Li Cheng-Fei, Xie Ling-Jie, Zhao Jia-Wei, Gu Lin-Fei, Tang Hai-Bo, Zheng Lirong, Li Gao-Ren
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.
Angew Chem Int Ed Engl. 2022 Apr 19;61(17):e202116934. doi: 10.1002/anie.202116934. Epub 2022 Mar 2.
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.
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。