Hierarchical Carbon Nanowire/Ni@MnO2 Nanocomposites for High-Performance Asymmetric Supercapacitors

被引:20
作者
Kang, Chenxia [1 ]
Fang, Ju [1 ]
Fu, Likang [1 ]
Li, Shuxian [1 ]
Liu, Qiming [1 ]
机构
[1] Wuhan Univ, Sch Phys & Technol, Minist Educ, Key Lab Artificial Micro & Nanostruct, Wuhan 430072, Peoples R China
关键词
carbon nanowires; electrochemistry; electrodeposition; hierarchical nanostructures; supercapacitors; POROUS CARBON; GRAPHENE OXIDE; MANGANESE OXIDE; RATE CAPABILITY; MNO2; FABRICATION; ELECTRODES; NANOSHEETS; NITROGEN; COMPOSITES;
D O I
10.1002/chem.202002724
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A 3D hierarchical carbon cloth/nitrogen-doped carbon nanowires/Ni@MnO2 (CC/N-CNWs/Ni@MnO2) nanocomposite electrode was rationally designed and prepared by electrodeposition. The N-CNWs derived from polypyrrole (PPy) nanowires on the carbon cloth have an open framework structure, which greatly increases the contact area between the electrode and electrolyte and provides short diffusion paths. The incorporation of the Ni layer between the N-CNWs and MnO2 is beneficial for significantly enhancing the electrical conductivity and boosting fast charge transfer as well as improving the charge-collection capacity. Thus, the as-prepared 3D hierarchical CC/N-CNWs/Ni@MnO2 electrode exhibits a higher specific capacitance of 571.4 F g(-1) compared with those of CC/N-CNWs@MnO2 (311 F g(-1)), CC/Ni@MnO2 (196.6 F g(-1)), and CC@MnO2 (186.1 F g(-1)) at 1 A g(-1) and remarkable rate capability (367.5 F g(-1) at 10 A g(-1)). Moreover, asymmetric supercapacitors constructed with CC/N-CNWs/Ni@MnO2 as cathode material and activated carbon as anode material deliver an impressive energy density of 36.4 W h kg(-1) at a power density of 900 W kg(-1) and a good cycling life (72.8 % capacitance retention after 3500 cycles). This study paves a low-cost and simple way to design a hierarchical nanocomposite electrode with large surface area and superior electrical conductivity, which has wide application prospects in high-performance supercapacitors.
引用
收藏
页码:16392 / 16401
页数:10
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