EM Radiation

Poynting Theorem

Starting from Maxwell’s equation (for macroscopic materials). Consider Faraday’s law ×E+Bt=0 and Ampere’s law ×HDT=J.

Multiplying Ampere’s law by E and subtracting, we get the exact equation,

(E×H)+HBt+EDt=JE(1)S+HBt+EDt=JE.

For linear media, E=\veE,B=μH. So,

S+μHHt+\veEEt=JES+t(12ED+12HB)=JES+t(uE+uM)=JE(2)S+ut=JE.

For no current, we get S+ut=0 gives a continuity equation. Hence currents become a source and S is an energy flux since u is an energy density.

Consider the integral form of the Poynting vector,

(3)\oiintSn^da=ddtudVJEdV(4)\oiintSn^da=ddtUρvEdV(5)\oiintSn^da=ddt(U+T)

So, if the energy in a region is not changing, then no radiation is emitting. If energy in a region is changing, radiation must be coming in or leaving.

Momentum of E&M Wave

Classically: F=q(E+v×B)=dpmechdt. Doing a volume integration of the system, dpmechdt+dpemdt=F with dpemdt=gdV where g=1c2S.

A photon has energy ω then the energy density is NωV then the flux is NωVc=S. So, the momentum is then (say we have a single photon in a unit volume), S=ωc so, g=ωc so the momentum is ωc=2πccλ=k.

Consider the harmonic field: F(x,t)=[F(x)exp(iωt)]=12(F(x)exp(iωt)+F(x)exp(iωt))

Then the product of two fields, F(x,t)G(x,t)=14(FG+FG+FGexp(2iωt)+FGexp(2iωt)).

If we time-average this, F(x,t)G(x,t)=14FG+FG=12(FG).

So, the Complex Poynting Theorem can be derived. ×E=iωB and ×J=JiωD. Taking the complex conjugate of the second equation and multiplying by E and multiplying the first by H,

H×E=iωBHE×H=EJiωDE.

Subtracting,

Misplaced &

So, S=12E×H. Then, ×S=iω2(EDBH)12JE. So, Sn^da=iω2dV(EDBH)12dVJE.

So, Sn^da=12IV=12|I|2R.

Note that the half comes from the time-average.

Then, Irms2R is the energy loss of the system.

Monochromatic Waves

It is useful to write E,B,D,Hexp(iωt).

Then the field, F(x,t)=F(x)exp(iωt).

F(x,t)G(x,t)time=12[F(x)G(x)].

(E×H)=S=iω(EDBH)JE. uE=14ED, uM=14BH.

Taking the real part, [S=iω(EDBH)JE].

When we have R,C,L components in a circuit, we have Vi=ZIi. Where Z=RiX and X relates to both the inductance and capacitance.

Note that iω(EDBH) relates to the reactance and JE relates to resistance. , relates to reactance and resistance.

Monochromatic Plane Waves

Stoke’s Paramters

  • S0=|E1|2+|E2|2I
  • S1=|E1|2|E2|2
  • S2=2(E1E2)=2a1a2cosδ
  • S3=2(E1E2)=2a1a2sinδ
  • S02=S12+S22+S32.

Say we have E1=a1,E2=a2exp(iδ). Then, S0=a12+a22 and S1=a12a22I1I2. From these, a1 and a2 are fully determinable. S2 can be determine by putting polarizers at 45 above and below the polarization basis vector ϵ^1, and measure the intensities, I+I=cosδ, hence you get |δ|. S3 can be measured with far away plate, λ/2, IRIL=sinδ.

Light-matter interaction: atom absorbs light then eventually radiates (thus light travels slower in a medium). For transparent materials, the loss of the light through the medium is very small.

When light hits a superconductor, light gets reflected. For a conductor, light gets mostly reflected.

Ohm’s Law

J=σE.

For J=02E=\veμ2Et2. For J02E=\veμ2Et2+μσEt.

Losses in Complex Refractive Media

For a monochromatic wave, E(x,t)=Eexp(i(kxωt)) but in the medium k becomes complex and thus introduces a loss. Then, k2=\veμω2+iμωσ. Thus, k=\veμω2+iμωσ=kr+iki=(nr+ini)ωc. Then we have the decaying wave, exp(ikz)=exp(ikr)exp(kiz).

Note, when the electron absorbs the light, it gets accelerated. From the defects in the material, it gets kicked around and the energy gets turned into thermal energy. Thus, the wave decays as it progresses through the medium.

\ver=n2=1\ve0μ0(\veμ+iμσω) Then, n2=nr2ni2+2nrnii. So, kr,i=nr,iωc.

We can write this as, exp(kiz)=exp(z/δ) were delta is called the transmission depth.

Suppose that μσω\veμ, then k2=iμσω so k=μσω12(1+i). Thus, the imaginary and real parts have the same magnitude.

For copper, ρ=1σ=1.7108Ωm. Then, δ=1ki=2μσω2μ0σω=6.5102ν m. For visible light, 10141016. Then, δ1091010 m. The wave has a wavelength of 106, so most get reflected. The penetration depth is much shorter than the wavelength.

Transmission and Reflection

Polarizations

For s-polarization, E,E,Ey^. E0+E0=E01+rs=ts and cB0t+cB0t=cB0t1rs=nncosθtcosθits. So, ts=2ncosθincosθi+ncosθt rs=1ts.

For p-polarization, B,B,By^. (E0E0)cosθi=E0cosθt and c(B+B=B)nE+nE=nE. Thus, tp=2ncosθincosθt+ncosθi rp=1tp.

Recall nsinθi=nsinθt hence θt depends on θi. Therefore, we have fully determined the system: cosθt=1n2n2sin2θi.

Special Angles

If θi=0 then, cosθt=1, ts=2nn+n=tp and rs=nnn+n=rp. For s-pol, Ey^. For p-pol, EEEx^.

The total reflectance is then, 20230515102213-em_radiation.org_20230526_103743.png

The brewster angle, when p-reflectance goes to zero, tanθB=nn. There is no reflectance since the dipoles are oscillating parallel to the reflected wave, which means it does not show up.

Total internal reflection: θi=θc at θt=90. That is, there is only reflected light: R=1. We get a decaying wave and from phase matching kx=kx. And k=kxx^+kzz^. We have the dispersion relation, k2=n2ω2c2=kx2+kz2. So, kz must be imaginary to make the phase matching possible above the critical angle. So, if we let kz=iδ. Then we get the decaying wave of exp(zδ). Further, kz=iksin2θisin2θc. So, δ=λ2πsin2θisin2θc.

For \(n'\theta_c\), cosθt=1n2n2sin2θc=1sin2θisin2θc=isin2θisinθc1. Then, r=aiba+ibR=|r|2=1.

Frequency Dispersion

k=nωc=ωvph.

Drude-Lorentz SHOM

  • Drude - Model for free electrons
  • Lorentz - Dielectric medium

Consider if you have an electron and atom. Apply a wave. The electron is initially in roughly a harmonic well, V(x)=12kx2. So for an ideal dielectric, F(x)=md2xdt2=eEkx. Realistically, we have a damping force, F(x)=md2xdt2=eEkxγdxdt. For a 1d system, d2xdt2+γdxdt+ω02x=emEx, where ω02=km. Using an electric dipole approximation for our wave, E=E0exp(i(kzωt))=E0exp(iωt). Then, for a 1d system, d2xdt2+γdxdt+ω02x=emE0exp(iωt), where ω02=km. Then, x(t)=x0exp(ωt) with x=emEω02ω2)iωγ. So, p=ex=e2mEω02ω2iωγ Then, P=Np=ε0χeE. So, χe(ω)=Ne2mε01ω02ω2iωγ.

For a collection of these oscillators, j=1z=fiω02ω2iωγ.

For γω0, χe(ω)Ne22mε0ω01ω0ωiγ2=Aω0ωiΓ.

k=kr+iki=β+iα2. Then, I|E0|2exp(αz). Also, k2=α2+β24+iαβ=n2ω2/c2=εrω2c2. So, α2+β24=ω2c2[εr]. αβ=ω2c2[εr].

For a gaseous medium. εr=1+χen1+12χe. Then, α=ωc=2πλ. So, nR1+12(χe)1 and nI12χe Then, β=ωcχe.

Drude Model

F=mdvdt=eEm]gammav Eexp(iωt),v=v0exp(iωt). v=em1γiωE

J=ρv=Neev=σE. Nee2m1γiω=σ. σ(ω)=Nee2m1γiω=Nee2mγ+iωγ2+ω2 Then the scattering time is, τ0=1γ. σ(ω)=Nee2mτ0+iωτ021+ω2τ02

In DC limit, ω=0, σ0=Nee2mτ0. For γ1014 Hz, waves even as high as 1012 Hz are still behaving with a DC ’constant’ resistance. ×H=J+Dt=σEiωεbE=iω(εb+iσω)E. εr=εbε0+iσε0ω.

At high-frequency, σ(ω)=Nee2miωτ02ω2τ02=Nee2miω εr(ω)=εbε0+iNee2mωε01γiω=εbε0N0e2ε0mω21N0e2ε0mω2=1ωP2ω2 Where this is called the plasma frequency.

For ω<ωp εr<0 so it is purely imaginary εr and so we get total reflectance. For ω>ωp εr>0.

Gaussian Pulse

E(t)=E0exp(at2)cos(ω0t). I0(t)=12ε0cnE02exp(2at2). Since if you Fourier transform a gaussian, you get a guassian. A well localized packet has a wide frequency spectrum.

When the group velocity is equal to the phase velocity, the pulse remains the same and just translates.

For vg<vph. then the gropu velocity stays with the peak but the fast oscillation moves past the peak at a faster speed. For vg>vph. then the gropu velocity stays with the peak but the slow oscillation moves past the peak backwards.

Beats Phenomena

E~tot(t)=E~0exp(iω1t)+E~0exp(iω2t). ωave=ω1+ω22,Δω=ω1ω22. Then, E~tot(t)=2E~0exp(iωavet)cosΔωt. The cosine gives the envelope.

Similarly with the wavenumbers, Etot(x,t)=2E0cos(ΔkxΔωt)exp(i(kavgxωavgt)). Group velocity: vg=dωdk. From the dispersion relation, vg=(dkdω)1=(1c(n+ωdndω))1=vph1+ωndndω Phase velocity: vph=ωavgkavg.

Author: Christian Cunningham

Created: 2024-05-30 Thu 21:20

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