Molecular structures of supported metal oxide catalysts under different environments

• Published in: Journal of Raman spectroscopy 2002-05, Vol.33 (5), p.359-380
• Main Authors: Bañares, M. A., Wachs, I. E.
• Format: Article
• Language: English
• ISSN: 0377-0486; 1097-4555
• DOI: 10.1002/jrs.866

The use of in situ Raman spectroscopy to study the molecular structures of supported metal oxide catalysts under different environments is reviewed. The molecular structures under ambient (hydrated) and dehydrated conditions are presented. The effect of moisture at elevated temperatures is also presented and discussed with regard to its implications for catalytic phenomena. The molecular structural transformations during C2–C4 lower alkane (LPG) oxidation, methane oxidation, methanol oxidation and selective catalytic reduction of NO with NH3 reaction conditions are presented. In situ spectroscopy during catalytic reaction with simultaneous activity/selectivity measurement (‘operando’ spectroscopy) is emphasized owing to its contribution to the fundamental understanding of catalytic performance. The reducibility of the different surface metal oxide species, the relevance of surface coverage (surface monomeric vs polymeric species) and the specific oxide support are discussed when LPG, methane, methanol or hydrogen is the reducing agent. In situ Raman spectroscopy provides molecular‐level information about the surface metal oxide species: structures, stability and transformations under different environments. In many cases, the use of complementary spectroscopic techniques results in a more complete understanding of the molecular structure–activity/selectivity relationships for supported metal oxide catalysts. Copyright © 2002 John Wiley & Sons, Ltd.