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A quasi in situ TEM grid reactor for decoupling catalytic gas phase reactions and analysis

MPS-Authors
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Masliuk,  Liudmyla
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Swoboda,  Manfred
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Algara-Siller,  Gerardo
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Schlögl,  Robert
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;
Heterogeneous Reactions, Max-Planck-Institute for Chemical Energy Conversion , Stiftstr. 34 - 36 45470 Mülheim an der Ruhr, Germany;

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Lunkenbein,  Thomas
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Fulltext (public)

Quasi in-situ TEM_rev_no_mark.pdf
(Any fulltext), 572KB

Supplementary Material (public)

SI_quasi_in-situ_TEM_rev_no_mark.pdf
(Supplementary material), 133KB

Citation

Masliuk, L., Swoboda, M., Algara-Siller, G., Schlögl, R., & Lunkenbein, T. (2018). A quasi in situ TEM grid reactor for decoupling catalytic gas phase reactions and analysis. Ultramicroscopy, 195, 121-128. doi:10.1016/j.ultramic.2018.09.001.


Cite as: https://hdl.handle.net/21.11116/0000-0002-6777-5
Abstract
We present a versatile grid reactor setup for transmission electron microscopy (TEM), which is able to track catalytic conversion on TEM amounts of sample. It is based on the concept of decoupling catalytic gas-phase reactions from the structural analysis of identical particles before and after reaction. The system has superior properties in terms of image resolution and long-term measurements compared to conventional in situ TEM analysis. Monitoring catalytic conversions on a TEM grid is enabled by proton-transfer reaction mass spectrometry. In addition, identical location imaging benefits from a secure transfer of the sample between TEM and the reactor system by vacuum transfer holders. Using Pt and Cu/ZnO/Al2O3 as an example we show that structural changes of identical particles or areas of a Pt foil before and after reactive experiments can be tracked. During catalytic testing the samples are exposed to homogeneous reaction conditions. The concept minimizes electron-sample and electron-atmosphere interactions and can prospectively be considered as complementary tool to in situ TEM analysis.