4.8 Article

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

期刊

CARBON
卷 171, 期 -, 页码 62-71

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.carbon.2020.09.004

关键词

N-rich spherical porous carbon; Zn-TDPAT MOFs; Supercapacitor; High specific capacitance; Ultra-high energy density

资金

  1. National Key Research and Development Program of China [2019YFC1908304]
  2. National Natural Science Foundation of China [21676022, 21706004]
  3. Fundamental Research Funds for the Central Universities [BHYC1701A]

向作者/读者索取更多资源

A new method to fabricate N-rich spherical porous carbon with high specific capacitance and cyclic stability is proposed. The material shows great potential for application in power supercapacitors.
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.

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