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Copyright by Kirsten Viering 2006 - Raizen Lab - The University of ...

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2.3 Interaction <strong>of</strong> a multi-level system with non-resonant light<br />

Although there are many cases where the two-level approximation is justified, we<br />

will now consider the more general case <strong>of</strong> a multi-level atom <strong>by</strong> going back to the<br />

Schrödinger-equation (eq.2.1) and using time-dependant perturbation theory to solve<br />

the differential equation.<br />

cm(t),<br />

In the second order expansion we get the following expression for the coefficients<br />

cm(t) − cm(0) = − 1<br />

2 t<br />

dt<br />

0<br />

′<br />

t ′<br />

dt<br />

0<br />

′′ <br />

k<br />

µnk E(r, t ′ )µkm E(r, t ′′ )e iω nkt ′<br />

e iω kmt ′′<br />

, (2.21)<br />

where the sum has to be evaluated over all possible states. For further analysis we insert<br />

the complex electric field E(t) = 1<br />

2 E0e iω lt + c.c., where we neglect the spatial dependance<br />

again. Thus we obtain<br />

cm(t) − cm(0) = − 1<br />

42 t<br />

dt<br />

0<br />

′<br />

t ′<br />

dt<br />

0<br />

′′ <br />

k<br />

µnkE0(t ′ ) e iωlt ′<br />

+ e −iωlt ′<br />

×µkmE0(t ′′ ) e iωlt ′′<br />

+ e −iωlt ′′ e iωnkt ′<br />

e iωkmt ′′<br />

, (2.22)<br />

where we have avoided the Rotating Wave Approximation.<br />

Assuming the atom to be in state |m〉 we can rewrite the coefficients as complex<br />

phase e iφ(t) . <strong>The</strong> equation above then reads<br />

1 · e iφ(t) − const. = − 1<br />

42 t<br />

dt<br />

0<br />

′<br />

t ′<br />

dt<br />

0<br />

′′ <br />

k<br />

µ nkE0(t ′ ) e iωlt ′<br />

+ e −iωlt ′<br />

×µkmE0(t ′′ ) e iωlt ′′<br />

+ e −iωlt ′′ e iωnkt ′<br />

e iωkmt ′′<br />

. (2.23)<br />

By differentiating and averaging over one period this becomes<br />

〈 ˙φ〉<br />

|E0| 2<br />

= −<br />

42 <br />

k<br />

|µkm| 2<br />

<br />

1<br />

ωkm + ωl 8<br />

<br />

1<br />

− . (2.24)<br />

ωkm − ωl

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