An aqueous route to the deposition of multicomponent metal oxide films
is based upon the complexation of precursor metal nitrate salts by gl
ycine, or other organic complexant, followed by spin-coating the homog
eneous solution onto pre-treated silica substrates. Glycine serves to
frustrate the formation of cation oxides, thus precipitation. Upon deh
ydration, a glassy matrix results through which metal cations and nitr
ate anions are homogeneously dispersed. Subsequent heating of coated s
ubstrates initiates an oxidation-reduction reaction, which removes the
organic matrix and residual nitrate leaving behind a film of the desi
red oxide composition. Using this method, Sm:YAG (Sm: Y3Al(5)O(12)-gar
net) films about 150 nm thick have been deposited. The respective phas
es have been confirmed by powder X-ray diffraction measurements and fl
uorescence spectroscopy. Analogous studies using powders generated by
the same technique provided the parameters for optimizing processing c
onditions to generate phase pure YAG films. The fluorescence emission
wavelength and related lifetime of certain electronic transitions aris
ing from metal cation dopants vary as a function of pressure and tempe
rature suggesting their use as optical sensors. This work suggests the
possible application of these films as pressure-temperature sensors i
n a planar waveguide configuration or as a coating material for optica
l fibers.