Published in

American Chemical Society, Journal of Physical Chemistry C, 15(113), p. 6208-6214, 2009

DOI: 10.1021/jp810403d

Links

Tools

Export citation

Search in Google Scholar

Adsorption and Reaction of Acetone over CeOx(111) Thin Films

Journal article published in 2009 by S. D. Senanayake, W. O. Gordon, S. H. Overbury ORCID, D. R. Mullins
This paper is available in a repository.
This paper is available in a repository.

Full text: Download

Green circle
Preprint: archiving allowed
  • Must obtain written permission from Editor
  • Must not violate ACS ethical Guidelines
Orange circle
Postprint: archiving restricted
  • Must obtain written permission from Editor
  • Must not violate ACS ethical Guidelines
Red circle
Published version: archiving forbidden
Data provided by SHERPA/RoMEO

Abstract

This study reports the interaction of acetone (CH3COCH3), the simplest ketone, with well ordered CeO2(111) thin film surfaces. The fully oxidized CeO2(111) surface shows a weak interaction with acetone with the sole desorption product (TPD) being acetone at 210 K. The chemisorbed molecule binds to the surface as the η1-acetone species rather than through a bridge-bonded dioxy-configuration. Exposure of a CeO2(111) surface to acetone at 600K removes oxygen as CO and results in the conversion of Ce4+ to Ce3+. Acetone chemisorbs strongly on reduced CeO2−x(111) with molecular acetone desorbing near 500 K. Decomposition also occurs with H2 desorbing between 450 and 600 K and C reacting with O in the ceria to desorb above 650 K. A stable species exists from 200 to 500 K on the reduced surface that has three unique types of C. High resolution C 1s XPS spectra indicate these are Ce−CH2, C−CH3 and C−O species. C k-edge NEXAFS indicates the presence of CC and CO bonds. It is postulated that the intermediate is a carbanion bonded through both O and C atoms to Ce cations.