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Tuning the dimensions and structures of nitrogen-doped carbon nanomaterials derived from sacrificial g-C3N4/metal-organic frameworks for enhanced electrocatalytic oxygen reduction
被引:107
|作者:
Wang, Ruwen
[1
]
Yan, Tingting
[1
]
Han, Lupeng
[1
]
Chen, Guorong
[1
]
Li, Hongrui
[1
]
Zhang, Jianping
[1
]
Shi, Liyi
[1
]
Zhang, Dengsong
[1
]
机构:
[1] Shanghai Univ, Sch Mat Sci & Engn, Res Ctr Nano Sci & Technol, Shanghai 200444, Peoples R China
基金:
中国国家自然科学基金;
关键词:
METAL-ORGANIC FRAMEWORKS;
HIGHLY-EFFICIENT;
POROUS CARBON;
GRAPHENE;
COORDINATION;
CATALYSTS;
NANOPARTICLES;
CONSTRUCTION;
COMPOSITES;
NANOSHEETS;
D O I:
10.1039/c8ta00439k
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:
Here we demonstrate a facile strategy for tuning the dimensions and structures of nitrogen-doped carbon nanomaterials via regulating the ratio of Co/Zn in zeolitic imidazolate framework (ZIF) arrays in situ grown on g-C3N4 nanosheets, followed by a pyrolysis process. One-dimensional nitrogen-doped bamboo-like carbon nanotube encapsulated Co nanoparticle (Co/N-BCNTs), two-dimensional nitrogen-doped carbon nanosheet (N-CNS) and three-dimensional nitrogen-doped carbon nanotube framework encapsulated Co nanoparticle (Co/N-CNTFs) electrocatalysts are successfully fabricated from Zn/Co-ZIF@g-C3N4, ZIF-8@g-C3N4 (Co free) and ZIF-67@g-C3N4 (Zn free), respectively. The resulting Co/N-BCNTs electrocatalyst exhibits a better oxygen reduction reaction (ORR) activity than the other two catalysts, with a half-wave potential of 0.83 V (versus the reversible hydrogen electrode) in alkaline solutions, which is superior to that of a commercial Pt/C catalyst. More importantly, the Co/N-BCNTs show much higher stability and better methanol-tolerance than the Pt/C catalyst in a 0.1 M KOH solution. It has been demonstrated that the enhanced catalytic performance of Co/N-BCNTs is attributed to their suitable surface area, well-dispersed N dopants, and Co encapsulated inside carbon nanotubes. The presented strategy offers new prospects in developing highly active electrocatalysts.
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页码:5752 / 5761
页数:10
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