Coverage-driven dissociation of azobenzene on Cu(111): a route towards defined surface functionalization

We investigate the surface-catalyzed dissociation of the archetypal molecular switch azobenzene on the Cu(111) surface. Based on X-ray photoelectron spectroscopy, normal incidence X-ray standing waves and density functional theory calculations a detailed picture of the coverage-induced formation of...

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Autori principali: Willenbockel, Martin (Autore) , Maurer, Reinhard J. (Autore) , Bronner, Christopher (Autore) , Schulze, Michael (Autore) , Stadtmüller, Benjamin (Autore) , Soubatch, Serguei (Autore) , Tegeder, Petra (Autore) , Reuter, Karsten (Autore) , Tautz, F. Stefan (Autore)
Natura: Article (Journal)
Lingua:inglese
Pubblicazione: 28 August 2015
In: Chemical communications
Year: 2015, Volume: 51, Fascicolo: 83, Pages: 15324-15327
ISSN:1364-548X
DOI:10.1039/C5CC05003K
Accesso online:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1039/C5CC05003K
Verlag, lizenzpflichtig, Volltext: https://pubs.rsc.org/en/content/articlelanding/2015/cc/c5cc05003k
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Note sull'autore:Martin Willenbockel, Reinhard J. Maurer, Christopher Bronner, Michael Schulze, Benjamin Stadtmüller, Serguei Soubatch, Petra Tegeder, Karsten Reuter and F. Stefan Tautz
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Riassunto:We investigate the surface-catalyzed dissociation of the archetypal molecular switch azobenzene on the Cu(111) surface. Based on X-ray photoelectron spectroscopy, normal incidence X-ray standing waves and density functional theory calculations a detailed picture of the coverage-induced formation of phenyl nitrene from azobenzene is presented. Furthermore, a comparison to the azobenzene/Ag(111) interface provides insight into the driving force behind the dissociation on Cu(111). The quantitative decay of azobenzene paves the way for the creation of a defect free, covalently bonded monolayer. Our work suggests a route of surface functionalization via suitable azobenzene derivatives and the on surface synthesis concept, allowing for the creation of complex immobilized molecular systems.
Descrizione del documento:Gesehen am 02.07.2020
Descrizione fisica:Online Resource
ISSN:1364-548X
DOI:10.1039/C5CC05003K