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Reactivity and Passivation of Fe Nanoclusters on h‐BN/Rh(111)

The reactivity of iron nanocluster arrays on h‐BN/Rh(111) was studied using in situ high‐resolution X‐ray photoelectron spectroscopy. The morphology and reactivity of the iron nanoclusters (Fe‐NCs) were investigated by CO adsorption. On‐top and hollow/edge sites were determined to be the available a...

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Detalles Bibliográficos
Autores principales: Waleska, Natalie J., Düll, Fabian, Bachmann, Philipp, Hemauer, Felix, Steinhauer, Johann, Papp, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9290904/
https://www.ncbi.nlm.nih.gov/pubmed/34342077
http://dx.doi.org/10.1002/chem.202102590
Descripción
Sumario:The reactivity of iron nanocluster arrays on h‐BN/Rh(111) was studied using in situ high‐resolution X‐ray photoelectron spectroscopy. The morphology and reactivity of the iron nanoclusters (Fe‐NCs) were investigated by CO adsorption. On‐top and hollow/edge sites were determined to be the available adsorption sites on the as‐prepared Fe‐NCs and CO dissociation was observed at 300 K. C‐ and O‐precovered Fe‐NCs showed no catalytic activity towards CO dissociation because the hollow/edge sites were blocked by the C and O atoms. Therefore, these adsorption sites were identified to be the most active sites of the Fe‐NCs.