Nickel-Induced Activation of Iron Foam for the Oxygen-Evolution Reaction: A Multimodal Study of Structure and Dynamics.

IF 4.3 2区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR
Negah Hashemi,Mohammad Mahdi Najafpour
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引用次数: 0

Abstract

Iron/nickel (hydr)oxides are widely recognized as efficient catalysts for the oxygen-evolution reaction (OER) in alkaline media. In this study, the effect of Ni on Fe foam toward OER activity is investigated. Treatment with nickel(II) nitrate induces the emergence of oxidation and reduction peaks, whose intensity and position are modulated by the nickel concentration on the iron foam surface. Remarkably, the OER onset potential exhibits a 240 mV reduction in overpotential upon the incorporation of nickel ions. In-situ Raman spectroscopy reveals the formation of γ-NiO(OH) during OER. Although substantial Fe ions are incorporated into the nickel (hydr)oxide matrix, reduced OER activity and a negative potential shift in the Ni(II)/(III) peak suggest Fe leaching during OER. Based on our findings, we propose a structure featuring multiple active sites, including nickel-doped iron hydroxide, iron oxide, nickel hydroxide, and mixed nickel/iron hydroxides with varying stoichiometries. This work highlights nickel-induced activation of iron foam to enhance OER performance, offering valuable insights for designing advanced, cost-effective, and durable electrocatalysts for applications such as water splitting and renewable energy storage systems.
镍诱导泡沫铁的析氧反应:结构和动力学的多模态研究。
铁/镍(氢)氧化物是碱性介质中析氧反应(OER)的高效催化剂。本研究考察了Ni对Fe泡沫塑料OER活性的影响。硝酸镍可诱导泡沫铁表面出现氧化还原峰,氧化还原峰的强度和位置受泡沫铁表面镍浓度的影响。值得注意的是,在镍离子掺入后,OER起始电位显示出240 mV的过电位降低。原位拉曼光谱揭示了OER过程中γ-NiO(OH)的形成。尽管大量铁离子被纳入镍(氢)氧化物基体中,但OER活性的降低和Ni(II)/(III)峰的负电位移动表明在OER过程中铁浸出。基于我们的发现,我们提出了一种具有多个活性位点的结构,包括掺杂镍的氢氧化铁、氧化铁、氢氧化镍和具有不同化学计量的混合镍/铁氢氧化物。这项工作强调了镍诱导泡沫铁活化以提高OER性能,为设计先进、经济、耐用的电催化剂提供了有价值的见解,可用于水分解和可再生能源存储系统等应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Inorganic Chemistry
Inorganic Chemistry 化学-无机化学与核化学
CiteScore
7.60
自引率
13.00%
发文量
1960
审稿时长
1.9 months
期刊介绍: Inorganic Chemistry publishes fundamental studies in all phases of inorganic chemistry. Coverage includes experimental and theoretical reports on quantitative studies of structure and thermodynamics, kinetics, mechanisms of inorganic reactions, bioinorganic chemistry, and relevant aspects of organometallic chemistry, solid-state phenomena, and chemical bonding theory. Emphasis is placed on the synthesis, structure, thermodynamics, reactivity, spectroscopy, and bonding properties of significant new and known compounds.
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