Improving the performance of cobalt-nickel hydroxidebased self-supporting electrodes for supercapacitors using accumulative approaches

被引:227
作者
Cheng, Yingwen [1 ,2 ]
Zhang, Hongbo [1 ]
Varanasi, Chakrapani V. [1 ,3 ]
Liu, Jie [1 ,2 ]
机构
[1] Duke Univ, Dept Chem, Durham, NC 27708 USA
[2] Duke Univ, CEINT, Durham, NC 27708 USA
[3] Army Res Off, Durham, NC 27703 USA
基金
美国国家科学基金会;
关键词
LAYERED DOUBLE HYDROXIDES; ASYMMETRIC SUPERCAPACITORS; ELECTROCHEMICAL-BEHAVIOR; ACTIVATED CARBON; GRAPHENE; COMPOSITE; CAPACITANCE; DEPOSITION; NI(OH)(2); ENERGY;
D O I
10.1039/c3ee41143e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this paper we describe an accumulative approach to move beyond simple incorporation of conductive carbon nanostructures, such as graphene and carbon nanotubes, to improve the performance of metal oxide/hydroxide based electrodes in energy storage applications. In this approach we first synthesize Co-Ni double hydroxides/graphene binary composites through a co-precipitation process. We then assemble these composites into films (similar to 6 mg cm(-2)) by integrating with carbon nanotubes that can be used directly as electrodes. Experimental results indicate that the synergistic contributions from nanotubes, graphene and cobalt substitution enabled electrodes with substantially improved energy storage performance metrics. With 50% Co and 50% Ni (i.e. Co0.5Ni0.5(OH)(2)), the composite exhibited a remarkable maximum specific capacitance of 2360 F g(-1) (360 mA h g(-1)) at 0.5 A g(-1) and still maintained a specific capacitance as high as 2030 F g(-1) at 20 A g(-1) (similar to 86% retention). More importantly, the double hydroxides exhibited tunable redox behavior that can be controlled by the ratio between cobalt and nickel. These results demonstrate the importance of the rational design of functional composites and the large-scale assembly strategies for fabricating electrodes with improved performance and tunability for energy storage applications.
引用
收藏
页码:3314 / 3321
页数:8
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