海水
电解质
催化作用
吸附
腐蚀
析氧
化学工程
氯化物
制作
材料科学
电极
无机化学
化学
气泡
氧气
电流密度
电流(流体)
纳米技术
电化学
作者
Luo Yu,Linyuan Chi,Y. Wang,Minghui Ning,Edmond Nasr,Shaowei Song,Jingyi Luan,Shuo Chen,Zhifeng Ren
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2025-10-23
卷期号:10 (11): 5664-5673
被引量:5
标识
DOI:10.1021/acsenergylett.5c02699
摘要
NiFe-based (oxy)hydroxides are widely recognized as the most active non-noble-metal oxygen evolution reaction (OER) catalysts, yet their application is constrained by poor stability under ampere-scale current densities and complicated, energy-intensive syntheses. Here, we introduce a one-step, room-temperature corrosion strategy applied to commercial stainless-steel mats to directly fabricate large-area MoO42–-modified NiFe (oxy)hydroxide (Mo-NiFeOOH/SSM) electrodes. The incorporation of MoO42– effectively regulates the electronic structure and charge distribution of NiFeOOH, which strengthens the adsorption of OER intermediates while suppressing the competitive adsorption of chloride ions. Combined with a porous, hydrophilic surface that facilitates electrolyte transport and bubble release, the electrodes exhibit robust corrosion resistance and high catalytic activity for seawater OER, sustaining operation at current densities of ≥1000 mA cm–2. This facile, scalable, and low-cost fabrication method highlights the potential of Mo-NiFeOOH/SSM as a practical electrode design for large-scale seawater electrolysis.
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