Titanium-doped copper oxide/ruthenium heterostructure constructed on Cu3Ti nanosheet for efficient hydrogen evolution reaction in alkaline media

被引:3
作者
Ma, Zhiyuan [1 ]
Wang, Qingbing [1 ]
Du, Yiyang [1 ]
Li, Zhaolong [1 ]
Dong, Junjie [1 ]
Qi, Zhengqiu [1 ]
Zhang, Xiaoyan [1 ]
Yu, Bo [1 ]
Guo, Bingshu [1 ]
Chen, Junchen [1 ]
Wang, Mingshan [1 ]
Jia, Yanlin [2 ]
Zhou, Liujiang [3 ]
Yi, Jiang [1 ,4 ]
Zhang, Jin [1 ]
Li, Xing [1 ]
Zhang, Jing [1 ]
机构
[1] Southwest Petr Univ, Sch New Energy & Mat, Chengdu 610500, Peoples R China
[2] Cent South Univ, Sch Mat Sci & Engn, Changsha 410083, Peoples R China
[3] Univ Elect Sci & Technol China, Sch Phys, Chengdu 610054, Peoples R China
[4] Southern Univ Sci & Technol, Dept Mech & Energy Engn, Shenzhen 518055, Peoples R China
基金
中国国家自然科学基金;
关键词
Water electrolysis; Heterostructure; Hydrogen evolution reaction; Water dissociation; Platinum group metals; ELECTROCATALYSTS; OXYGEN; WATER; CUO; ADSORPTION; RUTHENIUM; SURFACES;
D O I
10.1016/j.apsusc.2023.158474
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
Platinum group metals (Pt, Ru, Ir, etc.) are the most active catalysts for acidic hydrogen evolution reaction (HER), yet they cannot deliver satisfactory performance in alkaline media owing to the high energy barrier of water dissociation. Here, we report the outstanding alkaline HER performance of Cu3Ti-supported Ti-doped CuO/Ru (Cu3Ti@CTO/Ru) heterostructure catalysts, which were fabricated simply by an impregnation-heat treatment method. Density functional theory calculation results indicate that the energy barriers of both water dissociation and hydrogen desorption at CTO/Ru heterointerface are significantly reduced relative to Ru catalyst alone. As a result, the Cu3Ti@CTO/Ru catalyst at the optimum Ru loading amount achieves a low overpotential of 34 mV at the current density of 10 mA cm-2 and an ultra-low Tafel slope of 29 mV dec-1 in 1 M KOH, outperforming the benchmark 20% Pt/C catalyst. This study provides new insight into the development of advanced alkaline HER catalysts.
引用
收藏
页数:10
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