Файл: Weber H., Herziger G., Poprawe R. (eds.) Laser Fundamentals. Part 1 (Springer 2005)(263s) PEo .pdf

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Ref. p. 40]

1.1 Fundamentals of the semiclassical laser theory

13

 

 

 

n1, n2 : density of states (atoms, molecules) in the lower/upper level, ∆n = n2 − n1 : inversion density,

n0 = n1 + n2 : total density, const.

The following assumptions are made:

Non-relativistic interaction. The velocity of the electrons is small compared with the velocity of light. This does not hold for inner-shell electrons, hot plasmas and free-electron lasers.

The wavelength of the light is large compared with the diameter of the atoms/molecules. It

means that in the domain of the atomic wave function the electromagnetic field is locally constant. Bohr’s radius with rB = 5.3 × 105 µm is a typical atomic dimension. The wavelength in the visible range of the spectrum is about 0.5 µm, thus this condition is fulfilled in the visible and UV-part of the spectrum. It is called the dipole approximation [97Scu].

The permanent dipole moments of the two-level system µ11 = µ22 are zero. Even if larger molecules have a permanent dipole moment, their response to the high-frequency field is small. Only for very strong fields are the permanent dipole moments of importance (see Part 4 on nonlinear optics). A dipole moment exists only for the transition from level 1 to 2 and vice versa. Non-degenerated levels are assumed with µ = µ12 = µ21.

The two-level system is completely described by its state vector , which in general is timedependent:

= c1(t) 1 exp

i

+ c2(t) 2 exp

i

 

,

(1.1.33)

 

 

E1t

 

 

E2t

 

 

 

with 1 , 2 the eigenfunctions and E1, E2 the energy eigenstates. The eigenfunctions are normalized, orthogonal and depend on the position vector r:

ϕ ϕ

dr =

 

ϕ

ϕ

2

 

= δ

ij

.

(1.1.34)

i j

 

1

 

 

 

 

The state vector has to fulfill the time-dependent Schr¨odinger equation:

i

∂ |ϕ

= (H

 

+ H

 

)

ϕ

 

,

(1.1.35)

 

∂t

 

0

 

int

|

 

 

 

with H0 the Hamilton operator of the undisturbed system (Hint = 0) and Hint the interaction energy. For the undisturbed system holds [89Yar]:

H0 i = Ei i , i = 1, 2 ,

(1.1.36)

which follows directly from (1.1.35) by replacing by i exp (iEit/ ). The parameters of interest, the inversion density ∆n = n2 − n1 and the macroscopic polarization

P A = n0 µ

(1.1.37)

are determined by the coe cients c1, c2. The probability of the system to be in the lower/upper state is given by |c1|2 , |c2|2 , respectively, which requires:

|c1|2 + |c2|2 = 1 .

(1.1.38)

The number of atoms in the lower/upper level is then given by:

n1 = n0 |c1|2 , n2 = n0 |c2|2 , n1 + n2 = n0

and hence the inversion density :

Landolt-B¨ornstein

New Series VIII/1A1


14

1.1.3 Interaction with two-level systems

[Ref. p. 40

 

 

 

n = n0

|c2|2 − |c1|2 .

(1.1.39)

The expectation value of the dipole moment µ = −e ϕrϕ is obtained from (1.1.33). Using the afore mentioned assumptions:

µ11 = −e ϕ11 = 0 , µ22 = −e ϕ22 = 0

one obtains finally for the polarization from (1.1.33), (1.1.34), (1.1.38)

P

A

= n

0 {

µ

12

 

c c

2

exp (

i ω

A

t) +

 

µ

21

 

c c exp (+i ω

A

t)

}

(1.1.40)

 

 

 

1

 

 

 

1 2

 

 

with µ12 , µ21 the dipole moment of the transition E1 ↔ E2 and vice versa. For non-degenerated transitions one has µ12 = µ21 = µA. In the following only µA will be used, which is a characteristic parameter of the specific transition:

µA = −e ϕ12 .

(1.1.41)

1.1.3.2.2 The interaction with a monochromatic field

The interaction Hamiltonian for a non-quantized real field Ereal corresponds to the classical energy of an electric dipole in an electric field. It reads [97Scu]:

Hint = µAEreal = µA

(E + E )

.

(1.1.42)

2

 

 

 

Substitution of (1.1.42) into (1.1.35), using the orthogonality (1.1.34) and (1.1.41) provides two

di erential equations for the coe cients c1, c2 of the state vector:

 

 

dc1

=

 

i

(E + E )

 

 

 

 

 

 

c2 exp (iωAt) µA

 

 

,

 

 

dt

 

2

 

 

dc2

=

 

i

c1 exp (+iωAt) µA

(E + E )

.

(1.1.43)

 

dt

 

 

2

 

 

 

 

 

 

 

The time dependence of inversion density and polarization is obtained from (1.1.39), (1.1.40) by di erentiating and applying (1.1.43). After some simple mathematics the following two equations

for the macroscopic parameters of the two-level-system result are obtained:

 

 

n

 

i

 

 

 

 

 

=

 

{(E + E ) (P A − P A)} ,

(1.1.44a)

 

∂t

 

 

∂P

 

 

 

µA

 

 

A

= i ωAP A +

 

µA (E + E ) ∆n .

(1.1.44b)

 

∂t

 

For E and P A the

SVE-approximations of (1.1.23), (1.1.25) are used.

Then in (1.1.44a),

(1.1.44b) terms with the frequency 2ω appear, which are neglected. This approach is called the rotating-wave approximation [97Scu, 72Cou]. The above equations simplify to

n

=

 

i

{

E P

 

 

E

P

}

,

(1.1.45a)

 

 

 

 

 

 

 

 

∂t

 

2

 

 

 

 

0

A0

 

0

A0

 

 

∂P A0

 

= i

δP A0 +

i µA

µAE0 n , δ = ω − ωA

(1.1.45b)

 

∂t

 

 

 

(rotating-wave approximation) with

µA: electric dipole moment of the transition, ω: frequency of the interacting field,

ωA: resonance frequency of the two-level system,= 1.0546 × 1034 Ws2: Planck’s constant.

Some typical values of dipole moments are given in Table 1.1.2.

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New Series VIII/1A1



Ref. p. 40]

1.1 Fundamentals of the semiclassical laser theory

15

 

 

 

Table 1.1.2. Typical values of dipole moments [01Men].

Transition

 

 

 

A| [As m]

Bohr’s radius × electron charge

 

 

1029

Hydrogen

1s – 2p

λ0

= 121 nm

0.8 × 1029

 

4f – 5g

λ0

= 4053 nm

8.3 × 1029

Chromium ions in ruby

4A2(3/2) – E levels

λ0

= 694 nm

1029

1.1.3.3 The Maxwell–Bloch equations

The idealized rotating-wave approximation is adapted to the real situation and combined with the SVE wave equation. Incoherent perturbations by the environment are taken into account.

So far the interaction of the two-level system with the electromagnetic field is purely coherent, no perturbations by external influences on the system are considered. Stochastic processes will modify the interaction considerably. Here only a very basic description is presented. A detailed analysis of these statistical processes is given in [70Hak, 97Scu].

1.1.3.3.1 Decay time T1 of the upper level (energy relaxation)

Three incoherent processes reduce or increase the upper-level population and have to be considered in (1.1.45a), (1.1.45b):

spontaneous emission,

interaction with the host material (collisions, lattice vibrations),

increase of the population by pumping (light, electron collisions, or other processes).

1.1.3.3.1.1 Spontaneous emission

The two-level system is coupled to the modes of the optical resonator or to the free-space modes. Spontaneous emission into these modes reduces the upper-level population. Moreover, by each spontaneous emission process the phase relation between the field and the two-level eigenfunction is destroyed. If the dimensions of the resonator are large compared with the wavelength, the decay is given by ∂n2/∂t = −n2/Tsp , with A21 = 1/Tsp , the Einstein coe cient of spontaneous emission. If the resonator dimensions are comparable with the wavelength, spontaneous emission is strongly influenced by the resonator geometry, it can be enhanced or reduced (see Chap. 8.1).

1.1.3.3.1.2 Interaction with the host material

This interaction reduces the population density. Energy is transferred to the host material and converted into heat. A simple approach for this decay is again an exponential ansatz ∂n2/∂t = −n2/TH . This decay time together with the spontaneous decay time delivers a resulting decay T1 of the upper-level population, also called energy relaxation time or longitudinal relaxation time.

Landolt-B¨ornstein

New Series VIII/1A1