Ultra-fine Ce:YAG phosphors were prepared by homogeneous precipitation under microwave irradiation method. The formation of Ce:YAG was investigated by means of XRD and DTA/TG. The purified YAG crystallized phase was o...Ultra-fine Ce:YAG phosphors were prepared by homogeneous precipitation under microwave irradiation method. The formation of Ce:YAG was investigated by means of XRD and DTA/TG. The purified YAG crystallized phase was obtained at a lower temperature (1100 ℃). Basically spherical Ce:YAG powders were indicated from TEM images, and the size of the particles is about 80 nm. Two peaks of 436 and 473 nm can be seen from the excitation spectrum in the range of 402~510 nm. A broad emission band located at 480~630 nm shows the phosphors prepared by this method have good emission properties.展开更多
The sub-micron sized YAG∶Ce phosphors were synthesized via a modified sol-gel method by peptizing nano-pesudoboehmite particulate. It is found that YAG phase from the dried gel powders appears at 1000 ℃ then the pur...The sub-micron sized YAG∶Ce phosphors were synthesized via a modified sol-gel method by peptizing nano-pesudoboehmite particulate. It is found that YAG phase from the dried gel powders appears at 1000 ℃ then the pure YAG phase exists at a relatively lower sintering temperature of 1400 ℃. The smaller sizes of phosphors in the ranges of 1~3 μm are obtained due to the contribution of seeding effects of nano-sized alumina particles to strengthen each step of the processes. Both the excitation and emission spectra of photoluminescence of the phosphor obtained at 1400 ℃ meet well with the spectroscopic requirements of the WLED phosphors.展开更多
A novel synthesis process, based on the polyacrylamide gel method, was used to prepare Ce-doped YAG phosphor powders. Effects of heat treatment parameters, temperature and holding time, the fluxes, and atmosphere on m...A novel synthesis process, based on the polyacrylamide gel method, was used to prepare Ce-doped YAG phosphor powders. Effects of heat treatment parameters, temperature and holding time, the fluxes, and atmosphere on microstructure and particle morphology as well as luminescent properties of YAG:Ce3+ phosphor powders were studied by X-ray powder diffractometry, scanning electron microscopy, and fluorescence spectrophotometry. The results show that the formation temperature (1 000 ℃) of pure YAG phase is significant low when being synthesized by the polyacrylamide gel method, compared with solid-state reaction. For luminescent properties, the intensity of emission of YAG:Ce3+ phosphor increases steadily with increasing temperature from 900 ℃ to 1 300 ℃ and prolonging holding time from 100 min to 400 min. But blue shift phenomenon is observed for 400 min calcination. Fluxes as BaF2 and H3BO3 can enhance the intensity of emission of phosphor due to the improvement of crystallization of YAG and the stabilization of trivalence cerium ion in YAG host lattice at high temperature. Weak reduction atmosphere can contribute to improvement of the emission intensity of YAG:Ce3+ phosphor powders.展开更多
YAG∶Ce 3+ phosphor particles were prepared using polyacrylamide gel method. The structure evolution of powders during annealing process was followed by X-ray diffraction determination. It is found that some intermedi...YAG∶Ce 3+ phosphor particles were prepared using polyacrylamide gel method. The structure evolution of powders during annealing process was followed by X-ray diffraction determination. It is found that some intermediate phases, including θ-Al2O3, YAM and YAP, are formed when calcining polyacrylamide gel, however, the pure YAG phase can be formed directly when calcining polyacrylamide gel with α-Al2O3 as seed crystal. These facts show that the existence of α-Al2O3 seed crystal can block the formation of θ-Al2O3, YAM and YAP, and accelerate its reaction with Y2O3 to form YAG phase directly at lower temperature. The emission peak of prepared YAG∶Ce 3+ phosphor is wide with maximum at 550 nm and the exitation band has two peaks, the major one is around at 460 nm, which matches the blue emission of GaN LED and is suitable for the assemble of white LED. Some fluxes can enhance the photoluminescence intensity of phosphor particles, that can be attributed both to the improvement of crystallization processes of YAG and to the stabilization of trivalence cerium ion in YAG∶Ce 3+.展开更多
Spherical YAG∶Ce3+ phosphor particles with narrow size distribution were prepared by spray pyrolysis. The effects of the concentration of solution, the flow rate of carrier gas and the annealing temperature on the ph...Spherical YAG∶Ce3+ phosphor particles with narrow size distribution were prepared by spray pyrolysis. The effects of the concentration of solution, the flow rate of carrier gas and the annealing temperature on the phosphor morphology were studied. The productivity of precursor particles shows a trend of drop after rising with the increase of concentration. Raising the flow rate of nitrogen can improve the productivity of the precursor particles. Phosphor prepared by spray pyrolysis has obviously higher emission intensity than that synthesized by solid state reaction, spray pyrolysis makes Ce3+ ions well distributed in the crystal lattice as the luminescent centers, and phosphor particles have regular sphericity and narrow size distribution.展开更多
基金Project supported by Foundation for the Excellent Middle-Aged or Young Scientists of Shandong Province (02BS049)
文摘Ultra-fine Ce:YAG phosphors were prepared by homogeneous precipitation under microwave irradiation method. The formation of Ce:YAG was investigated by means of XRD and DTA/TG. The purified YAG crystallized phase was obtained at a lower temperature (1100 ℃). Basically spherical Ce:YAG powders were indicated from TEM images, and the size of the particles is about 80 nm. Two peaks of 436 and 473 nm can be seen from the excitation spectrum in the range of 402~510 nm. A broad emission band located at 480~630 nm shows the phosphors prepared by this method have good emission properties.
文摘The sub-micron sized YAG∶Ce phosphors were synthesized via a modified sol-gel method by peptizing nano-pesudoboehmite particulate. It is found that YAG phase from the dried gel powders appears at 1000 ℃ then the pure YAG phase exists at a relatively lower sintering temperature of 1400 ℃. The smaller sizes of phosphors in the ranges of 1~3 μm are obtained due to the contribution of seeding effects of nano-sized alumina particles to strengthen each step of the processes. Both the excitation and emission spectra of photoluminescence of the phosphor obtained at 1400 ℃ meet well with the spectroscopic requirements of the WLED phosphors.
文摘A novel synthesis process, based on the polyacrylamide gel method, was used to prepare Ce-doped YAG phosphor powders. Effects of heat treatment parameters, temperature and holding time, the fluxes, and atmosphere on microstructure and particle morphology as well as luminescent properties of YAG:Ce3+ phosphor powders were studied by X-ray powder diffractometry, scanning electron microscopy, and fluorescence spectrophotometry. The results show that the formation temperature (1 000 ℃) of pure YAG phase is significant low when being synthesized by the polyacrylamide gel method, compared with solid-state reaction. For luminescent properties, the intensity of emission of YAG:Ce3+ phosphor increases steadily with increasing temperature from 900 ℃ to 1 300 ℃ and prolonging holding time from 100 min to 400 min. But blue shift phenomenon is observed for 400 min calcination. Fluxes as BaF2 and H3BO3 can enhance the intensity of emission of phosphor due to the improvement of crystallization of YAG and the stabilization of trivalence cerium ion in YAG host lattice at high temperature. Weak reduction atmosphere can contribute to improvement of the emission intensity of YAG:Ce3+ phosphor powders.
文摘YAG∶Ce 3+ phosphor particles were prepared using polyacrylamide gel method. The structure evolution of powders during annealing process was followed by X-ray diffraction determination. It is found that some intermediate phases, including θ-Al2O3, YAM and YAP, are formed when calcining polyacrylamide gel, however, the pure YAG phase can be formed directly when calcining polyacrylamide gel with α-Al2O3 as seed crystal. These facts show that the existence of α-Al2O3 seed crystal can block the formation of θ-Al2O3, YAM and YAP, and accelerate its reaction with Y2O3 to form YAG phase directly at lower temperature. The emission peak of prepared YAG∶Ce 3+ phosphor is wide with maximum at 550 nm and the exitation band has two peaks, the major one is around at 460 nm, which matches the blue emission of GaN LED and is suitable for the assemble of white LED. Some fluxes can enhance the photoluminescence intensity of phosphor particles, that can be attributed both to the improvement of crystallization processes of YAG and to the stabilization of trivalence cerium ion in YAG∶Ce 3+.
基金Project supported by National "The Tenth Five-Year"plan (2003BA316A01-03-05) and "The Tenth Five-Year"Plan(BE2004021) of Jiangsu provicce
文摘Spherical YAG∶Ce3+ phosphor particles with narrow size distribution were prepared by spray pyrolysis. The effects of the concentration of solution, the flow rate of carrier gas and the annealing temperature on the phosphor morphology were studied. The productivity of precursor particles shows a trend of drop after rising with the increase of concentration. Raising the flow rate of nitrogen can improve the productivity of the precursor particles. Phosphor prepared by spray pyrolysis has obviously higher emission intensity than that synthesized by solid state reaction, spray pyrolysis makes Ce3+ ions well distributed in the crystal lattice as the luminescent centers, and phosphor particles have regular sphericity and narrow size distribution.
文摘荧光粉是制备白光发光二极管(LED)关键材料之一,其性能直接影响着白光LED亮度、色度、色温及显色指数.但是,现有荧光粉由于稳定性差、光衰严重等问题,使白光LED不能达到预期目标,迫切需要改进其制备工艺.采用高温固相合成法制备YAG:Ce3+黄色荧光粉,研究温度、Ce添加量等对荧光粉粒度、荧光强度等理化性质影响规律,并评价该荧光粉与蓝光LED芯片组合形成白光LED的性能.结果表明,烧结温度高于1400℃时,荧光粉呈立方结构纯YAG晶相;温度越高,形成的粉末粒径越大,发光强度越高;Ce掺杂量x=0.06时,烧结的荧光粉发光强度最大;封装形成的Φ3 mm白光LED亮度为5581 cd/m2,色坐标x=0.2626,y=0.2753,色温Tc=13000 K.