Superior capacitive performances of binary nickel-cobalt hydroxide nanonetwork prepared by cathodic deposition

被引:109
作者
Chen, Jia-Cing [1 ]
Hsu, Chun-Tsung [1 ]
Hu, Chi-Chang [1 ]
机构
[1] Natl Tsing Hua Univ, Dept Chem Engn, Lab Electrochem & Adv Mat, Hsinchu 30013, Taiwan
关键词
Nickel-cobalt hydroxide; Cathodic deposition; Porous nanonetwork; Superior capacitive performances; Asymmetric supercapacitor; LAYERED DOUBLE HYDROXIDES; ELECTROCHEMICAL DEPOSITION; ELECTRODE MATERIALS; CYCLIC VOLTAMMETRY; ALKALINE-SOLUTION; OXYGEN EVOLUTION; ACTIVE MATERIAL; OXIDE; BEHAVIOR; CO;
D O I
10.1016/j.jpowsour.2013.12.073
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
Binary nickel-cobalt hydroxides (denoted as NixCo1-x(OH)(2)) with advanced capacitive performances, such as the superior rate capability, energy efficiency, and capacitance rate-/cycle-retention, are synthesized by cathodic deposition. The effects of deposition variables are systematically investigated and discussed. The deposition current density has been found to determine the morphology of hydroxides whereby a small current density facilitates the formation of porous nanonetwork microstructures. Both pH and temperature of the precursor solution affect the Co/Ni ratio of hydroxides, which in turn influence the capacitive performances. Eventually, Ni0.32Co0.68(OH)(2) synthesized under our proposed deposition condition exhibits a specific capacitance value of ca. 1000 F g(-1) at 5 mV s(-1), 100% capacitance cycle-retention over 1000 cycles, and 69% capacitance rate-retention (varying from 5 to 500 mV s(-1)). These superior capacitive performances make Ni0.32Co0.68(OH)(2) a promising material of the positive electrode for an asymmetric supercapacitor with an energy efficiency of 90% at 10 A g(-1). (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:205 / 213
页数:9
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