US EPA

1126164 

Journal Article 

Methanol oxidation over model cobalt catalysts: Influence of the cobalt oxidation state on the reactivity 

Zafeiratos, S; Dintzer, T; Teschner, D; Blume, R; Havecker, M; Knop-Gericke, A; Schlogl, R 

2010 

Yes 

Journal of Catalysis
ISSN: 0021-9517
EISSN: 1090-2694 

269 

2 

309-317 

10.1016/j.jcat.2009.11.013 

WOS:000275587000007 

X-ray photoelectron and absorption spectroscopies (XPS and XAS) combined with on-line mass spectrometry were applied under working catalytic conditions to investigate methanol oxidation on cobalt. Two cobalt oxidation states (Co(3)O(4) and CoO) were prepared and investigated as regards their influence on the catalytic activity and selectivity. In addition adsorbed species were monitored in the transition of the catalyst from a non-active state, to an active one. It is shown that the surface oxidation state of cobalt is readily adapted to the oxygen chemical potential in the CH(3)OH/O(2) reaction mixture. In particular, even in oxygen-rich mixtures the Co(3)O(4) surface is partially reduced, with the extent of surface reduction following the methanol concentration. The reaction selectivity depends on the cobalt oxidation state, with the more reduced samples favouring the partial oxidation of methanol to formaldehyde. In the absence of oxygen, methanol effectively reduces cobalt to the metallic state, also promoting H(2) and CO production. Direct evidence of methoxy and formate species adsorbed on the surface upon reaction was found by analysing the O 1s and C 1s photoelectron spectra. However, the surface coverage of those species was not proportional to the catalytic activity, indicating that they might also act as reaction inhibitors. (C) 2009 Elsevier Inc. All rights reserved. 

Cobalt catalyst; Cobalt oxides; Methanol oxidation; In Situ XPS; In Situ XAS; Reaction intermediates; Fischer-Tropsch synthesis