The complex fluoride LiBaF3 is solvothermally synthesized at 180degreesC and characterized by means of X-ray powder diffraction, scanning electron microscopy, thermogravimetric analysis and infrared spectroscopy. In t...The complex fluoride LiBaF3 is solvothermally synthesized at 180degreesC and characterized by means of X-ray powder diffraction, scanning electron microscopy, thermogravimetric analysis and infrared spectroscopy. In the solvothermal process, the solvents, mole ratios of initial mixtures and reaction temperature play important roles in the growth of the single crystal.展开更多
KMgF3 doped with Eu was synthesized by mild hydrothermal method at 240C for the first time. The excitation and emission spectra of the KMgF3 : Eu2+ phosphor were measured. Comparing with the sample synthesized throu...KMgF3 doped with Eu was synthesized by mild hydrothermal method at 240C for the first time. The excitation and emission spectra of the KMgF3 : Eu2+ phosphor were measured. Comparing with the sample synthesized through solid state reaction, the variation in the excitation spectra at 360 nm resulted from the existences of VK color centers; the low emission intensity was due to Eu2+ having transferred part energy to VK color centers.展开更多
基金This work was supported by the State Key Project of Foundation Research (G1998061306) theNational Natural Science Foundation of China (50072031).
文摘The complex fluoride LiBaF3 is solvothermally synthesized at 180degreesC and characterized by means of X-ray powder diffraction, scanning electron microscopy, thermogravimetric analysis and infrared spectroscopy. In the solvothermal process, the solvents, mole ratios of initial mixtures and reaction temperature play important roles in the growth of the single crystal.
文摘KMgF3 doped with Eu was synthesized by mild hydrothermal method at 240C for the first time. The excitation and emission spectra of the KMgF3 : Eu2+ phosphor were measured. Comparing with the sample synthesized through solid state reaction, the variation in the excitation spectra at 360 nm resulted from the existences of VK color centers; the low emission intensity was due to Eu2+ having transferred part energy to VK color centers.