The evolution equation for a particle in a homogeneous fluid is generalized to the case of many particles. The correct limiting expressions are obtained for the case of one particle and of random a priori phases.
Recently, the Fokker-Planck (F-P) equation, satisfied by the phase-space distribution function of a Brownian (B) particle, has been derived from the Liouville equation, satisfied by the phase-space distribution function of the composite system, B particle plus fluid. We have started from a strictly quantum-mechanical formulation of the problem, using a density-matrix description of the composite system, and have shown that in an appropriate classical limit the F-P equation results. To lowest order in $\ensuremath{\hbar}$, our technique gives the same expression for the friction coefficient obtained earlier from the Liouville equation. In principle it yields corrections to the F-P equation to all orders in $\ensuremath{\hbar}$. We have shown that for a uniform fluid, the quantum corrections to the F-P equation to first order in $\ensuremath{\hbar}$ appear only as a shift in the friction coefficient. If the classical friction coefficient ${\ensuremath{\zeta}}_{0}$ is replaced by ${\ensuremath{\zeta}}_{0}+\ensuremath{\hbar}{\ensuremath{\zeta}}_{1}$, with an appropriate ${\ensuremath{\zeta}}_{1}$, then the F-P equation is given correctly to order $\ensuremath{\hbar}$. There is a difference in the mass dependence of ${\ensuremath{\zeta}}_{0}$ and ${\ensuremath{\zeta}}_{1}$ which suggests the existence of an isotope effect in the mobility of a particle moving through a quantum fluid. The technique employed in the derivation is to consider the expectation value of the density matrix of the system in a state in which the position and momentum of the particles are known with maximum accuracy (Kennard packet). This expectation value $\ensuremath{\mu}$ is an appropriate, positive, semiclassical phase-space distribution function. An appropriate equation is derived for $\ensuremath{\mu}$, which to lowest order in $\ensuremath{\hbar}$ is the Liouville equation. The remainder of the derivation is similar to the derivation in the classical case (a suitable projection technique is used).
Abstract A density operator analysis is made of the particle‐ejection (e.g., photoionization) problem in the “generalized sudden approximation” for the case in which the ejected particle is detected but its dynamical properties are not observed. It is shown that the resultant statistical density operator may be derived from that obtained in a particle‐conserving Hamiltonian‐evolution linear‐response model with a random impulse perturbation, and that the physical applicability of the latter model embraces the range of applicability of the former. The initial value of the statistical density operator for the above particle‐ejection problem is shown to be the N – (1)‐particle reduced density operator of the initial state; and the initial value of the statistical density operator for the excitations in the random impulse model is shown to be the N‐particle Hermitian operator whose matrix representation is the G matrix of Garrod and Percus. The significance of the eigenvalue spectrum of these operators to the excitation properties of the system is discussed, especially for the random impulse model, where a large eigenvalue of the G matrix can signal strong preferential excitation to its corresponding particle‐hole collective state, even for a random perturbation. Extensions of these ideas to excitations from states with a large eigenvalue of the two‐particle reduced density operator (e.g., superconducting states) are mentioned. The The applicability of these density matrices to the description of the excitation spectrum due to a well‐defined perturbation is discussed. The relationship of these time‐dependent density operators to the one‐particle propagator and the particle–hole propagator (polarization propagator) is established.