Surface stratification determines the interfacial water structure of simple electrolyte solutions

被引:33
|
作者
Litman, Yair [1 ,2 ]
Chiang, Kuo-Yang [1 ]
Seki, Takakazu [1 ]
Nagata, Yuki [1 ]
Bonn, Mischa [1 ]
机构
[1] Max Planck Inst Polymer Res, Mainz, Germany
[2] Univ Cambridge, Yusuf Hamied Dept Chem, Cambridge, England
基金
欧洲研究理事会;
关键词
SUM-FREQUENCY GENERATION; AQUEOUS NAOH SOLUTIONS; MOLECULAR-DYNAMICS; VIBRATIONAL SPECTROSCOPY; HALIDE SOLUTIONS; SALT-SOLUTIONS; IONS; HYDRATION; SPECTRA; PROTONS;
D O I
10.1038/s41557-023-01416-6
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The distribution of ions at the air/water interface plays a decisive role in many natural processes. Several studies have reported that larger ions tend to be surface-active, implying ions are located on top of the water surface, thereby inducing electric fields that determine the interfacial water structure. Here we challenge this view by combining surface-specific heterodyne-detected vibrational sum-frequency generation with neural network-assisted ab initio molecular dynamics simulations. Our results show that ions in typical electrolyte solutions are, in fact, located in a subsurface region, leading to a stratification of such interfaces into two distinctive water layers. The outermost surface is ion-depleted, and the subsurface layer is ion-enriched. This surface stratification is a key element in explaining the ion-induced water reorganization at the outermost air/water interface.
引用
收藏
页码:644 / 650
页数:9
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