Piñeiro-García Alexis, Wu Xiuyu, Canto-Aguilar Esdras J, Kuzhikandathil Alice, Rafei Mouna, Gracia-Espino Eduardo
Department of Physics, Umeå University, SE-901 87 Umeå, Sweden.
ACS Appl Mater Interfaces. 2024 Dec 25;16(51):70429-70441. doi: 10.1021/acsami.4c10234. Epub 2024 Oct 13.
Robust electrocatalysts required to drive the oxygen evolution reaction (OER) during water electrolysis are still a missing component toward the path for sustainable hydrogen production. Here a new family of OER active quaternary mixed-oxides based on X-Sn-Mo-Sb (X = Mn, Fe, Co, or Ni) is reported. These nonstoichiometric mixed oxides form a rutile-type crystal structure with a random atomic motif and diverse oxidation states, leading to the formation of cation vacancies and local disorder. The successful incorporation of all cations into a rutile structure was achieved using oxidizing agents that facilitates the formation of Sb required to form the characteristic octahedral coordination in rutile. The mixed oxides exhibit enhanced stability in both acidic and alkaline environments under anodic potentials with no changes in their crystal structure after extensive electrochemical stress. The improved stability of these mixed oxides highlights their potential application as scaffolds to host and stabilize OER active metals.
在水电解过程中驱动析氧反应(OER)所需的强大电催化剂仍然是可持续制氢道路上缺失的一环。在此,报道了基于X-Sn-Mo-Sb(X = Mn、Fe、Co或Ni)的一类新型OER活性四元混合氧化物。这些非化学计量混合氧化物形成具有随机原子基序和多种氧化态的金红石型晶体结构,导致阳离子空位和局部无序的形成。使用促进形成金红石中形成特征八面体配位所需的Sb的氧化剂,成功地将所有阳离子掺入金红石结构中。在阳极电位下,这些混合氧化物在酸性和碱性环境中均表现出增强的稳定性,经过广泛的电化学应力后其晶体结构没有变化。这些混合氧化物稳定性的提高突出了它们作为承载和稳定OER活性金属的支架的潜在应用。