Integrating MXene nanosheets with cobalt-tipped carbon nanotubes for an efficient oxygen reduction reaction

被引:221
作者
Chen, Jianian [1 ]
Yuan, Xiaolei [1 ]
Lyu, Fenglei [1 ]
Zhong, Qixuan [1 ]
Hu, Huicheng [1 ]
Pan, Qi [1 ]
Zhang, Qiao [1 ]
机构
[1] Soochow Univ, Joint Int Res Lab Carbon Based Funct Mat & Device, Jiangsu Key Lab Carbon Based Funct Mat & Devices, Inst Funct Nano & Soft Mat FUNSOM, 199 Renai Rd, Suzhou 215123, Jiangsu, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
METAL-ORGANIC FRAMEWORKS; ELECTROCATALYSTS; EVOLUTION; DESIGN; PRINCIPLES; CATALYSIS; SURFACE; HYBRID; OXIDES; FE;
D O I
10.1039/c8ta10574j
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 oxygen reduction reaction (ORR) plays a key role in many renewable energy conversion and storage technologies. As the state-of-the-art ORR electrocatalysts, Pt-based electrocatalysts suffer from high price, low earth abundance and poor stability. Developing high performance noble-metal-free ORR electrocatalysts as alternatives for Pt is highly desirable but still remains a significant challenge. In this work, we reported a metal-organic-framework- engaged strategy for the fabrication of cobalt-tipped carbon nanotube/Ti3C2 nanosheet composites (Co-CNT/Ti3C2), in which ZIF-67 particles were in situ grown on Ti3C2 nanosheets and then were converted to cobalt-tipped carbon nanotubes through a pyrolysis process. The Ti3C2 nanosheets not only served as two-dimensional conductive scaffolds for the growth of Co-CNTs but also balanced the tradeoff between graphitization of carbon and the surface area. Benefiting from the abundant Co-N/C active sites, reasonably high graphitization of carbon and suitable surface areas, the optimized Co-CNT/Ti3C2 manifested comparable ORR activity (half-wave potential of 0.82 V and diffusion-limiting current density of 5.55 mA cm(-2)) but superior stability to commercial Pt/C (half-wave potential of 0.82 V and diffusion-limiting current density of 5.30 mA cm(-2)), providing great opportunity for its application in renewable conversion and storage technologies.
引用
收藏
页码:1281 / 1286
页数:6
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