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Projekt Druckansicht

Oxidkatalysatoren für selektive Hydrierungsreaktionen

Fachliche Zuordnung Physikalische Chemie von Festkörpern und Oberflächen, Materialcharakterisierung
Förderung Förderung von 2017 bis 2023
Projektkennung Deutsche Forschungsgemeinschaft (DFG) - Projektnummer 321623572
 
Erstellungsjahr 2022

Zusammenfassung der Projektergebnisse

Inspired by work published in literature, we designed and carried out experiments and theoretical investigations to better understand the role of ceria as a heterogeneous catalyst for the hydrogenation of alkenes and alkynes to alkanes and alkenes. In order to get closer to a fundamental understanding we combined surface science studies on single crystalline samples with those on powder samples (Chinese Partner Group). The former allowed us, by combining a number of different experimental techniques, to prove the strong influence of oxygen vacancies on the interaction of hydrogen from the gasphase with the solid surface, by comparing stoichiometric and reduced, non-stoichiometric CeO2(111) surfaces. It has been demonstrated, that non-stoichiometric ceria interacts with hydrogen by forming hydroxyl species at the surface, and by getting oxidized (Ce3+ - Ce4+) via the formation of hydride species underneath the surface. It was possible through theoretical calculations to demonstrate, that, indeed, the energetics favor such a reaction route. Based on those findings work on powder samples were started in the partner group and it was jointly demonstrated that the same phenomena also apply to those samples. It became clear, that, although, the surface hydride formation is the kinetically favorable process at relatively low temperatures, the resulting surface hydride may diffuse into the bulk region and be stabilized therein. At higher temperatures, surface hydroxyls can react to produce water and create additional oxygen vacancies, increasing its concentration, which then controls the H2/CeO2 interaction. The results demonstrate a large diversity of reaction pathways, which have to be taken into account for a better understanding of the reactivity of ceria-based catalysts in a hydrogen-rich atmosphere. In addition to the interaction of hydrogen with ceria we also studied water adsorption and the interaction with hydrocarbons with single crystalline stoichiometric and non-stoichiometric samples. Extensive studies on reactivity have been carried out on powder samples by the partner group, and the obtained results with the model systems turned out to allow for a mechanistic understanding of the observed reactions.

Projektbezogene Publikationen (Auswahl)

 
 

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