Crystalline/amorphous CoP/MnOx heterostructure derived from phase separation for electrochemical catalysis of alkaline hydrogen evolution reaction

被引:7
|
作者
Yu, Rui [1 ]
Du, Ying-Xia [1 ,2 ]
Zhao, Heng-Fan [3 ,4 ,5 ]
Cao, Fei-Fei [1 ]
Lu, Wang-Ting [3 ,4 ,5 ]
Zhang, Geng [1 ]
机构
[1] Huazhong Agr Univ, Coll Sci, Dept Chem, Wuhan 430070, Peoples R China
[2] Huazhong Agr Univ, Coll Resources & Environm, Wuhan 430070, Peoples R China
[3] Jianghan Univ, State Key Lab Precis Blasting, Wuhan 430056, Peoples R China
[4] Jianghan Univ, Key Lab Optoelect Chem Mat & Devices, Minist Educ, Wuhan 430056, Peoples R China
[5] Jianghan Univ, Inst Interdisciplinary Res, Sch Optoelect Mat & Technol, Wuhan 430056, Peoples R China
基金
中国国家自然科学基金;
关键词
Water splitting; Alkaline HER; Phase separation; Interface effect; Crystal refinement; CARBON NANOTUBES; EFFICIENT; PHOSPHIDE; COP; ELECTROCATALYST; PERFORMANCE; OXIDATION; HYBRIDS; OXIDES; NI;
D O I
10.1016/j.ijhydene.2022.10.049
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
The electrochemical water splitting in alkaline media is troubled by the lack of efficient electrocatalysts for hydrogen evolution reaction (HER). Herein, a crystalline/amorphous CoP/MnOx heterostructure is converted from a single-phase bimetallic Co-Mn oxide by phase separation strategy. The CoP/MnOx heterostructure only requires an overpotential of 135 mV to reach 10 mA cm-2 in 1 M KOH, which is lower than that of CoP (184 mV). The interface effect between CoP and MnOx is beneficial to the improvement of HER activity, which is confirmed by means of selective etching of MnOx and infrared spectroscopy. Moreover, the crystal size of CoP phase in the heterostructure is lower than that of the mono-component CoP. Furthermore, the decrease of precursor crystal size will give rise to a decrease in the CoP crystal size of heterostructure. The decline of crystal size results in higher active surface area and greater number of interfaces.(c) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:2593 / 2604
页数:12
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