A cell design for correlative hard X-ray nanoprobe and electron microscopy studies of catalysts under in situ conditions

纳米探针 纳米技术 材料科学 原位 透射电子显微镜 光束线 纳米颗粒 化学 光学 物理 梁(结构) 有机化学
作者
Julia E. Parker,Miguel A. Gomez‐Gonzalez,Yolanda Van Lishout,Husn Islam,Desirée Durán‐Martín,Doğan Özkaya,Paul D. Quinn,M. Schuster
出处
期刊:Journal of Synchrotron Radiation [International Union of Crystallography]
卷期号:29 (2): 431-438 被引量:10
标识
DOI:10.1107/s1600577521013576
摘要

To improve the understanding of catalysts, and ultimately the ability to design better materials, it is crucial to study them during their catalytic active states. Using in situ or operando conditions allows insights into structure-property relationships, which might not be observable by ex situ characterization. Spatially resolved X-ray fluorescence, X-ray diffraction and X-ray absorption near-edge spectroscopy are powerful tools to determine structural and electronic properties, and the spatial resolutions now achievable at hard X-ray nanoprobe beamlines make them an ideal complement to high-resolution transmission electron microscopy studies in a multi-length-scale analysis approach. The development of a system to enable the use of a commercially available gas-cell chip assembly within an X-ray nanoprobe beamline is reported here. The novel in situ capability is demonstrated by an investigation of the redox behaviour of supported Pt nanoparticles on ceria under typical lean and rich diesel-exhaust conditions; however, the system has broader application to a wide range of solid-gas reactions. In addition the setup allows complimentary in situ transmission electron microscopy and X-ray nanoprobe studies under identical conditions, with the major advantage compared with other systems that the exact same cell can be used and easily transferred between instruments. This offers the exciting possibility of studying the same particles under identical conditions (gas flow, pressure, temperature) using multiple techniques.
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