Ni0.85Se Inducing Strong Metal-Support Interaction Promotes Alkaline Hydrogen Electrooxidation on Ru

被引:2
|
作者
Feng, Youkai [1 ]
Fu, Luhong [2 ,3 ,4 ]
Yang, Fulin [1 ]
Feng, Ligang [1 ]
Luo, Wei [2 ]
机构
[1] Yangzhou Univ, Sch Chem & Chem Engn, Yangzhou 225002, Peoples R China
[2] Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China
[3] Kunming Univ Sci & Technol, Fac Mat Sci & Engn, Kunming 650093, Peoples R China
[4] Huaqiao Univ, Coll Mat Sci & Engn, Xiamen 361021, Peoples R China
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2024年 / 128卷 / 33期
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
OXIDATION REACTION; EXCHANGE MEMBRANE; FUEL-CELLS; EVOLUTION; ELECTROCATALYSTS; NANOPARTICLES; CATALYSTS; OXIDES; ACID;
D O I
10.1021/acs.jpcc.4c03778
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
Strong metal-support interaction (SMSI) is widely recognized as an effective strategy for designing high-performance electrocatalysts but suffers from a loss in the number of active sites during the high-temperature process. Herein, a Ru-catalyst supported on Ni0.85Se nanosheets has been fabricated through a facile microwave-assisted synthesis. Spectral characterizations and theoretical calculations confirm that the SMSI is formed under mild conditions at the metal-support interfaces, resulting in well-regulated electronic structures of the active Ru species and a downshifted d-band center. It significantly weakens the binding strength to the oxygenated species, which alleviates the competitive adsorption of H-ad and OHad on Ru surfaces and hence increases the tolerance to form the OHad-monolayer adsorbed (poisoned) Ru surfaces. As a result, the obtained catalyst exhibits a 7-fold enhanced mass activity compared to the conventional carbon black supported Ru as well as the enlarged effective potential window toward the alkaline hydrogen oxidation reaction. This work provides a facile strategy to construct SMSI under mild conditions for the design of high-performance electrocatalysts and can be expanded to other metal/metalloid compounds
引用
收藏
页码:13702 / 13710
页数:9
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