The dielectric function profile across the water interface through surface-specific vibrational spectroscopy and simulations

被引:35
作者
Chiang, Kuo-Yang [1 ]
Seki, Takakazu [1 ]
Yu, Chun-Chieh [1 ]
Ohto, Tatsuhiko [2 ]
Hunger, Johannes [1 ]
Bonn, Mischa [1 ]
Nagata, Yuki [1 ]
机构
[1] Max Planck Inst Polymer Res, Mol Spect Dept, D-55128 Mainz, Germany
[2] Osaka Univ, Grad Sch Engn Sci, Div Frontier Mat Sci, Toyonaka, Osaka 608531, Japan
基金
欧洲研究理事会; 日本科学技术振兴机构; 日本学术振兴会;
关键词
interfacial water; dielectric function; vibrational spectroscopy; molecular dynamics simulation; MOLECULAR-ORIENTATION;
D O I
10.1073/pnas.2204156119
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The dielectric properties of interfacial water on subnanometer length scales govern chemical reactions, carrier transfer, and ion transport at interfaces. Yet, the nature of the interfacial dielectric function has remained under debate as it is challenging to access the interfacial dielectric with subnanometer resolution. Here we use the vibrational response of interfacial water molecules probed using surface-specific sum-frequency generation (SFG) spectra to obtain exquisite depth resolution. Different responses originate from water molecules at different depths and report back on the local interfacial dielectric environment via their spectral amplitudes. From experimental and simulated SFG spectra at the air/water interface, we find that the interfacial dielectric constant changes drastically across an similar to 1 angstrom thin interfacial water region. The strong gradient of the interfacial dielectric constant leads, at charged planar interfaces, to the formation of an electric triple layer that goes beyond the standard double-layer model.
引用
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页数:7
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