Investigation of electrochemical behavior of Mn-Co doped oxide electrodes for electrochemical capacitors

被引:46
作者
Babakhani, Banafsheh [1 ]
Ivey, Douglas G. [1 ]
机构
[1] Univ Alberta, Dept Chem & Mat Engn, Edmonton, AB T6G 2V4, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Electrochemical capacitors; Co-doped Mn oxide electrode; Electrochemical characterization; Microstructural characterization; MANGANESE OXIDE; THIN-FILMS; OXIDE/PEDOT ELECTRODES; AMORPHOUS MNO2; MIXED OXIDES; DIOXIDE; NANOWIRES; MECHANISM; GROWTH; NANOCRYSTALLITES;
D O I
10.1016/j.electacta.2011.03.008
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 nanocrystalline Co-doped Mn oxide electrodes were investigated to determine the relationship between physicochemical feature evolution and the corresponding electrochemical behavior of synthesized electrodes. Co-doped Mn oxide electrodes with a rod-like morphology and antifluorite-type structure were synthesized by anodic electrodeposition on Au coated Si substrates from a dilute solution of 0.01 M Mn acetate (Mn(CH3COO)(2)) and 0.001 M Co sulphate (CoSO4). Electrochemical characterization of synthesized electrodes, with and without a conducting polymer (PEDOT) coating, was performed with electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV) at different scan rates. In addition, structural characterization of as-deposited and cycled electrodes was conducted using SEM, TEM and XPS. Capacitance values for all deposits increased with increasing scan rate to 100 mV s(-1), and then decreased after 100 mV s(-1). The Mn-Co oxide/PEDOT electrodes showed improved specific capacity and electrochemical cyclability relative to uncoated Mn-Co oxides. Mn-Co oxide/PEDOT electrodes with rodlike structures had high capacitances (up to 310 Fg(-1)) at a scan rate of 100 mV s(-1) and maintained their capacitance after 500 cycles in 0.5 M Na2SO4 (91% retention). Capacitance reduction for the deposits was mainly due to the loss of Mn ions by dissolution in the electrolyte solution. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4753 / 4762
页数:10
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