Introduction to Electrodynamics David J. Griffiths Fourth Edition

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Transcription:

Introduction to Electrodynamics David J. Griffiths Fourth Edition

Pearson Education Limited Edinburgh Gate Harlow Essex CM20 2JE England and Associated Companies throughout the world Visit us on the World Wide Web at: www.pearsoned.co.uk Pearson Education Limited 2014 All rights reserved. No part of this publication may be reproduced, stored in a retrieval system, or transmitted in any form or by any means, electronic, mechanical, photocopying, recording or otherwise, without either the prior written permission of the publisher or a licence permitting restricted copying in the United Kingdom issued by the Copyright Licensing Agency Ltd, Saffron House, 6 10 Kirby Street, London EC1N 8TS. All trademarks used herein are the property of their respective owners. The use of any trademark in this text does not vest in the author or publisher any trademark ownership rights in such trademarks, nor does the use of such trademarks imply any affiliation with or endorsement of this book by such owners. ISBN 10: 1-292-02142-X ISBN 13: 978-1-292-02142-3 British Library Cataloguing-in-Publication Data A catalogue record for this book is available from the British Library Printed in the United States of America

a given volume is equal and opposite to the amount that has been pushed out through the surface. The latter (by the same reasoning we used before) is P ˆn per unit area, so V ρ b dτ = Since this is true for any volume, we have S P da = ρ b = P, V ( P) dτ. confirming, again, the more rigorous conclusion of Sect. 2.1. Example 3. There is another way of analyzing the uniformly polarized sphere (Ex. 2), which nicely illustrates the idea of a bound charge. What we have, really, is two spheres of charge: a positive sphere and a negative sphere. Without polarization the two are superimposed and cancel completely. But when the material is uniformly polarized, all the plus charges move slightly upward (the z direction), and all the minus charges move slightly downward (Fig. 15). The two spheres no longer overlap perfectly: at the top there s a cap of leftover positive charge and at the bottom a cap of negative charge. This leftover charge is precisely the bound surface charge σ b. + + + + + + + + + ++ + d + FIGURE 15 The field in the region of overlap between two uniformly charged spheres is calculated as E = 1 qd 4πɛ 0 R, 3 where q is the total charge of the positive sphere, d is the vector from the negative center to the positive center, and R is the radius of the sphere. We can express this in terms of the polarization of the sphere, p = qd = ( 4 3 π R3 )P, as E = 1 3ɛ 0 P. 178

Meanwhile, for points outside, it is as though all the charge on each sphere were concentrated at the respective center. We have, then, a dipole, with potential V = 1 p ˆr 4πɛ 0 r. 2 (Remember that d is some small fraction of an atomic radius; Fig. 15 is grossly exaggerated.) These answers agree, of course, with the results of Ex. 2. Problem 13 A very long cylinder, of radius a, carries a uniform polarization P perpendicular to its axis. Find the electric field inside the cylinder. Show that the field outside the cylinder can be expressed in the form E(r) = [2(P ŝ)ŝ P]. 2ɛ 0 s2 [Careful: I said uniform, not radial!] a2 Problem 14 When you polarize a neutral dielectric, the charge moves a bit, but the total remains zero. This fact should be reflected in the bound charges σ b and ρ b. Prove from Eqs. 11 and 12 that the total bound charge vanishes. 2.3 The Field Inside a Dielectric 4 I have been sloppy about the distinction between pure dipoles and physical dipoles. In developing the theory of bound charges, I assumed we were working with the pure kind indeed, I started with Eq. 8, the formula for the potential of a perfect dipole. And yet, an actual polarized dielectric consists of physical dipoles, albeit extremely tiny ones. What is more, I presumed to represent discrete molecular dipoles by a continuous density function P. How can I justify this method? Outside the dielectric there is no real problem: here we are far away from the molecules (r is many times greater than the separation distance between plus and minus charges), so the dipole potential dominates overwhelmingly and the detailed graininess of the source is blurred by distance. Inside the dielectric, however, we can hardly pretend to be far from all the dipoles, and the procedure I used in Sect. 2.1 is open to serious challenge. In fact, when you stop to think about it, the electric field inside matter must be fantastically complicated, on the microscopic level. If you happen to be very near an electron, the field is gigantic, whereas a short distance away it may be small or may point in a totally different direction. Moreover, an instant later, as the atoms move about, the field will have altered entirely. This true microscopic field would be utterly impossible to calculate, nor would it be of much interest if you could. Just as, for macroscopic purposes, we regard water as a continuous fluid, ignoring its molecular structure, so also we can ignore the microscopic 4 This section can be skipped without loss of continuity. 179

bumps and wrinkles in the electric field inside matter, and concentrate on the macroscopic field. This is defined as the average field over regions large enough to contain many thousands of atoms (so that the uninteresting microscopic fluctuations are smoothed over), and yet small enough to ensure that we do not wash out any significant large-scale variations in the field. (In practice, this means we must average over regions much smaller than the dimensions of the object itself.) Ordinarily, the macroscopic field is what people mean when they speak of the field inside matter. 5 It remains to show that the macroscopic field is what we actually obtain when we use the methods of Sect. 2.1. The argument is subtle, so hang on. Suppose I want to calculate the macroscopic field at some point r within a dielectric (Fig. 16). I know I must average the true (microscopic) field over an appropriate volume, so let me draw a small sphere about r, of radius, say, a thousand times the size of a molecule. The macroscopic field at r, then, consists of two parts: the average field over the sphere due to all charges outside, plus the average due to all charges inside: E = E out + E in. The average field (over a sphere), produced by charges outside, is equal to the field they produce at the center, so E out is the field at r due to the dipoles exterior to the sphere. These are far enough away that we can safely use Eq. 9: V out = 1 4πɛ 0 outside P(r ) ˆr r 2 dτ. (17) The dipoles inside the sphere are too close to treat in this fashion. But fortunately all we need is their average field, and that is E in = 1 p 4πɛ 0 R, 3 regardless of the details of the charge distribution within the sphere. The only relevant quantity is the total dipole moment, p = ( 4 3 π R3 ) P: E in = 1 P. (18) 3ɛ 0 r R FIGURE 16 5 In case the notion of macroscopic fields sounds suspicious to you, let me point out that you do exactly the same averaging whenever you speak of the density of a material. 180

Now, by assumption, the sphere is small enough that P does not vary significantly over its volume, so the term left out of the integral in Eq. 17 corresponds to the field at the center of a uniformly polarized sphere, to wit: (1/3ɛ 0 )P (Eq. 14). But this is precisely what E in (Eq. 18) puts back in! The macroscopic field, then, is given by the potential V (r) = 1 P(r ) ˆr dτ 4πɛ 0 r, (19) 2 where the integral runs over the entire volume of the dielectric. This is, of course, what we used in Sect. 2.1; without realizing it, we were correctly calculating the averaged, macroscopic field, for points inside the dielectric. You may have to reread the last couple of paragraphs for the argument to sink in. Notice that it all revolves around the curious fact that the average field over any sphere (due to the charge inside) is the same as the field at the center of a uniformly polarized sphere with the same total dipole moment. This means that no matter how crazy the actual microscopic charge configuration, we can replace it by a nice smooth distribution of perfect dipoles, if all we want is the macroscopic (average) field. Incidentally, while the argument ostensibly relies on the spherical shape I chose to average over, the macroscopic field is certainly independent of the geometry of the averaging region, and this is reflected in the final answer, Eq. 19. Presumably one could reproduce the same argument for a cube or an ellipsoid or whatever the calculation might be more difficult, but the conclusion would be the same. 3 THE ELECTRIC DISPLACEMENT 3.1 Gauss s Law in the Presence of Dielectrics In Sect. 2 we found that the effect of polarization is to produce accumulations of (bound) charge, ρ b = P within the dielectric and σ b = P ˆn on the surface. The field due to polarization of the medium is just the field of this bound charge. We are now ready to put it all together: the field attributable to bound charge plus the field due to everything else (which, for want of a better term, we call free charge, ρ f ). The free charge might consist of electrons on a conductor or ions embedded in the dielectric material or whatever; any charge, in other words, that is not a result of polarization. Within the dielectric, the total charge density can be written: and Gauss s law reads ρ = ρ b + ρ f, (20) ɛ 0 E = ρ = ρ b + ρ f = P + ρ f, where E is now the total field, not just that portion generated by polarization. 181

It is convenient to combine the two divergence terms: (ɛ 0 E + P) = ρ f. The expression in parentheses, designated by the letter D, D ɛ 0 E + P, (21) is known as the electric displacement. In terms of D, Gauss s law reads D = ρ f, (22) or, in integral form, D da = Q fenc, (23) where Q fenc denotes the total free charge enclosed in the volume. This is a particularly useful way to express Gauss s law, in the context of dielectrics, because it makes reference only to free charges, and free charge is the stuff we control. Bound charge comes along for the ride: when we put the free charge in place, a certain polarization automatically ensues, by the mechanisms of Sect. 1, and this polarization produces the bound charge. In a typical problem, therefore, we know ρ f, but we do not (initially) know ρ b ; Eq. 23 lets us go right to work with the information at hand. In particular, whenever the requisite symmetry is present, we can immediately calculate D by the standard Gauss s law methods. Example 4. A long straight wire, carrying uniform line charge λ, is surrounded by rubber insulation out to a radius a (Fig. 17). Find the electric displacement. λ L s a Gaussian surface FIGURE 17 Solution Drawing a cylindrical Gaussian surface, of radius s and length L, and applying Eq. 23, we find D(2πsL) = λl. 182