A highly-efficient and durable Pt-based electrocatalyst decorated by Co2C-Mo2C@CS composite for methanol oxidation reaction

被引:9
|
作者
Wei, Shuang [1 ]
Xie, Fei [1 ]
Gan, Mengyu [1 ]
Ma, Li [1 ]
Wu, Taichun [1 ]
Fu, Qinglan [1 ]
Li, Tingting [1 ]
Yang, Yanlin [1 ]
Zhan, Wang [1 ]
机构
[1] Chongqing Univ, Coll Chem & Chem Engn, Chongqing 400044, Peoples R China
基金
中国国家自然科学基金;
关键词
Pt-based electrocatalyst; Methanol oxidation reaction; Molybdenum carbide; Synergistic effect; Impregnation-reduction-annealing method; ENHANCED CATALYTIC-ACTIVITY; REDUCED GRAPHENE OXIDE; HIGH-INDEX FACETS; TUNGSTEN CARBIDE; NONPRECIOUS CATALYST; CARBON NANOFIBERS; OXYGEN REDUCTION; ANODE CATALYST; CO TOLERANCE; PLATINUM;
D O I
10.1016/j.synthmet.2021.116878
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Designing highly efficient electrocatalysts for the methanol electro-oxidation is an ongoing challenge. Herein, we report that molybdenum carbide (Mo2C) and cobalt carbide (Co2C) are grown in situ on the surface of carbon spheres to form Co2C-Mo2C@CS carrier material by the impregnation-reduction-annealing process, and then Pt nanoparticles are deposited on the Co2C-Mo2C@CS surface through sodium borohydride reduction method. In-depth material characterizations and electrochemical analyses demonstrate that the introduction of small-sized Mo2C-Co2C composites can facilitate mass transfer and increase the solid-liquid interface area. As expected, the resulting Pt/Co2C-Mo2C@CS catalyst displays excellent methanol oxidation activity (1504.5 mA mgPt(-1)), enhanced CO tolerance and stability comparing with other catalysts, which mainly derived from the metal-support interaction between Co2C-Mo2C and small-sized Pt NPs. The rational design of Pt/Co2C-Mo2C@CS catalyst provides a feasible strategy for boosting the overall performance of Pt-based catalysts towards methanol oxidation, and broadens the potential applications of metal carbides.
引用
收藏
页数:11
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