Higher permittivity of Ni-doped lead zirconate titanate,Pb[(Zr0.52Ti0.48)(1-x) Nix]O3, ceramics

The paper reports highest obtained dielectric constant for Ni-doped Lead Zirconate Titanate [PZT, Pb(Zr_0.52Ti_0.48)O₃] ceramics. The Ni-doped PZT ceramic pellets were prepared via conventional solid-state reaction method with Ni content chosen in the range 0–20?at%. X-ray diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopy were employed to investigate the crystal structure of the prepared ceramics. The X-ray diffraction analysis indicated that the ceramic pellets had crystallized into tetragonal perovskite structure. A minute displacement of XRD peaks was detected in the diffraction spectra of Ni-doped PZT ceramic samples which when examined by size-strain plot (SSP) method revealed presence of homogenous strain that decreased with increase in concentration of Ni. In FTIR the maximum absorption at 597?cm^?1, 608?cm^?1, 611?cm^?1, 605 and 613?cm^?1 for Ni?=?0, 5, 10, 15 and 20?at%, respectively, confirmed the formation of perovskite structure in all the compositions and the slight shift suggests decrease in cell size on doping. The values of dielectric constant (ε′) & tanδ as a function of frequency and temperature were measured for the prepared ceramics and it revealed highest ever reported dielectric constant for Ni - doped PZT with Ni?=?5?at%. The dielectric variation with temperature exhibited a diffused type ferroelectric–paraelectric phase transition for the doped samples. Also, the maximum dielectric constant value (ε′_max) decreased while the phase transition temperature increased with increase in doping concentration of Ni. The estimated activation energy of different compositions was found to increase from 0.057 to 0.068?eV for x?=?0.00 to x?=?0.20 in ferroelectric phase. The piezoelectric, ferroelectric and magnetic properties were also investigated.     

Correlation between structural,ferroelectric, piezoelectric and dielectric properties of Ba0.7Ca0.3TiO3-xBaTi0.8Zr0.2O3 (x = 0.45, 0.55) ceramics

We report on the correlation between structural, ferroelectric, piezoelectric and dielectric properties of the (1-x)Ba_0.7Ca_0.3TiO₃-xBaTi_0.8Zr_0.2O₃ (x?=?0.45, 0.55; abbreviated as 55BCT30 and 45BCT30) ceramics close to morphotropic phase boundary (MPB) region. The 55BCT30 and 45BCT30 ceramics were synthesized by the standard, high-temperature solid state ceramic method. X-ray diffraction (XRD) along with Rietveld refinement indicate that the 55BCT30 ceramics exhibit rhombohedral (R, space group R3m), orthorhombic (O, space group Amm2) and tetragonal (T, space group P4mm) phases while 45BCT30 ceramics exhibit only T and O phases. The temperature dependent Raman spectroscopy measurements confirm the structure and phase transformations observed from XRD. All the ceramics are chemically homogeneous and exhibit a dense microstructure with a grain size of 5–7?µm. The presence of polarization-electric field and strain-electric field hysteresis loops confirm the ferroelectric and piezoelectric nature of the ceramics. The polarization current density-electric field curves show the presence of two sharp peaks in opposite directions indicating the presence of two stable states with opposite polarity. Higher values of direct piezoelectric coefficient (d₃₃ ~?360 pC/N) were observed due to the existence of low energy barrier near MPB region and polymorphism. The 55BCT30 ceramics exhibit a higher value of electrostrictive coefficient (Q₃₃ ~?0.1339?m⁴/C²) compared to the well-known lead-based materials. The temperature dependent dielectric measurements indicate the O to T phase transition for 55BCT30 and 45BCT30. These ceramics exhibit a Curie temperature (T_c) of 380?K with a dielectric maximum of ~ 4500.     

Large strain of temperature insensitive in (1–x)(0.94Bi0.5Na0.5TiO3–0.06BaTiO3) –xSr0.7La0.2TiO3 lead-free ceramics

Novel (1–x)(0.94Bi_0.5Na_0.5TiO₃–0.06BaTiO₃)–xSr_0.7La_0.2TiO₃ ternary lead-free ceramics (BNBT–xSL, x?=?0.00–0.08) were fabricated by the widely used solid-state sintering technique. The crystal phase, microstructure, dielectric relaxation, piezoelectric, and electromechanical properties of each composition were systematically analyzed. It is found that the addition of SL has little effect on the crystal phase and grain morphology, but it can remarkably improved the relaxation property of the ceramic sample and gave rise to favourable dielectric properties in a wide range of temperatures. In addition, as the SL content increases, the ferroelectric to relaxor temperature (T_F-R) is adjusted to below ambient temperature. More importantly, the decay of ferroelectric phase resulted in a significant increase in strain value: the large strain of 0.5% with normalized strain of 625?pm/V was obtained at 80kv/cm and x?=?0.04. Finally, the composition exhibited high strain of temperature insensitivity range from room temperature to 100?°C, the strain value remained above 0.4% and kept within 5%. The results are due to the coexistence of rhombohedral polar-nanoregions (PNRs) and tetragonal PNRs during the relaxor region. This result is of great importance to the developments of temperature-insensitive strain sensors and actuators.     

Physical properties of the (K0·44Na0·52Li0.04)0.97La0·01Nb0·9Ta0·1O3 ceramic with coexisting tetragonal and orthorhombic monocrystalline grains at room temperature

A structural and physical properties study on ferroelectric (K_0·44Na_0·52Li_0.04)_0.97La_0·01Nb_0·9Ta_0·1O₃ ceramics with monocrystalline grains of orthorhombic (O) and tetragonal (T) perovskite phases coexisting at room temperature (RT) is presented. Different sintering temperatures were evaluated. XRD analysis demonstrates high crystalline quality of both phases with volume fractions depending of the sintering temperature. SEM shows grain facets and morphologies of both phases in all samples. Raman analysis confirms the dopant incorporation and the coexistence of both phases. The contributions of each phase in the dielectric response are deconvoluted using the frequency-temperature dielectric analysis. The orthorhombic-to-tetragonal (T_O-T) and tetragonal-to-cubic (T_T-C) phase transition temperatures shift ~100 °C below those reported for pure-KNN in all samples, as consequence of the Li, La, and Ta doping combination. Li doping promotes T-phase grain growth and decreases T_O-T below RT. La incorporation promotes the O-phase grain growth and decreases T_O-T and T_T-C. The optimal sintering temperature is 1180 °C with 50-50 volume fractions of T-O phases. Piezoresponse studies show a complex 180°-domain structure.     

High electromechanical strain properties by the existence of nonergodicity in LiNbO3–modified Bi1/2Na1/2TiO3–SrTiO3 relaxor ceramics

This study investigated the effect of LiNbO₃ modification on the dielectric, ferroelectric and electromechanical strain properties of Bi_1/2Na_1/2TiO₃–SrTiO₃ (BNT–ST) lead–free relaxor ceramics. The sintering temperature for lead–free BNT–ST relaxor ceramics was slightly decreased from 1175?°C to 1050?°C by modifying with LiNbO₃. We found that the sintering temperature affects the dielectric behavior of 0.76BNT–(0.24?x)ST–xLiNbO₃ (BNST–100xLN) ceramics at high temperature (near dielectric maximum temperature, T_m). The T_m for the low–temperature sintered sample was shifted to relatively higher temperature by comparison with the high–temperature sintered samples. Furthermore, the degradation of dielectric behavior near T_m in low–temperature sintered BNST–2LN ceramics was revealed after poling treatment and seem to be related to the existence of a high temperature stabilized nonergodic relaxor phase. Accordingly, we assume that the stabilized nonergodic relaxor phase is responsible for the relatively late transition from ferroelectrics to the relaxor. Therefore, we obtained the improved d₃₃^* of 616?pm/V as the highest value in low–temperature sintered BNST–2LN ceramics.     

Effect of Li addition on phase formation behavior and electrical properties of (K0.5Na0.5)NbO3 lead free ceramics

In this work, Li-modified KNN ceramic compositions ((K_0.5Na_0.5)_1−xLi_x)NbO₃ with x = 0.03, 0.04, 0.05, 0.06, 0.65 and 0.07 were prepared by a conventional solid-state mixed-oxide method. The structural phase formation and microstructure were characterized by X-ray diffraction technique (XRD) and scanning electron microscopy (SEM). It has been found that a morphotropic phase boundary (MPB) between orthorhombic phase and tetragonal phases should exist between compositions with Li contents of 6-6.5%. The Curie temperature (T_c) of the ceramics shifted to higher temperature with increasing Li content. The room temperature dielectric constant was also seen to be higher than the pure KNN ceramics. In addition, the ferroelectric properties were found to enhance at near MPB compositions. This study clearly showed that the addition of Li could improve the dielectric and ferroelectric properties in (K_0.5Na_0.5)NbO₃ ceramics.     

Crystal structure,impedance and broadband dielectric spectra of ordered scheelite-structured Bi(Sc1/3Mo2/3)O4 ceramic

Bi(Sc_1/3Mo_2/3)O₄ ceramics were prepared via solid state reaction method. It crystallized with an ordered scheelite-related structure (a?=?16.9821(9)?Å, b?=?11.6097(3)?Å, c?=?5.3099(3)?Å and β?=?104.649(2)°) with a space group C12/C1, in which Bi³⁺, Sc³⁺ and Mo⁶⁺ are ?8, ?6 and ?4 coordinated, respectively. Bi(Sc_1/3Mo_2/3)O₄ ceramics were densifiedat 915?°C, giving a permittivity (ε_r) ～24.4, quality factor (Qf, Q?=?1/dielectric loss, f?=?resonant frequency) ～48, 100?GHz and temperature coefficient of resonant frequency (TCF)?～??68?ppm/°C. Impedance spectroscopy revealed that there was only a bulk response for conductivity with activation energy (E_a) ～0.97?eV, suggesting the compound is electrically and chemically homogeneous. Wide band dielectric spectra were employed to study the dielectric response of Bi(Sc_1/3Mo_2/3)O₄ from 20?Hz to 30?THz. ε_r was stable from 20?Hz to the GHz region, in which only ionic and electron displacive polarization contributed to the?ε_r.     

MgO-modified Sr0.7Ba0.3Nb2O6 ceramics for energy storage applications

We explored the phase structure, microstructure, dielectric and energy storage properties of MgO-modified strontium barium niobate Sr_0.7Ba_0.3Nb₂O₆-xwt%MgO (SBNMx; x?=?0–5) ceramics fabricated via conventional solid-state sintering precess. X-ray diffraction analysis indicates Mg²⁺ incorporates into lattice at x?=?0.5 and secondary phases come into formation for samples at x?≥?1, which results in the decrease of dielectric constant. There is also significant reduction of dielectric loss up to 0.002. Compared with pure SBN ceramics, the grain size of SBNMx ceramics becomes denser and more uniform, moreover, the dielectric breakdown strength shows increasing trend from 137?kV/cm to 226?kV/cm, which is in favor of the energy storage. SBNM0.5 ceramics presents the optimal energy storage performance: energy storage density of 0.93?J/cm³ and energy storage efficiency of 89.4% at 157?kV/cm, indicating that SBNM ceramics are prospective candidates for high voltage capacitor applications.     

Enhanced piezoelectric,electrocaloric and energy storage properties at high temperature in lead-free Bi0.5(Na1-xKx)0.5TiO3 ceramics

The piezoelectric, electrocaloric and energy storage properties were systemically investigated in lead-free Bi_0.5(Na_1-xK_x)_0.5TiO₃ ceramics from room temperature to high temperature region. These ceramics can be poled completely to obtain large piezoelectric coefficient (104–153 pC/N) at low electric field of ~30?kV/cm. The piezoelectric property shows good thermal stability due to high depolarization temperature (T_d). For BNKT₂₀, a large low electric field-induced strain of 0.36% is obtained at 120?°C under 50?kV/cm, the corresponding normalized strain coefficient is up to 720?pm/V, which is larger than other BNT-based ceramics at high temperature region. The electrocaloric properties of these ceramics are studied via indirect and direct methods. Large EC value (~1.08?K) in BNKT₂₀ ceramic is obtained at 50?kV/cm using indirect calculation. Above 100?°C, the dielectric energy storage density and efficiency of BNKT₂₀ is still up to ~0.85?J/cm³ and 0.75, respectively. The BNKT_x ceramics may become promising candidates in the fields of actuators, electrocaloric cooling and energy storage at high temperature region.     

Structural and electrical properties of 0.56Pb(Ni1/3Nb2/3)O3-0.10Pb(Zn1/3Nb2/3)O3-0.34PbTiO3 ceramics prepared by different ceramic processings

The ternary system of 0.56Pb(Ni_1/3Nb_2/3)O₃-0.10Pb(Zn_1/3Nb_2/3)O₃-0.34PbTiO₃ (0.56PNN-0.10PZN-0.34PT) ceramics were prepared by conventional solid-state reaction method via straight mixed oxide method, columbite precursor method and B-site oxide mixing route. X-ray diffraction (XRD) measurement demonstrated that both the tetragonal and rhombohedral phases coexist in the B-site oxide mixing route prepared ceramics accompanied by the largest content of perovskite phase of 95.18%. The 0.56PNN-0.10PZN-0.34PT ceramics prepared by the straight mixed oxide method and the B-site oxide mixing route exhibit rather homogeneous microstructure. As a comparison, in the columbite precursor method prepared ceramics nebulous granules and octahedral or other polyhedral morphology grains are observed. All the sintered ceramics exhibit diffused ferroelectric phase transition where the dielectric response peaks are broad, diffused and strongly frequency dependent. However, the temperature of dielectric maximum (T_m) increases greatly from 398.0 K of the 0.56PNN-0.10PZN-0.34PT ceramics prepared by the B-site oxide mixing route to 423.3 K of the ones prepared by the straight mixed oxide method. Saturated and symmetric P-E hysteresis loops are observed in all the sintered ceramics, where the B-site oxide mixing route prepared ceramics exhibit large value of remanent polarization (P_r) of 17.13 μC/cm² and the least value of coercive field (E_c) of 11.99 kV/cm. Piezoelectric constant (d₃₃) exhibits the largest value of 449 pC/N for the ceramics prepared by the B-site oxide mixing route. Such results are related to the phase composition, density and porosity of the ceramics.     

Structural,dielectric, piezoelectric,ferroelectric and electro-caloric properties of Ba1−xCaxTi0.975(Nb0.5Yb0.5)0.025O3 lead-free ceramics

Polycrystalline samples of Ba_1?xCa_xTi_0.975(Nb_0.5Yb_0.5)_0.025O₃ (where x = 0.15, 0.2 and 0.3, abbreviated as BCTYN) were prepared by the conventional solid state reaction method. The effect of calcium (Ca) substitution in BaTi_0.975(Nb_0.5Yb_0.5)_0.025O₃ (abbreviated as BTYN25) on the structural, dielectric, piezoelectric and ferroelectric properties and electro-caloric effects (ECE) was investigated. X-ray diffraction (XRD) results at room temperature showed that the BCTYN samples in the composition x < 0.3 exhibited a pure tetragonal perovskite structure. Dielectric measurements showed a classical ferroelectric behavior for all samples. With the increase of the Ca content, the Curie temperature (T_C) was still maintained with a small shift towards low temperature. The evolution of the Raman spectra was studied as a function of compositions and temperatures. The Raman bands confirmed the structure and the phase transition of the BCTYN ceramics. By adding Ca, the piezoelectric properties and the remanent polarization (P_r) are relatively maintained for the compositions x = 0.15 and x = 0.2. A piezoelectric coefficient of d₃₃ = 130 pC/N and a planar electromechanical coupling factor of k_p = 28% were obtained for these compositions. Two different methods were used to calculate the electro-caloric coefficients of the BCTYN ceramics. The incorporation of Ca was found to enhance the electro-caloric strength (ξ = ΔT/ΔE) within a broad temperature range with a best value of ξ = 0.2?Kmm/kV for x = 0.2.     

Piezoelectric properties of (1-x)BZT-xBCT system for energy harvesting applications

In this study, we investigated (1-x)Ba(Zr_0.2Ti_0.8)O₃–x(Ba_0.7Ca_0.3)TiO₃ lead-free piezoelectric ceramics for energy harvester applications. The (1-x)BZT-xBCT ceramic is a promising lead-free piezoelectric material in the field of piezoelectric energy harvesting. Piezoelectric and energy properties of (1-x)BZT-xBCT ceramics were analyzed to confirm the possibility of using them as energy-harvesting materials. Especially, the vicinity of the phase convergence region was investigated to improve their piezoelectric properties. In the phase convergence region, cubic, rhombohedral, orthorhombic, and tetragonal regions co-exist within the narrow region. Near the phase transition region between the orthorhombic and tetragonal phase, the highest piezoelectric property d₃₃?=?464 pC/N and the highest energy density of 158.5 μJ/cm³ were observed. This output energy density of 158.5 μJ/cm³ is the recorded highest value among lead-free ceramics. We found that the optimal sintering temperature was 1475?°C and the optimal composition was BZT-0.5BCT.     

Improvement of dielectric breakdown strength and energy storage performance in Er2O3–modified 0.95Sr0.7Ba0.3Nb2O6-0.05CaTiO3 lead-free ceramics

In this study, 0.95?Sr_0.7Ba_0.3Nb₂O₆-0.05CaTiO₃-x wt% Er₂O₃ ceramics (SBNCTEx; x?=?0–5) were synthesized using traditional solid-state method, and we investigated the microstructure, energy storage properties as well as the relationship between dielectric breakdown strength and interfacial polarization. As compared with pure 0.95?Sr_0.7Ba_0.3Nb₂O₆-0.05CaTiO₃ ceramics, the Er₂O₃ dopants suppressed the grain growth of SBNCTEx, and the doped ones showed the dense microstructure. The secondary phase was found for x?≥?1 according to the EDS results, and the influence of the secondary phase on relative dielectric breakdown strength has also been studied. The dielectric breakdown strength increased from 18.1?kV/mm to 34.4?kV/mm, which is good for energy storage. The energy storage density of 0.28?J/cm³ and the energy storage efficiency of 91.4% were obtained in the SBNCTE5 ceramics. The results indicate that SBNCTE ceramics can be used as energy storage capacitors.     

Structure and electrical properties of Ca2+-doped (Na0.47Bi0.47Ba0.06)TiO3 lead-free piezoelectric ceramics

The lead-free piezoelectric ceramics (Na_.47Bi_.47Ba_.06)_1-xCa_xTiO₃ (x?=?0, 0.01, 0.02, 0.03, 0.05, and 0.08, abbreviated as BNBTC/0, BNBTC/1, BNBTC/2, BNBTC/3, BNBTC/5, and BNBTC/8, respectively) were obtained using the solid-state reaction method. The structure, electric conductivity, and dielectric, ferroelectric, and piezoelectric properties of the Ca²⁺-doped (Na_.47Bi_.47Ba_.06)TiO₃ ceramics were thoroughly investigated. The ceramics sintered at 1200?°C exhibit dense microstructures, having relative densities higher than 96%. The X-ray diffraction results demonstrate that all ceramics have a pure perovskite structure. The mean grain sizes of the ceramics are related to the Ca²⁺ quantity. A small quantity of Ca²⁺ ions (x?≤?0.03) improves the piezoelectric and ferroelectric properties of the samples. The dielectric behavior of the samples is sensitive to the Ca²⁺ content and electric poling. The results demonstrate that the electrical properties of the (Na_.47Bi_.47Ba_.06)TiO₃ lead-free ceramics can be well tuned by varying the Ca²⁺ quantity.     

Fabrication and electrical properties of Pb(Co1/3Nb2/3)O3 ceramics

Pb(Co_1/3Nb_2/3)O₃ (PCN) ceramics have been produced by sintering PCN powders synthesized from lead oxide (PbO) and cobalt niobate (CoNb₂O₆) with an effective method developed for minimizing the level of PbO loss during sintering. Attention has been focused on relationships between sintering conditions, phase formation, density, microstructural development, dielectric and ferroelectric properties of the sintered ceramics. From X-ray diffraction analysis, the optimum sintering temperature for the high purity PCN phase was found at approximately 1050 and 1100 °C. The densities of sintered PCN ceramics increased with increasing sintering temperature. However, it is also observed that at very high temperature the density began to decrease. PCN ceramic sintered at 1050 °C has small grain size with variation in grain shape. There is insignificant change of dielectric properties with sintering temperature. The P–E hysteresis loops observed at −70 °C are of slim-loop type with small remanent polarization values, which confirmed relaxor ferroelectric behavior of PCN ceramics.     

Effects of sintering temperature and KBT content on microstructure and electrical properties of (Bi.5Na.5)TiO3-BaTiO3-(Bi.5K.5)TiO3 Pb-free ceramics

A route exploring the morphotropic phase boundaries (MPB) region in (Bi_.5Na_.5)TiO₃-BaTiO₃-(Bi_.5K_.5)TiO₃ ternary system has been designed based on the phase diagram. X-ray diffraction (XRD) has been performed to determine the phases of the prepared samples. The dielectric, ferroelectric, and piezoelectric properties of [(1-x) 0.9363(Bi_.5Na_.5)TiO₃–0.0637BaTiO₃]-x(Bi_.5K_.5)TiO₃ (BNKBT100x) ternary lead-free piezoelectric ceramics are investigated as the functions of x and sintering temperature. When x was varied from 0 to 0.11, the BNKBT100x ceramics show single perovskite structure sintered at 1130–1210?°C. These ceramics show large dielectric permittivity, small dielectric loss, and diffused phase transition behavior. Well-defined ferroelectric polarization-electric field (P-E) hysteresis loop and relative large piezoelectric and electromechanical coefficients are also found in these ceramics. When increasing x, the electrical performances first increase, then decrease. The same rule is found when varying the sintering temperature. The optimized composition and sintering temperature are finally obtained.     

Large electrocaloric effect in lead-free Ba1-xCaxTi1-yZryO3 ceramics under strong electric field at room-temperature

In this study, lead-free Ba_1-xCa_xZr_yTi_1-yO₃ (BCTZ(x, y)) ceramics were prepared by means of the classic solid-state reaction method. The morphotropic phase transition (MPB) from the orthorhombic to the tetragonal phase (O-T) was identified in this composition. Besides, the identification of those two structures at room temperature (RT) was made possible thanks to an X-ray diffraction (XRD) study. In order to determine the phase transitions dielectric measurements were conducted. Based on Maxwell equation, the electrocaloric (EC) effect in the studied ceramics was performed via the indirect method. The compositions gave maximum EC temperature changes (ΔT) at above their T_C on application of a 3?kV/mm electric field. These temperature changes are ΔT?=?0.565?K at T_EC=?392?K, ΔT?=?0.548?K at T_EC=?365?K and ΔT?=?0.235?K at T_EC=?307?K for BCZT(10%,5%), BCZT(13%,10%) and BCZT(20%,15%), respectively. At RT, these compositions provided a very interesting EC coefficient (ξ?=?ΔT/ΔE) compared to the pure BaTiO₃ (BT). These values, lying between 0.105 Kmm/kV and 0.188Kmm/kV for ΔE?=?3?kV/mm, are also greater than those related to some lead-based ferroelectric.     

Phase Diagram and Properties of High TC/TR−T Pb(In1/2Nb1/2) O3–Pb(Zn1/3Nb2/3)O3–PbTiO3 Ferroelectric Ceramics

A ternary ferroelectric ceramic system, (1?x?y)Pb(In_1/2Nb_1/2)O₃–xPb(Zn_1/3Nb_2/3)O₃–yPbTiO₃ (PIN–PZN–PT, x = 0.21, 0.27, 0.36, 0.42), was prepared using a two‐step precursor method. The phase structure, dielectric, piezoelectric, and ferroelectric properties of the ternary ceramics were systematically investigated. A morphotropic phase boundary (MPB) was identified by X‐ray diffraction. The optimum piezoelectric and electromechanical properties were achieved for a composition close to MPB (0.5PIN–0.21PZN–0.29PT), where the piezoelectric coefficient d₃₃, planar electromechanical coupling factor k_p, and remnant polarization P_r are 660 pC/N,72%, and 45 μC/cm², respectively. The Curie temperature T_C and rhombohedral to tetragonal phase transition temperature T_R?T were also derived by temperature dependence of dielectric measurements. The strongly “bended” MPB in the PIN–PT system was found to be “flattened” after addition of PZN in the PIN–PT–PZN system. The results demonstrate a possibility of growing ferroelectric single crystals with high electromechanical properties and expanded range of application temperature.     

Sol-gel synthesized and microwave heated Pb0.8-yLayCo0.2TiO3 (y = 0.2–0.8) nanoparticles: Structural,morphological and dielectric properties

In this work, the Pb_0.8-yLa_yCo_0.2TiO₃ (y?=?0.2–0.8) (PLCT) nanoparticles were prepared by sol-gel method and further subjected to microwave heating. The formed tetragonal reflection planes of PLCT samples were on par with PbTiO₃ (PT) and lanthanum cobalt titanate (LCT) tetragonal phases. Especially, for y?=?0.2–0.4, PLCT attained the PT structure while for y?=?0.6–0.8, PLCT acquired the LCT structure. That is, the structural transformation occurred from tetragonal PT to tetragonal LCT phases at higher La-contents. The high resolution transmission electron microscope (HRTEM) and field emission scanning electron microscopes (FESEM) showed complete formation of nanofibers at y?=?0.8 which may reveal drug delivery system applications. The Fourier transform infrared spectra (FTIR) were recorded in order to find the presence of metal oxide bonds. The dielectric properties evidenced that the transition temperatures (T_c) were found to be increasing from 713 to 783?K with increase of y-value. Furthermore, the temperature and frequency dependence of dielectric constant (ε′), dielectric loss (ε′′), ac-electrical conductivity (σ_ac), real (M′) and imaginary (M′′) parts of complex dielectric modulus (M*) was described. The Power law was used to fit the logσ_ac versus logω plots in order to determine the dc-conductivity (σ_dc) and exponent (n) values of the samples at room temperature (RT). Later on, the Arrhenius plots (lnσ_ac versus T^?1 plots) were drawn to find the activation energies. The results expressed the existence of two activation energies at low and high temperature regions due to slope change before and after T_c.     

A novel ((Bi0.5Na0.5)0.94Ba0.06)1-x (K0.5Nd0.5)xTiO3 lead-free relaxor ferroelectric ceramic with large electrostrains at wide temperature ranges

Novel ((Bi_0.5Na_0.5)_0.94Ba_0.06)_1-x(K_0.5Nd_0.5)_xTiO₃(x = 0.0, 0.02, 0.04, 0.06) lead-free ceramics (BNBT–xKN) were prepared by the solid-state reaction method. The effects of A-site (K_0.5Nd_0.5)²⁺ complex-ion substitution on their phase structure, dielectric, piezoelectric, and electromechanical properties were studied. The X-ray diffraction results indicate that all compositions are located in the morphotropic phase boundary (MPB) region where the tetragonal phase coexists with the rhombohedral phase. In addition, as the KN content increases, the ferroelectric order transform to relaxor order, which is characterized by a degeneration of maximum polarization, remnant polarization and correspondingly adjusts the ferroelectric-relaxor transformation temperature (T_F-R) to room temperature. Interestingly, the disruption of ferroelectric phase caused a significant improvement of strains. A maximum strain of ~ 0.52% corresponding to normalized strain of ~ 612 pm/V appeared at 85 kv/cm for the x = 0.04 composition. Particularly, the composition of x = 0.04 exhibited high electrostrains of temperature insensitivity, which remained above 0.4% and kept within 10% from ambient temperature up to 110 °C. It can be ascribed to the coexistence of non-ergodic and ergodic states in the relaxor region. As a result, the systematic investigations on the BNBT–xKN ceramics can benefit the developments of temperature-insensitive “on-off” actuators.