Ultrafast IR laser control of photodissociation: single- vs. multi-pulse schemes
Abstract
Analytical laser pulses are designed to break the H–Co bond of HCo(CO)4 in the electronic ground state. The potential energy surface is taken from a pseudo-triatomic model of this compound. Single- and two-pulse dissociations are shown to be equally efficient in their ability to dissociate the molecule within two picoseconds at moderate field strengths. The isotope TCo(CO)4 is considered as well and results of a three-pulse laser interaction are presented. Laser selective isotope separation is demonstrated to be feasible over a wide range of frequencies using a single driving field.