| Home > Publications database > Electrocatalytical properties of Au(111-25nm) - Pd quasi-single crystal film electrodes as probed by ATR-SEIRAS > print |
| 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 |2 DataCite |
| 336 | 7 | _ | |a Journal Article |0 0 |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 |c P42 |2 G:(DE-HGF) |0 G:(DE-Juel1)FUEK412 |x 0 |
| 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 |p VDB |
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| 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 |z 381 |0 I:(DE-Juel1)VDB381 |x 1 |
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| 980 | _ | _ | |a UNRESTRICTED |
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