Many of the chemistry-based processing routes for functional ceramics inevi
tably involve calcining the chemical-derived precursors at an intermediate/
high temperature, in order to form the designed ceramic phase. This is very
undesirable, although widely used, as the calcination can result in an ext
ensive degree of crystal growth and particle coarsening at the calcination
temperature and therefore ruins almost all the advantages offered by the ch
emistry-based processing routes, such as an ultrafine particle size and hig
h sintering-reactivity. Using a specifically designed PZT precursor prepare
d by co-precipitation, it is demonstrated that the precursor-to-ceramic con
version can alternatively be realized by mechanical activation. In this con
nection, a single phase, nanocrystalline perovskite PZT powder has been suc
cessfully derived from an amorphous hydroxide precursor by mechanical activ
ation. The resulting PZT powder was well dispersed, and the particle size w
as in the range of 30-50 nm, as observed using the scanning electron micros
copy and transmission electron microscopy. This is in contrast to the poor
particle characteristics, represented by very coarse and irregular particle
and agglomerate sizes, for the powder derived from calcination at 750 degr
ees C. The activation-triggered PZT powder was sintered to a density of 97.
6% theoretical density at 1150 degrees C for 1 h. Sintered PZT ceramic exhi
bits a dielectric constant of 927 at room temperature and a peak dielectric
constant of similar to 9100 at the Curie point of 380 degrees C when measu
red at the frequency of 1 kHz. (C) 2000 Elsevier Science S.A. All rights re
served.