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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.
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页码:4024 / 4030
页数:7
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