KNO3-mediated synthesis of high-surface-area polyacrylonitrile-based carbon material for exceptional supercapacitors

被引:41
|
作者
Li, Yao [1 ]
Liang, Yeru [1 ]
Hu, Hang [1 ]
Dong, Hanwu [1 ]
Zheng, Mingtao [1 ]
Xiao, Yong [1 ]
Liu, Yingliang [1 ]
机构
[1] South China Agr Univ, Coll Mat & Energy, Guangzhou 510642, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Polyacrylonitrile; KNO3-mediated synthesis; Porous carbon; Supercapacitor; HIERARCHICAL POROUS CARBON; STABILIZATION; FIBERS; GRAPHITIZATION; FABRICATION; ACTIVATION; NANOFIBERS; ELECTRODES; TEMPLATE; BIOMASS;
D O I
10.1016/j.carbon.2019.06.001
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
Exploration of effective ways to highly porous carbon is a critical but remains challenging issue for high-performance supercapacitors. Here, we propose a new and facile strategy to synthesize polyacrylonitrile-based porous carbon (PPC) material. The as-prepared PPC not only possesses a well-defined hierarchical pore structure, but also exhibits the highest BET surface area of 3751 m(2) g(-1) and the largest pore volume of 2.48 cm(3) g(-1) among all the materials derived from polyacrylonitrile. The key to this preparation strategy is utilization of KNO3 as a mediator for pre-oxidation of polyacrylonitrile, which leads to construction of a fluffy and rigid semi-carbonized framework for the easy accessibility of activator KOH. Benefiting from the well-developed porosity, the PPC electrode exhibits an unusually high capacitance of 448 F g(-1) at 0.5 A g(-1) and an outstanding long-term stability of 96.5% capacitance retention after 10000 cycles in 1.0 V aqueous supercapacitors. Additionally, a remarkable energy density of 23.6 Wh kg(-1) can be delivered at a high out-put power density of 220 W kg(-1) in 1.8 V aqueous supercapacitors. These attractive electrochemical properties enable PPC to go far beyond many reported carbonaceous electrodes, which is expected to be as competitive candidate for high-performance supercapacitor electrode. (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:120 / 127
页数:8
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