摘要
A series of CaMoO_4:Tb^(3+),Eu^(3+) phosphors were prepared by the method of precipitation. The structure and morphology of the phosphors were characterized by the X-ray diffraction(XRD) and field emission scanning electron microscopy(FE-SEM). The photoluminescence properties of the prepared products were researched, and the energy transfer from Tb^(3+) to Eu^(3+) in CaMoO_4 phosphors was studied. By adjusting the doping concentration of Eu^(3+) ions in CaMoO_4:Tb^(3+),Eu^(3+) phosphors, the emitting color of the phosphors could be easily tuned from green to red. With Tb^(3+) doped in the phosphors, the red luminescence of Eu^(3+) by near UV excitation was significantly enhanced. The energy transfer efficiency, rate and average distance between Tb^(3+) and Eu^(3+) in CaMoO_4:5%Tb^(3+),x%Eu^(3+)(mole percent) phosphors(x=0.3-10) were calculated. It was found that the interaction type between Tb^(3+) and Eu^(3+) was electric dipole-dipole interaction in the phosphors.
A series of CaMoO_4:Tb^(3+),Eu^(3+) phosphors were prepared by the method of precipitation. The structure and morphology of the phosphors were characterized by the X-ray diffraction(XRD) and field emission scanning electron microscopy(FE-SEM). The photoluminescence properties of the prepared products were researched, and the energy transfer from Tb^(3+) to Eu^(3+) in CaMoO_4 phosphors was studied. By adjusting the doping concentration of Eu^(3+) ions in CaMoO_4:Tb^(3+),Eu^(3+) phosphors, the emitting color of the phosphors could be easily tuned from green to red. With Tb^(3+) doped in the phosphors, the red luminescence of Eu^(3+) by near UV excitation was significantly enhanced. The energy transfer efficiency, rate and average distance between Tb^(3+) and Eu^(3+) in CaMoO_4:5%Tb^(3+),x%Eu^(3+)(mole percent) phosphors(x=0.3-10) were calculated. It was found that the interaction type between Tb^(3+) and Eu^(3+) was electric dipole-dipole interaction in the phosphors.
基金
supported by the National Natural Science Foundation of China(51002041)
Natural Science Foundation of Heilongjiang Province(F201202)