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Translationally and rotationally resolved excitation of CO[sub 2](00[sup 0]2) by collisions with hot hydrogen atoms

Journal Article · · Journal of Chemical Physics; (United States)
DOI:https://doi.org/10.1063/1.464833· OSTI ID:6697653
; ;  [1];  [2]
  1. Department of Chemistry and Columbia Radiation Laboratory, Columbia University, New York, New York 10027 (United States)
  2. Department of Chemistry, Brookhaven National Laboratory, Upton, New York 11973 (United States)

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]2) vibrational state by collisions with translationally hot hydrogen atoms. The 00[sup 0]2 rotational population distribution and rotationally resolved linewidths are remarkably similar to those previously obtained for 00[sup 0]1. Within the context of a simple physical model used to interpret the data, the similar rotational distributions and translational recoils for 00[sup 0]1 and 00[sup 0]2 suggest that these two states are excited by similar collision trajectories, wherein asymmetric stretching excitation is optimized when H strikes near the end of the O--C--O molecule. The magnitude of population scattered into 00[sup 0]2 is [similar to]21 times smaller than that scattered into 00[sup 0]1.

DOE Contract Number:
FG02-88ER13937
OSTI ID:
6697653
Journal Information:
Journal of Chemical Physics; (United States), Journal Name: Journal of Chemical Physics; (United States) Vol. 98:8; ISSN JCPSA6; ISSN 0021-9606
Country of Publication:
United States
Language:
English

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