Elucidating intrinsic contribution of d-orbital states to oxygen evolution electrocatalysis in oxides.

Abstract

Although numerous studies on oxide catalysts for an efficient oxygen evolution reaction have been carried out to compare their catalytic performance and suggest new compositions, two significant constraints have been overlooked. One is the difference in electronic conduction behavior between catalysts (metallic versus insulating) and the other is the strong crystallographic surface orientation dependence of the catalysis in a crystal. Consequently, unless a comprehensive comparison of the oxygen-evolution catalytic activity between samples is made on a crystallographically identical surface with sufficient electron conduction, misleading interpretations on the catalytic performance and mechanism may be unavoidable. To overcome these limitations, we utilize both metallic (001) LaNiO₃ epitaxial thin films together with metal dopants and semiconducting (001) LaCoO₃ epitaxial thin films supported with a conductive interlayer. We identify that Fe, Cr, and Al are beneficial to enhance the catalysis in LaNiO₃ although their perovskite counterparts, LaFeO₃, LaCrO₃, and LaAlO₃, with a large bandgap are inactive. Furthermore, semiconducting LaCoO₃ is found to have more than one order higher activity than metallic LaNiO₃, in contrast to previous reports. Showing the importance of facilitating electron conduction, our work highlights the impact of the near-Fermi-level d-orbital states on the oxygen-evolution catalysis performance in perovskite oxides.