Abstract
Despite the dominance of lead-based piezoelectric materials with ultrahigh electric-field-induced strain in actuating applications, seeking eco-friendly substitutes with an equivalent performance remains an urgent demand. Here, a strategy of regulating the irreversible non-180° domain via phase engineering is introduced to optimize the available strain (the difference between the maximum strain and the remnant strain in a unipolar strain curve) in the lead-free potassium–sodium niobate-based piezoelectric ceramics. In situ synchrotron X-ray diffraction and Rayleigh analysis reveal the contribution of the non-180° domain to available strain in the tetragonal–orthorhombic–rhombohedral phase boundary. The reducing orthorhombic phase and increasing rhombohedral/tetragonal phase accompanied by the reduced irreversible non-180° domain are obtained with increasing doping of Sb5+, resulting in an enlarged available strain due to the significantly lowered remnant strain. This optimization is mainly attributed to the reduced irreversible non-180° domain wall motion and the increased lattice distortion, which are beneficial to decrease extrinsic contribution and enhance intrinsic contribution. The mesoscopic structure of miniaturized nanosized domain with facilitated domain switching also contributes to the enhancement of available strain due to the improved random field and decreased energy barrier. The study will shed light on the design of lead-free high-performance piezoelectric ceramics for actuator applications.
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Introduction
Piezoelectric materials with the unique functionality of interconverting mechanical and electric energies, play a significant role in applications of many aspects, such as medicine, electronics, military, etc.1,2,3,4,5,6,7,8,9. The market demand for piezoelectric applications is expected to grow to a multi-billion-dollar with an annual growth of 13.2%10. As the most representative, piezoelectric actuators which can convert the electrical signal to displacement precisely, are expected to grow to 35.4 billion USD by 202611,12,13,14,15,16,17,18,19,20,21,22. For several decades, lead zirconate titanate [Pb(Zr, Ti)O3, PZT]-based piezoelectric actuators have dominated the market because of their outstanding performance11. Recently, restrictions on the use of lead in electronic devices have gradually come into practice due to ever-increasing ecological and environmental concerns, inducing great attention to lead-free piezoelectric materials8,9,10.
Electric field-induced-strain (or electrostrain) performance is one of the most important figure-of-merits for piezoelectric actuators12,13. Many breakthroughs have been made via microstructure manipulation in lead-free ceramics, including phase engineering, defect engineering, etc.15,16,17,18,19,20,21,22. For example, the giant electrostrain values of 0.7% (d33* ~1400 pm/V) and 1.05% (d33* ~2100 pm/V) have been achieved in bismuth sodium titanate [(Bi, Na)TiO3, BNT] and potassium–sodium niobate [(K, Na)NbO3, KNN]-based ceramics due to the electric field-induced phase transition and the interaction between defect dipoles and domain switching, respectively, leading to a new wave of research on this topic15,17. However, there remain critical challenges for practical applications, such as hysteresis and nonlinearity of electrostrain11,12,13. Additionally, a crucial issue of lead-free piezoelectric actuators is to obtain large available strain performance that is comparable to the lead-based ones. Generally, the actuating performance is assessed merely by the difference between poling strain (Spol) and remanent strain (Srem) (See Fig. 1a), which can be estimated via the following equation12:
where the Emax is the maximum electric field and d33* is the converse piezoelectric coefficient. Obviously, the higher Spol and the lower Srem, the better actuating performance. Namely, the actuating performance can be modified by enhancing Spol and/or restricting Srem. Spol can originate from multiple mechanisms, including the converse piezoelectric effect, non-180° domain wall motion, electrostriction, and possible electric field-induced phase transition11,12,13. On the other hand, the Srem is mainly generated by irreversible non-180° domain evolution which can keep the orientation after withdrawing the electric field12. Compared to the complex mechanisms for Spol, Srem with a rather straightforward contribution of the irreversible non-180° domain might be easier to regulate. Modifying the irreversible non-180° domain could be an effective approach to optimize available strain.
It is known that a change in lattice symmetry can lead to a variation in domain morphology, which can be accompanied by phase engineering and defect engineering23,24,25,26,27,28,29,30. Among them, phase engineering has been demonstrated to be the most promising approach3. KNN-based lead-free ceramics with multiphase boundary, which exhibit excellent piezoelectric response, are a great candidate for piezoelectric applications but there are challenges ahead27. Of the utmost importance, the mechanism for Srem needs to be urgently revealed, especially the connection between available strain (Suni–Srem) and irreversible non-180° domain for improving the practical actuating strain12. Here, the contribution of the irreversible non-180° domain to available strain is revealed via adjusting the rhombohedral–orthorhombic–tetragonal (R–O–T) phase boundary in high-performance KNN-based ceramics (Fig. 1b). Significantly, a high available strain is realized with reduced irreversible non-180° domain and decreased domain size based on increased R/T and decreased O phase. The underlying mechanism of enhancement is discussed based on the reduced extrinsic contribution of domain evolution and elevated intrinsic contribution of phase transition, accompanied by decreased domain size and facilitated domain switching. This work demonstrates an effective approach to the design of high-strain performance piezoelectric materials for actuators.
Results
Phase structure and macro-performance
A typical perovskite structure is obtained without any impurity phase in all the ceramics (Supplementary Fig. 1a, b)3. Room temperature phase transitions including TR–O and TO–T are observed for x = 0.035–0.055, indicating the R–O–T phase boundary (Supplementary Figs. 1c, 2 and Supplementary Table 1) which is verified by the Rietveld refinement (Fig. 2a, Supplementary Fig. 3, and Supplementary Table 2). The modified phase structure and pronounced diffusion behavior in phase transition are achieved by the increasing TR–O and decreasing TO–T as well as the enlarged compositional/structural heterogeneity (Supplementary Table 1 and Supplementary Fig. 4). The dominant R and O phases coexist with little T phase because of the much higher TO–T for x = 0.035, while the R–O–T phase boundary with strongly diffused behavior is obtained for x = 0.055 along with obviously diffused XRD and dielectric peaks. Samples with appropriate R–O–T phase structure (x = 0.04–0.05) are adopted to explore the effect on domain evolution from phase content. Significantly, the R and T phases increase as the O phase decreases with increasing Sb5+ content (Fig. 2b). It is known that the R phase contains spontaneous polarizations along 8 directions of <111>, which leads to the formation of 0°, 71°, 90°, 109°, and 180° domain walls31. For the O phase, there are 12 directions along <011> which leads to the formation of 0°, 60°, 90°, 120°, and 180° domain walls, while for the T phase, there are 6 directions along <001>, which leads to the formation of 0°, 90°, and 180° domain walls, respectively (Fig. 2c–e)31. The R–O–T phase boundary gradually changes to the O–T phase, T phase, and cubic phase finally with increasing temperature, leading to the reduced non-180° domain and weakened domain response (Fig. 2f)3. Thus, the domain characteristics depend on phase content correspondingly. Especially, the variation of the non-180° domain could yield different performances (Supplementary Table 3 and Fig. 5). Improved piezoelectric and ferroelectric properties are achieved for x = 0.045. Meanwhile, strain evolution is further emphasized since it is a figure of merit for piezoelectric actuators. From the unipolar strain curves (Fig. 2g), Srem drops from 0.024% to 0.019% when x increases from 0.04 to 0.05 along with little changed Suni (~0.206%), contributing to enhanced Suni–Srem, where the largest value of 0.187% is observed for x = 0.05 (Fig. 2h, i). The high available strain achieved is favorable for the piezoelectric actuating applications12,13.
Characterization of irreversible non-180° domain
The electrostrain originates from both intrinsic lattice strain and extrinsic strain from the non-180° domain, where the latter often plays a major role12,21. Thus, the evolution of domains upon applied electric field is explored. In situ, X-ray diffraction (XRD) has been recognized as a powerful approach to structure analysis during poling for piezoelectric materials32,33,34,35,36,37,38,39,40,41,42,43,44. Notably, the shift of diffraction peak position and variation of peak intensity can reflect the piezoelectric lattice strain due to the change of the unit cell and non-180° domain switching, respectively34. Of particular interest, the XRD patterns of (111) and (200) reflections are specifically investigated34,43. The domain evolution under different electric fields [virgin: 0 kV/mm→in situ: 3Ec (coercive electric field)→poled: 0 kV/mm] is revealed with well-fitted diffraction with R, O, and T phases (Fig. 3a and Supplementary Fig. 6). The volume fractions (F) of phases within the R–O–T multiphase coexistence can be approximately derived according to the following formula45:
where SIR, SIR, and SIR are the sums of peak intensities of (200) reflections for R, O, and T phases, respectively. The volume fractions of the phases are obtained from the characterization of the virgin state. Increasing R and T phases, as well as the decreasing O phase, are revealed due to increasing Sb5+ content (Supplementary Fig. 7), which conforms to the result from the Rietveld refinement of XRD patterns. Importantly, a considerably enhanced volume fraction of non-180° domains parallel to the electric field direction is observed during the application of external electric field in all samples, which is evidenced by the changed peak intensity ratios between the 111R/11-1R, 202o/020o, and 002T/200T reflections for the R, O, and T phases, respectively34,43. The volume fraction (f) of domains parallel to the electric field direction for R, O, and T phases can be expressed by the following equation34:
The fR, fO, and fT first increase and then decrease in the ceramics within the applied electric field process from 0 kV/mm to 3Ec, and subsequently to 0 kV/mm (Supplementary Fig. 8), which can be ascribed to the reorientation of the non-180° domain under electric field. Significantly, the volume fraction of domains parallel to the electric field direction depends on the phase content for multiphase coexistence. Thus, for the ceramics with R–O–T phase boundary, the f can be modified as follows34:
For the virgin state, the f shows a decreasing trend from 50.5% to 39.2% with increasing Sb5+ content (Fig. 3b). Compared with the virgin state, f exhibits a relatively large improvement with an electric field of 3Ec. The biggest f is up to 81.8% for x = 0.04, which is probably ascribed to the high O phase content with spontaneous polarization of more available directions. After removal of the electric field, f drops due to the depolarization process. Notably, the f of the poled state is still larger than that of the virgin state, suggesting the contribution of the irreversible non-180° domain switching. The contribution of non-180° domain switching under various electric fields can be quantitatively analyzed according to the following equations36:
where Δf1 and Δf2 are the degree of reversible and irreversible non-180° domain switching, respectively, and Δf3 is the degree of total non-180° domain switching. Δf1, Δf2, and Δf3 decrease with increasing Sb5+ content (Fig. 3c), corresponding with the variation of O phase content, implying reducing extrinsic contribution. In particular, the reduced irreversible non-180° domain switching is responsible for the decreased Srem. The strain from reversible domain switching can be calculated based on the assumption that the change of strain is proportional to the poling texture change, and it is determined by the following equation36:
where Sneg is obtained from bipolar strain curves (Supplementary Fig. 5). It is obvious that the S value first increases and then decreases with a level of 0.095–0.120% in the ceramics (Fig. 3d).
To further explore the contribution of irreversible domain switching, Rayleigh law based on phenomenological theory is also used to reveal the origin of strain46,47,48,49,50,51,52. The domain structure remains unchanged with the AC field cycle of 1/2Ec to 1/3Ec during the Raleigh region, leading to an increase linearly piezoelectric constant under the sub-switching conditions50. Their Rayleigh relationship can be expressed as follows50:
where S is strain value, E is the driving electric field, E0 is the maximum electric field, dinit is the initial reversible piezoelectric response, α is the piezoelectric Rayleigh coefficient, and αE0 describes the irreversible piezoelectric response caused by the irreversible domain response. The S–E loops are measured at an AC electric field with a maximum amplitude of 3 kV/cm after poling at a high electric field. The fitting results suggest a high reliability for Rayleigh parameters in the ceramics (Fig. 3e and Supplementary Fig. 9a, d). The Rayleigh parameters of dinit and α, corresponding to the reversible and irreversible piezoelectric response, can be calculated by linear fitting of measured d33* as a function of electric field (Fig. 3f and Supplementary Fig. 9b, e), while d33* is obtained according to the following equation50:
where \({x}_{{{{{{\rm{p}}}}}}-{{{{{\rm{p}}}}}}}\) is the difference between positive and negative strain values. The dinit first increases and then decreases with increasing Sb5+ (Fig. 3g). The enhancement when x increases from 0.04 to 0.045 is ascribed to the modified R–O–T boundaries with flatter Gibbs free energy, while the decline for x = 0.05 results from the relative excessive diffusion behavior. The irreversible piezoelectric coefficient α decreases with the increasing content of Sb5+, which is due to the decreased extrinsic contribution from irreversible domain evolution with decreasing O phase and strengthened diffusion behavior. Combining with the calculated dinit and α, d33* can be gained according to Eq. (15) with E0 = 3 kV/cm (Fig. 3i). Then, the unipolar S–E curve is measured at large electric fields for characterizing the intrinsic piezoelectric activity caused by the lattice distortion, while the domains are almost clamped and supply little contribution of domain switching or the motion of domain wall to the piezoelectric response. The slope for the linear part of S–E loops is calculated as the intrinsic piezoelectric coefficient (dlatt) (Fig. 3h and Supplementary Fig. 9c, f). The dlatt slightly increases first and then drops after adding Sb5+ (Fig. 3i). In addition, the contribution of reversible domain wall motion (drever-DW) can be calculated as follows50:
Similar to the variation of dlatt and dinit, the contribution of reversible domain wall motion also first increases and then decreases in the ceramics (Supplementary Fig. 10).
Thus, the proportion of intrinsic contribution (Cintri) from the lattice deformation can be calculated as50:
The Cintri increases with elevating Sb5+, implying an enlarged contribution of lattice distortion (Fig. 3j), and the extrinsic contribution from the irreversible domain response can be evaluated as follows50:
The decreased Cirrever manifests that the weakened irreversible domain response is caused by the decreased amount of non-180° domain with decreasing O and increasing R/T phase, which is consistent with the results of in situ synchrotron XRD.
Characterization of domain morphology
With optimized available strain from the modified irreversible non-180° domain, the domain morphology as well as switching behavior under bias is further explored50. The virgin domain structure is characterized as presented in Fig. 4a–c. Combining with the amplitude and phase images (Supplementary Fig. 11a–c), a refined domain is observed with increasing Sb5+ content, due to the reduced O phase and strengthened diffusion instead of grain evolution that changes little (Supplementary Fig. 12). Then, the lithography process is adopted at the regions under the bias of 2–8 V to analyze the domain switching behavior (Fig. 4d). Notably, although domain switching obvious happened at 4 V for x = 0.04 and 0.045 while little switching is found at 2 V, better switching is obtained for x = 0.045 than that for x = 0.04 (Fig. 4e, f and Supplementary Fig. 11d, e). The promoted domain switching is mainly generated by the modified phase content and diffusion behavior with a lowered energy barrier, which is also the origin of high piezoelectric performance (Supplementary Table 3). However, poor domain switching is observed for x = 0.05 due to diffused behavior which can make the domain recover easily after withdrawing bias (Fig. 4g and Supplementary Fig. 11f). Meanwhile, optimized piezoelectric response is also gained with the bias voltage-induced piezoresponse hysteresis and phase loops (Fig. 4h, i).
To reveal the domain morphology more accurately, TEM images are supplied as presented in Fig. 4j–l. A nano-sized stripe domain pattern is observed in all the ceramics along with uniformly distributed elements (Supplementary Fig. 13), conforming to the reported system with high performance from diffused R–O–T phase boundary26,53,54,55. The nano-sized stripe domain is further verified according to a regular fluctuated intensity at the regions marked by dotted lines (Fig. 4m–o), and the domain size decreases from 27 nm for x = 0.04 to 17 nm for x = 0.045, and 9 nm for x = 0.05 finally (Fig. 4p).
Discussion
The contribution of the irreversible non-180° domain to available strain is closely associated with the phase content for multiphase coexistence. When the O phase decreases with increasing R and T phases, the irreversible non-180° domain gradually reduces because of the reduced non-180° domain wall, generating decreased Srem values. Meanwhile, large Suni is maintained well because of the existence of the R–O–T phase boundary which contains a strong converse piezoelectric effect and flexible domain response. Then, optimized available strain is realized with reduced O phase in the ceramics. By further decreasing the O phase and increasing the R and T phase (x = 0.05), not only the irreversible non-180° domain decrease, but also the diffusion is strengthened which signifies the enlarged random field that can accelerate the domain recovery after withdrawing the electric field, yielding to further increased Suni–Srem along with lowered Srem.
In addition, the irreversible non-180° domain evolution is also affected by the external field which induces structure transformation. Both Srem and Suni–Srem gradually increase under elevating electric fields as Pr and small signal d33 increase rapidly when E ≤ 20 kV/cm and almost stay high values when E ≥ 25 kV/cm, which is due to the enhanced effective field applied on the irreversible non-180° domain with increasing electric field (Supplementary Fig. 14). Therefore, it can be noted that the higher electric field, the more sufficient domain switching and weaker domain reversion, manifesting that application of high electric field is beneficial of promoting available strain from increasing irreversible of the non-180° domain. With increasing temperature, the Srem and Suni–Srem reduce owing to reduced irreversible non-180° domain wall from increased T phase and decreased R and O phases and lowered polarity as well as impeded polarization rotation (Supplementary Fig. 15). And small signal d33 also decline sharply due to gradually vanished phase boundary, limited domain switching and reduced polarizability. Notably, strongly dropped Srem happens at the second cycle because most irreversible non-180° domains have been switched during the first cycle (Supplementary Fig. 16). Furthermore, little change is observed after three cycles, indicating little recovery of switched irreversible non-180° domains. Significantly, Suni–Srem and Pr exhibit slight fluctuation with increasing cycles, owing to sufficient domain switching for every cycle. The little change of Sneg is observed when n ≥ 2, which is attributed to the switched irreversible non-180° domain along the direction of the negative electric field after the first cycle. And, increasing Srem and Suni–Srem are observed for the ceramics with increasing frequency, while Pr presents a decreasing tendency (Supplementary Fig. 17), indicating the decline of the irreversible non-180° domain. The higher the frequency, the poorer the sufficiency of domain switching. The lowered contribution of the irreversible non-180° domain appears accordingly.
In summary, the contribution of the non-180° domain to available strain is revealed based on the R–O–T phase boundary in KNN-based ceramics. Enlarged Suni–Srem is achieved with significantly lowered Srem via reducing O and increasing R/T phase along with declined irreversible non-180° domain. According to the evolution of phase and domain structure, enhanced intrinsic and lowered extrinsic contributions are obtained to strain with increasing content of Sb5+, attributing to the strengthened lattice distortion and reduced irreversible non-180° domain wall motion along with the improved random field. The mesoscopic manifestation is refined domain size and easy domain switching under external electric fields. Therefore, the modification of the irreversible non-180° domain is an effective method for designing high-performance functional materials for piezoelectric actuators.
Methods
Sample preparation
The ceramics with multiphase coexistence: 0.965K0.48Na0.52Nb1−xSbxO3–0.02Bi0.5Na0.5ZrO3–0.015CaZrO3–0.4%Fe2O3 (x = 0.035, 0.04, 0.045, 0.05, and 0.055) were prepared via conventional solid-state method. The raw materials including K2CO3 (99.0%), Na2CO3 (99.8%), Nb2O5 (99.5%), Sb2O3 (99.99%), Bi2O3 (99.999%), ZrO2 (99%), CaCO3 (99%), and Fe2O3 (99%) produced by Sinopharm Chemical Reagent Co., Ltd., were ball milled for 24 h with both ZrO2 ball media and alcohol after weighed according to the formula. The dried powders were calcined at 850 °C for 6 h with a heating rate of 3 °C min−1, which were made into a disk with a diameter of ~10.0 mm and a thickness of ~1.0 mm under a pressure of 10 MPa with 8% PVA as a binder by the dry pressing process. After burning off the PVA of the disk, the specimens were sintered at 1070–1090 °C for 3 h with a heating rate of 3 °C min−1 in air. Furthermore, the upper and under surface of the ceramics were covered by silver paste and then were sintered at 600 °C for 10 min. Finally, a direct current electric field of 3–4 kV/mm for 30 min was applied to the samples in a silicon oil bath.
Structure characterizations
The XRD patterns were gained by XRD machine with Cu kα radiation in the θ-2θ scan mode (Bruker D8 Advanced XRD, Bruker AXS Inc., Madison, WI). The Materials Analysis Using Diffraction (MAUD) program was used to refine the XRD data to analyze the crystal structure parameters by selecting KNbO3 (tetragonal P4mm, orthorhombic Amm2, and rhombohedral R3m) as the initial model. In situ, synchrotron XRD under 0 and 3Ec was performed using Source BL02U2 (photon energy 18 keV) beamline in Shanghai Synchrotron Radiation Facility. A thermally stimulated depolarization current was measured by an electrometer (Keithley 6517B, Keithley Instruments, Inc., Cleveland, OH). A conductive Pt–Ir-coated cantilever PPP-NCHPt (Nanosensors, Switzerland) was applied to the Vertical Piezoresponse Force Microscopy (VPFM) with a commercial microscope (MFP-3D, Asylum Research, Goleta, CA). During the litho process, a negative voltage of 20 V was used first, and then a series of positive voltages (2, 4, 6, and 8 V) were employed in the oriented region. The triangular-wave high voltage was applied to obtain the local piezoresponse loops by the Switching Spectroscopy Piezoresponse Force Microscopy (SS-PFM) mode. The argon-ion beam milling (Gatan PIPS 695, Gatan Inc., USA) with an operating voltage of 0.1–6 kV to reach electron transparency was used for Transmission Electron Microscopy (TEM) specimen with mechanical polishing to around 20 μm in thickness. A high-resolution transmission electron microscope (JEOL 2100F, JEOL, Japan) operated at 200 kV was used for the TEM. The morphology of the surface was carried out using the Field-emission Scanning Electron Microscope (FE-SEM) (JSM-7500, Japan).
Electrical property measurements
The dielectric properties as a function of temperature in the range of −120–150 °C and 50–400 °C were gained by an LCR analyzer (E4980A, Keysight, USA). An impedance analyzer (Impedance Analyzer, PV70A, Beijing, China) was used to measure the planar electromechanical coupling factor (kp) by a resonance-antiresonance method. A commercial Berlincourt-type d33 meter (ZJ-3A, China) was applied to obtain the d33 of the poled samples. A ferroelectric tester (aixACC TF Analyzer 2000E, Germany) was used for measuring the ferroelectric hysteresis (P–E) loops, d33–E, and strain curves (S–E). The bipolar electric fields with amplitudes smaller than 1/2 Ec were applied to the samples according to the Rayleigh relationship under the sub-switching conditions. Then the unipolar S–E curve under a large electric field with the slope of a linear part can be realized from the increasing applied electric fields.
Data availability
The source data generated in this study are provided in the Source Data file. More relevant data sets generated during and/or analyzed during the current study are available from the first authors and corresponding authors on reasonable request. Source data are provided with this paper.
References
Jaffe, B., Cook, W. R. & Jaffe, H. Piezoelectric Ceramics (Academic Press, London, 1971).
Zhang, S. J. et al. Advantages and challenges of relaxor-PbTiO3 ferroelectric crystals for electroacoustic transducers—a review. Prog. Mater. Sci. 68, 1–66 (2015).
Wu, J. G., Xiao, D. Q. & Zhu, J. G. Potassium–sodium niobate lead-free piezoelectric materials: past, present, and future of phase boundaries. Chem. Rev. 115, 2559–2595 (2015).
Li, J. F., Wang, K., Zhu, F. Y., Cheng, L. Q. & Yao, F. Z. (K, Na)NbO3-based lead-free piezoceramics: fundamental aspects, processing technologies, and remaining challenges. J. Am. Ceram. Soc. 96, 3677–3696 (2013).
Lv, X., Zhu, J. G., Xiao, D. Q., Zhang, X. X. & Wu, J. G. Emerging new phase boundary in potassium sodium niobate-based ceramics. Chem. Soc. Rev. 49, 671–707 (2020).
Sun, Z. X. et al. Ultrahigh energy storage capacity in multilayer-structured cellulose-based dielectric capacitors caused by interfacial polarization-coupled Schottky barrier height. J. Mater. Chem. A 11, 20089–20101 (2023).
Sun, Z. X. et al. Achieving ultrahigh energy storage density in super relaxor BCZT-based lead-free capacitors through multiphase coexistence. Appl. Phys. Lett. 122, 263904 (2023).
Shrout, T. R. & Zhang, S. J. Lead-free piezoelectric ceramics: Alternatives for PZT? J. Electroceram. 19, 113–126 (2007).
Rödel, J. & Li, J. F. Lead-free piezoceramics: status and perspectives. MRS Bull. 43, 576–580 (2018).
Hong, C. H. et al. Lead-free piezoceramics–Where to move on? J. Materiomics 2, 1–24 (2016).
Hao, J. G., Li, W., Zhai, J. & Chen, H. Progress in high-strain perovskite piezoelectric ceramics. Mater. Sci. Eng. Rep. 135, 1–57 (2019).
Jo, W. et al. Giant electric-field-induced strains in lead-free ceramics for actuator applications—status and perspective. J. Electroceram. 29, 71–93 (2012).
Acosta, M. Strain Mechanisms in Lead-Free Ferroelectrics for Actuators (Springer International Publishing, New York, 2016).
Narayan, B. et al. Electrostrain in excess of 1% in polycrystalline piezoelectrics. Nat. Mater. 17, 427–431 (2018).
Liu, X. & Tan, X. Giant strains in non-textured (Bi1/2Na1/2)TiO3-based lead-free ceramics. Adv. Mater. 28, 574–578 (2016).
Hu, C. et al. Ultra-large electric field–induced strain in potassium sodium niobate crystals. Sci. Adv. 6, eaay5979 (2020).
Huangfu, G. et al. Giant electric field-induced strain in lead-free piezoceramics. Science 378, 1125–1130 (2022).
Piezoelectric devices market with COVID-19 impact analysis by material (piezoelectric ceramics, polymers), product (piezoelectric actuators, transducers, motors), application (aerospace & defense, industrial, consumer), and region-global forecast to 2026. Piezoelectric Devices Market (Markets and Markets, 2021).
Ren, X. B. Large electric-field-induced strain in ferroelectric crystals by point-defect-mediated reversible domain switching. Nat. Mater. 3, 91–94 (2004).
Zhao, Z. H., Lv, Y. K., Dai, Y. J. & Zhang, S. J. Ultrahigh electro-strain in acceptor-doped KNN lead-free piezoelectric ceramics via defect engineering. Acta. Mater. 200, 35–41 (2020).
Liu, Y. X., Thong, H. C., Cheng, Y. Y. S., Li, J. W. & Wang, K. Defect-mediated domain-wall motion and enhanced electric-field-induced strain in hot-pressed K0.5Na0.5NbO3 lead-free piezoelectric ceramics. J. Appl. Phys. 129, 024102 (2021).
Wu, B. et al. Facilitated reversible domain switching at multiphase boundary in periodically orthogonal poled KNN-based ceramics: strain vs. non-180° domain. J. Am. Ceram. Soc. 107, 1009–1019 (2024).
Zhang, M. H. et al. Deciphering the phase transition-induced ultrahigh piezoresponse in (K,Na)NbO3-based piezoceramics. Nat. Commun. 13, 3434 (2022).
Tao, H. et al. Ultrahigh performance in lead-free piezoceramics utilizing relaxor slush polar state with multiphase coexistence. J. Am. Chem. Soc. 141, 13987–13994 (2019).
Gao, X. Y. et al. The mechanism for the enhanced piezoelectricity in multi-elements doped (K,Na)NbO3 ceramics. Nat. Commun. 12, 881 (2021).
Wu, B. et al. Giant piezoelectricity and high curie temperature in nanostructured alkali niobate lead-free piezoceramics through phase coexistence. J. Am. Chem. Soc. 138, 15459–15464 (2016).
Wang, K., Malic, B. & Wu, J. G. Shifting the phase boundary: potassium sodium niobate derivates. MRS Bull. 43, 607–611 (2018).
Bell, A. J. & Deubzer, O. Lead-free piezoelectrics-The environmental and regulatory issues. MRS Bull. 43, 581–587 (2018).
Zhao, Z., Dai, Y., Li, X., Zhao, Z. & Zhang, X. The evolution mechanism of defect dipoles and high strain in MnO2-doped KNN lead-free ceramics. Appl. Phys. Lett. 108, 172906 (2016).
Feng, Y. et al. Defects and aliovalent doping engineering in electroceramics. Chem. Rev. 120, 1710–1787 (2020).
Marton, P., Rychetsky, I. & Hlinka, J. Domain walls of ferroelectric BaTiO3 within the Ginzburg–Landau–Devonshire phenomenological model. Phys. Rev. B 81, 144125 (2010).
Liu, Y., Liu, H., Sun, S., Wang, L. & Chen, J. Direct observation of electric field-induced tetragonal-orthorhombic phase transition in KNN-based piezoelectric ceramics via in-situ synchrotron diffraction. Scr. Mater. 207, 114283 (2022).
Hall, D. A., Steuwer, A., Cherdhirunkorn, B., Mori, T. & Withers, P. J. A high energy synchrotron X-ray study of crystallographic texture and lattice strain in soft lead zirconate titanate ceramics. J. Appl. Phys. 96, 4245–4252 (2004).
Fu, J., Zuo, R. Z., Xu, Y. D., Li, J. F. & Shi, M. Investigations of domain switching and lattice strains in (Na,K)NbO3-based lead-free ceramics across orthorhombic-tetragonal phase boundary. J. Eur. Ceram. Soc. 37, 975–983 (2017).
Jones, J. L., Slamovich, E. B. & Bowman, K. J. Domain texture distribution in tetragonal lead zirconate titanate by X-ray and neutron diffraction. J. Appl. Phys. 97, 034113 (2005).
Kungl, H. et al. Estimation of strain from piezoelectric effect and domain switching in morphotropic PZT by combined analysis of macroscopic strain measurements and synchrotron X-ray data. Acta Mater 55, 1849–1861 (2007).
Hinterstein, M. et al. Interplay of strain mechanisms in morphotropic piezoceramics. Acta Mater 94, 319–327 (2015).
Fan, L. L. et al. Unique piezoelectric properties of the monoclinic phase in Pb(Zr, Ti)O3 ceramics: large lattice strain and negligible domain switching. Phys. Rev. Lett. 116, 027601 (2016).
Khatua, D. K., Lalitha, K. V., Fancher, C. M., Jones, J. L. & Ranjan, R. Anomalous reduction in domain wall displacement at the morphotropic phase boundary of the piezoelectric alloy system PbTiO3–BiScO3. Phys. Rev. B 93, 104103 (2016).
Jones, J. L., Hoffman, M. & Bowman, K. J. Saturated domain switching textures and strains in ferroelastic ceramics. J. Appl. Phys. 98, 024115 (2005).
Reszat, J. T., Glazounov, A. E. & Hoffmann, M. J. Analysis of intrinsic lattice deformation in PZT-ceramics of different compositions. J. Eur. Ceram. Soc. 21, 1349–1352 (2001).
Hall, D. A., Steuwer, A., Cherdhirunkorn, B., Mori, T. & Withers, P. J. Analysis of elastic strain and crystallographic texture in poled rhombohedral PZT ceramics. Acta Mater 54, 3075–3083 (2006).
Zuo, R. Z., Qi, H., Xie, A. W. & Zheng, D. G. Anomalously large lattice strain contributions from rhombohedral phases in BiFeO3-based high-temperature piezoceramics estimated by means of in-situ synchrotron X-ray diffraction. J. Eur. Ceram. Soc. 38, 4653–4658 (2018).
Zuo, R. Z., Qi, H., Fu, J., Li, J. F. & Li, L. T. Multiscale identification of local tetragonal distortion in NaNbO3–BaTiO3 weak relaxor ferroelectrics by Raman, synchrotron X-ray diffraction, and absorption spectra. Appl. Phys. Lett. 111, 132901 (2017).
Ahn, C. W. et al. Correlation between phase transitions and piezoelectric properties in lead-free (K, Na, Li)NbO3-BaTiO3 ceramics. Jpn, J. Appl. Phys. 47, 8880–8883 (2008).
Tutuncu, G., Forrester, J. S., Chen, J. & Jones, J. L. Extrinsic contributions to piezoelectric Rayleigh behavior in morphotropic PbTiO3–BiScO3. Acta Mater 137, 45–53 (2017).
Kobayashi, K., Hatano, K., Mizuno, Y. & Randall, C. A. Rayleigh behavior in the lead free piezoelectric Lix(Na0.5K0.5)(1‑x)NbO3 ceramic. Appl. Phys. Exp. 5, 031501 (2012).
Damjanovic, D. Ferroelectric, dielectric and piezoelectric properties of ferroelectric thin films and ceramics. Rep. Prog. Phys. 61, 1267 (1998).
Damjanovic, D. Logarithmic frequency dependence of the piezoelectric effect due to pinning of ferroelectric–ferroelastic domain walls. Phys. Rev. B 55, R649–R652 (1997).
Xing, J., Mo, M. Y., Cheng, Y., Tan, Z. & Zhu, J. G. Decoding the piezo-contributions of potassium sodium niobate ceramics. J. Phys. Chem. C 128, 658–666 (2024).
Kim, D. J., Maria, J. P., Kingon, A. I. & Streiffer, S. K. Evaluation of intrinsic and extrinsic contributions to the piezoelectric properties of Pb(Zr1−xTix)O3 thin films as a function of composition. J. Appl. Phys. 93, 5568–5575 (2003).
Gao, J. et al. Major contributor to the large piezoelectric response in (1−x)Ba(Zr0.2Ti0.8)O3−x(Ba0.7Ca0.3)TiO3 ceramics: domain wall motion. Appl. Phys. Lett. 104, 252909 (2014).
Xu, K. et al. Superior piezoelectric properties in potassium–sodium niobate lead-free ceramics. Adv. Mater. 28, 8519–8523 (2016).
Liu, Q. et al. Practical high-performance lead-free piezoelectrics: structural flexibility beyond utilizing multiphase coexistence. Natl. Sci. Rev. 7, 355–365 (2020).
Lv, X., Zhang, X. X. & Wu, J. G. Nano-domains in lead-free piezoceramics: a review. J. Mater. Chem. A 8, 10026–10073 (2020).
Acknowledgements
K.W. acknowledges the support of the National Key Research and Development Program of China (No. 2020YFA0711700). H.T. acknowledges the support of the National Natural Science Foundation of China (No. 52202149), the Foundation of Sichuan Province Science and Technology Support Program (No. 2023NSFSC0968, 2021YJ0560, 22ZDYF3306, 2022NSFSC1970), and the Fundamental Research Funds for the Central Universities, Southwest Minzu University (No. ZYN2023110). S.-D.W acknowledges the support by the National Natural Science Foundation of China (No. 82202349), the Beijing Natural Science Foundation (No. L222066), and Peking University People’s Hospital research and development funds (No. RDJP2022-44). B.H. acknowledges the support of the National Natural Science Foundation of China (No. 51972005, U21A2055). F.-Y. Zhu acknowledges the support of the National Natural Science Foundation of China (No. 52032005). We acknowledge W.-J.W. for the provision of PFM (MFP-3D, Asylum Research, Goleta, CA) experimental facilities, and the BL02U2 beamline of SSRF is acknowledged for the provision of experimental beamtime.
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B.W., H.T., S.-D.W., B.H., and K.W. conceived the idea of this work. B.W., L.Z., and J.-Q.F. prepared the KNN ceramics while Y.-T. Z., X.-L.S., Z.X., J.-T.L., and F.-Y.Z. performed the electrical and structural measurements and analyzed the data with J.M., H.T., and K.W. guided the project. J.M., S.-D.W., B.H., and K.W. provided financial and technical support for this work and provided indispensable suggestions together with Y.-X.L.
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Wu, B., Zhao, L., Feng, J. et al. Contribution of irreversible non-180° domain to performance for multiphase coexisted potassium sodium niobate ceramics. Nat Commun 15, 2408 (2024). https://doi.org/10.1038/s41467-024-46800-z
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DOI: https://doi.org/10.1038/s41467-024-46800-z
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