Wang Yue, Feliciano Gustavo T, Kumar Ashwani, Auer Alexander A, Tüysüz Harun
Department of Heterogeneous Catalysis, Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, D-45470, Mülheim an der Ruhr, Germany.
Department of Molecular Theory and Spectroscopy, Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, D-45470, Mülheim an der Ruhr, Germany.
ChemSusChem. 2025 Jul 27;18(15):e202500281. doi: 10.1002/cssc.202500281. Epub 2025 Jun 24.
The development of low-cost electrocatalysts for the oxygen evolution reaction (OER) of water electrolysis is crucial for large-scale green hydrogen production. NiFe-based electrocatalysts have garnered significant attention due to their high OER activity; however, the need for a rapid and efficient electrode fabrication method and a clear understanding of the role of Fe in enhancing OER activity remains unresolved. Herein, a highly active NiFe-based OER electrocatalyst self-supported on carbon fiber paper (CFP) is developed using a versatile and rapid thermal shock method, requiring only 30 s of heat treatment. The as-prepared FeNi/CFP shows a current density of 493 mA/cm at 1.7 V vs reversible hydrogen electrode (RHE) and a low overpotential of 247 mV at 10 mA/cm, with excellent long-term durability in alkaline conditions. In situ Raman spectroscopy, pH-dependance activity test, and electronic structure calculations reveal that Fe not only promotes the oxidation of adjacent Ni but also accelerates the deprotonation of adsorbed -OH groups and stabilizes oxo-intermediates, thus, displaying both direct and indirect effects and enhancing the overall OER performance. This article provides a foundation for developing cost-effective electrocatalysts for hydrogen production and other sustainable energy applications while enhancing the understanding of the role of Fe in NiO catalysts.
开发用于水电解析氧反应(OER)的低成本电催化剂对于大规模绿色制氢至关重要。镍铁基电催化剂因其高OER活性而备受关注;然而,快速高效的电极制备方法以及对铁在增强OER活性中作用的清晰理解仍未得到解决。在此,使用一种通用且快速的热冲击方法开发了一种自支撑在碳纤维纸(CFP)上的高活性镍铁基OER电催化剂,仅需30秒的热处理。所制备的FeNi/CFP在相对于可逆氢电极(RHE)的1.7 V下显示出493 mA/cm的电流密度,在10 mA/cm下具有247 mV的低过电位,在碱性条件下具有出色的长期耐久性。原位拉曼光谱、pH依赖性活性测试和电子结构计算表明,铁不仅促进相邻镍的氧化,还加速吸附的-OH基团的去质子化并稳定氧代中间体,从而显示出直接和间接效应并提高整体OER性能。本文为开发用于制氢和其他可持续能源应用的经济高效电催化剂提供了基础,同时增进了对铁在NiO催化剂中作用的理解。