001     49365
005     20200402210040.0
024 7 _ |2 pmid
|a pmid:16331729
024 7 _ |2 DOI
|a 10.1002/cphc.200500198
024 7 _ |2 WOS
|a WOS:000234002300021
037 _ _ |a PreJuSER-49365
041 _ _ |a eng
082 _ _ |a 540
084 _ _ |2 WoS
|a Chemistry, Physical
084 _ _ |2 WoS
|a Physics, Atomic, Molecular & Chemical
100 1 _ |a Beltramo, G. L.
|b 0
|u FZJ
|0 P:(DE-Juel1)128800
245 _ _ |a Oxidation of Formic Acid an Carbon Monoxide on Gold Electrodes Studies by Surface-Enhanced Raman Spectroscopy and Density Functional Theory
260 _ _ |a Weinheim
|b Wiley-VCH Verl.
|c 2005
300 _ _ |a 2597 - 2606
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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336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a article
|2 DRIVER
440 _ 0 |a ChemPhysChem
|x 1439-4235
|0 10582
|v 6
500 _ _ |a Record converted from VDB: 12.11.2012
520 _ _ |a The oxidation of formic acid and carbon monoxide was studied at a gold electrode by a combination of electrochemistry, in situ surface-enhanced Raman spectroscopy (SERS), differential electrochemical mass spectrometry, and first-principles DFT calculations. Comparison of the SERS results and the (field-dependent) DFT calculations strongly suggests that the relevant surface-bonded intermediate during oxidation of formic acid on gold is formate HCOO- ad*. Formate reacts to form carbon dioxide via two pathways: at low potentials, with a nearby water to produce carbon dioxide and a hydronium ion; at higher potentials, with surface-bonded hydroxyl (or oxide) to give carbon dioxide and water. In the former pathway, the rate-determining step is probably related to the reaction of surface-bonded formate with water, as measurements of the reaction order imply a surface almost completely saturated with adsorbate. The potential dependence of the rate of the low-potential pathway is presumably governed by the potential dependence of formate coverage. There is no evidence for CO formation on gold during oxidation of formic acid. The oxidation of carbon monoxide must involve the carboxyhydroxyl intermediate, but SERS measurements do not reveal this intermediate during CO oxidation, most likely because of its low surface coverage, as it is formed after the rate-determining step. Based on inconclusive spectroscopic evidence for the formation of surface-bonded OH at potentials substantially below the surface oxidation region, the question whether surface-bonded carbon monoxide reacts with surface hydroxyl or with water to form carboxyhydroxyl and carbon dioxide remains open. The SERS measurements show the existence of both atop and bridge-bonded CO on gold from two distinguishable low-frequency modes that agree very well with DFT calculations.
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, Pubmed
650 _ 7 |a J
|2 WoSType
653 2 0 |2 Author
|a density functional calculations
653 2 0 |2 Author
|a electrochemistry
653 2 0 |2 Author
|a gold
653 2 0 |2 Author
|a oxidation
653 2 0 |2 Author
|a Raman spectroscopy
700 1 _ |a Shubina, T. E.
|b 1
|0 P:(DE-HGF)0
700 1 _ |a Koper, M. T. M.
|b 2
|0 P:(DE-HGF)0
773 _ _ |a 10.1002/cphc.200500198
|g Vol. 6, p. 2597 - 2606
|p 2597 - 2606
|q 6<2597 - 2606
|0 PERI:(DE-600)2025223-7
|t ChemPhysChem
|v 6
|y 2005
|x 1439-4235
856 7 _ |u http://dx.doi.org/10.1002/cphc.200500198
909 C O |o oai:juser.fz-juelich.de:49365
|p VDB
913 1 _ |k M02
|v Kondensierte Materie
|l Kondensierte Materie
|b Materie
|0 G:(DE-Juel1)FUEK242
|x 0
914 1 _ |y 2005
915 _ _ |0 StatID:(DE-HGF)0010
|a JCR/ISI refereed
920 1 _ |k ISG-4
|l Institut für biologisch-anorganische Grenzflächen
|d 31.12.2001
|g ISG
|0 I:(DE-Juel1)VDB44
|x 0
970 _ _ |a VDB:(DE-Juel1)77276
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980 _ _ |a ConvertedRecord
980 _ _ |a journal
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980 _ _ |a UNRESTRICTED
981 _ _ |a I:(DE-Juel1)IBI-2-20200312
981 _ _ |a I:(DE-Juel1)ICS-7-20110106


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