Simulation of ionic resistivity of ultra-thin passivating films on metals during their galvanostatic transient growth

Detalhes bibliográficos
Autor(a) principal: D'Alkaine,Carlos V.
Data de Publicação: 2002
Outros Autores: Tulio,Paulo C., Brito,Gilberto A. O., Salvador,José 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=S0103-50532002000400020
Resumo: Differential equations describing the evolution of defect concentrations inside ultra-thin films are developed and numerically resolved for the growth of passivating films under transient galvanostatic conditions. For this, the injection and recombination of defects together with the increase of the film thickness are taken into account. In the simulation, the defect concentrations pass through a maximum during the growth and increase with the current, becoming independent of it for higher values. To obtain reasonable values of defect concentrations the work shows the need to consider that only a part of the current is used in defect generation. For the film, the specific ionic resistivity passes through a minimum and the overpotential increases almost linearly with thickness. Analysis of the transients leads to the idea that the recombination rate constant can depend on the current density. All these aspects are analyzed and discussed from a physical point of view.
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spelling Simulation of ionic resistivity of ultra-thin passivating films on metals during their galvanostatic transient growthsimulationgalvanostatic transientspassivating filmsdefect concentrationionic resistivityDifferential equations describing the evolution of defect concentrations inside ultra-thin films are developed and numerically resolved for the growth of passivating films under transient galvanostatic conditions. For this, the injection and recombination of defects together with the increase of the film thickness are taken into account. In the simulation, the defect concentrations pass through a maximum during the growth and increase with the current, becoming independent of it for higher values. To obtain reasonable values of defect concentrations the work shows the need to consider that only a part of the current is used in defect generation. For the film, the specific ionic resistivity passes through a minimum and the overpotential increases almost linearly with thickness. Analysis of the transients leads to the idea that the recombination rate constant can depend on the current density. All these aspects are analyzed and discussed from a physical point of view.Sociedade Brasileira de Química2002-08-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532002000400020Journal of the Brazilian Chemical Society v.13 n.4 2002reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532002000400020info:eu-repo/semantics/openAccessD'Alkaine,Carlos V.Tulio,Paulo C.Brito,Gilberto A. O.Salvador,José A.eng2002-09-06T00:00:00Zoai:scielo:S0103-50532002000400020Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2002-09-06T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Simulation of ionic resistivity of ultra-thin passivating films on metals during their galvanostatic transient growth
title Simulation of ionic resistivity of ultra-thin passivating films on metals during their galvanostatic transient growth
spellingShingle Simulation of ionic resistivity of ultra-thin passivating films on metals during their galvanostatic transient growth
D'Alkaine,Carlos V.
simulation
galvanostatic transients
passivating films
defect concentration
ionic resistivity
title_short Simulation of ionic resistivity of ultra-thin passivating films on metals during their galvanostatic transient growth
title_full Simulation of ionic resistivity of ultra-thin passivating films on metals during their galvanostatic transient growth
title_fullStr Simulation of ionic resistivity of ultra-thin passivating films on metals during their galvanostatic transient growth
title_full_unstemmed Simulation of ionic resistivity of ultra-thin passivating films on metals during their galvanostatic transient growth
title_sort Simulation of ionic resistivity of ultra-thin passivating films on metals during their galvanostatic transient growth
author D'Alkaine,Carlos V.
author_facet D'Alkaine,Carlos V.
Tulio,Paulo C.
Brito,Gilberto A. O.
Salvador,José A.
author_role author
author2 Tulio,Paulo C.
Brito,Gilberto A. O.
Salvador,José A.
author2_role author
author
author
dc.contributor.author.fl_str_mv D'Alkaine,Carlos V.
Tulio,Paulo C.
Brito,Gilberto A. O.
Salvador,José A.
dc.subject.por.fl_str_mv simulation
galvanostatic transients
passivating films
defect concentration
ionic resistivity
topic simulation
galvanostatic transients
passivating films
defect concentration
ionic resistivity
description Differential equations describing the evolution of defect concentrations inside ultra-thin films are developed and numerically resolved for the growth of passivating films under transient galvanostatic conditions. For this, the injection and recombination of defects together with the increase of the film thickness are taken into account. In the simulation, the defect concentrations pass through a maximum during the growth and increase with the current, becoming independent of it for higher values. To obtain reasonable values of defect concentrations the work shows the need to consider that only a part of the current is used in defect generation. For the film, the specific ionic resistivity passes through a minimum and the overpotential increases almost linearly with thickness. Analysis of the transients leads to the idea that the recombination rate constant can depend on the current density. All these aspects are analyzed and discussed from a physical point of view.
publishDate 2002
dc.date.none.fl_str_mv 2002-08-01
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=S0103-50532002000400020
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532002000400020
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532002000400020
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.13 n.4 2002
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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