Bogoliubov Excitations of Inhomogeneous Bose-Einstein ...
Bogoliubov Excitations of Inhomogeneous Bose-Einstein ...
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 />
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