Construction of a Pt-CeOx Interface for the Electrocatalytic Hydrogen Evolution Reaction

被引:8
作者
Yu, Shen-Wei [1 ]
Kwon, Soonho [2 ]
Chen, Yizhen [1 ]
Xie, Zhenhua [3 ]
Lu, Xiner [4 ]
He, Kai [4 ]
Hwang, Sooyeon [5 ]
Chen, Jingguang G. [3 ]
Goddard, William A., III [2 ]
Zhang, Sen [1 ]
机构
[1] Univ Virginia, Dept Chem, Charlottesville, VA 22904 USA
[2] CALTECH, Mat & Proc Simulat Ctr, Pasadena, CA 91125 USA
[3] Columbia Univ, Dept Chem Engn, New York, NY 10027 USA
[4] Univ Calif Irvine, Dept Mat Sci & Engn, Irvine, CA 92697 USA
[5] Brookhaven Natl Lab, Ctr Funct Nanomat, Upton, NY 11973 USA
基金
美国国家科学基金会;
关键词
electrolysis; hydrogen evolution reaction; metal-metal oxide interface; Pt-CeOx; METAL-CATALYSTS; WATER; NICKEL; SURFACE; NANOPARTICLES; DISSOCIATION; ELECTROLYSIS;
D O I
10.1002/adfm.202402966
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The creation of metal-metal oxide interfaces is an important approach to fine-tuning catalyst properties through strong interfacial interactions. This article presents the work on developing interfaces between Pt and CeOx that improve Pt surface energetics for the hydrogen evolution reaction (HER) within an alkaline electrolyte. The Pt-CeOx interfaces are formed by depositing size-controlled Pt nanoparticles onto a carbon support already coated with ultrathin CeOx nanosheets. This interface structure facilitates substantial electron transfer from Pt to CeOx, resulting in decreased hydrogen binding energies on Pt surfaces, and water dissociation for the HER, as predicted by the density functional theory (DFT) calculations. Electrochemical testing indicates that both Pt specific activity and mass activity are improved by a factor of 2 to 3 following the formation of Pt-CeOx interfaces. This study underscores the significance and potential of harnessing robust interfacial effects to enhance electrocatalytic reactions.
引用
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页数:8
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