过电位
塔菲尔方程
材料科学
电催化剂
无定形固体
铂金
电化学
氧化物
氢
化学工程
过渡金属
无机化学
物理化学
催化作用
结晶学
有机化学
电极
冶金
化学
工程类
作者
Jie Xu,Chaoxiong Zhang,Haoxuan Liu,Jiaqiang Sun,Ruicong Xie,Yuan Qiu,Fang Lü,Yifan Liu,Longchao Zhuo,Xijun Liu,Jun Luo
出处
期刊:Nano Energy
[Elsevier BV]
日期:2020-01-24
卷期号:70: 104529-104529
被引量:177
标识
DOI:10.1016/j.nanoen.2020.104529
摘要
Abstract It is highly desirable to develop Pt single-atom (SA) catalysts with an optimized mass activity for acidic hydrogen evolution reaction (HER), but it remains a significant challenge. In this study, a new Pt SA strongly coupled with amorphous MoOX (Pt-SA/ɑ-MoOx) is rationally designed. The synergistic effect between unsaturated Pt atoms and defective MoOx can significantly lower the reaction barrier contributing to the fast HER reaction kinetics. Hence, Pt-SA/ɑ-MoOx exhibits an ultrahigh mass activity of 52.0 A mgPt−1 at an overpotential of 50 mV, corresponding to better acidic HER activity than those reported previously for Pt SA-based catalysts. Furthermore, Pt-SA/ɑ-MoOx shows Pt-like kinetics with a small Tafel slope of 123 mV dec−1 and outstanding long-term electrochemical stability for 20 h. This developed synthetic method is also extended for the fabrication of other amorphous MoOx-supported SA catalysts (e.g. Ir, Au and Pb). As far as we know, our study reports the first example of the combination of metal SA and amorphous oxide for highly efficient electrocatalysis.
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