Li-Qian Cheng*a,
Ze Xua,
Chunlin Zhaob,
Hao-Cheng Thongb,
Zhen-Yong Cenb,
Wei Lu*c,
Yu Lanc and
Ke Wangb
aDepartment of Materials Science and Engineering, China University of Mining & Technology (Beijing), Beijing 100083, China. E-mail: chenglq@cumtb.edu.cn
bState Key Laboratory of New Ceramics and Fine Processing, School of Materials Science and Engineering, Tsinghua University, Beijing 100084, China
cAcoustic Science and Technology Laboratory, Harbin Engineering University, Harbin 150001, China. E-mail: luwei@hrbeu.edu.cn
First published on 17th October 2018
A high-performance piezoelectric material, 0.95Pb(Zr0.52Ti0.48)O3-0.05Pb(Mn1/3Nb2/3)O3 (PZT-PMnN) ceramic, was prepared by using a spark plasma sintering (SPS) method. By systematically comparing the electrical properties, the spark-plasma-sintered sample was demonstrated to be superior to a conventionally sintered sample. With respect to conventionally sintered ceramic, the d33 of spark-plasma-sintered ceramic increases from 323 pC/N to 412 pC/N, and the increases from 318 pm V−1 to 553 pm V−1. More importantly, the mechanical quality factor (Qm) reaches 583, which is three times higher than the conventionally sintered sample (Qm ∼ 182). Furthermore, the SPS method was found to be capable of promoting other electrical properties simultaneously. Therefore, the SPS method is proposed to be an effective processing method to fabricate PZT-PMnN ceramics of higher performance.
It is mostly accepted that the criteria for practical applications include an excellent piezoelectric coefficient, good temperature stability, low dielectric loss, and high mechanical quality factor.6–8 However, some of these properties are not necessarily required to be outstanding under certain circumstances, e.g. a high mechanical quality factor is more important than a high piezoelectric coefficient in the application of high-frequency ultrasonic transducers. In 1954, Jaffe discovered the PbZrO3-PbTiO3 system, possessing high piezoelectricity.9,10 Different elements, acting as a soft or hard doping, when they were doped in PZT ceramics, can improve the ferroelectric properties of ceramics.11 On the other hand, Priya et al. analyzed and proved that Pb(Zr, Ti)O3-Pb(Mn1/3Nb2/3)O3 is suitable for applications, on the basis of the dielectric and piezoelectric magnitudes.12
However, PZT ceramics still face many problems, such as the volatilization of lead at the high sintering temperature.13–16 Spark plasma sintering (SPS) could be favorable in suppressing the lead loss because of the rapid heating rate, lower sintering temperature and shorter sintering time.17 It is well known that SPS is an effective tool to achieve dense and fine-grained ceramics at a relatively low temperature.18 For example, Han et al. demonstrated that SPS can reduce the sintering temperature of Pb(Zr0.52Ti0.42Sn0.02Nb0.04)O3 ceramic by about 200–300 °C while maintaining a high relative density (>99%).19 Besides, the SPS method is capable of promoting the performance of piezoceramics. For example, Shen et al. improved the electrical and mechanical properties of (Na0.535K0.485)1−xLix(Nb0.8Ta0.2)O3 (x = 0.02–0.07) ceramic using SPS method.20 This provides a promising alternative to fabricate lead-based ceramics with high mechanical strength and homogeneous fine-grain sizes.21 However, there is barely a few papers which systematically investigate and compare the comprehensive electrical properties of spark-plasma-sintered (SPSed) and conventionally sintered (CSed) ceramics.
In this work, Mn and Nb co-doped PZT ceramics with the composition 0.95Pb(Zr0.52Ti0.48)O3-0.05Pb(Mn1/3Nb2/3)O3 (PZT-PMnN) were prepared by the SPS method at 900–1000 °C. For comparison, the similar composition was prepared by using the conventional sintering (CS) method at 1250 °C. Both ceramic samples were systematically studied. A dense microstructure and high piezoelectric performance are obtained in the SPSed ceramic. This work herein suggests that SPS is an effective method for fabricating high-performance piezoceramics at a low sintering temperature, which is believed to be beneficial for further development of the piezoceramics.
The density of the samples was determined by the Archimedes method. A high-resolution X-ray diffractometer (Rigaku, D/Max2500, Tokyo, Japan) is implemented to examine the crystal structure. Microstructures of sintered disks were examined by using a scanning electron microscopy (SEM, JSM-6460LV, JEOL, Tokyo, Japan). The quasi-static piezoelectric coefficient d33 of the poled samples was measured using a quasi-static d33 meter (ZJ-3A, Institute of Acoustics, Beijing, China). Field-dependent parameters were measured by a ferroelectric tester (aixACCT TF Analyzer 1000, Germany), bipolar/unipolar strain curves (S–E) and ferroelectric hysteresis (P–E) loops were included. The dielectric properties were measured at a frequency of 1 kHz using an impedance analyzer (TH2827, Changzhou Tonghui Electronic Co, China). Resistance |Z| and phase angle θ were measured at room temperature, using an Agilent 4294A precision impedance analyzer.
It can be seen from the SEM images (Fig. 2) that the SPSed ceramic possesses a denser microstructure than CSed ceramic. A lot of pores can be found in the CSed ceramic, as shown in Fig. 2(a), while there is no visible pore in SPSed ceramic, as shown in Fig. 2(d). Hence, the density of SPS-prepared ceramic is obviously larger than the CS-prepared ceramic (see Table 1).27 In addition, SPS-prepared ceramic has a suitable grain size distribution [see Fig. 2(f)], so that the grains can distribute more densely. The average grain size of the CSed ceramic is about 6.0 μm, while the average grain size of SPSed ceramic is about 4.6 μm. This is in agreement with the previous reports because the relatively short holding time during SPS will limit the grain growth.19 It is proposed that electrical properties depend on the grain size.31 At an appropriate grain size, the electrical properties can be highly enhanced. As shown in Table 1, it can improve piezoelectric coefficient and strain of ceramics with decreased grain size and porosity.17 The piezoelectric effect of the piezoelectric ceramics is affected by the 90° domain wall movement.32 It is because that domain wall area will change as a function of grain size. A smaller domain can react strongly to the applied electric field as it can rotate more easily.31 The piezoelectric coefficients d33 of CSed and SPSed samples were measured by using a quasi-static d33 meter, as shown in Table 1. SPSed sample was found to possess an unexceptionally high d33 when compared to the CSed sample. Therefore, it is conjectured that the smaller grain size achieved by using SPS method helps reduce the domain size, which potentially plays a significant role on the enhancement of piezoelectric performance.
Fig. 4 shows P–E hysteresis loops of PZT-PMnN prepared by different sintering methods. Typical ferroelectric loops were observed for both ceramics. Maximum polarization (Pmax), residual polarization (Pr) and coercive field (EC) were summarized in Table 1. It can be seen that the SPSed ceramic possesses a better ferroelectric performance (Pmax = 28.2 μC cm−2 and Pr = 18.8 μC cm−2) than the CSed ceramic (Pmax = 20.1 μC cm−2 and Pr = 11.9 μC cm−2). In addition, the coercive field of SPSed ceramic is also higher than that of CSed ceramic. It is generally believed that the coercive field is related to the flexibility of domain and domain walls, and the coercive field of T-phase is generally larger than that of R-phase.29 SPS ceramic shows higher EC (1.49 kV mm−1) than CS ceramic (0.92 kV mm−1). This phenomenon is consistent with their XRD conclusions, and the XRD of SPS shows more obvious T-phase. It can be found that the content of the T phase in the coexisting phase affects the piezoelectric properties of the ceramic.
Fig. 5 shows temperature-dependent dielectric constant and loss of both SPSed and CSed PZT-PMnN ceramics. It can be seen from Fig. 5(a) that the Curie temperatures of the ceramics are quite similar. The Curie temperature of the SPSed ceramic is only 5 °C lower than that of the CSed ceramic. On the other hand, SPS can significantly increase the peak dielectric constant and the dielectric constant at room temperature. The dielectric constant at Curie temperature was increased from 21000 to 37000 and it was increased from 472 to 824 at room temperature. Besides, in Fig. 5(b), it can be seen that the SPS can largely reduce the dielectric loss of ceramic in various temperature ranges, and the loss was reduced from 0.0045 to 0.0018 at room temperature.
Fig. 5 Dielectric constants and losses of PZT-PMnN ceramics prepared by different sintering methods. |
Fig. 6(a) shows bipolar strain curves of PZT-PMnN ceramics. It can be observed that the strain value of SPSed ceramic at room temperature is almost twice that of the CSed ceramic. In order to verify the thermal stability of the strain performance, the unipolar strain was measured at various temperatures, ranging from 25 °C to 200 °C. The unipolar strain can be normalized as , which is also known as the converse piezoelectric coefficient. Similar to bipolar strain performance, a higher (553 pm V−1) is observed in SPSed ceramic at room temperature, when compared to the CSed ceramic (318 pm V−1). As shown in Fig. 6(b), when the temperature rises from 25 °C, the unipolar strain of CSed ceramic greatly increases from 0.08% to 0.17% (variation of 112.5%) while the SPSed ceramic only changes from 0.13% to 0.17% (variation of 33%). The result suggests that SPSed ceramic possesses a thermally stable strain performance.
According to the above comparison, it is easy to find that the performance of PZT-PMnN ceramics can be optimized via SPS method. And SPSed ceramic has the higher strain, d33, εr, Pr, EC, compactness, and lowest loss. The R–T phase structure with more T phase and denser and finer grain distribution are the main reasons for improving the ferroelectric properties of SPS ceramics. Hence, SPS not only reduced the sintering temperature by 300 °C, but also greatly improved the ceramic performance. This work provides a powerful reference for future researchers, how to improve the d33 and Qm while the performance requirements getting bigger in practical applications. SPS may be a reliable means.
This journal is © The Royal Society of Chemistry 2018 |