dc.contributor.author
Feldt, Christoph D.
dc.contributor.author
Kirschbaum, Thorren
dc.contributor.author
Low, Jian Liang
dc.contributor.author
Riedel, Wiebke
dc.contributor.author
Risse, Thomas
dc.date.accessioned
2022-03-31T14:12:54Z
dc.date.available
2022-03-31T14:12:54Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/34206
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-33924
dc.description.abstract
Methanol oxidation on the stepped Au(332) surface was investigated by pulsed isothermal molecular beam (MB) experiments. The effect of the surface temperature as well as the influence of changes in the methanol and atomic oxygen flux on the partial oxidation to methyl formate was studied. A maximum in methyl formate formation is observed at 250 K under the applied single collision conditions. Increasing the methanol to oxygen ratio was found to increase the selectivity to methyl formate and decrease unwanted overoxidation to surface deactivating formate detected by in situ infrared reflection absorption spectroscopy (IRAS). The results show evidence for the importance of an additional deactivation mechanism for methyl formate formation connected to methanol which is active under oxygen-deficient conditions at low temperatures. Moreover, the measurements suggest a small number of sites to be highly reactive for methyl formate formation which are preferentially blocked under oxygen-deficient conditions.
en
dc.format.extent
11 Seiten
dc.rights.uri
https://creativecommons.org/licenses/by-nc/4.0/
dc.subject
methanol oxidation
en
dc.subject
methyl formate selectivity
en
dc.subject
surface deactivation
en
dc.subject.ddc
500 Naturwissenschaften und Mathematik::540 Chemie::540 Chemie und zugeordnete Wissenschaften
dc.title
Methanol oxidation on Au(332): methyl formate selectivity and surface deactivation under isothermal conditions
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.doi
10.1039/D1CY02034J
dcterms.bibliographicCitation.journaltitle
Catalysis Science & Technology
dcterms.bibliographicCitation.number
5
dcterms.bibliographicCitation.pagestart
1418
dcterms.bibliographicCitation.pageend
1428
dcterms.bibliographicCitation.volume
12
dcterms.bibliographicCitation.url
https://doi.org/10.1039/D1CY02034J
refubium.affiliation
Biologie, Chemie, Pharmazie
refubium.affiliation.other
Institut für Chemie und Biochemie
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.isPartOf.eissn
2044-4761
refubium.resourceType.provider
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