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Polarization- and time-resolved DFWM spectroscopy of the A (2)Sigma(+) - X (2)Pi (0,0) band transitions of nascent OH radicals generated by 266nm laser photolysis of H2O2. / Maksyutenko, P.; Radi, P. P.; Kozlov, D. N.; Kouzov, A. P.
в: Journal of Raman Spectroscopy, Том 44, № 10, 2013.Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование
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TY - JOUR
T1 - Polarization- and time-resolved DFWM spectroscopy of the A (2)Sigma(+) - X (2)Pi (0,0) band transitions of nascent OH radicals generated by 266nm laser photolysis of H2O2
AU - Maksyutenko, P.
AU - Radi, P. P.
AU - Kozlov, D. N.
AU - Kouzov, A. P.
PY - 2013
Y1 - 2013
N2 - The potential of a non-linear spectroscopic technique - degenerate four-wave mixing (DFWM) spectroscopy - for photo-dissociation studies is investigated. By applying a carefully considered control of the input beam polarizations, the technique is used to measure the line shapes of specific rovibrational transitions in the A(2)sigma(+)-X-2 (0,0) band of nascent OH radicals upon pulsed photo-dissociation of H2O2. The photofragmentation is performed by linearly polarized radiation at 266nm, and DFWM spectra are observed at various time delays. In contrast to linear spectroscopic methods, isotropic and anisotropic components of the non-linear susceptibility tensor are separately accessible by using appropriate polarization geometries. In particular, four-wave mixing signals can be generated that are exclusively due to the occurrence of the transient anisotropy of the recoil velocity and angular momentum vector distributions of the fragments emerging from the dissociation reaction. The observed line shapes in isot
AB - The potential of a non-linear spectroscopic technique - degenerate four-wave mixing (DFWM) spectroscopy - for photo-dissociation studies is investigated. By applying a carefully considered control of the input beam polarizations, the technique is used to measure the line shapes of specific rovibrational transitions in the A(2)sigma(+)-X-2 (0,0) band of nascent OH radicals upon pulsed photo-dissociation of H2O2. The photofragmentation is performed by linearly polarized radiation at 266nm, and DFWM spectra are observed at various time delays. In contrast to linear spectroscopic methods, isotropic and anisotropic components of the non-linear susceptibility tensor are separately accessible by using appropriate polarization geometries. In particular, four-wave mixing signals can be generated that are exclusively due to the occurrence of the transient anisotropy of the recoil velocity and angular momentum vector distributions of the fragments emerging from the dissociation reaction. The observed line shapes in isot
U2 - 10.1002/jrs.4299
DO - 10.1002/jrs.4299
M3 - Article
VL - 44
JO - Journal of Raman Spectroscopy
JF - Journal of Raman Spectroscopy
SN - 0377-0486
IS - 10
ER -
ID: 7544871