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Ultrafine Co@nitrogen-doped carbon core-shell nanostructures anchored on carbon nanotubes for highly efficient oxygen reduction
被引:23
作者:
Quan, Li
[1
]
Yu, Xuelian
[1
]
Wang, Tao
[1
]
Yin, Wenchao
[1
]
Liu, Jianqiao
[1
]
Wang, Lin
[1
]
Zhang, Yihe
[1
]
机构:
[1] China Univ Geosci, Sch Mat Sci & Technol, Beijing Key Lab Mat Utilizat Nonmetall Minerals &, Natl Lab Mineral Mat, Beijing 100083, Peoples R China
关键词:
Core-shell;
Electrocatalysts;
Electronic coupling;
Oxygen reduction reaction;
Metal-organic frameworks;
ELECTROCATALYTIC ACTIVITY;
CATALYSTS;
HYBRID;
FRAMEWORKS;
D O I:
10.1016/j.apsusc.2019.07.157
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
The rational design of non-noble-metal electrocatalysts for oxygen reduction reaction (ORR) with both excellent activity and robust stability still remains a key challenge nowadays. Herein, N-doped carbon wrapped Co nanoparticles core-shell nanostructures grafted on carbon nanotubes (Co@NC@CNTs) were achieved by a simple pyrolysis process using ZIF-67 and CNTs as precursors. Most importantly, this unique structure of Co@NC@CNTs is beneficial to increase the contact area of N-doped carbon and Co, inhibit the aggregation of Co@NC core-shell nanoparticles and protect the Co from dissolution, thus improving the electrocatalytic performance and stability for ORR. As a result, the well-defined Co@NC@CNTs electrocatalyst exhibits excellent ORR activity with a high onset potential, half-wave potential and limited current density, comparable to the commercial Pt/C in alkaline electrolyte. Furthermore, the Co@NC@CNTs electrocatalyst presents outstanding electrochemical durability and methanol tolerance in comparison with Pt/C. This strategy will open a new avenue toward the development of nonprecious high-performance ORR catalysts.
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页码:691 / 699
页数:9
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