中国物理B ›› 2022, Vol. 31 ›› Issue (2): 28202-028202.doi: 10.1088/1674-1056/ac2b15
Long-Xing Zhou(周龙兴)1,2, Yang Liu(刘洋)1,2, Shen He(贺屾)1,2, Da-Shuai Gao(高大帅)1,2, Xing-Chen Shen(沈星晨)1,2, Qi Chen(陈淇)1,2, Tao Yu(于涛)1,2, Hang Lv(吕航)1,2,†, and Hai-Feng Xu(徐海峰)1,2,‡
Long-Xing Zhou(周龙兴)1,2, Yang Liu(刘洋)1,2, Shen He(贺屾)1,2, Da-Shuai Gao(高大帅)1,2, Xing-Chen Shen(沈星晨)1,2, Qi Chen(陈淇)1,2, Tao Yu(于涛)1,2, Hang Lv(吕航)1,2,†, and Hai-Feng Xu(徐海峰)1,2,‡
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'-X2A" 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.
中图分类号: (Pump probe studies of photodissociation)