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Coherent Backscattering from Multiple Scattering Systems - KOPS ...

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5.1 Conservation of energy in coherent backscattering<br />

sample R [mm] L [mm] A (eqn. 5.4) A (eqn. 5.6)<br />

a-1 7.5 1.35 0.994 0.994<br />

a-2 7.5 1.03 0.995 0.995<br />

NIX-2 7.5 1.26 0.990 0.990<br />

NIX-3 7.5 1.75 0.992 0.992<br />

R700 (DuPont) 7.5 1.0 0.995 0.995<br />

R700 + gypsum 7.5 0.95 0.950 0.951<br />

R900 (DuPont) 7.5 0.5 0.994 0.994<br />

R902 (DuPont) 7.5 0.5 0.991 0.991<br />

S-25 7.5 0.5 0.993 0.993<br />

Teflon (D = 27500 m 2 /s) 20 50 0.901 0.890<br />

Teflon (D = 16500 m 2 /s) 20 50 0.922 0.918<br />

Teflon (D = 13300 m 2 /s) 20 50 0.930 0.927<br />

Ti-pure (Aldrich) 7.5 1.8 0.998 0.998<br />

Table 5.1: Albedos. The albedos for the samples with radius R and thickness L<br />

were calculated using eqns. 5.4 and 5.6. For other sample parameters see tab. 4.1 and<br />

sec. 4.2.2. The albedo of the teflon reference was calculated for the three different<br />

diffusion coefficients mentioned in sec. 4.2.2.<br />

solution of the wave equation by Green’s functions. This description would be exact, but<br />

it can not be solved for a system of millions and billions of randomly distributed particles,<br />

all of whose positions in addition would have to be known exactly. To turn it into a useful<br />

mathematical form, one therefore has to find a collective description of the multiple scattering<br />

medium by choosing exactly the right approximations.<br />

To describe multiple scattering, one must consider the products of Green’s functions corresponding<br />

to all possible scattering sequences. However, the coherent backscattering cone is<br />

observed in the averaged intensity, where most of the pairs of Green’s functions vanish, as<br />

their phase difference is large and random. In the so-called Drude-Boltzmann approximation,<br />

where the average over the product of two Green’s functions can be approximated by the<br />

product over the two averaged functions, the average intensity can therefore be written as<br />

∫∫ 〈Ψin<br />

I d (⃗r,⃗ r ′ ) ∝ (⃗r,⃗r 1 ) 〉 · 〈Ψ<br />

in(⃗r,⃗r ∗ 1 ) 〉 · Γ(⃗r 1 ,⃗r 2 ) · 〈G(⃗r<br />

2 ,⃗ r ′ ) 〉 · 〈G ∗ (⃗r 2 ,⃗ r ′ ) 〉 d⃗r 1 d⃗r 2<br />

where we introduce the structure factor or vertex function Γ(⃗r 1 ,⃗r 2 ), which takes into account<br />

all possible scattering sequences between the first and the last scattering site,⃗r 1 and⃗r 2 .<br />

One contribution that is not taken into account by the diffuson approximation are timeinverted<br />

photon paths, for which the phase difference also vanishes. It is given by<br />

∫∫ 〈Ψin<br />

I c (⃗r,⃗ r ′ ) ∝ (⃗r,⃗r 1 ) 〉 · 〈Ψ<br />

in(⃗r,⃗r ∗ 2 ) 〉 · Γ(⃗r 1 ,⃗r 2 ) · 〈G(⃗r<br />

2 ,⃗ r ′ ) 〉 · 〈G ∗ (⃗r 1 ,⃗ r ′ ) 〉 d⃗r 1 d⃗r 2<br />

In the limit of dilute systems with approximately spherical scatterers, where the Green’s<br />

functions are spherical waves and the transport mean free path is well described by the l ∗<br />

derived in sec. 2.3, this contribution is equivalent to the cooperon derived in sec. 2.7. The<br />

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