海水
电解
材料科学
过电位
化学工程
双功能
阳极
析氧
无机化学
图层(电子)
催化作用
兴奋剂
电解水
电极
电化学
纳米技术
化学
电解质
物理化学
光电子学
有机化学
工程类
地质学
海洋学
作者
Minghui Xing,Shitao Wang,Jimmy Yun,Dapeng Cao
出处
期刊:Small
[Wiley]
日期:2024-08-09
标识
DOI:10.1002/smll.202402852
摘要
Abstract The seawater electrolysis to produce hydrogen is a significant topic on alleviating the energy crisis. Here, the Fe, Nb‐Ni 3 S 2 catalyst is prepared by metal‐doping strategy, and it shows high oxygen evolution reaction (OER) activity in alkaline medium, and only needs 1.491 V to deliver a current density of 100 mA cm −2 in simulated seawater. Using Fe, Nb‐Ni 3 S 2 as a bifunctional catalyst, the two‐electrode electrolyzer only requires a voltage of 1.751 V (without impedance compensation) to drive the current density of 50 mA cm −2 , and can run over 150 h stably in the simulated seawater. Importantly, In situ Raman test demonstrates that the outstanding performance of Fe, Nb‐Ni 3 S 2 in simulated seawater is ascribed to the in situ formed sulfate protective layer induced by Nb doping, which can effectively inhibit the corrosion of chloride ion, while the protective layer is absent for Fe‐Ni 3 S 2 . The stable operation of simulated seawater electrolysis under industrial current density further confirms the stability improvement mechanism of forming protective layer. In short, this study provides a new strategy of using Nb dopants inducing the formation of protective layer to enhance the stability of seawater electrolysis.
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