Piezoelectric and ferroelectric properties of lead-free [Bi1−y(Na1−x−yLix)]0.5BayTiO3 ceramics

Lead-free [Bi_1−y(Na_1−x−yLi_x)]_0.5Ba_yTiO₃ (BNLB-x/y) piezoelectric ceramics were prepared by sintering the constituent oxides, and their piezoelectric and ferroelectric properties studied. The results of X-ray diffraction (XRD) suggest that Li⁺ and Ba²⁺ diffuse into the Bi_0.5Na_0.5TiO₃ (BNT) lattices to form a solid solution with a single-phase perovskite structure. The ceramics can be well sintered at 1100–1150 °C. The introduction of Li⁺ and Ba²⁺ into Bi_0.5Na_0.5TiO₃ significantly decreases the coercive field, E_c but maintains the large remanent polarization, P_r of the materials. The ceramics exhibit relatively good piezoelectric properties and very strong ferroelectricity: piezoelectric constant, d₃₃ = 208 pC/N, planar electromechanical coupling factor, k_p = 37.0%, remanent polarization, P_r = 38.5 μC/cm², coercive field, E_c = 3.27 kV/mm. The depolarization temperature, T_d of BNLB-0.075/0.04 ceramics is about 190 °C.     

High-temperature dielectric and relaxation behavior of Yb-doped Bi0.5Na0.5TiO3 ceramics

Microstructure, phase transition and dielectric properties of Yb-doped Bi_0.5Na_0.5TiO₃ (BNT) ceramics were investigated. It is found that ytterbium promotes the grain growth and densification of the ceramics while Ti-rich impurity appears due to the compensation of Ti-vacancy. The dielectric operational temperature range of the ceramics with a±15% tolerance was greatly broaden until 500 °C by ytterbium doping. Meanwhile, the diffuseness of the diffuse phase transition increases with the increase of doping Yb. BNT ceramics with 3 mol% Yb doping shows a near-plateau dielectric behavior in a broad temperature range from 147 to 528 °C and a low dielectric loss (<0.025) from 154 to 356 °C, indicating that it is a promising material for applications in high-temperature capacitor.     

Microstructure,ferroelectric and piezoelectric properties of Bi0.5K0.5TiO3-modified BiFeO3–BaTiO3 lead-free ceramics with high Curie temperature

The effects of composition, sintering temperature and dwell time on the microstructure and electrical properties of (0.75 ? x)BiFeO₃–0.25BaTiO₃–xBi_0.5K_0.5TiO₃ + 1 mol% MnO₂ ceramics were studied. The ceramics sintered at 1000 °C for 2 h possess a pure perovskite structure and a morphotropic phase boundary of rhombohedral and pseudocubic phases is formed at x = 0.025. The addition of Bi_0.5K_0.5TiO₃ retards the grain growth and induces two dielectric anomalies at high temperatures (T₁ ～ 450–550 °C and T₂ ～ 700 °C, respectively). After the addition of 2.5 mol% Bi_0.5K_0.5TiO₃, the ferroelectric and piezoelectric properties of the ceramics are improved and very high Curie temperature of 708 °C is obtained. Sintering temperature has an important influence on the microstructure and electrical properties of the ceramics. Critical sintering temperature is 970 °C. For the ceramic with x = 0.025 sintered at/above 970 °C, large grains, good densification, high resistivity and enhanced electrical properties are obtained. The weak dependences of microstructure and electrical properties on dwell time are observed for the ceramic with x = 0.025.     

Intermediate-temperature conductivity of B-site doped Na0.5Bi0.5TiO3-based lead-free ferroelectric ceramics

Na_0.5Bi_0.5TiO₃ (NBT) based oxide-ion conductor ceramics have great potential applications in intermediate-temperature solid oxide fuel cells (SOFCs) and oxygen sensors. Na_0.5Bi_0.49Ti_1−xMg_xO_3−δ ceramics with x=0, 0.01, 0.02, 0.03, 0.05 and 0.08 were prepared by conventional solid-state reaction. XRD measurement and SEM analysis revealed the formation of pure perovskite structures without secondary phase. MgO doping greatly decreased the sintering temperature and inhibited grain growth. AC impedance spectroscopy measurement was adopted to measure the total conductivity, which was found to increase with MgO doping content ranging from 0 to 3 mol% and subsequently to decrease. High oxygen ionic conductivity σ_t=0.00629 S/cm was achieved for sample doped with 3 mol% MgO at 600 °C in air atmosphere.     

Dielectric and ferroelectric properties of (1 − x)BaTiO3–xBi0.5Na0.5TiO3 ceramics

Lead-free (1 − x)BaTiO₃–xBi_0.5Na_0.5TiO₃ (x = 0.01, 0.02, 0.05, 0.1, 0.2, 0.3) ferroelectric ceramics were fabricated by the conventional ceramic technique. Sintering was made at 1200 °C for 2–4 h in air atmosphere. The crystal structure was investigated by X-ray diffraction. The dielectric and ferroelectric properties were also studied. Room temperature permittivity was found to decrease as Bi_0.5Na_0.5TiO₃ (BNT) content increases. Only the sample with 0.3 mol BNT was found to have relaxor behaviour. The T_c shifted slightly only for BNT addition lower than 0.1 mol. The highest T_c (about 150 °C) was obtained for 0.2 mol BNT addition. The remanent polarization, P_r, decreases whereas the coercive field, E_c, increases monotonously as the BNT content increases.     

Low-temperature-sintered Bi0.5Na0.5TiO3-based lead-free ferroelectric ceramics with good piezoelectric properties

Li₂CO₃ has been used as a sintering aid for fabricating lead-free ferroelectric ceramic 0.93(Bi_0.5Na_0.5TiO₃)-0.07BaTiO₃. A small amount (0.5 wt%) of it can effectively lower the sintering temperature of the ceramic from 1200 °C to 980 °C. Unlike other low temperature-sintered ferroelectric ceramics, the ceramic retains its good dielectric and piezoelectric properties, giving a high dielectric constant (1570), low dielectric loss (4.8%) and large piezoelectric coefficient (180 pC/N). The “depolarization” temperature is also increased to 100 °C and the thermal stability of piezoelectricity is improved. Our results reveal that oxygen vacancies generated from the diffusion of the sintering aid into the lattices are crucial for realizing the low temperature sintering. Owing to the low sintering temperature and good dielectric and piezoelectric properties, the ceramics, especially of multilayered structure, should have great potential for practical applications.     

Effects of Li2CO3 addition on the microstructure and magnetic properties of low-temperature-fired NiCuZn ferrites

NiCuZn ferrites doped with 0.5 wt% Bi₂O₃ and different Li₂CO₃ contents (0–0.25 wt%) were sintered at 900 °C. The microstructure and magnetic properties of these materials were investigated. The addition of low-melting-point Li₂CO₃ led to large and uniform grains. However, excess Li₂CO₃ addition produced abnormal grains and many closed pores, thereby reducing density. Permeability initially increased and then decreased at the Li₂CO₃ content of >0.2 wt%. Maximum magnetic flux density (431.1 mT at room temperature, 339.6 mT at 100 °C) and minimum power loss were achieved at 0.2 wt% Li₂CO₃. These findings suggested the suitability of 0.2 wt% Li₂CO₃ for applications in low-temperature co-fired ceramic magnetic power components and modules.     

Lead-free BaTiO3-Bi0.5Na0.5TiO3-Na0.73Bi0.09NbO3 relaxor ferroelectric ceramics for high energy storage

A series of (1-x)(0.65BaTiO₃-0.35Bi_0.5Na_0.5TiO₃)-xNa_0.73Bi_0.09NbO₃ ((1-x)BBNT-xNBN) (x = 0–0.14) ceramics were designed and fabricated using the conventional solid-state sintering method. The microstructure, dielectric property, relaxor behavior and energy storage property were systematically investigated. X-ray diffraction results reveal a pure perovskite structure and dielectric measurements exhibit a relaxor behavior for the (1-x)BBNT-xNBN ceramics. The slim polarization electric field (P-E) loops were observed in the samples with x ≥ 0.02 and the addition of Na_0.73Bi_0.09NbO₃ (NBN) could decrease the remnant polarization (P_r) of the (1-x)BBNT-xNBN ceramics obviously. The sample with x = 0.08 exhibits the highest energy storage density of 1.70 J/cm³ and the energy storage efficiency of 82% at 172 kV/cm owing to its submicron grain size and high relative density. These results show that the (1-x)BBNT-xNBN ceramics may be promising lead-free materials for high energy storage density capacitors.     

High performance lead-free piezoelectric 0.96(K0.48Na0.52)NbO3-0.03[Bi0.5(Na0.7K0.2Li0.1)0.5]ZrO3-0.01(Bi0.5Na0.5)TiO3 single crystals grown by solid state crystal growth and their phase relations

0.96(K_0.48Na_0.52)NbO₃-0.03[Bi_0.5(Na_0.7K_0.2Li_0.1)_0.5]ZrO₃-0.01(Bi_0.5Na_0.5)TiO₃ single crystals were grown for the first time by the solid state crystal growth method, using [001] or [110]-oriented KTaO₃ seed crystals. The grown single crystal shows a dielectric constant of 2720 and polarization-electric field loops of a lossy normal ferroelectric, with P_r = 45 μC/cm² and E_c = 14.9 kV/cm, while the polycrystalline samples with a dielectric constant of 828 were too leaky for P-E measurement due to humidity effects. The single crystal has orthorhombic symmetry at room temperature. Dielectric permittivity peaks at 26 °C and 311 °C, respectively, are attributed to rhombohedral-orthorhombic and tetragonal–cubic phase transitions. Additionally, Raman scattering shows the presence of an orthorhombic-tetragonal phase transition at ∼150 °C, which is not indicated in the permittivity curves but by the loss tangent anomalies. A transition around 700 °C in the high temperature dc conductivity is suggested to be a ferroelastic-paraelastic transition.     

Enhanced microstructure and electrical properties of Mn-modified Bi0.5(Na0.65K0.35)0.5TiO3 ferroelectric ceramics

Bi_0.5(Na_0.65K_0.35)_0.5TiO₃ (BNKT) and Mn-modified Bi_0.5(Na_0.65K_0.35)_0.5(Mn_xTi_1−x)O₃ (BNKMT-10³x), (x=0.0–0.5%) ferroelectric ceramics were synthesized by solid-state reaction method. Optimization of calcination temperature in Mn-doped ceramics was carried out for the removal of secondary phases observed in XRD analysis. BNKMT ceramics sintered at 1090 °C showed enhanced dielectric, piezoelectric and ferroelectric properties in comparison to pure BNKT. The average grain size was found to increase from 0.35 μm in BNKT to 0.52 μm in Bi_0.5(Na_0.65K_0.35)_0.5(Mn_0.0025Ti_0.9975)O₃ (BNKMT-2.5) ceramics. The dielectric permittivity maximum temperature (T_m) was increased to a maximum of 345 °C with Mn-modification. AC conductivity analysis was performed as a function of temperature and frequency to investigate the conduction behavior and determine activation energies. Significant high value of piezoelectric charge coefficient (d₃₃=176 pC/N) was achieved in BNKMT 2.5 ceramics. Improved temperature stability of ferroelectric behavior was observed in the temperature dependent P–E hysteresis loops as a result of Mn-incorporation. The fatigue free nature along with enhanced dielectric and ferroelectric properties make BNKMT-2.5 ceramic a promising candidate for replacing lead based ceramics in device applications.     

Development of texture in Bi0.5Na0.5TiO3 prepared by reactive-templated grain growth process

The effect of sodium concentration on texture development in Bi_0.5Na_0.5TiO₃ [BNT] bulk ceramics was examined. The 〈1 0 0〉-textured specimens were prepared by the reactive-template grain growth process using platelike Bi₄Ti₃O₁₂ particles. Texture did not extensively develop in stoichiometric and Na-deficient BNT, but excess Na promoted extensive texture development together with densification. The role of excess Na was discussed based on the formation of a liquid phase.     

Fabrication of transparent electro-optic (K0.5Na0.5)1−xLixNb1−xBixO3 lead-free ceramics

Lead-free transparent electro-optic ceramics (K_0.5Na_0.5)_1?xLi_xNb_1?xBi_xO₃ have been fabricated by hot-press sintering. Owing to the effective suppression of grain growth, the Li and Bi co-modified ceramics generally possess a dense and fine-grained structure. The co-modification also causes the ceramics to transform into a nearly cubic structure with minimal optical anisotropy. A diffuse phase transformation is also induced, causing the ceramics to become more relaxor-like and contain more polar nano-regions. These would reduce the light scattering by the grains, at the grain boundaries and at the domain walls, respectively, and thus making the ceramics become optically transparent. For the ceramic modified with 5 mol% Li⁺ and Bi⁵⁺, the optical transmittance reaches a high value of 60% in the near-IR region. The ceramics also exhibit a strong linear EO response, giving a large effective linear EO coefficient in the range of 120–200 pm/V.     

Effects of Nb-doping on the micro-structure and dielectric properties of (Bi0.5Na0.5)TiO3 ceramics

Bismuth sodium titanate [(Bi_0.5Na_0.5)TiO₃ or BNT] ceramics incorporated with 0, 1, 5, 10, 15 and 20 mol% niobium were prepared by conventional solid state reaction method. The green bodies were sintered at 1050 °C for 2 h to obtain dense ceramics. The effects of substitution of niobium ion for titanium ion in BNT ceramics on micro-structure and dielectric properties were investigated. X-ray diffraction analysis showed the presence of a secondary phase when more than 5 mol% niobium was added. Within the solubility limit, Nb doping caused the grain size of BNTNb to be smaller than the undoped sample. The investigation of the dielectric properties showed that the transition temperature (T_c) was found to shift towards lower temperature as the content of Nb increased. In this research, the donor-type behavior and induced charged defects had significant influence on the electrical properties of Nb-doped BNT ceramics.     

0-3 type magnetoelectric 0.94Na0.5Bi0.5TiO3-0.06BaTiO3:CoFe2O4 composite ceramics with a deferred thermal depolarization

Developing Na_0.5Bi_0.5TiO₃-based magnetoelectric (ME) coupling composites with higher depolarization temperature is highly valuable for the environment-friendly smart electronic devices. We have developed a new kind of 0-3 type 0.94Na_0.5Bi_0.5TiO₃-0.06BaTiO₃:xCoFe₂O₄ (NBTBT:xCFO, x = 0, 0.1, 0.2, 0.3) composite ceramics with a deferred depolarization temperature, together with an additional strong ME coupling of 9.2 mV/cm·Oe for the NBTBT:0.2CFO. The basic structure, ferroelectric/ferromagnetic properties, and the depolarization temperature of the NBTBT:xCFO composite ceramics were investigated. It was found that an enhancement of depolarization temperature (>25 °C) was obtained in these 0-3 type composites relative to the pure NBTBT ones (115 °C vs 90 °C). The mechanism of the enhanced depolarization temperature of the composites is discussed. The present results demonstrate that NBTBT:xCFO composites have great potential for ME devices.     

Microstructure and piezoelectric properties of textured (Na0.84K0.16)0.5Bi0.5TiO3 lead-free ceramics

Textured (Na,K)_0.5Bi_0.5TiO₃ ceramics were fabricated by reactive-templated grain growth in combination with tape casting. The effects of sintering conditions on the grain orientation and the piezoelectric properties of the textured (Na,K)_0.5Bi_0.5TiO₃ ceramics were investigated. The results show that the textured ceramics have microstructure with plated-like grains aligning in the direction parallel to the casting plane. The ceramics exhibit {h 0 0} preferred orientation and the degree of orientation is larger than 0.7. The degree of grain orientation increases with the increasing sintering temperature. The textured ceramics show anisotropy dielectric and piezoelectric properties in the directions of parallel and perpendicular to the casting plane. The ceramics in the perpendicular direction exhibit better dielectric and piezoelectric properties than those of the nontextured ceramics with the same composition. The optimized sintering temperature is 1150 °C where the maximum d₃₃ of 134 pC/N parallel to casting plane, the maximum k₃₁ of 0.31, and the maximum Q_m of 154 in perpendicular direction were obtained.     

Grain size control of lead-free Li0.06(Na0.5K0.5)0.94NbO3 piezoelectric ceramics by Ba and Ti doping

In this study, Ba- and Ti-doped Li_0.06(Na_0.5K_0.5)_0.94NbO₃ [(1 ? x)Li_0.06(Na_0.5K_0.5)_0.94NbO₃–xBaTiO₃ (x = 0–0.07)] ceramics were prepared by using conventional solid state reaction method, and the microstructure and electric properties of these samples were investigated. The grain size distribution of non-doped Li_0.06(Na_0.5K_0.5)_0.94NbO₃ ceramics was relatively wide. The microstructure was composed of grains ranging 1.1–5.0 μm in size. However, with increasing Ba and Ti content, the grain size distribution became narrow and the average grain size decreased from 2.0 to 0.9 μm in size. In particular, the microstructure of x = 0.07 sample was composed of grains ranging 0.5–2.2 μm in size. As a result, the frequency dispersion of dielectric constant for the (1 ? x)Li_0.06(Na_0.5K_0.5)_0.94NbO₃–xBaTiO₃ (x = 0–0.07) ceramics was reduced and the mechanical quality factor Q_m was enhanced with increasing Ba and Ti content.     

Dielectric,ferroelectric and field-induced strain behavior of K0.5Na0.5NbO3-modified Bi0.5(Na0.78K0.22)0.5TiO3 lead-free ceramics

Lead-free piezoelectric (1 ? x)Bi_0.5(Na_0.78K_0.22)_0.5TiO₃–xK_0.5Na_0.5NbO₃ (BNKT–xKNN, x = 0–0.10) ceramics were synthesized using a conventional, solid-state reaction method. The effect of KNN addition on BNKT ceramics was investigated through X-ray diffraction (XRD), dielectric, ferroelectric and electric field-induced strain characterizations. XRD revealed a pure perovskite phase with tetragonal symmetry in the studied composition range. As the KNN content increased, the depolarization temperature (T_d) as well as maximum dielectric constant (?_m) decreased. The addition of KNN destabilized the ferroelectric order of BNKT ceramics exhibiting a pinched-type hysteresis loop with low remnant polarization (11 μC/cm²) and small piezoelectric constant (27 pC/N) at 3 mol% KNN. As a result, at x = 0.03 a significant enhancement of 0.22% was observed in the electric field-induced strain, which corresponds to a normalized strain (S_max/E_max) of ～434 pm/V. This enhancement is attributed to the coexistence of ferroelectric and non-polar phases at room temperature.     

Ferroelectric properties and core shell domain structures of Fe-modified 0.77Bi0.5Na0.5TiO3-0.23SrTiO3 ceramics

The crystal structure, domain patterns, and ferroelectric properties of Fe-modified BNT-ST [0.77(Bi_0.5Na_0.5)TiO₃-0.23Sr(Ti_1-xFe_x)O₃] ceramics, fabricated by a conventional solid-state reaction, were investigated. Core-shell structures were observed and the volume fractions of the core-domain and shell (relaxor-matrix) were found to be dependent on Fe-modification content. The crystal structures of the core-domain and the relaxor-matrix were rhombohedral with the space group R3c, and the tetragonal with the space group P4bm, respectively. Compositional inhomogeneity, specifically, the enrichment of Bi³⁺ and Na⁺ and the considerable depletion of Sr²⁺, were observed in the core-domain region, and was reduced by substituting Ti⁴⁺ with Fe³⁺. The Fe-modification of the BNT-23ST ceramics promoted the diffusion of Sr²⁺ ions into the core region and shifted ferroelectric behaviour towards ergodic-relaxor behaviour. This improved the effective d₃₃* of BNT-23ST ceramics to over 500 pm/V at 2 kV/mm.     

Microwave dielectric properties and microstructures of Nb2O5-Zn0.95Mg0.05TiO3 + 0.25TiO2 ceramics with Bi2O3 addition

The effects of Bi₂O₃ addition on the microwave dielectric properties and the microstructures of Nb₂O₅-Zn_0.95Mg_0.05TiO₃ + 0.25TiO₂ (Nb-ZMT′) ceramics prepared by conventional solid-state routes have been investigated. The results of X-ray diffraction (XRD) indicate the presence of four crystalline phases, ZnTiO₃, TiO₂, Bi₂Ti₂O₇, and (Bi_1.5Zn_0.5)(Ti_1.5Nb_0.5)O₇ in the sintered ceramics, depending upon the amount of Bi₂O₃ addition. In addition, in order to confirm the existence of (Bi_1.5Zn_0.5)(Ti_1.5Nb_0.5)O₇ phase in the samples, the microstructure of Nb-ZMT′ ceramic with 5 wt.% B₂O₃ addition was analyzed by using a transmission electron micrograph. The dielectric constant of Nb-ZMT′ samples was higher than ZMT′ ceramics. The Nb-ZMT′ ceramic with 5 wt.% Bi₂O₃ addition exhibits the optimum dielectric properties: Q × f = 12,000 GHz, ?_r = 30, and τ_f = ?12 ppm/°C. Unlike the ZMT′ ceramic sintered at 900 °C, the Nb-ZMT′ ceramics show higher Q value and dielectric constant. Moreover, there is no Zn₂TiO₄ existence at 960 °C sintering. To understand the co-sinterability between silver electrodes and the Nb-ZMT′ dielectrics, the multilayer samples are prepared by multilayer thick film processing. The co-sinterability (900 °C) between silver electrode and Nb-ZMT′ dielectric are well compatible, because there are no cracks, delaminations, and deformations in multilayer specimens.     

Approaches for preparing 〈1 1 1〉-textured Bi0.5Na0.5TiO3-based ceramics by hetero-templated grain growth

The preparation of 〈1 1 1〉-textured Bi_0.5Na_0.5TiO₃ (BNT) ceramics was attempted by the templated grain growth method. This method uses anisometric grains as the template for texture development. In this work, plate-like BaTiO₃ grains with the 〈1 1 1〉 direction perpendicular to the plate faces were used. A mixture of the plate-like BaTiO₃ grains and equiaxed BNT grains was consolidated by tape casting to prepare green compacts in which the plate-like BaTiO₃ grains were dispersed in the matrix of the BNT grains and were aligned with their plate faces parallel to the casting direction. The textured BNT ceramics could not be obtained by the sintering of the green compacts, because of the disappearance of the plate-like BaTiO₃ grains by dissolution in the BNT grains. Several approaches were examined to obtain 〈1 1 1〉-textured ceramics. They included the use of plate-like (Sr, Ba)TiO₃ grains as the template, the use of equiaxed grains of BNT–BaTiO₃ and BNT–Bi_0.5K_0.5TiO₃ solid solutions as the matrix, and the addition of excess Na₂CO₃ and Bi₂O₃ to form liquid phases. The only approach successful in obtaining the textured ceramics was the one involving the addition of excess Na₂CO₃. The excess Na₂CO₃ formed a liquid phase and promoted the formation of a shell of BNT grains around a plate-like BaTiO₃ grain, prior to the dissolution of the BaTiO₃ grain. The BNT shell had the same crystallographic orientation as the BaTiO₃ grain and acted as the template for texture development.