Mode-dependent vibrational autoionization of NO2

被引:14
|
作者
Bell, P
Aguirre, F
Grant, ER
Pratt, ST
机构
[1] Argonne Natl Lab, Argonne, IL 60439 USA
[2] Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA
[3] Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2003年 / 119卷 / 19期
关键词
D O I
10.1063/1.1618218
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
Triple-resonance excitation and high-resolution photoelectron spectroscopy were combined to study the mode dependence of vibrational autoionization in Rydberg states of NO2. Photoselection isolates vibrational autoionization via the symmetric stretching vibration, nu(1), and the bending vibration, nu(2). The previously characterized Fermi resonance between one quantum of nu(1) and two quanta of nu(2) [H. Matsui , J. Mol. Spectrosc. 175, 203 (1996)] allows the comparison of the vibrational autoionization matrix elements for these two modes. The squared matrix element for vibrational autoionization via the symmetric stretch is found to be approximately 35 times greater than that for the bend, which is also consistent with previous results. The results are discussed in terms of existing theoretical models for the autoionization process. (C) 2003 American Institute of Physics.
引用
收藏
页码:10146 / 10157
页数:12
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