Chattot Raphaël, Martens Isaac, Mirolo Marta, Ronovsky Michal, Russello Florian, Isern Helena, Braesch Guillaume, Hornberger Elisabeth, Strasser Peter, Sibert Eric, Chatenet Marian, Honkimäki Veijo, Drnec Jakub
European Synchrotron Radiation Facility, ID 31 Beamline, BP 220, 38043 Grenoble, France.
Univ. Grenoble Alpes, Univ. Savoie Mont Blanc, CNRS, Grenoble INP, LEPMI, 38000 Grenoble, France.
J Am Chem Soc. 2021 Oct 20;143(41):17068-17078. doi: 10.1021/jacs.1c06780. Epub 2021 Oct 8.
The theoretical design of effective metal electrocatalysts for energy conversion and storage devices relies greatly on supposed unilateral effects of catalysts structure on electrocatalyzed reactions. Here, by using high-energy X-ray diffraction from the new Extremely Brilliant Source of the European Synchrotron Radiation Facility (ESRF-EBS) on device-relevant Pd and Pt nanocatalysts during cyclic voltammetry experiments in liquid electrolytes, we reveal the near ubiquitous feedback from various electrochemical processes on nanocatalyst strain. Beyond challenging and extending the current understanding of practical nanocatalysts behavior in electrochemical environment, the reported electrochemical strain provides experimental access to nanocatalysts absorption and adsorption trends (i.e., reactivity and stability descriptors) . The ease and power in monitoring such key catalyst properties at new and future beamlines is foreseen to provide a discovery platform toward the study of nanocatalysts encompassing a large variety of applications, from model environments to the device level.
用于能量转换和存储设备的高效金属电催化剂的理论设计在很大程度上依赖于催化剂结构对电催化反应的假定单向影响。在此,通过在液体电解质中进行循环伏安实验时,利用欧洲同步辐射装置(ESRF-EBS)新的极亮光源产生的高能X射线衍射对与器件相关的钯和铂纳米催化剂进行研究,我们揭示了各种电化学过程对纳米催化剂应变几乎普遍存在的反馈。除了挑战和扩展目前对电化学环境中实际纳米催化剂行为的理解之外,所报道的电化学应变还为纳米催化剂的吸收和吸附趋势(即反应性和稳定性描述符)提供了实验途径。预计在新的和未来的光束线上监测此类关键催化剂特性的简便性和强大功能将为研究涵盖从模型环境到器件层面等各种应用的纳米催化剂提供一个发现平台。