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Steven Errede
LECTURE NOTES 7
The general solution of this differential equation for the free charge density is of the form:
free r , t free r , t 0 e C t free r , t 0 e t relax i.e. a damped exponential !!!
Characteristic damping time: relax C = charge relaxation time {aka time constant}.
Thus, the continuity equation J free r , t free r , t t inside a conductor tells us that any
free charge density free r , t 0 initially present at time t = 0 is exponentially damped /
dissipated in a characteristic time relax C = charge relaxation time {aka time constant},
such that at when: t relax C : free r , t relax free r , t 0 e 1 0.369 free r , t 0
Cu
relax
Cu Cu Cu Cu 4.5 1019 sec !!!
However, the characteristic (aka mean} collision time of free electrons in pure copper is
Cu
coll
coll
Cu
Cu
vthermal where Cu
coll
3.9 108 m = mean free path (between successive collisions) in
pure copper, and vthermal
Cu
3k BT me 12 105 m sec and thus we obtain: coll
Cu
3.2 1013 sec .
Hence we see that the calculated charge relaxation time in pure copper, Cu
relax
4.5 1019 sec
is than the calculated collision time in pure copper, coll
Cu
3.2 1013 sec .
So in reality, if we are willing to wait a short time (e.g. t ~ 1ps 1012 sec ) then, any initial
free charge density free r , t 0 accumulated inside a good conductor at t = 0 will have
dissipated away/damped out, and from that time onwards, free r , t 0 can be safely assumed.
Note: For a poor conductor C 0 , then: relax C !!! Please keep this in mind
After many charge relaxation time constants, e.g. 20 relax t 1 ps 1012 sec , Maxwells
steady-state equations for a good conductor become {with free r , t t 0 from then onwards}:
1) E r , t 0 2) B r , t 0 Maxwells equations for a
charge-equilibrated conductor
B r , t E r , t E r , t
3) E r , t 4) B r , t C E r , t C E r , t
t t t
These equations are different from the previous derivation(s) of monochromatic plane EM
waves propagating in free space/vacuum and/or in linear/homogeneous/isotropic non-conducting
materials {n.b. only equation 4) has changed}, hence we re-derive {steady-state} wave equations
for E & B from scratch. As before, we apply to equations 3) and 4):
E t
B B C E
t
E
E B 2 B
= E E C E
2
B B C
= 2
2
t t t t
2 E E 2 B B
= E 2 C
2
2 B 2 C
=
t t t t
2 E r , t E r , t 2 B r , t B r , t
Again: E r , t
2
C B r , t
2
and: C
t 2 t t 2 t
Note that the {steady-state} 3-D wave equations for E and B in a conductor have an
additional term that has a single time derivative which is analogous e.g. to a velocity-dependent
damping term associated with the motion of a 1-D mechanical harmonic oscillator.
The general solution(s) to the above {steady-state} wave equations are usually in the form of
an oscillatory function a damping term (i.e. a decaying exponential) in the direction of the
propagation of the EM wave, complex plane-wave type solutions for E and B associated with
the above wave equation(s) are of the general form:
i kz t i kz t 1 k
E r , t Eo e and: B r , t Bo e k E r , t k E r , t
v
where: k e k and m k and corresponding complex wave vector
Physically, k e k is associated with wave propagation, and m k
is associated with wave attenuation (i.e. dissipation).
i kz t i kz t
We plug E r , t Eo e and B r , t Bo e into their respective wave equations
above, and obtain from each wave equation the same/identical characteristic equation
{aka a dispersion relation} between complex k and {please work this out yourselves!}:
k 2 2 i C
k 2 k i k 2 2 2ik 2 i C
2
k 2 k i k 2 2 2ik 2 i C
2
for any/all values of {any of} the parameters involved. The only in-general way that this relation
can hold is if both k 2 2 2 0 .and. 2k C 0 . Then:
k 2 2 2 and: 2k C
From the latter relation, we see that: 12 C k . Plug this result into the other relation:
1 1
k 2 2 k 2 12 C k k 2 2 2
C 2
2 2
Then multiply by k 2 and rearrange the terms to obtain the following relation:
k 4 2 k 2 12 C 0
2
This may look like a scary equation to try to solve (i.e. a quartic equation - eeekkk!), but its
actually just a quadratic equation! {So, its really just a leprechaun, masquerading as a unicorn!}
b b 2 4ac 1 2
x or: k 2 2 2 2
4 12 C
2a 2
1 2
k 1 1 4
2 C2 2
1
C2 1
2
2 1 1 2 2 2 1 1
2 2 2 C
2
4 2 2 4 2
Having thus solved for k (or equivalently, k 2 ), we can use either of our original two relations to
solve for , e.g. k 2 2 2 , thus:
1 C
2
1 C
2
2 k 2 2
2
2
1 1
2
2
2
1 1
2 2 2 2
k e k 1 C 1
and: m k 1 C 1
2
2
The above two relations clearly show the frequency dependence of both the real and imaginary
components of the complex wavenumber k k i . This physically means that EM
wave propagation in a conductor is dispersive (i.e. EM wave propagation is frequency dependent).
1 1
i.e. sc E z sc , t Eo e1e
i kz t
1
2 2
1 C 1
B z sc , t Bo e 1ei kz t
2
The real part of k , i.e. k e k determines the spatial wavelength ,
the phase speed v and also the group speed vg of the monochromatic EM plane wave
in the conductor:
2 2
k
e k
v() = propagation speed
v
Phase (kz t) = constant.
k e k
of a point on waveform A constant phase point on the
that has constant phase . waveform moves: z(t) = /k + v t.
1
1 dk vg() = propagation
vg speed of energy /
dk d d information.
We will discuss phase speed v and the group speed vg more later
The above plane wave solutions satisfy the above EM wave equations(s) for any choice of Eo .
As we have also seen before, it can similarly be shown here that Maxwells equations 1) and 2)
E 0 and B 0 rule out the presence of any {longitudinal} z-components for E and B .
For EM waves propagating in a conductor, E and B are {still} purely transverse!
If we consider e.g. a linearly polarized monochromatic plane EM wave propagating in the
k z -direction in a conducting medium, e.g. E r , t E e z e
i kz t
o x , then:
k k k i z i kz t
B r , t k E r , t E o e z e
i kz t
y Eo e e y
E r , t B r , t k z ( k z = propagation direction of EM wave, here)
m k
|k|
k
k
k e k
k k 2 2
E r , t E o e z e
i kz t
Then we see that: x has: E o Eo ei E k |k|eik
k k |k|eik
and that: B r , t B0 e e
z i kz t
y E o e z ei kz t y has: Bo Bo ei B E o Eo ei E
|k|eik |k| k2 2
Eo e
i E k
Eo e
i i E k
Thus, we see that: Bo e B Eo ei B
i.e., inside a conductor, E and B are no longer in phase with each other!!!
Phases of E and B : B E k
With phase difference: B E B E k magnetic field lags behind electric field!!!
1
Bo |k| C
2 2
1
We also see that: 1
Eo c
The real/physical E and B fields associated with linearly polarized monochromatic plane
EM waves propagating in a conducting medium are exponentially damped:
E r, t E e
E r , t e o
z
cos kz t E x B E k
B r , t e B r, t B e o
z
cos kz t B y Bo e z cos kz t E k y
1 1
Bo |k | C
2 2 C
2 2
1 where: k k 1
2 2
Eo
B E k , k tan 1 and: k k i z , k k i
k
The time-averaged power per unit volume in the conductor is: p r , t t 12 Eo2 e2 z po e z
i.e. is the independent variable {always plotted on the axis of abscissas (i.e. the x-axis)}
k is the dependent variable {always plotted on the axis of ordinates (i.e. the y-axis)}
Thus, the technically correct way is to plot k vs. : {because k depends on , not vice-versa!}
1
dk dk
Then: vg 1 i.e. vg 1 slope of k vs. graph
d d
See below:
Another way to think about this issue is to remember that the angular frequency and
wavenumber k are Fourier transforms of time t and position z t , respectively. In the space-
time domain, clearly the space position z t is the dependent variable, time t is the independent
variable. The Fourier transform of the dependent variable z t is the dependent variable k ,
the Fourier transform of the independent variable t is the independent variable .
Thus here, for the physics associated with propagation of EM plane waves in a conductor,
with frequency-dependent real-component wavenumber k :
2 2
C
k e k 1
2
1
1
The phase speed: v
k 1
2 2
1 C 1
2
1
1
2
1 dk d
1
C
2
The group speed: vg 1 1
dk d d d 2
So lets work out what the group speed vg is for an EM plane wave propagating in a conductor.
Using the chain rule of differentiation:
1 1
dk d
2 2 2 2
1 C 1 1 C 1
d 2 2 d
2
1 1 1 1
2 C 3
2 2
1 C 1
2 2
1
2 2 2
C
2
2
1 1 1 C
2
1 C
C
2 1
2
1
1
2 2 2
1
2
C
2
C
2
1 1 1
2
1 C
2 2
1
1 C 1 1
2 2
2
2
1 C 1 1 C
The group speed of an EM plane wave propagating in a conductor is: (eeek!!!)
1
dk 1 1
vg
d
1
2 2
1 C 1
2
C
2 1
1
2
2 2
C C
1 1 1
The relation between phase speed vs. group speed of an EM plane wave propagating in a conductor is:
1 1
v vg v
k 1
2 2
1 C 1
2
C
2 1
1
2
2
2
1 C 1 1 C
If the electric and magnetic fields associated with the EM wave propagating in the conductor are:
k k
E r , t E o e z e x and: B r , t k E r , t E o e z e
i kz t i kz t
y
Then:
k * * z i kz t
E o e z e
i kz t
x E e e y
o
Z r , t;
2
k
E o e e
y
i kz t
z
2
k * E o e 2 z k*
|k |2
z z Ohms
|k |2 2
E o e 2 z
k*
Note that {again}: Z r , t ; 2
z
has no explicit time dependence
|k |
Complex
k* k i impedance is
Z r , z 2 z Ohms . manifestly a
|k |
2
k 2
complex
frequency-domain
quantity
and: k tan 1 B E
k
k* k e ik
Z r , z z
|k |2 | |2
k
i B E i E B
z z
|k |
e e
|k |
k 1 1 1
2 2 2 2 2
and:
1 1 1
C
2 2
C
2 2
C C C
2
1 1 1
2 2 2 2 2
In a good conductor C 1 :
C 1 2
k and skin depth: sc .
2 C
FORMULAS FOR EM WAVE PROPAGATION IN A GOOD CONDUCTOR C 1
C 1 2
k and: sc skin depth
2 C
2 2 2 2
Wavenumber, k 2 sc 2
k C
n.b. in a perfect conductor: C k B E tan 1 tan 1
1
k
C
k But: tan 1 45
1
2 4
2
0 B E 45
k 4
1 2
sc 0 B lags E by 45 in a good conductor.
C
n.b. In a perfect conductor: C , 45 4
For optical frequencies/visible light region: 1016 radians sec . A good conductor typically has
C 107 Siemens m and 3 o , and at optical frequencies: C 37.7 1 is satisfied.
If the conductor is non-magnetic (e.g. copper, aluminum, gold, silver, platinum etc.)
o 4 107 Henrys /m .
1
C o C
1016 4 107 107 2
Then:
k
2.51108 radians /m
2 2 2
And: 2 k = wavelength in good conductor 2.51108 m 25.1nm
2 2 c c 2 3 108
cf w/ vacuum wavelength: o 1.885 107 m 188.5 nm
ko f 10 16
25.1nm good
conductor o 188.5 nm wavelength
vacuum
188.5 nm
Vacuum/conductor -ratio: o 7.52 at optical frequencies, 1016 rad/sec.
25.1 nm
1
Skin depth: sc 4.0 109 m 4.0 nm !!!
2
This explains why metals are opaque at optical frequencies, 1016 radians/sec
{and also e.g. explains why/how silvered sunglasses work!}
Compare these results for EM waves propagating in conductors at optical frequencies to those
for EM waves propagating in conductors, but instead at very low frequencies e.g. the AC line
frequency, f AC 60 Hz AC 2 f AC 120 rad/sec , where the criterion for a good
conductor, C 1015 1 is certainly well-satisfied:
AC 0.129 m
60 Hz AC skin depth: AC AC 2.05 102 m 2.05 cm !!
sc
2
C
Given that: k in a good conductor, where: C 1
2
The phase speed and group speed in a good conductor are respectively:
1
dk 1 1 2
v and: vg 2v !!!
k C d C 1 1 C
2 2 2 2
Complex impedance in a Good conductor:
k* |k | e ik ik
Z r , z z Ohms
|k |
z e
|k |
2 |k | 2
C
Since: k Then: |k | = k 2 2 2k C
2
k tan 1 B lags E by 45
tan 1 45 B E
1
And:
k in a good conductor.
good i B E i E B i E B
Z cond r , e
z e z e z
C C C
i E B C i E B
e z e z Ohms
C
Z
1
C C
2
Define {real scalar}: Z med
lin
Then {real scalar} Z cond
good
lin
Z med
lin
med
We see the phase of the complex wave impedance for a good conductor is:
Z tan 1 tan 1 45 E B B E k
1
C
Instantaneous EM Wave Energy Densities in a Good Conductor: 1
1 1 2 1 1 k B E
45
uEM u EM
u EM
E2 B EE B B 4
2 2 2
E M
2 {in a good conductor}
E r , t Eo e z cos kz t E x and B r , t Bo e z cos kz t E y
|k | C
2 2
C C
Where: Bo
Eo 1 Eo Eo E for a good conductor,
o
C
And: k ,
2
2
v for a good conductor.
k C C
2
Then:
1 1 1
uEEM r , t E 2 E E Eo2 e 2 z cos 2 kz t E and:
2 2 2
1 2 1 1 2 2 z
uMEM r , t B B B Bo e cos 2 kz t E k C Eo2 e2 z cos 2 kz t E k
2 2 2 2
1
Time-averaging these quantities over one complete cycle: u r , t u r , t dt
0
1 1 1
u EEM r , t Eo2 e 2 z cos 2 kz t E d Eo2 e 2 z
2 4
0
12
1 1 1
uMEM r , t C Eo2 e 2 z cos 2 kz t E k d C Eo2 e2 z C Eo2 e2 z
2 4
0
4
12
EM
r , t uEEM r , t uMEM r , t 1 C Eo2e2 z n.b. Exponentially attenuated in z !!!
1
uTot
4
EM 1 1 2 2 z
But: C 1 for a good conductor, uTot r , t C Eo e
2 2
uMEM r , t C
i.e. the ratio: EM
1 or: uMEM r , t uEEM r , t for a good conductor.
uE r , t
Vast majority of EM wave energy is carried by the magnetic field in a good conductor !!!
1 1 1
Poyntings Vector: S E B S r ,t EB Eo Bo e 2 z cos k z k
2 4
1 1 2 2 z |k|
EM wave intensity (aka irradiance): I r S r , t Eo Bo e 2 z cos k Eo e cos k
2 2
|k|cos k
C
k C 1 k 2 2 z 1 C 2 2 z
But: 2
I r S r ,t Eo e Eo e
2 2 2 2
b.) Special/Limiting Case of a Fair Conductor: C 1 Must use exact formulae!
Here: C 1 . Conductivity of poor conductor: C 0 i.e.C 1 C .
Complex wavenumber: k k i , with: k k e k and: m k .
Noting that to 1st order in the Taylor series expansion: 1 1 12 for 1 , thus:
1 1 1
2
2 2 2 2 2
C 1 C 1 C
k 1 1 1 1 2
2 2 2
2
2
1 1
2
2 2 2
C 1 C C2 1
1 1 1 1 C
2 2
2 4
2 2
2
1
k and: C for a poor conductor.
2
2 C
1
C 1
In a poor conductor 1 , the ratio: k C 1 i.e. k .
2
1 1 C 1 C
Phase angle in a poor conductor: k B E tan 1 tan ~ 0 1
k 2 2
B E k E , i.e. B and E are nearly in phase with each other in a poor conductor
(i.e. dissipation/losses very small in a poor conductor).
The conductivity of pure water is: CH 2O 1 CH 2O 1 2.5 105 -m 4.0 106 Siemens m
at P 1 ATM and T 20 C . Thus, the criteria for a poor conductor C 2.54 1011 1
is certainly satisfied at optical frequencies.
The wavenumber in pure H 2O at optical frequencies is:
188.5 nm
Note that the optical wavelength ratio: o
H O 1.333 nH 2O for a poor conductor.
2 141.3 nm
1 1
Skin depth: sc for a poor conductor C 1 .
1
2 C
1 1 o 1 1 4 107
H 2O C C 5
5.65 104 rad m
2 2 2 2.5 10 1.777 8.85 10 12
1
H 2O 2 C 1 1 1 1
Ratio: C 1.27 1011 1
kH O 2 2 2.5 10 1.777 8.85 10 10
5 12 16
2
H O
Phase difference: k B E tan 1 2 1.27 1011 radians 1 i.e. B E k E
kH O
2
B and E are nearly in phase with each other in pure H2O at optical frequencies.
For pure H2O at low frequencies e.g. 60 Hz AC line frequency AC 2 f AC 120 rad sec :
4.0 106
Note that the criteria for a poor conductor: AC C 15 1
H O AC 80 8.85 10 12
120
2
AC AC
H O
C
2
AC o C 120 4 107 4 106
H 2O
k AC AC
H 2O
3.08 105 rads m
2 2 2
2 2 c
AC
H O
2
2.04 105 m cf w/ vacuum wavelength: o c f AC 5.00 106 m
k H 2O
AC AC
o 5.00 106 m
Vacuum/good conductor wavelength ratio: H 2O 24.495
AC 2.04 10 m
5
Skin depth for pure H2O at 60 Hz AC line frequency: HAC2O 1 HAC2O 3.25 104 m 32.5km
This may seem like a large distance scale associated with the attenuation of the 60 Hz EM
waves propagating in pure water, however compare the skin depth to the wavelength at this
frequency: HAC2O 32.5km vs. AC
H 2O
1.77 106 m , i.e. we see that HAC2O HAC2O , as we expect
for the case of a good conductor !!!
The ratio HAC2O k HAC2O 1 for pure H2O at 60 Hz AC line frequency, which is what we expect for
a good conductor {this ratio should be 1 for a poor conductor!}.
Thus, the phase difference is: k B E tan 1 HAC2O k HAC2O tan 1 1 45o
4
o
which again is what we expect for a good conductor, i.e. B lags E by 45 !
1
Given that: k and: C in a poor conductor, where: C 1
2
k* k e ik
Z r , z z e ik z Ohms
|k |
2
|k | 2
|k |
1
But: k and: C in a poor conductor, where: C 1
2
poor
Hence in a poor conductor: Z cond r , z Z cond
poor
z . Define {real scalar}: Z med
lin
.
Then {real scalar} characteristic longitudinal EM wave impedance for a poor conductor is:
o
poor
Z cond Z med
lin
Ohms n.b. Compare to free space: Z o 376.8 Ohms
o
i B
Since {in general} the complex impedance is: Z r , Z r , e Z z Z r , e E
i
z .
The phase of the complex wave impedance for a poor conductor is:
1 1 C
Z tan 1 tan 0 E B
k 2
Instantaneous EM energy densities in a poor conductor: C 1
1 1 2 1 1
uEM r , t uEEM r , t uMEM r , t E 2 B EE B B
2 2 2 2
The physical/instantaneous purely real time-domain E and B fields are:
E r , t Eo e z cos kz t E x and: B r , t Bo e z cos kz t E k y
1
|k| C
2 2
where: Bo Eo 1 Eo Eo for a poor conductor, C 1 .
1
k where: v for a poor conductor.
v k
1
and: c k , |k| for a poor conductor.
2
1 1 1 2 2 z
then: uEEM r , t E 2 cE E Eo e cos 2 kz t E and:
2 2 2
1 2 1 1 2 2 z
uMEM r , t B B B Bo e cos 2 kz t E k
2 2 2
1 2 2 z
uEEM r , t Eo e H 2O 1 o
4 1 tan 1
1 H 2O c k H 2O o
uM r , t 1 2 2 z
k B E
EM
Eo e k H 2O 2
4
EM wave energy is shared equally by the E and B fields in a poor conductor!
Instantaneous Poyntings Vector for EM waves propagating in a poor conductor:
1 1 1 2 2 z
S r,t E r ,t B r ,t S r ,t E r ,t B r ,t Eo e cos k z
2 o
1
1 2 2 z
Intensity of EM waves propagating in a poor conductor: I r S r , t Eo e
2 o
BC 3): (normal B at interface): B1 B2 0 B1 B2
1 || 1 ||
BC 4): (tangential H at interface): B1 B2 K free n
1 2 21
where n is a unit vector to the interface, pointing from medium (2) into medium (1).
21
1
B k E
v
1
and: Binc r , t E oinc e 1 y
Einc r , t E oinc ei k1z t x
i k z t
Incident EM wave {medium (1)}:
v1
1
Reflected EM wave {medium (1)}: Erefl r , t E orefl e 1 x and: Brefl r , t E orefl e 1 y
i k z t i k z t
v1
i k z t k i k z t
Transmitted EM wave {medium (2)}: Etrans r , t E otrans e 2 x and: Btrans r , t 2 E otrans e 2 y
n.b. complex wavenumber in {conducting} medium (2): k2 k2 i 2
In medium (1) EM fields are: ETot1 r , t Einc r , t Erefl r , t and: BTot1 r , t Binc r , t Brefl r , t
In medium (2) EM fields are: ETot2 r , t Etrans r , t and: BTot2 r , t Btrans r , t
BC 3): B1 B2 but: B1 B1z 0 and: B2 B2 z 0 0 0
k
BC 4):
1
1
B1||
1
2
B2|| K free n
21
but: K free 0
1
1v1
2
Eoinc E orefl 2 E otrans 0
v k v
or: E oinc E orefl E otrans with: 1 1 2 1 1 k2
2 2
1 2
Thus we obtain: E orefl Eoinc and: E otrans E oinc
1
1
E orefl 1 E otrans 2 v k v
and: with: 1 1 2 1 1 k2
1
or:
E o
inc Eoinc
1 2 2
Note that these Fresnel relations for reflection/transmission of EM waves at normal incidence
on a non-conductor/conductor boundary/interface are identical to those obtained for reflection /
transmission of EM waves at normal incidence on a boundary/interface between two linear non-
conductors, except for the replacement of with a now complex for the present situation.
v k v
Note also that here, is frequency-dependent, i.e. 1 1 2 1 1 k2 .
2 2
Thus, for a perfect conductor, we see that: E orefl E oinc and: E trans 0
Thus, for a perfect conductor, the reflection and transmission coefficients are:
2 2 *
Eo E orefl E orefl E orefl
R refl 1 and: T 1 R 0
Eo Eoinc E o E o
inc inc inc
We also see that for a perfect conductor, for normal incidence, the reflected wave undergoes
a 180o phase shift with respect to the incident wave at the interface/boundary at z = 0 in the x-y
plane. A perfect conductor screens out all EM waves from propagating in its interior.
For the case of a good conductor, the conductivity C is finite-large, but not infinite.
The reflection coefficient R for monochromatic plane EM waves at normal incidence on a good
conductor is not unity, but very close to it. {This is why good conductors make good mirrors!}
2 2 *
E orefl E o E orefl 2 *
Eorefl 1 1 1
For a good conductor: R refl
E E 1
Eoinc Eoinc
oinc oinc 1 1
v k v 2 C
Where: 1 1 2 1 1 k2 and: k2 k2 i 2 . For a good conductor: k2 2
2 2 2
1v1 1v1 2 C C
Thus: k2 1 i 1v1 1 i
2 2 2 2 2
C
Define: 1v1 Then: 1 i
2 2
Thus, the reflection coefficient R for monochromatic plane EM waves at normal incidence on
a good conductor is {n.b. frequency-dependent!}:
2
E o 1
2 * 2
1 1 1 1 i 1 i 2
R refl
E 1
1
1 1 1 i 1 i
2 2
oinc
C
with: 1v1
2 2
Note that the transmitted wave is exponentially attenuated in the z-direction; the E and B
fields in the good conductor fall to 1/e of their initial {z = 0} values (at/on the interface) after the
monochromatic plane EM wave propagates a distance of one skin depth in z into the conductor:
1 2
sc
2 2 C
Note also that the energy associated with the transmitted monochromatic plane EM wave is
ultimately dissipated in the conducting medium as heat.
In {bulk} metals, since the transmitted wave is {rapidly} absorbed/attenuated in the metal,
experimentally we are only able to study/measure the reflection coefficient R. A full/detailed
mathematical description of the physics of reflection from the surface of a metal conductor as a
function of angle of incidence i.e. R , inc and also requires the use of a complex dispersion
relation k v c n with complex k k i and a complex
propagation speed v v iv c n with accompanying complex index of refraction
n n i , and is hence commensurately more mathematically complicated.
So-called ellipsometry measurements of the EM radiation reflected from the surface of the metal
as a function of angle of incidence yields information on the real and imaginary parts of the
complex index of refraction of the metal n n i , and thus the real and imaginary
parts of the complex dielectric constant and/or the complex electric susceptibility of the metal,
since n o 1 e or n 2 o 1 e .
If interested in learning more about this, e.g. please see/read Physics 436 Lect. Notes 8, and e.g.
please see/read Optics, M.V. Klein, p. 588-592, Wiley, 1970 {P436 reference book on reserve in the
Physics library}. Please also tsee/read he UIUC P402 Optics/Light Lab Ellipsometry Lab Handout C4
and especially the references at the end. Available at: http://online.physics.uiuc.edu/courses/phys402/exp/C4/C4.pdf
We will discuss the dispersive nature of dielectric, non-conducting materials in the next lecture
But first, we need to remind the reader of the full Maxwells equations in matter
All four of these quantities are macroscopically averaged - i.e. the microscopic fluctuations
due to atomic/molecular makeup of matter have been smoothed out.
The four above quantities are related to the macroscopic E and B fields by the four Maxwell
equations for matter (see Physics 435 Lect. Notes 24, p. 14):
1
1) Gauss Law: E Tot free bound , where: bound
o o
Auxiliary relation: D o E & constitutive relation: D E
Electric polarization o E 0 e E , electric susceptibility: e 1
o
D o E free
2) No magnetic charges/monopoles: B 0
1
Auxiliary relation: H B H M & constitutive relation: B H
o
B H M
3) Faradays Law: E 0 0
t t t
Magnetization: M= 1 H m H , magnetic susceptibility: m 1
o o
E
4) Amperes Law: B o J ToT o J D with: J D o
t
mag P mag P P
Total current density: J ToT J free J bound J bound J bound M J bound
t
P E
B o J free o M o o o
t t
D
H o J free o
t
We also have Ohms Law: J C E and the 3 continuity equation(s): J
t
associated with subscript index for free, bound and total electric charge conservation.
For many/most (but not all!!!) physics problems, e.g. in optics/condensed matter physics,
materials of interest are frequently non-magnetic (or negligibly magnetic) and have no free
charge densities present, i.e. free 0 . If o , then: M 0 and thus: H B o in such
non-magnetic materials.
Then Maxwells equations in matter, for free 0 and M 0 reduce to:
1
1) Gauss Law: D 0 or: E P bound
o o
2) No magnetic charges: B 0
B
3) Faradays Law: E
t
E P
4) Amperes Law: B o o o o J free
t t
We also have Ohms Law J free c E and the Continuity eqn. J free 0 {here}.
J free E
For good conductors (e.g. metals), the conduction term o o C is the most
t t
important, because it explains the opacity of metals (e.g. in the visible light region) and also
explains the high reflectance of metals.
All source terms on the RHS of the above inhomogeneous wave equation are of importance for
semi-conductors however a proper/more complete physics description of EM wave propagation
in semiconductors also requires the addition of quantum theory for rigorous treatment