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Neutral dissociation of hydrogen following photoexcitation of HCl at the chlorineKedge
Author(s) -
D. L. Hansen,
M. E. Arrasate,
J. Cotter,
G. R. Fisher,
K. T. Leung,
J. C. Levin,
Rolf Martin,
P. Neill,
R. C. C. Perera,
I. A. Sellin,
M. Simon,
Yasushi Uehara,
Brett J. Vanderford,
S. B. Whitfield,
D. W. Lindle
Publication year - 1998
Publication title -
physical review a
Language(s) - English
Resource type - Journals
eISSN - 1094-1622
pISSN - 1050-2947
DOI - 10.1103/physreva.57.2608
Subject(s) - physics , excited state , atomic physics , photoexcitation , glauber , dissociation (chemistry) , scattering , chemistry , quantum mechanics
Time-of-flight mass spectroscopy was used to study the relaxation dynamics of HCl following photoexcitation in the vicinity of the Cl K edge ({approximately}2.8keV) using monochromatic synchrotron radiation. At the lowest resonant excitation to the 6{sigma}{sup {asterisk}} antibonding orbital, almost half of the excited molecules decay by emission of a neutral H atom, mostly in coincidence with a highly charged Cl{sup n+} ion. The present work demonstrates that neutral-atom emission can be a significant decay channel for excited states with very short lifetimes (1 fs). {copyright} {ital 1998} {ital The American Physical Society}

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