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The Dynamic Structure of Au(38)(SR)(24) Nanoclusters Supported on CeO(2) upon Pretreatment and CO Oxidation

[Image: see text] Atomically precise thiolate protected Au nanoclusters Au(38)(SC(2)H(4)Ph)(24) on CeO(2) were used for in-situ (operando) extended X-ray absorption fine structure/diffuse reflectance infrared fourier transform spectroscopy and ex situ scanning transmission electron microscopy–high-a...

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Detalles Bibliográficos
Autores principales: Pollitt, Stephan, Truttmann, Vera, Haunold, Thomas, Garcia, Clara, Olszewski, Wojciech, Llorca, Jordi, Barrabés, Noelia, Rupprechter, Günther
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7295362/
https://www.ncbi.nlm.nih.gov/pubmed/32551181
http://dx.doi.org/10.1021/acscatal.0c01621
Descripción
Sumario:[Image: see text] Atomically precise thiolate protected Au nanoclusters Au(38)(SC(2)H(4)Ph)(24) on CeO(2) were used for in-situ (operando) extended X-ray absorption fine structure/diffuse reflectance infrared fourier transform spectroscopy and ex situ scanning transmission electron microscopy–high-angle annular dark-field imaging/X-ray photoelectron spectroscopy studies monitoring cluster structure changes induced by activation (ligand removal) and CO oxidation. Oxidative pretreatment at 150 °C “collapsed” the clusters’ ligand shell, oxidizing the hydrocarbon backbone, but the S remaining on Au acted as poison. Oxidation at 250 °C produced bare Au surfaces by removing S which migrated to the support (forming Au(+)-S), leading to highest activity. During reaction, structural changes occurred via CO-induced Au and O-induced S migration to the support. The results reveal the dynamics of nanocluster catalysts and the underlying cluster chemistry.