Asymmetric supercapacitors based on β-Ni(OH)2 nanosheets and activated carbon with high energy density

被引:265
|
作者
Huang, Jichun [1 ]
Xu, Panpan [1 ]
Cao, Dianxue [1 ]
Zhou, Xiaobin [1 ]
Yang, Sainan [1 ]
Li, Yiju [1 ]
Wang, Guiling [1 ]
机构
[1] Harbin Engn Univ, Coll Mat Sci & Chem Engn, Minist Educ, Key Lab Superlight Mat & Surface Technol, Harbin 150001, Peoples R China
关键词
Nickel hydroxide; Activated carbon; Aqueous electrolyte; Asymmetric supercapacitors; MANGANESE-DIOXIDE; NICKEL-HYDROXIDE; HIGH-POWER; ELECTROCHEMICAL CHARACTERISTICS; AQUEOUS-ELECTROLYTES; NANOWIRE ARRAY; V; ELECTRODES; PERFORMANCE; CAPACITOR;
D O I
10.1016/j.jpowsour.2013.07.105
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
Ni(OH)(2) nanosheets are directly grown on nickel foam by a simple template-free growth process. Their microstructure and surface morphology are studied by X-ray diffraction spectroscopy and scanning electron microscopy. The XRD and SEM results show that Ni(OH)(2) has a beta-phase structure and covers the nickel foam skeleton with nanosheets. This beta-Ni(OH)(2)/Ni-foam electrode exhibits a high specific electric quantity of 790.3 C g(-1), approaching the theoretical value (1040.6 C g(-1)) and high electrochemical activity. Asymmetric supercapacitor has been fabricated successfully using beta-Ni(OH)(2)/Ni-foam nanosheets as positive electrode and activated carbon as negative electrode in a KOH aqueous electrolyte. The electrochemical capacitances of this supercapacitor are investigated by cyclic voltammetry, galvanostatic charge/discharge and electrochemical impedance spectroscopy. An asymmetric supercapacitor AC/6 mol L-1 KOH/beta-Ni(OH)(2)/Ni-foam could be cycled reversibly in the high-voltage region of 0-1.6 V and displays intriguing performances with a specific capacitance of 105.8 F g(-1) and high energy density of 36.2 W h kg(-1). Importantly, this asymmetric supercapacitor device exhibits an excellent long cycle life along with 92% specific capacitance retained after 1000 cycles. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:371 / 376
页数:6
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