In this study, green barium strontium silicate phosphor (BaSrSiO4:Eu3+, Eu2+) was synthesized using a solid-statereaction method in air and reducing atmosphere. Investigation of the firing temperature indicates that a single phase of BaSrSiO4is formed when the firing temperature is higher than 1400oC. The effect of firing temperature and doping concentration onluminescent properties are investigated. The light-emitting property was the best when the molar content of Eu2O3 was 0.025mol. Also, the luminescent brightness of the BaSrSiO4 fluorescent substance was the best when the particle size of the bariumwas 0.5µm. BaSrSiO4 phosphors exhibit the typical green luminescent properties of Eu3+ and Eu2+. The characteristics of thesynthesized BaSrSiO4:Eu3+, Eu2+ phosphor were investigated using X-ray diffraction (XRD) and scanning electron microscopy.The maximum emission band of the BaSrSiO4:Eu3+, Eu2+ was 520nm.

The effect of BaF2 flux in Y3Al5O12:Ce3+(YAG:Ce) formation was investigated. Phase transformation ofY3Al5O12(YAG) was characterized by using XRD, SEM, and TEM-EDS, and it was revealed that the sequential formation ofthe Y4Al2O9(YAM), YAlO3(YAP) and Y3Al5O12(YAG) in the temperature range of 1000-1500oC. Single phase of YAG wasrevealed from 1300oC. In order to find out the effect of BaF2 flux, three modeling experiments between starting materials(1.5Al2O3−2.5Y2O3, Y2O3−BaF2, and Al2O3−BaF2) were done. These modeling experiments showed that the nucleationprocess occurs via the dissolution-precipitation mechanism, whereas the grain growth process is controlled via the liquid-phasediffusion route. YAG:Ce phosphor particles prepared using a proposed technique exhibit a spherical shape, high crystallinity,and an emission intensity. According to the experimental results conducted in this investigation, 5% of BaF2 was the bestconcentration for physical, chemical and optical properties of Y3Al5O12:Ce3+(YAG:Ce) that is approximately 10-15% greaterthan that of commercial phosphor powder.

[ Zn2(1-x)MnxSiO4 ]0.07≤x≤0.15) green phosphor was prepared by solid state reaction. The first heating was at 900˚C-1250˚C in air for 3 hours and the second heating was at 900˚C in N2/H2(95%/5%) for 2 hours. The size effect of SiO2 in forming Zn2SiO4 was investigated. The temperature for obtaining single phase Zn2SiO4 was lowered from 1100˚C to 1000˚C by decreasing the SiO2 particle size from micro size to submicro size. The effect of the activators for the Photoluminescence (PL) intensity of Zn2SiO4:Mn2+ was also investigated. The PL intensity properties of the phosphors were investigated under vacuum ultraviolet excitation (147 nm). The emission spectrum peak was between 520 nm and 530 nm, which was involved in green emission area. MnCl2·4H2O, the activator source, was more effective in providing high emission intensity than MnCO3. The optimum conditions for the best optical properties of Zn2SiO4:Mn2+ were at x = 0.11 and 1100˚C. In these conditions, the phosphor particle shape was well dispersed spherical and its size was 200 nm.

In this study, high purity fine powders were prepared by SHS (Self-propagating High-temperature Synthesis). We would examinate the study of sintering properties and characteristics as a function of temperature with various additives (binder, sintering agent). In separately binder addition, the green and sintered density of specimen were increased as binder content increases. The increased porosity resulted in fine grain size due to the inhibition of grain boundary moving. The and MgO playa role of increasing dielectric constants at room temperature. These values were decreased at curie temperature. In case of , the Curie temperature was decreased. In this study, a high dielectric ceramic capacitor material with temperature stability was synthesized by using various additives