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.
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页数:5
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