When we formulated our description of how electromagnetic waves move through linear media, we relied on the stipulation that the free charge density ρf and free current density Jf were zero. In the case of conductors, we're going to need to re-visit that assumption.
As a refresher, when we last took a good look at conductors we had just moved beyond the electrostatic picture. In statics, we could assume that the field within a conductor is always zero, because any field would eventually (quickly) cause the free changes to arrange in such a way as to cancel the field. Now, we want to see how the conductor responds when we have a varying electric field.
So, what do we already know about electric fields in matter?
∇⋅E=ϵρf(Gauss’ Law in media)
∇⋅Jf+∂t∂ρf=0(Continuity)
Jf=σE(Ohm’s Law)
→∇⋅(σJf)=ϵρf
→σ1(−∂t∂ρf)=ϵρf
→∂t∂ρf=−ϵσρf
We see differential equations like this all the time - it's the equation for an exponential decay. The decay timescale of the free charge density is
τ1/e=σϵ
Applying to the situation of a very good conductor where σ is very large, e.g. copper, the time constant is around 10−19 seconds. This means that if a little bit of free charge has accumulated at any time, then from that point charge will flow to suppress that field on the timescale of 10−19 seconds. So, for the vast majority of radiation (wave period up to ≈10−18), the time constant is fast enough that the conductor is effectively impermeable, and all our previous descriptions of conductors are still sound. Namely, the Maxwell equations look like
∇⋅E=0
∇⋅B=0
∇×E=−∂t∂B
∇×B=μϵ∂t∂E+μσE(σE=J)
As before, to get our wave equations, apply ∇×(∇×E) and ∇×(∇×B)
∇(∇⋅E)−∇2E=−∇×(∂t∂B)=−∂t∂(∇×B)
→−∇2E=−μϵ∂t2∂2E−μσ∂t∂E
→∇2E=μϵ∂t2∂2E+μσ∂t∂E
As σ→0, we recover the wave equation for linear media as we'd expect. We now have a "lossy" wave equation, since there is attenuation of the wave over time.
From ∇×(∇×B) we get
∇2B=μϵ∂t2∂2B+μσ∂t∂B
Recall that for σ=0 the wave equation supports waves of the form ei(k⋅r−ωt). For propagation along the z-axis, ei(kz−ωt). To solve the lossy version, we'll look for solutions by introducing an imaginary component to k in order to satisfy the damping term.
→k~=k+iκ
For the one-dimensional case, let's plug our new wave solution in
∇2E=μϵ∂t2∂2E+μσ∂t∂E
→−k~2=μϵ(−ω2)+μσ(−iω)
→k2−κ2+2ikκ=μϵω2+iμσω
→k2−κ2=μϵω2kκ=μσω
→k=2κμσω(2κμσω)2−κ2=μϵω2
→κ4+μϵω2κ2−(2μσω)2=0
We just write down the solution to the quadratic equation in κ
κ=2−μϵω2±(μϵω2)2+(μσω)2
Because we enforce that κ is real, and all of the parameters within the square root are positive, we need to choose the + sign
κ=2(μϵω2)2+(μσω)2−μϵω2
→κ=2μϵω21+(ϵωσ)2−1
→κ=ω2ϵμ[1+(ϵωσ)2−1]1/2
Plugging κ back in to our expression for k and doing some algebraic manipulation,
k=ω2ϵμ[1+(ϵωσ)2+1]1/2
So the fields look like
E(z,t)=E0e−κzei(kz−ωt)
B(z,t)=B0e−κzei(kz−ωt)
As a check, if σ→0, κ→0, k→ω2ϵμ2=ωϵμ=ω/v and we are back to the linear medium we started with. In the case of a really good conductor (where 1/ω≫ϵ/σ), both k and κ will converge
k≈κ→ω2ϵμ[ϵωσ]1/2=ω2ϵμϵσ=2ωμσ
For a good conductor, both E and B get damped over a distance scale given by 1/κ, which can be quite short. Since kκ we can relate this "skin depth" to the wavelength
λ=k2π→d=κ1=2πλ
Before, we had a real proportionality factor between E0 and B0. If we go through the same motions here with our new lossy solution,
∇×E=−∂t∂B→B0=ωk~E0
Because k~ is a complex number, this ratio will also be a complex number. For our phasor expressions for the fields, this amounts to a phase shift between the two.
In conductors, there is a phase difference between the E and B fields. For a good conductor, the phase shift is 45∘
9.4.2: Reflection at a Conducting Surface
In this situation, we consider a wave traveling through a linear medium (or vacuum) impinging on a conducting surface at a normal to the surface. We can go ahead and write down the general boundary conditions:
For a conductor obeying Ohm's law Jf=σE. So, since E is finite, we will have a finite Jf, so we have kf must go to zero, which takes care of the right hand side of equation (iv). Since we know that E and B are transverse to the wave,
E1⊥=E2⊥=0→σf=0
Putting all of these together, we have the boundary conditions for a conducting-linear interface:
Apply boundary condition at z=0 and set the time phase factors equal to each other (as they must be)
E~0,I+E~0,R=E~0,T
μ1v11E~0,I−μ1v11E~0,R=μ21ωk2~E~0,T
E~0,I−E~0,R=β~E~0,Tβ~=μ2ωμ1v1k2~
Manipulating these together,
E~0,T=(1+β~2)E~0,I
E~0,R=(1+β~1−β~)E~0,I
For a good conductor (where σ/ϵω≫1), β~ will approach
β~→μ2ωμ1v12ωσμ2(1+i)
For σ→∞ (a perfect conductor),
E~0,R→−E~0,I
E~0,T→0
Which is to say, a perfect conductor is a perfect reflector with a 180∘ phase change at the interface. The obvious applications are silvered mirrors and fully metal mirrors.
9.4.3: The Frequency Dependence of Permittivity
For electromagnetic radiation, dispersion is a measure of the frequency response of a propagating wave on the permittivity, permeability, and conductivity of the medium it is propagating through.
Permittivity:ϵ→ϵ(ω)
The majority of radiation that we interact with is not monochromatic, and every real radiation source has some non-zero linewidth. The spectrum of frequencies contained in the radiation will broaden and "disperse" depending on the dispersion relation of the material the wave propagates through. This makes it very important to consider the dispersion properties of whatever material a wave is propagating through, no matter what the source is.
As usual, we'll start with the simplest case: the linear relation
Linear dispersion in free space: ω=ck
Actually, many real media are have very nearly a linear dispersion relationship. Since the wave velocity depends on ϵ and μ, we now have a velocity which is a function of frequency. In general, there are two velocities that we care about: the wave/phase velocityv=ω/k and the group velocityvg=dkdω. We can think of the phase velocity as the velocity at which each individual sinusoidal component of a wave packet travels, while the group velocity defines the speed of the overall packet/envelope.
What gives rise to the real relationship? Well, as a wave propagates through some medium, the atoms that make up the medium will have their own resonances depending on their state. In general, any mildly complex medium will have many many resonances, and the shape of the permittivity curve will be defined by the full composition of all of the resonances and can be quite complicated.
Because the mass of the electron is so much smaller than the mass of the nucleus, the electron responds as if it were tied to a central potential like a spring with damping.
mdt2d2x+mγdtdx+mω02x=qE0cos(ωt)
where γ is a damping term. There are many potential mechanisms by which the system can lose energy, and we lump them all together into the simple damping term.
Setting up shop back in our phasor space,
x≡Re[x~]
dt2d2x~+γdtdx~+mω02x~=mqE0e−iωt
Plugging in the form for x~ we know we're going to get (a response with the same frequency as the driving field)
x~=x~0e−iωt
[−ω2−iγω+ω02]x~e−iωt=mqE0e−iωt
→x~0=(ω02−ω2)−iγωqE0/mx0=Re[x~0]
What's the dipole moment of the system of the electron moving up and down with the wave? We will see that the dipole moment can be connected to the permittivity of the system through the polarization, and from there we'll get our dispersion relation.
p~(t)==qx~(t)(ω02−ω2)−iγωq2/mE0e−iωt
If we assume we have N molecules per unit volume and multiple resonances j:ωj,γj, and oscillator "strength" fj (where we lump together the oscillation response of the resonance), the polarization P is
P~(t)=mNq2(j∑(ωj2−ω2)−iγjωfi)E~
Recall the relation between polarization and susceptibility
So that's how the electron response to a wave can be connected with the index of refraction, but we've got a complex permittivity & dielectric constant. What does the generalized wave equation tell us about how this changes our solutions?
∇2E~=ϵ~μ0∂t2∂2E
Again, insert a plane wave solution
E~=E~0ei(k~z−ωt)
→−k~2=ϵ~μ0(−ω2)
→k~2=ϵ~μ0ω2
and
k~=ϵ~μ0ω=k+iκ
When n2−1 is small compared to 1, then we can expand n as
n=n~=1+2mϵ0Nq2j∑(ωj2−ω02)−iγjωfj
E~=E~0e−κzei(kz−ωt)
"n2−1 is small compared to 1" just means the larger term on the RHS is small compared to 1, and this is true for many gaseous systems resulting in an index of refraction close to 1. We often compare the frequency response to the so-called absorption coefficientα=2κ, because the intensity is proportional to E2 which goes as e−2κz so the characteristic width of the distribution is 2κ. For gases (diffuse media),