Issue 5, 2022

Direct evidence of cobalt oxyhydroxide formation on a La0.2Sr0.8CoO3 perovskite water splitting catalyst

Abstract

Understanding the mechanism of the oxygen evolution reaction (OER) on perovskite materials is of great interest for the development of more active catalysts. Despite a lot of literature reports, the complexity of catalytic systems and scarce in situ and operando surface sensitive spectroscopic tools render the detection of active sites and the understanding of reaction mechanisms challenging. Here, we carried out and compared in situ and ex situ ambient pressure X-ray photoelectron spectroscopy experiments on a La0.2Sr0.8CoO3−δ perovskite OER catalyst. The experimental results show that segregated surface strontium, which is present in the as prepared sample, is leached into the electrolyte after immersion, leading to surface cobalt active site enrichment. Such a cobalt-enriched oxide surface evolves into a new phase, whose spectral feature is detected in situ and after the OER. With the help of theoretical simulations, such a species is assigned to cobalt oxyhydroxide, providing direct evidence of its formation and surface segregation during the oxygen evolution reaction.

Graphical abstract: Direct evidence of cobalt oxyhydroxide formation on a La0.2Sr0.8CoO3 perovskite water splitting catalyst

Supplementary files

Article information

Article type
Paper
Submitted
11 Jun 2021
Accepted
13 Okt 2021
First published
13 Okt 2021

J. Mater. Chem. A, 2022,10, 2434-2444

Direct evidence of cobalt oxyhydroxide formation on a La0.2Sr0.8CoO3 perovskite water splitting catalyst

A. Boucly, L. Artiglia, E. Fabbri, D. Palagin, D. Aegerter, D. Pergolesi, Z. Novotny, N. Comini, J. T. Diulus, T. Huthwelker, M. Ammann and T. J. Schmidt, J. Mater. Chem. A, 2022, 10, 2434 DOI: 10.1039/D1TA04957G

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