Zhao Jia-Wei, Yue Kaihang, Zhang Hong, Wei Shu-Yin, Zhu Jiawei, Wang Dongdong, Chen Junze, Fominski Vyacheslav Yu, Li Gao-Ren
College of Materials Science and Engineering, Sichuan University, Chengdu, 610065, China.
School of Chemistry, Sun Yat-sen University, Guangzhou, 510275, China.
Nat Commun. 2024 Apr 4;15(1):2928. doi: 10.1038/s41467-024-46801-y.
Electrocatalytic water splitting is a promising route for sustainable hydrogen production. However, the high overpotential of the anodic oxygen evolution reaction poses significant challenge. SrIrO-based perovskite-type catalysts have shown great potential for acidic oxygen evolution reaction, but the origins of their high activity are still unclear. Herein, we develop a Co-doped SrIrO system to enhance oxygen evolution reaction activity and elucidate the origin of catalytic activity. In situ experiments reveal Co activates surface lattice oxygen, rapidly exposing IrO active sites, while bulk Co doping optimizes the adsorbate binding energy of IrO. The Co-doped SrIrO demonstrates high oxygen evolution reaction electrocatalytic activity, markedly surpassing the commercial IrO catalysts in both conventional electrolyzer and proton exchange membrane water electrolyzer.
电催化水分解是可持续制氢的一条有前景的途径。然而,阳极析氧反应的高过电位带来了重大挑战。基于SrIrO的钙钛矿型催化剂在酸性析氧反应中显示出巨大潜力,但其高活性的来源仍不清楚。在此,我们开发了一种Co掺杂的SrIrO体系,以提高析氧反应活性并阐明催化活性的来源。原位实验表明,Co激活了表面晶格氧,迅速暴露出IrO活性位点,而体相Co掺杂优化了IrO的吸附质结合能。Co掺杂的SrIrO表现出高析氧反应电催化活性,在传统电解槽和质子交换膜水电解槽中均明显超过商业IrO催化剂。