In situ STM study of electrocrystallization of Ag on Ag(111)
Autor(a) principal: | |
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Data de Publicação: | 2004 |
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=S0103-50532004000600020 |
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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Journal of the Brazilian Chemical Society (Online) |
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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 |
format |
article |
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 |
_version_ |
1750318166103293952 |