Structural Characterization and Physical Properties of Double Perovskite La2FeReO6+δ Powders

The structural, optical, dielectric, and magnetic properties of double perovskite La2FeReO6+δ (LFRO) powders synthesized by solid-state reaction method under CO reduced atmosphere are reported on in this paper. Reitveld refinements on the XRD data revealed that the LFRO powders crystallized in an orthogonal structure (Pbnm space group) with column-like morphology. The molar ratios of La, Fe, and Re elements were close to 2:1:1. XPS spectra verified the mixed chemical states of Fe and Re ions, and two oxygen species in the LFRO powders. The LFRO ceramics exhibited a relaxor-like dielectric behavior, and the associated activation energy was 0.05 eV. Possible origins of the dielectric relaxation behavior are discussed based on the hopping of electrons among the hetero-valence ions at B-site, oxygen ion hopping through the vacant oxygen sites, and the jumping of electrons trapped in the shallower level created by oxygen vacancy. The LFRO powders display room temperature ferromagnetism with Curie temperature of 746 K. A Griffiths-like phase was observed in the LFRO powders with a Griffiths temperature of 758 K. The direct optical band gap of the LFRO powders was 2.30 eV, deduced from their absorption spectra, as confirmed by their green photoluminescence spectra with a strong peak around 556 nm.

Microwave dielectric properties of Na+-substituted CaMg0.9Li0.2Si2O6 ceramics

Ceramics with low dielectric constant are widely used in high frequency substrates. The low temperature sintered CaMg0.9-xNa2xLi0.2Si2O6(x = 0–0.05 and 0.1) ceramics with low dielectric constant and dielectric loss were prepared by the traditional solid-state reaction method, with 0.5wt%LBSCA additive. The XRD patterns of the samples were obtained by X-ray diffraction and it was found that there were three ceramic components, CaMgSi2O6, CaSiO3 and Na2MgSiO4, which indicated that the experimental sample was a multiphase ceramic system. Through the trend of bulk density as functions of the content of substitution and the change of SEM morphology, it could be found that appropriate amount of Na+ substitution can promote the grain growing and the densification of ceramics. Results demonstrated that both the Q × f and εr were relevant to bulk density and the second phase. The τf was also affected by the second phase to some extent. In particular, the ceramics sintered at 925 °C for 3h possessed the desirable microwave dielectric properties for LTCC application: εr = 7.03, Q × f = 17,956 GHz, and τf= −79 ppm/°C.

PHASE ANALYSIS AND PHYSICAL PROPERTIES OF B2O3-ADDED ZIRCON CERAMICS SINTERED AT 1300 °C

This study was aimed to know the effect of B2O3(boria) addition on the phase composition and physical properties of zircon ceramics.The raw zircon powder used in the study was a purified natural zircon sand from Kereng Pangi, Central Kalimantan, Indonesia. The zircon ceramics were prepared by a solid state reaction method with variation of B2O3 addition of 3 wt%, 6 wt% and 9 wt% and sintered at 1300 °C for 5h. The phase composition, density and microstructure were characterized using X-ray diffraction (XRD), densimeter and Scanning Electron Microscope (SEM), respectively. Vickers Hardness measurement was perfomed at the polished surface of the ceramics. Results showed that all samples contained pure zircon phase, i.e. there was no effect of B2O3 addition on the phase composition. In general, the density and hardness increased with increasing B2O3 addition, but addition up to 9 wt% is not optimum to achieve ultra-dense zircon ceramics. Furthermore, the SEM image also showed no significant difference in average grain size. The crystallite size has grown nearly eight times (325 nm) of its original powder. The Vickers hardness of the ceramics is not significantly influenced by the addition of boria. It appears that the boria failure to increase densification also results in the extent of contact between grains which then produces relatively large zircon grains.

Developments of crystal structures and photoluminescence properties of Sr0.85Eu0.15Al12O19 green phosphors using different synthesis parameters

First, a solid-state reaction method was used to synthesize a [Formula: see text] phosphor at 1250[Formula: see text]C–1400[Formula: see text]C for 1 h, and its crystal structures and photoluminescence properties were investigated as a function of synthesis temperature. When the furnace reached the synthesis temperature, the 5% [Formula: see text] reduction atmosphere was infused and the reduction atmosphere was removed as the temperature was dropped to 800[Formula: see text]C. When 1200[Formula: see text]C was used as the synthesis temperature, the [Formula: see text], [Formula: see text], and [Formula: see text] phases co-existed; only one weak emission peak was observed in the photoluminescence excitation (PLE) spectra, and two weak emission peaks were observed in the photoluminescence emission (PL) spectra. When the [Formula: see text] phosphors were synthesized at a temperature higher than 1200[Formula: see text]C, the diffraction intensities of [Formula: see text], [Formula: see text], and [Formula: see text] phases were almost unchanged, but the crystal sizes of [Formula: see text] powders increased. For [Formula: see text] phosphors, PLE spectra had one broad exciting band with two centered wavelengths of 317 and 365 nm, and PL spectra had one emission band with one centered wavelength of 513 nm. As the synthesis temperature rose, the emission intensities of PLE and PL spectra increased. Second, we show that the removed temperature of reduction atmosphere of [Formula: see text] phosphors had an apparent effect on their emission properties of PLE and PL spectra.

A density-wave-like transition in the polycrystalline V3Sb2 sample with bilayer kagome lattice

Recently, transition-metal-based kagome metals have aroused much research interest as a novel platform to explore exotic topological quantum phenomena. Here we report on the synthesis, structure, and physical properties of a bilayer kagome lattice compound V3Sb2. The polycrystalline V3Sb2 samples were synthesized by conventional solid-state-reaction method in a sealed quartz tube at temperatures below 850 ℃. Measurements of magnetic susceptibility and resistivity revealed consistently a density-wave-like transition at T dw ≈ 160 K with a large thermal hysteresis, even though some sample-dependent behaviors are observed presumably due to the different preparation conditions. Upon cooling through T dw, no strong anomaly in lattice parameters and no indication of symmetry lowering were detected in powder x-ray diffraction measurements. This transition can be suppressed completely by applying hydrostatic pressures of about 1.8 GPa, around which no sign of superconductivity is observed down to 1.5 K. Specific-heat measurements reveal a relatively large Sommerfeld coefficient γ = 18.5 mJ/mol-K2, confirming the metallic ground state with moderate electronic correlations. Density functional theory calculations indicate that V3Sb2 shows a non-trivial topological crystalline property. Thus, our study makes V3Sb2 a new candidate of metallic kagome compound to study the interplay between density-wave-order, nontrivial band topology, and possible superconductivity.

Physical and Mechanical Properties of Non-Stoichiometric Cordierite with Treated FGD Sludge Addition Sintered at 1250°C

The effects of addition treated FGD sludge in non-stoichiometric cordierite, by benefiting from its high mechanical strength and good thermal performance, can hold promise for more practical applications of non-stoichiometric cordierite. Treated FGD sludge waste from borosilicate glass industrial were used as a flux to reduce the sintering temperature of cordierite. Cordierite ceramics were prepared using silica (SiO2), alumina (Al2O3), talc, kaolin, magnesia (MgO) and treated FGD sludge via solid-state reaction method. The cordierite were prepared by adjusting the ratio of FGD sludge and magnesia in the cordierite composition, respectively. 4 composition of cordierite with 0%, 1.5%, 3.0% and 4.5% of FGD sludge were prepared to obtain the formation of α-cordierite that can be determine by X-ray diffraction (XRD) analysis. Porosity, density, shrinkage and flexural strength for each of cordierite composition were determined to obtain the best composition of treated FGD sludge required for sintering aids of cordierite. Only FGD 3.0% able to synthesis pure α-cordierite while FGD 1.5 % shows an improvement in both porosity and density. The increasing amount of treated FGD sludge lead to decreasing in mechanical strength of cordierite ceramic due to porous formation.

Influence of Sintering Time on Superconducting Properties of Bi, Pb-2223 Compound Doped with Indium

This work was performed to investigate the effect of sintering time on superconducting properties of Bi1.7In0.3Pb0.3Sr2Ca2Cu3O10+d samples prepared by solid state reaction method. The samples properties have been investigated structurally by X-ray diffraction and morphologically by scanning electron microscopy. Structural analysis showed that two superconducting phases coexist in the samples. High temperature Bi-2223 and low-temperature phase 2212 with orthorhombic structure for all samples. Four point probe method used to study the electrical properties of the samples and the results showed that increasing sintering time yields superconductor samples. The sintering time 140 h improves the microstructure of the superconductor and produces greater size platelets as well as leading to the highest TC value of 113 K and highest oxygen content value. Scanning electron microscopy shows increasing sintering time changed morphology of samples. Moreover plate grains of the high Bi-2223 phase appeared in most micrographs of the superconducting samples.