旋转-振动耦合
振动能量弛豫
离域电子
分子物理学
弯曲
拉曼光谱
分子振动
化学物理
放松(心理学)
联轴节(管道)
分子间力
模耦合
消散
飞秒
原子物理学
正常模式
分子动力学
材料科学
红外线的
热带
化学
分子
计算化学
振动
物理
光学
激光器
热力学
心理学
社会心理学
有机化学
量子力学
冶金
复合材料
作者
Chun‐Chieh Yu,Kuo-Yang Chiang,Masanari Okuno,Takakazu Seki,Tatsuhiko Ohto,Xiaoqing Yu,Vitaly I. Korepanov,Hiro‐o Hamaguchi,Mischa Bonn,Johannes Hunger,Yuki Nagata
标识
DOI:10.1038/s41467-020-19759-w
摘要
Coupling between vibrational modes is essential for energy transfer and dissipation in condensed matter. For water, different O-H stretch modes are known to be very strongly coupled both within and between water molecules, leading to ultrafast dissipation and delocalization of vibrational energy. In contrast, the information on the vibrational coupling of the H-O-H bending mode of water is lacking, even though the bending mode is an essential intermediate for the energy relaxation pathway from the stretch mode to the heat bath. By combining static and femtosecond infrared, Raman, and hyper-Raman spectroscopies for isotopically diluted water with ab initio molecular dynamics simulations, we find the vibrational coupling of the bending mode differs significantly from the stretch mode: the intramode intermolecular coupling of the bending mode is very weak, in stark contrast to the stretch mode. Our results elucidate the vibrational energy transfer pathways of water. Specifically, the librational motion is essential for the vibrational energy relaxation and orientational dynamics of H-O-H bending mode.
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