4.8 Article

Heterogeneous lamellar-edged Fe-Ni(OH)2/Ni3S2 nanoarray for efficient and stable seawater oxidation

期刊

NANO RESEARCH
卷 14, 期 4, 页码 1149-1155

出版社

TSINGHUA UNIV PRESS
DOI: 10.1007/s12274-020-3164-3

关键词

lamellar edges; Fe-Ni(OH)(2)/Ni3S2 seawater oxidation; chlorine electrochemistry; electrocatalysis

资金

  1. National Natural Science Foundation of China [91963113]

向作者/读者索取更多资源

The study presents a heterostructure of Ni3S2 nanoarray with Fe-Ni(OH)(2) edges for efficient catalysis in seawater electrolysis, demonstrating high Faraday efficiency for oxygen evolution reaction and good stability. The introduction of Fe activator and heterostructure design offer massive active and selective sites, providing insights for the rational design of high-performance Fe-based electrodes for industrial seawater electrolysis.
Development of efficient non-precious catalysts for seawater electrolysis is of great significance but challenging due to the sluggish kinetics of oxygen evolution reaction (OER) and the impairment of chlorine electrochemistry at anode. Herein, we report a heterostructure of Ni3S2 nanoarray with secondary Fe-Ni(OH)(2) lamellar edges that exposes abundant active sites towards seawater oxidation. The resultant Fe-Ni(OH)(2)/Ni3S2 nanoarray works directly as a free-standing anodic electrode in alkaline artificial seawater. It only requires an overpotential of 269 mV to afford a current density of 10 mA center dot cm(-2) and the Tafel slope is as low as 46 mV center dot dec(-1). The 27-hour chronopotentiometry operated at high current density of 100 mA center dot cm(-2) shows negligible deterioration, suggesting good stability of the Fe center dot Ni(OH)(2)/Ni3S2@NF electrode. Faraday efficiency for oxygen evolution is up to similar to 95%, revealing decent selectivity of the catalyst in saline water. Such desirable catalytic performance could be benefitted from the introduction of Fe activator and the heterostructure that offers massive active and selective sites. The density functional theory (DFT) calculations indicate that the OER has lower theoretical overpotential than Cl-2 evolution reaction in Fe sites, which is contrary to that of Ni sites. The experimental and theoretical study provides a strong support for the rational design of high-performance Fe-based electrodes for industrial seawater electrolysis.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据