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  Dynamics of palladium single-atoms on graphitic carbon nitride during ethylene hydrogenation

Vennewald, M., Sackers, N. M., Iemhoff, A., Kappel, I., Weidenthaler, C., Meise, A., et al. (2023). Dynamics of palladium single-atoms on graphitic carbon nitride during ethylene hydrogenation. Journal of Catalysis, 421(5), 134-144. doi:10.1016/j.jcat.2023.03.011.

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 Creators:
Vennewald, Maurice1, Author
Sackers, Nina Michelle1, Author
Iemhoff, Andree1, Author
Kappel, Isabella2, Author           
Weidenthaler, Claudia2, Author           
Meise, Ansgar3, Author
Heggen, Marc3, Author
Dunin-Borkowski, Rafal E.3, Author
Keenan, Luke4, Author
Palkovits, Regina1, 5, Author
Affiliations:
1Chair of Heterogeneous Catalysis and Chemical Technology, ITMC, RWTH Aachen University, Worringerweg 2, DE-52074 Aachen, Germany, ou_persistent22              
2Research Group Weidenthaler, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1950291              
3Ernst Ruska-Centre for Microscopy and Spectroscopy with Electrons (ER-C), Forschungszentrum Jülich GmbH, DE-52428 Jülich, Germany, ou_persistent22              
4Diamond Light Source, Harwell Science and Innovation Campus, Didcot OX110DE, United Kingdom, ou_persistent22              
5Max-Planck-Institute for Chemical Energy Conversion, Stiftstraße 34-36, DE-45470 Mülheim an der Ruhr, Germany, ou_persistent22              

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 Abstract: Single-atoms on carbon–nitrogen supports are considered catalysts for a multitude of reactions. However, doubts remain whether really these species or subnanometer clusters formed under reaction conditions are the active species. In this work, we investigate the dynamics of palladium single-atoms on graphitic carbon nitride during ethylene hydrogenation and H2-D2 exchange. By employing aberration-corrected scanning transmission electron microscopy, x-ray photoelectron spectroscopy and x-ray absorption spectroscopy, we will show that palladium, originally present as single-atoms, agglomerates to clusters at 100 °C in a gas atmosphere that contains both ethylene and hydrogen. This agglomeration goes in hand with the emergence of catalytic activity in both ethylene hydrogenation and H2-D2 exchange, suggesting that clusters, rather than single-atoms, are the active species. The results presented herein highlight the potential of analytics over the course of reaction to identify the active species and provide new insights into the influence of gas atmosphere on metal speciation.

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Language(s): eng - English
 Dates: 2022-11-302023-03-082023-05-01
 Publication Status: Issued
 Pages: 11
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1016/j.jcat.2023.03.011
 Degree: -

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Title: Journal of Catalysis
  Abbreviation : J. Catal.
Source Genre: Journal
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Publ. Info: Amsterdam : Elsevier
Pages: - Volume / Issue: 421 (5) Sequence Number: - Start / End Page: 134 - 144 Identifier: ISSN: 0021-9517
CoNE: https://pure.mpg.de/cone/journals/resource/954922645027