Self-supported iron-based bimetallic phosphide catalytic electrode for efficient hydrogen evolution reaction at high current density

被引:3
|
作者
Zuo, Ziteng [1 ]
Zhang, Xian [2 ]
Peng, Ouwen [1 ]
Shan, Lianwei [3 ]
Xiang, Shengling [1 ]
Lian, Qing [1 ]
Li, Ningxue [1 ]
Mi, Guojun [1 ]
Amini, Abbas [4 ]
Cheng, Chun [1 ,5 ]
机构
[1] Southern Univ Sci & Technol, Dept Mat Sci & Engn, Shenzhen 518055, Peoples R China
[2] Wuhan Univ Technol, Sch Resources & Environm Engn, Wuhan 430070, Peoples R China
[3] Harbin Univ Sci & Technol, Sch Mat Sci & Chem Engn, Harbin 150040, Peoples R China
[4] Univ Western Sydney, Ctr Infrastruct Engn, Sydney, NSW 2751, Australia
[5] Southern Univ Sci & Technol, Guangdong Prov Key Lab Energy Mat Elect Power, Shenzhen 518055, Peoples R China
基金
中国国家自然科学基金;
关键词
Iron (Fe)-based materials; which are abundant in Earth's crust; can be competent candidates as electrocatalysts for large-scale and sustainable alkaline hydrogen evolution reaction (HER); however; unlocking their huge potential critically relies on the rational integration of their structures and electrode materials. Herein; we report the construction of FeP-based bimetallic electrodes through a facile soaking-phosphorization approach. The hierarchical structure of porous iron foam (IF)-nanosheet arrays (NAs) endows enhanced reaction kinetics under high current densities. Modification with different transition metal cations evidently improves the intrinsic catalytic activity of FeP; among which cobalt-modified FeP (CoFe-P) shows the best performance. The optimized CoFe-P NAs/IF electrode exhibits an outstanding catalytic performance in the HER in alkaline media; with a current density of 10 mA cm−2 at an extremely low overpotential of 40 mV. Additionally; at high current densities of 500 and 1000 mA cm−2; the electrode requires impressively low overpotentials of 151 and 162 mV; respectively; Furthermore; the catalytic performance experiences minimal degradation after a stability test at 500 mA cm−2 for 200 hours; suggesting the exceptional stability of the CoFe-P NAs/IF electrode. © 2024 The Royal Society of Chemistry;
D O I
10.1039/d3ta06035g
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
Iron (Fe)-based materials, which are abundant in Earth's crust, can be competent candidates as electrocatalysts for large-scale and sustainable alkaline hydrogen evolution reaction (HER); however, unlocking their huge potential critically relies on the rational integration of their structures and electrode materials. Herein, we report the construction of FeP-based bimetallic electrodes through a facile soaking-phosphorization approach. The hierarchical structure of porous iron foam (IF)-nanosheet arrays (NAs) endows enhanced reaction kinetics under high current densities. Modification with different transition metal cations evidently improves the intrinsic catalytic activity of FeP, among which cobalt-modified FeP (CoFe-P) shows the best performance. The optimized CoFe-P NAs/IF electrode exhibits an outstanding catalytic performance in the HER in alkaline media, with a current density of 10 mA cm-2 at an extremely low overpotential of 40 mV. Additionally, at high current densities of 500 and 1000 mA cm-2, the electrode requires impressively low overpotentials of 151 and 162 mV, respectively. Furthermore, the catalytic performance experiences minimal degradation after a stability test at 500 mA cm-2 for 200 hours, suggesting the exceptional stability of the CoFe-P NAs/IF electrode. Cheap Fe foam (IF) was entirely transformed to the robust and high output CoFe-P NAs/IF electrode via facile soaking-phosphorization approach. The as-prepared CoFe-P NAs/IF exhibits remarkable HER activity and stability under industrial conditions.
引用
收藏
页码:5331 / 5339
页数:9
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