In Situ Self-Supporting Cobalt Embedded in Nitrogen-Doped Porous Carbon as Efficient Oxygen Reduction Electrocatalysts

被引:6
|
作者
Gao, Yuan [1 ]
Gong, Xiaoman [1 ]
Zhong, Haihong [1 ]
Li, Dianqing [1 ]
Tang, Pinggui [1 ]
Alonso-Vante, Nicolas [2 ]
Feng, Yongjun [1 ,3 ]
机构
[1] Beijing Univ Chem Technol, Beijing Engn Ctr Hierarch Catalysts, State Key Lab Chem Resource Engn, 15 Beisanhuan East Rd, Beijing 100029, Peoples R China
[2] UMR CNRS 7285, IC2MP, F-86022 Poitiers, France
[3] Beijing Univ Chem Technol, Anqing Res Inst, 8 Huanhu West Rd, Anqing City 24600, Anhui, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
oxygen reduction reaction; Co-II; EDTA chelate; porous structure; pore formation; non-noble electrocatalysts; METAL-ORGANIC FRAMEWORK; BIFUNCTIONAL ELECTROCATALYST; ACTIVE-SITES; CATALYST; NANOPARTICLES; ORR; PHTHALOCYANINE; SPHERES; OER;
D O I
10.1002/celc.202001090
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
A facile two-step chemical route using cobalt ions coordinated with EDTA (Co-II/EDTA chelate complex supported on glucose mixture), followed by the in situ pyrolysis process, from 500 to 900 degrees C, was developed to prepare Co embedded in N-doped porous carbon hybrids (Co@C-T). The EDTA chelating agent served as both the N source and pore former. The physicochemical characterization results revealed that the pore structure, graphitization degree, and relative content of active centers, e. g., cobalt-based components and nitrogen species, for Co@C-T electrocatalysts, were tailored by controlling the temperature of pyrolysis. The optimized material generated at 600 degrees C (Co@C-600), showed an excellent oxygen reduction reaction activity with an onset potential of 0.91 V vs. RHE, and a half-wave potential of 0.80 V vs. RHE. In addition, the Co@C-600 catalyst showed superior durability and stability compared to the benchmark Pt/C.
引用
收藏
页码:4024 / 4030
页数:7
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