Chee See Wee, Lunkenbein Thomas, Schlögl Robert, Cuenya Beatriz Roldan
Department of Interface Science, Fritz Haber Institute of the Max Planck Society, 14195 Berlin, Germany.
Department of Inorganic Chemistry, Fritz Haber Institute of the Max Planck Society, 14195 Berlin, Germany.
J Phys Condens Matter. 2021 Feb 26;33(15). doi: 10.1088/1361-648X/abddfd.
This review features state-of-the-artandelectron microscopy (EM) studies of heterogeneous catalysts in gas and liquid environments during reaction. Heterogeneous catalysts are important materials for the efficient production of chemicals/fuels on an industrial scale and for energy conversion applications. They also play a central role in various emerging technologies that are needed to ensure a sustainable future for our society. Currently, the rational design of catalysts has largely been hampered by our lack of insight into the working structures that exist during reaction and their associated properties. However, elucidating the working state of catalysts is not trivial, because catalysts are metastable functional materials that adapt dynamically to a specific reaction condition. The structural or morphological alterations induced by chemical reactions can also vary locally. A complete description of their morphologies requires that the microscopic studies undertaken span several length scales. EMs, especially transmission electron microscopes, are powerful tools for studying the structure of catalysts at the nanoscale because of their high spatial resolution, relatively high temporal resolution, and complementary capabilities for chemical analysis. Furthermore, recent advances have enabled the direct observation of catalysts under realistic environmental conditions using specialized reaction cells. Here, we will critically discuss the importance of spatially-resolvedmeasurements and the available experimental setups that enable (1) correlated studies where EM observations are complemented by separate measurements of reaction kinetics or spectroscopic analysis of chemical species during reaction or (2) real-time studies where the dynamics of catalysts are followed with EM and the catalytic performance is extracted directly from the reaction cell that is within the EM column or chamber. Examples of current research in this field will be presented. Challenges in the experimental application of these techniques and our perspectives on the field's future directions will also be discussed.
本综述重点介绍了在反应过程中,对气液环境中多相催化剂进行的最先进的电子显微镜(EM)研究。多相催化剂是在工业规模上高效生产化学品/燃料以及用于能量转换应用的重要材料。它们在确保我们社会可持续未来所需的各种新兴技术中也发挥着核心作用。目前,由于我们对反应过程中存在的工作结构及其相关性质缺乏深入了解,催化剂的合理设计在很大程度上受到了阻碍。然而,阐明催化剂的工作状态并非易事,因为催化剂是亚稳态功能材料,会动态适应特定的反应条件。化学反应引起的结构或形态变化也可能局部不同。对其形态的完整描述要求所进行的微观研究跨越多个长度尺度。电子显微镜,尤其是透射电子显微镜,由于其高空间分辨率、相对较高的时间分辨率以及化学分析的互补能力,是研究纳米级催化剂结构的强大工具。此外,最近的进展使得能够使用专门的反应池在实际环境条件下直接观察催化剂。在这里,我们将批判性地讨论空间分辨测量的重要性以及可用的实验装置,这些装置能够实现:(1)相关研究,即通过反应动力学的单独测量或反应过程中化学物种的光谱分析来补充电子显微镜观察;(2)实时研究,即利用电子显微镜跟踪催化剂的动态变化,并直接从电子显微镜柱或腔室内的反应池中提取催化性能。将展示该领域当前研究的实例。还将讨论这些技术在实验应用中的挑战以及我们对该领域未来方向的展望。