Experimental and theoretical determination of rotational-translational state-to-state rate constants for N2:He collisions at low temperature (3<T<20 K)

被引:15
作者
Maté, B
Thibault, F
Ramos, A
Tejeda, G
Fernández, JM
Montero, S
机构
[1] CSIC, Inst Estructura Mat, Madrid 28006, Spain
[2] Univ Rennes 1, Lab Phys Atomes Lasers Mol & Surfaces, UMR CNRS 6627, F-35042 Rennes, France
关键词
D O I
10.1063/1.1543945
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We present an experimental determination of state-to-state rotational-translational (RT) rate constants of N-2:He collisions in the vibrational ground state as a function of temperature in the range 3<T<20 K. Raman spectroscopy in supersonic expansions of N-2/He mixtures is used to determine the primary data that, together with the N-2:N-2 state-to-state RT rates previously determined [Ramos et al., Phys. Rev. A 66, 022702 (2002)], are needed to solve the master equation according to a procedure that does not impose any particular scaling law. We also report first principle calculations of the N-2:He state-to-state RT rate constants performed using the full three-dimensional potential energy surface of Reid [J. Chem. Phys. 107, 2329 (1997)], in the 3<T<300 K temperature range. The coupled-channel method, and the coupled-states approximation, were applied in the low (0-610 cm(-1)) and in the high (610-1500 cm(-1)) energy limits, respectively. A good agreement between theoretical and experimental results is found in the temperature range where comparison is possible. (C) 2003 American Institute of Physics.
引用
收藏
页码:4477 / 4486
页数:10
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