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Facile Synthesis of Co-N4-Doped Mesoporous Carbon for Oxygen Reduction Reaction
被引:17
作者:
Zhao, Hong
[1
,2
]
Su, Caina
[3
]
Hui, K. N.
[4
]
Hui, K. S.
[1
]
机构:
[1] Univ East Anglia, Sch Math, Norwich NR4 7TJ, Norfolk, England
[2] Hong Kong Univ Sci & Technol, Dept Mech Engn, Kowloon, Hong Kong, Peoples R China
[3] Shanxi Datong Univ, Inst Appl Chem, Sch Chem & Environm Engn, Datong 037009, Peoples R China
[4] Univ Macau, Inst Appl Phys & Mat Engn, Ave Univ, Taipa, Macau, Peoples R China
关键词:
NITROGEN-DOPED CARBON;
FUEL-CELLS;
COMPOSITE ELECTROCATALYST;
METHANOL OXIDATION;
RECENT PROGRESS;
ALKALINE MEDIA;
ACTIVE-SITES;
CATALYST;
GRAPHENE;
NANOPARTICLES;
D O I:
10.1149/2.1611704jes
中图分类号:
O646 [电化学、电解、磁化学];
学科分类号:
081704 ;
摘要:
The oxygen reduction reaction (ORR) is a critical factor in fuel cells that has attracted significant research attention. Non-precious metal catalysts have improved the ORR activity considerably, but they still exhibit poorer ORR performance than commercial Pt-based catalysts. In this study, Co-N-4-doped mesoporous carbon (Co-N-4-MC) was prepared for the ORR using cobalt-azides as the Co-N-4-containing precursor, and ordered mesoporous silica SBA-15 as a template for achieving mesoporous structures. The Co-N-4-MC electrode exhibited remarkable ORR activity in an alkaline medium (a half-wave potential of -0.15 V vs. MMO, only similar to 19 mV deviation from the commercial Pt/C catalyst), high selectivity (electron-transfer number similar to 4) and excellent electrochemical stability (similar to 8 mV negative shift of the half-wave potential after 1000 cycles). The good performance of the Co-N-4- MC electrode was attributed to the synergetic effects of N-4, C and Co. In particular, the existence of graphitic pores in the Co-N-4-MC catalyst facilitated the diffusion of O-2 to the catalytic active sites, which benefited the progression of the ORR on the Co-N-4-MC catalyst. (C) 2017 The Electrochemical Society.
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页码:F412 / F417
页数:6
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