State-to-state ArHBr photodissociation quantum dynamics

被引:16
|
作者
Lepetit, B [1 ]
Lemoine, D
机构
[1] Univ Toulouse 3, IRSAMC, LCAR, F-31062 Toulouse, France
[2] CNRS, UMR 5589, F-31062 Toulouse, France
[3] Univ Lille 1, Ctr Etud & Rech Lasers & Applicat, CNRS,UMR 8523, Lab Phys Lasers Atomes & Mol, F-59655 Villeneuve Dascq, France
来源
JOURNAL OF CHEMICAL PHYSICS | 2002年 / 117卷 / 19期
关键词
D O I
10.1063/1.1514213
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 report quantum dynamical calculations on the photodissociation process: ArHBr+hnu-->H+ArBr or Ar+Br+H. Jacobi coordinates associated with the product arrangement H+ArBr have been used as well as a pseudospectral wave packet propagation method. The radial singularity at the origin is either analytically lifted with a discrete Bessel transform approach, or treated within a sine transform strategy. The relative fraction of a bound ArBr product state is high (of the order of 50%) and decreases with energy. Product vibrational populations decrease with vibrational energies. Rotational distributions show oscillatory patterns characteristic of rotational rainbows, whereas angular distributions have maxima at rainbow angles. (C) 2002 American Institute of Physics.
引用
收藏
页码:8676 / 8685
页数:10
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