Synthesis of Long Afterglow Phosphor CaAl2Si2O8 ：Eu^2＋, Dy^3＋ via Sol-Gel Technique and Its Optical Properties

The long afterglow phosphor CaAl2Si2O8：Eu^2＋ , Dy^3＋ was prepared by a sol-gel method. The sol-gel process and the structure of the phosphor were investigated by means of X-ray diffraction analysis （XRD）. It is found that the single anorthite phase formed at about 1000 %, which is 300 % lower than that required for the conventional solid state reaction. The obtained phosphor powders are easier to grind than those of solid state method and the partical size of phosphor has a relative narrow distribution of 200 to 500 nm. The photoluminescence and afterglow properties of the phosphor were also characterized. An obvious blue shift occurs in the excitation and emission spectra of phosphors obtained by sol-gel and solid state reaction methods. The change of the fluorescence spectra can be attributed to the sharp decrease of the crystalline grain size of the phosphor resulted from the sol-gel technique.     

Characterization and Stability of La0.5Sr0.5CoO2.91 Perovskite-Type Oxide

Compositely doped oxide La0.5Sr0.5CoO2.91 （LSC） was synthesized using solid state reaction and citric acid-nitrate low temperature self-propagating combustion methods. The crystal structure and the particle size micrograph of LSC powders synthesized by different methods were investigated with XRD and SEM. The experimental results show that the single perovskite phase of LSC can be synthesized by solid state reaction method, but LaSrCoO4 phase appears in LSC powder synthesized by citric acid-nitrate low temperature self-propagating combustion method. The LSC particle by citric acid-nitrate low temperature self- propagating combustion method has smaller size. To analyze the character of cathode material based on Ceo.gGdo.101.95（GDC） electrolyte, two types of cathode wafers were fabricated with the two kinds of LSC and GDC powders at the mass rate of 6：4, respectively. The electrical conductivity of the sintered samples was measured by four probe DC method from 300 to 800 ℃. The cathode with LSC particle by citric acid- nitrate low temperature self-propagating combustion method has higher electrical conductivity. In order to investigate the stability, the two samples were put into the muffle furnace to heat up in air at 800℃for 800 h. To analysis the reason for reduced electrical conductivity, the crystal structure and the particle micrograph of the cathode wafers before and after an exposure were investigated with XRD and SEM. The result shows that new crystal structure appears in both the two kinds of cathode wafers and crystal micrographs change a lot.     

Effect of different synthesis techniques on structural,magnetic and magneto-transport properties of Pr0.7Sr0.3MnO3 manganite

We investigated the effect of different synthesis techniques on the structural, magnetic and magneto-transport properties of Pr0.7Sr0.3MnO3 (PSMO) samples. The samples were synthesized by three different techniques: solid state reaction, sol-gel and chemical Co-precipitation method. XRD studies confirmed the single phase formation of PSMO by all three techniques. It was also found that the magnetotransport properties of PSMO strongly depended on the synthesis techniques. A substantial decrease in the insula...     

Preparation and Characterization of Red Luminescent Ca0.8 Zn0.2 TiO3 ： Pr3 ＋ , Na^＋ Nanophosphor

Nanophosphor with the nominal composition of Ca0.8 Zn0.2 TiO3 ： Pr3 ＋ , Na^＋ （CZTOPN） was synthesized at relatively low temperature by the sol-gel method. Metal ions were dispersed by citric acid in ethylene glycol solvent and then react with Ti（OC4H9）4 to form sol and gel. The decomposition process of the precursor, and crystallization and particle size of CZTOPN were examined by thermal analysis （TG-DSC）, powder X-ray diffraction （XRD）, and scan election microscopy （SEM）. Results of TG-DSC and XRD reveal that the composition of Ca0.8 Zn0.2 TiO3 ： Pr3 ＋ , Na^＋ changes with the sintering temperature. SEM data indicate that the diameter of particles is under 50 nm even if the sintering temperature increases to 1000 ℃. In contrast to a solid state reaction, the excitation spectra of samples synthesized by the sol-gel method shift blue about 10 nm and the emission intensity at 617 nm increases significantly.     

Synthesis and Luminescent Properties of Novel Red Long-Lasting Phosphor Ca2Zn4Ti15O36：Pr^3＋

A novel red long-lasting phosphor Ca2Zn4Ti15O36:Pr were synthesized by solid state reaction and by sol-gel method. It is a new type of Pr^3 -doped titanate red long lasting phosphor. It is difficult to make pure Ca2Zn4Ti15O36 crystalline by solid state reaction and it must be sintered at 1200℃ for 96 h.The analysis results of thermogravimetric curve and Xray powder diffraction revealed that Ca2Zn4Ti15O36 canbe formed by sintering precursor at 700℃ for 12 h,     

Preparation and Characterization of Y_3Sc_2Ga3O（12） Nano-Polycrystalline Powders by Co-Precipitation Method

In order to grow high-quality gallium garnet crystals,polycrystalline materials were used as starting materials.YSGG precursor was synthesized by co-precipitation method using aqueous ammonia as a precipitator,and the precursor was then sintered at different temperatures.The results showed that the feasible pH range was 8.3～9.84 in the process of co-precipitation reaction.The YSGG precursor and the powders sintered at different temperatures were characterized by IR,XRD and TEM methods.It was found that the precursor transformed to pure YSGG polycrystalline phase at 800 ℃.YSGG nano-polycrystalline powders sintered at 800～1000 ℃ were well dispersed and the sizes of the YSGG grains were about 40～100 nm.     

Preparation of CaS：Eu^2＋ , Sm^3＋ by Solid Reaction Method and Its Photostimulated Luminescence

The CaS:Eu^2 , Sm^3 powders were prepared by high-temperature solid method in a reducing atmosphere. The influences of temperature and fired-time on properties of samples were studied. XRD analysis shows that crystal structure of CaS has formed at 700℃. Spectrum analysis results show that the samples which were stimulated by 980 nm laser after excited by ultraviolet lamp emit red luminescence peaking at 649 nm.     

Preparation and Electrical Transport Properties of Perovskite Oxide Ln0.5Sr0.5CoO3

The superfine powders of Ln0.5 Sr0.5 CoO3 （Ln = La, Pr, Nd, Sm, Eu） were obtained by solid state reactions. The crystal structure and electrical transport properties of samples doped with different rare earth elements as well as the forming process of the Perovskite structure were studied. The result shows that when the temperature reaches 1200 ℃, the samples will become a steady and unitary Perovskite phase by solid state reactions. The conductive behavor at low temperature is consistent with small polaron mechanism （i. e., localized electronic carriers having a thermally activated mobility）. However, the maximum of conductivity appears at about 700 ℃, and the conductivity of La0.5Sr0.5CoO3 is the biggest in the intermediate-temperature （600 - 850 ℃ ）, so it is fit for cathode material of intermediate-temperature solid oxide fuel cells.     

Preparation of Perovskite-Type Oxides La1-x Srx Fe1-y Coy O3 Using EDTA Sol-Gel Method

Two series of perovskite-type oxides with composition La1-xSrxFeO3 (x≤0.8)and La1-xSrxFe1-yCoyO3( x = 0.2；y = 0.2, 0.4 ) powder productions were synthesized by EDTA complexing sol-gel method. The products were characterized by XRD, TEM, SEM, BET method (N2 adsorption)and laser granularity analysis for different synthesis conditions to obtain the optimum conditions for the preparation process. Single-phased, uniform perovskite-type oxides with small particle size were obtained by EDTA sol-gel process with high stability and repeatability,and the process temperature is much lower than that of solid state reaction method.     

Synthesis and Luminescence Properties of Gd2O3：Eu^3＋ Phosphors

Gd2O3: Eu^3 phosphors were prepared by urea homogeneous precipitation with different surfactant and sol-gel method. XRD patterns show that all the obtained samples are in cubic Gd2O3, and the results of FTIR and fluorescent spectra conformed that OP is a good surfactant for preparing the Gd2O3:Eu^3 phosphors. The SEM photographs show that the particles prepared by urea homogeneous precipitation method are all spherical and well-dispersed, and grain morphology can be controlled by different surfactant. XRD and SEM indicate that the particle sizes prepared by sol-gel method are in the range of 5-30 nm, and the grain sizes increase with increasing of heated temperatures. Luminescence spectra indicat that the main emission peaks of all samples are at 610 nm, the intensities are different from samples prepared with different surfactant and the luminescence intensities increase with increasing of annealed temperatures.     

Structure properties and sintering densification of Gd2Zr2O7 nanoparticles prepared via different acid combustion methods

Gadolinium zirconate(Gd2Zr2O7) nanocrystals were prepared via two different combustion methods: citric acid combustion(CAC) and stearic acid combustion(SAC). The effects of the different preparation methods on the phase composition, microtopography, and sintering densification of the resulting Gd2Zr2O7 nanopowders were investigated by thermal-gravimetric and differential thermal analysis(TG-DTA), Fourier transform infrared spectroscopy(FTIR), X-ray diffraction(XRD), and transmission electron microscopy(TEM) techniques. The results indicated that both methods could produce Gd2Zr2O7 nanopowders with an excellent defective fluorite structure. The reaction time was reduced by the SAC method, compared with the CAC method. The nanopowders synthesized by the two methods were different in grain size distribution. The resulting nanoparticle diameter was about 50 nm for CAC and 10 nm for SAC. After vacuum sintering, the sintered bodies also had a different relative density of about 93% and 98%, respectively. Thus the preparation of Gd2Zr2O7 nanopowders by SAC was the first choice to achieve the desired sintering densification.     

Influence of oxygen non-stoichiometry on physical properties of NdSr2Mn2O7±δ

Nd Sr2Mn2O7+δ compounds were synthesized by ceramic method under three different cooling conditions. The Nd Sr2Mn2O7+δ samples were characterized by powder X-ray diffraction(XRD). Oxygen non-stoichiometry data for the studied powders were determined by using gravimetric and X-ray photoelectron spectroscopy(XPS) methods. The correlation of cooling method and oxygen as non-stoichiometry was established. The electroconductivity in samples was studied by using four-point probe method, and the strong correlation with non-stoichiometry was found out. Magnetization measurements were carried out. It was found that the magnetic and transport properties of the samples were also influenced by oxygen non-stoichiometry. The evolution of the magnetic properties could be explained by the formation of magnetic clusters in the vicinity of oxygen vacancies(OV) and strong competition between the superexchange and double exchange interactions.     

Preparation of Sr_2Fe_(1-x)Sc_xMoO_(6-δ) nanopowders and its electrical conductivity

Double-perovskite Sr2Fe1-xScxMoO6-δ (x=0, 0.05, 0.1, 0.2, 0.3, 0.4) powders applied to the cathode of solid oxide electrolysis cells were synthesized by the sol-gel citrate combustion method. Initial powders were calcined at different temperatures under different atmosphere (air, H2(4 vol.%)/Ar), and the effects of the preparation process on the structure and the morphology of the powders were investigated by thermal analysis (TG/DSC), X-ray diffraction (XRD), scanning electron microscopy (SEM) and surface area analysis. The electric conductiv-ity of the materials was measured by electrochemical work station using wafers prepared by dry pressing. It was found that the formation of perovskite structure was related to the content of Sc and combustion improver (NH4NO3), pH value, calcining temperature and atmosphere. A single perovskite phase of Sr2Fe1-xScxMoO6-δ could be formed after 3 h calcining in reducing atmosphere of H2 (4 vol.%)/Ar at 1100 oC. The electrical property indicated that, this material had a potential to be used in medium/high temperature solid oxide fuel cells or electrolysis cells.     

Thermoelectric Properties of （Ce, La）yFe1.0Co3.0Sb12 Compounds Syntiesized by Solid State Reaction

The filled Skutterudite compounds (Ce,La)yFexCo4-xSb12 with x= 1.0 and y=0-0.3 were synthesized by solid state reaction and Spark PlasmaSintefing (SPS) using powders of Co, Sb, Fe and rare earth Ce, La as starting materials. The thermoe-lectric properties of the compounds were also studied.It is shown that the almost single phase Skutterudite compounds (Ce, La)yFex Co4-xSb12 are synthesized at900-1000K and all samples show p-type.     

Solid state reaction synthesis and total electrical conductivity of La_(0.7)Sr_(0.3)Cr_yMn_zCo_(1-y-z)O_(3-δ)

The La0.7Sr0.3CryMnzCo(1-y-z)O3-δ samples were prepared by solid state reaction.The phases,microstructure and properties of the samples were investigated by XRD,SEM,DC four-probe method and iodometry method.The single orthorhombic phase La0.7Sr0.3CryMnzCo(1-y-z)O3-δ perovskite oxides were obtained when sintered at l350 °C for 10 h.The oxygen nonstoichiometry of the materials varied inversely with the total electronic conductivity.The sample with composition of La0.7Sr0.3Cr0.5Mn0.35 Co0.15O3-δ had the maximal total electronic conductivity and the lowest oxygen nonstoichiometry which were 22.4 S/cm and 0.040 at 850 °C,respectively.The low total electronic conductivity is related to the low relatively density of the samples directly.The activation energy of conduction changed at 550 °C,and the activation energy of conduction at high temperature(T550 °C) was higher than that at low temperature range(T550 °C).     

Enhancement of secondary emission property of molybdenum cathode co-doped with La_2O_3 and Y_2O_3

La2O3 and Y2O3 co-doped Mo secondary emitters were prepared by three kinds of doping method combined with high temperature plasma sintering.The secondary electron emission property and microstructure of the cathodes were studied.It showed that the cathode prepared by liquid-liquid doping method exhibited the best emission property among all the samples prepared by liquid-solid doping,solid-solid doping and liquid-liquid doping methods due to a uniform distribution of different substances.RE2O3 existed unifo...     

Thermoluminescence characteristics and dosimetric aspects of fluoroperovskites （NaMgF3：Eu2＋,Ce3＋）

The perovskite-like NaMgF3 polycrystalline powder samples, pure and rare earth doped, were synthesized by conventional solid state reaction method. The perovskite material was doped with 0.2 mol.% of EuF3 and CeF3 impurity. Phase purity of synthe-sized compounds was analyzed by powder X-ray diffraction technique. The thermoluminescence response of polycrystalline samples showed a linear response up to 12 Gy and then became sub linear at higher doses. The order of kinetics （b）, activation energy （E） and other trapping parameters were calculated using peak shape method and variable heating rate method. From glow curve analysis the symmetric factor was calculated. The glow curve showed two peaks at 404 and 488 K, and both of them confirmed the thermolumi-nescence in the phosphor, which obeyed second-order kinetics. The experimental resulted showed that this phosphor could have po-tential applications in radiation dosimetry.     

Luminescence Properties of Tb^3＋ -Doped LuAG Films Prepared by Pechini Sol-Gel Method

Lu3Al5O12（LuAG） thin films with different Tb^3＋ concentration were prepared on carefully cleaned （111 ） silicon wafer by a Peehini process and dip-coating technique. Heat treatment was performed in the temperature range from 800 to 1100 ℃. The crystal structure was analyzed by XRD. The results show that LuAG film starts to crystallize at about 900 ℃, and the particle size increases with the sintering temperature. Excitation and emission spectra of Tb^3＋ doped LuAG films were measured. The effects of heat-treatment temperature and doping concentration of Th3 ＋ on the luminescent properties were also investigated. For a comparison study, Th^3＋-doped LuAG powders were also prepared by the same sol-gel method.     

Microstructures and properties of CuZrAl and CuZrAlTi medium entropy alloys prepared by mechanical alloying and spark plasma sintering

Equiatomic CuZrAl and CuZrAlTi medium entropy alloys were designed and synthesized by mechanical alloying and spark plasma sintering technique.The alloying behavior,phase evolutions,microstructures and properties of samples were investigated by X-ray diffraction,differential scanning calorimetry,field emission scanning electron microscopy,microscopy/Vickers hardness testing and electrochemical polarization measurement.The results indicate that the final products of as-milled alloys consist of amorphous phases.Ti addition improves the glass forming ability of as-milled alloys.The as-sintered CuZrAl alloy contains face-centered cubic(fcc)solid solution,Al_(1.05)Cu_(0.95) Zr and AlZr_2 phases at different sintering temperatures.With Ti addition,the as-sintered sample is only composed of intermetallics at 690°C,while fcc1,fcc2 and CuTi3phases are formed at 1100°C.CuZrAlTi-1100°C alloy exhibits the highest hardness value of 1173HV0.2owing to the high sintering density,solid solution strengthening and homogeneous precipitation of nano-size crystalline phase.CuZrAlTi-690°C alloy presents a similar corrosion resistance with304 Lstainless steel in seawater solution and further possesses the lower corrosion rate.     

Preparation of transparent Y2O3 ceramic by slip casting and vacuum sintering

In the present work transparent Y2O3 ceramics were made by slip casting and vacuum sintering of nanopowders with sodium poly-acrylic acid(PAA-Na) as dispersant.The rheological properties of Y2O3 nanopowder slurry were investigated using different amounts of dis-persant and solid contents.The microstructures and transmittance of the sintered ceramics were also studied by means of scanning electron microscopy(SEM) and ultra-violet visible spectrometry.The results showed that rheological behaviors of the Y2O3 nanopowder slurry were effectively promoted by sodium polyacrylic acid.Highly dispersive and stable slurries were obtained as the dispersant was added over 1.0 dwb% under the fixed conditions of pH 11 and 45 wt.% solid content.All the slip cast green bodies were sintered into highly dense ceramics after sintering at 1700 oC for 5 h in vacuum,wherein the sample added with 1.1% sodium polyacrylic acid exhibited the highest relative den-sity of 99.36% and transmission of 30% at 800 nm wavelength.