16), the susceptibility is defined via P = ϵ0χE, where E is the macroscopic
field. The polarization is always based on the combined behavior of all of the dipoles P = N qe re (see (2.31)). Equating these two expressions for P and inserting (2.70), we find that the susceptibility is given by χ(ω) = Nα(ω) ϵ0 1− Nα(ω) 3ϵ0 (2.71) This is known as the Clausius-Mossotti relation. In Section 2.4, we only included the numerator of (2.71). The extra term in the denominator becomes important when N is sufficiently large, which is the case for liquid or solid densities. Since we neglect absorption, from (2.25) we have χ = n 2−1, and we may write n 2 −1 = Nα/ϵ0 1− Nα/3ϵ0 (2.72) In this case, we may invert the relation to write Nα/ϵ0 in terms of the index:17 Nα ϵ0 = 3 n 2 −1 n 2 +2 (2.73) 16In principle, the detailed fields of nearby dipoles should also be considered rather than representing their influence with the macroscopic field. However, if they are symmetrically distributed the result is the same. See J. D. Jackson, Classical Electrodynamics, 3rd ed., Sect. 4.5 (New York: John Wiley, 1999). 17This form of Clausius-Mossotti relation, in terms of the refractive index, was renamed the Lorentz-Lorenz formula, but probably undeservedly so, since it is essentially the same formula. 64 Chapter 2 Plane Waves and Refractive Index Example 2.5 Xenon vapor at STP (density 4.46×10−5mol/cm3 ) has index n = 1.000702 measured at wavelength 589nm. Use (a) the Clausius-Mossotti relation (2.71) and (b) the uncorrected formula (i.e. numerator only) to predict the index for liquid xenon with density 2.00×10−2mol/cm3 . Compare with the measured value of n = 1.332.18 Solution: At the low density, we may safely neglect the correction in the denominator of (2.72) and simply write Natmα/ϵ0 = 1.0007022 − 1 = 1.404 × 10−3 . The liquid density Nliquid is 2.00 × 10−2 /4.46 × 10−5 = 449 times greater. Therefore, Nliquidα/ϵ0 = 449×1.404×10−3 = 0.630. (a) According to Clausius-Mossotti (2.72), the index is n = r 1+ 0.630 1−0.630/3 = 1.341 (b) On the other hand, without the correction in the denominator, we get n = p 1+0.630 = 1.277 The Clausius-Mossotti formula gets much closer to the measured value. Figure 2.12 The field lines surrounding a dipole. Average Field Produced by a Dipole Consider a dipole comprised of point charges ±qe separated by spacing re = zˆd. If the dipole is centered on the origin, then by Coulomb’s law the field surrounding the point charges is E = qe 4πϵ0 r−zˆd/2 |r−zˆd/2| 3 − qe 4πϵ0 r+zˆd/2 |r+zˆd/2| 3 We wish to compute the average field within a cubic volume V = L 3 that symmetrically encompasses the dipole.19 We take the volume dimension L to be large compared to the dipole dimension d. Integrating the field over this volume yields Z Ed v = qe 4πϵ0 ZL/2 - L/2 d x ZL/2 - L/2 d y ZL/2 - L/2 d z " xxˆ + yyˆ +(z −d/2)zˆ £ x 2 + y 2 +(z −d/2) 2 ¤3/2 − xxˆ + yyˆ +(z +d/2)zˆ £ x 2 + y 2 +(z +d/2) 2 ¤3/2 # = −zˆ qe 2πϵ0 ZL/2 - L/2 d x ZL/2 - L/2 d y 1 q x 2 + y 2 +(L −d) 2 /4 − 1 q x 2 + y 2 +(L +d) 2 /4 18D. H. Garside, H. V. Molgaard, and B. L. Smith, “Refractive Index and Lorentz-Lorenz function of Xenon Liquid and Vapour,” J. Phys. B: At. Mol. Phys. 1, 449-457 (1968). 19Authors often obtain the same result using a spherical volume with the (usually unmentioned) conceptual awkwardness that spheres cannot be closely packed to form a macroscopic medium without introducing voids. 2.C Energy Density of Electric Fields 65 The terms multiplying xˆ and yˆ vanish since they involve odd functions integrated over even limits on either x or y, respectively. On the remaining term, the integration on z has been executed. Before integrating the remaining expression over x and y, we make the following approximation based on L ≫ d: 1 q x 2 + y 2 +(L ±d) 2 /4 ∼= 1 p x 2 + y 2 +L 2/4 1 q 1± Ld/2 x 2+y 2+L 2/4 ∼= 1 p x 2 + y 2 +L 2/4 · 1∓ Ld/4 x 2 + y 2 +L 2/4¸ which will make integration considerably easier.20 Then integration over the y dimension brings us to21 Z Ed v = −zˆ qed 4πϵ0 ZL/2 -L/2 d x ZL/2 -L/2 Ld y £ x 2 + y 2 +L 2/4¤3/2 = −zˆ qed 4πϵ0 ZL/2 -L/2 L 2d x ¡ x 2 +L 2/4¢p x 2 +L 2/2 The final integral is the same as twice the integral from 0 to L/2. Then, with x > 0, we can employ the variable change s = x 2+L 2 /4 ⇒ 2d x = d s/ p s −L 2/4 and obtain Z Ed v = −zˆ qed 4πϵ0 L 2 Z /2 L 2/4 L 2d s s p s 2 −L 4/16 = −zˆ qed 4πϵ0 4π 3 Reinstalling re = zˆd and dividing by the volume 1/N, allotted to individual dipoles, brings us to the anticipated result (2.68). Appendix 2.C Energy Density of Electric Fields In this appendix we show that the term ϵ0E 2 /2 in (2.53) corresponds to the energy density of an electric field.22 The electric potential φ(r) (in units of energy per 20One might be tempted to begin this calculation with the well-known dipole field E = qe 4πϵ0r 3 r−zˆd/2 h 1−zˆ · rˆ d r + d 2 4r 2 i3/2 − r+zˆd/2 h 1+zˆ · rˆ d r + d 2 4r 2 i3/2 ∼= qed 4πϵ0r 3 [3rˆ (zˆ · rˆ)−zˆ] which relies on the approximation h 1±zˆ · rˆd/r +d 2 /4r 2 i−3/2 ∼= [1±zˆ · rˆd/r ] −3/2 ∼= 1∓ 3dzˆ · rˆ 2r This dipole-field expression, while useful for describing the field surrounding the dipole, contains no information about the fields internal to the dipole. Note that we integrate z through the origin, which would violate the above assumption r ≫ d. Alternatively, the influence of the internal fields on our integral could be accomplished using a delta function as is done in J. D. Jackson, Classical Electrodynamics, 3rd ed., p. 149 (New York: John Wiley, 1999). 21Two useful integral formulas are (0.61) and (0.61). 22J. R. Reitz, F. J. Milford, and R. W. Christy, Foundations of Electromagnetic Theory 3rd ed., Sect. 6-3 (Reading, Massachusetts: Addison-Wesley, 1979). 66 Chapter 2 Plane Waves and Refractive Index charge, or volts) describes the potential energy that a charge would experience if placed at any given point in the field. The electric field and the potential are connected through E(r) = −∇φ(r) (2.74) The energy U necessary to assemble a distribution of charges (owing to attraction or repulsion) can be written in terms of a summation over all of the charges (or charge density ρ (r)) located within the potential: U = 1 2 Z V φ(r)ρ (r)d v (2.75) We consider the potential to arise from the charges themselves. The factor 1/2 is necessary to avoid double counting. To appreciate this factor consider just two point charges: We only need to count the energy due to one charge in the presence of the other’s potential to obtain the energy required to bring the charges together. A substitution of (1.1) for ρ (r) into (2.75) gives U = ϵ0 2 Z V φ(r)∇·E(r)d v (2.76) Next, we use the vector identity in P0.9 and get U = ϵ0 2 Z V ∇· £ φ(r)E(r) ¤ d v − ϵ0 2 Z V E(r)· ∇φ(r)d v (2.77) An application of the divergence theorem (0.11) on the first integral and a substitution of (2.74) into the second integral yields U = ϵ0 2 I S φ(r)E(r)·nˆd a + ϵ0 2 Z V E(r)·E(r)d v (2.78) We can consider the volume V (enclosed by S) to be as large as we like, say a sphere of radius R, so that all charges are contained well within it. Then the surface integral over S vanishes as R → ∞ since φ ∼ 1/R and E ∼ 1/R 2 , whereas d a ∼ R 2 . Then the total energy is expressed solely in terms of the electric field: U = Z All Space uE (r)d v (2.79) where uE (r) ≡ ϵ0E 2 2 (2.80) is interpreted as the energy density of the electric field. 2.D Energy Density of Magnetic Fields 67 Appendix 2.D Energy Density of Magnetic Fields In a derivation similar to that in appendix 2.C, we consider the energy associated with magnetic fields.23 The magnetic vector potential A(r) (in units of energy per charge×velocity) describes the potential energy that a charge moving with velocity v would experience if placed in the field. The magnetic field and the vector potential are connected through B(r) = ∇ ×A(r) (2.81) The energy U necessary to assemble a distribution of currents can be written in terms of a summation over all of the currents (or current density J(r)) located within the vector potential field: U = 1 2 Z V J(r)·A(r)d v (2.82) As in (2.75), the factor 1/2 is necessary to avoid double counting the influence of the currents on each other. Under the assumption of steady currents (no variations in time), we may substitute Ampere’s law (1.21) into (2.82), which yields U = 1 2µ0 Z V [∇ ×B(r)]·A(r)d v (2.83) Next we employ the vector identity P0.8 from which the previous expression becomes U = 1 2µ0 Z V B(r)·[∇ ×A(r)]d v − 1 2µ0 Z V ∇·[A(r)×B(r)]d v (2.84) Upon substituting (2.81) into the first equation and applying the Divergence theorem (0.11) on the second integral, this expression for total energy becomes U = 1 2µ0 Z V B(r)·B(r)d v − 1 2µ0 I S [A(r)×B(r)]·nˆ d a (2.85) As was done in connection with (2.78), if we choose a large enough volume (a sphere with radius R → ∞), the surface integral vanishes since A ∼ 1/R and B ∼ 1/R 2 , whereas d a ∼ R 2 . The total energy (2.85) then reduces to U = Z Al l Space uB (r)d v (2.86) where uB (r) ≡ B 2 2µ0 (2.87) is the energy density for a magnetic field. 23J. R. Reitz, F. J. Milford, and R. W. Christy, Foundations of Electromagnetic Theory 3rd ed., Sect. 12-2 (Reading, Massachusetts: Addison-Wesley, 1979. 68 Chapter 2 Plane Waves and Refractive Index Exercises Exercises for 2.4 The Lorentz Model of Dielectrics P2.1 Verify that (2.35) is a solution to (2.34). P2.2 Derive the Sellmeier equation n 2 = 1+ Aλ 2 vac λ2 vac −λ 2 0,vac from (2.39) for a gas with negligible absorption (i.e. γ ∼= 0, valid far from resonance ω0), where λ0,vac corresponds to frequency ω0 and A is a constant. Many materials (e.g. glass, air) have strong resonances in the ultraviolet. In such materials, do you expect the index of refraction for blue light to be greater than that for red light? Make a sketch of n as a function of wavelength for visible light down to the ultraviolet (where λ0,vac is located). P2.3 In the Lorentz model, take N = 1028 m−3 for the density of bound electrons in an insulator, and a single transition at ω0 = 6×1015 rad/sec (in the UV), and damping γ = ω0/5 (quite broad). Assume that the magnitude of E0 is 104 V/m. For three frequencies i) ω = ω0 − 2γ, ii) ω = ω0, and iii) ω = ω0 +2γ find: (a) the amplitude and phase of the charge displacement re (2.35) relative to the phase of E0e i(k·r−ωt) . (b) the magnitude and complex phase of the susceptibility χ(ω). Does χ(ω) depend on the strength of the E-field? (c) n and κ at the three frequencies via (2.29) and (2.27). Answer: i) n = 1.53, κ = 0.0817, ii) n = 1.66, κ = 1.33, iii) n = 0.470, κ = 0.263. (d) the three speeds of light in terms of c and how far light penetrates into the material before only 1/e of the amplitude of E remains. P2.4 (a) Use a computer to plot n and κ as a function of ω for a dielectric (i.e. obtain graphs such as the ones in Fig. 2.5). Use the Lorentz model and the following parameters: ω0 = 10ωp, and γ = ωp; plot your function from ω = 0 to ω = 20ωp. No need to choose a value for ωp; your horizontal axis will be in units of ωp. (b) Plot n and κ as a function of frequency for a material that has three resonant frequencies: ω01 = 10ωp, γ1 = ωp, f1 = 0.5; ω02 = 15ωp, γ2 = ωp, f2 = 0.25; and ω03 = 25ωp, γ3 = 3ωp, f3 = 0.25. Plot the results from ω = 0 to ω = 30ωp. Exercises 69 Exercises for 2.5 Index of Refraction of a Conductor P2.5 For silver, the complex refractive index is charact
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