Microwave dielectric properties of Sr<Subscript>0.7</Subscript>Ce<Subscript>0.2</Subscript>TiO<Subscript>3</Subscript>–Sr(Mg<Subscript>1/3</Subscript>Nb<Subscript>2/3</Subscript>)O<Subscript>3</Subscript> ceramics

xSr_0.7Ce_0.2TiO₃–(1???x)Sr(Mg_1/3Nb_2/3)O₃ ceramics, referred to xSCT–(1???x)SMN, were successfully produced by conventional solid-state sintered technology. The compounds, belonging to perovskites with a secondary phase of CeO₂, can be detected even with x down to 0.1 of SCT composition. The overall trend for grain growth illustrates the increase with increasing SCT doping level. The Raman peak at 825 cm^?1 splits into two peaks and causes red shift phenomenon. XPS spectra indicate that Ti and Nb ions exist respectively in tetravalence and pentavalence, and Ce ions exist in trivalence and tetravalence. Dielectrics constant (ε _r ) of SCT–SMN ceramics gradually increases with increasing theoretical dielectric polarizabilities. A wider width of the 825 cm^?1 for FWHM of A_1g mode Raman peaks suggests to a lower Q?×?f value. The increasing tolerance factor in agreement with temperature coefficient of resonant frequency (τ _f ), denotes that the rise of perovskite symmetry. The 0.1SCT–0.9SMN ceramic sintered at 1450?°C for 4 h illustrates excellent microwave dielectric properties with ε _r ?~?35.4, Q?×?f?~?11282 GHz and τ _f ?~?1.7 ppm/°C. Activation energies of 0.1SCT–0.9SMN ceramic at 100, 300 and 500 V, are ~0.436, 0.427 and 0.331 eV, respectively, indicative of a decreased trend with external electric field.     

SmAlO<Subscript>3</Subscript> + Ba(Zn<Subscript>1/2</Subscript>Nb<Subscript>2/3</Subscript>)O<Subscript>3</Subscript>: microwave ceramic composite

The 0.1SmAlO₃ + 0.9Ba(Zn_1/2Nb_2/3)O₃ composite is prepared through the solid state ceramic route. The structure of the materials is studied using X-Ray diffraction analysis. The microstructure is studied using scanning electron microscopy and the elemental composition by energy dispersive spectrometry. The dielectric properties in the radio and microwave frequencies are measured. The photoluminescence property of the sample is also analyzed. The material has dielectric constant (ε _r ) = 37, temperature coefficient of resonant frequency (τ _f ) = +25 ppm/°C and high quality factor. The measured values of ε _r and τ _f are compared with the corresponding theoretical values. The composite is useful in the field of optoelectronics and microwave communication.     

Electrical properties of B site substituted (K<Subscript>0.48</Subscript>Na<Subscript>0.52</Subscript>)(W<Subscript>2/3</Subscript>Bi<Subscript>1/3</Subscript>)<Subscript>x</Subscript>Nb<Subscript>1−x</Subscript>O<Subscript>3</Subscript> piezoceramics

Lead-free (K_0.48Na_0.52)(W_2/3Bi_1/3)_xNb_1−xO₃ (KNN-WBi) piezoceramics with x ranging from 0.004 to 0.010 were synthesized by conventional ceramic processing. The sintered KNN-WBi ceramics showed perovskite structure without detectable secondary phase containing W and Bi. With increasing x, the orthorhombic-tetragonal phase transition temperature (T _O-T) decreased from 200 to 184 °C whereas, the tetragonal-cubic phase transition temperature (T _C) decreased slightly. With the doping of (W_2/3Bi_1/3), the piezoelectric properties were greatly improved and the piezoelectric constants d ₃₃, k _p, Q _m exhibited maximum values of 136 pC/N, 43.3% and 175, respectively at x = 0.008. The KNN-WBi ceramics also exhibited good ferroelectric properties with remnant polarizations P _r higher than 25 μC/cm² and coercive fields E _c lower than 1,000 V/mm. The results strongly suggest that the B site doping of constructed quinquevalent element is an effective method for the investigation of potassium sodium niobate system.     

Structural and electrical properties of Bi<Subscript>1/2</Subscript>Na<Subscript>1/2</Subscript>TiO<Subscript>3</Subscript>–BaTiO<Subscript>3</Subscript>–Sr<Subscript>3</Subscript>CuNb<Subscript>2</Subscript>O<Subscript>9</Subscript> lead-free piezoelectric ceramics

The structure, microstructure, field-induced strain, ferroelectric, piezoelectric and dielectric properties of (1 ? x) (Bi_0.5Na_0.5)_0.935Ba_0.065TiO₃–xSr₃CuNb₂O₉ (BNT-BT6.5–xSCN, with x = 0, 0.003, 0.006, 0.009) ceramics were investigated. X-ray diffraction patterns show that all samples are pure perovskite structure and Sr₃CuNb₂O₉ (SCN) effectively diffused into the 0.935Bi_0.5Na_0.5TiO₃–0.065BaTiO₃ (BNT–BT6.5) solid solution which also reflected in the Raman spectra and the energy disperse spectroscopy (EDS) analysis. With the increases of SCN content, the coercive field (E _c  = 18.41 kV/cm) decreases greatly, whereas the remnant polarization (P _r  = 29.11 μC/cm²) increases a little at x = 0.003 which is showed in the polarization hysteresis (P–E) loops, the result indicate that the ferroelectric order would be disrupted. Around critical composition (x = 0.003) at a driving field of 60 kV/cm, a large unipolar strain of 0.29 % with a normalized strain (d ₃₃ ^*  = 483 pm/V) is obtained at room temperature. The results indicate that BNT-BT6.5-xSCN ceramics with excellent properties are promising to replace lead-based piezoelectric ceramics and can be used in practical applications.     

BaFe<Subscript>12</Subscript>O<Subscript>19</Subscript> films produced from BaFe<Subscript>2</Subscript>O<Subscript>4</Subscript>/α-Fe<Subscript>2</Subscript>O<Subscript>3</Subscript> heterostructures

BaFe₁₂O₁₉ hexaferrite films have been produced on thermally oxidized single-crystal silicon (SiO₂/Si) substrates by sequential ion-beam sputtering of BaFe₂O₄ and α-Fe₂O₃ targets in an argon-oxygen atmosphere. Their crystal structure has been studied, and the origin of the impurity phases forming during heat treatment has been identified. The results show that heat treatment may lead to the formation of eutectic melts. As a result, the hexaferrite films may contain spherulites.     

System ZnO ⋅ B<Subscript>2</Subscript>O<Subscript>3</Subscript>-CuO ⋅ B<Subscript>2</Subscript>O<Subscript>3</Subscript>

Differential thermal analysis and x-ray diffraction data indicate that the ZnO B₂O₃-CuO B₂O₃ join of the ternary system CuO-B₂O₃-ZnO is pseudobinary, with eutectic phase relations and a liquid-liquid miscibility gap in the composition range 25–35 mol % CuO.Translated from Neorganicheskie Materialy, Vol. 41, No. 3, 2005, pp. 339–340.Original Russian Text Copyright © 2005 by Kasumova, Bananyarly.This revised version was published online in April 2005 with a corrected cover date.This revised version was published online in April 2005 with a corrected cover date.     

Variable—Range hopping in Fe<Subscript>2</Subscript>O<Subscript>3</Subscript>-Bi<Subscript>2</Subscript>O<Subscript>3</Subscript>-K<Subscript>2</Subscript>B<Subscript>4</Subscript>O<Subscript>7</Subscript> glasses

The dc conductivity of the glasses in the Fe₂O₃-Bi₂O₃-K₂B₄O₇ system was studied at temperatures between 223 and 393 K. At temperatures from 300 to 223 K, T^–1/4 (T is temperature) dependence of the conductivity was found, however, both Mott variable-range hopping and Greaves intermediate range hopping models are found to be applicable. Mott and Greaves parameters analysis gave the density of states at Fermi level N (E_F) = 3.13 × 10²⁰–21.01 × 10²⁰ and 1.93 × 10²¹–16.39 × 10²¹ cm^–3eV^–1 at 240 K, respectively. The variable-range hopping conduction occurred in the temperature range T = 300–223 K, since W_D was found to be large (W_D = 0.08–0.14 eV for these glasses) and dominated the conduction at T < 300 K.     

Structural and electrical properties of Ho<Superscript>3+</Superscript>-modified Pb(Zn<Subscript>1/3</Subscript>Nb<Subscript>2/3</Subscript>)O<Subscript>3</Subscript>–9PbTiO<Subscript>3</Subscript> single crystals

Ho³⁺-modified Pb(Zn_1/3Nb_2/3)O₃–9PbTiO₃ (PZN–9PT) single crystals were grown through a flux method. Phase structure and microstructural morphology of the as-grown single crystals were performed by X-ray diffraction analysis and scanning electron microscopy. The refinement of the lattice parameters were obtained by the Rietveld method. The electrical properties of PZN–9PT single crystals were improved significantly by the modification of Ho³⁺ ions. The rhombohedral–tetragonal phase transition temperature, Curie temperature, coercive field at 15 kV cm^?1, and remnant polarization of Ho³⁺-modified PZN–9PT single crystals were increased by 14, 42 K, 2.4 kV cm^?1, and 7.5 μC cm^?2, respectively (i.e., 375.45, 448.45 K, 5.9 kV cm^?1, and 38.40 μC cm^?2, respectively). Furthermore, Lorentz-type law was used to describe the dielectric relaxor behavior of the as-grown single crystals.     

Kinetics of Thermal Transformation of Mg<Subscript>3</Subscript>(PO<Subscript>4</Subscript>)<Subscript>2</Subscript> · 8H<Subscript>2</Subscript>O to Mg<Subscript>3</Subscript>(PO<Subscript>4</Subscript>)<Subscript>2</Subscript>

The kinetics of thermal dehydration of Mg₃(PO₄)₂ · 8H₂O was investigated using thermogravimetry at four different heating rates. The activation energies of the dehydration step of Mg₃(PO₄)₂ · 8H₂O were calculated through the isoconversional Ozawa and Kissinger-Akahira-Sunose (KAS) methods and iterative methods, which were found to be consistent and indicate a single mechanism. The possible conversion function of the dehydration reaction for Mg₃(PO₄)₂ · 8H₂O has been estimated through the Coats and Redfern integral equation, and a better kinetic model such as random nucleation of the “Avrami–Erofeev equation (A _3/2 model)” was found. The thermodynamic functions (ΔH*, ΔG*, and ΔS*) of the dehydration reaction are calculated by the activated complex theory and indicate that it is a non-spontaneous process when the introduction of heat is not connected.     

Spectroscopic characterisation of local structure in Y<Subscript>2</Subscript>O<Subscript>3</Subscript>–B<Subscript>2</Subscript>O<Subscript>3</Subscript>–Bi<Subscript>2</Subscript>O<Subscript>3</Subscript> glasses doped with gadolinium

Gadolinium doped bismuth borate glasses containing up to 30 mol% Y₂O₃ were prepared by fast melt quenching method. The effect of yttrium on the local order in 3B₂O₃ · Bi₂O₃ and B₂O₃ · Bi₂O₃ glass matrices, particularly on the bismuth sites, was investigated by infrared (IR) spectroscopy and electron paramagnetic resonance (EPR) of Gd³⁺ ions. The IR results show that the local structure is more ordered in the glass system with higher bismuth content and the progressive addition of yttrium increases the local disorder in both bismuth–borate glass matrices. The EPR results indicate that Gd³⁺ ions occupy both bismuth and yttrium sites and reflect the same structural disorder like that suggested by IR results.     

Phase equilibria in the system “CaAl<Subscript>2</Subscript>Si<Subscript>3</Subscript>O<Subscript>10</Subscript>”-Na<Subscript>2</Subscript>Al<Subscript>2</Subscript>Si<Subscript>3</Subscript>O<Subscript>10</Subscript>-H<Subscript>2</Subscript>O

The phase equilibria in the “CaAl₂Si₃O₁₀”-Na₂Al₂Si₃O₁₀-H₂O system are analyzed using structural and thermal analysis data, and the ideal gonnardite structure is modeled. The results suggest that, to ensure a better correlation with the structures of the zeolites in this series, a new structural model of the gonnardite-based solid solution must be selected, with the structure rotated through 45° about the c axis in the ab plane.     

Catalytic combustion of methane over Pt and PdO-supported CeO<Subscript>2</Subscript>–ZrO<Subscript>2</Subscript>–Bi<Subscript>2</Subscript>O<Subscript>3</Subscript>/γ-Al<Subscript>2</Subscript>O<Subscript>3</Subscript> catalysts

Catalytic combustion of methane was investigated on Pt and PdO-supported CeO₂–ZrO₂–Bi₂O₃/γ-Al₂O₃ catalysts prepared by a wet impregnation method in the presence of polyvinylpyrrolidone. The catalysts were characterized by X-ray fluorescence analysis, X-ray powder diffraction, X-ray photoelectron spectra, transmission electron microscopy, and BET specific surface area measurements. The Pt/CeO₂–ZrO₂–Bi₂O₃/γ-Al₂O₃ and PdO/CeO₂–ZrO₂–Bi₂O₃/γ-Al₂O₃ catalysts were selective for the total oxidation of methane into carbon dioxide and steam, and no by-products such as HCHO, CO, and H₂ were obtained. The catalytic activities of the PdO/CeO₂–ZrO₂–Bi₂O₃/γ-Al₂O₃ catalysts were relatively higher than those of the Pt-supported catalysts, due to the facile re-oxidation of metallic Pd into PdO based on lattice oxygen supplied from the CeO₂–ZrO₂–Bi₂O₃ bulk. A decrease in the calcination temperature during the preparation process was found to be effective in enhancing the specific surface area of the catalysts, whereby particle agglomeration was inhibited. Optimization of the PdO amount and calcination temperature enabled complete oxidation of methane at temperatures as low as 320 °C on the 11.6 wt% PdO/CeO₂–ZrO₂–Bi₂O₃/γ-Al₂O₃ catalyst prepared at 400 °C.     

A physicochemical study of the Sb<Subscript>2</Subscript>Se<Subscript>3</Subscript>–Nd<Subscript>2</Subscript>Se<Subscript>3</Subscript> system

We have studied phase relations in the Sb₂Se₃–Nd₂Se₃ system and mapped out its T–x phase diagram using differential thermal analysis, X-ray diffraction, microstructural analysis, microhardness tests, and density measurements. The system contains one compound, with the composition NdSbSe₃, which melts incongruently at 865 K and crystallizes in orthorhombic symmetry with the following lattice parameters: а = 12.77(1) Å, b = 14.08(1) Å, and c = 5.82(5) Å (Z = 8, ρ_meas = 6.20 g/cm³, ρ_x = 6.38 g/cm³). At room temperature, the Nd₂Se₃ solubility in Sb₂Se₃ is 5 mol % and the Sb₂Se₃ solubility in Nd₂Se₃ is 2.5 mol %. The Sb₂Se₃–Nd₂Se₃ system has a eutectic located at 15 mol % Nd₂Se₃, with a melting point at 755 K. The electrical conductivity and thermoelectric power of the (Sb₂Se₃)_1–x (Nd₂Se₃) _x solid solutions have been measured as functions of temperature.     

Effect of excess Pb in PbTiO<Subscript>3</Subscript> precursors on ferroelectric and fatigue property of sol–gel derived PbTiO<Subscript>3</Subscript>/PbZr<Subscript>0.3</Subscript>Ti<Subscript>0.7</Subscript>O<Subscript>3</Subscript>/PbTiO<Subscript>3</Subscript> thin films

A series of Pb_(1+x)TiO₃/PbZr_0.3Ti_0.7O₃/Pb_(1+x)TiO₃ (PTO/PZT/PTO) and PbZr_0.3Ti_0.7O₃ (PZT) thin films were prepared by a sol–gel method. Different excess Pb content (x) (x = 0, 0.05, 0.10, 0.15, 0.20) were added to the PbTiO₃ (PTO) precursors to investigate their effect on ferroelectric and fatigue properties of the PTO/PZT/PTO thin films. X-ray diffraction results show that the crystallization behavior of the PTO/PZT/PTO thin films is greatly affected by the excess Pb content (x) in PTO precursors. Topographic images show that the PTO/PZT/PTO thin films with excess Pb content x = 0.10 appears the densest and the most uniform grain size surface morphology. The ferroelectric and fatigue properties of the films correlate straightforwardly to the crystallization behaviors and excess Pb content (x) in the PTO precursors. The excess Pb content (x) in the PTO layers which acts as a nucleation site or seeding layer for PZT films affects the crystallization of the PTO layer and ultimately affects the perovskite phase formation of the PZT films. With the proper excess Pb content (x = 0.10–0.15) in the PTO precursors, the pure perovskite structure PTO/PZT/PTO thin films, with dense, void-free, and uniform fine grain size are obtained, and a well-saturated hysteresis loop with higher remnant polarization is achieved. Using an appropriate Pb content, the fatigue has been avoided by controlling the inter-diffusion and surface volatilization.     

Aging and thermal stability of [001]<Subscript>c</Subscript>- and [111]<Subscript>c</Subscript>-poled 0.63Pb(Mg<Subscript>1/3</Subscript>Nb<Subscript>2/3</Subscript>)O<Subscript>3</Subscript>–0.37PbTiO<Subscript>3</Subscript> single crystals

The aging characteristics and thermal stability of [001]_c- and [111]_c-poled tetragonal 0.63Pb(Mg_1/3Nb_2/3)O₃–0.37PbTiO₃ single crystals have been studied. For [001]_c-poled crystal, the d₃₃, \(\varepsilon _{{33}}^{T}\), k_t, and k₃₃ increase slightly during the aging process due to the gradual depolarization of the single-domain state. On the contrary, the electromechanical properties of [111]_c-poled crystal decrease quickly with the aging time due to the growth and combination of micro-domains. The temperature-dependent electromechanical properties indicate that the [111]_c-poled multi-domain crystal is more stable than [001]_c-poled single-domain crystal. In addition, the second poling can effectively enhance the piezoelectric constant d₃₃ of the [111]_c-oriented multi-domain crystals from 1032 pC/N after the first poling to 1247 pC/N.     

Angular-Dependent Vortex Pinning Properties of YBa<Subscript>2</Subscript>Cu<Subscript>3</Subscript>O<Subscript>7−<Emphasis Type="Italic">δ</Emphasis></Subscript>/Y<Subscript>2</Subscript>O<Subscript>3</Subscript> Quasi-Multilayers

A series of quasi-multilayers of YBa₂Cu₃O_7?δ (YBCO)/Y₂O₃ specifically 70 × (m YBCO/n Y₂O₃) were prepared on SrTiO₃ single crystal using pulsed-laser deposition (PLD) with a controlled deposition pulses of m = 40 and n = 2, 5, and 10 for YBCO and Y₂O₃, respectively. The x-ray diffraction patterns indicate that all the present quasi-multilayers exhibit good c-axis orientation. The angular dependence of critical current density (J _c ) on applied magnetic field directions are systemically measured to study the anisotropic vortex pinning performances for those quasi-multilayers. It is revealed that compared with the pure YBCO films, the quasi-multilayers with n = 2, i.e., a proper constituent pulse of Y₂O₃, exhibits the enhanced vortex pinning abilities in all angles between c-axis orientation and the applied magnetic field direction. As well, such a quasi-multilayer film (n = 2) shows the higher lift factor J _c (Θ)/ J _c (90°) and much better vortex pinning properties at high fields and high temperatures, showing promising potential for coated conductor application.     

Optical properties and crystallization of glasses in the system Bi<Subscript>2</Subscript>O<Subscript>3</Subscript>–MoO<Subscript>3</Subscript>–B<Subscript>2</Subscript>O<Subscript>3</Subscript>

The purpose of this work is to study the optical properties and crystallization of glasses in the ternary system Bi₂O₃–MoO₃–B₂O₃. In order to verify the obtaining of bismuth borate crystal phases several glass compositions have been selected for crystallization. The obtained samples were characterized by X-ray diffraction, scanning electron microscopy and UV–Vis spectroscopy. The UV–Vis spectroscopy showed that the obtained glasses are transparent in the visible region. The values of optical band gap (E _opt) and changes in cut-off (λ_c) depending on composition are reported. It was established that the increase in the MoO₃ content led to decreasing the transmittance of the glasses. Moreover, the absorption edge shifts towards longer wavelength.     

The crystallographic orientation relationship between Al<Subscript>2</Subscript>O<Subscript>3</Subscript> and MgAl<Subscript>2</Subscript>O<Subscript>4</Subscript> in the composite material Al<Subscript>2</Subscript>O<Subscript>3</Subscript>/Al–Mg–Si alloy

The formation mechanism of spinels on Al₂O₃ particles in the Al₂O₃/Al–1.0 mass% Mg₂Si alloy composite material has been investigated by transmission electron microscopy (TEM) in order to determine the crystallographic orientation relationship. A thin sample of the Al₂O₃/Al–Mg–Si alloy composite material was obtained by the FIB method, and the orientation relationship between Al₂O₃ and MgAl₂O₄, which was formed on the surface of Al₂O₃ particles, was discovered by the TEM technique as follows:

Structure and piezoelectric properties of new ternary K<Subscript>0.5</Subscript>Na<Subscript>0.5</Subscript>NbO<Subscript>3</Subscript>–LiSbO<Subscript>3</Subscript>–CaTiO<Subscript>3</Subscript> lead-free piezoceramics

New ternary (1−x)K_0.5Na_0.5NbO₃–x(0.80LiSbO₃–0.20CaTiO₃) lead-free ceramics were fabricated by a conventional ceramic technique and their structure and piezoelectric properties were studied. The results of X-ray diffraction reveal that LiSbO₃ and CaTiO₃ diffuse into the K_0.5Na_0.5NbO₃ lattices to form a new solid solution with a perovskite structure. After the addition of LiSbO₃ and CaTiO₃, the cubic-tetragonal and tetragonal-orthorhombic phase transitions shift to lower temperatures. Coexistence of the orthorhombic and tetragonal phases is hence formed in the ceramics with 0.03 < x < 0.07 at room temperature, leading to a significant enhancement of the piezoelectric properties. For the ceramics with x = 0.04–0.06, the piezoelectric properties become optimum: d ₃₃ = 172–253 pC/N, k _P = 49.9–55.5%, k _t = 49.2–52.1% and T _C = 348–373 °C. The ceramic with x = 0.04 also exhibits a good thermal stability of piezoelectric properties.     

Enhanced dielectric and piezoelectric properties of (100) oriented Bi<Subscript>0.5</Subscript>Na<Subscript>0.5</Subscript>TiO<Subscript>3</Subscript>–BaTiO<Subscript>3</Subscript>–SrTiO<Subscript>3</Subscript> thin films

The (100) oriented and random oriented 0.755Bi_0.5Na_0.5TiO₃–0.065BaTiO₃–0.18SrTiO₃ (BNT–BT–ST) thin films were deposited on LaNiO₃ (LNO) buffered Pt(111)/Ti/SiO₂/Si substrates by the sol–gel processing technique. The orientation is controlled by the concentration of solution. The structure, dielectric and piezoelectric properties of the thin films are significantly affected by the crystallographic orientation. The (100) oriented BNT–BT–ST thin film has improved dielectric and piezoelectric properties. For the (100) oriented and random oriented BNT–BT–ST thin films, the dielectric constants are 660 and 550, the dielectric losses are 0.045 and 0.076 and the effective piezoelectric coefficients are 140 and 110 pm/V, respectively. The large piezoelectric response is attributed to the uniform microstructure and increased lattice distortion along (100) direction.