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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and<br />
c ′ g(t) = cg(t) (2.12)<br />
c ′ e(t) = ce(t)e −iδt , (2.13)<br />
where δ = ωl − ωa defines the detuning from resonance. By making this substitution<br />
and making the Rotating Wave Approximation [9] one derives the following equations<br />
[10]<br />
and<br />
i dc′ g(t)<br />
dt = c′ e(t) Ω<br />
2<br />
(2.14)<br />
i dc′ e(t)<br />
dt = c′ g(t) Ω<br />
2 − c′ eδ. (2.15)<br />
It is now possible to diagonalize the matrix for the perturbative part <strong>of</strong> the<br />
Hamiltonian to the following form<br />
H ′ = <br />
2<br />
thus the shifted energy levels are given <strong>by</strong><br />
<br />
−2δ Ω<br />
Ω 0<br />
, (2.16)<br />
Eg,e = <br />
2 (−δ ± Ω′ ), (2.17)<br />
where Ω ′ ≡ √ Ω 2 + δ 2 . If we assume Ω ≪ δ the energy levels are shifted <strong>by</strong><br />
respectively.<br />
∆Eg,e = ± Ω2<br />
4δ<br />
Similarly, if we assume Ω ≫ |δ| the levels shift <strong>by</strong><br />
∆Eg,e = ±sgn(δ) Ω<br />
2<br />
A schematic for the two-level energy shift is shown in fig. 2.1.<br />
6<br />
(2.18)<br />
. (2.19)