In situ STM study of electrocrystallization of Ag on Ag(111)

Detalhes bibliográficos
Autor(a) principal: García,Silvana G.
Data de Publicação: 2004
Outros Autores: Mayer,Carlos E., Salinas,Daniel R., Staikov,Georgi
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=S0103-50532004000600020
Resumo: The electrocrystallization process was studied in the system Ag(111)/Ag+, SO4= by in situ scanning tunneling microscopy (STM). The results show that Ag deposition occurs preferentially at step edges following a layer-by-layer growth mechanism, but polarization and imaging conditions greatly affect the local kinetics of this process. At STM-tip potentials more positive than the Ag/Ag+ equilibrium potential, a local dissolution of the substrate underneath the tip is observed even at low negative substrate overpotentials, at which the overall substrate current density is cathodic. An in situ STM imaging of Ag deposition was possible at sufficiently high negative substrate overpotentials. An estimation of the local deposition current density, however, indicates that the deposition rate underneath the STM-tip is reduced. These results are explained by the presence of an electric field between the STM-tip and the substrate, which affects the potential distribution directly underneath the tip, producing a large shielding of the diffusive flux of Ag+ ions.
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spelling In situ STM study of electrocrystallization of Ag on Ag(111)Scanning Tunneling MicroscopySTM-tip shielding effectsilver depositiontip-induced dissolutionThe electrocrystallization process was studied in the system Ag(111)/Ag+, SO4= by in situ scanning tunneling microscopy (STM). The results show that Ag deposition occurs preferentially at step edges following a layer-by-layer growth mechanism, but polarization and imaging conditions greatly affect the local kinetics of this process. At STM-tip potentials more positive than the Ag/Ag+ equilibrium potential, a local dissolution of the substrate underneath the tip is observed even at low negative substrate overpotentials, at which the overall substrate current density is cathodic. An in situ STM imaging of Ag deposition was possible at sufficiently high negative substrate overpotentials. An estimation of the local deposition current density, however, indicates that the deposition rate underneath the STM-tip is reduced. These results are explained by the presence of an electric field between the STM-tip and the substrate, which affects the potential distribution directly underneath the tip, producing a large shielding of the diffusive flux of Ag+ ions.Sociedade Brasileira de Química2004-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532004000600020Journal of the Brazilian Chemical Society v.15 n.6 2004reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532004000600020info:eu-repo/semantics/openAccessGarcía,Silvana G.Mayer,Carlos E.Salinas,Daniel R.Staikov,Georgieng2005-01-24T00:00:00Zoai:scielo:S0103-50532004000600020Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2005-01-24T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv In situ STM study of electrocrystallization of Ag on Ag(111)
title In situ STM study of electrocrystallization of Ag on Ag(111)
spellingShingle In situ STM study of electrocrystallization of Ag on Ag(111)
García,Silvana G.
Scanning Tunneling Microscopy
STM-tip shielding effect
silver deposition
tip-induced dissolution
title_short In situ STM study of electrocrystallization of Ag on Ag(111)
title_full In situ STM study of electrocrystallization of Ag on Ag(111)
title_fullStr In situ STM study of electrocrystallization of Ag on Ag(111)
title_full_unstemmed In situ STM study of electrocrystallization of Ag on Ag(111)
title_sort In situ STM study of electrocrystallization of Ag on Ag(111)
author García,Silvana G.
author_facet García,Silvana G.
Mayer,Carlos E.
Salinas,Daniel R.
Staikov,Georgi
author_role author
author2 Mayer,Carlos E.
Salinas,Daniel R.
Staikov,Georgi
author2_role author
author
author
dc.contributor.author.fl_str_mv García,Silvana G.
Mayer,Carlos E.
Salinas,Daniel R.
Staikov,Georgi
dc.subject.por.fl_str_mv Scanning Tunneling Microscopy
STM-tip shielding effect
silver deposition
tip-induced dissolution
topic Scanning Tunneling Microscopy
STM-tip shielding effect
silver deposition
tip-induced dissolution
description The electrocrystallization process was studied in the system Ag(111)/Ag+, SO4= by in situ scanning tunneling microscopy (STM). The results show that Ag deposition occurs preferentially at step edges following a layer-by-layer growth mechanism, but polarization and imaging conditions greatly affect the local kinetics of this process. At STM-tip potentials more positive than the Ag/Ag+ equilibrium potential, a local dissolution of the substrate underneath the tip is observed even at low negative substrate overpotentials, at which the overall substrate current density is cathodic. An in situ STM imaging of Ag deposition was possible at sufficiently high negative substrate overpotentials. An estimation of the local deposition current density, however, indicates that the deposition rate underneath the STM-tip is reduced. These results are explained by the presence of an electric field between the STM-tip and the substrate, which affects the potential distribution directly underneath the tip, producing a large shielding of the diffusive flux of Ag+ ions.
publishDate 2004
dc.date.none.fl_str_mv 2004-12-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532004000600020
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532004000600020
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532004000600020
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.15 n.6 2004
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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