Zhang Hongbo, Zhao Yiting, Cheng Zhenfeng, Jiang Jingyun, Fu Jianwei, Xu Qun
School of Materials Science and Engineering, Zhengzhou University, Zhengzhou, 450052, P. R. China.
Henan Institute of advanced technology, Zhengzhou University, Zhengzhou, 450052, P. R. China.
Small. 2024 Nov;20(47):e2405225. doi: 10.1002/smll.202405225. Epub 2024 Aug 19.
To meet the industrial demand for overall water splitting, oxygen evolution reaction (OER) electrocatalysts with low-cost, highly effective, and durable properties are urgently required. Herein, a facile confined strategy is utilized to construct 2D NiFeO/Ni(OH) heterostructures-based self-supporting electrode with surface-interfacial coengineering, in which abundant and ultrastable interfaces are developed. Under the high molar ratio of Ni/Fe, both spinel oxide and hydroxides phases are formed simultaneously to obtain 2D NiFeO/Ni(OH) heterostructure. The in-depth analysis indicates that the NiFeO/Ni(OH) interface displays strong electronic interactions and triggers the formation of crystalline-amorphous coexisting catalytic active NiOOH. Meanwhile, the stable catalyst-collector interface favors the electron transfer and oxygen molecules transport. The resultant 2D NiFeO/Ni(OH)@CP electrode exhibits superior OER performance, including a low overpotential of 389 mV and a long operating time of 12 h at 1 A cm. This work paves a novel method for fabricating efficient and low-cost electrocatalysts for electrochemical conversation devices.
为满足工业对整体水分解的需求,迫切需要具有低成本、高效且耐用性能的析氧反应(OER)电催化剂。在此,采用一种简便的受限策略来构建基于二维NiFeO/Ni(OH)异质结构的自支撑电极,并进行表面-界面协同工程,其中形成了丰富且超稳定的界面。在高镍/铁摩尔比下,同时形成尖晶石氧化物和氢氧化物相,从而获得二维NiFeO/Ni(OH)异质结构。深入分析表明,NiFeO/Ni(OH)界面表现出强烈的电子相互作用,并引发结晶-非晶共存的催化活性NiOOH的形成。同时,稳定的催化剂-集流体界面有利于电子转移和氧分子传输。所得的二维NiFeO/Ni(OH)@CP电极表现出优异的OER性能,包括在1 A cm下低至389 mV的过电位和12小时的长运行时间。这项工作为制造用于电化学转换装置的高效低成本电催化剂开辟了一种新方法。