Chen Xiaokang, Zhang Xiaohui, Zhuang Linzhou, Zhang Wei, Zhang Naichi, Liu Hongwei, Zhan Tianrong, Zhang Xiaoli, She Xilin, Yang Dongjiang
School of Environmental Science and Engineering, State Key Laboratory of Bio-fibers and Eco-textiles, Collaborative Innovation Center of Marine Biobased Materials, Qingdao University, Qingdao, 266071, P. R. China.
School of Chemical Engineering, East China University of Science and Technology, Shanghai, 200237, P. R. China.
Chem Asian J. 2020 Dec 1;15(23):3995-3999. doi: 10.1002/asia.202000468. Epub 2020 Oct 28.
Oxygen evolution reaction (OER) as the rate-determining reaction of water splitting has been attracting enormous attention. At present, only some noble-metal oxide materials (IrO and RuO ) have been reported as efficient OER electrocatalysts for OER. However, the high cost and scarcity of these noble-metal oxide materials greatly hamper their large-scale practical application. Herein, we synthesize 100% (111) faceted NiFe O single crystals with multiple vacancies (cation vacancies and O vacancies). The (111) facets can supply enough platform to break chemical bonds and enhance electrocatalytic activity, due to its high density of atomic steps and kink atoms. Compared to NiFe O (without vacancies), the as-synthesized NiFe O -Ar (with vacancies) exhibits a dramatically improved OER activity. The NiFe O -Ar-30 shows the lowest onset potential (1.45 V vs RHE) and the best electrocatalytic OER activity with the lowest overpotential of 234 mV at 50 mA cm . Furthermore, based on the theoretical calculations that the introduction of multiple vacancies can effectively modulate the electronic structure of active centers to accelerate charge transfer and reaction intermediates adsorption, which can reduce the reaction energy barrier and enhance the activity of electrochemical OER.
析氧反应(OER)作为水分解的速率决定反应,一直备受关注。目前,仅有一些贵金属氧化物材料(IrO和RuO)被报道为用于OER的高效析氧电催化剂。然而,这些贵金属氧化物材料的高成本和稀缺性极大地阻碍了它们的大规模实际应用。在此,我们合成了具有多种空位(阳离子空位和氧空位)的100%(111)面的NiFeO单晶。(111)面由于其高密度的原子台阶和扭结原子,能够提供足够的平台来断裂化学键并增强电催化活性。与NiFeO(无空位)相比,合成的NiFeO -Ar(有空位)表现出显著提高的析氧活性。NiFeO -Ar-30具有最低的起始电位(相对于可逆氢电极,为1.45 V),并且在50 mA cm时具有最低过电位234 mV的最佳析氧电催化活性。此外,基于理论计算,多种空位的引入可以有效地调节活性中心的电子结构,以加速电荷转移和反应中间体吸附,从而降低反应能垒并增强电化学析氧的活性。