High area-specific capacitance of Co(OH)2/hierarchical nickel/nickel foam supercapacitors and its increase with cycling

被引:85
|
作者
Yu, Zheyin [1 ]
Cheng, Zhenxiang [1 ]
Wang, Xiaolin [1 ]
Dou, Shi Xue [1 ]
Kong, Xiangyang [2 ]
机构
[1] Univ Wollongong, Inst Superconducting & Elect Mat, Wollongong, NSW 2500, Australia
[2] Shanghai Jiao Tong Univ, Sch Mat Sci & Engn, Shanghai 200240, Peoples R China
基金
澳大利亚研究理事会;
关键词
PERFORMANCE ELECTROCHEMICAL CAPACITORS; ULTRAHIGH CAPACITANCE; ELECTRODE MATERIALS; SOLUBILITY PRODUCT; TEMPLATE SYNTHESIS; NICKEL-HYDROXIDE; ARRAY ELECTRODES; ENERGY DENSITY; CO(OH)(2); FILM;
D O I
10.1039/c7ta00719a
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
Supercapacitors are an important energy storage systems due to their high power compared to batteries, giving them unique applications. The search for low-cost and high-surface-area pseudocapacitive metal oxides/hydroxides with good conductivity as supercapacitor materials is a developing trend. In this work, the nanometer-scale active material Co(OH) 2 was deposited on well-designed hierarchical nickel/nickel foam (current collector) with significantly enhanced conductivity, and the electrodes exhibited excellent electrochemical performance, displaying a high area-specific capacitance of 3.17 F cm(-2) under the current density of 5 mA cm(-2). Importantly, the capacitance increased to 9.62 F cm(-2) after 2000 cycles of galvanostatic charging-discharging, which is 3.03 times as great as the initial value. Such a capacitance increase could be attributed to the formation of porous Ni-Co mixed hydroxide with a micro/nanostructure during cycling, which was confirmed by scanning and transmission electron microscopy investigations. The formation mechanism of Ni-Co mixed hydroxide is also proposed. This result demonstrates that the electrochemical reactions during galvanostatic charging-discharging could represent a novel fabrication method to synthesize mixed hydroxides for energy storage and conversion materials in the future.
引用
收藏
页码:7968 / 7978
页数:11
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