Sun Yan, Wu Cheng-Rong, Ding Tian-Yi, Gu Jian, Yan Jia-Wei, Cheng Jun, Zhang Kelvin H L
State Key Laboratory of Physical Chemistry of Solid Surfaces, iChEM, College of Chemistry and Chemical Engineering, Xiamen University Xiamen 361005 China
Innovation Laboratory for Sciences and Technologies of Energy Materials of Fujian Province (IKKEM) Xiamen 361005 China.
Chem Sci. 2023 May 2;14(22):5906-5911. doi: 10.1039/d2sc07034k. eCollection 2023 Jun 7.
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 LaNiO (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)/NiOOH redox transformation by quantifying STM images. Our findings demonstrate that 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.
镍基过渡金属氧化物因其储量丰富且活性高,是很有前景的析氧反应(OER)催化剂。识别和调控催化剂表面真实活性相的化学性质对于改善OER的反应动力学和效率至关重要。在此,我们利用电化学扫描隧道显微镜(EC-STM)直接观察了LaNiO(LNO)外延薄膜在OER过程中的结构动力学。基于对LNO表面终端不同组成的动态形貌变化的比较,我们提出表面形貌的重构源于OER过程中LNO表面终端上镍物种的转变。此外,通过对STM图像进行量化,我们表明LNO表面形貌的变化是由Ni(OH)/NiOOH氧化还原转变引起的。我们的研究结果表明,对薄膜进行可视化和量化表征对于揭示电化学条件下催化剂界面的动态性质非常重要。该策略对于深入理解OER的内在催化机制以及合理设计高效电催化剂至关重要。