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  The formation of a NO-NH3 coadsorption complex on a Pt(111) surface: a NEXAFS study

Esch, F., Greber, T., Kennou, S., Siokou, A., Ladas, S., & Imbihl, R. (1996). The formation of a NO-NH3 coadsorption complex on a Pt(111) surface: a NEXAFS study. Catalysis Letters, 38(3-4), 165-170. doi:10.1007/BF00806563.

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 Creators:
Esch, F.1, Author           
Greber, T.1, 2, Author           
Kennou, S.1, 3, Author           
Siokou, A.1, 4, Author           
Ladas, S.1, 4, Author           
Imbihl, R.5, Author
Affiliations:
1Fritz Haber Institute, Max Planck Society, ou_24021              
2Physik-Institut der Universität Zürich, CH-8057, Zurich, Switzerland, ou_persistent22              
3Physics Department, University of loannina, GR-45110 loannina, Greece, ou_persistent22              
4FORTH-ICE/HT and Chemical Engineering Department, University of Patras,, GR-26500 Rion, Patras, Greece, ou_persistent22              
5Institut für Physikalische Chemie und Elektrochemie, Universität Hannover, Callinstrasse 3-3a, D-30167 Hannover, Germany, ou_persistent22              

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 Abstract: The adsorption of NO and the coadsorption of NO and NH3 on Pt(l11) has been studied with TDS, work function measurements and near-edge X-ray absorption fine structure spectroscopy (NEXAFS). Pure NO was found to be adsorbed upright at low coverages (θno < 0.25) with a bond length of 1.24 ±0.05 Å which corresponds to an elongation by 0.1 Å as compared to the gas phase. An additional tilted species forms at high coverages. The formation of a coadsorption complex of NH3 and low coverage NO shows up in an elongation of NO to 1.28 ±0.05 Å. In the coadsorption complex NO is adsorbed upright. The formation of such a complex which is held together by strong attractive interactions explains the high abundance of the mixed14N15N reaction product in experiments with isotopically labeled educts in the NO + NH3 reaction.

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Language(s): eng - English
 Dates: 1995-01-171996-01-171996-09
 Publication Status: Issued
 Pages: 6
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1007/BF00806563
 Degree: -

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Title: Catalysis Letters
  Abbreviation : Catal. Letters
Source Genre: Journal
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Publ. Info: New York : Springer
Pages: 6 Volume / Issue: 38 (3-4) Sequence Number: - Start / End Page: 165 - 170 Identifier: ISSN: 1011-372X
CoNE: https://pure.mpg.de/cone/journals/resource/954925586300