Temperature-stable and low loss Fe-containing dielectrics in BaO-Ln<Subscript>2</Subscript>O<Subscript>3</Subscript>-Fe<Subscript>2</Subscript>O<Subscript>3</Subscript>-Ta<Subscript>2</Subscript>O<Subscript>5</Subscript> system

Polycrystalline samples of Ba₄Ln₂Fe₂Ta₈O₃₀ (Ln = La and Nd) were prepared by a high temperature solid-state reaction technique. The formation, structure, dielectric and ferroelectric properties of the compounds were studied. Both compounds are found to be paraelectrics with filled tetragonal tungsten bronze (TB) structure at room temperature. Dielectric measurements revealed that the present ceramics have exceptional temperature stability, a relatively small temperature coefficient of dielectric constant (τ _ε ) of −25 and −58 ppm/°C, with a high dielectric constant of 118 and 96 together with a low dielectric loss of 1.2 × 10⁻³ and 2.8 × 10⁻³ (at 1 MHz) for Ba₄La₂Fe₂Ta₈O₃₀ and Ba₄Nd₂Fe₂Ta₈O₃₀, respectively. The measured dielectric properties indicate that both materials are possible candidates for the fabrication of discrete multilayer capacitors in microelectronic technology.     

Electrical conductivity of Bi<Subscript>2</Subscript>O<Subscript>3</Subscript>-Tm<Subscript>2</Subscript>O<Subscript>3</Subscript>-Nb<Subscript>2</Subscript>O<Subscript>5</Subscript> solid solutions

New solid solutions, Bi_2?x?y Tm _x Nb _y O_3+δ, with tetragonal and cubic structures have been synthesized in the Bi₂O₃-Tm₂O₃-Nb₂O₅ system, and their electrical conductivity has been measured at temperatures from 670 to 1020 K. The 1020-K conductivity of the tetragonal solid solution Bi_1.8Tm_0.15Nb_0.05O_3+δ is comparable to that of Bi_1.75Tm_0.25O₃, the best conductor in the Bi₂O₃-Tm₂O₃ system.     

Phase equilibria in the La<Subscript>2</Subscript>O<Subscript>3</Subscript>-Nb<Subscript>2</Subscript>O<Subscript>5</Subscript>-Nb system and thermal stability of LaNb<Subscript>7</Subscript>O<Subscript>12</Subscript>

The phase equilibria in the ternary system La₂O₃-Nb₂O₅-Nb have been studied at subsolidus temperatures in vacuum (6.65 × 10^?3 Pa), and the temperature stability limits of LaNb₇O₁₂ have been determined in vacuum and during heating in air.     

Enhancement in electrical conductivity of Li<Subscript>2</Subscript>O: B<Subscript>2</Subscript>O<Subscript>3</Subscript>: V<Subscript>2</Subscript>O<Subscript>5</Subscript> glasses

The study of electrical conductivity of 30Li₂O: (70 − x) B₂O₃: xV₂O₅ glass samples has been carried out. The results have been explained by dividing the temperature range into two regions. In region I, conductivity shows Arrhenius behaviour for all the samples. The conductivity increases with addition of V₂O₅. The results have been explained in the light of Anderson and Stuart Model. In region II, an anomalous enhancement in the conductivity is observed for all the samples up to certain temperature beyond which the conductivity decreases. The enhancement in the conductivity in the annealed glass sample has been attributed to nanocrystallization.     

Crystallization from high-temperature solutions in the K<Subscript>2</Subscript>O-P<Subscript>2</Subscript>O<Subscript>5</Subscript>-V<Subscript>2</Subscript>O<Subscript>5</Subscript>-Bi<Subscript>2</Subscript>O<Subscript>3</Subscript> system

We have studied general trends of crystallization from high-temperature solutions in the K₂O-P₂O₅-V₂O₅-Bi₂O₃ system at P/V = 0.5?2.0, K/(P + V) = 0.7?1.4, and Bi₂O₃ contents from 25 to 50 wt % and identified the stability regions of BiPO₄, K₃Bi₅(PO₄)₆, K₂Bi₃O(PO₄)₃, and K₃Bi₂(PO₄)_{3 ? x} (VO₄) _x (x = 0?3) solid solutions. The synthesized compounds have been characterized by X-ray powder diffraction and IR spectroscopy, and the structure of two solid solutions has been determined by single-crystal X-ray diffraction (sp. gr. C ₂/c): K₃Bi₂(PO₄)₂(VO₄), a = 13.8857(8), b = 13.5432(5), c = 6.8679(4) Å, β = 114.031(7)°; K₃Bi₂(PO₄)_1.25(VO₄)_1.75, a = 13.907(4), b = 13.615(2), c = 6.956(2) Å, β = 113.52(4)°.     

Low-firing Li<Subscript>2</Subscript>ZnTi<Subscript>3</Subscript>O<Subscript>8</Subscript> microwave dielectric ceramics with BaCu(B<Subscript>2</Subscript>O<Subscript>5</Subscript>) additive

Phase purity, microstructure, sinterability and microwave dielectric properties of BaCu(B₂O₅)-added Li₂ZnTi₃O₈ ceramics and their cofireability with Ag electrode were investigated. A small amount of BaCu (B₂O₅) can effectively reduce the sintering temperature from 1075°C to 925°C, and it does not induce much degradation of the microwave dielectric properties. Microwave dielectric properties of ε _r = 23·1, Q × f = 22,732 GHz and τ _f = − 17·6 ppm/°C were obtained for Li₂ZnTi₃O₈ ceramic with 1·5 wt% BaCu(B₂O₅) sintered at 925°C for 4 h. The Li₂ZnTi₃O₈ +BCB ceramics can be compatible with Ag electrode, which makes it a promising microwave dielectric material for low-temperature co-fired ceramic technology application.     

Reactions of V<Subscript>2</Subscript>O<Subscript>5</Subscript>, Nb<Subscript>2</Subscript>O<Subscript>5</Subscript>, and Ta<Subscript>2</Subscript>O<Subscript>5</Subscript> with AlN

Reactions of vanadium, niobium, and tantalum pentoxides with aluminum nitride have been studied using X-ray diffraction. At temperatures from 1000 to 1600°C, we have identified various V, Nb, and Ta nitrides. The composition of the niobium and tantalum nitrides depends on the reaction temperature. The tendency toward nitride formation becomes stronger in the order V₂O₅ < Ta₂O₅ < Nb₂O₅.     

Subsolidus phase relations in the system Tm<Subscript>2</Subscript>O<Subscript>3</Subscript>-Rh<Subscript>2</Subscript>O<Subscript>3</Subscript>

The Tm₂O₃-Rh₂O₃ system has been studied by x-ray diffraction, thermal analysis, and chemical analysis of annealed and quenched samples. The results have been used to construct a schematic subsolidus phase diagram of the system. Only one double oxide, TmRhO₃, has been identified. Some of its physicochemical properties are reported.     

Calcium bismuth borates in the CaO-Bi<Subscript>2</Subscript>O<Subscript>3</Subscript>-B<Subscript>2</Subscript>O<Subscript>3</Subscript> system

The 600°C (subsolidus) section of the CaO-Bi₂O₃-B₂O₃ phase diagram has been studied by x-ray diffraction and differential thermal analysis. A new calcium bismuth borate of composition CaBi₂B₄O₁₀ has been identified, and the existence of CaBi₂B₂O₇ has been confirmed. According to T-x phase diagram data, these compounds form peritectically at 700±5 and 783±5°C, respectively.     

Electrochemical properties of Li<Subscript>4</Subscript>Ti<Subscript>5</Subscript>O<Subscript>12</Subscript>/C and Li<Subscript>4</Subscript>Ti<Subscript>5</Subscript>O<Subscript>12</Subscript>/C/Ag nanomaterials

We have prepared and characterized lithium titanate-based anode materials, Li₄Ti₅O₁₂/C and Li₄Ti₅O₁₂/C/Ag, using polyvinylidene fluoride as a carbon source. The formation of such materials has been shown to be accompanied by fluorination of the lithium titanate surface and the formation of a highly conductive carbon coating. The highest electrochemical capacity (175 mAh/g at a current density of 20 mA/g) is offered by the Li₄Ti₅O₁₂-based anode materials prepared using 5% polyvinylidene fluoride. The addition of silver nanoparticles ensures a further increase in electrical conductivity and better cycling stability of the materials at high current densities.     

Glass formation in the Bi<Subscript>2</Subscript>O<Subscript>3</Subscript>-B<Subscript>2</Subscript>O<Subscript>3</Subscript>-BaO system

The physicochemical properties of BaO-Bi₂O₃-B₂O₃ glasses have been studied. The effect of KBF₄ additions on the properties of the glasses has been examined. The transmission of the glasses has been correlated with their local structure and composition.     

Electrical properties of perovskite-like compounds in the Bi<Subscript>2</Subscript>O<Subscript>3</Subscript>-Fe<Subscript>2</Subscript>O<Subscript>3</Subscript>-TiO<Subscript>2</Subscript> system

The electrical properties of layered perovskite-like compounds with the general formula Bi _{m + 1}Fe _{m − 3}Ti₃O_{3m + 3} have been studied in relation to their physicochemical properties and structure.     

Investigation on the stability of Li<Subscript>5</Subscript>La<Subscript>3</Subscript>Ta<Subscript>2</Subscript>O<Subscript>12</Subscript> lithium ionic conductors in humid environment

In this paper, the stability in humid air of Li₅La₃Ta₂O₁₂ lithium ionic conductors synthesized by conventional solid-state reaction was investigated by internal friction, conductivity, weight variation, X-ray diffraction, and thermogravimetric analysis methods. It was found that when the Li₅La₃Ta₂O₁₂ samples were aged in open air at room temperature, the internal friction peaks associated with the short-distance diffusion of lithium vacancies gradually shift toward higher temperature and increase in height, while the weight of the sample increases and impurity phases of LiOH·H₂O appear. These results reveal that the Li₅La₃Ta₂O₁₂ compounds are unstable against moisture in open air at room temperature. It was suggested that the protons from the moisture substitute the lithium ions in Li₅La₃Ta₂O₁₂ samples to form Li₂O and new protonic derivatives, Li_5?x La₃Ta₂O_12?x (OH) _x (0<x<2.15), and the resultant Li₂O may react further with water to form LiOH·H₂O.     

Synthesis of anisometric KSr<Subscript>2</Subscript>Nb<Subscript>5</Subscript>O<Subscript>15</Subscript> particles in the SrNb<Subscript>2</Subscript>O<Subscript>6</Subscript>–Nb<Subscript>2</Subscript>O<Subscript>5</Subscript>–KCl system

Anisometric and agglomerate-free template particles are important for fabrication of grain-oriented ceramics. In the present work, preparation of acicular KSr₂Nb₅O₁₅ (KSN) particles was firstly explored in the SrNb₂O₆–Nb₂O₅–KCl system by molten salt synthesis (MSS) method. It was found that the molar ratio of SrNb₂O₆ to Nb₂O₅, the amount of KCl salt and synthesis time could significantly affect the phase structure and morphology of KSN particles. When calcined at 1,150 °C for 6 h with the molar ratio of SrNb₂O₆ to Nb₂O₅ was 1 and the weight ratio of salt to oxide source was 1.50, pure KSN particles with well-developed acicular morphology were successfully obtained in this system. They were agglomerate-free and with proper scale in the size range of 5–30 μm, which made them the ideal templates for fabricating textured ceramics. In addition, some new reaction and growth mechanisms were proposed in this work.     

Nano-domain structure of Li<Subscript>4</Subscript>Mn<Subscript>5</Subscript>O<Subscript>12</Subscript> spinel

XRD-pure Li₄Mn₅O₁₂ spinels are obtained below 600 °C from oxalate and acetate precursors. The morphology consists of nanometric particles (about 25 nm) with a narrow particle size distribution. HRTEM and electron paramagnetic resonance (EPR) spectroscopy of Mn⁴⁺ are employed for local structure analysis. The HRTEM images recorded on nano-domains in Li₄Mn₅O₁₂ reveal its complex structure. HRTEM shows one-dimensional structure images, which are compatible with the (111) plane of the cubic spinel structure and the (001) plane of monoclinic Li₂MnO₃. For Li₄Mn₅O₁₂ compositions annealed between 400 and 800 °C, EPR spectroscopy shows the appearance of two types of Mn⁴⁺ ions having different metal environments: (i) Mn⁴⁺ ions surrounded by Li⁺ and Mn⁴⁺ and (ii) Mn⁴⁺ ions in Mn⁴⁺-rich environment. The composition of the Li⁺, Mn⁴⁺-shell around Mn⁴⁺ mimics the local environment of Mn⁴⁺ in monoclinic Li₂MnO₃, while the Mn⁴⁺-rich environment is related with that of the spinel phase. The structure of XRD-pure Li₄Mn₅O₁₂ comprises nano-domains with a Li₂MnO₃-like and a Li_4/3−x Mn_5/3+x O₄ composition rather than a single spinel phase with Li in tetrahedral and Li_1/3Mn_5/3 in octahedral spinel sites. The annealing of Li₄Mn₅O₁₂ at temperature higher than 600 °C leads to its decomposition into monoclinic Li₂MnO₃ and spinel Li_4/3−x Mn_5/3+x O₄.     

Effect of Eu<Subscript>2</Subscript>O<Subscript>3</Subscript> doping on the crystallization behavior of BaO-Bi<Subscript>2</Subscript>O<Subscript>3</Subscript>-B<Subscript>2</Subscript>O<Subscript>3</Subscript> glasses

We gave studied the crystallization behavior of 30BaO · 25Bi₂O₃ · 45B₂O₃ glasses doped with Eu₂O₃ to different levels. At a Eu₂O₃ content of 7 mol % or higher, the glasses undergo volume crystallization. The only precipitating phase is a solid solution between europium and bismuth oxides. With increasing europium concentration in the glass, the structure of the crystallites changes from cubic to rhombohedral. We have investigated the morphology, physicochemical properties, and luminescence spectra of the glasses and glass-ceramics.     

Chemical reactions in the Mo-W-Al<Subscript>2</Subscript>O<Subscript>3</Subscript> system at 2400 K and 100 Pa

We examine the behavior of the Mo-W-Al₂O₃ system at T = 2400 K and p = 100 Pa and identify the main chemical reactions that lead to the oxidation of Mo and W. The results indicate that, under these thermodynamic conditions, direct reaction between Mo, W, and molten Al₂O₃ is impossible, and oxidation processes are indirect and involve vapor species. For a Mo: W: Al₂O₃ molar ratio of 1: 1: 1, we calculate the gas-phase composition and demonstrate that the predominant vapor species are Al, AlO, Al₂O, MoO, MoO₂, and WO₃.     

Preparation of magnetic composites through SrO-Fe<Subscript>2</Subscript>O<Subscript>3</Subscript>-Al<Subscript>2</Subscript>O<Subscript>3</Subscript>-B<Subscript>2</Subscript>O<Subscript>3</Subscript> glass crystallization

Glasses with nominal compositions 11SrO · 5.5Fe₂O₃ · 4.5Al₂O₃ · 4B₂O₃ (1) and 15SrO · 5.5Fe₂O₃ · 4.5Al₂O₃ · 4B₂O₃ (2) were prepared by rapidly quenching oxide melts between counterrotating steel rollers. The glasses were then heat-treated in the range 650–950°C to produce glass-ceramic samples. The samples were characterized by X-ray diffraction, electron microscopy, and magnetic measurements. The phase composition of the glass-ceramics was determined, and their microstructure and magnetic properties were studied. The annealing temperature was shown to have a strong effect on the coercivity of the materials, which reaches 650 and 570 kA/m for compositions 1 and 2, respectively.     

Subsolidus Phase Relations in the System Dy<Subscript>2</Subscript>O<Subscript>3</Subscript>-Rh<Subscript>2</Subscript>O<Subscript>3</Subscript>

The Dy₂O₃-Rh₂O₃ system is studied by thermal analysis, x-ray diffraction, and chemical analysis of annealed and quenched samples. The results are used to construct a schematic subsolidus phase diagram of the system. Only one double oxide, DyRhO₃, is obtained. Some of its physicochemical properties are reported.__________Translated from Neorganicheskie Materialy, Vol. 41, No. 8, 2005, pp. 960–965.Original Russian Text Copyright © 2005 by Skrobot, Ugolkov, Grebenshchikov, Gusarov.