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The influence of the Mg 2+ codoping and annealing in the air on the scintillation and luminescence characteristics of Pr-doped lutetium-aluminum garnet crystals (LuAG) was studied to find a possible positive effect of Pr 4+ . The overall scintillation efficiency under X-ray excitation of the annealed Pr- doped samples decreased with increasing Mg concentration. This was explained by increased overlap of the Pr 3+ 5d-4f emission with the charge-transfer (CT) absorption band of the Pr 4+ ion stabilized by Mg 2+ . This absorption caused even greater decrease of the light yield, as the light is collected from the whole sample volume in the pulse-height spectrum measurement. Electron centers based on oxygen vacancies (F + centers) which can have negative influence on scintillation mechanism were revealed by the electron paramagnetic resonance (EPR) experiments. The O - hole center was detected as well and the temperature dependences of the EPR spectra showed that its thermal stability was decreased by Mg codoping. Negligible changes in the decay time of Pr 3+ 5d-4f photoluminescence exclude the non-radiative energy transfer from relaxed 5d 1 excited state of Pr 3+ towards CT absorption transition of Pr 4+ and suggest that simple reabsorption of the emitted light takes place. Unlike for the Ce-doped analogs, promoting the Pr 3+ luminescence center to the tetravalent state by divalent ion co-doping and air annealing did not improve scintillation properties of Pr-doped LuAG. [ABSTRACT FROM AUTHOR]

Driven by the pursuit of optimizing the luminescent properties of garnet-based single crystals for X-ray imaging applications, this work reports on the successful synthesis and in-depth characterization of GYAGG crystals doped with Ce³⁺ or Tb³⁺ ions, and doubly-doped with both of them. Micro-pulling down synthesis yielded crystals with a single cubic phase confirmed by X-ray diffraction. Photoluminescence (PL) and radioluminescence (RL) measurements on Ce³⁺,Tb³⁺ co-doped GYAGG revealed bidirectional energy transfer processes. Characteristic broadband 5d 1 →4f emission of Ce³⁺ centers peaking at 530 nm and narrow 4f→4f emission lines of Tb³⁺ ions starting from 5D 4 level within 480–630 nm were observed. At higher doping levels, cross-relaxation in Tb³⁺ pairs resulted depleted 5D 3 state and only the emission from 5D 4 one was observed in the spectra. Analysis of PL decay characteristics corroborated the spectral observations, confirming progressively decreasing Ce³⁺ decay time (down to 40 ns at 15 % Tb3+) due to enhanced Ce³⁺→Tb³⁺ energy transfer. Similarly, the Tb³⁺ decay time accelerated by more than 60 % after the Ce³⁺ co-doping. Notably, co-doping with 0.5 % Ce³⁺ and 10–15 % Tb³⁺ doubled the luminescence intensity of RL spectra compared to 0.5 % Ce³⁺-doping alone, attributed to the increased density of emitting centers. • High-quality and crack-free GYAGG:Ce,Tb single crystals were successfully grown. • The photoluminescence spectra revealed Ce³⁺↔Tb³⁺ bidirectional energy transfer. • At lower Tb³⁺ doping (0.5 %), the bidirectional energy transfer was inefficient. • High Tb³⁺ doping (15 %) significantly enhanced energy transfer. • Co-doping yielded a two-fold radioluminescence intensity compared to sole doping. [ABSTRACT FROM AUTHOR]