Issue 22, 2023

Direct observation of the dynamic reconstructed active phase of perovskite LaNiO3 for the oxygen-evolution reaction

Abstract

Ni-based transition metal oxides are promising oxygen-evolution reaction (OER) catalysts due to their abundance and high activity. Identification and manipulation of the chemical properties of the real active phase on the catalyst surface is crucial to improve the reaction kinetics and efficiency of the OER. Herein, we used electrochemical-scanning tunnelling microscopy (EC-STM) to directly observe structural dynamics during the OER on LaNiO3 (LNO) epitaxial thin films. Based on comparison of dynamic topographical changes in different compositions of LNO surface termination, we propose that reconstruction of surface morphology originated from transition of Ni species on LNO surface termination during the OER. Furthermore, we showed that the change in surface topography of LNO was induced by Ni(OH)2/NiOOH redox transformation by quantifying STM images. Our findings demonstrate that in situ characterization for visualization and quantification of thin films is very important for revealing the dynamic nature of the interface of catalysts under electrochemical conditions. This strategy is crucial for in-depth understanding of the intrinsic catalytic mechanism of the OER and rational design of high-efficiency electrocatalysts.

Graphical abstract: Direct observation of the dynamic reconstructed active phase of perovskite LaNiO3 for the oxygen-evolution reaction

Supplementary files

Article information

Article type
Edge Article
Submitted
23 Dec 2022
Accepted
02 May 2023
First published
02 May 2023
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2023,14, 5906-5911

Direct observation of the dynamic reconstructed active phase of perovskite LaNiO3 for the oxygen-evolution reaction

Y. Sun, C. Wu, T. Ding, J. Gu, J. Yan, J. Cheng and K. H. L. Zhang, Chem. Sci., 2023, 14, 5906 DOI: 10.1039/D2SC07034K

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