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@ARTICLE{Garcia:46694,
author = {Garcia, S. G. and Mayer, C. E. and Salinas, D. R. and
Staikov, G.},
title = {{I}n {S}itu {STM} {S}tudy of {E}lectrocrystallization of
{A}g on {A}g(111)},
journal = {Journal of the Brazilian Chemical Society},
volume = {15},
issn = {0103-5053},
address = {São Paulo},
publisher = {SBQ},
reportid = {PreJuSER-46694},
pages = {917},
year = {2004},
note = {Record converted from VDB: 12.11.2012},
abstract = {The electrocrystallization process was studied in the
system Ag(111)1Ag(+). SO4= by in situ scanning tunneling
microscopy (STM). The results show that Ag deposition occur
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 sire 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.},
keywords = {J (WoSType)},
cin = {ISG-3},
ddc = {540},
cid = {I:(DE-Juel1)VDB43},
pnm = {Kondensierte Materie},
pid = {G:(DE-Juel1)FUEK242},
shelfmark = {Chemistry, Multidisciplinary},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000226205000020},
url = {https://juser.fz-juelich.de/record/46694},
}