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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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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 |
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. |
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