Synthesis,luminescence, and effect of heat treatment on the properties of Y<Subscript>3</Subscript>Al<Subscript>5</Subscript>O<Subscript>12</Subscript>:Ce phosphor

YAG:Ce nanosized spherical precursors were synthesized by coprecipitation using ammonium hydrogen carbonate as precipitant. Composition, phase transition, morphologies, and luminescence properties of the powders during calcination were studied. The precursors directly convert to pure YAG structure at about 900°C. The mean size of precursors is about 100 nm, and the grain size increases with increase of calcination temperature. When calcined above 1400°C, the grain size comes into a micrometer. With increase of calcination temperature, the luminescent intensity increases, and the emission band shows a redshift, while the lifetime increases.     

Synthesis,crystal structure and luminescence in Ca<Subscript>3</Subscript>Al<Subscript>2</Subscript>O<Subscript>6</Subscript>

Bluish green emitting phosphor, Ca₃Al₂O₆:Ce³⁺, is prepared by low-temperature combustion method. X-ray diffraction, photoluminescence, scanning electron microscopy techniques are used to characterize the synthesized phosphor. The most efficient bluish green (483 nm) emission is observed under the excitation by near UV light. The emission characteristics are credited to 5d → 4f type transitions in Ce³⁺. The luminescence properties of Eu²⁺ are predicted for the first time from those of Ce³⁺. Also, photoluminescence of Eu³⁺ is studied in the same host. The emission spectrum of Ca₃Al₂O₆:Eu³⁺ shows the peak at 592 (orange) and 614 nm (red) wavelengths. Ca₃Al₂O₆:Ce³⁺phosphor can be a potential blue phosphor for field emission display, solid-state lighting and LED.     

Microstructure and high-temperature strength of Al<Subscript>2</Subscript>O<Subscript>3</Subscript>/Er<Subscript>3</Subscript>Al<Subscript>5</Subscript>O<Subscript>12</Subscript>/ZrO<Subscript>2</Subscript> ternary melt growth composite

A new Al₂O₃/Er₃Al₅O₁₂(EAG)/ZrO₂ ternary MGC (Melt Growth Composite) with a novel microstructure has been fabricated by unidirectional solidification. This ternary MGC has a microstructure consisting of continuous networks of single-crystal Al₂O₃, single-crystal EAG and fine cubic-ZrO₂ phases without grain boundaries. The ternary MGC has also characteristic dimensions of the microstructure of around 2–4 m for EAG phases, around 2–4 m for Al₂O₃ phases reinforced with around 0.4–0.8 m cubic-ZrO₂ phases. No amorphous phases are formed at interfaces between phases in the ternary MGC. The ternary MGCs flexural strength at 1873 K is approximately 700 MPa, more than twice the 330 MPa of the Al₂O₃/EAG binary MGC. The fracture manner of the Al₂O₃/EAG/ZrO₂ ternary MGC at 1873 K shows the same intergranular fracture as the Al₂O₃/EAG binary MGC, but is significantly different from the transgranular fracture of the sintered ceramic.     

Luminescence properties and preparation of Lu<Subscript>3</Subscript>Al<Subscript>5</Subscript>O<Subscript>12</Subscript> powder doped with Ce and Pr ions

Lu₃Al₅O₁₂:Ce³⁺ phosphor powder, which exhibits green emission band, was synthesized by the high-temperature solid-state reaction method with a flux BaF₂. X-ray diffraction (XRD), photoluminescence (PL) spectra, and fluorescent lifetime spectra were used to characterize the structure and luminescent properties of the sample. The XRD patterns indicated that when prepared at 1550 °C for 3 h with 4 wt% flux, Lu₃Al₅O₁₂:Ce³⁺ phosphors powder is the garnet cubic crystal system structure. Photoluminescence (PL) spectra showed that the Lu₃Al₅O₁₂:Ce³⁺ phosphor powder can be effectively excited by near ultraviolet and blue light, emitting broad band peaking at 505 nm, which is attributed to ²F_5/2?→?²D_5/2 transition. The self-concentration quenching mechanism of Ce³⁺ is the dipole–dipole interaction. Small amount of Pr³⁺ increased red light emission at 610 nm. Photoluminescence (PL) spectra and fluorescent lifetime spectra indicated that there was an efficient energy transfer process between Ce³⁺ and Pr³⁺.     

Ultrafine Cr-Doped Al<Subscript>2</Subscript>O<Subscript>3</Subscript> Prepared by Detonation Synthesis

Data are presented on the phase composition, particle size distribution, EPR, and luminescence of ultrafine chromium-doped alumina powders prepared by detonation synthesis. The largest particles in the powders are shown to consist mainly of a Cr₂O₃ solid solution in α-Al₂O₃. The luminescence spectrum of fine particles shows, in addition to lines characteristic of ruby, extra lines which are tentatively attributed to Cr³⁺ ions incorporated substitutionally into θ-Al₂O₃.__________Translated from Neorganicheskie Materialy, Vol. 41, No. 8, 2005, pp. 948–954.Original Russian Text Copyright © 2005 by Lyamkina, Chiganova, Slabko, Vorotynov, Taranova.     

Directional solidification and growth characteristics of Al<Subscript>2</Subscript>O<Subscript>3</Subscript>/Er<Subscript>3</Subscript>Al<Subscript>5</Subscript>O<Subscript>12</Subscript>/ZrO<Subscript>2</Subscript> ternary eutectic ceramic by laser floating zone melting

Directionally solidified Al₂O₃/Er₃Al₅O₁₂/ZrO₂ ternary eutectic ceramic in situ composite rods with length of 110 mm have been fabricated by laser floating zone melting. The microstructural characteristics of steady growth zone, initial growth zone and solid/liquid interface are investigated under high temperature gradient. In the steady growth zone, the eutectic spacing (λ) is rapidly decreased as increasing the growth rate (V), and the corresponding relationship between growth rate and eutectic spacing is determined to be λ = 11.14 × V ^?1/2. The temperature gradient has been measured to be about 5.3 × 10³ K/cm. In the initial growth zone, the melting process and temperature distribution are recorded by infrared thermal imager, and several unstable complex microstructures are observed. In the quenched zone, the regular eutectics with minimum eutectic spacing of 200 nm are obtained. Moreover, the solid/liquid interface during solidification shows convex interface morphology and the interface height is gradually decreased as increasing the growth rate. The eutectic growth behaviors at the center and edge of the as-grown rod are compared and discussed.     

Production of the Y<Subscript>3</Subscript>Al<Subscript>5</Subscript>O<Subscript>12</Subscript> transparent nanostructured ceramics

The nanocrystalline Y₃Al₅O₁₂ ceramics with different phase compositions, microstructures, and optical characteristics have been prepared by low-temperature consolidation of the Y₃Al₅O₁₂ powder at pressures from 6 to 7.7 GPa in the temperature range from 250 to 550°C. The conditions have been defined for obtaining transparent nanostructured ceramics Y₃Al₅O₁₂ having grains of size 20–40 nm and a transmission coefficient in the visible region of 40–45%. The criteria for the transparency of the nanostructured ceramics have been formulated and the ways of an improvement of its optical characteristics are discussed.     

Electron traps in Gd<Subscript>3</Subscript>Ga<Subscript>3</Subscript>Al<Subscript>2</Subscript>O<Subscript>12</Subscript>:Ce garnets doped with rare-earth ions

The curves of thermally stimulated luminescence of Gd₃Ga₃Al₂O₁₂:Ce³⁺ ceramics (a nominally pure sample and samples doped with rare-earth ions) are measured in the temperature range of 80–550 K. The depth and the frequency factor of electron traps established by Eu and Yb impurities are determined. An energy-level diagram of rare-earth ions in the bandgap of Gd₃Ga₃Al₂O₁₂ is presented.     

Recombination processes in the Y<Subscript>3</Subscript>Al<Subscript>5</Subscript>O<Subscript>12</Subscript>:Ce<Superscript>3+</Superscript> scintillator

The roentgenoluminescence spectra, temperature-dependent activator luminescence, optically stimulated luminescence, and the effect of IR irradiation on the yield and spectral composition of the low-temperature roentgenoluminescence and thermoluminescence curves of the Y₃Al₅O₁₂:Ce³⁺ scintillator have been studied in the temperature range 85–295 K. The results, coupled with earlier data, suggest that the Ce³⁺ ions in the garnet crystal studied form Ce³⁺ p hole centers and increase the concentration of electronic F ^?-centers responsible for the IR stimulation band at 940 nm. The reduction in roentgenoluminescence yield on cooling Y₃Al₅O₁₂:Ce³⁺ to below 230 K is due to the significant localization of excited carriers at defects, which show up in thermoluminescence peaks and optical stimulation spectra. The low-temperature Ce³⁺ luminescence in Y₃Al₅O₁₂:Ce₃₊ seems to result from the recombination of activator-bound excitons.     

Anelastic behavior of 8Y-FSZ/Al<Subscript>2</Subscript>O<Subscript>3</Subscript> composite

This paper has clarified the anelasticity of 8Y-FSZ/α-alumina composites wherein the 8Y-FSZ phases are dispersed like islands. The amount of anelastic strain generated and the manner of anelastic deformation were compared to those of monolithic 8Y-FSZ. The anelastic strains of six kinds of 8Y-FSZ/α-alumina, as well as of monolithic 8Y-FSZ and monolithic α-alumina, were measured. The results showed that the anelastic strain was produced even in the composite where 8Y-FSZ phases existed as islands, and that the more the anelastic strain produced, the higher the volume fraction of 8Y-FSZ. In addition, the composition with a fully densified alumina phase had the effect of inhibiting anelastic strain in the 8Y-FSZ phase.     

Fabrication of Cr<Subscript>2</Subscript>O<Subscript>3</Subscript>/Al<Subscript>2</Subscript>O<Subscript>3</Subscript> composite nanofibers by electrospinning

PVA(Polyvinyl alcohol)/chromium nitrate/aluminum nitrate composite nanofibers were prepared by using sol–gel processing and electrospinning technique. By high temperature calcinating the above precursor fibers, Cr₂O₃/Al₂O₃ composite nanofibers were successfully obtained. The fibers were characterized by XRD, IR, and SEM, respectively. The results showed that the crystalline phase and the morphology of the fibers depended on the calcination temperatures.     

Temperature-Dependent Thermal Boundary Conductance at Al/Al<Subscript>2</Subscript>O<Subscript>3</Subscript> and Pt/Al<Subscript>2</Subscript>O<Subscript>3</Subscript> interfaces

With the ever-decreasing size of microelectronic devices, growing applications of superlattices, and development of nanotechnology, thermal resistances of interfaces are becoming increasingly central to thermal management. Although there has been much success in understanding thermal boundary conductance at low temperatures, the current models applied at temperatures more common in device operation are not adequate due to our current limited understanding of phonon transport channels. In this study, the scattering processes in Al and Pt films on Al₂O₃ substrates are examined by transient thermoreflectance testing at high temperatures. At high temperatures, traditional models predict the thermal boundary conductance to be relatively constant in these systems due to assumptions about phonon elastic scattering. Experiments, however, show an increase in the conductance indicating potential inelastic phonon processes.     

Crystallization and microstructures of Y-Si-Al-O-N glass-ceramics containing main crystal phase Y<Subscript>3</Subscript>Al<Subscript>5</Subscript>O<Subscript>12</Subscript>

A glass with the nominal composition of 28Y48Si24Al83O17N (in equal percentage) was chosen as parent glass in this paper to prepare Y₃Al₅O₁₂-based glass-ceramics. Differential scanning calorimetry (DSC), X-ray diffraction (XRD) and scanning electron microscopy (SEM) were used to assess the crystallization process of the parent glass. YAG as the only crystalline phase appears in all glass-ceramics produced under 1250°C. A small amount of O’-Sialon secondary phase starts to precipitate from parent glass samples as heat treatment temperature increases to 1250°C. Grain size of the dendrite crystal which corresponds to YAG phase increases and the dendrite branches get thickened as heat treatment temperature increases. Moreover, grain size of YAG phase resulting from two-stage heat treatment is much smaller than that of YAG phase obtained by one-stage heat treatment. The results are relevant to developing improved crystallization treatments for glasses with potential for crystallization to YAG-based glass-ceramics and for heat treatments of YAG/β-SiAlON materials.     

Kinetics of mechanically activated P<Subscript>2</Subscript>O<Subscript>5</Subscript> incorporation into Al<Subscript>2</Subscript>O<Subscript>3</Subscript>

The incorporation of phosphoric anhydride into - and -aluminas during mechanical activation is investigated. An empirical equation is proposed for the kinetics of P₂O₅ incorporation. The effect of the specific power of the mill on the amount of bound P₂O₅ is analyzed.Translated from Neorganicheskie Materialy, Vol. 41, No. 3, 2005, pp. 321–323.Original Russian Text Copyright © 2005 by Kosenko, Smirnova, Denisova.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.     

Synthesis and thermoluminescence/optically stimulated luminescence properties of CaB<Subscript>4</Subscript>O<Subscript>7</Subscript>:Ce phosphor

In this report, we presented the luminescence properties of CaB₄O₇:Ce phosphor synthesized by solid state method. The structural property was studied through X-ray diffraction and surface morphology was studied through scanning electronic microscope. Additionally, the photoluminescence (PL), thermoluminescence (TL) and optically stimulated luminescence (OSL) behaviors of CaB₄O₇:Ce phosphor was studied. Prepared phosphor was found to be in monoclinic structure, with the space group P21/n (14). The TL sensitivity of CaB₄O₇:Ce phosphor was 0.8 time than that of TLD-100 and kinetics parameters such as activation energy (eV), frequency factors (s) and order of kinetics were calculated by using peak shape method. The phosphor shows OSL sensitivity about 0.46 times than that of α-Al₂O₃:C (BARC). The decay pattern of prepared phosphor was faster than decay pattern of α-Al₂O₃:C phosphor. In OSL mode dose–response was almost linear in the range of measurement. Minimum detectable dose was found to be 35.40 mGy with 3σ of background. The effective atomic number (Z_eff) of prepared phosphor is nearly similar to Z_eff of Al₂O₃:C phosphor. The PL spectrum of CaB₄O₇:Ce showed emission in near blue region for the excitation of 290 nm under UV source.     

Nucleation of the Plasticity at Nanodeformation of the Y<Subscript>3</Subscript>Al<Subscript>5</Subscript>O<Subscript>12</Subscript> Yttrium-Aluminum Garnet

The nanoindentation in the continuous stiffness measurement (CSM) mode was used to study the nucleation of the plasticity at the nanodeformation of the yttrium-aluminium garnet (YAG) having a low ((111) YAG single crystal after the annealing at the temperature of 1300°C) and a high (polycrystalline yttrium-aluminium garnet with a grain size of ~ 20 μm after the mechanical polishing) density of dislocations. For a sample having a high dislocations density a smooth elastoplastic transition was observed in the nanocontact as a result of the motion and multiplication of dislocations that are already present in the sample. For (111) YAG single crystal after annealing at the temperature of 1300°C an abrupt elastoplastic transition (pop-in) caused by a homogeneous nucleation of dislocations in the region under the contact was observed.     

Effect of grain size on the strength of Y<Subscript>3</Subscript>Al<Subscript>5</Subscript>O<Subscript>12</Subscript> optical ceramics

Using micro- and nanoindentation techniques, we have studied the mechanical properties of Y₃Al₅O₁₂ optical ceramics: coarse-grained, prepared by vacuum sintering, and nanostructured, prepared by high-pressure, low-temperature sintering. The effect of grain size on the strength of the ceramics has been analyzed.     

Formation and structural phase transitions of mesoporous Al<Subscript>2</Subscript>O<Subscript>3</Subscript> and TiO<Subscript>2</Subscript>/Al<Subscript>2</Subscript>O<Subscript>3</Subscript> xerogels under hydrothermal conditions

We have studied the effect of the hydrothermal synthesis temperature on Al₂O₃ structure formation and examined the role of the phase composition of the precursor gel and surfactant in the formation of the pore structure of Al₂O₃. A technique has been proposed for the synthesis of TiO₂/Al₂O₃ binary xerogels, and the effect of TiO₂ content on the pore structure parameters and adsorption properties of TiO₂/Al₂O₃ has been investigated.     

Synthesis,tunable luminescence and thermal stability of Mg<Subscript>2</Subscript>Al<Subscript>4</Subscript>Si<Subscript>5</Subscript>O<Subscript>18</Subscript>:Ce<Superscript>3+</Superscript>/Mn<Superscript>2+</Superscript> phosphors

Ce³⁺/Mn²⁺ singly doped and codoped Mg₂Al₄Si₅O₁₈ phosphors were synthesized by a solid state reaction. The phase, luminescent properties and thermal stability of the synthesized phosphors were investigated. Ce³⁺ and Mn²⁺ singly doped Mg₂Al₄Si₅O₁₈ phosphors show emission bands locating in blue and yellow–red regions, respectively. In Ce³⁺ and Mn²⁺ codoped Mg₂Al₄Si₅O₁₈, tunable luminescence was obtained because of the energy transfer from Ce³⁺ to Mn²⁺. In Mg₂Al₄Si₅O₁₈:Ce³⁺/Mn²⁺ phosphors with a fixed Ce³⁺ concentration, energy transfer efficiency increases with the increasing Mn²⁺ concentration, which is confirmed by the continually decreasing intensity and shortening decay time of Ce³⁺ emission. Moreover, the luminescent properties and thermal stability provide a great significance on the applications in the field of light emitting diodes.