Copyright by Kirsten Viering 2006 - Raizen Lab - The University of ...
Copyright by Kirsten Viering 2006 - Raizen Lab - The University of ...
Copyright by Kirsten Viering 2006 - Raizen Lab - The University of ...
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with the perturbation H ′ (t) = −µ·E(t). <strong>The</strong> set <strong>of</strong> differential equations, eq. 2.4, specifies<br />
to<br />
∂cm(t)<br />
∂t<br />
= i<br />
<br />
where µmn describes the dipole matrix element 〈m|µ|n〉.<br />
<br />
µmnE(t)cn(t)e iωmnt<br />
, (2.6)<br />
n<br />
Let us first consider the analytically solvable case <strong>of</strong> a two-level atom. <strong>The</strong> more<br />
general treatment <strong>of</strong> a multi-level system will be presented in chapter 2.3. In a two-level<br />
atom there are two coupled differential equations<br />
and<br />
∂cg(t)<br />
∂t<br />
∂ce(t)<br />
∂t<br />
i<br />
= µgeE(t)ce(t)e iωat<br />
<br />
i<br />
= µeg E(t)cg(t)e<br />
iωat<br />
<br />
(2.7)<br />
(2.8)<br />
with the resonant absorption frequency ωa = ωe − ωg. <strong>The</strong> ground and excited states<br />
are labeled <strong>by</strong> the indices g and e respectively. By introducing the Rabi frequency for a<br />
two-level atom<br />
these differential equations can be simplified to<br />
and<br />
Ω = E<br />
〈e|µ|g〉, (2.9)<br />
<br />
∂cg(t)<br />
∂t = iΩ∗ ce(t)e −iωat<br />
(2.10)<br />
∂ce(t)<br />
∂t = iΩcg(t)e iωat , (2.11)<br />
where we have ignored the spatial dependance <strong>of</strong> the oscillating electric field.<br />
Generally it is possible to solve these equations <strong>by</strong> transforming them into a<br />
rotating frame. Here we will follow another ansatz [8] and substitute the coefficients<br />
cg(t) and ce(t) with<br />
5