Facile Synthesis of N-Doped Graphene-Like Carbon Nanoflakes as Efficient and Stable Electrocatalysts for the Oxygen Reduction Reaction

被引:0
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作者
Daguo Gu
Yao Zhou
Ruguang Ma
Fangfang Wang
Qian Liu
Jiacheng Wang
机构
[1] Yancheng Institute of Technology,School of Materials Engineering
[2] Shanghai Institute of Ceramics,State Key Laboratory of High Performance Ceramics and Superfine Microstructure
[3] Chinese Academy of Sciences,undefined
[4] Shanghai Institute of Materials Genome,undefined
来源
Nano-Micro Letters | 2018年 / 10卷
关键词
Nitrogen doping; Graphene-like; Carbon nanoflakes; Electrocatalyst; Oxygen reduction reaction;
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学科分类号
摘要
A series of N-doped carbon materials (NCs) were synthesized by using biomass citric acid and dicyandiamide as renewable raw materials via a facile one-step pyrolysis method. The characterization of microstructural features shows that the NCs samples are composed of few-layered graphene-like nanoflakes with controlled in situ N doping, which is attributed to the confined pyrolysis of citric acid within the interlayers of the dicyandiamide-derived g-C3N4 with high nitrogen contents. Evidently, the pore volumes of the NCs increased with the increasing content of dicyandiamide in the precursor. Among these samples, the NCs nanoflakes prepared with the citric acid/dicyandiamide mass ratio of 1:6, NC-6, show the highest N content of ~6.2 at%, in which pyridinic and graphitic N groups are predominant. Compared to the commercial Pt/C catalyst, the as-prepared NC-6 exhibits a small negative shift of ~66 mV at the half-wave potential, demonstrating excellent electrocatalytic activity in the oxygen reduction reaction. Moreover, NC-6 also shows better long-term stability and resistance to methanol crossover compared to Pt/C. The efficient and stable performance are attributed to the graphene-like microstructure and high content of pyridinic and graphitic doped nitrogen in the sample, which creates more active sites as well as facilitating charge transfer due to the close four-electron reaction pathway. The superior electrocatalytic activity coupled with the facile synthetic method presents a new pathway to cost-effective electrocatalysts for practical fuel cells or metal–air batteries. [graphic not available: see fulltext]
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