期刊
JOURNAL OF CHEMICAL PHYSICS
卷 135, 期 3, 页码 -出版社
AMER INST PHYSICS
DOI: 10.1063/1.3610415
关键词
-
资金
- Engineering and Physical Sciences Research Council (EPSRC) [EP/G00224X/1]
- ICONIC Marie Curie Initial Training Network
- European Research Council (ERC)
- Engineering and Physical Sciences Research Council [EP/G00224X/1] Funding Source: researchfish
- EPSRC [EP/G00224X/1] Funding Source: UKRI
Kr+ and Xe+ formation following photodissociation of NO-RG ( RG = Kr or Xe) molecules via the (A) over tilde-(X) over tilde electronic transition in the 44 150-44 350 cm(-1) region has been investigated using velocity map imaging. Nuclear kinetic energy release (nKER) spectra indicate that the NO cofragment is produced in multiple vibrational states of the electronic ground state, with a high degree of rotational excitation. Photofragment angular distributions and nKERs are consistent with photo-induced charge transfer at the two-photon level followed by dissociative ionization at the three-photon level. RG(+) angular distributions showing highly parallel character relative to the laser polarization axis are indicative of a high degree of molecular alignment in the dissociating species. (C) 2011 American Institute of Physics. [doi:10.1063/1.3610415]
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据