Frank Sara, Ceccato Marcel, Jeppesen Henrik S, Marks Melissa J, Nielsen Mads L N, Lu Ronghui, Gammelgaard Jens Jakob, Quinson Jonathan, Sharma Ruchi, Jensen Julie S, Hjelme Sara, Friberg Klysner Cecilie, Billinge Simon J L, Just Justus, Gjørup Frederik H, Catalano Jacopo, Lock Nina
Department of Biological and Chemical Engineering Aarhus University Åbogade 40 8200Aarhus N Denmark.
Deutsches Elektronen-Synchrotron (DESY) Notkestrasse 85 22607Hamburg Germany.
J Appl Crystallogr. 2024 Sep 20;57(Pt 5):1489-1502. doi: 10.1107/S1600576724007817. eCollection 2024 Oct 1.
Understanding the structure-property relationship in electrocatalysts under working conditions is crucial for the rational design of novel and improved catalytic materials. This paper presents the Aarhus University reactor for electrochemical studies using X-rays (AUREX) electrocatalytic flow cell, designed as an easy-to-use versatile setup with a minimal background contribution and a uniform flow field to limit concentration polarization and handle gas formation. The cell has been employed to measure total scattering, diffraction and absorption spectroscopy as well as simultaneous combinations thereof on a commercial silver electrocatalyst for proof of concept. This combination of techniques allows for monitoring of the short-, medium- and long-range structure under working conditions, including an applied potential, liquid electrolyte and local reaction environment. The structural transformations of the Ag electrocatalyst are monitored with non-negative matrix factorization, linear combination analysis, the Pearson correlation coefficient matrix, and refinements in both real and reciprocal space. Upon application of an oxidative potential in an Ar-saturated aqueous 0.1 KHCO/KCO electrolyte, the face-centered cubic (f.c.c.) Ag gradually transforms first to a trigonal AgCO phase, followed by the formation of a monoclinic AgCO phase. A reducing potential immediately reverts the structure to the Ag (f.c.c.) phase. Following the electrochemical-reaction-induced phase transitions is of fundamental interest and necessary for understanding and improving the stability of electrocatalysts, and the cell proves a versatile setup for probing this. In addition, it is demonstrated that, when studying electrochemical reactions, a high energy or short exposure time is needed to circumvent beam-induced effects.
了解工作条件下电催化剂的结构-性能关系对于合理设计新型和改进的催化材料至关重要。本文介绍了用于电化学研究的奥胡斯大学X射线电化学流动池(AUREX),它被设计成一种易于使用的通用装置,背景贡献最小,流场均匀,以限制浓度极化并处理气体生成。该流动池已用于在商业银电催化剂上测量总散射、衍射和吸收光谱以及它们的同时组合,以进行概念验证。这种技术组合允许在工作条件下监测短程、中程和长程结构,包括施加的电势、液体电解质和局部反应环境。通过非负矩阵分解、线性组合分析、皮尔逊相关系数矩阵以及实空间和倒易空间中的精修来监测银电催化剂的结构转变。在氩气饱和的0.1 KHCO/KCO水性电解质中施加氧化电势时,面心立方(f.c.c.)银首先逐渐转变为三角AgCO相,随后形成单斜AgCO相。还原电势立即将结构恢复到Ag(f.c.c.)相。跟踪电化学反应诱导的相变具有根本重要性,对于理解和提高电催化剂的稳定性是必要的,并且该流动池证明是用于探测此现象的通用装置。此外,还表明,在研究电化学反应时,需要高能量或短曝光时间来规避束流诱导效应。