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催化反应过程中的原位表面光谱学与显微镜技术:从团簇经纳米颗粒到中尺度聚集体

Operando Surface Spectroscopy and Microscopy during Catalytic Reactions: From Clusters via Nanoparticles to Meso-Scale Aggregates.

作者信息

Rupprechter Günther

机构信息

Institute of Materials Chemistry, Technische Universität Wien, Getreidemarkt 9/BC/01, Vienna, 1060, Austria.

出版信息

Small. 2021 Jul;17(27):e2004289. doi: 10.1002/smll.202004289. Epub 2021 Mar 10.

DOI:10.1002/smll.202004289
PMID:33694320
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11475487/
Abstract

Operando characterization of working catalysts, requiring per definitionem the simultaneous measurement of catalytic performance, is crucial to identify the relevant catalyst structure, composition and adsorbed species. Frequently applied operando techniques are discussed, including X-ray absorption spectroscopy, near ambient pressure X-ray photoelectron spectroscopy and infrared spectroscopy. In contrast to these area-averaging spectroscopies, operando surface microscopy by photoemission electron microscopy delivers spatially-resolved data, directly visualizing catalyst heterogeneity. For thorough interpretation, the experimental results should be complemented by density functional theory. The operando approach enables to identify changes of cluster/nanoparticle structure and composition during ongoing catalytic reactions and reveal how molecules interact with surfaces and interfaces. The case studies cover the length-scales from clusters via nanoparticles to meso-scale aggregates, and demonstrate the benefits of specific operando methods. Restructuring, ligand/atom mobility, and surface composition alterations during the reaction may have pronounced effects on activity and selectivity. The nanoscale metal/oxide interface steers catalytic performance via a long ranging effect. Combining operando spectroscopy with switching gas feeds or concentration-modulation provides further mechanistic insights. The obtained fundamental understanding is a prerequisite for improving catalytic performance and for rational design.

摘要

对工作催化剂进行原位表征(根据定义需要同时测量催化性能)对于确定相关的催化剂结构、组成和吸附物种至关重要。文中讨论了常用的原位技术,包括X射线吸收光谱、近常压X射线光电子能谱和红外光谱。与这些面积平均光谱不同,光发射电子显微镜原位表面显微镜可提供空间分辨数据,直接可视化催化剂的不均匀性。为了进行全面解释,实验结果应以密度泛函理论作为补充。原位方法能够识别正在进行的催化反应过程中团簇/纳米颗粒结构和组成的变化,并揭示分子如何与表面和界面相互作用。案例研究涵盖了从团簇到纳米颗粒再到介观尺度聚集体的长度尺度,并展示了特定原位方法的优势。反应过程中的结构重组、配体/原子迁移率和表面组成变化可能对活性和选择性产生显著影响。纳米级金属/氧化物界面通过长程效应控制催化性能。将原位光谱与切换气体进料或浓度调制相结合可提供更多的机理见解。所获得基本认识是提高催化性能和进行合理设计的先决条件。

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