Breaking the activity and stability bottlenecks for acid hydrogen evolution by strong metal-support interaction between Pt nanoparticles and amorphous MoOx

被引:1
|
作者
Ning, Bo [1 ,2 ]
Huang, Zhen-Feng [1 ,2 ,3 ]
Shi, Chengxiang [1 ,2 ,3 ]
Pan, Lun [1 ,2 ,3 ]
Gao, Ruijie [1 ,2 ,3 ]
Zhang, Xiangwen [1 ,2 ,3 ]
Zou, Ji-Jun [1 ,2 ,3 ]
机构
[1] Tianjin Univ, Inst Mol Plus, Sch Chem Engn & Technol, Key Lab Green Chem Technol,Minist Educ, Tianjin 300072, Peoples R China
[2] Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 300072, Peoples R China
[3] Haihe Lab Sustainable Chem Transformat, Tianjin 300192, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
HIGHLY EFFICIENT; OXYGEN VACANCIES; ELECTROCATALYST; NANOSHEETS;
D O I
10.1039/d4cy00114a
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
Commercial Pt/C is the best electrocatalyst for electrocatalytic hydrogen evolution due to its high activity and fast electron transfer kinetics. However, the poor stability under high current density and high cost limits its large-scale application. Here, we managed to fabricate a stable catalyst where MoOx stabilized Pt nanoparticles is supported on Ketjen Black via impregnation-annealing method. This catalyst exhibited a low overpotential of 4 mV (@10 mA cm(-2)) and 29 mV (@100 mA cm(-2)) and considerable long-term stability for 100 h toward acid hydrogen evolution reaction, outperforming commercial 20 wt% Pt/C. The excellent catalytic performances can be assigned to the existence of amorphous MoOx which can transport electrons to Pt nanoparticles and prevent Pt nanoparticles from agglomeration. This work provided a simple synthesis strategy to synthesize an amorphous MoOx protected Pt nanoparticles catalyst with good activity and stability, which can be an alternative to commercial Pt/C for acid hydrogen evolution reaction.
引用
收藏
页码:2218 / 2225
页数:8
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