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Abstract: Calcium aluminate powders co-doped with Yb3+ and Eu3+: Ca1−x−y Yb x Eu y Al4O7 (x = 0.02–0.06; y = 0.02), Ca1−x−y Yb x Eu y Al4O7 (x = 0.05, y = 0.01–0.07) were synthesized by a modified Pechini citrate process and their optical properties at 298 K and 77 K were investigated. Direct excitation of Yb3+ by means of 2F7/2 → 2F5/2 absorption at 980 nm leads to bluish-green luminescence centered around 488 nm due to the cooperative emission of Yb3+ and red emission of Eu3+ corresponding to 5D0 → 7F J (J = 0–4) transitions. The near-infrared to red up-conversion luminescence of Eu3+ was assigned to a cooperative sensitization mechanism. The effect of activators concentration and charge compensation by co-doping with Na+ ions on luminescence properties were studied in detail. Na+ addition led to narrowing of luminescence bands, suggesting smaller disturbance/distribution of activator ions local symmetries. This was associated with significantly enhanced luminescence brightness of Eu3+ under UV excitation and, surprisingly, with noticeably reduced efficiency of Eu UC emission upon near-infrared excitation. It was also concluded that Yb3+ pairs transfer preferentially their excitation energy to Eu3+ ions with the local symmetry perturbed by certain defects present in the crystal lattice. [Copyright &y& Elsevier]

Abstract: Results of structural and spectroscopic measurements of Sm3+ doped calcium aluminates: Ca1−x Sm x Al4O7 and Ca1−2x Sm x Na x Al4O7 (x=0.0005, 0.002, 0.01, 0.02, 0.03, 0.05) obtained by the modified Pechini method are presented. All samples yield intense orange–red emission under violet excitation (404.5nm). Narrow bands corresponding to characteristic f–f intraconfigurational transition of Sm3+ in excitation and emission spectra were observed. The influences of the concentration of Sm3+ as well as charge compensation by co-doping with Na+ ions on the luminescent properties of the phosphor were investigated. Detailed analysis of the emission spectra of Sm3+ doped and Sm3+,Na+ co-doped CaAl4O7 powders proved that activator ions substitute Ca2+ in the host. Co-doping with Na+ ions enhanced greatly the intensity of the luminescence. Concentration dependencies of the intensity of luminescence and its decay kinetics proved the emission quenching at higher dopant contents due to cross-relaxation processes between Sm3+ ions. Fitting of the 4G5/2 state fluorescence decay to the Inokuti–Hirayama model indicated dipole–dipole interaction as the dominant mechanism of the cross-relaxation processes. [Copyright &y& Elsevier]

Abstract: HfO2 and HfO2:Eu powders were synthesized with Pechini method at temperatures in the range of 600–1500°C. Structural, radioluminescence and photoluminescence properties of the powders were investigated. The highest light output of about 20% of the efficiency of commercial GOS:Eu was found for materials containing 0.5% of Eu and prepared at 1500°C. The data shows, that further improvement of light output could be obtained if materials are processed at yet higher temperatures. Emission spectra indicate that Eu3+ experiences variety of symmetries of its surroundings. Undoped materials produce broad band emission peaking at 480nm and showing a significant afterglow. [Copyright &y& Elsevier]

Abstract: A comparative analysis of the luminescent properties of YAG and YAG:Ce nanopowders (NP) in comparison with single crystalline film (SCF) and single crystal (SC) analogues was performed under excitation by a pulsed synchrotron and X-ray radiation. It was shown that the natural defects concentration in NP was between the SC with a large (∼0.18–0.19at.%) concentration of YAl antisite defects (AD) and SCF of these garnets where YAl AD were completely absent. At the same time, Ce3+ doped YAG NP showed luminescent properties close to those of YAG:Ce SCF. [Copyright &y& Elsevier]