Semiclassical Green function calculation of four wave mixing in polarizable clusters and liquids

Abstract

A theory for the nonlinear optical response of an assembly of four level atoms representing an s–p transition, with dipole–dipole interactions is developed. Simulation results for two-pulse ultrafast four wave mixing measurements in atomic clusters and in liquids demonstrate that the electronic density of states can be obtained by combining absorption and four wave mixing experiments. We show that a sensitive direct probe for interatomic interactions and correlations is provided by reversing the pulse time ordering in a photon echo sequence. The effect of nuclear motions on the linear absorption spectrum is investigated.