Structure analysis on the Ba3Mg(Ta1−xNbx)2O9 ceramics: Coexistence of order and disorder

The Ba₃ZnTa₂O₉ (BZT) and Ba₃MgTa₂O₉ (BMT) ceramics, a family of A₃B²⁺B⁵⁺₂O₉ complex perovskites, are extensively utilized in mobile based technologies due to their intrinsic high unloaded quality factor, high dielectric constant and a low (near-zero) resonant frequency temperature coefficient at microwave frequencies. The preparation conditions as well as size and nature of B cations have a profound effect on the final dielectric properties. In this article, we report the effect of Nb⁵⁺ at the Ta⁵⁺ site on the BMT structure prepared at four synthesis temperatures (1300, 1400, 1500 and 1600 °C). The analysis has been carried out using the Rietveld technique on the X-ray powder diffraction data. Results suggest that both the preparation temperatures and Nb⁵⁺ content have significant effect on the ordering of B cations in the Ba₃Mg(Ta_1−xNb_x)₂O₉ solid solution. A disordered (cubic) structure is preferred by the 1300 °C compounds. The weight percentage of the ordered (trigonal) phase escalates, for a given composition, with increasing calcination temperature. A fully ordered trigonal arrangement exists only for x = 0.0 and 0.2 compounds calcined at 1600 °C, and the rest are biphasic (cubic and trigonal). The increase in the cubic fraction upon Nb⁵⁺ augmentation suggests that the solid solution leans more toward the disordered structural arrangement of B²⁺ and B⁵⁺ cations.     

Synthesis and microwave dielectric properties of Sr3Zn1−xMgxNb2O9 phases

Oxides of the type, Sr₃Zn_1−xMg_xNb₂O₉ (0≤x≤1) have been obtained by the ceramic method. These oxides crystallize in the hexagonal cell corresponding to ordered triple perovskites. Sintered disks show nearly frequency-independent dielectric constant for all the compositions. Compositions sintered at 1425°C yield dielectric constant of 20-22 at ∼6 GHz, with quality factor ranging from 1300 to 1500. Sr₃Zn_0.5Mg_0.5Nb₂O₉ shows a very low temperature coefficient of resonant frequency (τ_f) of +4 ppm/°C.     

Structural and electrical properties of La2−xBaxMo2O9−x/2 (x = 0-0.18)

La_2−xBa_xMo₂O_9−x/2 (x ≤ 0.18) have been prepared by solid state reaction method. The lattice parameter of La_2−xBa_xMo₂O_9−x/2 (x ≤ 0.18) determined by XRD data refinement shows a linear dependence on the dopant Ba content x. For the specimen with a La/Ba molar ratio of 0.18-0.2, additional reflection of secondary phase exists in the XRD pattern, so the value of solubility limit for Ba in La₂Mo₂O₉ is defined in range of 0.18 < x < 0.2. As the replacement degree of La³⁺ by Ba²⁺ increases, the bulk conductivity of La_2−xBa_xMo₂O_9−x/2 (x ≤ 0.18) decreases initially and then increases, a minimum value at La_1.9Ba_0.1Mo₂O_8.95 exists. Hebb-Wagner studies in argon atmosphere, which use an oxide-ion blocking electrode, show that La_2−xBa_xMo₂O_9−x/2 (x ≤ 0.18) are predominantly oxide-ion conducting in the temperature ranging from 773 to 1173 K. The average thermal expansion coefficient of La_1.84Ba_0.16Mo₂O_8.92 determined by high-temperature XRD was deduced as great as 17.5 × 10⁻⁶ K⁻¹ between 298 and 1173 K.     

Novel transparent conducting oxide: Anatase Ti1−xNbxO2

Single-crystalline Ti_1−xNb_xO₂ (x = 0.2) films of 40 nm thickness were deposited on SrTiO₃ (100) substrates by the pulsed laser deposition (PLD) technique. X-ray diffraction measurement confirmed epitaxial growth of anatase (001) film. The resistivity of Ti_1−xNb_xO₂ films with x ≥ 0.03 is 2-3 × 10^− 4 Ω cm at room temperature. The carrier density of Ti_1−xNb_xO₂, which is almost proportional to the Nb concentration, can be controlled in a range of 1 × 10¹⁹ to 2 × 10²¹ cm^− 3. Optical measurements revealed that internal transmittance in the visible and near-infrared region for films with x = 0.03 was more than 97%. These results demonstrate that the presently developed anatase Ti_1−xNb_xO₂ is one of the promising candidates for the practical TCOs.     

R3Mn1.5CuV0.5O9 (R = Y, Ho, Er, Tm, Yb and Lu) and Lu3Mn3−3xCu2xVxO9: New noncentrosymmetric oxides related to YMnO3

We report formation of new noncentrosymmetric oxides of the formula, R₃Mn_1.5CuV_0.5O₉ for R = Y, Ho, Er, Tm, Yb and Lu, possessing the hexagonal RMnO₃ (space group P6₃cm) structure. These oxides could be regarded as the x = 0.5 members of a general series R₃Mn_3−3xCu_2xV_xO₉. Investigation of the Lu-Mn-Cu-V-O system reveals the existence of isostructural solid solution series, Lu₃Mn_3−3xCu_2xV_xO₉ for 0 < x ≤ 0.75. Magnetic and dielectric properties of the oxides are consistent with a random distribution of Mn³⁺, Cu²⁺ and V⁵⁺ atoms that preserve the noncentrosymmetric RMnO₃ structure.     

Effect of Nb substitution on the structural, dielectric and magnetic properties of multiferroic BiFe1−xNbxO3 ceramics

Polycrystalline BiFe_1−xNb_xO₃ ceramics have been synthesized by standard solid-state reaction method. The effect of Nb substitution on the dielectric, magnetic and magnetoelectric properties of the BiFeO₃ multiferroic perovskite was studied. X-ray diffraction pattern revealed that all the samples with x = 0.00-0.10 showed rhombohedral perovskite structure. We obtained single phase upto doping concentration of x = 0.05 and with further increase in Nb concentration, some impurity peaks appeared. An anomaly in the dielectric constant (?) and dielectric loss (tan (δ)) in the vicinity of the antiferromagnetic Néel temperature (T_N) was observed. Nb substitution reduced the antiferromagnetic Néel temperature (T_N) in BiFe_1−xNb_xO₃. Proper amount of Nb could decrease the dielectric loss. Magnetic hysteresis loops measured at 5 K/300 K and temperature dependent magnetization curves indicated ferromagnetism in Nb substituted BiFeO₃ ceramics. The room temperature magnetic moment was found to increase with increase in Nb concentration. The dependence of dielectric constant on the magnetic field is an evidence of magnetoelectric coupling in BiFe_1−xNb_xO₃ ceramics.     

Microwave dielectric properties of Ba2 − xSrxLa3Ti3NbO15 ceramics

High dielectric constant and low loss ceramics in the system Ba_2 − xSr_xLa₃Ti₃NbO₁₅ (x = 0-1) have been prepared by conventional solid-state ceramic route. Ba_2 − xSr_xLa₃Ti₃NbO₁₅ solid solutions adopted A₅B₄O₁₅ cation-deficient hexagonal perovskite structure for all compositions. The materials were characterized at microwave frequencies. They show a linear variation of dielectric properties with the value of x. Their dielectric constant varies from 48.34 to 43.03, quality factor Q_u × f from 20,291 to 39,088 GHz and temperature variation of resonant frequency from 8 to 1.39 ppm/°C as the value of x increases. These low loss ceramics might be used for dielectric resonator (DR) applications.     

Dielectric and pyroelectric anisotropy in melt-quenched BaBi2(Nb1 − xVx)2O9 ceramics

The (0 0 l) textured BaBi₂(Nb_1 − xV_x)₂O₉ (where x = 0, 0.03, 0.07, 0.1 and 0.13) ceramics were fabricated via the conventional melt-quenching technique followed by high temperature heat-treatment (800-1000 °C range). The influence of vanadium content and sintering temperature on the texture development and relative density were investigated. The samples corresponding to the composition x = 0.1 sintered at 1000 °C for 10 h exhibited the maximum orientation of about 67%. The Scanning electron microscopic studies revealed the presence of platy grains having the a-b planes perpendicular the pressing axis. The dielectric constant and the pyroelectric co-efficient values in the direction perpendicular to the pressing axis were higher. The anisotropy in the dielectric constant is about 100 (at 100 kHz) at the dielectric maximum temperature and anisotropy in the pyroelectric co-efficient is about 50 μC cm⁻² °C⁻¹ in the vicinity of pyroelectric anomaly for the sample corresponding to the composition x = 0.1 sintered at 1000 °C. Higher values of the dielectric loss and electrical conductivity were observed in the direction perpendicular to the pressing axis which is attributed to the high oxygen ion conduction in the a-b planes.     

Dielectric properties of a new ceramic system (1 − x)Mg4Nb2O9-xCaTiO3 at microwave frequency

The microstructures and the microwave dielectric properties of the (1 − x)Mg₄Nb₂O₉-xCaTiO₃ ceramic system were investigated. In order to achieve a temperature-stable material, CaTiO₃ (τ_f ∼ 800 ppm/°C) was chosen as a τ_f compensator and added to Mg₄Nb₂O₉ (τ_f ∼ −70 ppm/°C) to form a two phase system. It was confirmed by the XRD and EDX analysis. By appropriately adjusting the x-value in the (1 − x)Mg₄Nb₂O₉-xCaTiO₃ ceramic system, near-zero τ_f value can be achieved. A new microwave dielectric material, 0.5Mg₄Nb₂O₉-0.5CaTiO₃ applicable in microwave devices is suggested and possesses the dielectric properties of a dielectric constant ?_r ∼ 24.8, a Q × f value ∼82,000 GHz (measured at 9.1 GHz) and a τ_f value ∼−0.3 ppm/°C.     

Lattice vibrations and dielectric functions of ferroelectric SrBi2−xNdxNb2O9 bismuth layer-structured ceramics determined by infrared reflectance spectra

Infrared optical properties of SrBi_2−xNd_xNb₂O₉ (SBNN) ceramics with different Nd compositions (from 0 to 0.2) have been investigated by near-normal incident reflectance technique. The experimental spectra in the wavenumbers range of 350-1500 cm⁻¹ were analyzed using the Lorentz oscillator model for five infrared-active phonon mode observed. It is found that the frequencies of the NbO₆ tilting and symmetric stretching modes linearly decrease with the Nd composition due to the octahedra distortion. The high-frequency dielectric constant varies in the range from 4.55 ± 0.04 to 4.80 ± 0.04. Owing to the contribution from the stronger electronic transitions, the real part of dielectric function Re(?) is estimated to about 4.0 in the high-frequency transparent region.     

Structural, spectroscopic and dielectric investigations on Ba8Zn(Nb6−xSbx)O24 microwave ceramics

Ba₈Zn(Nb_6−xSb_x)O₂₄ (x = 0, 0.3, 0.6, 0.9, 1.2, 1.5, 1.8 and 2.4) ceramics were prepared through the conventional solid-state route. The materials were calcined at 1250 °C and sintered in the range 1400-1425 °C. The structure of the system was analyzed by X-ray diffraction, Fourier transform infrared and Raman spectroscopic methods. The theoretical and experimental densities were calculated. The microstructure of the sintered pellets was analyzed using scanning electron microscopy. The low frequency dielectric properties were studied in the frequency range 50 Hz-2 MHz. The dielectric constant (?_r), temperature coefficient of resonant frequency (τ_f) and the unloaded quality factor (Q_u) are measured in the microwave frequency region using cavity resonator method. The τ_f values of the samples reduced considerably with the increase in Sb concentration. The materials have intense emission lines in the visible region. The compositions have good microwave dielectric properties and photoluminescence and hence are suitable for dielectric resonator and ceramic laser applications.     

Order-disorder phase transitions and high-temperature oxide ion conductivity of Er2+xTi2−xO7−δ (x = 0, 0.096)

The Er_2+xTi_2−xO_7−δ (x = 0.096; 35.5 mol% Er₂O₃) solid solution and the stoichiometric pyrochlore-structured compound Er₂Ti₂O₇ (x = 0; 33.3 mol% Er₂O₃) are characterized by X-ray diffraction (phase analysis and Rietveld method), thermal analysis and optical spectroscopy. Both oxides were synthesized by thermal sintering of co-precipitated powders. The synthesis study was performed in the temperature range 650-1690 °C. The amorphous phase exists below 700 °C. The crystallization of the ordered pyrochlore phase (P) in the range 800-1000 °C is accompanied by oxygen release. The ordered pyrochlore phase (P) exists in the range 1000−1200 °C. Heat-treatment at T ≥ 1600 °C leads to the formation of an oxide ion-conducting phase with a distorted pyrochlore structure (P2) and an ionic conductivity of about 10⁻³ S/cm at 740 °C. Complex impedance spectra are used to separately assess the bulk and grain-boundary conductivity of the samples. At 700 °C and oxygen pressures above 10⁻¹⁰ Pa, the Er_2+xTi_2−xO_7−δ (x = 0, 0.096) samples are purely ionic conductors.     

Study on properties of BaxSmyTi7O20 ceramics with CaO-SiO2-B2O3 glass

The effect of CaO-SiO₂-B₂O₃ (CSB) glass addition on the sintering temperature and dielectric properties of Ba_xSm_yTi₇O₂₀ ceramics has been investigated using X-ray diffraction, scanning electron microscopy and differential thermal analysis. The CSB glass starts to melt at about 970 °C, and a small amount of CSB glass addition to Ba_xSm_yTi₇O₂₀ ceramics can greatly decrease the sintering temperature from about 1350 to about 1260 °C, which is attributed to the formation of liquid phase. It is found that the dielectric properties of Ba_xSm_yTi₇O₂₀ ceramics are dependent on the amount of CSB glass and the microstructures of sintered samples. The product with 5 wt% CSB glass sintered at 1260 °C is optimal in these samples based on the microstructure and the properties of sintering product, when the major phases of this material are BaSm₂Ti₄O₁₂ and BaTi₄O₉. The material possesses excellent dielectric properties: ?_r = 61, tan δ = 1.5 × 10⁻⁴ at 10 GHz, temperature coefficient of dielectric constant is −75 × 10⁻⁶ °C⁻¹.     

Microstructure and microwave dielectric characteristics of (1 − x)Ba(Zn1/3Ta2/3)O3-xBaTi4O9 ceramics

(1 − x)Ba(Zn_1/3Ta_2/3)O₃-xBaTi₄O₉ (0.1 ≤ x ≤ 0.85) composites are prepared by mixing 1150 °C-calcined BaTi₄O₉ with 1150 °C-calcined Ba(Zn_1/3Ta_2/3)O₃ powders. The crystal structure, microwave dielectric properties and sinterabilites of the (1 − x)Ba(Zn_1/3Ta_2/3)O₃-xBaTi₄O₉ ceramics have been investigated. X-ray diffraction patterns reveal that BaTi₄O₉, ordered and disordered Ba(Zn_1/3Ta_2/3)O₃ phases exist independently over the whole compositional range. The sintering temperatures of (1 − x)Ba(Zn_1/3Ta_2/3)O₃-xBaTi₄O₉ ceramics are about 1240 - 1320 °C and obviously lower than those of Ba(Zn_1/3Ta_2/3)O₃ ceramics. The dielectric constants (?_r) and the temperature coefficient of resonant frequency (τ_f) of (1 − x)Ba(Zn_1/3Ta_2/3)O₃-xBaTi₄O₉ ceramics increase with the increase of BaTi₄O₉ content. Nevertheless, the bulk densities and the quality values (Q × f) of (1 − x)Ba(Zn_1/3Ta_2/3)O₃-xBaTi₄O₉ ceramics increase with the increase of Ba(Zn_1/3Ta_2/3)O₃ content. The results are attributed to the higher density and quality value of Ba(Zn_1/3Ta_2/3)O₃ ceramics, the better grain growth, and the densification of sintered specimens added a small BaTi₄O₉ content. The (1 − x)Ba(Zn_1/3Ta_2/3)O₃-xBaTi₄O₉ ceramic with x = 0.1 sintered at 1320 °C exhibits a ?_r value of 31.5, a maximum Q × f value of 68500 GHz and a minimum τ_f value of 4.1 ppm/°C.     

Synthesis and characterization of Ba1−xNdxF2+x (0.00 ≤ x ≤ 1.00)

A series of mixed fluorides with general composition Ba_1−xNd_xF_2+x (0.00≤x≤1.00) was prepared by vacuum heat treatment of the mixture of starting fluorides, and analyzed by powder XRD. From the XRD analysis, the low temperature phase equilibria in BaF₂-NdF₃ system is elucidated. The initial compositions in this series, that is, up to the nominal composition Ba_0.65Nd_0.35F_2.35 (x≤0.35) exist as cubic fluorite-type solid solution. Beyond the solid solution limit, that is, x>0.35, a rhombohedral fluorite related ordered phase is observed. Further, NdF₃-rich compositions (x≥0.50) exist as a mixture of rhombohedral ordered phase and NdF₃ (tysonite)-type phase. About 10 mol% of BaF₂ could be retained in the NdF₃ lattice, forming a tysonite-type solid solution, under the short annealed and slow cooled conditions.     

Structural and transport properties of stoichiometric Mn-doped magnetite: Fe3−xMnxO4

The polycrystalline samples of Fe_3−xMn_xO₄ (0.10 ≤ x ≤ 0.50) were prepared by a solid-state route reaction method. X-ray diffraction pattern shows that Mn²⁺ doped magnetites are in single phase and possess cubic inverse spinel structure. The resistivity measurements (10 < T < 300 K) for x = 0.0 and 0.01 confirms the first order phase transition at the Verwey transition T_V = 123 K and 117 K, respectively. No first order phase transition was evidenced for Fe_3−xMn_xO₄ (0.10 ≤ x ≤ 0.50). Small polaron model has been used to fit the semiconducting resistivity behavior and the activation energy ?_a, for samples x = 0.10 and 0.50 is about 72.41 meV and 77.39 meV, respectively. The Raman spectra of Fe_3−xMn_xO₄ at room temperature reveal five phonons modes for Fe_3−xMn_xO₄ (0.01 ≤ x ≤ 0.50) as expected for the magnetite (Fe₃O₄). Increased Mn²⁺ doping at Fe site leads to a gradual changes in phonon modes. The Raman active mode for Fe_3−xMn_xO₄ (x = 0.50) at ≅641.5 cm⁻¹ is shifted as compared to parent Fe₃O₄ at ≅669.7 cm⁻¹, inferring that Mn⁺² ions are located mostly on the octahedral sites. The laser power is fixed to 5 mW causes the bands to broaden and to undergo a small shift to lower wave numbers as well as increase in the full width half maxima for A_1g phonon mode with the enhancement of Mn²⁺ doping. Mössbauer spectroscopy probes the site preference of the substitutions and their effect on the hyperfine magnetic fields confirms that Mn⁺² ions are located mostly on the octahedral sites of the Fe_3−xMn_xO₄ spinel structure.     

Structural and dielectric properties of ferroelectric Sr1−xBaxBi2(Nb0.5Ta0.5)2O9 and Sr0.5Ba0.5Bi2(Nb1−yTay)2O9 ceramics

Ferroelectric Sr_1−xBa_xBi₂(Nb_0.5Ta_0.5)₂O₉ and Sr_0.5Ba_0.5Bi₂(Nb_1−yTa_y)₂O₉ were synthesized by solid state reaction route. X-ray diffraction studies confirm the formation of single phase layered perovskite solid solutions over a wide range of compositions (x=y=0.0, 0.25, 0.50, 0.75 and 1). The lattice parameters and the Curie temperature (T_c) have been found to have linear dependence on x and y. Transmission electron microscopy (TEM) suggest the lowering of orthorhombic distortion with increasing Ba²⁺ substitution. Variations in microstructural features as a function of x and y were monitored by scanning electron microscopy (SEM). The dielectric constant at room temperature increases with increase in both x and y. Interestingly Ba²⁺ substitution on Sr²⁺ site induces diffused phase transition and diffuseness increases with increasing Ba²⁺ concentration.     

Correlation of crystal structure and microwave dielectric properties for Zn(Ti1−xSnx)Nb2O8 ceramics

The correlation of crystal structure and microwave dielectric properties for Zn(Ti_1−xSn_x)Nb₂O₈ ceramics were investigated. The Zn(Ti_1−xSn_x)Nb₂O₈ ceramics contained ZnTiNb₂O₈ and an unknown Columbite-type phase. The columbite structure phase with increasing degree of ordering led to decrease of dielectric constant, increase of Qf and τ_f. The ZnTiNb₂O₈ with decreasing cation valence led to increase of τ_f. The typical values were: ? = 30.88, Qf = 43,500 GHz, τ_f = −54.32 × 10⁻⁶/ °C.     

Synthesis and characterizations of A-site deficient perovskite Sr0.9Ti0.8−xGaxNb0.2O3

The effects of reduction and Ga-doping on the physicochemical properties of A-site deficient perovskites Sr_0.9Ti_0.8−xGa_xNb_0.2O₃ (x = 0, 0.05, 0.1, 0.15 and 0.2) are reported. With 10% Ga doping, the sample sintered in air and treated at 1400 °C in H₂ atmosphere exhibits the highest electrical conductivity. It is found that the Ga-doping lowers the sinterability but promotes the reduction of Sr_0.9Ti_0.8−xGa_xNb_0.2O₃. The XRD analysis on the reduced samples suggests that some cations are reduced during the treatment. However, without high temperature pre-reduction, the improvement of Ga-doping is limited and the overall cell performance using Sr_0.9Ti_0.8−xGa_xNb_0.2O₃ as an anode without catalysts is still relatively low.     

Structural, magnetic and dielectric properties of Bi5−xLaxTi3Co0.5Fe0.5O15 ceramics

The Bi_5−xLa_xTi₃Co_0.5Fe_0.5O₁₅ (0 ≤ x ≤ 0.4) ceramics were successfully synthesized by a modified Pechini process. The samples were characterized by X-ray diffraction and no impurity phase has been detected. The cell volume of the composites increases monotonously with the increase of La content, which indicates that La ions have been incorporated into the lattice of Bi₅Ti₃Co_0.5Fe_0.5O₁₅. The magnetic measurements show that La doping on Bi sites has enhanced the magnetization of Bi_5−xLa_xTi₃Co_0.5Fe_0.5O₁₅ (0 ≤ x ≤ 0.4). Both the dielectric constants and loss tangent of all the samples decrease on increasing frequency and then become almost constant at room temperature. The La doped Bi₅Ti₃Co_0.5Fe_0.5O₁₅ samples exhibit improved dielectric and ferroelectric properties, with higher dielectric constant enhanced remnant polarization and lower losses at room temperature.