Structure from Dynamics: Vibrational Dynamics of Interfacial Water as a Probe of Aqueous Heterogeneity

被引:49
|
作者
Cyran, Jenee D. [1 ]
Backus, Ellen H. G. [1 ]
Nagata, Yuki [1 ]
Bonn, Mischa [1 ]
机构
[1] Max Planck Inst Polymer Res, Ackermannweg 10, D-55128 Mainz, Germany
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2018年 / 122卷 / 14期
基金
欧洲研究理事会;
关键词
SUM-FREQUENCY GENERATION; HYDROGEN-BOND DYNAMICS; AIR/WATER INTERFACE; LIQUID WATER; SPECTRAL DIFFUSION; MOLECULAR-REORIENTATION; VAPOR/WATER INTERFACE; ULTRAFAST DYNAMICS; ISOTOPIC DILUTION; ENERGY TRANSFER;
D O I
10.1021/acs.jpcb.7b10574
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The structural heterogeneity of water at various interfaces can be revealed by time-resolved sum-frequency generation spectroscopy. The vibrational dynamics of the O-H stretch vibration of interfacial water can reflect structural variations. Specifically, the vibrational lifetime is typically found to increase with increasing frequency of the O-H stretch vibration, which can report on the hydrogen-bonding heterogeneity of water. We compare and contrast vibrational dynamics of water in contact with various surfaces, including vapor, biomolecules, and solid interfaces. The results reveal that variations in the vibrational lifetime with vibrational frequency are very typical, and can frequently be accounted for by the bulk-like heterogeneous response of interfacial water. Specific interfaces exist, however, for which the behavior is less straightforward. These insights into the heterogeneity of interfacial water thus obtained contribute to a better understanding of complex phenomena taking place at aqueous interfaces, such as photocatalytic reactions and protein folding.
引用
收藏
页码:3667 / 3679
页数:13
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