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
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/268044
Ver los metadatos del registro completo
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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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1842270110705778688 |
score |
13.13397 |