Surface structure and electron transfer dynamics of the self-assembly of cyanide on Au{111}

A vibronic resonance between Au{111} surface states and adsorbed CN vibrations has been predicted, which we target for study. We have formed stable monolayers of cyanide on Au{111} and observe a hexagonal close-packed lattice with a nearest neighbor distance of 3.8 ± 0.5 Å. Cyanide orients normal t...

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Main Authors: Guttentag, Andrew I. (Author) , Wächter, Tobias (Author) , Barr, Kristopher K. (Author) , Abendroth, John M. (Author) , Song, Tze-Bin (Author) , Sullivan, Nichole F. (Author) , Yang, Yang (Author) , Allara, David L. (Author) , Zharnikov, Michael (Author) , Weiss, Paul S. (Author)
Format: Article (Journal)
Language:English
Published: October 17, 2016
In: The journal of physical chemistry. C, Energy, materials, and catalysis
Year: 2016, Volume: 120, Issue: 47, Pages: 26736-26746
ISSN:1932-7455
DOI:10.1021/acs.jpcc.6b06006
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1021/acs.jpcc.6b06006
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Author Notes:Andrew I. Guttentag, Tobias Wächter, Kristopher K. Barr, John M. Abendroth, Tze-Bin Song, Nichole F. Sullivan, Yang Yang, David L. Allara, Michael Zharnikov, and Paul S. Weiss

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520 |a A vibronic resonance between Au{111} surface states and adsorbed CN vibrations has been predicted, which we target for study. We have formed stable monolayers of cyanide on Au{111} and observe a hexagonal close-packed lattice with a nearest neighbor distance of 3.8 ± 0.5 Å. Cyanide orients normal to the surface attached via a Au-C bond. We show that the substrate-molecule coupling is particularly strong, leading to ultrafast electron transfer from the cyanide molecules to the Au{111} substrate as measured by resonant Auger spectroscopy using the core-hole clock method. The CN/Au{111} system is a simple example of a strongly interacting adsorbate-substrate system and will be the subject of a number of further studies, as discussed. 
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