Article

Properties of the Sr 3 MoO 6 electroceramic for RF/microwave devices

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Abstract

The Sr3MoO6 (SMO) double perovskite has been studied due to its photoluminescence properties. Herein, the aim of this work is to study the dielectric properties of the SMO in radiofrequency (RF). From impedance spectra, we proposed an equivalent circuit using three associations of R-CPE in parallel. We also evaluated its performance as a microwave device (dielectric resonator antenna - DRA). The SMO-based DRA operated at 3.71 GHz (frequency of operation antenna), with reasonable gain (5.00 dBi) and directivity (5.70 dBi), where these values are close to the ones presented by commercial antennas. Additionally, a numerical simulation is performed to obtain the main parameters for proper device application. Based on our results, SMO electroceramic shows important properties, which can be used for devices operating in the S-band such as weather radar, surface ship radar and communications satellites.

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... For example, the decrease in R values due to the temperature rise is associated with the increase of conductivity. These results confirmed that the profile found in the arcs reduced diameters with the temperature rise [9]. Furthermore, all samples presented a decrease in n values with temperature increasing, indicating a resistive behavior contribution for CPE elements. ...
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... It is important that the reflection coefficient (S 11 ) of the DRA is below −10 dB in order to operate efficiently as an antenna, with less return loss [28]. As shown in Fig. 6a, all of the DRAs had good S 11 values, which were below −40 dB. ...
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We report multiferroic behavior in double perovskite Y2CoMnO6 with ferroelectric transition temperature Tc = 80K. The origin of ferroelectricity is associated with magnetic ordering of Co2+ and Mn4+ moments in a up-up-down-down arrangement. The saturation polarization and magnetization are estimated to be 65 uC/m2 and 6.2 Bohr magneton/f.u. respectively. The magnetoelectric coupling parameter, on the other hand, is small as a 5 Tesla field suppresses the electric polarization by only ~8%. This is corroborated with observed hysteretic behaviour at 5K that remains unsaturated even upto 7 Tesla. A model based on exchange-striction is proposed to explain the observed high temperature ferroelectricity.
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In this paper is reported an experimental and numerical investigation of the microwave dielectric properties of BiFeO3 (BFO) ceramic matrix added with 3 and 10 wt% of Bi2O3 or PbO, obtained through a new procedure based on the solid-state method. The experimental and theoretical characteristics of the resonator like return loss, bandwidth, input impedance are in good agreement. The simulations of radiation patterns are presented. For BFO reference sample, frequency response bandwidth is of 6.40% (simulated) and 7.18% (experimental) for frequency operation around 2.94 GHz. The BFO reference sample showed a dielectric permittivity around 25, with loss around 10(-2). The adding of bismuth oxide (3 and 10 wt%) reduced the value of the dielectric permittivity as well as lead oxide 3 wt%, otherwise only the adding of 10 wt% increases its value. The temperature coefficient of resonant frequency (tau(f)) was also measured for all dielectric samples. The values obtained were in the range of -517 ppm degrees C-1 to -222 ppm degrees C-1. With the addition of lead oxide was observed a deterioration of the thermal stability of the ceramic, with respect to the central frequency of resonance. The results obtained confirm the necessity of producing composites of this material with others positive tau(f) materials for obtaining dielectric resonator antennas with tau(f) similar to 0.
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Potentiodynamic electrochemical impedance spectroscopy (PDEIS) employs virtual instruments for probing the interface and gives, in real time and in a single potential scan, the multidimensional spectra that characterise complex impedance of the interface as a function of frequency and the electrode potential, along with the potentiodynamic voltammogram. The built-in equivalent electric circuit analyser provides semi-automatic extraction of the potential dependencies of the double layer capacitance, components of Faraday impedance (charge transfer resistance and Warburg impedance) and some additional impedance elements from the impedance spectra extended for the variable potential. PDEIS has been applied to probe the electrochemical response of metal monolayers and nanostructures on various supports.
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In this work, barium zirconate (BaZrO3) ceramics synthesized by solid state reaction method and sintered at 1670 8C for 4 h were characterized by X-ray diffraction (XRD), Rietveld refinement, and Fourier transform infrared (FT-IR) spectroscopy. XRD patterns, Rietveld refinement data and FT-IR spectra which confirmed that BaZrO3 ceramics have a perovskite-type cubic structure. Optical properties were investigated by ultraviolet– visible (UV–vis) absorption and photoluminescence (PL) measurements. UV–vis absorption spectra suggested an indirect allowed transition with the existence of intermediary energy levels within the band gap. Intense visible green PL emission was observed in BaZrO3 ceramics upon excitation with a 350 nm wavelength. This behavior is due to a majority of deep defects within the band gap caused by symmetry breaking in octahedral [ZrO6] clusters in the lattice. The microwave dielectric constant and quality factor were measured using the method proposed by Hakki– Coleman. The dielectric resonator antenna (DRA) was investigated experimentally and numerically using a monopole antenna through an infinite ground plane and Ansoft’s high frequency structure simulator software, respectively. The required resonance frequency and bandwidth of DRA were investigated by adjusting the dimension of the same material.
Article
Layered oxides, A2B'B"O6, with small ions at A-site mostly occupied by unusual-metals like transitional metals are of great importance due to their strong and unusual magnetic interactions and technical applications. Due to small tolerance factors it is very difficult to synthesize such materials in ambient pressure and temperature. Depending upon the variation in temperature and pressure, same composition of the above mentioned materials can be crystallized with different structural arrangements. The effect of pressure and synthetic condition of different materials has been described in this review. The literature data on the effects of the A-site occupation by small ions on the structure and properties are summarized. Finally structural changes and dissimilar properties of high temperature and pressure synthesized recent developed materials are compared with the materials with usual B-site ordered double perovskite.
Article
We investigate the dependence of magnetic properties on the B-site cation ordering for a series of (Sr0.5Ba0.5)2FeSbO6 double-perovskite samples for which the Fe/Sb long-range ordering ranges from nearly nonexisting to essentially complete. Also the size of crystallographically ordered domains varies among the samples. All the samples are antiferromagnetic at low temperatures independent of the level of ordering, indicating multiple co-existing exchange and/or superexchange interactions. Nevertheless, a clear trend is seen for the Néel temperature and the effective magnetic moment both increasing with increasing degree of order and the size of the ordered domains.
Article
Eu³⁺-activated BaLaMgNbO6 red-emitting phosphors were synthesized by a high-temperature solid-state reaction method. Phase analysis and luminescence were characterized by X-ray diffraction (XRD) and photoluminescence excitation and emission spectra. The XRD patterns showed that BaLaMgNbO6 had a monoclinic structure with space group P21/n. The excitation spectra consisted of a broad charge-transfer band and some sharp f-f absorption peaks characteristic of Eu³⁺. The intensity ratio of I615/I590 was used to detect the chemical environment of Eu³⁺. The chromaticity coordinates of BaLa0.7Eu0.3MgNbO6 were (0.67, 0.33), indicating that the BaLaMgNbO6:Eu³⁺ phosphors were excellent red-emitting phosphors. Under excitation by near-ultraviolet (UV) and blue light, the phosphor not only exhibited intense red emission but also showed high color quality. The Ozawa and Dexter energy-transfer theories were employed to calculate the theoretical quenching concentration and determine the concentration quenching mechanism. In addition, the activation energy of BaLa0.7Eu0.3MgNbO6 was calculated through the Arrhenius equation. A configurational coordinate diagram was used to explain the thermal quenching mechanism.
Article
A BiCu2PO6 microwave dielectric ceramic was prepared using a solid-state reaction method. As the sintering temperature increased from 800°C to 880°C, the bulk density of BiCu2PO6 ceramic increased from 6.299 g/cm³ to 6.366 g/cm³; the optimal temperature was 860°C. The best microwave dielectric properties [permittivity (ɛr) = ∼16, a quality factor (Q × f) = ∼39,110 GHz and a temperature coefficient of resonant frequency (τf) = ∼−59 ppm/°C] were obtained in the ceramic sintered at 860°C for 2 h. Then, TiO2 with a positive τf (∼+400 ppm/°C) was added to compensate the τf value. The composite material was found to have a near-zero τf (+2.7 ppm/°C) and desirable microwave properties (ɛr = 19.9, Q × f = 24,885 GHz) when synthesized at a sintering temperature of 880°C. This system could potentially be used for low-temperature co-fired ceramics technology applications.
Article
Novel members of the R2NiRuO6 family of double perovskites have been prepared via a nitrate-citrate route, followed by annealing treatments in air in the 1100-1300 °C temperature range. The crystal and magnetic structures were characterized from neutron powder diffraction (NPD) data at 300 K and 2 K. All the samples are monoclinic, P21/n space group, with a √2a0×√2a0×2a0 unit-cell, compared to the simple perovskite a0 edge. Ni²⁺ and Ru⁴⁺ ions occupy distinct octahedral positions, with a certain antisite disordering. The magnetic structures are defined by the propagation vector k = 0. The magnetic moments of the Ni²⁺ cations are antiparallel to the spins of the Ru⁴⁺ sublattice; the structure can be described as ferromagnetic [011] layers antiferromagnetically (AFM) coupled to each other. For R = Ho and Er perovskites, the rare-earth moments participate in the magnetic structure: Ho³⁺ cations are ordered along the direction (010) in alternate planes AFM coupled and the magnetic moments of Er³⁺ are ferromagnetically ordered along the c axis.
Article
Environmental friendly, non-toxic double perovskite Sr 2 TiMoO 6 (STM) ceramics were synthesized using solid-state reaction route for high temperature thermoelectric applications. XRD and SEM studies confirmed the presence of single-phase solid solution with highly dense microstructure, which were achieved by optimizing sintering temperature and atmosphere. Effect of sintering atmosphere on the structure of STM samples was studied. Rietveld refinement of XRD data confirmed cubic structure of this double perovskite with space-group Pm3m. Temperature dependent thermoelectric measurement showed that STM ceramics converted from p-type into n-type behavior around 550 K. Conductivity mechanism of this double perovskite was further explained by small polaron hopping model.
Article
The effect of calcium on the properties of SmBa1–xCaxCoCuO5+δ (x = 0.0–0.3) as a cathode material for intermediate-temperature solid oxide fuel cells (IT-SOFCs) is evaluated systematically. Samples exhibit a highly crystalline double perovskite phase, and their cell volumes decrease as x is changed from 0.0 to 0.3. The oxygen content and average thermal expansion coefficient (TEC) of SmBa1–xCaxCoCuO5+δ decreases as the calcium content increased. An average TEC of as low as 15.3 × 10⁻⁶ °C⁻¹ is obtained for SmBa0.7Ca0.3CoCuO5+δ. The area specific resistances at 700 °C decrease by approximately 50% when the calcium content is increased from x = 0.0 (0.173 Ω cm²) to x = 0.3 (0.086 Ω cm²). The maximum power densities of SmBa1−xCaxCoCuO5+δ-based single cells at 800 °C increase from 635 mW cm⁻² (x = 0.0) to 939 mW cm⁻² (x = 0.3).
Article
Two microwave dielectric ceramics ReVO4 (Re = Nd, Sm) prepared through a conventional solid-state reaction method were investigated. X-ray diffraction (XRD) and scanning electron microscopy (SEM) analysis revealed that pure and dense NdVO4 and SmVO4 ceramics with tetragonal structure could be obtained when sintered in the temperature range 1100°C-1180°C for 4 h. The samples sintered at 1160°C exhibited the best densification with relative densities larger than 96%. NdVO4 ceramic exhibited promising microwave dielectric properties with a relative permittivity (εr) of 12.0, a quality factor (Q × f) of 36,440 GHz, and a negative temperature coefficient of resonance frequency (τf) of −44.3 ppm/°C. SmVO4 had a εr ∼ 11.7, a Q × f ∼ 38,620 GHz and a τf ∼ −48.4 ppm/°C.
Article
Double perovskite R2NiMnO6 (R=Pr, Nd, Tb, Ho and Y) composites are prepared via solid state synthesis or nitrate route. Isothermal magnetic entropy change ( ) and relative cooling power (RCP) for all systems are calculated and compared. All of them possess relatively high values of and RCP as compared to many perovskite and double perovskite systems reported previously. Ho2NiMnO6 has the highest value for and RCP as 8.4 at 70 kOe and 59.18 JKg⁻¹ at 20 kOe respectively. This study highlights the potential of magnetocaloric refrigerant materials at low temperature.
Article
LiLaMgWO6:Eu³⁺ phosphors have been synthesized by high-temperature solid-state reaction and their structure, ultraviolet-visible diffuse reflectance spectra, photoluminescence and decay properties have been investigated as a function of the Eu³⁺ concentration. The XRD results indicated that all the prepared phosphors can be assigned to a monoclinic double perovskite structure in space group C2/m. LiLaMgWO6:Eu³⁺ phosphor has exhibited excellent red emission and efficient excitation, consisting of a broad band ranging from 250 to 350 nm as well as several narrow excitation peaks between 450 and 580 nm. The presence of dominant red emission band centered at 615 nm suggested that Eu³⁺ enters in the lattice site without inversion symmetry. The quenching concentration of Eu³⁺ is up to 30 mol%. The theoretical quenching concentration and quenching mechanism were discussed herein. Moreover, the thermal quenching, CIE chromaticity coordinates, quantum yield, Judd-Ofelt analysis and energy transfer mechanism are discussed in detail.
Article
There is a growing global interest for the development of green technologies that allow the use of products with less damage to environment, as well as for maximum and sustainable use of natural resources. The main aim of this study was to develop superparamagnetic nano-biocomposites for application as dielectric resonator antennas, from a combination of a cardanol-based thermoset plastic, chemically modified sponge gourd fibers (NaOH 10% and NaClO 1 wt%), and magnetite nanoparticles in different contents (1, 5, and 10 wt%). The magnetite particles exhibited nanometric size, high purity and crystallinity, and superparamagnetic character. All nano-biocomposites showed superparamagnetic behavior, excellent thermal stability, good biodegradation rates, and better mechanical strength for the material with magnetite 10 wt%. All dielectric resonator antennas showed satisfactory return loss and suitability for technological applications, especially for performance in broadband.
Article
Double perovskite related oxides A2ZnTiO6 (A = Pr, Gd) have been successfully synthesized by solid state reaction and investigated as photocatalysts for the first time. The two layered titanates mainly demonstrate absorbances under UV irradiation, except for several sharp absorption bands above 400 nm for Pr2ZnTiO6. Therefore, a series of photocatalysts by doping A2ZnTiO6 (A = Pr, Gd) with Cr have been developed in the hope to improve their absorption in the visible light region. The successful incorporation of Cr was detected by XRD and XPS, and the prepared samples have also been characteriazed by SEM, UV–vis DRS and PL. The characterization results suggested that Cr was present mainly in the form of Cr3+, with only a small amount of Cr6+ species. It served as an efficient dopant for the extension of visible light absorbance and improved photocatalytic activities under solar light irradiation. For both Pr2ZnTiO6 and Gd2ZnTiO6, the valence band (VB) was composed of hybridized states of the Zn 3d, O 2p and the conduction band (CB) has major contribution from Zn 4s, Ti 3d orbitals. For Cr doped samples, the newly formed spin-polarized valence band in the middle of the band gap that primarily arise from Cr 3d orbitals was responsible for the improved optical and photocatalytic properties.
Article
A new glass free low temperature sinterable CuMoO4 ceramic was prepared by solid state ceramic route. The structural, microstructural, electron dispersive spectrum and X-ray photoelectron spectroscopy analysis revealed the quality of the material synthesized. The CuMoO4 ceramic sintered at 650 oC exhibits densification of 96 % and low coefficient of thermal expansion (CTE) of 4.6 ppm/oC in the temperature range of 25-500 oC. It has relative permittivity (εr) of 7.9, quality factor (Qf) of 53000 GHz and temperature coefficient of resonant frequency (τf) of -36 ppm/oC (25-85 oC) at 12.7 GHz. The sintered ceramic also shows εr of 11 and low dielectric loss (tanδ) of 2.7 ×10-4 at a frequency of 1 MHz. The full width half maximum (FWHM) of A1g Raman mode of CuMoO4 ceramic at different sintering temperatures correlate well with the Qf values. The low sintering temperature, low relative permittivity, high-quality factor and matching coefficient of thermal expansion to that of Si make CuMoO4 a suitable candidate for ultra-low temperature cofired ceramic (ULTCC) applications.
Article
Polycrystalline Pr2CuTiO6 (PCT) ceramics exhibits dielectric, impedance and modulus characteristics as a possible material for microelectronic devices. PCT was synthesized through the standard solid-state reaction method. The dielectric permittivity, impedance and electric modulus of PCT have been studied in a wide frequency (100 Hz–1 MHz) and temperature (303–593 K) range. Structural analysis of the compound revealed a monoclinic phase at room temperature. Complex impedance Cole–Cole plots are used to interpret the relaxation mechanism, and grain boundary contributions towards conductivity have been estimated. From electrical modulus formalism polarization and conductivity relaxation behavior in PCT have been discussed. Normalization of the imaginary part of impedance (Z″) and the normalized imaginary part of modulus (M″) indicates contributions from both long-range and localized relaxation effects. The grain boundary resistance along with their relaxation frequencies are plotted in the form of an Arrhenius plot with activation energy 0.45 eV and 0.46 eV, respectively. The ac conductivity mechanism has been discussed.
Article
This work reports the dielectric properties of Sr3WO6 (SWO) double perovskite at radio frequencies as a function of the temperature and a study in microwaves range to evaluate the material as a novel dielectric resonator. Thermo-activated charge transfer process for SWO ceramic was observed and two resistor–capacitor associations were fitted for the Nyquist diagram. SWO presented negative values of temperature coefficient of capacitance (TCC) and the activation energies of dielectric relaxation processes were measured by conductivity (1.35 eV), imaginary modulus (1.38 eV) and imaginary impedance (1.36 eV). For the microwave range, SWO shows high dielectric permittivity (13.57) and dielectric loss (0.0281). The dielectric resonator antenna (DRA) fabricated from SWO ceramic presented an operation frequency in 4.1 GHz and return loss below −40 dB. It was possible to evaluate the performance of the antenna from numerical simulation. From these results, the SWO based DRA shows good properties to be used as a novel microwave dielectric resonator.
Article
Despite the remarkable rise in efficiencies of solar cells containing the lead-halide perovskite absorbers RPbX3 (R = organic cation; X = Br(-) or I(-)), the toxicity of lead remains a concern for the large-scale implementation of this technology. This has spurred the search for lead-free materials with similar optoelectronic properties. Here, we use the double-perovskite structure to incorporate nontoxic Bi(3+) into the perovskite lattice in Cs2AgBiBr6 (1). The solid shows a long room-temperature fundamental photoluminescence (PL) lifetime of ca. 660 ns, which is very encouraging for photovoltaic applications. Comparison between single-crystal and powder PL decay curves of 1 suggests inherently high defect tolerance. The material has an indirect bandgap of 1.95 eV, suited for a tandem solar cell. Furthermore, 1 is significantly more heat and moisture stable compared to (MA)PbI3. The extremely promising optical and physical properties of 1 shown here motivate further exploration of both inorganic and hybrid halide double perovskites for photovoltaics and other optoelectronics.
Book
Modern Antenna Handbook represents the most current and complete thinking in the field of antennas. The handbook is edited by one of the most recognizable, prominent, and prolific authors, educators, and researchers on antennas and electromagnetics. Each chapter is authored by one or more leading international experts and includes cover-age of current and future antenna-related technology. The information is of a practical nature and is intended to be useful for researchers as well as practicing engineers. From the fundamental parameters of antennas to antennas for mobile wireless communications and medical applications, Modern Antenna Handbook covers everything professional engineers, consultants, researchers, and students need to know about the recent developments and the future direction of this fast-paced field. In addition to antenna topics, the handbook also covers modern technologies such as metamaterials, microelectromechanical systems (MEMS), frequency selective surfaces (FSS), and radar cross sections (RCS) and their applications to antennas, while five chapters are devoted to advanced numerical/computational methods targeted primarily for the analysis and design of antennas.
Article
We have studied the effect of addition of titania, as a sintering agent, to alumina on the dielectric characteristics of the ceramic composites obtained. The dielectric properties of the titania–alumina composites were studied by use of impedance spectroscopy and the Hakki–Coleman method in the radio-frequency and microwave regions, respectively. The temperature coefficient of the resonant frequency (τ f ) was also studied. Dielectric permittivity (ε′) was increased and the dielectric loss (tan δ) was improved by addition of titania, as a result of better sintering; addition of 10 wt.% titania resulted in ε′ = 12.68 and tan δ = 8.23 × 10−4 in the microwave region. Increasing the concentration of TiO2 led to inversion of the τ f signal; values were positive when the concentration of TiO2 was >7.5 wt.%. The ceramic composites were evaluated as antennas; for all samples the return loss (S 11) was <−10 dB and the gain was approximately 3 dBi. Addition of 7.5 wt.% titania to the Al2O3 improved antenna performance. In conclusion, addition of the TiO2 to alumina improves its dielectric properties, resulting in the possibility of use of such composites as dielectric resonator antennas (DRA).
Article
The polycrystalline sample of Ba2BiNbO6 (a member of double perovskite family) was synthesized by a high-temperature solid-state reaction method (calcination at 910 °C, and sintering at 950 °C). Preliminary analysis of room temperature X-ray data pattern of the sample confirms the formation of a single phase compound in orthorhombic crystal system. The room temperature scanning electron microscope image of the pellet sample clearly shows the uniform distribution of grains and formation of a high density sample. Detailed studies of dielectric and polarization characteristics with temperature confirmed the existence of ferroelectricity in the material. Studies of electrical properties exhibits a strong correlation with the micro-structure and resistive properties of the material. The electrical transport shows the existence of non-exponential-type of conductivity relaxation in the material. This lead-free ferroelectric has many interesting characteristics as compared to that of their lead-based counterpart, Pb2BiNbO6.
Article
The B-site substituted perovskite oxides A2B′B″O6 have in the recent decades gained an increasing amount of interest due to their various interesting properties and possible applications. Here we survey the literature for ca. one thousand A2B′B″O6 perovskite compounds. Crystal structures and the various crystal chemistry features such as ordering and valence mixing of the B cations characteristic to these compounds are reviewed, together with their electronic and magnetic properties. Most importantly, the thorough examination of the research so far carried out allows us to make predictions for a number of new A2B′B″O6 compounds yet to be synthesized and reveal exciting but not yet fully explored puzzles related to this family of functional oxide materials.
Article
Sr3−xEuxMoO6 and Sr2.7Eu0.3Mo1−yWyO6 red phosphors were successfully synthesized by solid-state reaction method at 1260 °C for 6 h. The photoluminescence (PL) properties of Eu3+ in this phosphor material were investigated by analyzing the excitation and emission spectra and the effect of Eu3+ concentration. X-ray diffraction (XRD) patterns indicate the formation of Sr3MoO6:Eu3+ pure phase. The excitation and emission spectra demonstrate that 30 mol% Eu3+:Sr3MoO6 shows a broad charge-transfer (CT) band at around 365 nm and an intense red emission (616 nm, 5D0→7F2 transition), with Commission Internationale de I׳Eclairage (CIE) chromaticity coordinates (0.619, 0.376). The substitution of Mo6+ with W6+ results in a considerable enhancement of luminescence intensity and improved red color purity. All the results imply that the studied phosphors may be a promising red component for the application in the white light emitting diodes.
Article
In the present work, the microwave dielectric ceramic (Ag0.5Bi0.5)(Mo0.5W0.5)O4 was prepared by using the solid-state reaction method. (Ag0.5Bi0.5)(Mo0.5W0.5)O4 was found to crystallize in the scheelite structure, in which Ag(+) and Bi(3+) occupy the A site randomly with 8-coordination while Mo(6+) and W(6+) occupy the B site with 4-coordination, at a sintering temperature above 500 °C, with lattice parameters a = b = 5.29469(2) Å and c = 11.62114(0) Å, space group I41/a (No. 88), and acceptable Rp = 9.38, Rwp = 11.2, and Rexp = 5.86. High-performance microwave dielectric properties, with permittivity ∼26.3, Qf value ∼10000 GHz, and temperature coefficient ∼+20 ppm/°C, were obtained in the sample sintered at 580 °C. Its chemical compatibility with aluminum at its sintering temperature was revealed and confirmed by both X-ray and energy dispersive spectrometer analysis. This ceramic could be a good candidate for ultralow-temperature cofired ceramics.
Article
A new microwave dielectric (AgBi)0.5WO4 ceramic with an ultralow firing temperature was prepared by the solid-state reaction method. (AgBi)0.5WO4 can be obtained as a dense single-phase bulk material with a calcination temperature of 500 °C and sintering temperatures of ca. 580 °C. The material has a microwave relative permittivity of ca. 35.9, a Qf value of ca. 13000 GHz, and a negative temperature coefficient of –69 ppm/°C at 7.5 GHz. The crystal structure of (AgBi)0.5WO4 was determined by a combination of X-ray and transmission electron microscopy (TEM) diffraction analysis. The compound crystallizes in the monoclinic C12/m1 (no. 12) space group with the lattice parameters a = 10.1330(8) Å, b = 11.0013(0) Å, c = 7.2756(4) Å, and β = 127.712(3)°. From an X-ray diffraction analysis, the (Ag0.5Bi0.5)WO4 ceramic reacts with silver after heat treatment at 560 °C to form new compounds, namely, Bi2WO6 and Ag2WO4. However, the (AgBi)0.5WO4 ceramic is chemically compatible with aluminum powder at 600 °C as an alternative cofired electrode material. All the results suggest that (AgBi)0.5WO4 ceramic is a promising new candidate material for ultralow-temperature cofired ceramic (ULTCC) technology.
Article
A sintering-aid system using melting of B-Li glass for barium strontium titanate (BST)-based compositions to be used in low-temperature cofired ceramic (LTCC) layers is introduced. The effects of the sintering aid on the microstructure, dielectric properties, and application in LTCC were investigated. The composition Ba0.5Sr0.5TiO3-SrMoO4 with 3 wt.% B-Li glass sintered at 950°C exhibits optimized dielectric properties, including low dielectric constant (368), low dielectric loss (0.007), and moderate tunability (13%, 60 kV/cm) at 10 kHz. At 1.44 GHz, it possesses a dielectric constant of 218 and Q value of 230. LTCC multilayer ceramic capacitors fabricated by the tape-casting process have steady relative tunability of 12% at 300 V, suggesting that BST50-SrMoO4-B-Li glass composite ceramic is a promising candidate for electrically tunable LTCC microwave device applications.
Article
A compositional dependence on the ferroelastic phase transition in scheelite solid-solution [(Li0.5Bi0.5)xBi1−x][MoxV1−x]O4 ceramics was characterized by the microwave dielectric data over the temperature range 10–420 K. As x values increased from 0.0 to 0.125, a dielectric temperature-dependent anomaly consistent with a phase transition decreased linearly from 528 K for the pure BiVO4 end member to 264 K for the solid-solution composition at x = 0.125. With further increasing x, the transition temperature decreased sharply to approximately 45 K and became stable for x ⩾ 0.52. The phase transition point for pure tetragonal (Li0.5Bi0.5)MoO4 ceramics is approximately 43 K. As the x value increases, the Raman band of the [(Li0.5Bi0.5)xBi1−x][MoxV1−x]O4 ceramics at room temperature broadens and overlaps. Ferroelastic domain structures were observed as a function of composition with diffraction contrast imaging and high-resolution imaging with transmission electron microscopy. Structure–property relations are inferred from the microscopy observations and the Raman spectra.
Article
The influence of long term milling in an attritor of a mixture of BaCO3 and TiO2 powders on the reaction synthesis of BaTiO3 was studied. Thermal analysis (TG and DTA) of the unmilled and milled powders and X-ray diffraction of powders calcined at different temperatures were undertaken. Milling does not change the reaction sequence between BaCO3 and TiO2. BaTiO3 and Ba2TiO4 are produced in both kinds of powders. However, milling reduces the formation temperature and accelerates the formation rate of these two phases. The production of final BaTiO3 is incomplete in the milled powder, probably because of the formation of big crystals of Ba2TiO4. As a consequence, the milled powder contains large amounts of Ba2TiO4 after calcination at 1200°C. Milling produces allotropic transformations in TiO2 from anatase phase, to α-PbO2-like phase and finally to rutile structure.
Article
Compound formation and compatibility relations have been studied for a portion of the system SrMoO at 1200°C. The ternary compounds were prepared: SrMoO4 with the tetragonal scheelite structure, SrMoO3 with the cubic perovskite structure and Sr3MoO6. This last compound, which had not been previously reported, gave X-ray powder data which could be indexed on a cubic unit cell with . It appeared to have a structure related to that of (NH4)3FeF6. X-ray powder data have been determined for SrMoO3 and Sr3MoO6. A previously reported fourth compound, Sr2MoO4, could not be prepared at 1000°C, 1200°C or 1400°C. The stable phase assemblage at its bulk composition was (Sr3MoO6 + Mo).
Article
Temperature dependent impedance spectroscopic analysis of fine-grained magnetoelectric Pb(Zr0.53Ti0.47)O3–(Ni0.5Zn0.5)Fe2O4 (PZT–NZFO) composites was investigated. Debye-like impedance relaxation peaks were observed at intermediate frequency range. Maxwell–Wagner (MW) relaxation model was used to explain the space charge effect due to heterogeneous PZT and NZFO grain boundary in finer structure. The total resistivity was dominated by the grain boundary resistance due to the blocking effect arisen from the glass phase additive. The small value of conductivity measured in this system suggested the glass additive markedly modified the grain boundary properties. Electric modulus spectra reflected the contributions from two different effects: the large resolved semicircle arc was caused by the grain effect and the small poorly resolved semicircle arc was attributed to the grain boundary. The activation energy calculated from the impedance spectra was consistent with value estimated from the modulus spectra. Investigation on dielectric spectra revealed a polydispersive dielectric relaxation existing in the system, which was also demonstrated in the ac conductivity spectra. Small polaron relaxation and MW-type polarization mechanism were discussed through the analysis on the ac conductivity spectra.
Article
The microwave dielectric properties of A5B4O15 (A=Ba, Sr, Mg, Ca, Zn; B=Nb, Ta) ceramics are investigated. The ceramics are prepared through the solid-state ceramic route. The dielectric properties are studied at microwave frequencies and structure and microstructure by XRD and scanning electron micrograph (SEM) methods. The ceramics show εr in the range 11–51, Q×f is in the range 2400–88,000 GHz and τf in the range −73–232 ppm/°C.
Article
A series of (ABi)1/2MoO4 (A=Li, Na, K, Rb, Ag) compositions were studied in regard to the sintering behavior, phase composition, microwave dielectric properties and chemical compatibility with silver and/or aluminum for electrodes. All the (ABi)1/2MoO4 (A=Li, Na, K, Rb, Ag) ceramics could be sintered below 700°C with relative densities above 93%. Whereas the (KBi)1/2MoO4 ceramic can be sintered to a high density at around 630°C/2hrs with a relative permittivity ∼37, a Qf value of 4000GHz and a temperature coefficient of resonant frequency (TCF)∼+117ppm/°C. Furthermore, from the XRD analysis of co-fired ceramics, the (KBi)1/2MoO4 ceramic reacts with silver but not with aluminum at its densification temperature. The (ABi)1/2MoO4 (A=Li, Na, K, Rb, Ag) type ceramics can all be considered into the new field of ultra-low temperature co-firing dielectrics for multilayer applications.
Chapter
Potentiodynamic electrochemical impedance spectroscopy (PDEIS) uses virtual instruments to acquire, by means of a common potentiostat, multidimensional dependencies that characterise variations of dc current and frequency response in the same potential scan. Unlike classical EIS, which finds the whole equivalent circuit in stationary states, PDEIS finds, in potentiodynamic systems, only those elements of equivalent circuits that are needed to decompose the ac response in a limited range of frequencies. The decomposition of ac response into components belonging to different elements is provided by a built-in spectrum analyser, which gives dependences of equivalent circuit parameters on variable potential. The new technique develops the idea, originally suggested by D.E. Smith, of versatile characterisation of the electrochemical response in a simple computerised experiment. PDEIS solves this problem with the use of multi-frequency potentiodynamic probing based on analysis of streams of wavelets. The use of the additional variable (electrode potential) helps to disambiguate the equivalent circuit analysis. The PDEIS performance is illustrated on systems of different kind: a reversible system (ferricyanide redox transformations on glassy carbon and platinum electrodes), a system that is locally reversible but shows different responses in forward and backward scans (Bi upd on Au) and strongly irreversible variable system (initial stages of aniline electropolymerisation on gold).
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Colossal magnetoresistance - a huge decrease in resistance in response to a magnetic field has recently been observed in manganese oxides with perovskite structure. This effect is attracting considerable interest from both fundamental and practical points of view. In the context of using this effect in practical devices, a noteworthy feature of these materials is the high degree of spin polarization of the charge carriers, caused by the half- metallic nature of these materials; this in principle allows spin-dependent carrier scattering processes, and hence the resistance, to be strongly influenced by low magnetic fields. This type of field control has been demonstrated for charge-carrier scattering at tunnelling junctions and at crystal-twin or ceramic grain boundaries, although the operating temperature of such structures is still too low (≤150K) for most applications. Here we report a material-Sr2FeMoO6, an ordered double perovskite exhibiting intrinsic tunnelling-type magnetoresistance at room temperature. We explain the origin of this behaviour with electronic-structure calculations that indicate the material to be half-metallic. Our results show promise for the development of ordered perovskite magnetoresistive devices that are operable at room temperature.
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