp lines of the "structural" scattering described in the preceding sections. Here we shall discuss these maxima of the thermal scattering (W. H. Zachariasen, 1940). The thermal oscillations of the crystal lattice can be represented as com- binations of "sound" waves. As we shall see, the maxima of the thermal scattering arise from wavelengths large compared with the lattice constant. t Corresponding to Debye and Scherrer's method (the powder method) in X-ray analysis. 27 408 Diffraction of X-rays in Crystals §99 The change in the electron density due to such a wave can be regarded, at any point, as due to a simple displacement of the lattice by an amount equal to the local value of the displacement vector u in the wave. Thus the change in the density {not averaged with respect to time) when a given sound wave passes can be expressed in terms of the mean density by Sn = «(r— u) — n(r) ^ —u-dn/dr. In considering diffuse scattering near a given line, we must replace n by « b exp(27rtb«r) with the appropriate b, so that 8n = - 2Wb • u« b exp(27rtb • r). (99.1) The scattering by density fluctuations is, of course, not coherent with that by the mean density, and the two therefore do not interfere. Hence the effective cross-section for diffuse scattering can be obtained from (97.10), substituting 8n for n and then carrying out the statistical averaging over fluctuations : da = 27T 2 ( |« b | 2 (l+ cos 2 #)x x | j b • u exp( - iK • r)d V\ 2 do', (99.2) where K = k' — k — 27rb. The scattered intensity is large for directions where K ^ 27rb. The integral j" u exp( — iK-r) dV gives the Fourier space component of u whose wave vector is K, and we can therefore take u to be simply the dis- placement vector in a sound wave having this wave vector. The inequality K <^ 2rrb therefore implies that the wavelength of the scattering sound wave is large compared with the dimension of the crystal lattice cell. Thus we can put u = i[uo exp(*K • r) + uo* exp( - iK • r)], (99.3) so that J(b«u) exp( — z*K*r) dV = ^Fb»uo and the effective cross-section is 2 / 2 \ 2 da = ^-(-^r-l \n b \ 2 (l + cos2&)bib k ^ k V2do'. (99.4) 2 \ mc 1 } The products of the components of uo are averaged as in §96 for a sound wave in an isotropic medium. The elastic energy per unit volume of a deformed crystal is WnimUikUim, where uoc is the strain tensor and Xikim the elastic modulus tensor, t Hence the mean elastic energy of the whole crystal is ^V^ncimiHkUim- We substitute 1 / dm dujc \ 2\ dxjc dxi J = £re {(iKkUQi + iKiUok) exp(^K • r)}. t See Theory of Elasticity, §10, Pergamon Press, London, 1959. §99 Diffuse thermal scattering of X-rays 409 The terms containing exp(±2iK«r) give zero on averaging. Using also the symmetry of the tensor Xikim with respect to interchange of i, k, or /, m, or i, k and /, m, we obtain iV\ ik i m K k K m uoiiioi* or £Vg ik uoiUok* , where gik = hlkmKiK m . (99.5) According to the general theory of thermodynamic fluctuations, we can at once write down the required mean values : f uowojc* = (4T!V)g~i ik , (99.6) where g^m is the tensor inverse to gt kl and the effective scattering cross- section is da = 2n*(—) TV\n b \2(l + cos?d-)bib k g-i ik od'. (99.7) \mc 2 } Thus the diffusely scattered intensity is, as we should expect, proportional to the volume of the crystal. A characteristic feature of this scattering is the way in which its intensity is distributed over the area of the spot. Apart from the factor 1 + cos 2 &, which is almost constant for a given spot, the intensity is given by the expression g'hkhh- This expression is the product of 1/K 2 and a fairly involved function of the direction of the vector K with respect to the crystal axes. For scattering near a principal maximum the diffusely scattered intensity is itself a maximum where K = (the expres- sion (99.7) becomes infinite for K = and is, of course, invalid). If the condition (97.15) b«k = — <nb 2 is not satisfied, however, K cannot be zero, and the maximum of the diffusely scattered intensity lies at some K different from zero, which in general does not coincide with the maximum of the structural scattering. In either case the diffuse scattering forms a background whose intensity falls off essentially as 1/K 2 , that is, considerably more slowly than the intensity in the sharp structural-scattering line superposed upon it. f See Statistical Physics, §110. If the prob abilit y distribution for fluctuating quantities xi, X2, ... is of the form exp(— ^Xncx t xje), then xtx* = A-^fc. A factor 2 in (99.6) appears because each of the complex moi involves two independent quantities. 27* APPENDIX CURVILINEAR CO-ORDINATES We give below, for reference, certain formulae relating to vector operations in curvilinear co-ordinates, both general and particular. In an arbitrary system of orthogonal curvilinear co-ordinates «i, u 2 , «3, the squared element of length is d/ 2 = h^&ufi + htf'&wg' + htf'&uz 2 , where the hi are functions of the co-ordinates. The element of volume is d V = hihzhz d«i du 2 dwg. The various vector operations can be expressed in terms of the functions h i as follows. For vector operations on a scalar : 1 8f (grad/), = -/-, hi cm 1 v d /h 2 h 3 3f 1 y /h 2 h 3 g/\ hxhzhz^- 1 dui\ hi du\l' where the summation is over cyclic interchanges of the suffixes 1, 2, 3. For vector operations on a vector : divA = irirSir^ 3 ^' 1 f 8 d I (curl A)! = — U(M,) - -r-(M2) • «2«3 L <7W2 ^3 J The remaining components of curl A are obtained by cyclic interchanges of the suffixes. Cylindrical co-ordinates r } <f>, z. Element of length: d/ 2 = dr 2 + r 2 d<£ 2 + da; 2 ; h r = 1, hf = r, h z = 1. Vector operations : _ 1 d I df\ i a 2 / a 2 / A ' = rSU/ + r 2 " &£2 + d^ 2 ' _ 1 a 1 dAf dA z r dr r d(f> dz 410 Curvilinear Co-ordinates 411 1 dAz 8A, 3A r dA z (curl AY* = — , v } * 8z Br 18 1 8A r (curlA), = -— (r4,) — , r or r c<p A r 2 8A 6 (AA) r =AA r -— - r 2 r 2 8<f> A, 2 8A r (AA) Z = AA Z . In the expressions for the components of AA, /\Ai signifies the result of the operator A acting on A\ regarded as a scalar. Spherical co-ordinates r, 6, </>. Element of length: d/2 = dr 2 + r 2 d0 2 + r 2 sin* d<f> 2 ; hr = 1, h e = r, h$ = r sin0. Vector operations : 1 8 ( 8f\ 1 8 l . 8f\ 1 a 2 / A/ = \r 2 — \ + sin0— + -, J r 2 8r\ 8rJ r 2 sin 9 80\ 86/ r 2 sin 2 8cf> 2 \ 8 \ 8 1 ZA* divA = ——(f*Ar) + ——-(A e sm0) + r 2 8r r sin 89 r sin 8<j> 1 [8 8A e -\ 1 8A r 1 8 (curl A), = -r-~ ~ ~ T (rA^ r sin 9 8<f) r or Ira 8A r l 2r 1 8 1 8A 6 -\ (AA) r = A ^r--Ur + -— -(Agsm0)+ . ' , r 2 L sin0 80 sinS a<£ J 2 ra^ r ^ C os0 a^i r 2 I 80 2 sin 2 sin 2 8<f> ] 2 [8A r 8A e A 6 I r 2 sin L a<6 a^ 2 sin J INDEX Absorption coefficient, 265 Absorption of electromagnetic waves by small particles, 303f. Acceleration, excitation of currents by, 210ff. Airy function, 286 Anisotropic media, electromagnetic waves in (XI), 313ff. Antiferromagnetic Curie point, 165f. Antiferromagnetics, 117 Barnett effect, 144 Bindrmal, 326 Biot and Savart's law, 122 Biradial, 326 Black-body radiation in a transparent medium, 367f. Bragg and Vul'f 's equation, 401 Bragg's method, 406n. Brewster angle, 276 Capacity, 4, 8f., 19f., 62, 202ff. coefficients, 4, 6, 8 of conducting ellipsoid, 24f. of conducting sphere, 62 mutual, 8, 17 Causality, 257, 260 Charge distribution on conducting disc, 27, 28 on conducting ellipsoid, 24, 28 on conductors, Iff., 18 Charges in a dielectric, 68 extraneous, 37 Cherenkov radiation, 357ff. Conduction current density, 120 Conductivity, electrical, 92 tensor, 93, 96 Conductors, Iff. cylindrical, 16, 17, 18, 125, 194 disc-shaped, 27, 28 electrostatics of (I), Iff. electrostriction of, 33ff. ellipsoidal, 20ff. forces on, 31ff., 62, 142ff., 221 motion in a magnetic field, 205ff. turbulent, 234ff. spherical, 15f., 34f., 95f., 193ff., 209f., 212 Conformal mapping, 14 method of, 12ff. Conical refraction external, 328 internal, 326, 328 413 Contact potential, 100 Cotton-Mouton effect, 336 Critical field, 173ff. Critical opalescence, 393ff. Critical state, 82f. Crystals biaxial, 59, 324ff. dielectric properties of, 58ff., 313ff. enantiomorphic, 341 magnetic properties of, 116ff. natural optical activity of, 341 f. piezoelectric, 76 pyroelectric, 60 uniaxial, 59, 321ff. negative, 322 positive, 322 X-ray diffraction in (XV), 398ff. general theory of, 398ff. Curie point antiferromagnetic, 165f. ferroelectric, 83 ferromagnetic, 146 Curie— Weiss law, 148 Current boundary conditions for, 92f. conduction, 120 constant (III), 92ff. magnetic field of, 119ff. in a crystal, 398 density, 92 eddy, 189ff. electric, 1 excitation by acceleration, 210ff. linear, 122; see also Linear current molecular, 120n. in a moving conductor, 206 superconductivity, 169ff. surface, 115 Curvilinear co-ordinates, 410f. Cylinder conducting, 16, 17, 18, 125, 194 dielectric, 43, 57, 58 Debye relaxation time, 392 Debye and Scherrer's method, 407n. Demagnetisation coefficients, 44n., 169 Depolarisation coefficients, 26f., 302 Depolarising field, 44n. Dielectric axes, principal, 316 Dielectric constant, see Dielectric permea- bility Dielectric crystals, 58ff., 313ff. 414 Index Dielectric cylinder, 43, 57 Dielectric disc, 43, 57, 58, 62 Dielectric ellipsoid, 42ff., 56f. Dielectric fluid, forces in, 64ff. Dielectric permeability analytical properties of, 256ff. of crystals, 313ff. dispersion of, 247ff. electrostatic, 38 at high frequencies, 251 at low frequencies, 250 of a mixture, 45ff. spatial variation of, 337ff. tensor, 58, 69ff., 329ff., 339, 385f. Dielectric polarisation, 36 Dielectrics, 1 electrostatics of (II), 36ff. electrostriction of isotropic, 55ff. moving, 243ff. boundary conditions, 245f. thermodynamics of, 47ff. total free energy of, 52ff. Dielectric solid, forces in, 69ff. Dielectric sphere, 42f., 45, 61, 62, 73, 246f. Dielectric susceptibility, 38 sign of, 63f. Dielectric tensor, 58; see also Dielectric permeability tensor Diffraction by a plane screen, 308ff. by a wedge, 304ff. of X-rays in crystals (XV), 398ff. general theory of, 398ff. Diffusion phenomena, HOff. Dipole moment of conducting cylinder, 16, 18f. of conducting disc, 28 of conducting sphere, 16 of conductor, 7 of dielectric, 36f., 54 Disc conducting, 27, 28 dielectric, 43, 57, 58, 62 superconducting, 173 Discontinuities in a magnetic fluid, 224ff. Discontinuity contact, 225 rotational, 226ff. tangential, 225ff. stability of, 227ff. Dispersion relation, 220 Displacement, electric, 37n. Dissipative function, 204 Domains, 87ff., 152ff., 158ff., 179ff. Double circular refraction, 335 Double refraction, 323 in an electric field, 329ff. Easy magnetisation, direction of, 150 Eddy currents, 189ff. Eikonal, 269, 317 Einstein-de Haas effect, 145 Elastic constant tensor, 75 Elastic-optical constants, 330 Electric displacement, 37n. Electric field, constant of conductors, Iff. boundary conditions, 2f., 39f., 92 energy of, 3ff. in dielectrics, 36ff. boundary conditions, 37ff. thermodynamics of, 47ff. See also Electromagnetic field Electric induction, 37 Electric moment, 37 Electrocaloric effect, 56ff. Electrocapillarity, 103f. Electromagnetic field boundary conditions, 273, 280f., 290 fluctuations, 361ff. in moving media, 243ff. quasi-static (VII), 186ff. in dielectrics, 239ff. variable, 247ff. Electromagnetic fluctuations (XIII), 360ff. Electromagnetic wave equations (IX), 239ff Electromagnetic waves, 239ff. absorption of, by small particles, 303f. in anisotropic media (XI), 313ff. extraordinary, 322ff. ordinary, 322 plane in an absorbing medium, 264f. in anisotropic media, 315ff. homogeneous, 264 inhomogeneous, 263 of a single frequency, 263ff., 268 in a transparent medium, 264 propagation of (X), 269ff. in an inhomogeneous medium, 284ff. in waveguides, 293ff. reflection and refraction of, 272ff. , 283f. in resonators, 290ff. scattering of (XIV), 377ff. by small particles, 299ff. Electromotive force, 101 Electrostatic induction coefficients, 4, 6 Electrostatics of conductors (I), Iff. of dielectrics (II), 36ff. Electrostriction of conductors, 33ff. of dielectrics, 55ff. Ellipsoid conducting, 20ff. dielectric, 42ff., 56f. ferromagnetic, 157f. superconducting, 169f., 182 Ellipsoidal co-ordinates, 20ff. E.m.f., 101 Index 415 Energy of conductors, 3ff., 124 of a system of currents, 13 Iff. of dielectrics, 48ff., 52ff., 79ff. of fields in dispersive media, 253ff. flux (Poynting vector) 124, 191, 242, 253, 271,274,280,314 in a plane wave, 264, 315f. in a resonator, 291f. in a waveguide, 295f. free self-, 132 interaction, 132 of magnetic substances, 129ff., 149ff., 156, 159ff. Ettingshausen effect, 109 E waves, 285f., 294ff. Extinction coefficient differential, 384 total, 384 Extraneous charges, 37 Extraordinary waves, 322ff. Faraday effect, 335 Faraday's law, 207 Fast particles, passage of through matter (XII), 344ff. Fermat's principle, 270 Ferroelectric axis, 83 Ferroelectrics, 83ff. domains in, 87f. Ferromagnetics, 117 near the Curie point, 146ff. domain structure of, 152ff., 158ff. thermodynamics of, 147 Ferromagnetism (V), 146ff. Fluctuations of anisotropy, 388 of current in linear circuits, 360f. electromagnetic (XIII), 360ff. electromagnetic field, 361ff. Fresnel ellipsoid, 321 Fresnel's equation, 317, 324ff. Fresnel's formulae, 273ff. Galvanic cell, lOlff. Geometrical optics, 269ff. Group velocity, 220, 270, 318 Gyration vector, 332n., 339 Gyromagnetic coefficients, 145 Gyromagnetic phenomena, 144f. Gyrotropic media, 319n., 332ff. Hall effect, 97 Hall's constant, 98 if waves, 285, 287f., 294ff. Hydromagnetic waves, 221n. absorption of, 223 Hysteresis, 151 Image, 9 force, 10, 40 Images, method of, 9ff. Impedance, 197ff. matrix, 201 surface, 280ff., 314f. Inductance mutual, 132 self-, 132 Induction electric, 37 extraneous fluctuating, 361 correlations of, 363ff. unipolar, 208f. Inversion method of, llf. radius of, 12 transformation, 12 Ionisation losses by fast particles, 344ff. relativistic, 349ff. Joule's law, 93 in a moving conductor, 206 Kerr effect, 329 Kinetic coefficients, 94 symmetry of, 94, 96, 314, 331, 338f. Kramer's and Kronig's formulae, 259ff., 282f. Laue's equation, 401 Laue's method, 405n. Leduc-Righi effect, 109 Linear currents, 122ff., 133ff., 197ff., 210, 212 fluctuations of, 360f. mutual inductance of, 133 self-inductance of, 136ff. Lorentz condition, 350 Losses electric, 254 magnetic, 254 Magnetic anisotropy energy, 146n., 148n., 149ff. Magnetic crystal classes, 118 Magnetic field, 114 boundary conditions, 115, 187f. conductor moving in, 205ff. constant (IV), 113ff. of constant current, 119ff. conducting fluid moving in, 213ff. forces on matter in, 141ff., 221 thermodynamics of, 126ff. See also Electromagnetic field Magnetic fluid dynamics (VIII), 213ff. Magnetic flux, 134 Magnetic induction, 113 Magnetic moment, 114 in variable field, 252 416 Index Magnetic-optical effects, 3 3 Iff. Magnetic permeability, 114 analytic properties of, 262 of crystals, 313 dispersion of, 25 Iff. tensor, 119 Magnetic polarisability tensor, 192 Magnetic space groups, 117 Magnetic structure, 116 Magnetic susceptibility, 114f. sign of, 115, 129 Magnetisation, 114 by rotation, 144f. regions of spontaneous, 152 Magneto-elastic energy, 156 Magnetostatics and electrostatics compared, 115, 116, 126ff., 141f., 146 Magnetostriction, 155ff. Mandershtam-Brillouin doublet, 390 Maxwell effect, 331 Maxwellian relaxation time, 392 Maxwell's equations, 2, 113, 315, 349 Maxwell stress tensor, 31 Mechanical-optical effects, 330f. Molecular attraction between solid bodies, 368ff. Momentum density, 242 Mutual inductance, 132 Natural optical activity, 248n., 337ff. of crystals, 341f. Nernst effect, 109 Ohm's law, 92, 200 Optical axis, 321, 326 Optical frequencies, 248 Optical ray axis, 326 Ordinary waves, 322 Oscillator strength, 261 Peltier coefficient, 108 Peltier effect, 107f. Penetration depth, 189, 279f. in a superconductor, 167 Phase velocity, 219, 270 Piezoelectricity, 60n., 70n., 73ff. Piezoelectric tensor, 74, 76ff. Piezomagnetism, 119 Polarisability tensor, 7f., 192 Polarisation, 36 coefficient, 38 of dielectric in variable field, 249 of electromagnetic waves in anisotropic medium, 319ff. in geometrical optics, 271 in gyrotropic medium, 335ff. in uniaxial crystal, 323 Ponderomotive forces , 64 Potential contact, 100 electric complex, 13 scalar, 2f., 350 vector, 13, 350 magnetic, vector, 120 Powder method, 407n. Poynting vector, see Energy flux Principal section, 322 Principal waves in waveguides, 296ff. damping of, 297ff. Pyroelectricity, 60f. Quadrupole moment tensor, 28 of conducting ellipsoid, 28 Quality of a resonator, 292n. Quasi-static fields, 186, 364 Raman-Landsberg-Mandel'shtam effect, 387 Ray surface, 317ff. Ray vector, 317ff. Reactance, 198n. Reciprocity theorem, 289f. Reflection coefficient, 274, 277ff., 283f. Refractive index, 264, 265, 269, 316n., 322, 368 Resistance, 198n. complex, 197 Resonators, 290ff. quality of, 292n. Rotation method, 406n. Scattering in amorphous solids, 395ff. anti-Stokes, 377 antisymmetrical, 383 combination, 387 effective cross-section for, 300ff. of electromagnetic waves (XIV), 377ff. by small particles, 299ff. by fluctuations, 388ff. principle of detailed balancing for, 383 ff. Rayleigh, in gases and liquids, 387ff. scalar, 383 with small change in frequency, 385ff. Stokes, 377 symmetrical, 383 Self-inductance, 132 of linear circuits, 136ff. of superconductors, 171 Shock waves in a magnetic fluid, 229ff. weak, 231 in weak magnetic fields, 231f. Skin effect, 136n., 195ff. Solenoid, 137, 140f. Index 417 Sphere conducting, 15f., 34f., 62, 95f., 193ff., 209f., 212 dielectric, 42f., 45, 61, 62, 73, 246f. Spheroidal co-ordinates oblate, 22 prolate, 22 Stewart-Tolman effect, 212 Stimulated emission, 377n. Stopping power, 346 Stress tensor, 65ff., 70f. Superconductivity (VI), 167ff. destruction of, 173ff. transition point, 167 Superconductors critical field in, 173ff. currents in, 168ff. ellipsoidal, 169f., 182 impedance of, 28 If. intermediate state of, 179ff. magnetic properties of, 167ff. multiply connected, 170ff. rotating, 212 self-inductance of, 171 thermodynamics of, 173ff. Telegrapher's equation, 298 Tensor ellipsoid, 59n. Thermodynamic inequalities, 81ff. Thermoelectric phenomena, 104ff. Thermoelectromotive force, 108 Thermogalvanomagnetic effects, 109f. Thomson coefficient, 107 Thomson effect, 107 Thomson's formula, 203 Thomson's relations, 108 Thomson's theorem, 7 Total polarisation, angle of, 276 Total reflection, 277 angle of, 277 Transparency ranges, 254 Transparent media, 266ff. black-body radiation in, 367f. Turbulence in conducting fluid, 234ff. Two-dimensional field, 12f. Unipolar induction, 208f. Velocity of light in moving medium, 271f. Waveguides, 293ff. Waves on a charged liquid surface, 35 electric-type, 294 electromagnetic, see Electromagnetic waves extraordinary, 322ff. hydromagnetic, 221n. absorption of, 223 magnetic-type, 294 ordinary, 322 principal, 296 shock, see Shock waves Wave-vector surface, 317ff., 322, 324ff., 334n. Wedge problem, 14f. Work function, 99 X-ray diffraction in crystals (XV), 398ff. general theory of, 398ff. X-rays, diffuse thermal scattering of, 407ff. 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