Ions Speciation at the Water-Air Interface

被引:17
|
作者
Seki, Takakazu [1 ]
Yu, Chun-Chieh [1 ]
Chiang, Kuo-Yang [1 ]
Greco, Alessandro [1 ]
Yu, Xiaoqing [1 ]
Matsumura, Fumiki [1 ]
Bonn, Mischa [1 ]
Nagata, Yuki [1 ]
机构
[1] Max Planck Inst Polymer Res, D-55128 Mainz, Germany
基金
欧盟地平线“2020”;
关键词
MOLECULAR-DYNAMICS; SUM-FREQUENCY; WATER/VAPOR INTERFACE; SALT-SOLUTIONS; SURFACE; SOLVATION; SPECTROSCOPY; CHEMISTRY; ANIONS;
D O I
10.1021/jacs.3c00517
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In typical aqueous systems, including naturally occurring sweet and salt water and tap water, multiple ion species are co-solvated. At the water-air interface, these ions are known to affect the chemical reactivity, aerosol formation, climate, and water odor. Yet, the composition of ions at the water interface has detected sum-frequency generation spectroscopy, we quantify the relative surface activity of two co-solvated ions in solution. We find that more hydrophobic ions are speciated to the interface due to the hydrophilic ions. Quantitative analysis shows that the interfacial hydrophobic ion population increases with decreasing interfacial hydrophilic ion population at the interface. Simulations show that the solvation energy difference between the ions and the intrinsic surface propensity of ions determine the extent of an ion's speciation by other ions. This mechanism provides a unified view of the speciation of monatomic and polyatomic ions at electrolyte solution interfaces.
引用
收藏
页码:10622 / 10630
页数:9
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