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Kinetic and internal energy distributions via velocity-aligned Doppler spectroscopy: The 193 nm photodissociation of H/sub 2/S and HBr

Journal Article · · J. Chem. Phys.; (United States)
DOI:https://doi.org/10.1063/1.453339· OSTI ID:6449802
We report center-of-mass kinetic energy distributions for the 193 nm photodissociation of H/sub 2/S and HBr using the method of velocity--aligned Doppler spectroscopy. Nascent H atoms are detected by sequential two-photon photoionization via Lyman-..cap alpha.. (121.6 nm + 364.7 nm), and internal SH(X /sup 2/Pi) and Br excitations are observed directly in the H-atom kinetic energy distributions. The kinetic energy resolution is much better than in ''conventional'' sub-Doppler resolution spectroscopy and results from detecting spatially selected species whose velocities are aligned with the wave vector of the probe radiation, k/sub probe/, thereby providing a kinetic energy distribution for a specific laboratory direction. This improved resolution is achieved in the present experiments by using pulsed, collimated, and overlapped photolysis and probe beams, but the vital aspect of the technique involves increasing the delay between the two lasers in order to discriminate against species having velocity components perpendicular to k/sub probe/.
Research Organization:
Chemistry Department, University of Southern California, Los Angeles, California 90089-0484
OSTI ID:
6449802
Journal Information:
J. Chem. Phys.; (United States), Journal Name: J. Chem. Phys.; (United States) Vol. 87:2; ISSN JCPSA
Country of Publication:
United States
Language:
English