氢铵
放射分析
化学
电离
离解(化学)
光化学
氧气
化学物理
溶剂化电子
亚稳态
电子转移
飞秒
氢键
分子间力
质子
水的自电离
激进的
离子
物理化学
分子
激光器
有机化学
光学
物理
量子力学
作者
Ming‐Fu Lin,Narendra Singh,Shiheng Liang,Mianzhen Mo,J. Pedro F. Nunes,Kathryn Ledbetter,Jie Yang,M. Kozina,Stephen Weathersby,Xiaozhe Shen,Amy A. Cordones,Thomas Wolf,C. D. Pemmaraju,Matthias Ihme,Xijie Wang
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2021-09-30
卷期号:374 (6563): 92-95
被引量:70
标识
DOI:10.1126/science.abg3091
摘要
The radiolysis of water is ubiquitous in nature and plays a critical role in numerous biochemical and technological applications. Although the elementary reaction pathways for ionized water have been studied, the short-lived intermediate complex and structural dynamic response after the proton transfer reaction remain poorly understood. Using a liquid-phase ultrafast electron diffraction technique to measure the intermolecular oxygen···oxygen and oxygen···hydrogen bonds, we captured the short-lived radical-cation complex OH(H3O+) that was formed within 140 femtoseconds through a direct oxygen···oxygen bond contraction and proton transfer, followed by the radical-cation pair dissociation and the subsequent structural relaxation of water within 250 femtoseconds. These measurements provide direct evidence of capturing this metastable radical-cation complex before separation, thereby improving our fundamental understanding of elementary reaction dynamics in ionized liquid water.
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