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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Tien, Eu Pin
Diamond Light Source
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (3/3 displayed)
- 2024Electron Beam and Thermal Stabilities of MFM-300(M) Metal-Organic Frameworkscitations
- 2017In Situ Industrial Bimetallic Catalyst Characterisation using Scanning Transmission Electron Microscopy and X-Ray Absorption Spectroscopy at One Atmosphere and Elevated Temperaturecitations
- 2017In Situ Industrial Bimetallic Catalyst Characterisation using Scanning Transmission Electron Microscopy and X-Ray Absorption Spectroscopy at One Atmosphere and Elevated Temperaturecitations
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article
In Situ Industrial Bimetallic Catalyst Characterisation using Scanning Transmission Electron Microscopy and X-Ray Absorption Spectroscopy at One Atmosphere and Elevated Temperature
Abstract
We have developed a new experimental platform for in situ scanning transmission electron microscope (STEM) energy dispersive X-ray spectroscopy (EDS) which allows real time, nanoscale, elemental and structural changes to be studied at elevated temperature (up to 1000°C) and pressure (up to 1 atm). Here we demonstrate the first application of this approach to understand complex structural changes occurring during reduction of a bimetallic catalyst, PdCu supported on TiO2, synthesized by wet impregnation. We reveal a heterogeneous evolution of nanoparticle size, particle distribution and composition with large differences in reduction behavior for the two metals. We show that the data obtained is complementary to in situ STEM electron energy loss spectroscopy (EELS) and when combined with in situ X-ray absorption spectroscopy (XAS) allows correlation of bulk chemical state with nanoscale changes in elemental distribution during reduction, facilitating new understanding of the catalytic behavior for this important class of materials.