Suppr超能文献

利用原位X射线光电子能谱揭示镍/钇稳定氧化锆固体氧化物电解池电极在水电还原中的关键界面特性

Unveiling Key Interface Characteristics of Ni/Yttria-Stabilized Zirconia Solid Oxide Cell Electrodes in HO Electroreduction Using Operando X-ray Photoelectron Spectroscopy.

作者信息

Zhang Jinming, Barreau Mathias, Dintzer Thierry, Haevecker Michael, Teschner Detre, Efimenko Anna, Luo Wen, Zafeiratos Spyridon

机构信息

Institut de Chimie et Procédés pour l'Energie, l'Environnement et la Santé (ICPEES), ECPM, UMR 7515 CNRS-Université de Strasbourg, 25 Rue Becquerel, 67087 Strasbourg Cedex 02, France.

Max-Planck-Institut für Chemische Energiekonversion (MPI-CEC), Stiftstrasse 34-36, D-45470 Mülheim an der Ruhr, Germany.

出版信息

ACS Appl Mater Interfaces. 2024 Jul 24;16(29):37915-37926. doi: 10.1021/acsami.4c05046. Epub 2024 Jul 11.

Abstract

Nickel/yttria-stabilized zirconia (YSZ) composites are the most commonly used fuel electrodes for solid oxide cells. While microstructural changes of Ni/YSZ during operational conditions have been thoroughly investigated, there is limited knowledge regarding Ni/YSZ surface chemistry under working conditions. In this study, we examine the interaction between Ni/YSZ electrodes and water vapor under open circuit and polarization conditions, utilizing near ambient pressure soft and hard X-ray photoelectron spectroscopies. Miniature cells with conventional porous Ni/YSZ composite cermet cathodes were modified to facilitate the direct spectroscopic observation of the functional electrode's areas close to the interface with the YSZ electrolyte. The results highlight dynamic changes in the oxidation state and composition of Ni/YSZ under H and HO atmospheres. We also quantify the accumulation of impurities on the electrode surface. Through adjustments in the pretreatment of the cell, the correlation between the nickel surface oxidation state and the cell's electrochemical performance during HO electroreduction is established. It is unequivocally shown that nickel surface oxidation in HO electrolysis favors NiO over Ni(OH), providing critical insights into the mechanism of Ni-phase redistribution within the electrode during long-term operation. Depth-dependent photoemission measurements, combined with theoretical quantitative simulations, reveal that NiO and Ni phases are uniformly mixed on the surface during HO electrolysis. This differs from the conventional expectation of a NiO-shell/Ni-core configuration in gas phase oxidation. These findings provide crucial insights into the surface chemistry of Ni/YSZ electrodes under conditions relevant to HO electrolysis, elucidating their impact on the electrochemical performance of the cell.

摘要

镍/氧化钇稳定氧化锆(YSZ)复合材料是固体氧化物电池中最常用的燃料电极。虽然已经对工作条件下Ni/YSZ的微观结构变化进行了深入研究,但关于工作条件下Ni/YSZ的表面化学的了解却很有限。在本研究中,我们利用近常压软X射线和硬X射线光电子能谱,研究了开路和极化条件下Ni/YSZ电极与水蒸气之间的相互作用。对具有传统多孔Ni/YSZ复合金属陶瓷阴极的微型电池进行了改进,以便直接对功能电极靠近YSZ电解质界面的区域进行光谱观察。结果突出了在H和HO气氛下Ni/YSZ氧化态和组成的动态变化。我们还对电极表面杂质的积累进行了量化。通过调整电池的预处理,建立了镍表面氧化态与HO电还原过程中电池电化学性能之间的相关性。明确表明,HO电解中的镍表面氧化有利于生成NiO而非Ni(OH),这为长期运行过程中电极内镍相重新分布的机制提供了关键见解。深度相关的光发射测量与理论定量模拟相结合,揭示了HO电解过程中NiO和Ni相在表面均匀混合。这与气相氧化中传统预期的NiO壳层/Ni核结构不同。这些发现为与HO电解相关条件下Ni/YSZ电极的表面化学提供了关键见解,阐明了它们对电池电化学性能的影响。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验