Different kinds of CuO-MO, mixtures were used to investigate their role in
the microstructure evolution, sintering densification and microwave propert
ies of Bi-2(Zn1/3Nb2/3)(2)O-7 (BZN) ceramics. Without the addition of CuO-M
O, mixtures, pure BZN ceramics have to be sintered above 900 degreesC. Howe
ver, a comparable bulk density to that of pure BZN ceramics sintered at 950
degreesC can be achieved for 2 wt% 0.29BaCO(3)-0.71 CuO-added at 850 degre
esC and 0.15CuO-0,85MoO(3)-added BZN ceramics at 800 degreesC, which was at
tributed to the liquid-phase sintering. A higher dielectric constant along
with a smaller Q factor was obtained in 0.29BaCO(3)-0.71CuO-added BZN ceram
ics because of the formation of the BaBi2Nb2O9 phase. On the other hand, a
larger Q factor of similar to 1500 can be obtained at about 850 degreesC fo
r 1 wt% 0.15CuO-0.85MoO(3)-added BZN ceramics. However, as the 0.2CuO-0.8GC
O(2) mixture was used, a partial transformation of pseudo-tetragonal Bi-2(Z
n1/3Nb2/3)(2)O-7 to cubic (Bi1.5Zn0.5)(Zn0.5Nb1.5)O-7 phase was induced pos
sibly because both Zn2+ and Ge4+ have similar ion radius and electronegativ
ity. With increasing 0.2CuO-0.8GeO(2) content, a decrease in microwave prop
erties was also obtained due to an inhibition of sintering densification si
nce a eutectic liquid phase was not formed.