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dc.date.accessioned 2022-06-13T15:05:26Z
dc.date.available 2022-06-13T15:05:26Z
dc.date.issued 2018
dc.identifier.uri http://sedici.unlp.edu.ar/handle/10915/137742
dc.description.abstract We have studied the adsorption of reduced sulfur species on the Au(001)-hex surface from diluted ethanolic sulfide solutions by STM, XPS, electrochemical techniques, and DFT calculations. Our results reveal the absence of S multilayers because all S species are bonded to Au surface atoms. Monomeric S adsorbs at hollow sites forming a (2 × 2) lattice, while S2 species either capture the gold adatoms (Auad) that result from the hex lifting or remove Auad from the substrate forming well-ordered S8-like structures. These are formed by four S2 species coordinated by a central Auad, with AuSS interatomic distances closely resembling those of a metal disulfide. Our results explain not only the predominant surface structures on the gold surface but also topographic features, like Auad islands and Au vacancy islands, and also the chemical nature of adsorbed species from XPS S 2p spectra. In contrast to the S heads of small aromatic thiols, which exhibit a low affinity for Auad, strongly reactive sulfide species react with the metal adatoms leading to well-ordered complexes. en
dc.format.extent 2207-2214 es
dc.language en es
dc.subject Adsorption es
dc.subject Chemical structure es
dc.subject Gold es
dc.subject Lattices es
dc.subject Scanning tunneling microscopy es
dc.title Role of Gold Adatoms in the Adsorption of Sulfide Species on the Gold(001)-hex Surface en
dc.type Articulo es
sedici.identifier.other doi:10.1021/acs.jpcc.7b11059 es
sedici.identifier.issn 1932-7447 es
sedici.identifier.issn 1932-7455 es
sedici.creator.person Maza, Flavia Emilia Lobo es
sedici.creator.person Carro, Pilar es
sedici.creator.person Vericat, Carolina es
sedici.creator.person Kern, Klaus es
sedici.creator.person Salvarezza, Roberto Carlos es
sedici.creator.person Grumelli, Doris Elda es
sedici.subject.materias Química es
sedici.description.fulltext true es
mods.originInfo.place Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas es
sedici.subtype Preprint es
sedici.rights.license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
sedici.rights.uri http://creativecommons.org/licenses/by-nc-sa/4.0/
sedici.description.peerReview peer-review es
sedici.relation.journalTitle The Journal of Physical Chemistry C es
sedici.relation.journalVolumeAndIssue vol. 122, no. 4 es


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Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) Excepto donde se diga explícitamente, este item se publica bajo la siguiente licencia Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)