Electrochemical characterization of MnO2-based composite in the presence of salt-in-water and water-in-salt electrolytes as electrode for electrochemical capacitors

被引:81
作者
Gambou-Bosca, Axel [1 ]
Belanger, Daniel [1 ]
机构
[1] Univ Quebec, Dept Chim, Case Postale 8888,Succursale Ctr Ville, Montreal, PQ H3C 3P8, Canada
关键词
MnO2; Aqueous electrolyte; Water-in-salt electrolyte; LiTFSI; Electrochemical supercapacitor; CHARGE STORAGE MECHANISM; MANGANESE-DIOXIDE; HYDROTHERMAL SYNTHESIS; FACILE SYNTHESIS; MNO2; PERFORMANCE; OXIDE; BEHAVIOR; ION; ALKALINE;
D O I
10.1016/j.jpowsour.2016.04.088
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
The effect of the electrolyte on the electrochemical utilization of manganese dioxide as active material for electrochemical capacitor was studied by cyclic voltammetry and electrochemical impedance spectroscopy. MnO2-based composite electrodes were characterized in salt-in-water (0.65 M K2SO4, 5 M LiNO3, 0.5 M LiNO3 and 0.5 M Ca(NO3)(2)) and water-in-salt (5 M LiTFSI (lithium bis-trifluoromethanesulfonimide)) electrolytes. Firstly, no effect of the cation valence on the specific capacitance was observed as similar values were measured in 0.5 M LiNO3 and 0.5 M Ca(NO3)(2) aqueous solutions at both low and high scan rate, when a MnO2-based composite electrode was cycled in the pseudocapacitive potential region. Secondly, it was found that in 5 M LiTFSI, a MnO2 electrode is characterized by an extended potential stability window of about 1.4 V and exhibits a high specific capacitance of 239 F g(-1) per active material mass at a scan rate of 2 mV s(-1). However due to the low ionic conductivity of this solution, the rate capability is limited at high scan rate. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:595 / 603
页数:9
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