Rate capability improvement of Co-Ni double hydroxides integrated in cathodically partially exfoliated graphite

被引:28
作者
Cai, Xiang [1 ]
Song, Yu [1 ]
Sun, Zhen [1 ]
Guo, Di [1 ]
Liu, Xiao-Xia [1 ]
机构
[1] Northeastern Univ, Dept Chem, Shenyang 110819, Liaoning, Peoples R China
基金
中国国家自然科学基金;
关键词
Cathodically-exfoliated graphene; Co-Ni double hydroxide; Hierarchical structure; High rate capability; LAYERED DOUBLE HYDROXIDES; NICKEL-COBALT HYDROXIDE; ASYMMETRIC SUPERCAPACITORS; ELECTROCHEMICAL EXPANSION; CYCLING STABILITY; POWER-DENSITY; HIGH-ENERGY; PERFORMANCE; NANOSHEETS; POLYPYRROLE;
D O I
10.1016/j.jpowsour.2017.08.039
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
In-situ growing of energy storage materials on graphene-based substrates/current collectors with low defect is a good way to boost electron transport and so enhance rate capability for the obtained electrode. Herein, high-quality graphene-like nanopetals are partially exfoliated from graphite foil (GF) through a facile and fast cathodic process. Three-dimensional porous structure is established for the afforded cathodically-exfoliated graphite foil (CEG), with many graphene-like nanopetals vertically anchoring on the graphite substrate. A hierarchical structure is constructed by the following electrochemical growth of Co-Ni double hydroxide nanopetals on the graphene atop CEG. The double hydroxide in the obtained electrode with the optimized Co2+/Ni2+ molar ratio, Co0.75Ni0.25(OH)(2)-CEG, displays much improved rate capability and so can deliver a high specific capacitance of 1460 F g(-1) at an ultra-high current density of 100 A g(-1). An asymmetric device is assembled by using Co0.75Ni0.25(OH)(2)-CEG as cathode, which demonstrates a high energy density of 31.6 Wh kg-1 at an ultra-high power density of 21.5 kW kg(-1), showing the potential of the hierarchical composite electrode for high power application. The device also displays good stability, it can retain more than 90% of its capacitance after 10000 galvanostatic charge-discharge cycles. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:126 / 133
页数:8
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