Estimating the Electrochemically Active Area: Revisiting a Basic Concept in Electrochemistry

Detalhes bibliográficos
Autor(a) principal: Coelho,Dyovani
Data de Publicação: 2021
Outros Autores: Luiz,Giuliana M., Machado,Sergio A. S.
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=S0103-50532021001001912
Resumo: The well-known electrochemical probe Fe(CN)63-/Fe(CN)64- is widely used for estimating the electrochemically active area of electrodes modified with carbon nanotubes, conductive polymers, enzymes, etc. In this study, we used the platinum electrode, smooth or platinized with different roughness factors, to demonstrate that such a redox couple fails to respond to a surface roughness variation. We determined the roughness factors of the Pt surfaces by atomic force microscopy (AFM) images, which yielded values between 2.72 and 25.91. Almost the same values were found by using the charge of the hydrogen monolayer desorption obtained from steady-state cyclic voltammetry experiments performed in an acid medium. They were then compared with those provided by peak current in voltammetry or chronoamperometry with Fe(CN)63-/Fe(CN)64- which all yielded values nearly to one. Such comparison demonstrates that the electrochemical behavior of the redox probe is an outer sphere reaction with a quite small interaction with the electrode surface, thus not being suitable to be related with active areas.
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spelling Estimating the Electrochemically Active Area: Revisiting a Basic Concept in Electrochemistryelectrochemical areapotassium ferrocyanideelectrode areacyclic voltammetrychronoamperometryThe well-known electrochemical probe Fe(CN)63-/Fe(CN)64- is widely used for estimating the electrochemically active area of electrodes modified with carbon nanotubes, conductive polymers, enzymes, etc. In this study, we used the platinum electrode, smooth or platinized with different roughness factors, to demonstrate that such a redox couple fails to respond to a surface roughness variation. We determined the roughness factors of the Pt surfaces by atomic force microscopy (AFM) images, which yielded values between 2.72 and 25.91. Almost the same values were found by using the charge of the hydrogen monolayer desorption obtained from steady-state cyclic voltammetry experiments performed in an acid medium. They were then compared with those provided by peak current in voltammetry or chronoamperometry with Fe(CN)63-/Fe(CN)64- which all yielded values nearly to one. Such comparison demonstrates that the electrochemical behavior of the redox probe is an outer sphere reaction with a quite small interaction with the electrode surface, thus not being suitable to be related with active areas.Sociedade Brasileira de Química2021-10-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532021001001912Journal of the Brazilian Chemical Society v.32 n.10 2021reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.21577/0103-5053.20210080info:eu-repo/semantics/openAccessCoelho,DyovaniLuiz,Giuliana M.Machado,Sergio A. S.eng2021-09-28T00:00:00Zoai:scielo:S0103-50532021001001912Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2021-09-28T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Estimating the Electrochemically Active Area: Revisiting a Basic Concept in Electrochemistry
title Estimating the Electrochemically Active Area: Revisiting a Basic Concept in Electrochemistry
spellingShingle Estimating the Electrochemically Active Area: Revisiting a Basic Concept in Electrochemistry
Coelho,Dyovani
electrochemical area
potassium ferrocyanide
electrode area
cyclic voltammetry
chronoamperometry
title_short Estimating the Electrochemically Active Area: Revisiting a Basic Concept in Electrochemistry
title_full Estimating the Electrochemically Active Area: Revisiting a Basic Concept in Electrochemistry
title_fullStr Estimating the Electrochemically Active Area: Revisiting a Basic Concept in Electrochemistry
title_full_unstemmed Estimating the Electrochemically Active Area: Revisiting a Basic Concept in Electrochemistry
title_sort Estimating the Electrochemically Active Area: Revisiting a Basic Concept in Electrochemistry
author Coelho,Dyovani
author_facet Coelho,Dyovani
Luiz,Giuliana M.
Machado,Sergio A. S.
author_role author
author2 Luiz,Giuliana M.
Machado,Sergio A. S.
author2_role author
author
dc.contributor.author.fl_str_mv Coelho,Dyovani
Luiz,Giuliana M.
Machado,Sergio A. S.
dc.subject.por.fl_str_mv electrochemical area
potassium ferrocyanide
electrode area
cyclic voltammetry
chronoamperometry
topic electrochemical area
potassium ferrocyanide
electrode area
cyclic voltammetry
chronoamperometry
description The well-known electrochemical probe Fe(CN)63-/Fe(CN)64- is widely used for estimating the electrochemically active area of electrodes modified with carbon nanotubes, conductive polymers, enzymes, etc. In this study, we used the platinum electrode, smooth or platinized with different roughness factors, to demonstrate that such a redox couple fails to respond to a surface roughness variation. We determined the roughness factors of the Pt surfaces by atomic force microscopy (AFM) images, which yielded values between 2.72 and 25.91. Almost the same values were found by using the charge of the hydrogen monolayer desorption obtained from steady-state cyclic voltammetry experiments performed in an acid medium. They were then compared with those provided by peak current in voltammetry or chronoamperometry with Fe(CN)63-/Fe(CN)64- which all yielded values nearly to one. Such comparison demonstrates that the electrochemical behavior of the redox probe is an outer sphere reaction with a quite small interaction with the electrode surface, thus not being suitable to be related with active areas.
publishDate 2021
dc.date.none.fl_str_mv 2021-10-01
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=S0103-50532021001001912
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532021001001912
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.21577/0103-5053.20210080
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.32 n.10 2021
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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