Simulation of ionic resistivity of ultra-thin passivating films on metals during their galvanostatic transient growth
Autor(a) principal: | |
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Data de Publicação: | 2002 |
Outros Autores: | , , |
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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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 |
_version_ |
1750318164930985984 |