材料科学
电解
腐蚀
海水
电极
无定形固体
催化作用
化学工程
膜
冶金
有机化学
电解质
化学
海洋学
遗传学
物理化学
生物
工程类
地质学
作者
Lin Wang,Kai Huang,Xiaohe Zheng,Yingnan Liu,Jiadong Wu,Qizhou Dai,Zhengfei Chen,Zhongjian Li,Bin Yang,Cheng Lian,Lecheng Lei,Yang Hou
标识
DOI:10.1002/adfm.202417603
摘要
Abstract The oxygen evolution reaction (OER) is integral to the production of green hydrogen via seawater electrolysis. However, it faces significant challenges, including suboptimal catalytic activity, pronounced corrosion induced by Cl − ions, and restricted operational lifetimes. In this study, a heterostructured hybrid catalyst composed of an amorphous NiFe‐layered double hydroxide (LDH) and a crystalline NiMoO₄ is presented. Leveraging the synergistic coupling interactions, the NiFe‐LDH/NiMoO₄ demonstrates a remarkable OER performance in seawater electrolysis, requiring a minimal overpotential of merely 339 mV to attain an industrial‐level current density of 500 mA cm − 2 . Experimental findings reveal that the constructed NiFe‐LDH/NiMoO₄ architecture significantly enhances electron transfer between the Ni and Fe sites, resulting in the formation of high‐valent Ni species that are beneficial for OER catalysis. A mechanistic analysis elucidates the phenomenon whereby the integration of NiFe‐LDH and NiMoO₄ mitigates Cl − ions corrosion and optimizes the adsorption of vital oxygen‐containing intermediates, accelerating the kinetics of alkaline seawater OER and improving catalytic performance during the seawater electrolysis process.
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