过电位
电解水
材料科学
电催化剂
纳米团簇
制氢
析氧
电解质
双金属片
分解水
化学工程
氢
催化作用
电化学
电解
无机化学
无定形固体
纳米技术
金属
电极
化学
冶金
物理化学
结晶学
有机化学
工程类
光催化
生物化学
作者
Qian Kong,Chengcheng Yu,Qing Lü,Xingyu Yang,Tongguang Xu,Qi Song,Huatong Li,Zhaoshuo Yuan,Hongyu Liu,Qian Qiao,Gang He,Yufan Wang,Linglong Yao,Xiaoping Dai,Yun Xiao
出处
期刊:Small
[Wiley]
日期:2025-07-10
标识
DOI:10.1002/smll.202503398
摘要
Abstract The electrolysis of water for hydrogen production has gained increasing attention as a sustainable and efficient method to obtain high‐purity green hydrogen. The development of efficient catalysts for hydrogen evolution is crucial in order to achieve this target under industrial conditions. The objective of this work is to synthesize a highly efficient F‐Co x Fe y (PO n ) z /IF catalyst with ultra‐low impedance for hydrogen evolution in electrolytic water by incorporating metal phosphatides into metal oxide nanoclusters through a controlled two‐step process involving melting and electrodeposition. The nano‐heterostructure of F‐Co x Fe y (PO n ) z /IF exhibits a low overpotential of 276 mV at a current density of 1000 mA cm −1 , while having an electrochemical impedance comparable to commercial Pt/C/CP (0.41 Ω), and long‐term stability up to 200 h in 1 M KOH electrolyte. The synergistic effect of crystal/amorphous heterojunctions, F doping, and oxygen vacancies further enhances the kinetics of water cracking. Impressively, when combined with NiFeCo LDH/NiS/NF as membrane electrodes, F‐Co x Fe y (PO n ) z /IF || NiFeCo LDH/NiS/NF achieves a water decomposition voltage of 2.03 V at a current density of 1000 mA cm −2 and demonstrates stable operation for over 500 h, showing great potential for large‐scale commercial production.
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