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A DISSERTATION
SUBMITTED TO
The degree of
MASTER OF SCIENCE
IN
PHYSICS
2016-18
DEPARTMENT OF PHYSICS
GURU NANK DEV UNIVERSITY, AMRITSAR-143005
CERTIFICATE
(Monika)
CONTENTS
1. Introduction 5
5. End result 23
References.
Introduction To Quantum Optics:
Quantum optics is a field of quantum physics that deals specifically with the
interaction of photons with matter. The study of individual photons is crucial to
understanding the behavior of electromagnetic waves as a whole. To clarify what
this means the word “quantum” refers to the smallest amount of any physical
entity that can interact with another entity. Quantum physics, therefore, deals
with the smallest particles; these are incredibly tiny sub-atomic particles which
behave in unique ways.
The word “optics” in physics, refers to the study of light .photons are the smallest
particles of light (though it is important to know that photons can behave as both
particles and waves.
.E 0 (1)
.B 0 (2)
B (3)
E (4)
t
E
B (1/ C 2 )
t
With these equations an electromagnetic vector potential A and a normal electric
potential can be associated . The field they obey the equations :=>
B A (5)
A
E (6)
t
1 A
( A) ( )
C 2 t t
1 2 A
.(. A) 2 A 2 2
C t
1 2 A
A 2 2
2
C t (8)
So in a vacuum the electromagnetic vector potential obeys a wave equation. Now
consider a cubic region space of length L. This region of space can be considered
as a box with arbitrary boundaries.
For this box the vector potential can be written as a Fourier expansion of the box
.This gives
A(r , t ) eK AK (t )eiK .r eK* AK* , (t )eiK .r (9)
K 1,2
Here is the polarization of the wave, K is the wave number and eK is the
polarization vector .The AK (t ) is the amplitude for each mode. The Wave number
K obeys the standard quantization condition
2 ni
Ki
L
ˆ K ' '
ˆ K
K.
ˆ K 0
Circularly polarized vectors
eiK .r
A(r , t ) AK (t ) K
K , V
We take potential as real no.
AK* , (t ) AK , (t )
*K , K ,
Substitute value of A in wave equation (9)
We have:
1 2 eiK .r
][ AK , (t ) K ,
2
0
C 2 t 2 K , V
1 2 eiKr eiK .t
( K , K , V
C 2 t 2 K ,
A (t ) 2
K ,
AK (t )
ˆ K ,
V
0
1 A (t )
2 K
A (t ) ˆ K , eiK .t / V K ( K 2 ) ˆ K , eiK .r 0
C K K V
AK (t ) C 2 K 2 AK , (t )
K2 AK , (t )
1 3 | B |2
2
H d r | E 2
|
0
0
1 3 A
2 d r[0 ( ) 2 C 2 0 | A |2
t
A A eiKr
E K , ˆ K ,
t K , t V
0 2 AK , (t ) AK ' , ' (t )
2
d 3
r | E |2
2V
K , K ', ' t u 2
K , K ' , '
'
'
d re V , K K
i( K K ' )r
3
0, otherwise
1 AK , (t ) A K , (t )
2
0 d 3 r | E |2 0
2
K, t t
0
2
| A
K,
K , (t ) |2
C 02
2 d 3 r | B 2 | 0
2
K,
K | AK , |2
0
| A (t ) | K2 | AK , (t ) |2
2
H K ,
2 K,
(C 2 0 ) / 2 d 3r | B 2 |0 /2 K | AK , |2
AK , AK , is
complex quantity ,we want a real value of E , So we introduce some
new real numbers:
QK(1), Re{ AK , }
QK(2), Im{ AK , }
QK(1), 2 QK(2), 2 , K Z 0
| AK , | (1) 2
2
QK , Q K , , K 0
(2) 2
Kx K y Kz
K ,
K Z 0, K K x , K y , K
K Z 0, K K x , K y , K z
K ( K x , K y ,| K z |)
| A |2 2 [QK(1), QK(2), 2 ]
2
K ,
K, K ,
2
K,
(QK , ) 2
K Z 0
0 QK , 0 QK ,
H
2
K, ,
[K2 | QK , |2 (
t
)2 ]
2
K, ,
[K2 (QK , ) (
t
)2 ]
QK ,
H 0 [
k,
2
K | QK , |2 (
t
)2 ]
Q is canonical postulate
P a Q
H H
Q , P
P Q
P2
H 0 [ Q 2 ] 2 2
K , , k z 0 a
H 2 0 P
Q
P a2
a 2 0
.
P 2 0 Q
1 2
H [0 2 Q2 P ]
4 0
(11)
Identify x Q ; p P ; m 2 0 we get equivalent harmonic oscillator equation.
To quantize it :=>
[Q , P ] i
Q (b b )
4 0 K
P 0 K (ib ib )
4 0 K
Substitute eq. (12) in eq. (11), we get
H K [b b 1/ 2]
2
Z
(b1 K ib2K )
, KZ 0
2
a K 1
(bK ibK ) , K 0
2
2
Z
(bK1 ibK2 )
, KZ 0
2
aK 1 2
(b K ib K ) , K 0
2
Z
1
H field K (a a )
K 2
0
H atom [| e e | | g g |]
2
0 Z
2
These are field and atomic Hamiltonian of Jaynes- Cumming model
Where u(R) is the mode function of the field at the center of mass coordinate R,
u ( R)
2 0 V
to be a real by a proper choice of phase.
Which contains 4 terms. To further simplify this , we involve the rotating wave
approximation and 1 and 3 terms. There are two ways to understand the RWA.
The above argument is rather heuristic .We can make it more rigorous . For this
purpose ,it is easiest to work in the interaction picture. Decompose the total
Hamiltonian as
H H 0 H INT
H0 H A H F
H INT e(iH0t )/ H INT e( iH0t )/
H INT ei ( H A H F )t / g (ˆ ˆ )(aˆ aˆ )ei ( H A H F )t /
g[eiH At / (ˆ ˆ )eiH At / ][eiH F t / (aˆ aˆ )eiH F t / ]
Now
eiH At / e iH At /
eiH At / | g e | e iH At /
and
H A 0 ee
Now
e | ei0 |ee|t e | (1 i | e e | t........)
e | i0 e | t..........
e | (1 i0t..........)
e | ei0t
Also
eiH At / | g eiot|e e| | g
(1 i0t | e e | .... ....) | g
| g i0t | e e | g ..... .....
| g
So
eiH At / | g e | e iH At /
| g e | e i0t
e i0t
e(iH At )/ e( iH At )/ e(iH At )/ | e g | e( H At )/ gg
H A 0 gg
ei0 | g g |t | e (1 i0 | g g | t ........) | e
| e i0 | g g | e t .......
| e
So g | ei |g g |t g | (1 i0 | g g | t ..........)
0
g | i0 g | .......
g | (1 i0t .......)
g | ei0t
thus
e(iH At )/ | e g | e( iH At )/ | e g | ei0t
ei0t
Similarly
eiH F t / aeiH F t / e it a
eiH F t / a eiH F t / eit a
(1)
H INT g (ei0t ei0t )(e it a eit a )
(1)
H INT g (e i ( 0 )t a e i ( 0 )t a ei ( 0 )t a ei ( 0 )t a )
Now, we note that terms 1 and 4 terms that do not conserve energy are
multiplied by oscillatory terms which involve the sum of the frequencies of the
field and the atomic transition , while other terms which do conserve energy are
multiplied by terms involving the difference of the two frequencies . For the near
resonant case we are most interested in , difference of frequencies.
Since the Schrodinger equation is a differential equation of first order in time we
have to integrate in time. This time integration brings the frequency sum and
difference into the denominator. Hence the dominant contribution must come
from the slowly varying part. The interaction Hamiltonian in the interaction
picture is then given by
Schrodinger equation
d |
i H INT
(1)
|
dt
(1)
H INT g ( a eit ae it )
Dressed states of Jaynes Cumming Model:
Lets back to Schrodinger picture under RWA Hamiltonian reads:
H 0 ee aa g ( a a)
/2
0
H ATOM [| e e | | g g |]
2
0 Z
2
H0 H A H F
0 Z
(a a)
2
Z Z
[ a a]
2 2
[ 0 ]
Where is applied frequencThe atom can be found | e , n> excited and |g , n+1 >
Now define a factor
Z
N aa
2
Now
Z
H JC N g (a a )
2
Z
[ H JC , N ] [ N g ( a a), N ]
2
Z
[ N , N ] [ , N ] g[ˆ aˆ ˆ aˆ , N ]
2 (14)
Now
[ N , N ] 0
Z Z Z
[ ,a a ] [ , a a]
2 2 2
[ [ z , z ] 0]
Z
[ , a a] 0 a a
2
Z
[ , a a] 0
2
[ a a involves field operators and Z represent atom operators and are
independent]
Z
[ a a, N ] [ a a, a a ]
2
1
[ a a, a a] [ a a, z ]
2
(15)
Consider a typical state | e | n | e | n
Now
1
[ a a, Z ] | e | n
2
1
{[ a a,| e e | | g g |] | e | n ]}
2
1
{[ a a,| e e | | g g |] | e | n ]}
2
1
[( a a )(| e e | | g g |) (| e e | | g g |)( a a )] | e | n
2
1
[( a a )(| e e | | g g |) (| e e | | g g |)( a a )] | e | n
2
1
[a | e g || e | n | g e || e | n | e e | a | g | n | g g | a | g | n
2
1
= [ a | g | n a | g | n ]
2
a | g | n (16)
= [(a a ), a a] | e | n
[(a a )a a a a(a a )] | e | n
[a a a a 2 a a a 2 a aa ] | e | n
a 2 a | g | n a aa | g | n
a [a a aa ] | g | n
a (1) | g | n
a | g | n (17)
[ a a, Z ] 0
Substituting the values of eq. (15),(16) and (17) in eq. (14), we have
[ H JC , N JC ] =0
N is conserved quantity and hence
Z
H0 H0 N
2
e, n | H 0 | e, n e, n | H INT | g , n 1
g , n 1| H | e, n g , n 1| H | g , n 1
INT 0
e, n | H 0 | e, n e, n | H INT | g , n 1
g , n 1| H INT | e, n g , n 1| H 0 | g , n 1
The H INT term only works on the off- diagonal elements , while the H 0 term
applies only on the diagonal terms . Applies only on the diagonal terms . Applying
the operators on the states gives for the Hamiltonian
e, n | H 0 | e, n e n | (| e e | | g g |) | e | n
2
[ e n || e | n 0]
2 2
Now
e n | H INT | g | n 1
g e | n | ( a | e | n 1 )
g e | | n n 1(| e | n )
g n 1
g n 1
H 2
g n 1
2
n
2
2
n
2 2
n n 2 g n 1
Where is Rabi frequency defined as
To find energy eigen values
| H I | 0
n
2 2
n =0
2 2
2
( )( ) n 0
2 2 4
2 2
2 n 0
4 4
n 2
2
2
4
2n
2
2
This gives
Rn
E
2
Rn 2 2n
Where Adding the conserved number terms gives for the full energy
Rn
E [ (n 1) ]
2
NEAR RESONANCE:=>
Z
H JC N g[ a a ]
2
[ 0 ,near resonance]
H JC N g ( a a )
H JC H1 H 2
Where
H1 N
H 2 g[ a a ]
Now
[ H1 , H 2 ] 0
|
is any arbitrary state of the system at any time t
| Ce (t )eiHt / |1 Cg (t )eiHt / | 2
e iHt / | 1 eiH 2t / e iH1t / | 1
Z
i[ ( a a )]t /
e iH1t /
| 1 e 2
| 1
|e e|| g g |
it [ a a ]
e 2
| 1
it
(|e e|| g g |)
[eia at
e 2
] | 1
i | g g |t
e 2
| 1
1
[Because |e><e| don’t act on ]
it
| (t ) e i a at (1 | e e | .....) | n | e
2
it
e i a at (| n | e | n | e .....)
2
it
| (t ) e i a at (1 | e e | ......) | n | e
2
it
e i a at (| n | e | n | e ......)
2
it
eia at e 2
|n |e
1
i ( a a ) t
e 2
| 1
eit |
Effect of H(1) is to give overall phase change and does nothing
From schrodinger equation we have
d |
i H 2 | (t )
dt
| (t ) C1 (t ) | 1 C2 (t ) | 2
Where
C1 (t ) Ce (t )eiHt / , C2 (t ) Cg (t )eiHt /
|
Pre multiply by
i C1 (t ) C1 (t ) g n 1
C1 (t ) igC2 (t ) n 1
i C2 (t ) C1 (t ) g n 1
C2 (t ) igC1 (t ) n 1
C1 (t ) ig n 1C2 (t )
C1 (t ) ig n 1(igC1 (t ) n 1)
C1 (t ) g 2 (n 1)C1 (t )
d 2C1 (t )
2
g 2 (n 1)C1 (t ) 0
dt
Similarly
C2 (t ) C cos( g n 1)t D sin( g n 1)t
Conclusion
We have considered a two level atom having two states initial and final state and
have energies Ei and E f , now when the field is quantized, transitions will occur
for the case Ei E f , even when no photons are present – the so called
spontaneous emission . This is the only one of several differences that will appear
in the atom-field dynamics in the comparison between cases when the field is
quantized and when it is not. This is obviously in agreement with the case of a
classical driving field – no field, no transition . But in the case of above equation ,
transition may occur even when no photons are present. This is spontaneous
emission and it has no semi classical counterpart .
In the classical case there must always be a field present initially . But in the
quantum –mechanical case there are Rabi oscillations even for the case when n=0
. These are vacuum field Rabi oscillations and ofcourse , they have no classical
counterpart . They are the result of the atom spontaneously emitting a photon
then re-observing it, re-emitting it, etc: an example of reversible spontaneous
emission . Thus the spontaneous-emission is explained by Jaynes-Cumming model
(quantum theory) which was not explained by semi-classical theory .
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