Nanophosphor with the nominal composition of Ca0.8 Zn0.2 TiO3 ： Pr3 ＋ , Na^＋ （CZTOPN） was synthesized at relatively low temperature by the sol-gel method. Metal ions were dispersed by citric acid in ethylene glyc...Nanophosphor with the nominal composition of Ca0.8 Zn0.2 TiO3 ： Pr3 ＋ , Na^＋ （CZTOPN） was synthesized at relatively low temperature by the sol-gel method. Metal ions were dispersed by citric acid in ethylene glycol solvent and then react with Ti（OC4H9）4 to form sol and gel. The decomposition process of the precursor, and crystallization and particle size of CZTOPN were examined by thermal analysis （TG-DSC）, powder X-ray diffraction （XRD）, and scan election microscopy （SEM）. Results of TG-DSC and XRD reveal that the composition of Ca0.8 Zn0.2 TiO3 ： Pr3 ＋ , Na^＋ changes with the sintering temperature. SEM data indicate that the diameter of particles is under 50 nm even if the sintering temperature increases to 1000 ℃. In contrast to a solid state reaction, the excitation spectra of samples synthesized by the sol-gel method shift blue about 10 nm and the emission intensity at 617 nm increases significantly.展开更多
Nb5＋ doped Ca0.8Zn0.2TiO3：Pr3＋ red long afterglow phosphors were synthesized by solid-state reaction methods. X-ray diffraction, photoluminescence spectroscopy and thermally stimulated spectrometry were used to inv...Nb5＋ doped Ca0.8Zn0.2TiO3：Pr3＋ red long afterglow phosphors were synthesized by solid-state reaction methods. X-ray diffraction, photoluminescence spectroscopy and thermally stimulated spectrometry were used to investigate the effects of Nb5＋ content on the crystal characteristics and luminescent properties of Ca0.8Zn0.2Ti1-xNbxO3：Pr3＋ phosphors. The results showed that the addition of a small quantity of Nb5＋ had negligible effect on the crystal characteristics of Ca0.8Zn0.2Ti1-xNbxO3：Pr3＋, but it could change the trapping parameters （the depth of trap, frequency factors and the concentration of trapped charges at t=0） of Ca0.8Zn0.2Ti1-xNbxO3：Pr3＋ phosphors, and then led to the enhance-ment of red fluorescence and phosphorescence at 612 nm originating from 1D2→3H4 transition of Pr3＋. Both of the red fluorescence intensity and afterglow time reached the largest values in the sample of Ca0.8Zn0.2Ti1-xNbxO3：Pr3＋ with x=0.05. The afterglow time of Ca0.8Zn0.2Ti0.95Nb0.05O3：Pr3＋ phosphors lasted for over 24 min （≥1 mcd/m2） when the excited source was cut off.展开更多
We investigated the effect of processing conditions on the structure and physical properties of the polycrystalline samples of Ca0.8Fe2Se2 prepared via solid state reaction. X-ray diffraction showed that the main phas...We investigated the effect of processing conditions on the structure and physical properties of the polycrystalline samples of Ca0.8Fe2Se2 prepared via solid state reaction. X-ray diffraction showed that the main phase became FeSe when the sintering temperature increased above 350 ℃. The temperature dependence of magnetization （M-T curves） recorded in zero-field-cooled mode by SQUID magnetometer showed some bumps at around 120 K to 140 K. These bumps moved to lower temperatures when the processing temperature increased above 550 ℃. On the other hand, pure FeSe materials produced at 900 ℃ for 24 h showed a sharp superconducting transition Tconset = 8.16 K and the critical current density of 6,252 A/cm2 at 5 K, self-field. SEM results indicated an enhanced grain connectivity.展开更多
文摘Nanophosphor with the nominal composition of Ca0.8 Zn0.2 TiO3 ： Pr3 ＋ , Na^＋ （CZTOPN） was synthesized at relatively low temperature by the sol-gel method. Metal ions were dispersed by citric acid in ethylene glycol solvent and then react with Ti（OC4H9）4 to form sol and gel. The decomposition process of the precursor, and crystallization and particle size of CZTOPN were examined by thermal analysis （TG-DSC）, powder X-ray diffraction （XRD）, and scan election microscopy （SEM）. Results of TG-DSC and XRD reveal that the composition of Ca0.8 Zn0.2 TiO3 ： Pr3 ＋ , Na^＋ changes with the sintering temperature. SEM data indicate that the diameter of particles is under 50 nm even if the sintering temperature increases to 1000 ℃. In contrast to a solid state reaction, the excitation spectra of samples synthesized by the sol-gel method shift blue about 10 nm and the emission intensity at 617 nm increases significantly.
基金Project supported by the National Natural Science Foundation of China (51072128)Key Research Project of Science and Technology of Shanxi (20110321040-01)Program for the Top Young Academic Leaders of Higher Learning Institutions of Shanxi
文摘Nb5＋ doped Ca0.8Zn0.2TiO3：Pr3＋ red long afterglow phosphors were synthesized by solid-state reaction methods. X-ray diffraction, photoluminescence spectroscopy and thermally stimulated spectrometry were used to investigate the effects of Nb5＋ content on the crystal characteristics and luminescent properties of Ca0.8Zn0.2Ti1-xNbxO3：Pr3＋ phosphors. The results showed that the addition of a small quantity of Nb5＋ had negligible effect on the crystal characteristics of Ca0.8Zn0.2Ti1-xNbxO3：Pr3＋, but it could change the trapping parameters （the depth of trap, frequency factors and the concentration of trapped charges at t=0） of Ca0.8Zn0.2Ti1-xNbxO3：Pr3＋ phosphors, and then led to the enhance-ment of red fluorescence and phosphorescence at 612 nm originating from 1D2→3H4 transition of Pr3＋. Both of the red fluorescence intensity and afterglow time reached the largest values in the sample of Ca0.8Zn0.2Ti1-xNbxO3：Pr3＋ with x=0.05. The afterglow time of Ca0.8Zn0.2Ti0.95Nb0.05O3：Pr3＋ phosphors lasted for over 24 min （≥1 mcd/m2） when the excited source was cut off.
文摘We investigated the effect of processing conditions on the structure and physical properties of the polycrystalline samples of Ca0.8Fe2Se2 prepared via solid state reaction. X-ray diffraction showed that the main phase became FeSe when the sintering temperature increased above 350 ℃. The temperature dependence of magnetization （M-T curves） recorded in zero-field-cooled mode by SQUID magnetometer showed some bumps at around 120 K to 140 K. These bumps moved to lower temperatures when the processing temperature increased above 550 ℃. On the other hand, pure FeSe materials produced at 900 ℃ for 24 h showed a sharp superconducting transition Tconset = 8.16 K and the critical current density of 6,252 A/cm2 at 5 K, self-field. SEM results indicated an enhanced grain connectivity.
