飞秒
激发态
电子
放松(心理学)
溶剂化电子
原子物理学
化学
激发
内部转换
女性化学
分子物理学
电子转移
化学物理
激光器
光化学
物理
激进的
光学
放射分析
心理学
社会心理学
有机化学
量子力学
作者
Madeline H. Elkins,Holly Williams,Alexander T. Shreve,Daniel M. Neumark
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2013-12-19
卷期号:342 (6165): 1496-1499
被引量:123
标识
DOI:10.1126/science.1246291
摘要
The relaxation dynamics of the photoexcited hydrated electron have been subject to conflicting interpretations. Here, we report time-resolved photoelectron spectra of hydrated electrons in a liquid microjet with the aim of clarifying ambiguities from previous experiments. A sequence of three ultrashort laser pulses (~100 femtosecond duration) successively created hydrated electrons by charge-transfer-to-solvent excitation of dissolved anions, electronically excited these electrons via the s→p transition, and then ejected them into vacuum. Two distinct transient signals were observed. One was assigned to the initially excited p-state with a lifetime of ~75 femtoseconds, and the other, with a lifetime of ~400 femtoseconds, was attributed to s-state electrons just after internal conversion in a nonequilibrated solvent environment. These assignments support the nonadiabatic relaxation model.
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