Control of the hydrolysis and condensation of soluble precursors of ti
tanium is shown to yield oxide coatings of well-defined morphology. A
''smooth'' coating, consisting of patches of titania on silica, causes
only a small increase in the surface area, from 130 m(2)/g for the un
coated silica gel to 154 m(2)/g. On the other hand, the ''rough'' coat
ing, which consists of 3 nm diameter titania particles dispersed over
the silica surface, results in an increase in the BET surface area to
350 m(2)/g. The specific titania surface area was determined via isopr
opanol dehydration activity and was found to be comparable to the BET
surface area indicating that the titania phase is responsible for the
increase in surface area. Small angle X-ray scattering (SAXS) and tran
smission electron microscopy (TEM) provide definitive evidence for the
coating morphology while X-ray photoelectron spectroscopy (XPS) was u
sed to determine the dispersion of the titania. The supported titania
maintains its surface area upon calcination at temperatures up to 873
K while unsupported titania looses much of its surface area. Also demo
nstrated in this work is a novel preparation method using titanium bis
-ammonium lactate dihydroxide (TALH), a water soluble precursor.