Ionic Liquids at Electrified Interfaces

被引:1050
|
作者
Fedorov, Maxim V. [1 ]
Kornyshev, Alexei A. [2 ]
机构
[1] Univ Strathclyde, Dept Phys, SUPA, Glasgow G4 0NG, Lanark, Scotland
[2] Univ London Imperial Coll Sci Technol & Med, Dept Chem, Fac Nat Sci, London SW7 2AZ, England
基金
英国工程与自然科学研究理事会;
关键词
DENSITY-FUNCTIONAL THEORY; SUM-FREQUENCY GENERATION; DOUBLE-LAYER CAPACITANCE; POLYMER-METAL COMPOSITES; ELECTRON-TRANSFER REACTIONS; IN-SITU STM; NONLOCAL DIELECTRIC RESPONSE; ELECTROCHEMICAL DOUBLE-LAYER; INTEGRAL-EQUATION THEORY; PORE-SIZE DISTRIBUTION;
D O I
10.1021/cr400374x
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The review discusses the properties of RTILs at different EIs, specifically the RTILs' response to charging of the interface and how it manifests itself in a range of selected applications. Response of an electrolyte to a charged electrode surface is described within the theory of electrical double layer (EDL). It overviews the current status of the theory of EDL in RTILs, showing that the structure of EDL there is different from that of a diluted electrolyte despite having certain common features with that of high-temperature molten salts (HTMS). It is well-known that the EDL plays a crucial role in electrodes and the potential drop across the EDL and its response to charging determines the electrical capacitance of the electrode/electrolyte interface and the energy stored in the EDL capacitors. The potential distribution in the EDL controls electrochemical kinetics, as the voltage difference between the electrode and the point where the reactant sits is the driving force of electrochemical reactions.
引用
收藏
页码:2978 / 3036
页数:59
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