Ultrafast dynamics and dissociative ionization of CS2 molecules studied via the femtosecond pump-probe method

被引:2
作者
Zhang DongDong [1 ]
Fan Zhen [1 ]
Sun ErPing [1 ]
Zhang JunFeng [1 ]
Liu Hang [1 ]
Xu HaiFeng [1 ]
Jin MingXing [1 ]
Ding DaJun [1 ]
机构
[1] Jilin Univ, Inst Atom & Mol Phys, Changchun 130012, Peoples R China
来源
CHINESE SCIENCE BULLETIN | 2011年 / 56卷 / 09期
基金
中国国家自然科学基金;
关键词
ultrafast dynamics; femtosecond; pump-probe; carbon disulfide; 2-PHOTON DISSOCIATION; ELECTRONIC STATES; CARBON-DISULFIDE; LASER-PULSES; SPECTROSCOPY; FIELD; IONIZATION/DISSOCIATION; PREDISSOCIATION; ABSORPTION; SPECTRA;
D O I
10.1007/s11434-010-4325-7
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The ultrafast dynamics and dissociative ionization of CS2 were studied using the pump-probe method with time-of-flight mass spectroscopy. The transient behavior of both parent ion (CS2 (+)) and fragment ions (S+ and CS+) was observed. It was found that all the ionic signals decay exponentially with lifetimes that were different for delay times, t > 0 and t < 0, which can be attributed to the evolution of different Rydberg states pumped by 267-nm and 400-nm laser pulses. The lifetimes of two Rydberg states were obtained simultaneously from one fitting of the transients. The fragment ions were produced by the dissociation of CS2 (+), and it is suggested that the final ionic state is the (CI)-I-2 (g) pound (+) state of CS2 (+) based on the measured S+/CS+ branching ratio. The S+/CS+ ratio is dependent on the delay time of the two lasers, indicating that the dissociation process of CS2 (+) is related to the evolution of the intermediate Rydberg state.
引用
收藏
页码:855 / 861
页数:7
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