
2.5 Lippmann–Schwinger Equation 51
where the diffusion constant D is given by
D =
K
Cρ
=
(thermal conductivity)
(specific heat) ×(density)
.
These two expressions, Eqs. (2.4.13) and (2.4.15), are related by the analytic contin-
uation, t →−it.ThediffusionconstantD plays the role of the inverse of the Planck
constant .
We shall devote the next section for the more formal discussion of the scattering
problem.
2.5
Lippmann–Schwinger Equation
In the nonrelativistic scattering problem of quantum mechanics, we have the
macroscopic causality of Stueckelberg: when we regard the potential V(t, r)asa
function of t, we have no scattered wave, ψ
scatt
(t, r) = 0, for t < T,ifV(t, r) = 0
for t < T. We employ the adiabatic switching hypothesis: we can take the limit
T →−∞after the computation of the scattered wave, ψ
scatt
(t, r). We derive the
Lippmann–Schwinger equation, and prove the orthonormality of the outgoing wave
and the incoming wave and the unitarity of the S matrix. We then discuss optical
theorem and asymptotic wavefunctions. Lastly, we discuss the rearrangement
collision and the final state interaction to get in touch with Born approximation.
Lippmann–Schwinger Equation: We shall begin with the time-dependent
Schr
¨
odinger equation with the time-dependent potential V(t, r),
i
∂
∂t
ψ(t, r) = [H
0
+ V(t, r)]ψ(t, r).
In order to use the macroscopic causality, we assume
V(t, r) =
V(r)fort ≥ T,
0fort < T.
For t < T, the particle obeys the free equation,
i
∂
∂t
ψ(t, r) = H
0
ψ(t, r). (2.5.1)
We write the solution of Eq. (2.5.1) as ψ
inc
(t, r). The wavefunction for the general
time t is written as
ψ(t, r) = ψ
inc
(t, r) + ψ
scatt
(t, r),