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Piezoelectric ceramics is a versatile functional material that can realize interconversion between electrical energy and mechanical energy. As the electrical properties of piezoelectric ceramics are extremely sensitive to the grain size variation, the investigation of grain size effect has attracted much attention. In this paper, the recent research progress of the grain size effect on perovskite piezoelectric ceramics, including barium titanate (BT), lead zirconate titanate (PZT), potassium sodium niobate (KNN), and sodium bismuth titanate (BNT), is comprehensively reviewed. We especially focus on topics including feasible ways of fabricating piezoelectric ceramics with the desired grain sizes, the influence of the grain size effect on piezoelectric properties, and the corresponding physical mechanisms. This review would be beneficial to understanding the influence of the grain size effect on piezoelectric properties. The review concludes with the prediction of the further investigation on the grain size effect.
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Keywords:
- piezoelectric ceramics /
- piezoelectric properties /
- grain size controlling /
- grain size effect
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图 3 BT压电陶瓷的晶粒形貌及晶粒尺寸对压电性能的影响 (a) BT陶瓷中不同尺寸(5 nm—100 μm)晶粒的扫描电子显微镜照片[27,30,52,54,63,93-95]; (b) 典型BT陶瓷中ε与d33[98]; (c) 双向极化应变曲线; (d) 电滞回线; (e) 单向极化应变曲线随晶粒尺寸的变化[99]
Figure 3. The grain size effect on BT ceramics: (a) A wide range of grain size varying from 5 nm to 100 μm can be obtained in BT ceramics[27,30,52,54,63,93-95]; (b) ε and d33[98]; (c) bipolar strain curve; (d) hysteresis loop; (e) unipolar strain loop measured as a function of grain size[99].
图 4 BT陶瓷中(a)畴尺寸、(b)介电常数ε及(c)压电常数d33随晶粒尺寸的变化趋势; (d)高能X射线衍射图谱显示不同晶粒尺寸的BT陶瓷中平均晶面间距及(002)和(200)衍射峰强度在电场激励下的变化[95]. “nano”, “micro”分别表示纳米级和微米级粒径的BT陶瓷粉体; “MS”, “HP”, “SPS”, “CS”和“TSS”分别表示微波烧结、热压烧结、等离子放电烧结、普通烧结及两步法烧结方法
Figure 4. (a) Ferroelectric domain size, (b) ε, and (c) d33 of BT ceramics summarized as a function of grain size; (d) extrinsic contribution was found maximized when the grain size of BT ceramic is around 2 μm in a high-energy XRD measurement[95]. Note: “nano” and “micro” implies that the raw materials are nano-sized and micro-sized BaTiO3 powders. “MS”, “HP”, “SPS”, “CS”, and “TSS” represents the microwave sintering, hot-pressing, spark plasma sintering, conventional sintering and two-step sintering, respectively.
图 5 采用不同方法制得的BT陶瓷和带有不同相结构的BT陶瓷中, 晶粒尺寸效应呈现显著的不同 (a) 不同陶瓷粉体粒径和烧结方法制备BT陶瓷中d33随晶粒尺寸的变化趋势[28]; (b) Ba(Ti0.96Sn0.04)O3 (BTS)和(Ba0.85Ca0.15)(Zr0.1Ti0.9)O3 (BCZT)陶瓷中d33与
${d}_{33}^{{*}}$ 随晶粒尺寸的变化趋势[119,120]Figure 5. Grain size effect can be different among BT ceramics with virous phase structure and by different preparation method: (a) Grain size dependence of d33 of BT ceramics prepared by using different sintering method[28]; (b) d33 and
$ {d}_{33}^{{*}} $ of Ba(Ti0.96Sn0.04)O3, (Ba0.85Ca0.15)(Zr0.1Ti0.9)O3 ceramics with different average grain sizes[119,120].图 6 (a) 通过控制烧结温度获得晶粒尺寸不同的PZT陶瓷[141]; (b) d33和d31随烧结温度的变化[141]; (c) 晶粒尺寸效应的“空间电荷模型”[132]
Figure 6. (a) Grain size evolution in PZT ceramics as a function of sintering temperature[141]; (b) piezoelectric coefficients of PZT ceramics measured as a function of sintering temperature[141]; (c) illustration of the “space-charge model” [132].
图 7 (a) PZT陶瓷的d33, d31, dh和Pr与晶粒尺寸的关系[25]; (b) PZT陶瓷的晶体四方性c/a与晶粒尺寸的关系[25]; (c) 晶粒尺寸为3.9 μm和10.4 μm的PZT陶瓷的压电力显微镜(PFM)图[150]; (d) 在细晶粒陶瓷的晶界上观察到比较强烈的局部矫顽场[150]; (e) 不同晶粒尺寸PZT陶瓷样品经过2000次电循环去老化后测量的电致应变曲线(左), 双极化应变Sbip和Pr与晶粒尺寸的关系(右)[150]
Figure 7. (a) d33, d31, dh, and Pr of PZT ceramics measured as a function of grain size[25]; (b) c/a ratio measured as a function of grain size[25]; (c) PFM amplitude images of PZT samples with average grain sizes of 3.9 μm and 10.4 μm[150]; (d) stronger local coercive voltages can be obtained at the grain boundary in the fine grain[150]; (e) bipolar strain and Pr of PZT ceramics measured as a function of grain size after de-aging[150].
图 8 (a) KNN-x Sr陶瓷中铁电畴尺寸随着晶粒尺寸的变化; 在总体畴壁密度提升的同时, 导电畴壁的数量也大幅增加[170]; (b) KNN基陶瓷的铁电与压电性能随着晶粒尺寸的变化[171]
Figure 8. (a) Variation of domain size as a function of grain size in KNN-x Sr ceramics; an increased amount of conductive domain wall is observed as the grain size decreases[170]; (b) evolution of ferroelectric and piezoelectric properties as a function of grain size in KNN-based ceramics[171].
图 9 (a) KNN陶瓷在高温烧结过程中产生液相导致的异常晶粒长大[176]; (b) 通过改变烧结气氛可以抑制陶瓷中的异常晶粒长大[177]; (c) 在KNN基陶瓷预烧粉末中观察到的异常晶粒长大[178]
Figure 9. (a) Abnormal grain growth in sintered KNN ceramics caused by the formation of the liquid phase at high temperature[176]; (b) abnormal grain growth in sintered ceramics can be suppressed by controlling sintering atmosphere[177]; (c) irregular grain growth observed in calcined KNN-based ceramic powder[178].
图 10 (a) 利用闪速烧结方式制备细晶粒BNT基陶瓷[191]; (b) BNT基陶瓷中晶粒尺寸效应的物理模型[196]; (c) BNT基陶瓷的压电性能随晶粒尺寸的变化[197]
Figure 10. (a) Fine-grained BNT-based ceramics prepared by flash sintering[191]; (b) a qualitative model of the grain size effect in BNT-based ceramics[196]; (c) variation of piezoelectric properties of BNT-based ceramics as a function of grain size[197].
表 1 不同粉体制备方法与最细粉体粒径
Table 1. Ceramic powders prepared by using different approaches.
表 2 不同烧结方法与晶粒尺寸
Table 2. Grain size variation among BT, PZT, and KNN ceramics prepared by using different sintering techniques.
烧结方法 晶粒尺寸/μm BT PZT KNN 普通烧结 0.5—100[51,52] 1—10[25] 0.5—4[53] 两步法烧结 0.005—8.6[27,54] 1.6—6.4[55] 1.6—3.8[56,57] 热压烧结 0.3—1.2[23] 2—5[58] ~0.31[57] 热等静压烧结 0.32—47.3[59,60] 2—4[61] ~0.34[62] 微波烧结 ~3.4[63] ~2[64] < 1[65] 等离子放电烧结 0.02—1.2[52,66,67] 0.3—0.5[68] 0.2—1[69-71] 闪速烧结 0.3—0.4[72] #0.168—1.4 (AC)[73]
0.269—4 (DC)[74]* < 0.5&4[75] 注: #AC指在交流电场下的闪速烧结, DC指在直流电场下的闪速烧结;
*晶粒尺寸呈现双峰分布. -
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