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Ultrafast Dynamics of Water Molecules Excited to Electronic ■ States:A Time-Resolved Photoelectron Spectroscopy Study

水分子■态超快动力学:时间分辨光电子能谱研究(英文)
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摘要 The ultrafast dynamics of water molecules excited to the two F states is studied by combining two-photon excitation and time-resolved photoelectron imaging techniques. The lifetimes of the F1A1 and F1B1 states of H2O (D2O) were derived to be 1.0±0.3 (1.9±0.4) and 10±3 (30±10) ps, respectively. We propose that the F1A1 state mainly decays through the D state, due to the nonadiabatic coupling between them, while the F1B1 state decays through the F1A1 state via Coriolis interaction.
作者 Dong-yuan Yang Yan-jun Min Zhen Chen Zhi-gang He Zhi-chao Chen Kai-jun Yuan Dong-xu Dai Guo-rong Wu Xue-ming Yang 杨栋元;闵彦钧;陈震;贺志刚;陈志超;袁开军;戴东旭;吴国荣;杨学明(中国科学院大连化学物理研究所,分子反应动力学国家重点实验室,大连116023;中国科学院大学,北京100049)
出处 《Chinese Journal of Chemical Physics》 SCIE CAS CSCD 2019年第1期53-58,I0001,共7页 化学物理学报(英文)
基金 supported by the National Natural Science Foundation of China (No.21573228, No.21833003, No.21673232, and No.21773236) the Strategic Priority Research Program of the Chinese Academy of Sciences (No.XDB17000000)
关键词 Photoelectron spectrum Pump/probe Femtosecond time-resolved sprctra 光电子能谱 泵浦/探测 飞秒时间分辨
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