Coincidence spectroscopy of molecular normal Auger decay by ultrashort x-ray pulses

被引:4
作者
Zhu, Yan Ping [1 ]
Zhao, Xi [1 ]
Liu, Xiao-Jing [2 ]
Kimberg, Victor [3 ]
Zhang, Song Bin [1 ]
机构
[1] Shaanxi Normal Univ, Sch Phys & Informat Technol, Xian 710119, Peoples R China
[2] ShanghaiTech Univ, Sch Phys Sci & Technol, Shanghai 201210, Peoples R China
[3] Royal Inst Technol, Theoret Chem & Biol, S-10691 Stockholm, Sweden
基金
瑞典研究理事会;
关键词
ROTATING-WAVE APPROXIMATION; SUDDEN APPROXIMATION; EXCITATION; RESONANCE; DYNAMICS; SPECTRUM; STATES;
D O I
10.1103/PhysRevA.106.023105
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
When a core-shell electron is ionized by coherent ultrashort x-ray pulses with varied duration, different nuclear wave packets of a cationic molecule are formed, which can be effectively studied by detecting the photoelectron -Auger electron-ion fragment as it is proposed in the present paper. We develop the theory for the photoelectron, i.e., Auger electron, ion fragment three-body coincidence spectroscopy, where dissociative Auger final states are considered. Simulations to display the HF molecule show that the coincidence spectra encode the detailed information of coherent nuclear wave-packet dynamics. Our work paves the way for using currently available coherent ultrashort x-ray pulses to investigate and manipulate molecular nuclear wave packets. Moreover, we discuss possibilities for high-resolution coincidence experimental techniques.
引用
收藏
页数:8
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