Spatial variations of the interface composition during surface chemical reactions

Research output: Contribution to journalConference articleResearchpeer review

Authors

  • S. Günther
  • H. Marbach
  • R. Hoyer
  • R. Imbihl
  • L. Gregoratti
  • M. Kiskinova

External Research Organisations

  • Sincrotrone Trieste
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Details

Original languageEnglish
Pages (from-to)989-996
Number of pages8
JournalJournal of Electron Spectroscopy and Related Phenomena
Volume114-116
Publication statusPublished - 8 Mar 2001
Event8th International Conference on Electronic Spectroscopy and Structure (ICESS-8) - Berkeley, CA, USA
Duration: 8 Aug 200012 Aug 2000

Abstract

The spatial distribution of potassium under reaction conditions on a composite Pt/Rh catalyst has been studied employing photoelectron spectromicroscopy as in situ method during the H2+O2 reaction. The composite catalyst consisted of a 70×70 μm2 Pt domain on a Rh(110) surface predosed with a submonolayer coverage of potassium. This catalyst was exposed to an O2+H2 atmosphere in the 10-7 mbar range. The combination of chemical specific imaging with a spatial resolution of 0.12 μm and micro-spot spectroscopy provided direct evidence for lateral re-distribution of potassium into a stationary concentration pattern under reaction conditions. The identity of the adsorbed species in the pattern and the changes in the chemical state of the substrate were determined.

ASJC Scopus subject areas

Cite this

Spatial variations of the interface composition during surface chemical reactions. / Günther, S.; Marbach, H.; Hoyer, R. et al.
In: Journal of Electron Spectroscopy and Related Phenomena, Vol. 114-116, 08.03.2001, p. 989-996.

Research output: Contribution to journalConference articleResearchpeer review

Günther S, Marbach H, Hoyer R, Imbihl R, Gregoratti L, Kiskinova M. Spatial variations of the interface composition during surface chemical reactions. Journal of Electron Spectroscopy and Related Phenomena. 2001 Mar 8;114-116:989-996. doi: 10.1016/S0368-2048(00)00262-0
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AU - Günther, S.

AU - Marbach, H.

AU - Hoyer, R.

AU - Imbihl, R.

AU - Gregoratti, L.

AU - Kiskinova, M.

N1 - Funding Information: The excellent technical support of D. Lonza is greatly acknowledged. This work was supported by Sincrotrone Trieste SCpA and partially by the EEC contract # ERBFMGECT950022.

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Y1 - 2001/3/8

N2 - The spatial distribution of potassium under reaction conditions on a composite Pt/Rh catalyst has been studied employing photoelectron spectromicroscopy as in situ method during the H2+O2 reaction. The composite catalyst consisted of a 70×70 μm2 Pt domain on a Rh(110) surface predosed with a submonolayer coverage of potassium. This catalyst was exposed to an O2+H2 atmosphere in the 10-7 mbar range. The combination of chemical specific imaging with a spatial resolution of 0.12 μm and micro-spot spectroscopy provided direct evidence for lateral re-distribution of potassium into a stationary concentration pattern under reaction conditions. The identity of the adsorbed species in the pattern and the changes in the chemical state of the substrate were determined.

AB - The spatial distribution of potassium under reaction conditions on a composite Pt/Rh catalyst has been studied employing photoelectron spectromicroscopy as in situ method during the H2+O2 reaction. The composite catalyst consisted of a 70×70 μm2 Pt domain on a Rh(110) surface predosed with a submonolayer coverage of potassium. This catalyst was exposed to an O2+H2 atmosphere in the 10-7 mbar range. The combination of chemical specific imaging with a spatial resolution of 0.12 μm and micro-spot spectroscopy provided direct evidence for lateral re-distribution of potassium into a stationary concentration pattern under reaction conditions. The identity of the adsorbed species in the pattern and the changes in the chemical state of the substrate were determined.

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JO - Journal of Electron Spectroscopy and Related Phenomena

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