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.
引用
收藏
页码:5752 / 5761
页数:10
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