Hierarchical Fe-based electrocatalyst for lattice oxygen mediated water oxidation with Industrial-Level activity

被引:0
|
作者
Yang, Rui [1 ]
Fu, Hao [1 ]
Han, Zimin [1 ]
Feng, Guoqing [1 ]
Liu, Huaizhi [1 ]
Gao, Yin [1 ]
Hu, Yangguang [3 ,4 ]
Wang, Zhongkai [1 ]
Huang, Yiyin [2 ]
机构
[1] Anhui Agr Univ, Anhui Prov Engn Ctr High Performance Biobased Nylo, Anhui Prov Engn Ctr Automot Highly Funct Fiber Pro, Sch Mat & Chem, Hefei 230036, Peoples R China
[2] Fujian Normal Univ, Coll Phys & Energy, Fujian Prov Key Lab Quantum Manipulat & New Energy, Fuzhou 350117, Peoples R China
[3] Univ Sci & Technol China, Sch Chem & Mat Sci, Hefei Natl Lab Phys Sci Microscale, iChEM, Hefei 230026, Anhui, Peoples R China
[4] Univ Sci & Technol China, Natl Synchrotron Radiat Lab, Hefei 230026, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
Hierarchical structure; Lattice oxygen mediated pathway; Oxygen evolution; Large current density; Long-term stability; EVOLUTION; HYDROGEN; PERFORMANCE; CATALYSTS;
D O I
10.1016/j.jcis.2025.01.210
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
Rational design transition metal-based electrocatalysts for oxygen evolution reaction (OER) at large current densities is vital for industrial applications of alkaline water electrolysis. Here, we present a three-dimensional catalyst comprises of Fe2O3 nanoparticles that are highly dispersed on FeMoO4 nanorods, supported on Ni foam, featuring a hierarchical heterostructure and array morphology. The resulting Fe2O3/FeMoO4/NF electrodes exhibit remarkable OER catalytic activity, achieving overpotentials of 315 mV and 352 mV at current densities of 1000 mA cm(-2) and 2000 mA cm(-2), respectively, while maintaining outstanding long-term durability (>900 h) at a current density of 500 mA cm(-2). In-situ Fourier-transform infrared (FTIR) spectroscopy and theoretical studies demonstrate the direct O-O radical coupling for lattice-oxygen-mediated mechanism (LOM)dominated O-2 evolution, thereby breaking the scaling relationship limitation and accelerating reaction kinetics. Operando electrochemical impedance spectroscopy implies fast charge transport. The superior OER performance can be attributed to the abundant heterointerfaces between the active phases in hierarchical structure and the enhanced intrinsic activity through the LOM mechanism. This work paves an avenue for constructing advanced electrocatalysts with industrial-level activity and offering a promising approach for practical applications in alkaline water electrolysis.
引用
收藏
页码:107 / 117
页数:11
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