Lutetium aluminum garnet （LuAG） precursors doped with different Pr^3＋ concentration （0.25at.%, 0.5at.%, 1.0at.%, 3.0at.%, 5.0at.%） were synthesized via a co-precipitation method using ammonium hydrogen carbonate as precipitant. The phase evolution and morphology of the precursor were characterized with X-ray diffractometer （XRD） and transmission electron microscopy （TEM）. The resultant LuAG：Pr^3＋ powder was sintered into translucent ceramic without any additives in vacuum at 1150 ℃ and then in nitrogen atmosphere at 1700 ℃. spectra of LuAG：Pr^3＋ powder and ceramic were measured at room temperature in vacuum ultraviolet （VUV） and ultraviolet （VU） region. For the 5d-4f transition of Pr^3＋ ions, dominant emission of ceramic samples peaking round 311 um had higher luminescence intensity. And the host absorption in ceramic samples was not as intensive as that in powder samples. The luminescent intensity of LuAG：Pr^3＋ varied with the Pr^3＋ contents and the quenching concentration was about 1.0at.% for ceramic and 3.0at.% for powder, which was much higher than 0.24at.% for LuAG：Pr^3＋ single crystals. This phenomenon showed that the ceramic had some superiority over single crystals.
Under 980 nm laser excitation,red emission(5D0-7FJ(J=0,1,2)) of Eu3+ was observed in cubic Y2O3 codoped with Eu3+ and Yb3+.The dependence of the upconverted emission on doping concentration and laser power was studied.Yb3+ emission around 1000 nm(2F5/2-2F7/2) was reported upon excitation of Eu3+ ions.The decay curves of 5DJ(J=0,2) emission of Eu3+ under excitation of 266 nm pulse laser were examined to investigate the Eu3+→Yb3+ energy transfer process.Cooperative energy transfer process was discussed as the...
Bi3＋ and Yb3＋ codoped cubic Y2O3 phosphors are prepared by pechini sol-gel method. Strong near-infrared （NIR） emission around 980 nm from Yb3＋ （2F5/2＋2 F7/2） is observed under ultraviolet light excitation. A broad excitation band ranging from 320 to 360 nm, owing to the 6s2→6s6p transition of Bi3＋ ions, is recorded when the Yb3＋ emission is monitored, which suggests a very efficient energy transfer from Bi3＋ ions to Yb3＋ ions. The Yb3＋ concentration dependences of both the Bi3＋ and the Yb3＋ emissions are investigated. The decay curve of Bi3＋ emission under the excitation of 355 nm pulse laser is used to explore the Bi3＋ →＋Yb3＋ energy transfer process. Cooperative energy transfer （CET） is discussed as a possible mechanism for the near-infrared emission.
Lutetium oxide nanocrystals codoped with Tm3＋ and Yb3＋ were synthesized by the reverse-like co-precipitation method, using ammonium hydrogen carbonate as precipitant. Effects of the Tm3＋, Yb3＋ molar fractions and calcination temperature on the structural and upconversion luminescent properties of the Lu2O3 nanocrystals were investigated. The XRD results show that all the prepared nanocrystals can be readily indexed to pure cubic phase of Lu2O3 and indicate good crystallinity. The experimental results show that concentration quenching occurs when the mole fraction of Tm3＋ is above 0.2%. The optimal Tm3＋ and Yb3＋ doped molar fractions are 0.2% and 2%, respectively. The strong blue （490 nm） and the weak red （653 nm） emissions from the prepared nanocrystals were observed under 980 nm laser excitation, and attributed to the 1G4→3H6 and IG4→3F4 transitions of Tm3＋, respectively. Power-dependent study reveals that the 1G4 levels of Tm3＋ can be populated by three-step energy transfer process. The upconversion emission intensities of 490 nm and 653 nm increase gradually with the increase of calcination temperature. The enhancement of the upconversion luminescence is suggested to be the consequence of reducing number of OH- groups and the enlarged nanoerystal size.
In order to sensitize the luminescence of Eu3+ ions in heavy metal glass,zinc lead borate glass samples containing various concentrations of Eu3+ and Tb3+ ions were prepared to study the Tb3+ to Eu3+ non-radiative energy transfer phenomena.Energy level structures of Tb3+ and Eu3+ ions were plotted to show the excitation and energy transfer routes.Efficient energy transfer from Tb3+ to Eu3+ was observed and studied qualitatively in terms of doping concentrations.The sensitization turned out to be less effective than expected.Further studies to characterize the oxidation of Tb3+ into tetravalent state and to examine the mechanism of energy transfer are proposed.
Li Li~(1,2),Wei Xiantao~1,Chen Yonghu~1,Guo Changxin~1,Yin Min~(1*) (1.Department of Physics,University of Science and Technology of China,Hefei 230026, P R China) (2.College of Mathematics and Physics,Chongqing University of Posts and Telecommunications, Chongqing 400065,P R China)
The precursor powders of LuAG∶Ce3+ transparent ceramics were synthesized by solvo-thermal method.The crystal structure and morphology of powders were analyzed by means of Fourier transform infra-red spectroscopy,X-ray diffraction and scanning electron microscopy.The precursor powders were sintered into transparent ceramics in vacuum and then in nitrogen without any additive.The surface morphology of the transparent unpolished ceramics was characterized using scanning electron microscopy.Some factors that affect the transparency of ceramics were discussed.The UV-Vis fluorescence excitation and emission spectra of LuAG∶Ce3+ transparent ceramics were measured.The vacuum ultraviolet spectra of transparent ceramics were investigated using the synchrotron radiation as the excitation source.The excitation mechanism of Ce3+ was discussed at different excitation wavelength.
WANG Lin-xiangZHU Heng-jiangWU Ling-yuanDENG Kai-moGUO Chang-xinYIN Min
(Y0.95La0.05)2O3: Ce3+ nano-powder was synthesized by co-precipitation method and sintered at 800 and 900 oC. All the samples were cubic phase characterized by X-ray diffraction (XRD) analysis. The samples sintered at the lower temperature exhibited luminescence. According to the distinguishable structure of Ce 3d peaks and the shift of O 1s lines in the X-ray photoelectron spectroscopy (XPS), luminescence was further confirmed to originate from Ce3+ ions. Effects of introducing La3+ into Y2O3 were discusse...
