Microstructure and microwave dielectric properties of (1 − y)Li3NbO4+yLi2TiO3(Li2SnO3) ceramics

Phase formation, microstructure and microwave dielectric properties of (1 − y)Li₃NbO₄ + yLi₂TiO₃(Li₂SnO₃) ceramics have been studied in this paper. The structure and microstructure of the compounds were investigated using X-ray powder diffractometer (XRD), scanning electron microscope (SEM), Raman spectrometer. The microwave dielectric properties of the ceramics were studied with a network analyzer at the frequency of about 8–12 GHz. Li₃NbO₄ formed ordered solid solutions with the addition of small amount of Li₂TiO₃ (y ≤ 0.2), whereas no solid solution formed with the addition of small amount of Li₂SnO₃. Small amount of Li₂TiO₃ doping suppressed the appearance of impurity phases caused by lithium evaporation for Li₃NbO₄. The Li₂TiO₃ doped compositions with 0.02 ≤ y ≤ 0.08 demonstrated homogeneous and dense microstructure after sintering at 1150 °C/2 h, in contrast the 0.2 ≤ y ≤ 0.6 specimens exhibited porous and subgrains microstructure after sintering at 1250 °C/2 h. Short range ordering was observed in the 0.2 ≤ y ≤ 0.6 compositions. Mechanical mixture phases of Li₃NbO₄ and Li₂SnO₃ based solid solution (Li₂SnO₃ (ss)) existed in the Li₂SnO₃ added specimens_. The dielectric permittivity increased with increasing Li₂TiO₃ addition, but decreased with the increase of Li₂SnO₃ content. All specimens exhibited negative τ_f value for the Li₂TiO₃ added specimens, although its absolute τ_f value decreased with the increase of Li₂TiO₃ addition. Whereas, the τ_f value changed from negative into positive with the increase of Li₂SnO₃ addition. Optimized combined microwave dielectric properties (?_r = 19.8, Q × f = 91,200 GHz, τ_f = −24 ppm/°C and ?_r = 16, Q × f = 75,300 GHz, τ_f = 3 ppm/°C) could be obtained for the Li₂TiO₃ added (y = 0.6) and Li₂SnO₃ added specimens(y = 0.7), respectively. The microwave dielectric properties of the Li₂SnO₃ end member are ?_r = 13.5, Q × f = 61,600 GHz, τ_f = 29 ppm/°C.     

Synthesis, low-temperature sintering and the dielectric properties of the ZnO-(1 − x)TiO2-xSnO2 (x = 0.04-0.2)

ZnO-(1 − x)TiO₂-xSnO₂ (x = 0.04-0.2) ceramics were prepared by conventional mixed-oxide method combined with a chemical processing. Fine particle powders were prepared by chemical processing to activate the formation of compound and to improve the sinterability. One wt.% of V₂O₅ and B₂O₃ with the mole ratios of 3:1 were used to lower the sintering temperature of ceramics. The effect of Sn content on phase structure and dielectric properties were investigated. The results show that the substituting Sn for Ti accelerates the hexagonal phase transition to cubic phase, and an inverse spinel structure Zn₂(Ti_1−xSn_x)O₄ solid solution forms. The best dielectric properties obtained at x = 0.12. The ZnO-0.88TiO₂-0.12SnO₂ ceramics sintered at 900 °C exhibit a good dielectric property: ?_r = 29 and tan δ = 9.86 × 10⁻⁵. Due to their good dielectric properties, low firing characteristics, ZnO-(1 − x)TiO₂-xSnO₂ (x = 0.04-0.2) can serve as the promising microwave dielectric capacitor.     

(5 − x)BaO-xMgO-2Nb2O5 ceramics prepared using a reaction-sintering process

(5 − x)BaO-xMgO-2Nb₂O₅ (x = 0.5 and 1; 5MBN and 10MBN) microwave ceramics prepared using a reaction-sintering process were investigated. Without any calcinations involved, the mixture of BaCO₃, MgO, and Nb₂O₅ was pressed and sintered directly. MBN ceramics were produced after 2-6 h of sintering at 1350-1500 °C. The formation of (BaMg)₅Nb₄O₁₅ was a major phase in producing 5MBN ceramics, and the formation of Ba(Mg_1/3Nb_2/3)O₃ was a major phase in producing 10MBN ceramics. As CuO (1 wt%) was added, the sintering temperature dropped by more than 150 °C. We produced 5MBN ceramics with these dielectric properties: ?_r = 36.69, Qf = 20,097 GHz, and τ_f = 61.1 ppm/°C, and 10MBN ceramics with these dielectric properties: ?_r = 39.2, Qf = 43,878 GHz, and τ_f = 37.6 ppm/°C. The reaction-sintering process is a simple and effective method for producing (5 − x)BaO-xMgO-2Nb₂O₅ ceramics for applications in microwave dielectric resonators.     

Crystal structure and electrical properties of new tungsten bronzes: BxWO3 (0.01 ≤ x ≤ 0.08)

Boron tungsten bronzes B_xWO₃ (0.01 ≤ x ≤ 0.08) were synthesized by hybrid microwave method from mixtures of WO₃ and amorphous boron powder. With the increase of boron content, the crystal structure of B_xWO₃ transforms from orthorhombic (x = 0.01) to tetragonal α (x = 0.048) and then to tetragonal β (0.07 ≤ x ≤ 0.08). The average size of crystallites is in the range of 1-10 μm. All samples show semiconducting behaviour in their temperature dependence of resistivity. The conduction behaviour above 80 K for samples with x = 0.01 and 0.08 can be explained using the variable-range hopping and thermally activated mechanism, respectively. Comparative experiments showed that boron bronze phases cannot be obtained by the microwave heating of pure WO₃ powder or a mixture of B₂O₃ and WO₃ under the same conditions.     

Synthesis of (1 − x)Ca2/5Sm2/5TiO3-xLi1/2Nd1/2TiO3 ceramic powder via ethylenediaminetetraacetic acid precursor

(1 − x)Ca_2/5Sm_2/5TiO₃-xLi_1/2Nd_1/2TiO₃ (CSLNT) ceramic powder was prepared by a liquid mixing method using ethylenediaminetetraacetic acid (EDTA) as the chelating agent. TG, DTA, XRD and TEM characterized the precursors and derived oxide powders. When x = 0.3, perovskite CSLNT was synthesized at 1000 °C for 3 h in air. The CSLNT (x = 0.3) ceramics sintered at 1200 °C for 3 h show excellent microwave dielectric properties of ?_r = 99, Q_f = 6200 GHz and τ_f = 9 × 10⁻⁶ °C⁻¹.     

Dielectric properties of Ba(Ti1 − xZrx)O3 solid solutions

This paper reports the structural and dielectric properties of Ba(Ti_1 − xZr_x)O₃ (x = 0-0.3) ceramics. Single-phase solid solutions of the samples were determined by X-ray diffraction. Microscopic observation by scanning electron microscope revealed dense, single-phase microstructure with large grains (20-60 μm). The evolution of dielectric behavior from a sharp ferroelectric peak (for x ≤ 0.08) to a round dielectric peak (for 0.15 ≤ x ≤ 0.25) with pinched phase transitions and successively to a ferroelectric relaxor (for x = 0.3) was observed with increasing Zr concentration. Compared with pure BaTiO₃, broaden dielectric peaks with high dielectric constant of 25,000-40,000 and reasonably low loss (tanδ: 0.01-0.06) in the Ba(Ti_1 − xZr_x)O₃ ceramics have been observed, indicating great application potential as a dielectric material.     

Rietveld refinements of the solid solution Li(1−2x)NixTiO(PO4) (0 ≤ x ≤ 0.50)

Li_(1−2x)Ni_xTiO(PO₄) oxyphosphates with 0 ≤ x ≤ 0.10 crystallize in the orthorhombic system with the space group Pnma, those with 0.10 < x ≤ 0.25 crystallize in the monoclinic system with the space group P2₁/c and compositions with 0.25 < x < 0.50 present a mixture of the limit of the solid solution Li_0.50Ni_0.25TiO(PO₄) and Ni_0.50TiO(PO₄). The structure of the compositions 0 ≤ x ≤ 0.25 is based on a three-dimensional anionic framework constructed of chains of alternating TiO₆ octahedra and PO₄ tetrahedra, with the lithium and nickel atoms in the cavities in the framework. The dominant structural units in the compositions are chains of tilted corner-sharing TiO₆ octahedra running parallel to one of the axis. The oxygen atoms of the shared corners, not implied in (PO₄) tetrahedra, justify the oxyphosphate designation. Titanium atoms are displaced from the geometrical center of the octahedra resulting in alternating long (≈2.25 Å) and short (≈1.71 Å) TiO(1) bonds. The four remaining TiO bond distances have intermediate values ranging from 1.91 to 2.06 Å.     

Microwave dielectric properties of Li2TiO3 ceramics sintered at low temperatures

Li₂TiO₃ ceramics were prepared at the sintering temperatures from 1050 to 1250 °C. The optimal microwave dielectric properties were ?_r = 23.29, Q × f = 15,525 GHz (5.9 GHz), and τ_f = 35.05 ppm/ °C for the sample sintered at 1200 °C. The microwave dielectric properties were improved obviously when the Li₂TiO₃ ceramics were sintered at low temperatures with small additions of H₃BO₃ (B₂O₃ in the form of H₃BO₃). Only monoclinic Li₂TiO₃ was found in the pure or H₃BO₃-doped Li₂TiO₃ ceramics. About 1.0 wt.% H₃BO₃ addition aided the sintering of Li₂TiO₃ ceramics effectively while excessive H₃BO₃ (≥2.5 wt.%) was not favorable. Typically the best microwave dielectric properties were ?_r = 23.28, Q × f = 37,110 GHz (6.3 GHz), and τ_f = 30.43 ppm/ °C for the 1.0 wt.% H₃BO₃-doped Li₂TiO₃ ceramic sintered at 920 for 3 h, which is promising for LTCC applications.     

Dielectric properties of (1−x)(Mg0.95Co0.05)TiO3-xCaTiO3 ceramic system at microwave frequency

The microwave dielectric properties and the microstructures of the (1−x)MgTiO₃-xCaTiO₃ ceramic system were investigated. With partial replacement of Mg by Co, dielectric properties of the (1−x)(Mg_0.95Co_0.05)TiO₃-xCaTiO₃ ceramics can be promoted. The microwave dielectric properties are strongly correlated with the sintering temperature. At 1275°C, the 0.95(Mg_0.95Co_0.05)TiO₃-0.05CaTiO₃ ceramics possesses excellent microwave dielectric properties: a dielectric constant ε_r of 20.3, a Q×f value of 107 000 ( at 7 GHz) and a τ_f value of −22.8 ppm/°C. By appropriately adjusting the x value in the (1−x)(Mg_0.95Co_0.05)TiO₃-xCaTiO₃ ceramic system, zero τ_f value can be achieved. With x=0.07, a dielectric constant ε_γ of 21.6, a Q×f value of 92 000 (at 7 GHz) and a τ_f value of −1.8 ppm/°C was obtained for 0.93(Mg_0.95Co_0.05)TiO₃-0.07CaTiO₃ ceramics sintered at 1275°C for 4 h.     

Microwave dielectric properties and microstructures of the 11Li2O-3Nb2O5-12TiO2 ceramics with B2O3 addition

The effects of B₂O₃ addition, as a sintering agent, on the sintering behavior, microstructure and microwave dielectric properties of the 11Li₂O-3Nb₂O₅-12TiO₂ (LNT) ceramics have been investigated. With the low-level doping of B₂O₃ (≤2 wt.%), the sintering temperature of the LNT ceramic could be effectively reduced to 900 °C. The B₂O₃-doped LNT ceramics are also composed of Li₂TiO₃ss and “M-phase” phases. No other phase could be observed in the 0.5-2 wt.% B₂O₃-doped ceramics sintered at 840-920 °C. The addition of B₂O₃ induced no obvious degradation in the microwave dielectric properties but increased the τ_f values. Typically, the 0.5 wt.% B₂O₃-doped ceramics sintered at 900 °C have better microwave dielectric properties of ?_r = 49.2, Q × f = 8839 GHz, τ_f = 57.6 ppm/°C, which suggest that the ceramics could be applied in multilayer microwave devices requiring low sintering temperatures.     

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.     

New dielectric material system of x(Mg0.95Zn0.05Ti)O3-(1 − x)Ca0.8Sm0.4/3TiO3 at microwave frequency

The microstructures and the microwave dielectric properties of the x(Mg_0.95Zn_0.05)TiO₃-(1 − x) Ca_0.8Sm_0.4/3TiO₃ ceramic system were investigated. In order to achieve a temperature-stable material, we studied a method of combining a positive temperature coefficient material with a negative one. Ca_0.8Sm_0.4/3TiO₃ has dielectric properties of dielectric constant ε_r ~ 120, Q × f value ~ 13,800 GHz and a large positive τ_f value ~ 400 ppm/°C. (Mg_0.95Zn_0.05)TiO₃ possesses high dielectric constant (ε_r ~ 16.21), high quality factor (Q × f value ~ 210,000 at 9 GHz) and negative τ_f value (− 59 ppm/°C). Sintering at 1300 °C with x = 0.9, 0.9(Mg_0.95Zn_0.05Ti)O₃ − 0.1 Ca_0.8Sm_0.4/3TiO₃ has a dielectric constant (ε_r) of 22.7, a Q × f value of 124,000 GHz and a temperature coefficient of resonant frequency (τ_f) of − 6.3 ppm/°C.     

Properties of the PLZTN x/54/46 (0.4 ≤ x ≤ 1.4) ceramic system

Even though the PZT ceramic system has been thoroughly studied and modified with different additives, no numerous reports have been published focusing on the PZT double ‘soft’ modification with La³⁺ and Nb⁵⁺ (PLZTN). In this paper, we explore the structural, morphological, dielectric, ferroelectric and piezoelectric properties of the PLZTN system for different doping levels (x_La3+ = x_Nb5+ = 0.4, 0.6, 0.8, 1.0 and 1.4 at.%) synthesized by conventional powders reaction. The temperature dependence of the piezoelectric response of poled ceramic disks is also analyzed and, according to its overall features, an optimum modification is proposed in order to develop PZT-based sensors for several applications.     

Phase formation, microstructure, and dielectric properties of (1 − x)PZT-(x)PCN ceramics

Ceramics in a PZT-PCN system with the formula (1 − x)Pb(Zr_1/2Ti_1/2)O₃-(x)Pb(Co_1/3Nb_2/3)O₃, where x = 0.0, 0.1, 0.2, 0.3, 0.4, 0.5, and 1.0, were prepared using a solid-state mixed-oxide technique with columbite−CoNb₂O₆ and wolframite−ZrTiO₄ precursors. The crystal structure of the specimens studied with X-ray diffraction (XRD) analysis showed a coexistence between tetragonal and pseudo cubic phases at composition x = 0.2. The SEM micrograph showed that the average grain size significantly decreased with increasing PCN content. A maximum dielectric constant was observed at composition x = 0.2, while the transition temperature strongly decreased with increasing PCN content. All ceramics also showed diffused phase transition behaviors with a minimum diffusivity at x = 0.2. The morphotropic phase boundary (MPB) lay at the 0.8PZT-0.2PCN composition.     

Influences of poling condition and sintering temperature on piezoelectric properties of (Na0.5Bi0.5)1 − xBaxTiO3 ceramics

The structure, ferroelectric characteristics and piezoelectric properties of (Na_0.5Bi_0.5)_1 − xBa_xTiO₃ (x = 0.04, 0.06, 0.10) ceramics prepared by conventional solid state method were investigated. The influences of poling condition and sintering temperature on the piezoelectric properties of the ceramics were examined. The piezoelectric properties of the ceramics highly depend on poling field and temperature, while no remarkable effect of poling time on the piezoelectric properties was found in the range of 5-25 min. Compared with (Na_0.5Bi_0.5)_0.96Ba_0.04TiO₃ and (Na_0.5Bi_0.5)_0.90Ba_0.10TiO₃, the piezoelectric properties of (Na_0.5Bi_0.5)_0.94Ba_0.06TiO₃ are more sensitive to poling temperature due to the relatively low depolarization temperature. Moderate increase of sintering temperature improved the poling process and piezoelectric properties due to the development of microstructural densification and crystal structure. With respect to sintering behavior and piezoelectric properties, a sintering temperature range of 1130-1160 °C was ascertained for (Na_0.5Bi_0.5)_0.90Ba_0.10TiO₃.     

Structural and microwave dielectric behavior of (Li1/4Nb3/4) substituted ZrxSnyTizO4 (x + y + z = 2) system

The phase structure, microwave dielectric properties, and their stability with different annealing conditions have been investigated in (Li_1/4Nb_3/4) substituted Zr_xSn_yTi_zO₄ system. The sintering temperature of Zr_xSn_yTi_zO₄ ceramic was lowered from 1500 to 1140 °C by (Li_1/4Nb_3/4) substitution. Both X-ray diffraction (XRD) analysis and electron diffraction (ED) analysis revealed that the (Li_1/4Nb_3/4) substituted Zr_xSn_yTi_zO₄ ceramic crystallized as the high-temperature disordered ZrTiO₄ phase. As the content of Sn increased from 0.10 to 0.30, the permittivity of the (Zr_1−xSn_x)(Li_1/4Nb_3/4)_0.4Ti_0.6O₄ ceramic decreased gradually from 35.5 to 31.5, the Q_f value increased from 37,800 to 58,300 GHz, and TCF value shifted slightly from −4.5 to −33.0 ppm °C⁻¹. Both the phase structure and microwave dielectric properties of (Zr_1−xSn_x)(Li_1/4Nb_3/4)_0.4Ti_0.6O₄ ceramics were stable with annealing conditions.     

Crystal structure and microwave dielectric properties of (1 − x)NdAlO3-xCaTiO3 ceramics

Crystal structure and microwave dielectric properties of (1−x)NdAlO₃-xCaTiO₃ ceramics have been investigated. Crystal structure of the specimens changed with the composition. Rhombohedral structure was found for the specimens with x≤0.1. When 0.3≤x≤0.7, the specimens had the tetragonal structure and it changed to the orthorhombic structure as x exceeded 0.7. Two types of the second phases were observed in (1−x)NdAlO₃-xCaTiO₃ ceramics. For the specimens with x≤0.5, Nd₄Al₂O₉ phase was observed and Al-rich phase was found in the specimens with x≥0.7. The dielectric constant (ε_r) and the temperature coefficient of the resonant frequency (τ_f) increased with the increase of x. The Q×f value of the specimen increased with x and exhibited the maximum value when x=0.5. The microwave dielectric properties of Q×f=45,000 GHz, ε_r=45 and τ_f=−1.5 ppm/°C were obtained for 0.3NdAlO₃-0.7CaTiO₃ ceramics.     

Structure and electrical properties of (1 − x)Bi0.5Na0.5TiO3-xBi0.5K0.5TiO3 ceramics near morphotropic phase boundary

The binary lead-free piezoelectric ceramics with the composition of (1 − x)Bi_0.5Na_0.5TiO₃-xBi_0.5K_0.5TiO₃ were synthesized by conventional mixed-oxide method. The phase structure transformed from rhombohedral to tetragonal phase in the range of 0.16 ≤ x ≤ 0.20. The grain sizes varied with increasing the Bi_0.5K_0.5TiO₃ content. Electrical properties of ceramics are significantly influenced by the Bi_0.5K_0.5TiO₃ content. Two phase transitions at T_t (the temperature at which the phase transition from rhombohedral to tetragonal occurs) and T_c (the Curie temperature) were observed in all the ceramics. Adding Bi_0.5K_0.5TiO₃ content caused the variations of T_t and T_c. A diffuse character was proved by the linear fitting of the modified Curie-Weiss law. Besides, the ceramics with homogeneous microstructure and excellent electrical properties were obtained at x = 0.18 and sintered at 1170 °C. The piezoelectric constant d₃₃, the electromechanical coupling factor K_p and the dielectric constant ?_r reached 144 pC/N, 0.29 and 893, respectively. The dissipation factor tan δ was 0.037.     

Structure and microwave dielectric characteristics of lithium-excess Ca0.6Nd0.8/3TiO3/(Li0.5Nd0.5)TiO3 ceramics

Compositions based on (1−x)Ca_0.6Nd_8/3TiO₃−x(Li_1/2Nd_1/2)TiO₃ + yLi (CNLNTx + yLi, x = 0.30–0.60, y = 0–0.05), suitable for microwave applications have been developed by systematically adding excess lithium in order to tune the microwave dielectric properties and lower sintering temperature. Addition of 0.03 excess-Li simultaneously reduced the sintering temperature and improved the relative density of sintered CNLNTx ceramics. The excess Li addition can compensate the evaporation of Li during sintering process and decrease the secondary phase content. The CNLNTx (x = 0.45) ceramics with 0.03 Li excess sintered at 1190 °C have single phase orthorhombic perovskite structure, together with the optimum combination of microwave dielectric properties of ɛ_r = 129, Q × f = 3600 GHz, τ_f = 38 ppm/°C. Obviously, excess-Li addition can efficiently decrease the sintering temperature and improve the microwave dielectric properties. The high permittivity and relatively low sintering temperatures of lithium-excess Ca_0.6Nd_0.8/3TiO₃/(Li_0.5Nd_0.5)TiO₃ ceramics are ideal for the development of low cost ultra-small dielectric loaded antenna.     

Low-temperature sintering and microwave dielectric properties of 5Li2O–0.58Nb2O5–3.23TiO2 ceramics

The effect of B₂O₃ addition on the sintering, microstructure and the microwave dielectric properties of the 5Li₂O–0.58Nb₂O₅–3.23TiO₂ (LNT) ceramics have been investigated. It is found that the LNT ceramics could be sintered well at ∼880 °C with low-level doping of B₂O₃ (≤2 wt.%). Only Li₂TiO₃ solid solution (Li₂TiO₃ss) crystal structure could be detected for all the ceramics with various amounts of B₂O₃ addition from the X-ray diffraction (XRD) results. And interestingly, two phases with different color in SEM images are observed in B₂O₃-doped LNT ceramics. EDS results suggest that the two different phases are two Li₂TiO₃ss phases with different amount of Nb. In addition, there is no much degradation in the microwave dielectric properties with the B₂O₃ adding. In the case of 0.5 wt.% B₂O₃-doped samples sintered at 880 °C, good microwave dielectric properties of ?_r = 22, Q × f = 32,000 GHz, τ_f = 9.5 ppm °C⁻¹ are obtained.