Nitrogen-doped hierarchical porous carbon derived from block copolymer for supercapacitor

被引:69
|
作者
Tong, Yun-Xiao [1 ,2 ]
Li, Xiao-Ming [1 ]
Xie, Li-Jing [1 ]
Su, Fang-Yuan [1 ]
Li, Jing-Ping [2 ]
Sun, Guo-Hua [1 ]
Gao, Yi-Dan [1 ]
Zhang, Nian [2 ]
Wei, Qiang [2 ]
Chen, Cheng-Meng [1 ]
机构
[1] Chinese Acad Sci, Inst Coal Chem, Key Lab Carbon Mat, Taiyuan 030001, Peoples R China
[2] Lanzhou Jiaotong Univ, Sch Chem & Biol Engn, Lanzhou 730070, Peoples R China
基金
中国国家自然科学基金;
关键词
Block copolymer; Nitrogen-doped hierarchical carbon; Self-template; Chemical activation; Supercapacitor;
D O I
10.1016/j.ensm.2016.02.005
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
Nitrogen-doped hierarchical porous carbon was successfully synthesized using block copolymers as precursor by a self-template method and subsequent KOH chemical activation. The self-template agent, polystyrene, promotes the formation of mesopores, which is favorable for the rapid transport of both electrons and electrolyte ions. The micropores of nitrogen-doped hierarchical carbons were then extensively developed by activation to provide large electrochemical double-layer capacitance. As the activation temperature increased from 600 degrees C to 900 degrees C, the specific surface area of the materials increased dramatically. Thus, the as-obtained nitrogen-doped hierarchical carbon (NHPC-800) possesses a high surface area of up to 2104.5 m(2)/g with nitrogen content of 5.79%. It exhibits a maximum specific capacitance of 257 F/g at a current density of 0.5 A/g in 6 M KOH aqueous electrolyte as measured in a three-electrode system. Furthermore, the nitrogen-doped hierarchical carbon electrode exhibits excellent rate capability with 128 F/g remaining at 20 A/g and good cycling stability of 90.38% retention over 10,000 cycles in a two-electrode system. The tunable porous structure and effective nitrogen doping via block polymer precursor shed a light for designing advanced electrode materials for a high-performance electrochemical energy system. (C) 2016 Elsevier B.V. All rights reserved
引用
收藏
页码:140 / 148
页数:9
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