Wang Yunmeng, Fu Luhong, Wu Jiawei, Yang Fulin, Feng Ligang
School of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou, 225002, China.
Faculty of Materials Science and Engineering, Kunming University of Science and Technology, Kunming, 650093, China.
ChemSusChem. 2025 Mar 15;18(6):e202401580. doi: 10.1002/cssc.202401580. Epub 2024 Nov 14.
FeNi-based hybrid materials are promising oxygen evolution reaction (OER) catalysts for water electrolysis in hydrogen generation. In this work, the coordination tuning of FeNi-HMT frameworks was achieved by simply changing the Fe/Ni ratios using hexamethylenetetramine (HMT) as an organic ligand, and the derived hybrid FeNi catalysts with varied compositions were probed for OER. Incorporating varying amounts of Fe by adjusting the Ni/Fe ratio results in different metal-organic framework (MOF) structures, and higher Fe feed leads to the formation of amorphous structures due to the coordination structure destruction from the weaker coordination capacity of Fe compared to Ni combining with the tertiary amine ligand. Among them, the FeNi-HMT (with the Fe/Ni molar ratio of 1/1) derived catalyst, consisting of FeNi alloy/NiFeO spinel oxide heterostructures supported by graphitized carbon matrix, exhibits the highest OER performance. The unique structure facilitates significant electron transfer at the alloy/spinel interface due to the large work function difference between each phase. This strong electronic effect downshifts the d-band center of the catalyst and optimizes the binding energies to the crucial oxygenated intermediates, thereby promoting the OER kinetics. This work highlights the importance of the coordination tuning of FeNi-HMT frameworks for highly efficient catalyst development.
铁镍基混合材料是用于水电解制氢中析氧反应(OER)的有前景的催化剂。在这项工作中,通过使用六亚甲基四胺(HMT)作为有机配体简单地改变铁/镍比例,实现了FeNi - HMT框架的配位调节,并对衍生的不同组成的混合铁镍催化剂进行了OER研究。通过调节镍/铁比例掺入不同量的铁会导致不同的金属有机框架(MOF)结构,并且由于与镍相比铁与叔胺配体结合的配位能力较弱,导致配位结构破坏,较高的铁投料量会导致非晶结构的形成。其中,由石墨化碳基质支撑的FeNi合金/NiFeO尖晶石氧化物异质结构组成的FeNi - HMT(铁/镍摩尔比为1/1)衍生催化剂表现出最高的OER性能。由于各相之间的功函数差异大,这种独特的结构促进了合金/尖晶石界面处的显著电子转移。这种强电子效应使催化剂的d带中心下移,并优化了与关键含氧中间体的结合能,从而促进了OER动力学。这项工作突出了FeNi - HMT框架的配位调节对高效催化剂开发的重要性。