Atomic level tailoring of the electrocatalytic activity of Au-Pt core-shell nanoparticles with controllable Pt layers toward hydrogen evolution reaction

被引:31
|
作者
Shi, Yi [1 ]
Zhai, Ting-Ting [1 ]
Zhou, Yue [1 ]
Xu, Wei-Xuan [1 ]
Yang, Dong-Rui [1 ]
Wang, Feng-Bin [1 ]
Xia, Xing-Hua [1 ]
机构
[1] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Analyt Chem Sci, Nanjing 210023, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Au-Pt core-shell nanoparticles; Underpotential deposition; Hydrogen evolution reaction; Controllable Pt layers; Electronic interaction; Electrocatalysis; OXYGEN REDUCTION REACTION; TUNGSTEN CARBIDE; PLATINUM; DEPOSITION; CATALYSTS; OXIDATION; ELECTRON; STRAIN; FILMS;
D O I
10.1016/j.jelechem.2017.12.006
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The hydrogen evolution reaction (HER) is a critical step in water splitting and demands efficient and low-cost catalysts for real applications. Pt catalyzes HER efficiently, however, its scarcity and high cost inspire researchers to explore metallic catalysts with core-shell nanostructures. Precise tailoring of Pt catalysts at atomic monolayer level would shed insights on the relationship between electronic structure and electrocatalytic properties. Herein, we report the preparation of Au-Pt core-shell nanoparticles deposited on graphene sheets with tunable Pt monolayer coverage by controlling Cu underpotential deposition (UPD)-Galvanic replacement cycles. The electrochemical results suggest that Au-Pt with monolayer Pt shows superior electrocatalytic activity toward HER. Increasing the thickness of Pt shell results in the decrease of the electrocatalytic activity, which might be attributed to the decreased electronic interactions of Au core with outmost surface Pt atoms as confirmed by X-ray photoelectron spectroscopic characterization. The present research would offer a design criterion for metallic nanostructures in realizing catalysts with high performance.
引用
收藏
页码:442 / 446
页数:5
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