Authors (3): A. Chutia, D. J. Willock, C. R. A. .Catlow
Themes: Design (2018)
DOI: 10.1039/c8fd00002f
Citations: 14
Pub type: article-journal
Publisher: Royal Society of Chemistry (RSC)
Issue:
License: http://creativecommons.org/licenses/by/3.0/
Publication date(s): 2018 (online)
Pages: 123-145
Volume: 208 Issue:
Journal: Faraday Discussions
Link: http://pubs.rsc.org/en/content/articlepdf/2018/FD/C8FD00002F
URL: http://dx.doi.org/10.1039/C8FD00002F
We use density functional theory with Hubbard corrections (DFT+U) to understand the local electronic properties of Au adatom and Au2 dimer adsorption on the CeO2 (110) surface. We show that, based on the initial geometries, we can observe Au species in a variety of charge states including Au+, Au−, Auδ− and Auδ+–Auδ−. We present a detailed discussion using Bader charge analysis and partial density of states to support our observations. We also discuss the influence of solvent on the adsorption of Au adatoms adsorbed on top of an O-vacancy, which shows interesting geometrical and electronic properties.
Name | Description | Publised |
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c8fd00002f1.pdf | Supl. data for The electronic properties of Au clusters on CeO2 (110) su... | 2018 |