Nitrogen-Doped Graphitic Porous Carbon Nanosheets Derived from In Situ Formed g-C3N4 Templates for the Oxygen Reduction Reaction

被引:52
|
作者
Li, Qi [1 ]
Xu, Dan [1 ]
Ou, Xu [1 ]
Yan, Feng [1 ]
机构
[1] Soochow Univ, Jiangsu Key Lab Adv Funct Polymer Design & Applic, Dept Polymer Sci & Engn, Coll Chem Chem Engn & Mat Sci, Suzhou 215123, Peoples R China
基金
中国国家自然科学基金;
关键词
carbon; electron transfer; nanostructures; nitrides; reduction; METAL-FREE ELECTROCATALYSTS; ACTIVE-SITES; HYDROTHERMAL SYNTHESIS; GRAPHENE OXIDE; EFFICIENT CATALYSTS; HYDROGEN EVOLUTION; NITRIDE; SULFUR; BORON; SUPERCAPACITOR;
D O I
10.1002/asia.201700586
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Heteroatom-doped carbon materials have been considered as potential substitutes for Pt-based electrocatalysts for the oxygen reduction reaction (ORR) in alkaline fuel cells. Here we report the synthesis of oxygen-containing nitrogen-doped carbon (ONC) nanosheets through the carbonization of a mixture that contained glucose and dicyandiamide (DCDA). In situ formed graphitic carbon nitride (g-C3N4) derived from DCDA provided a nitrogen-rich template, thereby facilitating the formation of ONC nanosheets. The resultant ONC materials with high nitrogen content, high specific surface areas, and highly mesoporous total volume displayed excellent electrochemical performance, including a similar ORR onset potential, half-potential, a higher diffusion-limited current, and excellent tolerance to methanol than that of the commercial Pt/C catalyst, respectively. Moreover, the ONC-850 nanosheet displayed high long-term durability even after 1000cycles as well as a high electron transfer number of 3.92 (4.0 for Pt/C). Additionally, this work provides deeper insight into these materials and a versatile strategy for the synthesis of cost-effective 2D N-doped carbon electrocatalysts.
引用
收藏
页码:1816 / 1823
页数:8
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