Formation, characterization and electrocatalytic activity of layer-by-layer self-assembled films containing polyoxomolybdate over Au surfaces

Autores
Volker, Edgar; Calvo, Ernesto Julio; Williams, Federico José
Año de publicación
2012
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
We describe a novel strategy for the controlled fabrication of well-defined multilayer films incorporating a polyoxomolybdate anion (PMo12 O3À , POM) via ion exchange on Au electrodes. Composite films were 40 thoroughly characterized by ellipsometry, X-ray photoelectron spectroscopy (XPS), FTIR-ATR, quartz crystal microbalance (QCM) and cyclic voltammetry (CV). XPS and FTIR-ATR measurements showed that the Keggin structure of polyoxomolybdates is maintained as they are incorporated into the film. QCM experiments demonstrated that larger amounts of POM are incorporated into thicker film electrodes. EQCM and XPS measurements further showed that part of the film is delaminated when the modified electrodes were submerged in acid or basic solutions, but after this initial loss of mass the electrodes remain stable in time and with electrochemical use. POM-modified electrodes showed a pH-dependent electrochemical behavior, with peak potentials shifting by À60 mV pHÀ1, characteristic of a 2e/2H+ redox process at room temperature. Furthermore, our results suggest that POM molecules in the film are not decomposed when the electrodes are immersed in solutions with pH = 4.8 a key finding as POM mole- cules in solution suffer from complete hydrolysis at this pH value. Finally, the performance of these POM-modified electrodes as electrocatalysts was assessed via the reduction of nitrite, chlorate and peroxodisulfate.
Fil: Volker, Edgar. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
Fil: Calvo, Ernesto Julio. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
Fil: Williams, Federico José. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
Materia
Polyoxomolybdate
layer-by-layer
ion exchange
electrocatalysis
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/268044

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spelling Formation, characterization and electrocatalytic activity of layer-by-layer self-assembled films containing polyoxomolybdate over Au surfacesVolker, EdgarCalvo, Ernesto JulioWilliams, Federico JoséPolyoxomolybdatelayer-by-layerion exchangeelectrocatalysishttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1We describe a novel strategy for the controlled fabrication of well-defined multilayer films incorporating a polyoxomolybdate anion (PMo12 O3À , POM) via ion exchange on Au electrodes. Composite films were 40 thoroughly characterized by ellipsometry, X-ray photoelectron spectroscopy (XPS), FTIR-ATR, quartz crystal microbalance (QCM) and cyclic voltammetry (CV). XPS and FTIR-ATR measurements showed that the Keggin structure of polyoxomolybdates is maintained as they are incorporated into the film. QCM experiments demonstrated that larger amounts of POM are incorporated into thicker film electrodes. EQCM and XPS measurements further showed that part of the film is delaminated when the modified electrodes were submerged in acid or basic solutions, but after this initial loss of mass the electrodes remain stable in time and with electrochemical use. POM-modified electrodes showed a pH-dependent electrochemical behavior, with peak potentials shifting by À60 mV pHÀ1, characteristic of a 2e/2H+ redox process at room temperature. Furthermore, our results suggest that POM molecules in the film are not decomposed when the electrodes are immersed in solutions with pH = 4.8 a key finding as POM mole- cules in solution suffer from complete hydrolysis at this pH value. Finally, the performance of these POM-modified electrodes as electrocatalysts was assessed via the reduction of nitrite, chlorate and peroxodisulfate.Fil: Volker, Edgar. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; ArgentinaFil: Calvo, Ernesto Julio. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; ArgentinaFil: Williams, Federico José. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; ArgentinaElsevier Science SA2012-05info: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/11336/268044Volker, Edgar; Calvo, Ernesto Julio; Williams, Federico José; Formation, characterization and electrocatalytic activity of layer-by-layer self-assembled films containing polyoxomolybdate over Au surfaces; Elsevier Science SA; Journal of Electroanalytical Chemistry; 673; 5-2012; 1-71572-6657CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/abs/pii/S1572665712001142info:eu-repo/semantics/altIdentifier/doi/10.1016/j.jelechem.2012.03.014info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:10:12Zoai:ri.conicet.gov.ar:11336/268044instacron: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:34982025-09-03 10:10:12.362CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Formation, characterization and electrocatalytic activity of layer-by-layer self-assembled films containing polyoxomolybdate over Au surfaces
title Formation, characterization and electrocatalytic activity of layer-by-layer self-assembled films containing polyoxomolybdate over Au surfaces
spellingShingle Formation, characterization and electrocatalytic activity of layer-by-layer self-assembled films containing polyoxomolybdate over Au surfaces
Volker, Edgar
Polyoxomolybdate
layer-by-layer
ion exchange
electrocatalysis
title_short Formation, characterization and electrocatalytic activity of layer-by-layer self-assembled films containing polyoxomolybdate over Au surfaces
title_full Formation, characterization and electrocatalytic activity of layer-by-layer self-assembled films containing polyoxomolybdate over Au surfaces
title_fullStr Formation, characterization and electrocatalytic activity of layer-by-layer self-assembled films containing polyoxomolybdate over Au surfaces
title_full_unstemmed Formation, characterization and electrocatalytic activity of layer-by-layer self-assembled films containing polyoxomolybdate over Au surfaces
title_sort Formation, characterization and electrocatalytic activity of layer-by-layer self-assembled films containing polyoxomolybdate over Au surfaces
dc.creator.none.fl_str_mv Volker, Edgar
Calvo, Ernesto Julio
Williams, Federico José
author Volker, Edgar
author_facet Volker, Edgar
Calvo, Ernesto Julio
Williams, Federico José
author_role author
author2 Calvo, Ernesto Julio
Williams, Federico José
author2_role author
author
dc.subject.none.fl_str_mv Polyoxomolybdate
layer-by-layer
ion exchange
electrocatalysis
topic Polyoxomolybdate
layer-by-layer
ion exchange
electrocatalysis
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv We describe a novel strategy for the controlled fabrication of well-defined multilayer films incorporating a polyoxomolybdate anion (PMo12 O3À , POM) via ion exchange on Au electrodes. Composite films were 40 thoroughly characterized by ellipsometry, X-ray photoelectron spectroscopy (XPS), FTIR-ATR, quartz crystal microbalance (QCM) and cyclic voltammetry (CV). XPS and FTIR-ATR measurements showed that the Keggin structure of polyoxomolybdates is maintained as they are incorporated into the film. QCM experiments demonstrated that larger amounts of POM are incorporated into thicker film electrodes. EQCM and XPS measurements further showed that part of the film is delaminated when the modified electrodes were submerged in acid or basic solutions, but after this initial loss of mass the electrodes remain stable in time and with electrochemical use. POM-modified electrodes showed a pH-dependent electrochemical behavior, with peak potentials shifting by À60 mV pHÀ1, characteristic of a 2e/2H+ redox process at room temperature. Furthermore, our results suggest that POM molecules in the film are not decomposed when the electrodes are immersed in solutions with pH = 4.8 a key finding as POM mole- cules in solution suffer from complete hydrolysis at this pH value. Finally, the performance of these POM-modified electrodes as electrocatalysts was assessed via the reduction of nitrite, chlorate and peroxodisulfate.
Fil: Volker, Edgar. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
Fil: Calvo, Ernesto Julio. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
Fil: Williams, Federico José. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina
description We describe a novel strategy for the controlled fabrication of well-defined multilayer films incorporating a polyoxomolybdate anion (PMo12 O3À , POM) via ion exchange on Au electrodes. Composite films were 40 thoroughly characterized by ellipsometry, X-ray photoelectron spectroscopy (XPS), FTIR-ATR, quartz crystal microbalance (QCM) and cyclic voltammetry (CV). XPS and FTIR-ATR measurements showed that the Keggin structure of polyoxomolybdates is maintained as they are incorporated into the film. QCM experiments demonstrated that larger amounts of POM are incorporated into thicker film electrodes. EQCM and XPS measurements further showed that part of the film is delaminated when the modified electrodes were submerged in acid or basic solutions, but after this initial loss of mass the electrodes remain stable in time and with electrochemical use. POM-modified electrodes showed a pH-dependent electrochemical behavior, with peak potentials shifting by À60 mV pHÀ1, characteristic of a 2e/2H+ redox process at room temperature. Furthermore, our results suggest that POM molecules in the film are not decomposed when the electrodes are immersed in solutions with pH = 4.8 a key finding as POM mole- cules in solution suffer from complete hydrolysis at this pH value. Finally, the performance of these POM-modified electrodes as electrocatalysts was assessed via the reduction of nitrite, chlorate and peroxodisulfate.
publishDate 2012
dc.date.none.fl_str_mv 2012-05
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/11336/268044
Volker, Edgar; Calvo, Ernesto Julio; Williams, Federico José; Formation, characterization and electrocatalytic activity of layer-by-layer self-assembled films containing polyoxomolybdate over Au surfaces; Elsevier Science SA; Journal of Electroanalytical Chemistry; 673; 5-2012; 1-7
1572-6657
CONICET Digital
CONICET
url http://hdl.handle.net/11336/268044
identifier_str_mv Volker, Edgar; Calvo, Ernesto Julio; Williams, Federico José; Formation, characterization and electrocatalytic activity of layer-by-layer self-assembled films containing polyoxomolybdate over Au surfaces; Elsevier Science SA; Journal of Electroanalytical Chemistry; 673; 5-2012; 1-7
1572-6657
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/abs/pii/S1572665712001142
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.jelechem.2012.03.014
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
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 Elsevier Science SA
publisher.none.fl_str_mv Elsevier Science SA
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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