Photoelectron spectromicroscopy of potassium redistribution in the O 2 + H2 reaction on Rh(110)

Research output: Contribution to journalArticleResearchpeer review

Authors

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

External Research Organisations

  • Sincrotrone Trieste
View graph of relations

Details

Original languageEnglish
Pages (from-to)15182-15191
Number of pages10
JournalJournal of Physical Chemistry B
Volume108
Issue number39
Early online date28 Aug 2004
Publication statusPublished - 1 Sept 2004

Abstract

The reversible condensation of potassium into large K + O coadsorption islands that occurs during the O2 + H2 reaction on a Rh(110) surface predosed with potassium has been studied in the 10-7 mbar range at temperatures between 533 and 623 K and with K coverages between 0.025 and 0.11 ML. Scanning photoelectron microscopy has been used as a spatially resolving in situ method to follow the development of the condensation process via calibrated K and O profiles. A Pt patch evaporated onto the Rh(110) surface served as a nucleation center for the reaction fronts. The coadsorbate phases evolving in the course of the condensation were characterized by local photoelectron spectra. Only at high enough temperature (∼580 K) is a nearly complete redistribution of the potassium by reaction fronts observed, whereas at low temperature, a substantial amount of the K + O coadsorbate remains on the reduced surface. The formation of a high-coverage (8 × 2) K + O phase characterized by an energy-shifted component in the Rh 3d and O 1s peaks appears to play a particular role in the condensation process.

ASJC Scopus subject areas

Cite this

Photoelectron spectromicroscopy of potassium redistribution in the O 2 + H2 reaction on Rh(110). / Marbach, H.; Günther, S.; Neubrand, T. et al.
In: Journal of Physical Chemistry B, Vol. 108, No. 39, 01.09.2004, p. 15182-15191.

Research output: Contribution to journalArticleResearchpeer review

Marbach, H, Günther, S, Neubrand, T, Hoyer, R, Gregoratti, L, Kiskinova, M & Imbihl, R 2004, 'Photoelectron spectromicroscopy of potassium redistribution in the O 2 + H2 reaction on Rh(110)', Journal of Physical Chemistry B, vol. 108, no. 39, pp. 15182-15191. https://doi.org/10.1021/jp048721y
Marbach, H., Günther, S., Neubrand, T., Hoyer, R., Gregoratti, L., Kiskinova, M., & Imbihl, R. (2004). Photoelectron spectromicroscopy of potassium redistribution in the O 2 + H2 reaction on Rh(110). Journal of Physical Chemistry B, 108(39), 15182-15191. https://doi.org/10.1021/jp048721y
Marbach H, Günther S, Neubrand T, Hoyer R, Gregoratti L, Kiskinova M et al. Photoelectron spectromicroscopy of potassium redistribution in the O 2 + H2 reaction on Rh(110). Journal of Physical Chemistry B. 2004 Sept 1;108(39):15182-15191. Epub 2004 Aug 28. doi: 10.1021/jp048721y
Marbach, H. ; Günther, S. ; Neubrand, T. et al. / Photoelectron spectromicroscopy of potassium redistribution in the O 2 + H2 reaction on Rh(110). In: Journal of Physical Chemistry B. 2004 ; Vol. 108, No. 39. pp. 15182-15191.
Download
@article{66bea5843f9f4f36aac47ac384973d38,
title = "Photoelectron spectromicroscopy of potassium redistribution in the O 2 + H2 reaction on Rh(110)",
abstract = "The reversible condensation of potassium into large K + O coadsorption islands that occurs during the O2 + H2 reaction on a Rh(110) surface predosed with potassium has been studied in the 10-7 mbar range at temperatures between 533 and 623 K and with K coverages between 0.025 and 0.11 ML. Scanning photoelectron microscopy has been used as a spatially resolving in situ method to follow the development of the condensation process via calibrated K and O profiles. A Pt patch evaporated onto the Rh(110) surface served as a nucleation center for the reaction fronts. The coadsorbate phases evolving in the course of the condensation were characterized by local photoelectron spectra. Only at high enough temperature (∼580 K) is a nearly complete redistribution of the potassium by reaction fronts observed, whereas at low temperature, a substantial amount of the K + O coadsorbate remains on the reduced surface. The formation of a high-coverage (8 × 2) K + O phase characterized by an energy-shifted component in the Rh 3d and O 1s peaks appears to play a particular role in the condensation process.",
author = "H. Marbach and S. G{\"u}nther and T. Neubrand and R. Hoyer and L. Gregoratti and M. Kiskinova and R. Imbihl",
year = "2004",
month = sep,
day = "1",
doi = "10.1021/jp048721y",
language = "English",
volume = "108",
pages = "15182--15191",
journal = "Journal of Physical Chemistry B",
issn = "1520-6106",
publisher = "American Chemical Society",
number = "39",

}

Download

TY - JOUR

T1 - Photoelectron spectromicroscopy of potassium redistribution in the O 2 + H2 reaction on Rh(110)

AU - Marbach, H.

AU - Günther, S.

AU - Neubrand, T.

AU - Hoyer, R.

AU - Gregoratti, L.

AU - Kiskinova, M.

AU - Imbihl, R.

PY - 2004/9/1

Y1 - 2004/9/1

N2 - The reversible condensation of potassium into large K + O coadsorption islands that occurs during the O2 + H2 reaction on a Rh(110) surface predosed with potassium has been studied in the 10-7 mbar range at temperatures between 533 and 623 K and with K coverages between 0.025 and 0.11 ML. Scanning photoelectron microscopy has been used as a spatially resolving in situ method to follow the development of the condensation process via calibrated K and O profiles. A Pt patch evaporated onto the Rh(110) surface served as a nucleation center for the reaction fronts. The coadsorbate phases evolving in the course of the condensation were characterized by local photoelectron spectra. Only at high enough temperature (∼580 K) is a nearly complete redistribution of the potassium by reaction fronts observed, whereas at low temperature, a substantial amount of the K + O coadsorbate remains on the reduced surface. The formation of a high-coverage (8 × 2) K + O phase characterized by an energy-shifted component in the Rh 3d and O 1s peaks appears to play a particular role in the condensation process.

AB - The reversible condensation of potassium into large K + O coadsorption islands that occurs during the O2 + H2 reaction on a Rh(110) surface predosed with potassium has been studied in the 10-7 mbar range at temperatures between 533 and 623 K and with K coverages between 0.025 and 0.11 ML. Scanning photoelectron microscopy has been used as a spatially resolving in situ method to follow the development of the condensation process via calibrated K and O profiles. A Pt patch evaporated onto the Rh(110) surface served as a nucleation center for the reaction fronts. The coadsorbate phases evolving in the course of the condensation were characterized by local photoelectron spectra. Only at high enough temperature (∼580 K) is a nearly complete redistribution of the potassium by reaction fronts observed, whereas at low temperature, a substantial amount of the K + O coadsorbate remains on the reduced surface. The formation of a high-coverage (8 × 2) K + O phase characterized by an energy-shifted component in the Rh 3d and O 1s peaks appears to play a particular role in the condensation process.

UR - http://www.scopus.com/inward/record.url?scp=6344244599&partnerID=8YFLogxK

U2 - 10.1021/jp048721y

DO - 10.1021/jp048721y

M3 - Article

AN - SCOPUS:6344244599

VL - 108

SP - 15182

EP - 15191

JO - Journal of Physical Chemistry B

JF - Journal of Physical Chemistry B

SN - 1520-6106

IS - 39

ER -