Unraveling the oxide layer on Mo2C as the active center for hydrogen evolution reaction

被引:49
作者
Huang, Xiang [1 ,2 ,3 ]
Wang, Jiong [3 ]
Tao, Hua Bing [4 ]
Tian, Hao [1 ]
Zhang, Zhe [1 ]
Xu, Hu [1 ]
机构
[1] Southern Univ Sci & Technol, Dept Phys, Shenzhen 518055, Peoples R China
[2] Wuhan Univ, Sch Phys & Technol, Wuhan 430072, Peoples R China
[3] Northwestern Polytech Univ, Sch Chem & Chem Engn, Inst Adv Synth IAS, Xian 710072, Peoples R China
[4] Nanyang Technol Univ, Sch Chem & Biomed Engn, 62 Nanyang Dr, Singapore 637459, Singapore
基金
中国国家自然科学基金;
关键词
beta-Mo2C; Hydrogen evolution reaction; Surface structures; Active site; Reaction mechanism; DENSITY-FUNCTIONAL THEORY; CARBIDE; TEMPERATURE; ADSORPTION; SURFACE; WATER; MOC; ELECTROCATALYSTS; BETA-MO2C; STABILITY;
D O I
10.1016/j.jcat.2020.06.020
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
Large-scale production of hydrogen fuels via electrochemical water splitting requires efficient and cost-effective electrocatalysts. Molybdenum carbide (Mo2C), as a promising substitute for expensive Pt-based catalysts, exhibits outstanding electrocatalytic performance toward hydrogen evolution reaction (HER). Herein, by combining theoretical studies and experimental measurements, we systematically investigate the surface stability and HER activity of Mo2C. We demonstrate that the Mo2C(100) surface is oxidized under HER turnover condition, and the HER activity shows a positive correlation with the oxidation degrees of this surface. The Mo2C(100) surface covered by a monolayer of oxygen atoms is verified as the most stable surface structure, which derives the optimum HER activity, and thus the surface chemisorbed oxygen atoms are identified as the active sites. This study provides new insights into developing efficient electrocatalysts for HER based on Mo2C. (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:461 / 467
页数:7
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