Solid state metathesis synthesis of BaTiO3, PbTiO3, K0.5Bi0.5TiO3 and Na0.5Bi0.5TiO3

A solid state metathesis approach has been applied to synthesize perovskite oxides such as BaTiO₃, PbTiO₃, K_0.5Bi_0.5TiO₃ and Na_0.5Bi_0.5TiO₃, these were characterized by powder XRD, IR and energy dispersive spectra (EDS). Potassium titanium oxalate and metal chlorides are used as the starting materials. X-ray analysis shows the formation of a single phase with tetragonal structure for BaTiO₃, PbTiO₃, K_0.5Bi_0.5TiO₃ and a monoclinic structure for Na_0.5Bi_0.5TiO₃. The Infrared spectra of these compounds show the characteristic band due to Ti–O octahedron for all the compounds. The EDS spectra show the relative ratio of the metal ions. The morphology of synthesized compounds was obtained from SEM measurements.     

Synthesis of Bi0.5(Na0.7K0.2Li0.1)0.5TiO3 powders through the molten salt method

The Bi_0.5(Na_0.7K_0.2Li_0.1)_0.5TiO₃ powder synthesis through molten salt method was investigated in the temperature range of 650–700 °C for 2–4 h. The XRD results indicated that the optimal synthesizing temperature for molten salt method was 700 °C, significantly lower than that for conventional processing route of solid state reaction method, where a calcining temperature of 850 °C was needed. The SEM results revealed better crystallization of the powders obtained through molten salt method, compared with those through the conventional processing route of solid state reaction method.     

The optimum conditions for preparing the lead-free piezoelectric ceramic of Bi0.5Na0.5TiO3 using the Taguchi method

Using the Taguchi method, this study analyzes the optimum conditions for preparing the disk of bismuth sodium titanate (Bi_0.5Na_0.5TiO₃), BNT, which is prepared using the mixed oxide method. The controllable factors used in this study consisted of the following: (1) the duration of milling; (2) the temperature of calcining; (3) the rotation speed of mill; and (4) the temperature of sintering. According to the optimum conditions, the confirmation experiment was carried out, and the relative density of the BNT disk, which was prepared without adding the additive, was up to 89.05%. The percentage contribution of each controllable factor was also determined. Most interestingly, the temperature of sintering is the most influential factor to press the BNT powder together tightly, and its value of percentage contribution is up to 94.94%.     

Effect of HfO2 content on the microstructure and piezoelectric properties of (Bi0.5Na0.5)0.94Ba0.06TiO3 lead-free ceramics

(Bi_0.5Na_0.5)_0.94Ba_0.06TiO₃–xHfO₂ [BNBT–xHfO₂] lead-free ceramics were prepared using the conventional solid-state reaction method. Effects of HfO₂ content on their microstructures and electrical properties were systematically studied. A pure perovskite phase was observed in all the ceramics with x=0–0.07 wt%. Adding optimum HfO₂ content can induce dense microstructures and improve their piezoelectric properties, and a high depolarization temperature was also obtained. The ceramics with x=0.03 wt% possess optimum electrical properties (i.e., d₃₃~168 pC/N, k_p~32.1%, Q_m~130, ε_r~715, tan δ~0.026, and T_d~106 °C, showing that HfO₂-modified BNBT ceramics are promising materials for piezoelectric applications.     

An efficient approach for direct synthesis of K0.5Na0.5NbO3 powders

Pure K_0.5Na_0.5NbO₃ powders were prepared at low temperatures by an efficient method using Na₂CO₃, K₂CO₃ and Nb₂O₅ as raw materials and urea as fuel. The phase evolution of the powders was investigated by X-ray diffractometer (XRD) and thermo gravimetric analysis-differential scanning calorimeter (TG-DSC). The phase composition and morphology of the powders were characterized by electron probe microanalysis (EPMA) and scanning electron microscope (SEM), respectively. The results reveal that single-phase K_0.5Na_0.5NbO₃ powder can be obtained at 550 °C by the method. The as-prepared powder is stoichimetric, fine and well-developed.     

(Ba0.5Sr0.5)TiO3 modification on etched aluminum foil for electrolytic capacitor

A new method was proposed to form (Ba_0.5Sr_0.5)TiO₃–Al₂O₃ composite oxide film on etched aluminum foils. The specimens were covered with (Ba_0.5Sr_0.5)TiO₃ (BST) layer by dip-coating in citrate solution and subsequent heat-treatment under 400–650 °C, finally by anodizing in a hot boracic acid and borate solution. The BST powders heated under different temperatures were characterized by X-ray diffraction (XRD) and the specific capacitance of the coated specimens heat-treated under different temperatures and times was measured. It is found that the specific capacitance increases initially with enhancing the temperature and reaches to maximum at 550 °C, but slightly decreases with the heat-treatment time. The capacitance was increased by about 35% after BST coating.     

Piezoelectric properties and microstructures of ZnO-doped Bi0.5Na0.5TiO3 ceramics

This article studies the microstructure and piezoelectric properties of a ceramic lead-free NBT under different amount of ZnO doping. X-ray diffraction shows that Zn²⁺ diffuses into the lattice of (Bi_0.5Na_0.5)TiO₃ to form a solid solution with a pure perovskite structure. By modifying the zinc oxide content, the sintering behavior of (Bi_0.5Na_0.5)TiO₃ ceramics was significantly improved and the grain size was increased. The piezoelectric coefficient d₃₃ for the 1.0 wt.% ZnO-doped (Bi_0.5Na_0.5)TiO₃ ceramics sintered at 1050 °C was found to be 95 pC/N, and the electromechanical coupling factor k_p = 0.13. However, the piezoelectric coefficient d₃₃ for the 0.5 wt.% ZnO-doped (Bi_0.5Na_0.5)TiO₃ ceramics sintered at 1140 °C was found to be 110 pC/N, and the electromechanical coupling factor k_p = 0.17.     

Study on Resistance Switching Properties of Na0.5Bi0.5TiO3 Thin Films Using Impedance Spectroscopy

The Na_0.5Bi_0.5TiO₃ (NBT) thin films sandwiched between Au electrodes and fluorine-doped tin oxide (FTO) conducting glass were deposited using a sol–gel method. Based on electrochemical workstation measurements, reproducible resistance switching characteristics and negative differential resistances were obtained at room temperature. A local impedance spectroscopy measurement of Au/NBT was performed to reveal the interface-related electrical characteristics. The DC-bias-dependent impedance spectra suggested the occurrence of charge and mass transfer at the interface of the Au/NBT/FTO device. It was proposed that the first and the second ionization of oxygen vacancies are responsible for the conduction in the low- and high-resistance states, respectively. The experimental results showed high potential for nonvolatile memory applications in NBT thin films.     

Investigations on the electrodeposition behaviors of Bi0.5Sb1.5Te3 thin film from nitric acid baths

The electrochemical reduction process of Bi³⁺, HTeO₂⁺, Sb^III and their mixtures in nitric acid medium was investigated by means of cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) measurements. The reduction products electrodeposited at various potentials were examined using X-ray diffraction (XRD) and energy dispersive spectroscopy (EDS). The results show that cathodic process in the nitric acid solution containing Bi³⁺, HTeO₂⁺ and Sb^III involves the following reduction reactions in different polarizing potential ranges: In low polarizing potential ranges, Te⁰ is formed firstly on the electrode surface through the electrochemical reduction of HTeO₂⁺; with the negative shift of the cathodic polarizing potential, the reduction reaction of Bi³⁺ with Te⁰ to form Bi₂Te₃ takes place; when the cathodic polarizing potential is negative enough, Bi³⁺ and Sb^III react with Te⁰ to form Bi_0.5Sb_1.5Te₃. The results indicate that Bi_0.5Sb_1.5Te₃ films can be fabricated by controlling the electrodepositing potential in a proper high potential ranges.     

Achieving excellent energy storage properties of Na0.5Bi0.5TiO3 - based ceramics by using a two-step strategy involving phase and polarization modification

Na_0.5Bi_0.5TiO₃-based ceramic specimens have been extensively investigated as ferroelectric materials. After being doped with CaTiO₃, the resulting Na_0.5Bi_0.5TiO₃-based ceramics exhibit relaxor characteristics, and improved energy storage density and efficiency. Based on these above results, CeO₂ was further employed to modify the polarization of the 0.85Na_0.5Bi_0.5TiO₃-0.15CaTiO₃ matrix ceramic to achieve better energy storage performance. The effective energy storage density was enhanced from 1.93 to 2.53 J/cm³ by using the appropriate doping concentration of CeO₂. Grain refinement effect can effectively enhance the electric-field strength from approximately 190 to 230 kV/cm. In particular, when doped with 2% CeO₂, the energy storage efficiency of the sample was maintained at approximately 90% at 30 °C-150 °C and at approximately 80% in the frequency range of 0.2–200 Hz. This combination has very excellent temperature stability and frequency stability, making it a promising candidate for energy storage applications.     

Study of crystal structure,dielectric, magnetic and magnetoelecrtic properties of xCoFe2O4-(1-x)Na0.5Bi0.5TiO3 composites

Multiferroic composites of spinel ferrite and ferroelectric xCoFe₂O₄ – (1-x)Na_0.5Bi_0.5TiO₃ (with x = 0.10,0.30,0.50) were efficiently prepared by standard solid state reaction mechanism. X-ray diffractometer was used to analyze crystal structure of the prepared composites. The observed XRD patterns of the composites comprise peaks of both the phases i.e. ferrite and ferroelectric, with no sign of secondary peaks. Rietveld refinement of XRD data further confirms the coexistence of these two phases with cubic (Fd3m) and rhombohedral (R3c) symmetry corresponding to ferrite and ferroelectric phase respectively. The 3-dimensional overview of crystal structure of pure CoFe₂O₄ and Na_0.5Bi_0.5TiO₃ and of composite 0.50CoFe₂O₄?0.50Na_0.5Bi_0.5TiO₃ is generated by using refined parameters. The dielectric constant (ε´) and dielectric loss (tanδ) values were recorded as a function of frequency ranging from 100?Hz to 7?MHz and at different temperatures. Both ε´ and tanδ follow dispersion pattern at lower frequencies while show frequency independent behavior at higher frequencies. The magnetic evaluation carried by analyzing M-H hysteresis loop reveals the ferrimagnetic characteristics of these composites. The highest value of magnetic moment is 1.12μ_B observed for composite 0.50CoFe₂O₄ – 0.50Na_0.5Bi_0.5TiO_3. Magnetoelectric (ME) voltage coefficient (α) was also demonstrated to observe the interaction between ferrite and ferroelectric phases. The highest value of α (72.72μV/Oe cm) is obtained for low ferrite composition 0.10CoFe₂O₄ – 0.90Na_0.5Bi_0.5TiO₃, which suggests the dependence of magnetoelectric response on the resistivity of the composites.     

Mechanism of Bi0.5Na0.5TiO3 and Bi4.5Na0.5Ti4O15 template synthesis during topochemical microcrystal conversion and texturing of Bi0.5(Na0.8K0.2)0.5TiO3 piezoelectric ceramics

The mechanism by which Bi_0.5Na_0.5TiO₃ and Bi_4.5Na_0.5Ti₄O₁₅ templates are synthesized via a topochemical microcrystal conversion method using Bi₄Ti₃O₁₂ precursor and TiO₂ particles was investigated based on their crystal structures. The Bi_0.5Na_0.5TiO₃ template consisted of a mixture of plate-like and equiaxed particles, whereas the Bi_4.5Na_0.5Ti₄O₁₅ template consisted only of plate-like particles. The size of the plate-like and equiaxed particles was dependent on the size of the Bi₄Ti₃O₁₂ precursor and TiO₂ particles, respectively. The Lotgering factor and piezoelectric constant of textured Bi_0.5(Na_0.8K_0.2)_0.5TiO₃ ceramics prepared using the Bi_0.5Na_0.5TiO₃ template were lower than those of the textured Bi_0.5(Na_0.8K_0.2)_0.5TiO₃ ceramics prepared from the Bi_4.5Na_0.5Ti₄O₁₅ template. This can be attributed to the small amount of plate-like particles in the Bi_0.5Na_0.5TiO₃ template caused by the inevitable co-existence of equiaxed particles.     

Rheology and physical properties of Bi0.5(Na0.82K0.18)0.5TiO3 piezoelectric thick films by aqueous gel-tape casting process

Piezoelectric Bi_0.5(Na_0.82K_0.18)_0.5TiO₃ thick films were prepared by aqueous gel-tape casting. Bi_0.5(Na_0.82K_0.18)_0.5TiO₃ nano-powder with perovskite structure prepared by sol–gel process was obtained. The average particle size was 200 nm. A stable Bi_0.5(Na_0.82K_0.18)_0.5TiO₃ suspension with 46 vol% solid loading and <1 Pa s viscosity was prepared when 0.8 wt% of ammonium polyacrylate was added with the pH value controlled in the range 7–9. The plasticizer glycerol had a positive effect on the fluidity of the suspensions. The tensile strength and strain to failure of the green tape were 0.42 MPa and 0.04 mm/mm when the addition of glycerol was 50 wt% of the premix solvent. The resulting about 100 μm thick films had relative permittivity of 910, dielectric loss of 4.9% at 10 kHz, remanent polarization of 24 μC/cm², coercive field of 56 kV/cm, and longitudinal effective piezoelectric coefficient d₃₃eff of 102 pC/N. The good performance illustrated that gel-tape casting was the effective way to prepare Bi_0.5(Na_0.82K_0.18)_0.5TiO₃ thick film.     

Formation of LiNi0.5Co0.5VO4 nano-crystals by solvothermal reaction

LiNi_0.5Co_0.5VO₄ nano-crystals were solvothermally prepared using a mixture of LiOH·H₂O, Ni(NO₃)₂·6H₂O, Co(NO₃)₂·6H₂O and NH₄VO₃ in isopropanol at 150–200 °C followed by 300–600 °C calcination to form powders. TGA curves of the solvothermal products show weight losses due to evaporation and decomposition processes. The purified products seem to form at 500 °C and above. The products analyzed by XRD, selected area electron diffraction (SAED), energy dispersive X-ray (EDX) and atomic absorption spectrophotometer (AAS) correspond to LiNi_0.5Co_0.5VO₄. V–O stretching vibrations of VO₄ tetrahedrons analyzed using FTIR and Raman spectrometer are in the range of 620–900 cm⁻¹. A solvothermal reaction at 150 °C for 10 h followed by calcination at 600 °C for 6 h yields crystals with lattice parameter of 0.8252 ± 0.0008 nm. Transmission electron microscope (TEM) images clearly show that the solvothermal temperatures play a more important role in the size formation than the reaction times.     

Temperature-stable dielectric ceramics based on Na0.5Bi0.5TiO3

Multiple ion substitutions to Na_0.5Bi_0.5TiO₃ give rise to favourable dielectric properties over the technologically important temperature range ?55?°C to 300?°C. A relative permittivity, ε_r,?=?1300?±?15% was recorded, with low loss tangent, tanδ?≤?0.025, for temperatures from 310?°C to 0?°C, tanδ increasing to 0.05 at ?55?°C (1?kHz) in the targeted solid solution (1–x)[0.85Na_0.5Bi_0.5TiO₃–0.15Ba_0.8Ca_0.2Ti_1-yZr_yO₃]–xNaNbO₃: x?=?0.3, y?=?0.2. The ε_r-T plots for NaNbO₃ contents x?<?0.2 exhibited a frequency-dependent inflection below the temperature of a broad dielectric peak. Higher levels of niobate substitution resulted in a single peak with frequency dispersion, typical of a normal relaxor ferroelectric. Experimental trends in properties suggest that the dielectric inflection is the true relaxor dielectric peak and appears as an inflection due to overlap with an independent broad dielectric peak. Process-related cation and oxygen vacancies and their possible contributions to dielectric properties are discussed.     

Microstructural,ferroelectric, and photoluminescent properties of (100)‐oriented Sm3+‐doped Na0.5Bi0.5TiO3 thin films

(100)_C‐oriented Na_0.5Bi_0.5‐xSm_xTiO₃ (NBST) lead‐free ferroelectric thin films were prepared on Pt/Ti/SiO₂/Si substrates by chemical solution deposition method, and their microstructural, dielectric, ferroelectric, and photoluminescent properties were studied. X‐ray diffraction and scanning electron microscopy analysis indicated that both the grain size and (100)_C orientation degree of NBST thin films were decreased by doping Sm³⁺ ions. Raman spectra showed that structural symmetry of NBST thin films decreased at low Sm³⁺ doping concentration and then increased at high doping concentration of Sm³⁺ ions. An appropriate amount of Sm³⁺ dopants was confirmed to enhance dielectric and ferroelectric properties of the NBST thin films. Among all the compositions, the Na_0.5Bi_0.492Sm_0.008TiO₃ thin film exhibited the largest remnant polarization (2P_r) of 27.3 μC/cm² and high dielectric constant of 1068, as well as a low dielectric loss of 0.04. Temperature‐ and frequency‐dependent dielectric characteristics illustrated the relaxor ferroelectric behavior of Na_0.5Bi_0.492Sm_0.008TiO₃ thin film. Meanwhile, the Na_0.5Bi_0.492Sm_0.008TiO₃ thin film also showed optimal orange‐red emission at 600 nm, which is originating from the ⁴G_5/2 → ⁴H_7/2 transition of Sm³⁺ ions.     

Carbon dioxide hydrogenation to methanol over the pre-reduced LaCr0.5Cu0.5O3 catalyst

The synthesis of methanol from CO₂ hydrogenation was carried out over the pre-reduced Cu-based LaCr_0.5Cu_0.5O₃ catalyst. It showed a much higher catalytic performance (X_CO2 = 10.4% and S_MeOH = 90.8%) at 250 °C than over 13% Cu/LaCrO₃ prepared by wet-impregnation method (X_CO2 = 4.8% and S_MeOH = 46.6%). XRD, H₂/CO₂-TPD and XPS measurements illustrated that hydrogen was adsorbed on the Cu^α+ sites and that CO₂ was activated on the medium basic sites for the reduced LaCr_0.5Cu_0.5O₃. This phenomenon was responsible for its catalytic activity.     

Texture development and dielectric relaxor behavior of 0.80Na0.5Bi0.5TiO3–0.20K0.5Bi0.5TiO3 ceramics templated by plate-like NaNbO3 particles

Plate-like NaNbO₃ particles were used as templates to fabricate grain-oriented 0.96(0.8Na_0.5Bi_0.5TiO₃–0.2 K_0.5Bi_0.5TiO₃)–0.04NaNbO₃ (NKBT) ceramics. The effects of the sintering temperature and the soaking time on the grain orientation and the microstructure of the textured NKBT ceramics were investigated, and the dielectric relaxor behavior is discussed. The results show that textured ceramics were successfully obtained with orientation factor more than 0.8. The textured ceramics have a microstructure with strip-like grains aligning in the direction parallel to the casting plane. The degree of grain orientation increases initially, then decreases with increasing sintering temperature, and increases continuously with increasing soaking time. The textured NKBT ceramics shows obvious dielectric relaxor characteristics which can be well explained by microdomain–macrodomain transition theory with calculating criterion K. The results show that formation of texture is beneficial to microdomain–macrodomain transition, which lead to weaken relaxor behavior and raise the dielectric constant at T_tr.     

Influence of the synthesis conditions on the dielectric properties in the Bi0.5Na0.5TiO3-KTaO3 system

A novel (1 − x)Bi_0.5Na_0.5TiO₃-xKTaO₃ system was characterized using X-ray powder diffraction, scanning electron microscopy, as well as dielectric and ferroelectric measurements. The results showed the formation of solid solutions across the whole concentration range; however, using a solid-state reaction method it was not possible to obtain single-phase ceramics. The secondary phases formed in the system were alkali-hexatitanate and -tetratantalate. The formation of the solid solutions initially starts with the formation of the Bi_0.5Na_0.5TiO₃- and KTaO₃-rich phases, which then react towards the nominal composition at higher temperatures. We observed that the structural and dielectric properties are strongly influenced by the heat-treatment conditions. Typical relaxor properties with a frequency dispersion of the dielectric maximum were obtained only after annealing at a higher temperature, which considerably improved the homogeneity of the perovskite phase. In accordance with the decreasing temperature of the permittivity maximum, ferroelectric measurements showed a changing of the properties from ferroelectric through relaxor to paraelectric with an increasing content of KTaO₃.     

Intermediate phases formation during the synthesis of Bi4Ti3O12 by solid state reaction

In this work, the formation of Bi₄Ti₃O₁₂ by solid state reaction from Bi₂O₃ and TiO₂ starting powders has been studied. The Bi₄Ti₃O₁₂ formation occurs through an intermediate Bi₁₂TiO₂₀ sillenite phase formed at temperatures sligthly over 300 °C. This sillenite phase is stable up to ∼750 °C, but in the presence of TiO₂ reacts to form Bi₄Ti₃O₁₂ at temperatures >500 °C. Raman spectroscopy has been used to evidence the amorphization of TiO₂, demonstrating that the Bi₄Ti₃O₁₂ formation occurs through the reaction of sillenite Bi₁₂TiO₂₀ and TiO₂.