Vibrational Relaxation of the Bending Mode of HDO in Liquid D2O

2005 ◽  
Vol 109 (24) ◽  
pp. 5303-5306 ◽  
Author(s):  
Pavol Bodis ◽  
Olaf F. A. Larsen ◽  
Sander Woutersen
2004 ◽  
Vol 121 (24) ◽  
pp. 12143 ◽  
Author(s):  
Olaf F. A. Larsen ◽  
Sander Woutersen

2004 ◽  
Vol 120 (18) ◽  
pp. 8866-8867 ◽  
Author(s):  
Gerhard Seifert ◽  
Toralf Patzlaff ◽  
Heinrich Graener

1969 ◽  
Vol 35 (1) ◽  
pp. 171-183 ◽  
Author(s):  
J. P. Hodgson ◽  
R. J. Hine

The vibrational relaxation frequency of carbon dioxide has been determined by measuring the rate of change of thermal emission in shock waves near 4±3μ. This method of measuring the relaxation frequency depends mainly on the degree of excitation of the asymmetric stretching mode of the molecule, and the results are compared with those of earlier density measurements made in the same shock tube. The gas samples used are not optically thin, and it is shown that self-absorption can be taken into account. The results imply that the relaxation frequency of the asymmetric stretching mode is about 70% of that of the bending mode.


1994 ◽  
Vol 14 (4) ◽  
pp. 191-200 ◽  
Author(s):  
M. A. Vazquez ◽  
M. L. Azcárate ◽  
E. J. Quel ◽  
L. Doyennette ◽  
C. Rinaldi ◽  
...  

The time variation of the 2ν5 fluorescence intensity was measured in CDCl3 excited in the ν4 C–D bending mode by a TEA CO2 laser operating on the 10P(48) line. A fast rise of the fluorescence, with a time constant ≤ 1 μs Torr, was first observed, showing that a fast equilibration of population occurs between the ν4 and ν5 modes through a ν4 ↔ ν5 Coriolis-assisted intermode transfer and a ν5 ↔ 2ν5 near-resonant ladder-climbing process. Then a first fast fluorescence decay was observed and attributed to a (ν4, ν5) → ν2 intermode transfer with a rate constant of (7.10 ± 1.13)ms-1 Torr-1. At last, a much slower decay, with a rate constant of 0.111 ± 0.015 ms-1 Torr-1, results from the less efficient intermode transfer and V–T,R deexcitation processes involving the ν3 and ν6 states, and which compete to relax the gas to a thermodynamic equilibrium.


2003 ◽  
Vol 771 ◽  
Author(s):  
C. Gadermaier ◽  
G. Cerullo ◽  
C. Manzoni ◽  
U. Scherf ◽  
E.J.W. List ◽  
...  

AbstractIn a novel modification of transient differential transmission spectroscopy, the first excited state S1 is reexcited via a second laser pulse towards a higher lying state Sn. The dynamics of the relaxation of this state Sn as well as the states created from Sn are revealed by a broad-band probe pulse.We find that the charge carrier generation efficiency from Sn is higher compared to S1. The push and probe durations below 20 fs enable the temporal resolution of the ultrafast relaxation of the Sn state and enables us to identify the two main contributions to enhanced charge generation from Sn, energy migration towards sites of high dissociation probability, and exciton dissociation during vibrational relaxation.


2009 ◽  
Vol E92-C (8) ◽  
pp. 1058-1065 ◽  
Author(s):  
Fuhliang WEN ◽  
Chao-Chun WEN ◽  
Ming-Hung LAI ◽  
Ichien HSU

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