Self-Supported Nanoporous Cobalt Phosphide Nanowire Arrays: An Efficient 3D Hydrogen-Evolving Cathode over the Wide Range of pH 0-14

被引:2195
作者
Tian, Jingqi [1 ,2 ]
Liu, Qian [1 ]
Asiri, Abdullah M. [3 ,4 ]
Sun, Xuping [1 ,3 ,4 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Changchun 130022, Jilin, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China
[3] King Abdulaziz Univ, Fac Sci, Dept Chem, Jeddah 21589, Saudi Arabia
[4] King Abdulaziz Univ, Ctr Excellence Adv Mat Res, Jeddah 21589, Saudi Arabia
基金
中国国家自然科学基金;
关键词
ACTIVE EDGE SITES; EVOLUTION REACTION; H-2; PRODUCTION; ELECTRONIC-STRUCTURE; GENERATING HYDROGEN; WATER; CATALYSTS; MOS2; CO; ELECTROCATALYST;
D O I
10.1021/ja503372r
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this Communication, we report the topotactic fabrication of self-supported nanoporous cobalt phosphide nanowire arrays on carbon cloth (Cop/CC) via low-temperature phosphidation of the corresponding Co(OH)F/CC precursor. The CoP/CC, as a robust integrated 3D hydrogen-evolving cathode, shows a low onset overpotential of 38 mV and a small Tafel slope of Si mV dec(-1), and it maintains its catalytic activity for at least 80 000 s in acidic media. It needs overpotentials (eta) of 67, 100, and 204 mV to attain current densities of 10, 20, and 100 mA cm(-2), respectively. Additionally, this electrode offers excellent catalytic performance and durability under neutral and basic conditions.
引用
收藏
页码:7587 / 7590
页数:4
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