In situ Raman spectroscopy is rapidly becoming a very popular catalyst char
acterization method because Raman cells are being designed that can combine
in situ molecular characterization studies with simultaneous fundamental q
uantitative kinetic studies. The dynamic nature of catalyst surfaces requir
es that both sets of information be obtained for a complete fundamental und
erstanding of catalytic phenomena under practical reaction conditions. Seve
ral examples are chosen to highlight the capabilities of in situ Raman spec
troscopy to problems in heterogeneous catalysis: the structural determinati
on of the number of terminal M=O bonds in surface metal oxide species that
are present in supported metal oxide catalysts; structural transformations
of the MoO3/SiO2 and MoO3/TiO2 supported metal oxide catalysts under variou
s environmental conditions, which contrast the markedly different oxide-oxi
de interactions in these two catalytic systems; the location and relative r
eactivity of the different surface M-OCH3 intermediates present during CH3O
H oxidation over V2O5/SiO2 catalysts; the different types of atomic oxygen
species present in metallic silver catalysts and their role during CH3OH ox
idation to H2CO and C2H4 epoxidation to C2H4O; and information about the ox
idized and reduced surface metal oxide species, isolated as well as polymer
ized species, present in supported metal oxide catalysts during reaction co
nditions. In summary, in situ Raman spectroscopy is a very powerful catalys
t characterization technique because it can provide fundamental molecular-l
evel information about catalyst surface structure and reactive surface inte
rmediates under practical reaction conditions.