ISSN:
1089-7690
Source:
AIP Digital Archive
Topics:
Physics
,
Chemistry and Pharmacology
Notes:
The photodissociation of HCl in solid Ar is studied by non-adiabatic Molecular Dynamics simulations, based on a surface-hopping treatment of transitions between different electronic states. The relevant 12 potential energy surfaces and the non-adiabatic interactions between them were generated by a Diatomics-in-Molecules (DIM) approach, which incorporated also spin-orbit coupling. The focus of the study is on the non-adiabatic transitions, and on their role both in the cage-exit of the H atom, and in the recombination process. It is found that non-adiabatic transitions occur very frequently. In some of the trajectories, all the 12 electronic states are visited during the timescale studied. At least one non-adiabatic transition was found to occur even in the fastest cage-exit events. The other main results are: (1) The total yields for photofragment separation (by cage exit of the H atom) and for H+Cl recombination onto the ground state are roughly equal in the conditions used. (2) The cage exit events take place in the time-window between ∼70 fs and ∼550 fs after the excitation pulse, and are thus all at least somewhat delayed. The recombination events span a much broader time-window, from almost immediately after excitation, and up to ∼1100 fs and beyond. (3) The electronic energy relaxation events during the process depend significantly on symmetry and interactions of the states involved, and not only on the energy gaps between them. (4) Different electronic states reached in the course of the process exhibit different propensities with regard to the recombination versus cage exit outcome. (5) Spin-orbit interactions, and spin-forbidden transitions play an important role in the process, especially for recombination events. © 1997 American Institute of Physics.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1063/1.473657
