Electroreduction of molecular oxygen on preferentially oriented platinum electrodes in acid solution

Autores
Zinola Sánchez, Carlos Fernando; Castro Luna Berenguer, Ana María del Carmen; Triaca, Walter Enrique; Arvia, Alejandro Jorge
Año de publicación
1994
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The oxygen electroreduction reaction was studied on two different preferentially oriented ((111)-type and (100)-type and on a conventional polycrystalline (PC) platinum rotating disc electrodes in acid solutions at 30 °C. At low overpotentials, Tafel lines of −0.060 V decade−1 were obtained on the three electrodes in oxygen-saturated 1.0m H2SO4 and 1.0m H2SO4 + y; m K2SO4 (0 ⩽y ⩽ 1). At high over-potentials the usual Tafel slope of -0.120V decade−1 was observed on both (111)-type and PC platinum electrodes in 1.0m H2SO4, whereas a slope of −0.165V decade−1 was found on (100)-type platinum. In oxygen-saturated 1.0m H2SO4 the surface coverage by O-containing adsorbates on (100)-type platinum was greater than on both (111)-type and PC platinum. Rotating ring-disc electrode data showed that a higher amount of H2O2 was produced on (100)-type platinum than on the other platinum surfaces. The overpotential against current density plots are influenced by the anion concentration depending on the type of preferentially oriented platinum.
Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas
Materia
Física
Química
oxygen electroreduction
conventional polycrystalline
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/134066

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network_name_str SEDICI (UNLP)
spelling Electroreduction of molecular oxygen on preferentially oriented platinum electrodes in acid solutionZinola Sánchez, Carlos FernandoCastro Luna Berenguer, Ana María del CarmenTriaca, Walter EnriqueArvia, Alejandro JorgeFísicaQuímicaoxygen electroreductionconventional polycrystallineThe oxygen electroreduction reaction was studied on two different preferentially oriented ((111)-type and (100)-type and on a conventional polycrystalline (PC) platinum rotating disc electrodes in acid solutions at 30 °C. At low overpotentials, Tafel lines of −0.060 V decade−1 were obtained on the three electrodes in oxygen-saturated 1.0m H2SO4 and 1.0m H2SO4 + y; m K2SO4 (0 ⩽y ⩽ 1). At high over-potentials the usual Tafel slope of -0.120V decade−1 was observed on both (111)-type and PC platinum electrodes in 1.0m H2SO4, whereas a slope of −0.165V decade−1 was found on (100)-type platinum. In oxygen-saturated 1.0m H2SO4 the surface coverage by O-containing adsorbates on (100)-type platinum was greater than on both (111)-type and PC platinum. Rotating ring-disc electrode data showed that a higher amount of H2O2 was produced on (100)-type platinum than on the other platinum surfaces. The overpotential against current density plots are influenced by the anion concentration depending on the type of preferentially oriented platinum.Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas1994info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf119-125http://sedici.unlp.edu.ar/handle/10915/134066enginfo:eu-repo/semantics/altIdentifier/issn/0021-891xinfo:eu-repo/semantics/altIdentifier/issn/1572-8838info:eu-repo/semantics/altIdentifier/doi/10.1007/bf00247782info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/4.0/Creative Commons Attribution 4.0 International (CC BY 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-29T11:31:52Zoai:sedici.unlp.edu.ar:10915/134066Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-29 11:31:52.287SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv Electroreduction of molecular oxygen on preferentially oriented platinum electrodes in acid solution
title Electroreduction of molecular oxygen on preferentially oriented platinum electrodes in acid solution
spellingShingle Electroreduction of molecular oxygen on preferentially oriented platinum electrodes in acid solution
Zinola Sánchez, Carlos Fernando
Física
Química
oxygen electroreduction
conventional polycrystalline
title_short Electroreduction of molecular oxygen on preferentially oriented platinum electrodes in acid solution
title_full Electroreduction of molecular oxygen on preferentially oriented platinum electrodes in acid solution
title_fullStr Electroreduction of molecular oxygen on preferentially oriented platinum electrodes in acid solution
title_full_unstemmed Electroreduction of molecular oxygen on preferentially oriented platinum electrodes in acid solution
title_sort Electroreduction of molecular oxygen on preferentially oriented platinum electrodes in acid solution
dc.creator.none.fl_str_mv Zinola Sánchez, Carlos Fernando
Castro Luna Berenguer, Ana María del Carmen
Triaca, Walter Enrique
Arvia, Alejandro Jorge
author Zinola Sánchez, Carlos Fernando
author_facet Zinola Sánchez, Carlos Fernando
Castro Luna Berenguer, Ana María del Carmen
Triaca, Walter Enrique
Arvia, Alejandro Jorge
author_role author
author2 Castro Luna Berenguer, Ana María del Carmen
Triaca, Walter Enrique
Arvia, Alejandro Jorge
author2_role author
author
author
dc.subject.none.fl_str_mv Física
Química
oxygen electroreduction
conventional polycrystalline
topic Física
Química
oxygen electroreduction
conventional polycrystalline
dc.description.none.fl_txt_mv The oxygen electroreduction reaction was studied on two different preferentially oriented ((111)-type and (100)-type and on a conventional polycrystalline (PC) platinum rotating disc electrodes in acid solutions at 30 °C. At low overpotentials, Tafel lines of −0.060 V decade−1 were obtained on the three electrodes in oxygen-saturated 1.0m H2SO4 and 1.0m H2SO4 + y; m K2SO4 (0 ⩽y ⩽ 1). At high over-potentials the usual Tafel slope of -0.120V decade−1 was observed on both (111)-type and PC platinum electrodes in 1.0m H2SO4, whereas a slope of −0.165V decade−1 was found on (100)-type platinum. In oxygen-saturated 1.0m H2SO4 the surface coverage by O-containing adsorbates on (100)-type platinum was greater than on both (111)-type and PC platinum. Rotating ring-disc electrode data showed that a higher amount of H2O2 was produced on (100)-type platinum than on the other platinum surfaces. The overpotential against current density plots are influenced by the anion concentration depending on the type of preferentially oriented platinum.
Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas
description The oxygen electroreduction reaction was studied on two different preferentially oriented ((111)-type and (100)-type and on a conventional polycrystalline (PC) platinum rotating disc electrodes in acid solutions at 30 °C. At low overpotentials, Tafel lines of −0.060 V decade−1 were obtained on the three electrodes in oxygen-saturated 1.0m H2SO4 and 1.0m H2SO4 + y; m K2SO4 (0 ⩽y ⩽ 1). At high over-potentials the usual Tafel slope of -0.120V decade−1 was observed on both (111)-type and PC platinum electrodes in 1.0m H2SO4, whereas a slope of −0.165V decade−1 was found on (100)-type platinum. In oxygen-saturated 1.0m H2SO4 the surface coverage by O-containing adsorbates on (100)-type platinum was greater than on both (111)-type and PC platinum. Rotating ring-disc electrode data showed that a higher amount of H2O2 was produced on (100)-type platinum than on the other platinum surfaces. The overpotential against current density plots are influenced by the anion concentration depending on the type of preferentially oriented platinum.
publishDate 1994
dc.date.none.fl_str_mv 1994
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Articulo
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://sedici.unlp.edu.ar/handle/10915/134066
url http://sedici.unlp.edu.ar/handle/10915/134066
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/issn/0021-891x
info:eu-repo/semantics/altIdentifier/issn/1572-8838
info:eu-repo/semantics/altIdentifier/doi/10.1007/bf00247782
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by/4.0/
Creative Commons Attribution 4.0 International (CC BY 4.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by/4.0/
Creative Commons Attribution 4.0 International (CC BY 4.0)
dc.format.none.fl_str_mv application/pdf
119-125
dc.source.none.fl_str_mv reponame:SEDICI (UNLP)
instname:Universidad Nacional de La Plata
instacron:UNLP
reponame_str SEDICI (UNLP)
collection SEDICI (UNLP)
instname_str Universidad Nacional de La Plata
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repository.name.fl_str_mv SEDICI (UNLP) - Universidad Nacional de La Plata
repository.mail.fl_str_mv alira@sedici.unlp.edu.ar
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