太赫兹辐射
氢键
材料科学
离子
分子间力
皮秒
化学物理
极化(电化学)
电场
克尔效应
激发
分子物理学
光学
化学
物理
物理化学
分子
光电子学
激光器
非线性系统
量子力学
有机化学
作者
Hang Zhao,Yong Tan,Rui Zhang,Yuejin Zhao,Cunlin Zhang,Liangliang Zhang
出处
期刊:Optics Letters
[Optica Publishing Group]
日期:2021-01-05
卷期号:46 (2): 230-230
被引量:15
摘要
The microscopic mechanism for ionic influence on the hydrogen bond network of water has not been fully understood. Here we employ the terahertz Kerr effect (TKE) technique to map the intermolecular hydrogen bond dynamics in a series of aqueous halide solutions at the sub-picosecond scale. Compared with pure water, the significantly enhanced bipolar TKE response associated with polarization anisotropy in an ionic aqueous solution is successfully captured. We decompose the measured TKE response into different molecular motion modes and demonstrate that the obviously increasing positive polarity response is mainly due to the anion–water hydrogen bond vibration mode with the resonant THz electric field excitation. Our measurement results provide an experimental basis for further insight into the effects of ions on the structure and dynamics of a hydrogen bond in water.
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