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Abstract Ca 0.66 Ti 0.66 Nd 0.34 Al 0.34 O 3 (CTNA) ceramics were prepared by solid-state reaction method and their sintering behavior, microwave dielectric properties, and microstructure were investigated. CTNA ceramics were examined by Raman scattering to reveal the correlation of perovskite structure with the microwave properties. It found that the area of peak A 1g (O) stretch mode reflects the quality factor Q × f value in the perovskite materials. This concludes that the oxygen octahedron plays an important role of the material's microwave performance. Sintering temperature affected the unit cell volume and the lattice parameters of the CTNA ceramics, the grain size distribution, the Gibbs free energy, the thermal expansion coefficient (CTE), and the dielectric properties (ε r , Q × f , τ f). The samples sintered at 1500 °C displayed the best dielectric constant and Q × f , as 44.94 and 41922.22 GHz, respectively. Highlights • The CTNA ceramics were sintered at different temperatures were investigated. • The thermal analysis detailed description of the stages of sintering process. • The unit cell volume is affected by the sintering temperature was confirmed by XRD. • Raman to reveal the correlation of structure with the microwave properties. • Relationship between grain size, Gibbs free energy, CTE, and dielectric properties. [ABSTRACT FROM AUTHOR]

The influence of substitution with rare earth elements in orthorhombic Ca 0.66 Ti 0.66 R 0.34 Al 0.34 O 3 (R = Sm, Nd, La) perovskite ceramics, which were successfully produced with a solid-state reaction method, on their crystal structure (analyzed with Rietveld refinement of X-ray diffractograms and Raman spectroscopy) and on the microwave dielectric properties was investigated. The dielectric constant (ε r ) increased due to the increase of cell volume, which was a result of the increase of the ionic radius of the rare earth cations incorporated in the host lattice R 3+ . The values of the quality factors were 43620.74, 41292.71, and 38389.57 GHz for the Sm-, Nd-, and La-containing ceramics, respectively. The decrease of these values is correlated to the level of distortion of the octahedral due to the incorporation of the three different rare earth cations. The temperature coefficient of resonant frequency increased from 4.99 for the Sm-ceramics to 9.92 ppm/ ° C for the La-ceramics, attributed to the increase of cell polarization. [ABSTRACT FROM AUTHOR]

Herein, Ce3+ and Ce3+/Dy3+ co-doped Ca 3 Al 2 O 6 phosphors have been designed and synthesized via a facile citrate-based sol-gel technique, and their structural, photoluminescence properties and energy transfer phenomenon were investigated comprehensively. The XRD analysis indicated that pure Ca 3 Al 2 O 6 phase can be synthesized at low temperature (1000 °C) for merely 2 h. The photoluminescence spectra showed the dominant emission of Ce3+ singly doped phosphors is located in the blue region even at low Ce3+ doping level, which indeed favors the energy transfer from Ce3+ to other luminescent centers. When Dy3+ is co-doped into Ca 3 Al 2 O 6 :Ce3+ phosphors, the remarkable sensitizing effect of Ce3+ on Dy3+ is validated by comparatively analyzing the excitation, emission spectra and average lifetimes of the series of samples. Through the concentration quenching theory, the critical distance between Ce3+ and Dy3+ is calculated to be 13.50 Å. Furthermore, the energy transfer mechanism between them is most likely ascribed to electric dipole-dipole interaction. In virtue of the variation of the emission intensities of Ce3+ and Dy3+, the emitting colors of Ca 3 Al 2 O 6 :Ce3+, Dy3+ phosphors can realize tunable luminescence from deep blue to bluish-white region through controlling the Dy3+ content. Based on these analysis, Ca 3 Al 2 O 6 :Ce3+, Dy3+ phosphors could potentially be applied as a single-phase color-tunable phosphors pumped by near-ultraviolet (n-UV) radiation. • Developed a facile sol-gel method to prepare successfully Ca 3 Al 2 O 6 compound. • The blue emission of as-prepared Ca 3 Al 2 O 6 :Ce3+ phosphors dominates, which favors the energy transfer process. • The possible mechanism for the dominance of blue emission was discussed. • The energy transfer phenomenon in Ca 3 Al 2 O 6 :Ce3+, Dy3+ phosphors was investigated in detailed. • Ca 3 Al 2 O 6 :Ce3+, Dy3+ can serve as a single-phase color-tunable phosphors excited by near-ultraviolet radiation. [ABSTRACT FROM AUTHOR]

Abstract: The crystal structure and photoluminescence properties of Eu2+ doped Li2Ca0.7Sr0.3SiO4 phosphors were investigated. The Li2Ca0.7Sr0.3SiO4 is not an alloy between the tetragonal Li2CaSiO4 and hexagonal Li2SrSiO4 but crystallizes in orthorhombic structure similar to Li2(CaSr)SiO4. Photoluminescence properties of the Li2Ca0.7Sr0.3SiO4:Eu2+ phosphors, summarized in effective excitation in the UV region, strong emission in the blue light range (with a peak at 427nm) and the CIE chromaticity coordinate (0.154, 0.038), indicate this phosphor has great potential in UV-chip pumped white LEDs. White light output by mixing the Li2Ca0.7Sr0.3SiO4:Eu2+ blue and Li2SrSiO4:Eu2+ yellow phosphor was attempted. With proper molar ratio of these two compound phosphors, warm white light with CIE chromaticity coordinate close to that of the nature white light (0.33, 0.33) and color temperature about 5000K was obtained. The results indicated that the Li2Ca0.7Sr0.3SiO4:Eu2+ may become an important phosphor candidate for ultra-violet chip pumped and multi-phosphors converted white LEDs. [Copyright &y& Elsevier]

• Polymer-matrix composites. • 3-Dimensional reinforcement. • Thermal properties. • Syntactic foams. • Hollow glass microspheres. Electronic packaging materials with low dielectric constant (D k) and high thermal conductivity (TC) are of vital importance in mitigating signal delay and enhancing heat dissipation efficiency in modern electronics. However, low D k and high TC are difficult to complement each other, because high TC filler usually possesses a high D k. Herein, we have newly designed a composite material simultaneously with low D k and high TC through hollow glass microspheres (HGMs), boron nitride particles, epoxy resin and reticulated porous ceramic (RPC). The composite material prepared by sintering HGMs and RPC is more effective in improving TC while keeping low D k. Specifically, the D k of the newly designed composite is lower than 3.0 with a large TC of 0.96 W/m·K. This new epoxy-matrix composite with both low D k and high TC can shed new light on designing electronic packaging materials for advanced miniaturized electronics. [ABSTRACT FROM AUTHOR]