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Bogoliubov Excitations of Inhomogeneous Bose-Einstein ...

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3.1. Optical speckle potential<br />

In continuous systems, however, there is no spacing, and the actual correlation<br />

length is important, so similar correlation lengths in all directions<br />

are desirable. This could be achieved by the superposition <strong>of</strong> several speckle<br />

fields, where at least a second speckle field for the third dimension is needed.<br />

This would achieve similar correlation lengths in all directions, but with an<br />

anisotropic correlation function. Ideally, the speckle pattern should be obtained<br />

in a closed cavity [23, 24], which restores the isotropy. In this case,<br />

the complex degree <strong>of</strong> coherence reads γ(k) = 2π 2 σ 2 δ(|k|−kL), which results<br />

in a k-space correlator C3(kσ) = (8πkσ) −1 Θ(2 − |kσ|) with a divergence at<br />

k = 0.<br />

Lacking a simple experimentally realized model, we prefer to follow Pilati<br />

et al. [118] and define the three-dimensional speckle disorder from a more<br />

abstract point <strong>of</strong> view. Independently <strong>of</strong> a possible experimental realization,<br />

we declare Eq. (3.7) the definition <strong>of</strong> the speckle field also in dimension three.<br />

This preliminary isotropic three-dimensional speckle field grasps the important<br />

features <strong>of</strong> laser speckles: the asymmetric intensity distribution (3.10)<br />

and the finite support <strong>of</strong> the correlator in k-space (3.12), see below. Like the<br />

two-dimensional speckle it might have to be adjusted to the experimental<br />

details <strong>of</strong> future experimental setups, in particular to anisotropies.<br />

3.1.3. Intensity and potential correlations<br />

In typical experimental setups, the laser frequency ωL is chosen to be close to<br />

an internal resonance ω0 <strong>of</strong> the atom such that ωL/ω0 ≈ 1, but far-detuned<br />

in the sense that the detuning ∆ = ωL −ω0 is larger than the line width Γ <strong>of</strong><br />

the transition or the inverse lifetime <strong>of</strong> the excited state. Then, the energy<br />

levels <strong>of</strong> the atoms are shifted due to the interaction <strong>of</strong> their induced dipole<br />

moment with the electric laser field [39]. This shift is proportional to the<br />

laser intensity I(r) = |E(r)| 2 , where the sign and the magnitude depend on<br />

the detuning<br />

∆E(r) = 3πc2 L<br />

2ω 3 0<br />

Γ<br />

∆ 2ɛ0cL I(r). (3.8)<br />

In this formula, ɛ0 is the vacuum permittivity and cL is the speed <strong>of</strong> light.<br />

The origin <strong>of</strong> energy is shifted such that the potential has zero mean<br />

V (r) = V0(I(r) − I0)/I0. (3.9)<br />

Here, the signed disorder strength is defined as V0 = 3πc 3 L ɛ0ΓI0/(ω 3 0∆).<br />

The magnitude <strong>of</strong> the parameter V0 is the rms value <strong>of</strong> V (r), V 2<br />

0 = V (r) 2 .<br />

Its sign is determined by the detuning <strong>of</strong> the laser frequency and states<br />

61

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