An electrochemical perspective on the interfacial width between two immiscible liquid phases

被引:12
作者
Voci, Silvia [1 ]
Dick, Jeffrey E. [2 ]
机构
[1] Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA
[2] Purdue Univ, Elmore Family Sch Elect & Comp Engn, W Lafayette, IN 47907 USA
基金
美国国家卫生研究院;
关键词
ION TRANSFER; MOLECULAR-DYNAMICS; LIQUID/LIQUID INTERFACES; WATER/1,2-DICHLOROETHANE INTERFACE; ELECTROLYTE-SOLUTIONS; WATER INTERFACE; GIBBS ENERGIES; MASS-TRANSFER; NITROBENZENE; SOLVATION;
D O I
10.1016/j.coelec.2023.101244
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
Molecular dynamics simulations and vibrational sumfrequency spectroscopy are historically the main techniques applied to the description of the molecular structure and dynamics of the immiscible liquidlliquid interface. A molecular sharpness is estimated for oillwater interfaces, with an interfacial width that extends from hundreds of angstrom to 1 nm. However, electrochemical studies have elucidated a deeper liquidlliquid interface on the order of several micrometers. The breaking down of single-entity electrochemistry into simpler systems and the combination of high-resolution microscopies is confirming a larger extension of the interface. What can be the role of the electrochemist in clarifying this fundamental question? We try to give a suggestion at the end of a brief historical overview of the liquidlliquid interface studies.
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页数:8
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