A comprehensive framework is developed for the study
of the molecular
configuration of (MoO
x
)
n
species supported on pure anatase-TiO2 as well
as on mixed CeO2–TiO2. The framework
first employs the equilibrium deposition filtration method to molecularly
control the nature of the active molybdenum sites on the surface of
the supports while ensuring loadings below monolayer coverage. Next,
we deploy in situ Raman spectroscopic characterization in combination
with the isotope 18O2/16O2 exchange technique for the molecular-level identification of (MoO
x
)
n
surface configurations.
Results show that the distribution of (MoO
x
)
n
species depends strongly on the pH
of the precursor solution and that on both the TiO2 and
CeO2–TiO2 supports, the dominant configuration
pertains to a mono-oxo arrangement. Distinctive spectral behaviors
of a multicomponent band in the vicinity of the ∼900 cm–1 band for supported (MoO
x
)
n
on CeO2–TiO2 are assigned to two separate vibrational modes that involve
different anchoring Mo-O-Support bonds. The framework
also extends to the coupling of pulse experimentation with operando
Raman spectroscopy (transient operando spectroscopy) to distinguish
the reactivity among oxygen sites. From the rationalization of combined
results, we show that upon H2 exposure, the initial removal
of surface oxygen predominantly happens at the terminal (MoO)
site, which is then followed by the breaking of some Mo-O-Support bonds. This mechanism allows for oxygen swapping
between different Mo–O bonds during reoxidation.