4.6 Article

KOH activation of biomass-derived nitrogen-doped carbons for supercapacitor and electrocatalytic oxygen reduction

期刊

ELECTROCHIMICA ACTA
卷 261, 期 -, 页码 49-57

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2017.12.107

关键词

Biomass; Nitrogen doping; Hierarchical structure; Supercapacitor; Oxygen reduction reaction

资金

  1. National Key Research and Development Program of China [2016YFB0700204]
  2. NSFC [51602332, 51502327]
  3. Science and Technology Commission of Shanghai Municipality [15520720400, 15YF1413800, 14DZ2261203, 16DZ2260603]
  4. One Hundred Talent Plan of Chinese Academy of Sciences

向作者/读者索取更多资源

Nitrogen-doped porous carbon has aroused extensive interests owing to its unique physical and chemical properties. However, the complicated nitrogen-doping method and high cost limit its practical application. In this work, the nitrogen-rich biomass soybean was used as a single precursor for both carbon and nitrogen source to prepare nitrogen-doped hierarchical micro-mesoporous carbon via templating carbonization coupling with subsequent KOH activation. The influence of KOH dosage on the morphology, structure and electrochemical performance (supercapacitor and oxygen reduction reaction (ORR)) was studied in detail. The optimized ANPC-3, synthesized under the KOH/carbon mass ratio of 3/1, possesses high specific surface area of 1749 m(2) g(-1), developed hierarchical micro-mesoporous structures as well as moderate nitrogen content (1.37 at.%). ANPC-3 exhibits a large energy density of 12.5 Wh kg(-1) at a power density of 450 W kg(-1) with excellent charge-discharge cyclic stability of 96.5% capacitance remaining after 5000 cycles. As an ORR electrocatalyst, it shows improved ORR activity as well as much better stability and methanol-tolerance capacity than commercial Pt/C catalyst. The unique hierarchical micro-mesoporous textures, high surface area and moderate N-doping level make biomass-derived ANPC-3 become an excellent electrode material in various applications. (c) 2017 Elsevier Ltd. All rights reserved.

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