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界面Fe-O-Ni-O-Fe键合通过铁掺杂和用FeOOH修饰来调节Ni-MOFs的活性镍位点,以实现超高效析氧。

Interfacial Fe-O-Ni-O-Fe Bonding Regulates the Active Ni Sites of Ni-MOFs via Iron Doping and Decorating with FeOOH for Super-Efficient Oxygen Evolution.

作者信息

Li Cheng-Fei, Xie Ling-Jie, Zhao Jia-Wei, Gu Lin-Fei, Tang Hai-Bo, Zheng Lirong, Li Gao-Ren

机构信息

School of Chemistry, Sun Yat-sen University, Guangzhou, 510275, China.

Beijing Synchrotron Radiation Facility, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing, 100049, P.R. China.

出版信息

Angew Chem Int Ed Engl. 2022 Apr 19;61(17):e202116934. doi: 10.1002/anie.202116934. Epub 2022 Mar 2.

Abstract

The integration of Fe dopant and interfacial FeOOH into Ni-MOFs [Fe-doped-(Ni-MOFs)/FeOOH] to construct Fe-O-Ni-O-Fe bonding is demonstrated and the origin of remarkable electrocatalytic performance of Ni-MOFs is elucidated. X-ray absorption/photoelectron spectroscopy and theoretical calculation results indicate that Fe-O-Ni-O-Fe bonding can facilitate the distorted coordinated structure of the Ni site with a short nickel-oxygen bond and low coordination number, and can promote the redistribution of Ni/Fe charge density to efficiently regulate the adsorption behavior of key intermediates with a near-optimal d-band center. Here the Fe-doped-(Ni-MOFs)/FeOOH with interfacial Fe-O-Ni-O-Fe bonding shows superior catalytic performance for OER with a low overpotential of 210 mV at 15 mA cm and excellent stability with ≈3 % attenuation after a 120 h cycle test. This study provides a novel strategy to design high-performance Ni/Fe-based electrocatalysts for OER in alkaline media.

摘要

证明了将铁掺杂剂和界面氢氧化铁整合到镍基金属有机框架(Fe掺杂-(Ni-MOFs)/FeOOH)中以构建Fe-O-Ni-O-Fe键,并阐明了镍基金属有机框架显著电催化性能的起源。X射线吸收/光电子能谱和理论计算结果表明,Fe-O-Ni-O-Fe键可以促进具有短镍-氧键和低配位数的镍位点的扭曲配位结构,并可以促进Ni/Fe电荷密度的重新分布,以有效地调节具有接近最佳d带中心的关键中间体的吸附行为。在此,具有界面Fe-O-Ni-O-Fe键的Fe掺杂-(Ni-MOFs)/FeOOH对析氧反应表现出优异的催化性能,在15 mA cm下过电位低至210 mV,并且在120小时循环测试后具有约3%的衰减,稳定性优异。该研究为设计用于碱性介质中析氧反应的高性能镍/铁基电催化剂提供了一种新策略。

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