Imaging state-to-state reactive scattering in the Ar+ + H2 charge transfer reaction

被引:14
|
作者
Michaelsen, Tim [1 ]
Bastian, Bjoern [1 ]
Carrascosa, Eduardo [1 ,2 ]
Meyer, Jennifer [1 ]
Parker, David H. [3 ]
Wester, Roland [1 ]
机构
[1] Univ Innsbruck, Inst Ionenphys & Angew Phys, Technikerstr 25-3, A-6020 Innsbruck, Austria
[2] Univ Melbourne, Melbourne, Vic 3010, Australia
[3] Radboud Univ Nijmegen, Inst Mol & Mat, Dept Mol & Laser Phys, Heyendaalseweg 135, NL-6525 AJ Nijmegen, Netherlands
来源
JOURNAL OF CHEMICAL PHYSICS | 2017年 / 147卷 / 01期
基金
奥地利科学基金会;
关键词
ION-MOLECULE REACTIONS; TRANSLATIONAL ENERGY-DEPENDENCE; CHARGE-TRANSFER; CROSS-SECTIONS; CYCLOTRON-RESONANCE; ARGON IONS; INTRAMOLECULAR ISOTOPE; GASEOUS MOLECULES; RATE COEFFICIENTS; H-2;
D O I
10.1063/1.4983305
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 charge transfer reaction of Ar+ with H-2 and D-2 has been investigated in an experiment combining crossed beams with three-dimensional velocity map imaging. Angle-differential cross sections for two collision energies have been obtained for both neutral species. We find that the product ions are highly internally excited. In the reaction with H-2, the spin-orbit excited Ar+ state's coupling to the "resonant" vibrationally excited product H-2(+) (v = 2) dominates for both investigated energies, in line with previous investigations. The observed angular distributions, however, show significantly less back-scattering than was found previously. Furthermore, we discovered that the product ions are highly rotationally excited. In the case of Ar+ reacting with D-2, the energetically closest lying vibrational levels are not strictly preferred and higher-lying vibrational levels are also populated. For both species, the backward-scattered products show higher internal excitation. Published by AIP Publishing.
引用
收藏
页数:8
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