In this work, the (K1-xAgx)(Ta0.8Nb0.2)O3 (x=0.1-0.4) ceramics were fabricated using mixed-oxide method, and their structural and electrical properties were measured. All specimens represented a pseudo cubic structure with the lattice constant of 0.3989 nm. When 0.4 mol of Ag was added, second phases induced from metallic Ag and K2(Ta,Nb)6O16 phase were observed. Dielectric constant and dielectric loss of K(Ta0.8Nb0.2)O3 specimen doped with 0.3 mol of Ag were 2,737 and 0.446, respectively. The curie temperature was about -5℃, which does not change with Ag addition. The remanent polarization began to decrease sharply around 12~15℃, and the temperature at which the remanent polarization began to decrease as the applied voltage increased shifted to the high temperature side. The electrocaloric effect (ΔT) and electrocaloric efficiency (ΔT/ΔE) of the (K0.7Ag0.3)(Ta0.8Nb0.2)O3 ceramics were 0.01024℃ and 0.01825 KmV-1, respectively.
The electrocaloric effect in 0.94(Bi0.5Na0.5)TiO3+0.06KNbO3+0.9 wt% G.F.ferroelectricceramics was observed in terms of the temperature change (ΔT) of the fabricated ceramics, Curie temperature Tc, and applied electric field. The specimens were fabricated by a conventional solid-state reaction. Tc appeared near 165∼170℃. The P-E hysteresis showed a tendency to slim down with a temperature increase and finally was slimmest near 150℃. With the increase of temperature, the polarization revealed a gradual decrease, and a sharp decline near Tc. When an electric field of 45 kV/cm was applied, the largest polarization was shown. The maximum value of the temperature change (ΔT=0.31℃) was obtained at 165℃ under an applied electric field of 45 kV/cm.
In this study, in order to develop relaxor ferroelectric ceramics for refrigeration device application with large electrocaloric effect and low sintering temperature, PLZT(8/65/35) ceramics was fabricated using conventional solid-state method with the variation of sintering temperature (1,050℃, 1,100℃, 1,200℃). The XRD pattern of all specimens indicated general perovskite structure with secondary phase. From the results of temperature dependence of dielectric constant, the TC (ferroelectric-paraelectric phase transition temperature) was shifted toward high temperature with increasing sintering temperature. When the specimen was sintered at 1,100℃, the optimal value of .T ∼0.349℃ in ambient temperature of 215℃ was appeared. It is considered that PLZT(8/65/35) ceramics possess the possibility of refrigeration device application.
In this study, in order to develop relaxor ferroelectric ceramics for refrigeration device application with large electrocaloric effect, PLZT(8/65/35) composition was fabricated using conventional solid-state method. The Curi temperature of this composition PLZT ceramics was 230℃, and the P-E hysteresis loops of the PLZT ceramics as a fuction of temperature became slim by degrees with higher temperatures. The maximum value of .T of 0.243°C in ambient temperature of 215°C with 30 kV/cm was appeared. It is considered that PLZT ceramics possess the possibility of refrigeration device application.
In this work, in order to develop the ceramics with an excellent electrocaloric effect, [Bi0.5(Na0.84K0.16)0.5]TiO3 ceramics were fabricated by conventional solid state reaction method. The ceramics was observed as rhombohedral phase by X-ray diffraction patterns. To investigate the electrocaloric effect of the ceramics, P-E hysteresis loops were measured at various temperature. The temperature change ΔT of these ceramics was calculated using the Maxwell``s relations. The maximum value of temperature change ΔT was obtained as 0.3 1℃ at 165℃ under applied electric fields 45 kV/cm.