Energetics and dissociative photodetachment dynamics of superoxide-water clusters:: O2-(H2O)n, n=1-6

被引:38
|
作者
Luong, AK
Clements, TG
Resat, MS
Continetti, RE
机构
[1] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
[2] Environm Mol Sci Lab, Richland, WA 99352 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2001年 / 114卷 / 08期
关键词
D O I
10.1063/1.1342221
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
The dissociative photodetachment of O-2(-)(H2O)(n=1-6) was studied at 388 and 258 nm using photoelectron-multiple-photofragment coincidence spectroscopy. Photoelectron spectra for the series indicate a significant change in the energetics of sequential solvation beyond the fourth water of hydration. Photoelectron-photofragment kinetic energy correlation spectra were also obtained for O-2(-)(H2O)(1-2), permitting a determination of the first and second energies of hydration for O-2(-) to be 0.85 +/-0.05 and 0.70 +/-0.05 eV, respectively. The correlation spectra show that the peak photofragment kinetic energy release in the dissociative photodetachment of O-2(-)(H2O) and O-2(-)(H2O)(2) are 0.12 and 0.25 eV, respectively, independent of the photon and photoelectron kinetic energies. The molecular frame differential cross section for the three-body dissociative photodetachment: O-2(-)(H2O)(2) + h nu -->O-2 + 2H(2)O + e(-) is also reported. The observed partitioning of momentum is consistent with either a sequential dissociation or dissociation from a range of initial geometries. (C) 2001 American Institute of Physics.
引用
收藏
页码:3449 / 3455
页数:7
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