A feasible kinetic model for the hydrogen oxidation on ruthenium electrodes

Autores
Rau, M.S.; Gennero, Maria Rosa; Chialvo, Abel Cesar
Año de publicación
2010
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The hydrogen oxidation reaction (hor) was studied on a polycrystalline ruthenium electrode in H2SO4 solution at different rotation rates (ω). The experimental polarization curves recorded on steady state show the existence of a maximum current with a non-linear dependence of the current density on ω1/2. On the basis of the Tafel-Heyrovsky-Volmer kinetic mechanism, coupled with a process of inhibition of active sites by the reversible electroadsorption of hydroxyl species, it was possible to appropriately describe the origin of the maximum current. The corresponding set of kinetic parameters was also calculated from the correlation of the experimental results with the proposed kinetic model.
Fil: Rau, M.S.. Universidad Nacional del Litoral. Facultad de Ingeniería Química. Programa de Electroquímica Aplicada e Ingeniería Electroquímica; Argentina
Fil: Gennero, Maria Rosa. Universidad Nacional del Litoral. Facultad de Ingeniería Química. Programa de Electroquímica Aplicada e Ingeniería Electroquímica; Argentina
Fil: Chialvo, Abel Cesar. Universidad Nacional del Litoral. Facultad de Ingeniería Química. Programa de Electroquímica Aplicada e Ingeniería Electroquímica; Argentina
Materia
ELECTROCATALYTIC ACTIVITY
HYDROGEN OXIDATION
KINETIC PARAMETERS
RUTHENIUM
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:11336/97604

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network_name_str CONICET Digital (CONICET)
spelling A feasible kinetic model for the hydrogen oxidation on ruthenium electrodesRau, M.S.Gennero, Maria RosaChialvo, Abel CesarELECTROCATALYTIC ACTIVITYHYDROGEN OXIDATIONKINETIC PARAMETERSRUTHENIUMhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1The hydrogen oxidation reaction (hor) was studied on a polycrystalline ruthenium electrode in H2SO4 solution at different rotation rates (ω). The experimental polarization curves recorded on steady state show the existence of a maximum current with a non-linear dependence of the current density on ω1/2. On the basis of the Tafel-Heyrovsky-Volmer kinetic mechanism, coupled with a process of inhibition of active sites by the reversible electroadsorption of hydroxyl species, it was possible to appropriately describe the origin of the maximum current. The corresponding set of kinetic parameters was also calculated from the correlation of the experimental results with the proposed kinetic model.Fil: Rau, M.S.. Universidad Nacional del Litoral. Facultad de Ingeniería Química. Programa de Electroquímica Aplicada e Ingeniería Electroquímica; ArgentinaFil: Gennero, Maria Rosa. Universidad Nacional del Litoral. Facultad de Ingeniería Química. Programa de Electroquímica Aplicada e Ingeniería Electroquímica; ArgentinaFil: Chialvo, Abel Cesar. Universidad Nacional del Litoral. Facultad de Ingeniería Química. Programa de Electroquímica Aplicada e Ingeniería Electroquímica; ArgentinaPergamon-Elsevier Science Ltd2010-07info: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/11336/97604Rau, M.S.; Gennero, Maria Rosa; Chialvo, Abel Cesar; A feasible kinetic model for the hydrogen oxidation on ruthenium electrodes; Pergamon-Elsevier Science Ltd; Electrochimica Acta; 55; 17; 7-2010; 5014-50180013-4686CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.electacta.2010.04.007info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:48:47Zoai:ri.conicet.gov.ar:11336/97604instacron: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 09:48:48.015CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv A feasible kinetic model for the hydrogen oxidation on ruthenium electrodes
title A feasible kinetic model for the hydrogen oxidation on ruthenium electrodes
spellingShingle A feasible kinetic model for the hydrogen oxidation on ruthenium electrodes
Rau, M.S.
ELECTROCATALYTIC ACTIVITY
HYDROGEN OXIDATION
KINETIC PARAMETERS
RUTHENIUM
title_short A feasible kinetic model for the hydrogen oxidation on ruthenium electrodes
title_full A feasible kinetic model for the hydrogen oxidation on ruthenium electrodes
title_fullStr A feasible kinetic model for the hydrogen oxidation on ruthenium electrodes
title_full_unstemmed A feasible kinetic model for the hydrogen oxidation on ruthenium electrodes
title_sort A feasible kinetic model for the hydrogen oxidation on ruthenium electrodes
dc.creator.none.fl_str_mv Rau, M.S.
Gennero, Maria Rosa
Chialvo, Abel Cesar
author Rau, M.S.
author_facet Rau, M.S.
Gennero, Maria Rosa
Chialvo, Abel Cesar
author_role author
author2 Gennero, Maria Rosa
Chialvo, Abel Cesar
author2_role author
author
dc.subject.none.fl_str_mv ELECTROCATALYTIC ACTIVITY
HYDROGEN OXIDATION
KINETIC PARAMETERS
RUTHENIUM
topic ELECTROCATALYTIC ACTIVITY
HYDROGEN OXIDATION
KINETIC PARAMETERS
RUTHENIUM
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv The hydrogen oxidation reaction (hor) was studied on a polycrystalline ruthenium electrode in H2SO4 solution at different rotation rates (ω). The experimental polarization curves recorded on steady state show the existence of a maximum current with a non-linear dependence of the current density on ω1/2. On the basis of the Tafel-Heyrovsky-Volmer kinetic mechanism, coupled with a process of inhibition of active sites by the reversible electroadsorption of hydroxyl species, it was possible to appropriately describe the origin of the maximum current. The corresponding set of kinetic parameters was also calculated from the correlation of the experimental results with the proposed kinetic model.
Fil: Rau, M.S.. Universidad Nacional del Litoral. Facultad de Ingeniería Química. Programa de Electroquímica Aplicada e Ingeniería Electroquímica; Argentina
Fil: Gennero, Maria Rosa. Universidad Nacional del Litoral. Facultad de Ingeniería Química. Programa de Electroquímica Aplicada e Ingeniería Electroquímica; Argentina
Fil: Chialvo, Abel Cesar. Universidad Nacional del Litoral. Facultad de Ingeniería Química. Programa de Electroquímica Aplicada e Ingeniería Electroquímica; Argentina
description The hydrogen oxidation reaction (hor) was studied on a polycrystalline ruthenium electrode in H2SO4 solution at different rotation rates (ω). The experimental polarization curves recorded on steady state show the existence of a maximum current with a non-linear dependence of the current density on ω1/2. On the basis of the Tafel-Heyrovsky-Volmer kinetic mechanism, coupled with a process of inhibition of active sites by the reversible electroadsorption of hydroxyl species, it was possible to appropriately describe the origin of the maximum current. The corresponding set of kinetic parameters was also calculated from the correlation of the experimental results with the proposed kinetic model.
publishDate 2010
dc.date.none.fl_str_mv 2010-07
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/11336/97604
Rau, M.S.; Gennero, Maria Rosa; Chialvo, Abel Cesar; A feasible kinetic model for the hydrogen oxidation on ruthenium electrodes; Pergamon-Elsevier Science Ltd; Electrochimica Acta; 55; 17; 7-2010; 5014-5018
0013-4686
CONICET Digital
CONICET
url http://hdl.handle.net/11336/97604
identifier_str_mv Rau, M.S.; Gennero, Maria Rosa; Chialvo, Abel Cesar; A feasible kinetic model for the hydrogen oxidation on ruthenium electrodes; Pergamon-Elsevier Science Ltd; Electrochimica Acta; 55; 17; 7-2010; 5014-5018
0013-4686
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1016/j.electacta.2010.04.007
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 Pergamon-Elsevier Science Ltd
publisher.none.fl_str_mv Pergamon-Elsevier Science Ltd
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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