Quaternary-metal phosphide as electrocatalyst for efficient hydrogen evolution reaction in alkaline solution

被引:12
|
作者
Zhou, Pengfei [1 ]
Liu, Dong [1 ]
Wen, Zhaorui [1 ]
Chen, Mingpeng [1 ]
Liu, Qingju [2 ]
Ke, Ye [3 ]
Li, Shengwen [1 ]
Chen, Shi [1 ]
Kwok, Chi Tat [3 ]
Wang, Shuangpeng [1 ]
Tang, Yuxin [4 ]
Pan, Hui [1 ]
机构
[1] Univ Macau, Inst Appl Phys & Mat Engn, Joint Key Lab Minist Educ, Macau 999078, Peoples R China
[2] Yunan Univ, Yunan Key Lab Miconano Mat & Technol, Sch Mat Sci & Engn, Kuming 650091, Peoples R China
[3] Univ Macau, Fac Sci & Technol, Dept Electromech Engn, Macau 999078, Peoples R China
[4] Fuzhou Univ, Coll Chem Engn, Fuzhou 350116, Peoples R China
关键词
Electrocatalysis; Multi-metals; Phosphides; Hydrogen evolution reaction; PH-UNIVERSAL ELECTROCATALYST; NANOWIRE ARRAYS; WATER; NI; CATALYSTS; ALLOY; DESIGN; MONOLAYERS; NANOSHEET; CATHODE;
D O I
10.1016/j.ijhydene.2021.03.040
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
Hydrogen evolution reaction (HER) is a critical process in electrocatalytic water splitting for hydrogen production. However, the development of low-cost electrocatalysts for highly efficient HER is still a huge challenge. Hence, we fabricate a multi-metal phosphide on Ni foam, FeCoNiNbxP, through a facile hydrothermal reaction followed by phosphorization. We find that Nb promotes the formation of metal phosphides, and the main phases of the catalysts with Nb are multiphase phosphides. Importantly, the Nb incorporation significantly improves the HER activity of FeCoNiP. We show that FeCoNiNb0.3P has the best HER activity, which only requires an overpotential of 78 mV to achieve a current density of 10 mA cm(-2) in 1 M KOH, and demonstrates excellent stability under both constant potential and varied current densities. Our findings show that the multiple-metal compounds are beneficial to the improvement of catalytic activity and provide guidance on the design of novel catalysts for applications. (c) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:18878 / 18886
页数:9
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