RuP nanoparticles on ordered macroporous hollow nitrogen-doped carbon spheres for efficient hydrogen evolution reaction

被引:16
|
作者
Luo Wenjie [1 ]
Wang Yijie [1 ]
Li Xianglin [2 ,3 ]
Cheng Chuanwei [1 ]
机构
[1] Tongji Univ, Sch Phys Sci & Engn, Shanghai Key Lab Special Artificial Microstruct M, Shanghai 200092, Peoples R China
[2] Hunan First Normal Univ, Changsha 410205, Hunan, Peoples R China
[3] Dongguan NanoFrontier Microelect Equipment Co Ltd, Dongguan 523808, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
macroporous structure; hollow carbon spheres; ruthenium phosphides; hydrogen evolution reaction; HIGHLY EFFICIENT; ELECTROCATALYSTS; NANOSHEETS; REDUCTION; PHOSPHIDE; ULTRAFINE; GRAPHENE; ARRAYS; OXYGEN;
D O I
10.1088/1361-6528/ab824b
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The design of highly active, Earth-abundant and stable electrocatalysts is important for efficient water splitting. In this work, we report the fabrication of RuP and Ru2P nanoparticles supported on ordered macroporous N-doped carbon hollow spheres (RuP/H-NC and Ru2P/H-NC) through a facile and scalable space-confined pyrolysis process. The RuP/H-NC catalyst exhibits Pt-like activity in alkaline electrolyte, by means of the macroporous structure with a larger specific area and more exposed active sites, as well as the synergistic effect between the RuP nanoparticles and N-doped carbon. Specifically, the RuP/H-NC catalyst yields superior hydrogen evolution reaction activity in terms of low overpotential of 19 mV in 1 M KOH to achieve a current density of 10 mA cm(-2) and excellent durability, outperforming Ru2P/H-NC and most of the reported non-Pt catalysts. Further density function theory calculation reveals that RuP is more intrinsically active with favorable hydrogen adsorption Gibbs free energy than that of Ru2P.
引用
收藏
页数:9
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