Measurement of orientational relaxation times of OH in a flame using picosecond time-resolved polarization spectroscopy
Year: 1995
Authors: Dreizler A., Tadday R., Suvernev A.A., Himmelhaus M., Dreier T., Foggi P.
Autors Affiliation: Physikalisch-Chemisches Institut, Im Neuenheimer Feld 253, D-69120 Heidelberg, Germany; European Laboratory for Non-Linear Spectroscopy (LENS), University of Florence, Largo E. Fermi, 50125 Florence, Italy
Abstract: Picosecond time-resolved polarization spectroscopy in the ultraviolet has been used to measure relaxation times of the laser-induced optical anisotropy of OH in an atmospheric pressure flame. OH radicals were produced in the post flame gases of a methane/air flame. Transient signals from absorption in theA2S-X2? (0-0) electronic transition were studied by pump-probe experiments using different P- and Q-branch transitions. A theoretical approach has been developed to interpret experimentally observed transient signals in terms of the relaxations of molecular orientation and alignment. The observed effective relaxation times for these flame conditions are of the order of 240-590 ps depending on the rotational state. We found slightly larger values for the relaxation times of molecular orientation than for molecular alignment. These results are relevant to the interpretation and modeling of four-wave mixing spectra.
Journal/Review: CHEMICAL PHYSICS LETTERS
Volume: 240 (4) Pages from: 315 to: 323
More Information: American Antiquarian Society, AAS. – The authors thank Professor J. Wolfrum for his interest in this work. AAS acknowledgetsh e financial support from DeutscheF orschungsgemeinscha(SftF B 359). AD and TD are grateful to the Deutsche Forschungsgemeinschfaofrt financial support.KeyWords: Spectral-line shapes; Rotattional relaxationDOI: 10.1016/0009-2614(95)00472-GCitations: 24data from “WEB OF SCIENCE” (of Thomson Reuters) are update at: 2024-11-10References taken from IsiWeb of Knowledge: (subscribers only)Connecting to view paper tab on IsiWeb: Click hereConnecting to view citations from IsiWeb: Click here