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dc.contributor.author
Goduljan, Aleksej
dc.contributor.author
Moreira de Campos Pinto, Leandro
dc.contributor.author
Juarez, Maria Fernanda
dc.contributor.author
Santos, Elizabeth del Carmen
dc.contributor.author
Schmickler, Wolfgang
dc.date.available
2018-07-13T20:27:31Z
dc.date.issued
2016-02-23
dc.identifier.citation
Goduljan, Aleksej; Moreira de Campos Pinto, Leandro; Juarez, Maria Fernanda; Santos, Elizabeth del Carmen; Schmickler, Wolfgang; Oxygen Reduction on Ag(100) in Alkaline Solutions - A Theoretical Study; Wiley VCH Verlag; Chemphyschem; 17; 4; 23-2-2016; 500-505
dc.identifier.issn
1439-4235
dc.identifier.uri
http://hdl.handle.net/11336/52110
dc.description.abstract
Silver is much more reactive to oxygen than gold; nevertheless, in alkaline solutions, the rates of oxygen reduction on both metals are similar. To explain this phenomenon, the first, rate-determining step of oxygen reduction on Ag(100) is determined by a combination of DFT, molecular dynamics, and electrocatalysis theory. In vacuum, oxygen is adsorbed on Ag(100), but in the electrochemical environment, the adsorption energy is offset by the loss of hydration energy as the molecule approaches the surface. As a result, the first electron transfer should take place in an outer-sphere mode. Previously, the same mechanism for oxygen reduction on Au(100) has been predicted, and these calculations have been repeated by using a more advanced version of the electrocatalysis theory discussed herein to confirm previous conclusions. The theoretical results compare well with experimental data.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Wiley VCH Verlag
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
Density Functional Calculations
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Electrochemistry
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Electron Transfer
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Oxygen
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Silver
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Otras Ciencias Químicas
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Ciencias Químicas
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CIENCIAS NATURALES Y EXACTAS
dc.title
Oxygen Reduction on Ag(100) in Alkaline Solutions - A Theoretical Study
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2018-07-03T21:54:42Z
dc.identifier.eissn
1439-7641
dc.journal.volume
17
dc.journal.number
4
dc.journal.pagination
500-505
dc.journal.pais
Alemania
dc.journal.ciudad
Weinheim
dc.description.fil
Fil: Goduljan, Aleksej. Universidad de Ulm; Alemania
dc.description.fil
Fil: Moreira de Campos Pinto, Leandro. Universidad de Ulm; Alemania
dc.description.fil
Fil: Juarez, Maria Fernanda. Universidad de Ulm; Alemania. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
dc.description.fil
Fil: Santos, Elizabeth del Carmen. Universidad de Ulm; Alemania. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Física Enrique Gaviola. Universidad Nacional de Córdoba. Instituto de Física Enrique Gaviola; Argentina
dc.description.fil
Fil: Schmickler, Wolfgang. Universidad de Ulm; Alemania
dc.journal.title
Chemphyschem
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/abs/10.1002/cphc.201501036
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1002/cphc.201501036
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