V. Jarý

Radiation-induced preparation of pure and Ce-doped lutetium aluminium garnet and its luminescent properties

Radiation-induced preparation of pure or doped lutetium aluminium garnet Lu3Al5O12 (LuAG) is reported as a simple and robust process, which is easy to control. Irradiation of an aqueous solution containing formate anions and soluble salts of both metal ions by ionizing radiation or UV light leads to precipitation of an amorphous solid phase. Subsequent calcination in the interval 850–1200 °C results in the crystallization of the LuAG with a well developed structure. Depending on the calcination temperature, the particle size ranges from 20 to 60 nm; the prepared LuAG nanopowder was also found to be easily compactable. The manufactured Ce-doped LuAG features intensive luminescence corresponding to Ce3+ 5d–4f transitions at 510 nm and its photoluminescence excitation spectrum comprises two Ce3+ 4f–5d1, 5d2 bands at 450 and 347 nm, respectively. The decay times of Ce3+ emission in nanopowders were substantially influenced by the nanomorphological character of the prepared material. Due to its high density, chemical stability, non-toxic character and excellent scintillation efficiency, the application of Ce-doped LuAG nanopowder in photodynamic therapy and in optical ceramics preparation is suggested.

Preparation and luminescence properties of ZnO:Ga – polystyrene composite scintillator

Highly luminescent ZnO:Ga-polystyrene composite (ZnO:Ga-PS) with ultrafast subnanosecond decay was prepared by homogeneous embedding the ZnO:Ga scintillating powder into the scintillating organic matrix. The powder was prepared by photo-induced precipitation with subsequent calcination in air and Ar/H2 atmospheres. The composite was subsequently prepared by mixing the ZnO:Ga powder into the polystyrene (10 wt% fraction of ZnO:Ga) and press compacted to the 1 mm thick pellet. Luminescent spectral and kinetic characteristics of ZnO:Ga were preserved. Radioluminescence spectra corresponded purely to the ZnO:Ga scintillating phase and emission of polystyrene at 300-350 nm was absent. These features suggest the presence of non-radiative energy transfer from polystyrene host towards the ZnO:Ga scintillating phase which is confirmed by the measurement of X-ray excited scintillation decay with picosecond time resolution. It shows an ultrafast rise time below the time resolution of the experiment (18 ps) and a single-exponential decay with the decay time around 500 ps.

Optical, Structural and Paramagnetic Properties of Eu-Doped Ternary Sulfides ALnS2 (A = Na, K, Rb; Ln = La, Gd, Lu, Y)

Eu-doped ternary sulfides of general formula ALnS2 (A = Na, K, Rb; Ln = La, Gd, Lu, Y) are presented as a novel interesting material family which may find usage as X-ray phosphors or solid state white light emitting diode (LED) lighting. Samples were synthesized in the form of transparent crystalline hexagonal platelets by chemical reaction under the flow of hydrogen sulfide. Their physical properties were investigated by means of X-ray diffraction, time-resolved photoluminescence spectroscopy, electron paramagnetic resonance, and X-ray excited fluorescence. Corresponding characteristics, including absorption, radioluminescence, photoluminescence excitation and emission spectra, and decay kinetics curves, were measured and evaluated in a broad temperature range (8–800 K). Calculations including quantum local crystal field potential and spin-Hamiltonian for a paramagnetic particle in D3d local symmetry and phenomenological model dealing with excited state dynamics were performed to explain the experimentally observed features. Based on the results, an energy diagram of lanthanide energy levels in KLuS2 is proposed. Color model xy-coordinates are used to compare effects of dopants on the resulting spectrum. The application potential of the mentioned compounds in the field of white LED solid state lighting or X-ray phosphors is thoroughly discussed.