001     53213
005     20180211172022.0
024 7 _ |2 DOI
|a 10.1134/S1023193506110048
024 7 _ |2 WOS
|a WOS:000242234800004
037 _ _ |a PreJuSER-53213
041 _ _ |a eng
082 _ _ |a 540
084 _ _ |2 WoS
|a Electrochemistry
100 1 _ |a Pronkin, S.
|b 0
|u FZJ
|0 P:(DE-Juel1)VDB22265
245 _ _ |a Electrocatalytical properties of Au(111-25nm) - Pd quasi-single crystal film electrodes as probed by ATR-SEIRAS
260 _ _ |a Moscow
|b MAIK Nauka/Interperiodica Publ.
|c 2006
300 _ _ |a 1177 - 1192
336 7 _ |a Journal Article
|0 PUB:(DE-HGF)16
|2 PUB:(DE-HGF)
336 7 _ |a Output Types/Journal article
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336 7 _ |a Journal Article
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|2 EndNote
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a article
|2 DRIVER
440 _ 0 |a Russian Journal of Electrochemistry
|x 1023-1935
|0 5387
|y 11
|v 42
500 _ _ |a Record converted from VDB: 12.11.2012
520 _ _ |a Electrochemical and electrocatalytic properties of thin films Au(111-25 nm), which are quasi-single-crystal electrodes 25 nm thick made of gold with the (I 11) preferential orientation, and same electrodes modified with a monolayer (ML) of palladium are studied in 0.1 M solutions of HClO4 and H2SO4 employing voltammetric techniques and surface enhanced infrared reflection absorption spectroscopy (ATR-SEIRAS). Spectroscopic experiments demonstrate strong adsorption of electrolyte species (H2O, OHads, anions) on the Pd surface. The weak and reversible adsorption of CO on Au(111-25 nm) does not change the interfacial-water structure. Adsorption of CO on the Pd-modified film results in an irreversibly adsorbed CO adlayer stabilized by co-adsorbed isolated water species. Various electrooxidation mechanisms are discussed. Electrochemical and spectroscopic investigations on the adsorption and electrooxidation of HCOOH on bare and I ML Pd-Au(111-25 nm) electrodes reveal that electrooxidation proceeds in both cases via a direct or dehydrogenation pathway. This mechanism involves the formation of formate as intermediate, which is detected by in situ ATR-SEIRAS. The reactivity on Pd-modified surfaces is higher than on bare gold. The specifically adsorbed anions (sulfate/bisulfate) and the oxide formation on the substrate surface lower the reactivity for CO and HCOOH on both surfaces.
536 _ _ |a Grundlagen für zukünftige Informationstechnologien
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588 _ _ |a Dataset connected to Web of Science
650 _ 7 |a J
|2 WoSType
653 2 0 |2 Author
|a SEIRAS
653 2 0 |2 Author
|a quasi-single-crystal Au(111-25 nm) films
653 2 0 |2 Author
|a palladium
653 2 0 |2 Author
|a interfacial water
653 2 0 |2 Author
|a carbon monoxide
653 2 0 |2 Author
|a formic acid
653 2 0 |2 Author
|a adsorption
653 2 0 |2 Author
|a electrooxidation
700 1 _ |a Hara, M.
|b 1
|u FZJ
|0 P:(DE-Juel1)VDB17031
700 1 _ |a Wandlowski, Th.
|b 2
|u FZJ
|0 P:(DE-Juel1)VDB9859
773 _ _ |a 10.1134/S1023193506110048
|g Vol. 42, p. 1177 - 1192
|p 1177 - 1192
|q 42<1177 - 1192
|0 PERI:(DE-600)2058211-0
|t Russian journal of electrochemistry
|v 42
|y 2006
|x 1023-1935
856 7 _ |u http://dx.doi.org/10.1134/S1023193506110048
909 C O |o oai:juser.fz-juelich.de:53213
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913 1 _ |k P42
|v Grundlagen für zukünftige Informationstechnologien
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|x 0
914 1 _ |y 2006
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
|g ISG
|0 I:(DE-Juel1)VDB43
|x 0
920 1 _ |k CNI
|l Center of Nanoelectronic Systems for Information Technology
|d 14.09.2008
|g CNI
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981 _ _ |a I:(DE-Juel1)PGI-3-20110106
981 _ _ |a I:(DE-Juel1)VDB381


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