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005     20180210132728.0
024 7 _ |2 DOI
|a 10.1016/j.elecom.2003.10.027
024 7 _ |2 WOS
|a WOS:000188507400007
037 _ _ |a PreJuSER-31348
041 _ _ |a eng
082 _ _ |a 540
084 _ _ |2 WoS
|a Electrochemistry
100 1 _ |a Staikov, G.
|b 0
|u FZJ
|0 P:(DE-Juel1)VDB13645
245 _ _ |a In situ STM Study of the Initial Stages of Electrochemical Oxide Formation at the Ag(111)/0.1M NaOH(aq) Interface
260 _ _ |a Amsterdam [u.a.]
|b Elsevier Science
|c 2004
300 _ _ |a 132 - 137
336 7 _ |a Journal Article
|0 PUB:(DE-HGF)16
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336 7 _ |a Journal Article
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336 7 _ |a ARTICLE
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336 7 _ |a JOURNAL_ARTICLE
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336 7 _ |a article
|2 DRIVER
440 _ 0 |a Electrochemistry Communications
|x 1388-2481
|0 1775
|v 6
500 _ _ |a Record converted from VDB: 12.11.2012
520 _ _ |a The atomic structure of surface layers and the local changes of surface morphology during the initial stages of anodic oxidation of Ag(111) in an aqueous 0.1 M NaOH solution have been investigated by in situ scanning tunneling microscopy (STM) under different polarization conditions. The surface oxide formation starts at underpotentials, i.e. at electrode potentials E below the Nernst-potential E-3DAg2O (vs. SHE) = 0.4 V for the formation of the three-dimensional (3D) bulk Ag2O phase. An ordered overlayer showing distinct Moire pattern is observed in the potential range -0.1 V < E (vs. SHE) < 0.1 V. The appearance of the Moire structure is assigned to the strong OH adsorption, which induces a stretching of the 2D lattice of the OH-terminated topmost Ag(111) monolayer. In situ STM imaging at higher potentials (0.1 V < E (vs. SHE) < 0.3 V) shows the occurrence of a Ag dissolution process followed by an underpotential oxide formation in agreement with previous electrochemical measurements and in situ X-ray absorption studies. (C) 2003 Elsevier B.V. All rights reserved.
536 _ _ |a Kondensierte Materie
|c M02
|2 G:(DE-HGF)
|0 G:(DE-Juel1)FUEK242
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588 _ _ |a Dataset connected to Web of Science
650 _ 7 |a J
|2 WoSType
653 2 0 |2 Author
|a silver
653 2 0 |2 Author
|a STM
653 2 0 |2 Author
|a adsorption
653 2 0 |2 Author
|a electrochemical oxide formation
653 2 0 |2 Author
|a solid/liquid interface
700 1 _ |a Kunze, J.
|b 1
|0 P:(DE-HGF)0
700 1 _ |a Strehblow, H.-H.
|b 2
|0 P:(DE-HGF)0
773 _ _ |a 10.1016/j.elecom.2003.10.027
|g Vol. 6, p. 132 - 137
|p 132 - 137
|q 6<132 - 137
|0 PERI:(DE-600)2027290-X
|t Electrochemistry communications
|v 6
|y 2004
|x 1388-2481
856 7 _ |u http://dx.doi.org/10.1016/j.elecom.2003.10.027
909 C O |o oai:juser.fz-juelich.de:31348
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913 1 _ |k M02
|v Kondensierte Materie
|l Kondensierte Materie
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914 1 _ |a Nachtrag
|y 2004
915 _ _ |0 StatID:(DE-HGF)0010
|a JCR/ISI refereed
920 1 _ |k ISG-3
|l Institut für Grenzflächen und Vakuumtechnologien
|d 31.12.2006
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|0 I:(DE-Juel1)VDB43
|x 0
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981 _ _ |a I:(DE-Juel1)PGI-3-20110106


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