Ultrafast dynamics of cationic electronic states of vinyl bromide by strong-field ionization-photofragmentation

被引:1
|
作者
Zhou, Long-Xing [1 ,2 ]
Liu, Yang [1 ,2 ]
He, Shen [1 ,2 ]
Gao, Da-Shuai [1 ,2 ]
Shen, Xing-Chen [1 ,2 ]
Chen, Qi [1 ,2 ]
Yu, Tao [1 ,2 ]
Lv, Hang [1 ,2 ]
Xu, Hai-Feng [1 ,2 ]
机构
[1] Jilin Univ, Inst Atom & Mol Phys, Changchun 130012, Peoples R China
[2] Jilin Univ, Jilin Prov Key Lab Appl Atom & Mol Spect, Changchun 130012, Peoples R China
基金
中国国家自然科学基金;
关键词
strong field ionization; ultrafast dynamics; vinyl bromide cation; TIME-RESOLVED PHOTOELECTRON; SMALL MOLECULES; EXCITED-STATE; SPECTROSCOPY; COHERENCE;
D O I
10.1088/1674-1056/ac2b15
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
Strong field ionization-photofragmentation (SFI-PF) with ultrafast pump-probe scheme is a powerful approach to study the dynamics of molecular cationic electronic states. Here we carry out a SFI-PF study on the cationic electronic states of vinyl bromide, C2H3Br. The yields of the parent C2H3Br+ and the formation of the fragment (Br+, C2H2+ and C2H3+) ions have been measured at different pump-probe delay time. Analysis provides experimental evidence of A2A'-X(2)A '' internal conversion of vinyl bromide cations which occurs in a time of about 220 fs, and the time of C2H3+ formation induced by the dissociation of the A2A' state around 300 fs. The study would add our knowledge of the behavior of electronic excited states of complex molecular cations.
引用
收藏
页数:5
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