Comparative Study of the Adsorption of Thiols and Selenols on Au(111) and Au(100)
- Autores
- Arisnabarreta, Nicolás; Ruano Sandoval, Gustavo Daniel; Lingenfelder, Magalí Alejandra; Patrito, Eduardo Martin; Cometto, Fernando Pablo
- Año de publicación
- 2017
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- The effect of the Au crystalline plane on the adsorption of different thiols and selenols is studied via reductive desorption (RD) and X-ray photoelectron spectroscopy (XPS) measurements. Self-assembled monolayers (SAMs) using aliphatic (ATs) and aromatic thiols (ArTs) on both Au(111) and Au(100) were prepared. The electrochemical stability of these SAMs on both surfaces is evaluated by comparing the position of the RD peaks. The longer the AT chain the more stable the SAM on Au(100) when compared to Au(111). By means of XPS measurements, we determine that the binding energy (BE) of the S 2p signal corresponding to the S atoms at the thiol/Au interface, commonly assigned at 162.0 eV, shifts 0.2 eV from Au(111) to Au(100) for SAMs prepared using thiols with the C∗ (C atom bonded to S) in sp3 hybridization, such as ATs. However, when the thiol presents the C∗ with an sp2 hybridization, such as in the case of ArTs, the BE remains at 162.0 eV regardless of the surface plane. Selenol-based SAMs were characterized comparatively on both Au(100) and Au(111). Our results show that selenol SAMs become even more electrochemically stable on Au(100) with respect to Au(111) than the analogue sulfur-based SAM. According to our results, we suggest that the electronic distribution around the Au-S/Se bond could be responsible for the different structural arrangements reported in the literature (gold adatoms, etc.), which should be dependent on the crystalline face (Au(hkl)-S) and the chemical nature of the environment of the adsorbates (sp3-C∗ vs sp2-C∗ and Au-SR vs Au-SeR).
Fil: Arisnabarreta, Nicolás. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina
Fil: Ruano Sandoval, Gustavo Daniel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Física del Litoral. Universidad Nacional del Litoral. Instituto de Física del Litoral; Argentina
Fil: Lingenfelder, Magalí Alejandra. Max Planck-EPFL Laboratory for Molecular Nanoscience; Suiza
Fil: Patrito, Eduardo Martin. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina
Fil: Cometto, Fernando Pablo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina - Materia
-
SAM
THIOLS
SELENOLS
XPS
CVA
ELECTROCHEMICAL STABILITY - Nivel de accesibilidad
- acceso embargado
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/37975
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Comparative Study of the Adsorption of Thiols and Selenols on Au(111) and Au(100)Arisnabarreta, NicolásRuano Sandoval, Gustavo DanielLingenfelder, Magalí AlejandraPatrito, Eduardo MartinCometto, Fernando PabloSAMTHIOLSSELENOLSXPSCVAELECTROCHEMICAL STABILITYhttps://purl.org/becyt/ford/1.3https://purl.org/becyt/ford/1The effect of the Au crystalline plane on the adsorption of different thiols and selenols is studied via reductive desorption (RD) and X-ray photoelectron spectroscopy (XPS) measurements. Self-assembled monolayers (SAMs) using aliphatic (ATs) and aromatic thiols (ArTs) on both Au(111) and Au(100) were prepared. The electrochemical stability of these SAMs on both surfaces is evaluated by comparing the position of the RD peaks. The longer the AT chain the more stable the SAM on Au(100) when compared to Au(111). By means of XPS measurements, we determine that the binding energy (BE) of the S 2p signal corresponding to the S atoms at the thiol/Au interface, commonly assigned at 162.0 eV, shifts 0.2 eV from Au(111) to Au(100) for SAMs prepared using thiols with the C∗ (C atom bonded to S) in sp3 hybridization, such as ATs. However, when the thiol presents the C∗ with an sp2 hybridization, such as in the case of ArTs, the BE remains at 162.0 eV regardless of the surface plane. Selenol-based SAMs were characterized comparatively on both Au(100) and Au(111). Our results show that selenol SAMs become even more electrochemically stable on Au(100) with respect to Au(111) than the analogue sulfur-based SAM. According to our results, we suggest that the electronic distribution around the Au-S/Se bond could be responsible for the different structural arrangements reported in the literature (gold adatoms, etc.), which should be dependent on the crystalline face (Au(hkl)-S) and the chemical nature of the environment of the adsorbates (sp3-C∗ vs sp2-C∗ and Au-SR vs Au-SeR).Fil: Arisnabarreta, Nicolás. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; ArgentinaFil: Ruano Sandoval, Gustavo Daniel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Física del Litoral. Universidad Nacional del Litoral. Instituto de Física del Litoral; ArgentinaFil: Lingenfelder, Magalí Alejandra. Max Planck-EPFL Laboratory for Molecular Nanoscience; SuizaFil: Patrito, Eduardo Martin. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; ArgentinaFil: Cometto, Fernando Pablo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; ArgentinaAmerican Chemical Society2017-12info:eu-repo/date/embargoEnd/2018-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/37975Arisnabarreta, Nicolás; Ruano Sandoval, Gustavo Daniel; Lingenfelder, Magalí Alejandra; Patrito, Eduardo Martin; Cometto, Fernando Pablo; Comparative Study of the Adsorption of Thiols and Selenols on Au(111) and Au(100); American Chemical Society; Langmuir; 33; 48; 12-2017; 13733-137390743-7463CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/http://pubs.acs.org/doi/10.1021/acs.langmuir.7b03038info:eu-repo/semantics/altIdentifier/doi/10.1021/acs.langmuir.7b03038info:eu-repo/semantics/embargoedAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-15T15:09:50Zoai:ri.conicet.gov.ar:11336/37975instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-10-15 15:09:50.713CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Comparative Study of the Adsorption of Thiols and Selenols on Au(111) and Au(100) |
title |
Comparative Study of the Adsorption of Thiols and Selenols on Au(111) and Au(100) |
spellingShingle |
Comparative Study of the Adsorption of Thiols and Selenols on Au(111) and Au(100) Arisnabarreta, Nicolás SAM THIOLS SELENOLS XPS CVA ELECTROCHEMICAL STABILITY |
title_short |
Comparative Study of the Adsorption of Thiols and Selenols on Au(111) and Au(100) |
title_full |
Comparative Study of the Adsorption of Thiols and Selenols on Au(111) and Au(100) |
title_fullStr |
Comparative Study of the Adsorption of Thiols and Selenols on Au(111) and Au(100) |
title_full_unstemmed |
Comparative Study of the Adsorption of Thiols and Selenols on Au(111) and Au(100) |
title_sort |
Comparative Study of the Adsorption of Thiols and Selenols on Au(111) and Au(100) |
dc.creator.none.fl_str_mv |
Arisnabarreta, Nicolás Ruano Sandoval, Gustavo Daniel Lingenfelder, Magalí Alejandra Patrito, Eduardo Martin Cometto, Fernando Pablo |
author |
Arisnabarreta, Nicolás |
author_facet |
Arisnabarreta, Nicolás Ruano Sandoval, Gustavo Daniel Lingenfelder, Magalí Alejandra Patrito, Eduardo Martin Cometto, Fernando Pablo |
author_role |
author |
author2 |
Ruano Sandoval, Gustavo Daniel Lingenfelder, Magalí Alejandra Patrito, Eduardo Martin Cometto, Fernando Pablo |
author2_role |
author author author author |
dc.subject.none.fl_str_mv |
SAM THIOLS SELENOLS XPS CVA ELECTROCHEMICAL STABILITY |
topic |
SAM THIOLS SELENOLS XPS CVA ELECTROCHEMICAL STABILITY |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.3 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
The effect of the Au crystalline plane on the adsorption of different thiols and selenols is studied via reductive desorption (RD) and X-ray photoelectron spectroscopy (XPS) measurements. Self-assembled monolayers (SAMs) using aliphatic (ATs) and aromatic thiols (ArTs) on both Au(111) and Au(100) were prepared. The electrochemical stability of these SAMs on both surfaces is evaluated by comparing the position of the RD peaks. The longer the AT chain the more stable the SAM on Au(100) when compared to Au(111). By means of XPS measurements, we determine that the binding energy (BE) of the S 2p signal corresponding to the S atoms at the thiol/Au interface, commonly assigned at 162.0 eV, shifts 0.2 eV from Au(111) to Au(100) for SAMs prepared using thiols with the C∗ (C atom bonded to S) in sp3 hybridization, such as ATs. However, when the thiol presents the C∗ with an sp2 hybridization, such as in the case of ArTs, the BE remains at 162.0 eV regardless of the surface plane. Selenol-based SAMs were characterized comparatively on both Au(100) and Au(111). Our results show that selenol SAMs become even more electrochemically stable on Au(100) with respect to Au(111) than the analogue sulfur-based SAM. According to our results, we suggest that the electronic distribution around the Au-S/Se bond could be responsible for the different structural arrangements reported in the literature (gold adatoms, etc.), which should be dependent on the crystalline face (Au(hkl)-S) and the chemical nature of the environment of the adsorbates (sp3-C∗ vs sp2-C∗ and Au-SR vs Au-SeR). Fil: Arisnabarreta, Nicolás. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina Fil: Ruano Sandoval, Gustavo Daniel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Santa Fe. Instituto de Física del Litoral. Universidad Nacional del Litoral. Instituto de Física del Litoral; Argentina Fil: Lingenfelder, Magalí Alejandra. Max Planck-EPFL Laboratory for Molecular Nanoscience; Suiza Fil: Patrito, Eduardo Martin. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina Fil: Cometto, Fernando Pablo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina |
description |
The effect of the Au crystalline plane on the adsorption of different thiols and selenols is studied via reductive desorption (RD) and X-ray photoelectron spectroscopy (XPS) measurements. Self-assembled monolayers (SAMs) using aliphatic (ATs) and aromatic thiols (ArTs) on both Au(111) and Au(100) were prepared. The electrochemical stability of these SAMs on both surfaces is evaluated by comparing the position of the RD peaks. The longer the AT chain the more stable the SAM on Au(100) when compared to Au(111). By means of XPS measurements, we determine that the binding energy (BE) of the S 2p signal corresponding to the S atoms at the thiol/Au interface, commonly assigned at 162.0 eV, shifts 0.2 eV from Au(111) to Au(100) for SAMs prepared using thiols with the C∗ (C atom bonded to S) in sp3 hybridization, such as ATs. However, when the thiol presents the C∗ with an sp2 hybridization, such as in the case of ArTs, the BE remains at 162.0 eV regardless of the surface plane. Selenol-based SAMs were characterized comparatively on both Au(100) and Au(111). Our results show that selenol SAMs become even more electrochemically stable on Au(100) with respect to Au(111) than the analogue sulfur-based SAM. According to our results, we suggest that the electronic distribution around the Au-S/Se bond could be responsible for the different structural arrangements reported in the literature (gold adatoms, etc.), which should be dependent on the crystalline face (Au(hkl)-S) and the chemical nature of the environment of the adsorbates (sp3-C∗ vs sp2-C∗ and Au-SR vs Au-SeR). |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017-12 info:eu-repo/date/embargoEnd/2018-06-01 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/37975 Arisnabarreta, Nicolás; Ruano Sandoval, Gustavo Daniel; Lingenfelder, Magalí Alejandra; Patrito, Eduardo Martin; Cometto, Fernando Pablo; Comparative Study of the Adsorption of Thiols and Selenols on Au(111) and Au(100); American Chemical Society; Langmuir; 33; 48; 12-2017; 13733-13739 0743-7463 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/37975 |
identifier_str_mv |
Arisnabarreta, Nicolás; Ruano Sandoval, Gustavo Daniel; Lingenfelder, Magalí Alejandra; Patrito, Eduardo Martin; Cometto, Fernando Pablo; Comparative Study of the Adsorption of Thiols and Selenols on Au(111) and Au(100); American Chemical Society; Langmuir; 33; 48; 12-2017; 13733-13739 0743-7463 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/http://pubs.acs.org/doi/10.1021/acs.langmuir.7b03038 info:eu-repo/semantics/altIdentifier/doi/10.1021/acs.langmuir.7b03038 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/embargoedAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
embargoedAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
American Chemical Society |
publisher.none.fl_str_mv |
American Chemical Society |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1846083246533640192 |
score |
13.221938 |