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A A '=A
B '=B 1 Lorenz
choose A =0
'= E '=E c2 t condition
t
2
2 1 2 2 1 A
2 2
= , A 2 2
= 0 J
c t 0 c t
uncouple the 2nd-order equations
6.3 Gauge Transformations, Lorenz Gauge, Coulomb Gauge
The transformation is called agauge transformation, and the invariance of the
fields under such transformations is called gauge invariance.
1
A 0 A '=A , '=
c2 t t
1 ' 1 2 1 2
A ' = 0= A
c2 t c2 t c2 t 2
2
2 1 1 the new potentials А ' , ' will satisfy
= A
c2 t2 c2 t the Lorenz condition and the wave eqns
1 1 '
A 2
=0 A '=A , '= A ' 2
=0
c t t c t
2 1 2
2 2
=0 restricted gauge transformation
c t
All potentials in this restricted class are said to belong to the Lorenz gauge.
The Lorenz gauge is commonly used because
(1) it leads to the wave eqs, which treat the potentials on equivalent footings;
(2) a concept indep. of the coordinate system and so fits into special relativity.
Coulomb, radiation, or transverse gauge A = 0 2 = Poisson
0 eqn
1 x',t
x ,t =
4
x 0 x '
d x'
3
instantaneous Coulomb potential 1
2
1 A 1
2 A 2 2
= 0 J 2
× =0 irrotational
c t c t t
J = J J t × J = 0 longitudinal, irrotational × × J = J
2
J
J t = 0 transverse, solenoidal
2 J = J
2 1
= 4 x x'
2
Jt = × × J x x '
1 'J x ' , t
J =
4
x x '
d3 x '
J = 0 1
t 2
= 0 J
1 J x' ,t c t
J t =
4
× × x x '
d x'3
1
2
2 1 A
A 2 2
= 0 J t
c t
the source for the wave equation for A can be expressed entirely in terms of the
transverse current.
The radiation gauge stems from that transverse radiation fields are given by the
vector potential alone, the Coulomb potential contributing only to the near fields.
it is the fields, not the potentials, that matter. Another is that the transverse
current extends over all space, even if J is localized.
6.4 Green Functions for the Wave Equation
2 2
k x , = 4 f x , inhomogeneous Helmholtz wave equation
k = / c
The Helmholtz wave eqn is an elliptic partial differential eqn similar to the
Poisson eqn to which it reduces for k=0.
1 R
= for k = nondispersive
R c c
±
G x ,t;x' ,t ' =
t'
[ t
x
c
x '
] G : retarded Green function
x x ' G : advanced Green function
the retarded Green function has a causal behavior: an effect observed at the
point x at time t is caused by the action of a source a distance R away at an
earlier or retarded time t'=t-R/c. Similar with the advanced Green function.
From the 2 eqns the E & B fields can be computed, but it is often useful to have
retarded integral solutions for the fields in terms of the sources.
[ ]
2
1 E 1 1 J 1 1 1 J
2 E
c2 t 2
=
0
c2 t
E x,t =
4 0
R '
c2 t '
3
d x'
ret
2
1 B 0 [ ' × J ]ret
2
B 2
c t
2
= 0 × J
4
B x ,t =
R
d3 x '
' [ f ]ret [ ' f ]ret : ' in the retarded bracket is a spatial gradient in x' with t'
fixed; ' outside the retarded bracket is a spatial gradient in x' with x and t fixed.
[ f x ' , t ' ]ret = f x ' , t R t ' / c = f x ' , t ' [t t' R t ' /c ] d t ' , = R/ R
R
R
R
[ ' ]ret = ' []ret [ ] ' t = ' []ret [ ]
t' c t ' c
ret ret
J R J
R
[ ' × J ]ret = ' ×[ J ]ret [ ] × ' t = ' ×[ J ]ret [ ] ×
t' ret c t' ret c
E x,t =
4
1
0
[ [ x ' , t ' ]ret
R
R
2
[ x' ,t '
t' ] ret cR
R
c2 R
1
[ J x' ,t '
t' ]]
ret
d3 x '
[ [ ] ]
0
R J x' ,t '
R
B x ,t = [ J x ' , t ' ]ret × 2
× d3 x '
4 R t ' ret cR
Jefimenko's generalizations of the Coulomb and Biot-Savart laws
1 R 3
E x =
4 0
x'
R
2
d x'
for , J are time-independent
0 R 3
B x =
4
J x' × 2d x'
R
[ f x' ,t'
t' ] ret
=
t
[ f x ' , t ' ]ret t ' = t
x
c
x '
x ' , t ' =q [x ' r0 t ' ] , J x ' , t ' = v t ' fora point charge
[[ ] [ ]]
Heaviside-Feynman expressions
q R 1 R v/c
E= 2
vR
4 0 R c t R =1 retardation factor
ret ret
2 c
B=
0 q
4 [[ ]R
v× R
2
ret
1
c t [ ]]
v× R
R ret
[t t '
R t'
c
]=
[t ' t ]
there is a difference between []ret/t and [/t]ret because x'r0(t'). The
fields are functions of x and t, with t'=t-|x-r0(t')|/c.
dt 1 dt' 1 dR dR
= = =1 v t' =
dt' dt c dt dt'
2
E=
q
4 0 [[ ]
R
R
2
ret
[ R]ret
c t R[ ]
R
2
ret
1 2
2
c t
2
[ R] ret
] Feynman's expression
B=
0 q
4 [[ ]
2
v× R
R 2
ret
1
c [ R]ret t [ ]]
v× R
ret
Heaviside's expression
For dimensions large compared to 10-14m, the nuclei and electrons can be
treated as point systems,
b
b = 0, ×e =0
t microscopic Maxwell equations
1 e
e = , ×b 2
= 0 j
0 c t
no corresponding fields d and h because all the charges are included in and j.
All the microscopic fluctuations are averaged out, giving smooth and slowly
varying macroscopic quantities, to appear in the macroscopic Maxwell equations.
[
3
f x = 3/ 4 R , r#R
2 examples
0, r$R
isotropic 2
r /R
2
f x =e R2 3/ 2
x , t = % q j [x x j t ]= free
bound
! n
x , t " = f x ' n
x x ' , t d3 x ' = % q j f x ' x x' xjn x n d3 x '
j n
=% qj f x xj n xn x j n : order of
j n atom dim
=% qj [ f x xn x j n f x x n
j n
1 2 f
% xjn & xjn ' x x n ]
2 &' x & x'
molecular charge qn = % q j
j n
* [ f )F ]= * [ f ] * [ F ]
convolution
faltung
f )F
f y F x y dy
* [ f F]=
* [ f ])* [ F]
2
1
!F x , t "=
2
3 (f k F
( k , t ei kx d 3 k * [! F x , t "]= (f k F
( k ,t
f x d3 x = 1 (f 0 =1 = f x e
i 0x
d3 x
3/2 r 2 / R2 k 2 R2 / 4
f= R
2
e Gaussian test function (f k = * [ f x ]= e
the Fourier transform of the averaged quantity contains only low wave numbers,
up to kmax=O(l/R), the inverse of the length scale of the averaging volume.
=q n f x xn p n f x x n
=! qn x xn " ! p n x x n "
%
&
x& [ 0 E & P & %
'
Q '& '
x'
=
] 0 E = ! x ,t "
Q '& '
D & = 0 E & P & % macroscopic displacement vector
' x'
j bound = % jn x , t jn x , t =% q j v j x xj
n molecues j n
! j n x , t " = % q j v j n vn f x xn xj n
j n
The final result for the averaged microscopic current density is
! j& x , t " = J & x , t [ D& x , t 0 E & x , t ] % & ' , M, x , t
t ', x'
% ! % [ pn & vn ' pn ' vn &] x xn "
' x' n molecules
2
1
% ! % [ Q 'n &'
vn , Q 'n ,'
vn &] x x n "
6 ', x' x, n molecules
J x , t =! % qj v j x xj % qn vn x x n " macroscopic
j free n molecules current density
1
% & ' , ! % Q 'n -'
vn , x x n "
6 ' ,- x- n molecules
Except the 1st term of RHS, the other terms are small since v's are small.
Q& ' 3 x & x ' r 2 & ' d3 x traceless molecular quadrupole moment
e rn=% qj x j n
2 2 2
Q 'n &'
= Qn &'
e r n & '
j n
1
Q ' & ' = Q& ' ! % e r 2n & ' x xn " macroscopic quadrupole density
6 n molecule
1
free ! % qn x xn " 2 ! % e r 2n x xn " **
n molecule 6 n molecule
the traceless quadrupole density replaces the quadrupole density and the charge
density is augmented by an additional term.
The molecular charge & mean square radius terms represent the 1st two terms
in an expansion of the =0 molecular multipole as we go beyond the static limit.
sin k r 1
F k 2 x !ei kx " =0 part d 3 x = x d3 x + d 3 x k2 r2 d3 x
kr 6
k. i **
6.7 Poynting's Theorem and Conservation of Energy & Momentum
for a System of Charged Particles and Electromagnetic Fields
For a single charge the rate of doing work by external EM fields is qv/E. The
magnetic field does no work, since the magnetic force is perpendicular to v.
the total rate of doing work by the fields in a finite volume is V JE d 3 x
It represents a conversion of EM energy into mechanical or thermal energy. It
must be balanced by a corresponding rate of decrease of energy in the EM field.
D
V
JE d x =
3
V
[ E × H E
t
3
]d x Ampere-Maxwell law
= V [ E × H E
D
t
H
B
t ]
d 3 x E × H = H × E
× E B/ t =0
E × H
The conservation of angular momentum of the system of particles & fields can
be treated in the same way as we have handled energy & linear momentum.
6.8 Poynting's Theorem in Linear Dispersive Media with Losses
Poynting's theorem was derived with linear media with no dispersion or losses,
with and real and frequency independent. Actual materials exhibit dispersion
and losses.
E x ,t =
E x , e it
d
with the linearity D x , = E x ,
D x , t = D x, e i t
d [B x , = H x , ]
reality of field E x , = E * x , , D x , = D* x , , = *
D D ED
E
t
= d E *
' E [ i ] e
i ' t
d' E
t
t 2
1
=
2
d E * ' E [i ' * ' i ]e i ' t
d'
'
'
assume E is dominated by frequency around ' + ' = = '
* d *
i' ' i =2 2 [ ] i ' [ ]
d
D
E
t
+ d
*
E ' E 2 [ ] e
i ' t
d '
1 d
2 t
d *
E ' E
d
[ * ] e i ' t
d' #
B
H
t
+
d
*
H ' H 2 [ ] e
i ' t
d '
1 d
2 t
d H* ' H
d
[ * ] e i ' t
d' @
If and are real and frequency independent we go back the the last section.
The 1st terms in (#) & (@) evidently represent the conversion of electrical
energy into heat, while the 2nd terms must be an effective energy density.
( t cos 0 t &
E=E ( 1
Let , and E t slowly varies relative to
( t cos 0 t '
H=H ( t
H 0
D B 2 2
ueff
! E H " = 0 {2 [ 0 ] ! E x , t " 2 [ 0 ] !H x , t "}
t t t
1 d 2 1 d 2
where u eff = 3[ 0 ] ! E x , t " 3[ 0 ] ! H x , t "
2 d 2 d
Poynting's theorem in these circumstances reads
u eff 2 2
S = JE 0 {2 [ 0 ] ! E x , t " 2 [ 0 ] ! H x , t "}
t
The 1st term in RHS describes the explicit ohmic losses, while the next terms
represent the absorptive dissipation in the medium, not counting conduction loss.
6.9 Poynting's Theorem for Harmonic Fields;
Field Definitions of Impedance and Admittance
assume that all fields and sources have a time dependence e-it
i t 1 it
E x , t = 3 [E x e ] [E x e E* x ei t ]
2
1 it * i t it * it
J x , t E x , t = [J x e J x e ][E x e E x e ]
4
1 2it
= 3 [ J * x E x J x E x e ]
2
For time averages of products, the convention is to take 1/2 of the real part of
the product of one complex quantity with the complex conjugate of the other.
B= 0, ×E i B=0
For harmonic fields the Maxwell equations
E = , × H i D = J
1 1 1
S E × H* , w e = ED* electric , w m = BH* magnetic
2 4 energy density 4 energy density
1
2
V
* 3
J E d x 2 i V
we wm d x
3
0 Sn d a = 0
S
Poynting theorem
The real part of the eqn gives the conservation of energy for the time-averaged
quantities and the imaginary part relates to the reactive or stored energy and its
alternating flow.
1
If V
we w m d 3 x is real
2
V
3 [ J *E] d3 x = 0 3 [Sn] d a
S
2 i V
we wm d3 x 0 S Si
Sn d a
If S-Si is taken to infinity, the surface integral is
real and represents escaping radiation.
R=
1
I i
2 {
3[
V
J *E d 3 x ]2 0 S Si
Sn d a 4 2 [ V
wm we d 3 x ]
}
X=
1
I i2
{
4 3[ V
wm we d x ]
3
2[ V
*
J E d x ]
3
}
2
I
2 0
S Si
Sn d a is the "radiation resistance," important at high frequencies.
i
At low frequencies, ohmic losses are the only appreciable source of dissipation.
1 4
R4
I i
2 V
- E2 d 3 x , X4 2
I i
V
wm we d3 x
Here - is the real conductivity, the energy densities are also real essentially.
B ' & ' = % a & , a ' B, are called 2nd-rank tensors or,
,,
commonly, tensors, like Maxwell stress tensor.
A = B×C A& = % & ' , B' C , A ' & = a % a& ' A ' a det 7a & '7
', '
Axial or pseudovectors: A ' & = a % a& ' A' & x x ' = x A A'=A
'
C. Time Reversal
The basic laws of physics are invariant to the sense of direction of time.
charge density is a scalar. And E is a polar vector, even under time reversal.
B
× E : pseudovector, even under time reversal ×E =0 Faraday's law
t
B : pseudovector, odd under time reversal
1 E
the Ampere-Maxwell eqn × B 0 = J polar vector, odd under time
reversal on both sides. 0 t
At low frequencies, the response of all material systems is via electric force
1 E 2 E 2 E
P = :0 E :1 × B0 : ' 2 B 0B0 2
: '3 2
B0 B0 more realistic
0 t t t
At optical frequencies this equation permits an understanding of the gyrotropic
behavior of waves in an isotropic medium in a constant magnetic field.
If there exist magnetic charge & current densities, then Maxwell eqns become
D e
D = e , ×H= Je J e = 0
t t
B m
B = m , ×E= Jm J m = 0
t t
transformation E =E ' cos 9 Z 0 H ' sin 9 , Z 0 D =Z 0 D ' cos 9 B ' sin 9
duality transformation:
;
impedance Z 0 = 0 / 0 Z 0 H = E ' sin 9 Z 0 H ' cos 9 , B = Z 0 D ' sin 9 B ' cos 9
For a real (pseudoscalar) angle 9, the transformation leaves quadratic forms like
E8H, (ED+H), and the components of the Maxwell stress tensor invariant.
Z 0 e =Z 0 ' e cos 9 ' m sin 9 , Z 0 J e =Z 0 J ' e cos 9 J ' m sin 9
Apply to the sources
m = Z 0 ' e sin 9 ' m cos 9 , J m = Z 0 J ' e sin 9 J ' m cos 9
the generalized Maxwell equations are invariant
D' B'
D ' = ' e , × H ' = J ' e , B ' = ' m , ×E ' = J 'm
t t
The invariance of the EM eqns under duality transformations shows that it is
only a convention to think of electric charge instead of magnetic charge.
Ifall particles have the same ratio of magnetic to electric charge, one can make
a duality transformation so that m=0, Jm=0, so we have the usual Maxwell eqns.
The conclusion is that the particles of ordinary matter possess only electric
charge or they all have the same ratio of magnetic to electric charge.
Since the symmetries of m under spatial inversion & time reversal are opposite
to those of e, then a particle with both electric & magnetic charges that space
inversion and time reversal are no longer valid symmetries of the laws of physics.
the present evidence is that the symmetry violation is extremely small and
associated with the weak interactions.
Considering the quantum mechanics of an electron near a magnetic monopole,
Dirac showed that consistency required the quantization condition,
g : magnetic charge
eg &g n
= = n = 0, ± 1, ± 2, e2 1
4< Z0 e 2 &= + fine structure const
4 0 < c 137
The discrete nature of electric charge thus follows from the existence of a
monopole. The magnitude of e is determined in terms of the magnetic charge g.
With the known value of the fine structure constant, we can also infer the
existence of magnetic monopoles with the magnetic "fine structure" constant
g2 n2 4 0 < c 137
= 2
= n2 Dirac monopoles
4 0 < c 4 e 4
The coupling strength is enormous, making their extraction from matter with dc
magnetic fields and their subsequent detection very simple in principle.
6.12 Discussion of the Dirac Quantization Condition
We consider the deflection at large impact parameters of a particle by the
field of a stationary magnetic monopole.
On the string the vector potential is singular, equivalent to a field B' in the
solenoid and bringing a return contribution of flux -g in along the string.
Bmonopole = × A B' B ' : exists only on the string (inside the solenoid)
g
AL ' x = AL x ?C x Problem 5.1
4
A A ' = A : ?C
1 : := g
'= 4
c t
a change in the gauge of the EM potentials leaves the form of the Schrodinger
en invariant, provided the wave function is transformed according to
e g ?C
[ ]
i
> ?C = 4 as an electron
i e :/ < 4<
[@ @ ' = @ e @ @ ' =@ e ]
crosses the surface S
eg
=2 n n = 0, ± 1, ± 2, the wave function is single-valued
<
The arguemnt follows from the general requirements of gauge invariance and
single-valuedness of the wave function, independent of the location of the
monopole's string.
6.13 Polarization Potentials (Hertz Vectors)
use potentials as auxiliary fields to determine the fundamental EM fields.
D= E P ext
P ext , M ext : external polarization densities
B = H 0 M ext
2 A 2
P ext
A = 0 × M ext
t
2
t
A =0
2
2 1 t
2
= P ext
t
Ae
A =: 0 × A m
t A e , A m : vector polarization potentials
1 Hertz vectors
=: A e
[
2 A e
2 A e
t
2 ]
P ext = 0
t [ 2 Ae
2 A e
t
2 ] [
P ext 0 × 2 A m
2 A m
t
2 ]
M ext = 0
2 A e 2 0
2
A e = Pext ×V
t
2
Am 2 V 9
2
A m = M ext
t t t
2 A e
2 A e = Pext
t2 the arbitrary functions V & 9 may be
2 A m 2
removed by a gauge transformation [Problem 6.23]
2
A m = M ext
t
2
1 Ae Am Am 1 1
E= A e 2
0 × = 0 × × × Ae P ext
t t t
Ae
B= × 0 × × A m
t
For a simple case
M ext = m t x x0 Am x , t =
m t ; R R =x x 0
4R
Selected problems: 6.1, 6.3, 6.10, 6.14, 6.18, 6.21