Coherent Backscattering from Multiple Scattering Systems - KOPS ...
Coherent Backscattering from Multiple Scattering Systems - KOPS ...
Coherent Backscattering from Multiple Scattering Systems - KOPS ...
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2 Theory<br />
cooperon<br />
1<br />
0.8<br />
0.6<br />
0.4<br />
l abs<br />
= 10 −5 m<br />
l abs<br />
= 3 ⋅ 10 −5 m<br />
l abs<br />
= 10 −4 m<br />
no absorption<br />
0.2<br />
0<br />
−90 −60 −30 0 30 60 90<br />
scattering angle [deg]<br />
Figure 2.13: <strong>Coherent</strong> backscattering with absorption. The graph shows the cooperon<br />
α c (θ, l abs ) calculated with eqn. 2.18 for different absorption lengths l abs = 3Dτ/l ∗ with<br />
λ = 590 nm, kl ∗ = 5, and non-reflective sample surface.<br />
function of time or respectively the pathlength. The longest photon paths have the narrowest<br />
Gaussians, while short paths have wide distributions.<br />
An infinite series of Gaussians creates a triangular cusp at the tip of the coherent backscattering<br />
cone. However, absorption as well as localization introduce a cutoff length for the photon<br />
paths, so that the narrowest Gaussians are eliminated. This explains why one observes a<br />
rounded conetip for absorbing or localizing samples (figs. 2.13, 3.4).<br />
The effect of absorption can be handled mathematically by introducing a substitution q 2 →<br />
q 2 + (Dτ) −1 in the cooperon [38]. With the correct normalization the cooperon for absorbing<br />
samples becomes<br />
α c (θ, τ) =<br />
(<br />
Dτ l ∗ +<br />
(<br />
l ∗ l ∗ + √ ) 2 (<br />
Dτ 1−e<br />
−2q abs z 0<br />
(<br />
1 − e − 2z 0<br />
q abs l ∗ + 2µ<br />
µ+1<br />
)<br />
) )<br />
√ √Dτ ( )<br />
Dτ q abs l ∗ + µ+1 2<br />
(2.18)<br />
2µ<br />
with q abs = √ q 2 + (Dτ) −1 .<br />
Anderson localization can be modeled by a transition <strong>from</strong> a constant diffusion coefficient D<br />
to a time-dependent coefficient D(t) ∝ t −1 at the localization time t loc [45]. As the ‘cutoff’<br />
mechanism is different, the resulting shape of the conetip also differs <strong>from</strong> that of a purely<br />
absorbing sample (fig. 3.4).<br />
22