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Reactive collision with excited states in a crossed beam experiment: O( sup 1 D )+H sub 2 ( v ) r arrow OH( A sup 2. Sigma. sup + )+H

Journal Article · · Journal of Chemical Physics; (USA)
DOI:https://doi.org/10.1063/1.458219· OSTI ID:6807227
; ; ;  [1];  [2]
  1. Centre d'Etudes Nucleaires de Saclay, DLPC-Service de Physique et de Physico-Chimie, Laboratoire des Jets Moleculaires, 91191 Gif-sur-Yvette Cedex, (France)
  2. Universite de Paris-Sud, Laboratoire de Chimie Theorique (CNRS, UA 506), 91405 Orsay Cedex, (France)
At least for its most probable mechanisms, the reaction O({sup 1}{ital D})+H{sub 2}({ital X} {sup 1}{summation}{sup +}{sub {ital g}}) {r arrow}OH({ital A} {sup 2}{summation}{sup +})+H(1 {sup 2}{ital S}) entirely takes place, from reagents to products, on electronically excited-state channels. Due to its endoergicity and to probable energy barriers ({ital E}*{approx}2.8 eV) encountered on these channels, the reaction can be produced in a crossed beam experiment only if the hydrogen molecule is excited on high vibrational levels ({ital v}{ge}5 or {ital v}{ge}7, according to the presence or the absence of energy barriers). This is obtained here by low-energy electron bombardment of the H{sub 2} molecular beam. The reaction is observed through the spontaneous fluorescence of the product OH. The measured spectrum corresponding to the 0--0 band of the {ital A} {sup 2}{summation}{sup +}{r arrow}{ital X} {sup 2}{Pi} transition is compared to simulated spectra, as obtained with a simple statistical model and with fitted rotational distribution for OH({ital A} {sup 2}{summation}{sup +},{ital v}=0): a broad rotational distribution and a strongly nonstatistical effect on the spin doublet populations are observed.
OSTI ID:
6807227
Journal Information:
Journal of Chemical Physics; (USA), Journal Name: Journal of Chemical Physics; (USA) Vol. 92:12; ISSN JCPSA; ISSN 0021-9606
Country of Publication:
United States
Language:
English