Activating CoP via spontaneous atomic palladium doping for efficient hydrogen evolution

被引:1
|
作者
Wang, Cheng [1 ,2 ,3 ]
Wang, Yibo [2 ]
Shi, Zhaoping [2 ]
Peng, Guowen [4 ]
Luo, Wenhua [1 ,3 ]
Xiao, Meiling [2 ]
Xing, Wei [2 ]
Sang, Ge [1 ,3 ]
Liu, Changpeng [2 ]
机构
[1] Sci & Technol Surface Phys & Chem Lab, Jiangyou 621908, Peoples R China
[2] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Jilin Prov Key Lab Low Carbon Chem Power, Changchun 130022, Peoples R China
[3] China Acad Engn Phys, Inst Mat, Jiangyou 621907, Peoples R China
[4] Univ South China, Sch Resources Environm & Safety Engn, Hengyang 421001, Peoples R China
基金
中国国家自然科学基金;
关键词
Hydrogen evolution reaction; Cobalt phosphide; Adsorption energy; Water electrolysis; Pd doping; CARBON; ELECTROCATALYSTS; NANOPARTICLES; MOF; IMMUNOSENSOR; PERFORMANCE; NANOSHEETS; CELL;
D O I
10.1016/j.ijhydene.2024.07.452
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
Electrocatalytic hydrogen evolution is an efficient and clean hydrogen production technology with simple process and high product purity. Searching for inexpensive alternatives to platinum will help popularize proton exchange membrane water electrolysis (PEMWE) technology. However, the alternative catalytic materials are essentially limited by low catalytic efficiency. Herein, we address this challenge through chemically activating cobalt phosphide (CoP) by doping a small amount of atomic palladium. Palladium substitution occurs at the cobalt site of CoP. Theoretical calculations manifest that the phosphorus atoms near the palladium sites exhibit almost zero hydrogen adsorption free energy. The final cobalt phosphide doped with only 2 wt% of palladium shows wonderful HER performance. Specifically, its overpotential at a current density of 10 mA cm-2 is only 37.5 mV in an acidic medium, and the corresponding Tafel slope is 56 mV dec- 1. This work provides a reference for preparing high performance non-platinum catalysts.
引用
收藏
页码:759 / 766
页数:8
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