析氧
塔菲尔方程
分解水
镍
催化作用
氢氧化物
无机化学
过电位
海水
化学工程
硫化物
材料科学
硫化镍
腐蚀
氢氧化钠
热液循环
化学
碱性电池
制氢
氧气
剥脱关节
硫代硫酸盐
碱性水电解
氢
水热合成
钝化
电解水
电化学
硫化氢
耐久性
作者
Bo Zheng,Yue Zhou,Chunlei Li,Zhaorui Pan,Xiaofeng Wang,Mei Shi,LiYang Fu,Mei Zhang,Wenjie Fei,G. X. Liu,Leiming Lang
出处
期刊:Langmuir
[American Chemical Society]
日期:2026-01-14
卷期号:42 (3): 2896-2906
被引量:3
标识
DOI:10.1021/acs.langmuir.5c05750
摘要
Developing low-cost, high-efficiency oxygen evolution reaction electrocatalysts is crucial for sustainable green hydrogen production via water electrolysis. Nonetheless, complex synthetic processes, low catalytic activity, and limited durability of catalysts pose significant challenges for industrial-scale applications, particularly in seawater electrolysis, where Cl – -induced chlorine oxidation and electrode corrosion are prominent issues. In this work, we present a one-step hydrothermal method to fabricate NiFe layered double hydroxide@Fe-doped nickel sulfide nanohybrids on nickel foam (NiFe LDH@Ni x Fe 3– x S 2 /NF) using sodium thiosulfate as a dual-function precursor (decomposing to S 2– for sulfide formation and SO 4 2– for LDH modification). The optimal catalyst demonstrates exceptional OER performance in alkaline freshwater (1 M KOH) with overpotentials of 191, 229, and 272 mV to achieve 10, 100, and 500 mA cm –2, respectively, alongside a low Tafel slope of 34.5 mV dec –1, while maintaining stability for 530 h at 500 mA cm –2 . In alkaline simulated seawater, it shows comparable activity (197/240/306 mV at the same current densities). Additionally, the self-assembled Pt/C/NF||NiFe LDH@Ni x Fe 3– x S 2 -2/NF couple delivers 10 mA cm –2 at 1.520 V for overall water splitting in an alkaline saline electrolyte. The enhanced performance is attributed to synergistic effects of hydroxide/sulfide nanointerfaces, low interfacial resistance, SO 4 2– -mediated Cl – repulsion/OOH* stabilization, and active β-NiOOH formation, underscoring its potential for practical seawater-based green hydrogen production.
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