Multiphoton fragmentation of H2+ and D2+ with coherent and incoherent fields.

Abstract

A theory of molecular photofragmentation is developed for coherent and incoherent light and for the case where dissociation lifetimes of field-induced resonances are shorter than pulse lengths. Using a mixed representation for the transition operator (a description of the initial state of the field with the coherent representation and of the final state with the number representation), we show how observables are modified at different field regimes by Poisson distributions. Applications to ${\mathrm{H}}_{2}^{+}$ and ${\mathrm{D}}_{2}^{+}$ are presented and discussed. They include line shapes and final distributions of kinetic energies for weak, intermediate, and strong fields. Results show that the interference of resonance states plays an important role even after averages over the field phases have been carried out to account for incoherent effects.