A novel in-situ preparation of N-rich spherical porous carbon as greatly enhanced material for high-performance supercapacitors

被引:82
作者
Gang, Xu [1 ]
Krishnamoorthy, Mohanapriya [1 ]
Jiang, Wenchao [1 ]
Pan, Junqing [1 ]
Pan, Zhigang [1 ,2 ]
Liu, Xiaoguang [1 ]
机构
[1] Beijing Univ Chem Technol, Coll Chem, Beijing Adv Innovat Ctr Soft Matter Sci & Engn, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
[2] Anhui Chilwee Power Ltd, Qingyang 242807, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
N-rich spherical porous carbon; Zn-TDPAT MOFs; Supercapacitor; High specific capacitance; Ultra-high energy density; METAL-ORGANIC FRAMEWORK; ELECTRODE MATERIALS; NITROGEN; GRAPHENE; COMPOSITES; ABSORPTION; NANOSHEETS; CATALYSTS;
D O I
10.1016/j.carbon.2020.09.004
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
Herein, a new approach to form the N-rich spherical porous carbon from direct carbonization of metal-organic framework based Zn-2,4,6-tris(3,5-dicarboxylphenylamino)-1,3,5-triazine structure without using any external doping and templates is proposed. During the carbonization process, Zn atoms, carboxyl and other functional groups are removed at high temperature, resulting in formation of mixed micro and mesopores with an increased surface area of 1826 m(2) g(-1) and nitrogen content of 11.37%. Benefiting from the high content of graphitic N and spherical structure, N-rich spherical porous carbon exhibits high specific capacitance of 386.3 F g(-1) at 1 A g(-1) along with superb cyclic stability of 97.8% capacitance retention after 100,000 cycles at 150 A g(-1). Besides, the N-rich spherical porous carbon-based symmetric supercapacitor offered specific capacitance values of 186.9 and 98.6 F g(-1) at 1 and 150 A g(-1), respectively. This device delivers an appreciable energy density (50.9 Wh kg(-1)) at the corresponding power density (1.6 kW kg(-1)), indicating that it will be a new approach for the preparation of spherical porous carbon derived from MOFs for the power supercapacitors. (C) 2020 Elsevier Ltd. All rights reserved.
引用
收藏
页码:62 / 71
页数:10
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