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State-resolved vibrational, rotational, and translational energy deposition in CO sub 2 (00 sup 0 1) excited by collisions with hot hydrogen atoms

Journal Article · · Journal of Chemical Physics; (USA)
DOI:https://doi.org/10.1063/1.457704· OSTI ID:7188737
; ;  [1];  [2]
  1. Department of Chemistry, Columbia University, New York, NY (USA) Columbia Radiation Laboratory, Columbia University, New York, New York 10027 (USA)
  2. Department of Chemistry, Brookhaven National Laboratory, Upton, New York 11973 (USA)

Time-domain tunable diode laser absorption spectroscopy has been used to measure rotationally resolved transient absorption line shapes and nascent rotational populations for CO{sub 2} molecules excited into the (00{sup 0}1) vibrational state by collisions with translationally hot hydrogen atoms. High-accuracy measurements were made at both 292 and 223 K, providing information about the initial-state dependence of the collision dynamics and about the (temperature-independent) state--to--state scattering cross sections. The nascent rotational population distribution is found to be nearly independent of temperature, indicating broad rotational inelasticity in the 00{sup 0}0{r arrow}00{sup 0}1 scattering process. The nascent populations and transient linewidths are interpreted in terms of two separate theoretical models which lend substantial insight into the H--CO{sub 2} collision dynamics.

DOE Contract Number:
FG02-88ER13937
OSTI ID:
7188737
Journal Information:
Journal of Chemical Physics; (USA), Journal Name: Journal of Chemical Physics; (USA) Vol. 92:8; ISSN JCPSA; ISSN 0021-9606
Country of Publication:
United States
Language:
English

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