1. Introduction
Lead-based piezoelectric materials have been intensively investigated for their excellent
piezoelectric (pC/N) and inverse piezoelectric (pm/V) properties. As a representative
piezoelectric material, (Pb,Zr)TiO3 has been extensively employed in industrial applications due to its excellent piezoelectric
and mechanical properties (d33 ~ 360 pC/N, kp ~ 0.51) with high Curie temperature (> 300 °C) [1-3]. Accordingly, this material has been tested for various applications including actuators,
sensors and transducers, which can be used in conditions of heavy load and mechanical
force. Despite these excellent mechanical and piezoelectric properties, lead based
piezoelectric materials also present environmental issues due to the toxic and harmful
properties of lead. To avoid these environmental problems, lead free alternatives
to replace lead-based piezoelectric materials have been widely and intensively investigated.
Among them Bi0.5Na0.5TiO3 (BNT), Na0.5K0.5NbO3 (NKN) and BaTiO3 (BT) are representative leadfree piezoelectric materials. NKN has a high piezoelectric
charge coefficient of 160 pC/N with a high Curie temperature of 420 °C [4,23]. But NKN has the drawback of being highly volatile because of the low melting temperatures
of Na and K [5]. Another alternative lead-free piezoelectric material candidate, BNT, has a very
high piezoelectric charge coefficient 230.8 pC/N, a relatively larger electromechanical
coupling factor (kp ~ 0.41), larger remanent polarization (Pr ~ 40 µC/cm2) and a better P–E hysteresis loop at relatively high temperature then other lead-free
piezoelectric ceramics [6-7]. However, its open stress vs strain curve means applied energy can accumulate, resulting
in high fatigue and lower reliability [8]. BT has shown promising properties, including a high piezoelectric charge coefficient
of more than 460 pC/N [9-10]. Therefore, in this research, a substitution type of BT material was selected to
investigate the relationship between activation energy and piezoelectric properties.
Piezoelectric ceramics have typically been fabricated with high density to achieve
a high d33 and reliable mechanical stability. In this paper, the activation energy of BZT-BCT
was derived from its shrinking behavior during the sintering process, and the sintering
temperature and BCT contents (0.4 ≤ x ≤ 0.5) were optimized. The Arrhenius equation
was adopted to derive activation energy from shrinking behavior. (1-x)Ba(Zr0.2Ti0.8)O3-x(Ba0.7Ca0.3)TiO3 has been intensively investigated for application in sensors and energy harvester
because of its high piezoelectric performance and properties [19-20]. A high piezoelectric charge coefficient d33 of 620 pC/N has been reported, and (1-x)Ba(Zr0.2Ti0.8)O3–x(Ba0.7Ca0.3)TiO3 (hereafter BZT-BCT) piezoelectric ceramics have been investigated to replace PZT
lead based piezoelectric materials [15]. One important feature of BZT-BCT is that the R-T phase transition is expected to
occur between BCT contents of 0.4 ≤ x ≤ 0.5. It is known that the phase transition
leads to high piezoelectric performance in materials such as PZT and PMN-PT [15,18,19,22].
In this study, we have focused on (1-x)BZT–xBCT materials with x(Ba0.7Ca0.3)TiO3 contents of x = 0.4, 0.425, 0.45, 0.475, 0.5 and sintering temperatures of 1475 °C,
1500 °C, and 1525 °C. This study has focused on the shrinkage mechanism and activation
energy of BZT-BCT ceramics to explain its outstanding piezoelectric properties. The
densification behavior of BZT-BCT and its microscopic surface were also measured.
3. Results and Discussion
Figure 1 shows the relative shrinkage ratio of the (1-x) BZT–xBCT ceramics sintered at temperatures
from 800 °C to 1525 °C. As shown in the figure, the porosity of the ceramic can be
decreased during the sintering process without melting. After the sintering process,
the relative shrinkage ratios of the (1-x)BZT–xBCT ceramics were measured. As shown
in Figure 1, the (1-x)BZT–xBCT ceramics started to shrink at 1200 °C. The BCT sample with a content
of 0.5 showed the highest shrinkage ratio in the temperature range of 800 °C -1200
°C, and the sample with the BCT content of 0.475 showed the highest shrinkage ratio
in the temperature range of 1200 °C - 1525 °C. The sintering process of the (1- x)BZT–xBCT
ceramics was completed near 1500 °C. The shrinkage rate of (1-x)BZT–xBCT was around
31.1% - 34.2 % at a sintering temperature of 1500 °C.
Figure 2 shows the isothermal shrinkage curves of the (1-x) BZT–xBCT ceramics depending on
holding time. Different holding times were analyzed using the kinetic equation [12-13]. Also, different sintering time depending on the sintering temperature was investigated.
Eq. (2) was employed to plot the
I
n
(
L
-
L
0
L
0
)
vs ln(t) data depending on the holding time. The exponent of n can be calculated
from the slopes (1/n) of the straight line fitted by the isothermal shrinkage in Figure 2. n can be related to material properties and the different shrinkage rates of the
sintered materials. As a result, the values of n were determined to be 7.83, 7.94,
8.01, 7.94 and 8.21 for the (1-x)BZT–xBCT ceramics, respectively. The different exponent
n indicates that each specimen has a distinctive shrinking behavior, which also leads
to their having their own distinct activation energy.
Figure 3 shows the activation energy of the (1-x)BZT–xBCT ceramics, simulated using the temperature
dependent shrinkage rate from Figure 1. Figure 3 shows the reconstructed curves for the relative shrinkage ratio of (1-x)BZT–xBCT
samples sintered at 1400 to 1525 °C which is translated to Arrhenius equation form.
Inverse temperature versus shrinkage rate gives the activation energy from the slope
in Figure 1. Since the calcination process was carried out at 1350 °C, lower than the 1300 °C
sintering temperature, the shrinkage ratio was not considered in calculating the shrinkage
mechanism. As a result, from the slope (Q / nRT) of the ln T
[
d
(
L
-
L
0
)
/
L
0
d
T
]
versus 1/T equation, the activation energy for the sintering process can be calculated
from the slope in Figure 2.
The calculated activation energies Q in the temperature range 1400 - 1525 °C were
around 404.9, 320.8, 276.3, 248.2 and 270.9 kJ/mol, respectively.
Table 1 lists the exponents of n and activation energies Q of the (1-x)BZT–xBCT ceramics.
The lowest n value was 7.83 for the 0.6BZT–0.4BCT ceramic. The activation energy of
the specimens means the internal energy needed to grow grains during the sintering
process. Therefore, the lowest activation energy leads to the most easily sintered
sample, compared with other specimens [12-14].
Figure 4 shows the X-ray diffraction θ-2θ patterns of the (1-x)BZT–xBCT ceramics sintered
at 1500 °C., to investigate their crystalline properties The patterns indicate that
all the specimens are single-phase. Samples with BCT contents of 0.4 ≤ x ≤ 0.45 exhibited
a rhombohedral structure. As shown in the figure, the split peak of (002)/(200) at
BCT contents (x) of 0.475 ≤ x ≤ 0.5 indicate a tetragonal structure, which is the
phase transition region between the rhombohedral phase and tetragonal phase [19]. Therefore, x approaching x = 0.45 (1-x)BZT–xBCT ceramics have a mixed phase of
rhombohedral and tetragonal structures.
Moreover, the Bragg reflections of the (002)/(200) planes showed that the position
of the (002) peak shifted to a slightly lower angle when the BCT content was increased
from 0.4 to 0.475, then shifted to a higher angle at a BCT content of 0.5. The (002)
peak shift to a lower angle means that the volume of the (1-x)BZT–xBCT ceramics increased,
since the two different rhombohedral and tetragonal phases are mixed near x = 0.45.
But when the BCT contents were increased further to x = 0.475, the (002)/(200) planes
moved to a higher position. This means the volume of the (1-x)BZT–xBCT ceramics decreased.
The atomic radius of Ba and Zr are sligthly larger than those of the Ca and Ti atoms.
As the x composition increased, Ba and Zr content decreased, while Ca and Ti were
increased. This has the effect of decreasing the volume of the (1-x)BZT–xBCT structure.
The atomic radius of Ba, Zr, Ca, Ti are 1.43, 1.06, 0.87, and 0.64 Å, respectively.
The position of the (002) peak at 45.02o relative to that that the lattice constant
c of the 0.525 BZT–0.475BCT implies it has increased relative to that of the other
specimens. In fact, the 0.525 BZT–0.475BCT had the highest c lattice parameter among
all specimens.
Figure 5 shows the enlarged X-ray diffraction pattern in the range of 43 to 46.5, where the
(002) and (200) planes exist. The symetric shape near 2θ = 45o, for BCT contents of
0.4 ≤ x ≤ 0.45, indicate a single rhombohedral structure, while the split peak of
(002)/(200) planes indicate that BCT contents of 0.475, 0.5 have a rhombohedral with
tetragonal structure. This represents a peak shift of (002) in the (1-x)BZT–xBCT ceramics.
As shown in the figure, 0.525BZT–0.475BCT show a split peak for the (002) and (200)
planes, indicating increased tetragonality. When the composition of x = 0.425, 0.45,
and 0.475, the peak positions were very similar. However, when the BCT contents were
0.5, then the (002) peak was shifted to a higher angle as the composition of the BCT
was increased. In the tetragonal structure, increased (002) peaks means that Ba, Zr,
which have larger ionic radii compared to Ca, Ti, decreased as the BCT contents increased,
reducing the lattice parameter according to Bragg’s law. Also, when x = 0.4, 0.425,
the rhombohedral structure peak was shifted to a lower angle. According to the crystal
geometry equation, α approaches 90 degrees, and an increase in the unit cell volume
can be seen.
Figure 6 shows the relative densities of the (1-x)BZT–xBCT samples sintered at 1475 °C, 1500
°C, 1525 °C. All sintering temperature showed that relative density increased up to
BCT contents of about x = 0.475 with 94.4%, and then decreased. This density increase
likely indicates the optimum BCT content and sintering temperature. In addition, this
bulk density is probably related to the degree of crystalization in the (1-x)BZT–xBCT
ceramics. Because the crystalization process is related to the BCT contents and sintering
temperature, the relative density is also related to BCT contents.
As the sintering temperature was increased from 1475 to 1500 °C, the crystalization
process progressed due to its low activation energy, as discussed in Figure 3. However, when the sintering temperature was further increased above 1500 °C, the
volume increased and weight might be decreased due to the low evaporation temperature
of Ca, at 1484 °C. The BZT-BCT material exhibited tricritical points in the phase
diagram, and near the tricritical points the x = 0.475 phase can be drastically changed.
With increasing BCT content, the BZT-BCT material forms rhombohedral, orthorombic,
and tetragonal structures. Due to this phase transition, relative density increased
up to the tricritical points at x = 0.475. However, relative density can be decreased
due to the phase transition with mixed phase [16].
Figure 7 shows Field emission scanning electron microscopy micrographs of the thermally etched
(1-x)BZT–xBCT ceramics sintered at 1500 °C. The (1-x)BZT–xBCT ceramic has an average
grain size of 9.5-11 μm. As shown in Fig 7(a), 0.6BZT–0.4BCT has a porous morphological surface, explaining the lower piezoelectric
charge coefficient. With increasing BCT content, the grain size becomes larger with
a clearer grain boundary, supporting the data in Figure 6, showing the bulk density of the (1-x)BZT–xBCT ceramics. For 0.525BZT–0.475BCT the
minimum activation energy needed to grow grains was assumed to be 201.88 kJ/mol, in
the temperature range of 1200 °C - 1525 °C, resulting in a dense, coarse-grain microstructure,
while 0.6BZT–0.4BCT needed the highest activation energy, 561.6468 kJ/mol, at a temperature
range of 1200 °C - 1525 °C, producing a fine, porous-grain microstructure.
Figure 8 displays the piezoelectric charge coefficients of (1-x)BZT–xBCT samples sintered
at 1475 °C, 1500 °C, 1525 °C. As shown in the figure, all of the specimens exhibit
an increasing piezoelectric charge coefficient up to 470 pC/N at a BCT content of
0.475, and then decrease. Among other sintering temperatures, the specimens sintered
at 1500 °C showed a relatively higher piezoelectric charge constant, indicating that
the optimized sintering temperature was 1500 °C from the perspective of energy harvesting.
Figure 9(a) displays the dielectric constants of (1-x)BZT–xBCT at 1kHZ (1475 °C, 1500 °C, 1525
°C). At all sintering conditions the samples exhibited the lowest dielectric constant
with BCT contents of 0.425, and then increased with increasing BCT contents. The lowest
dielectric constant of (1-x)BZT–xBCT was 2431.95 for the sample sintered at 1500 °C.
Fig 9(b) displays the piezoelectirc voltage constants of (1-x)BZT–xBCT ceramics at 1 kHz (1475
°C, 1500 °C, 1525 °C). The specimens sintered at a temperature of 1500 °C had a relatively
higher piezoelectric charge constant specimens then the other sintering temperatures,
and showed the highest piezoelectric voltage constant. Also, the sample with the BCT
content of 0.475 had the highest piezoelectric voltage constant under all sintering
temperature conditions. The highest value was 19.34 mVm/N at a BCT content of 0.475.