Electrochemical performance of dispersed Pt-M (M =V, Cr and Co) nanoparticles for the oxygen reduction electrocatalysis

Detalhes bibliográficos
Autor(a) principal: Lima,Fabio H. B.
Data de Publicação: 2005
Outros Autores: Giz,M. Janete, Ticianelli,Edson A.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532005000300006
Resumo: The kinetics of the oxygen reduction reaction (ORR) was studied in KOH electrolyte on ultra thin layer electrodes formed by Pt-V, Pt-Cr and Pt-Co electrocatalysts dispersed on a carbon powder (Pt-M/C). The electronic and structural features of the materials were studied by in situ XANES (X-ray Absorption Near Edge Structure) and EXAFS (Extended X-ray Absorption Fine Structure). Cyclic voltammograms and steady state polarization curves for the ORR were obtained using the rotating ring/disk electrode technique. The XANES results for the composites in the oxidized state have shown an increase of the occupancy of the Pt 5d band while the EXAFS analyses showed some reduction of the Pt-Pt interatomic distance in the different metal alloys compared to Pt/C. The electrochemical measurements indicated that the 4-electrons mechanism is mainly followed for the ORR in these platinum alloys. The highest electrocatalytic activity was shown by the Pt-V/C alloy, after treated at 850 ºC under hydrogen atmosphere.
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spelling Electrochemical performance of dispersed Pt-M (M =V, Cr and Co) nanoparticles for the oxygen reduction electrocatalysisoxygen reductionplatinum alloysX-ray absorptionThe kinetics of the oxygen reduction reaction (ORR) was studied in KOH electrolyte on ultra thin layer electrodes formed by Pt-V, Pt-Cr and Pt-Co electrocatalysts dispersed on a carbon powder (Pt-M/C). The electronic and structural features of the materials were studied by in situ XANES (X-ray Absorption Near Edge Structure) and EXAFS (Extended X-ray Absorption Fine Structure). Cyclic voltammograms and steady state polarization curves for the ORR were obtained using the rotating ring/disk electrode technique. The XANES results for the composites in the oxidized state have shown an increase of the occupancy of the Pt 5d band while the EXAFS analyses showed some reduction of the Pt-Pt interatomic distance in the different metal alloys compared to Pt/C. The electrochemical measurements indicated that the 4-electrons mechanism is mainly followed for the ORR in these platinum alloys. The highest electrocatalytic activity was shown by the Pt-V/C alloy, after treated at 850 ºC under hydrogen atmosphere.Sociedade Brasileira de Química2005-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532005000300006Journal of the Brazilian Chemical Society v.16 n.3a 2005reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532005000300006info:eu-repo/semantics/openAccessLima,Fabio H. B.Giz,M. JaneteTicianelli,Edson A.eng2005-07-18T00:00:00Zoai:scielo:S0103-50532005000300006Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2005-07-18T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Electrochemical performance of dispersed Pt-M (M =V, Cr and Co) nanoparticles for the oxygen reduction electrocatalysis
title Electrochemical performance of dispersed Pt-M (M =V, Cr and Co) nanoparticles for the oxygen reduction electrocatalysis
spellingShingle Electrochemical performance of dispersed Pt-M (M =V, Cr and Co) nanoparticles for the oxygen reduction electrocatalysis
Lima,Fabio H. B.
oxygen reduction
platinum alloys
X-ray absorption
title_short Electrochemical performance of dispersed Pt-M (M =V, Cr and Co) nanoparticles for the oxygen reduction electrocatalysis
title_full Electrochemical performance of dispersed Pt-M (M =V, Cr and Co) nanoparticles for the oxygen reduction electrocatalysis
title_fullStr Electrochemical performance of dispersed Pt-M (M =V, Cr and Co) nanoparticles for the oxygen reduction electrocatalysis
title_full_unstemmed Electrochemical performance of dispersed Pt-M (M =V, Cr and Co) nanoparticles for the oxygen reduction electrocatalysis
title_sort Electrochemical performance of dispersed Pt-M (M =V, Cr and Co) nanoparticles for the oxygen reduction electrocatalysis
author Lima,Fabio H. B.
author_facet Lima,Fabio H. B.
Giz,M. Janete
Ticianelli,Edson A.
author_role author
author2 Giz,M. Janete
Ticianelli,Edson A.
author2_role author
author
dc.contributor.author.fl_str_mv Lima,Fabio H. B.
Giz,M. Janete
Ticianelli,Edson A.
dc.subject.por.fl_str_mv oxygen reduction
platinum alloys
X-ray absorption
topic oxygen reduction
platinum alloys
X-ray absorption
description The kinetics of the oxygen reduction reaction (ORR) was studied in KOH electrolyte on ultra thin layer electrodes formed by Pt-V, Pt-Cr and Pt-Co electrocatalysts dispersed on a carbon powder (Pt-M/C). The electronic and structural features of the materials were studied by in situ XANES (X-ray Absorption Near Edge Structure) and EXAFS (Extended X-ray Absorption Fine Structure). Cyclic voltammograms and steady state polarization curves for the ORR were obtained using the rotating ring/disk electrode technique. The XANES results for the composites in the oxidized state have shown an increase of the occupancy of the Pt 5d band while the EXAFS analyses showed some reduction of the Pt-Pt interatomic distance in the different metal alloys compared to Pt/C. The electrochemical measurements indicated that the 4-electrons mechanism is mainly followed for the ORR in these platinum alloys. The highest electrocatalytic activity was shown by the Pt-V/C alloy, after treated at 850 ºC under hydrogen atmosphere.
publishDate 2005
dc.date.none.fl_str_mv 2005-06-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532005000300006
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532005000300006
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532005000300006
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.16 n.3a 2005
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
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