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Exceptionally active iridium evolved from a pseudo-cubic perovskite for oxygen evolution in acid

Exploring robust catalysts for water oxidation in acidic electrolyte is challenging due to the limited material choice. Iridium (Ir) is the only active element with a high resistance to the acid corrosion during water electrolysis. However, Ir is rare, and its large-scale application could only be p...

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Detalles Bibliográficos
Autores principales: Chen, Yubo, Li, Haiyan, Wang, Jingxian, Du, Yonghua, Xi, Shibo, Sun, Yuanmiao, Sherburne, Matthew, Ager, Joel W., Fisher, Adrian C., Xu, Zhichuan J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6362036/
https://www.ncbi.nlm.nih.gov/pubmed/30718514
http://dx.doi.org/10.1038/s41467-019-08532-3
Descripción
Sumario:Exploring robust catalysts for water oxidation in acidic electrolyte is challenging due to the limited material choice. Iridium (Ir) is the only active element with a high resistance to the acid corrosion during water electrolysis. However, Ir is rare, and its large-scale application could only be possible if the intrinsic activity of Ir could be greatly enhanced. Here, a pseudo-cubic SrCo(0.9)Ir(0.1)O(3-δ) perovskite, containing corner-shared IrO6 octahedrons, is designed. The Ir in the SrCo(0.9)Ir(0.1)O(3-δ) catalyst shows an extremely high intrinsic activity as reflected from its high turnover frequency, which is more than two orders of magnitude higher than that of IrO(2). During the electrochemical cycling, a surface reconstruction, with Sr and Co leaching, over SrCo(0.9)Ir(0.1)O(3-δ) occurs. Such reconstructed surface region, likely contains a high amount of structural domains with corner-shared and under-coordinated IrO(x) octahedrons, is responsible for the observed high activity.