The Electrochemical Behavior of 1-Ethyl-3-Methyl Imidazolium Tetracyanoborate Visualized by In Situ X-ray Photoelectron Spectroscopy at the Negatively and Positively Polarized Micro-Mesoporous Carbon Electrode

被引:16
|
作者
Kruusma, Jaanus [1 ]
Tonisoo, Arvo [2 ]
Parna, Rainer [2 ]
Nommiste, Ergo [2 ]
Kuusik, Ivar [2 ]
Vahtrus, Mikk [2 ]
Tallo, Indrek [1 ]
Romann, Tavo [1 ]
Lust, Enn [1 ]
机构
[1] Univ Tartu, Inst Chem, EE-50411 Tartu, Estonia
[2] Univ Tartu, Inst Phys, EE-51011 Tartu, Estonia
关键词
TEMPERATURE IONIC LIQUIDS; DOUBLE-LAYER CAPACITORS; CHEMICAL-COMPOSITION; STABILITY LIMITS; SUPERCAPACITORS; PERFORMANCE; FUNDAMENTALS; GRAPHITE; SOLVENTS; ENERGY;
D O I
10.1149/2.1861713jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The electrochemical properties of the C(Mo2C) vertical bar EMImB(CN)(4) system have been analyzed using cyclic voltammetry, in situ X-ray photoelectron spectroscopy and electrochemical impedance spectroscopy techniques. The cyclic voltammetry and electrochemical impedance measurements indicated that the tetracyanoborate anions started to electrooxidize and electropolymerize at E = 2.12 V (vs. Ag/AgCl in EMImBF(4)). However, despite of the formation of compact dielectric polymer layer at the micro-mesoporous C(Mo2C) electrode surface very slow electrochemical polymerization of tetracyanoborate anions continued further at E > 2.12 V leading to the blocking of the C(Mo2C) electrode porous structure and to the reduction of the electrochemically active surface area necessary for the construction of the high energy density supercapacitors. Thus, the tetracyanoborate anion based ionic liquids can be used as the electrolytes for the initial formation of the passivating solid-electrolyte interface for the very wide cell potential supercapacitor positive electrodes, as an electrolyte additives for the solid-electrolyte interface formation or for the correction of the solid-electrolyte interface damages. (c) The Author(s) 2017. Published by ECS. All rights reserved.
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页码:A3393 / A3402
页数:10
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