Structural Forces in Ionic Liquids: The Role of Ionic Size Asymmetry

被引:34
作者
de Souza, J. Pedro [1 ]
Pivnic, Karina [2 ]
Bazant, Martin Z. [1 ,3 ]
Urbakh, Michael [2 ]
Kornyshev, Alexei A. [4 ,5 ]
机构
[1] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[2] Tel Aviv Univ, Sackler Ctr Computat Mol & Mat Sci, Sch Chem, IL-6997801 Tel Aviv, Israel
[3] MIT, Dept Math, Cambridge, MA 02139 USA
[4] Imperial Coll London, Dept Chem, Mol Sci Res Hub, London W12 0BZ, England
[5] Imperial Coll London, Thomas Young Ctr Theory & Simulat Mat, South Kensington Campus, London SW7 2AZ, England
基金
以色列科学基金会; 英国工程与自然科学研究理事会; 美国国家科学基金会;
关键词
ELECTRIC DOUBLE-LAYER; PRIMITIVE MODEL ELECTROLYTES; FUNCTIONAL THEORY MODEL; ELECTROTUNABLE FRICTION; CAPACITANCE; ADSORPTION; MICROSCOPY;
D O I
10.1021/acs.jpcb.1c09441
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
Ionic liquids (ILs) are charged fluids composed of anions and cations of different size and shape. The ordering of charge and density in ILs confined between charged interfaces underlies numerous applications of IL electrolytes. Here, we analyze the screening behavior and the resulting structural forces of a representative IL confined between two charge-varied plates. Using both molecular dynamics simulations and a continuum theory, we contrast the screening features of a more-realistic asymmetric system and a less-realistic symmetric one. The ionic size asymmetry plays a nontrivial role in charge screening, affecting both the ionic density profiles and the disjoining pressure distance dependence. Ionic systems with size asymmetry are stronger coupled systems, and this manifests itself both in their response to the electrode polarization and spontaneous structure formation at the interface. Analytical expressions for decay lengths of the disjoining pressure are obtained in agreement with the pressure profiles computed from molecular dynamics simulations.
引用
收藏
页码:1242 / 1253
页数:12
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