Technological factors and processes contributing to the scintillation mechanism have been considered in quaternary garnet ceramics doped with Ce(Gd,Lu)₃Al₂Ga₃O₁₂. The super-stoichiometric additive of gadolinium in the material composition or its co-doping with a low concentration of Mg were found to be effective tools to suppress phosphorescence in the quaternary garnet, confirming that it is not an intrinsic property of the material. The Monte-Carlo simulation of electronic excitation transfer demonstrates that the hopping migration along the gadolinium sublattice plays an essential role in forming the scintillation kinetic parameters. Breaking the integrity of the gadolinium sublattice by substitution with heavier lutetium ions increases the role of self-trapped states in the excitation of Ce³⁺ ions, which ensures both an increase in the fraction of short ~20 ns and very long ~600 ns components in the scintillation kinetics.

A series of (Gd, Y, Yb, Tb, Ce)3Al2Ga3O12 compositionally disordered compounds with a garnet structure were prepared in the form of ceramics by sintering in oxygen at 1650 °C for 2 h and studied for the luminescent properties and interaction of ions entering the matrix host. The luminescence features of Ce3+ ions were found to be strongly dependent on the Yb concentration. Photoluminescence and scintillation kinetics are characterized by subnanosecond kinetics when the Yb index in the compound exceeds X = 0.3. It opens an opportunity to create an extremely fast and dense scintillation material emitting in a visible range. A further decrease in the Yb index in the compound leads to an increase in the intensity of Yb3+ infrared (IR) emission, whereas Ce3+ and Tb3+ ions contribute to the luminosity of the material by overlapping intra- and intereconfiguration luminescence bands in the spectral range of 300–700 nm. This finding opens an opportunity to create converter materials tolerant to the corpuscular radiation of isotope sources, providing a high efficiency of electric current production when coupled with a silicon photovoltaic element. The compounds were engineered at the nanoscale level, providing control over electronic excitation transfer between luminescent ions.

GYAGG:Tb (Ce) scintillators have been confirmed to be promising sources of light emission when excited by an intense 150 keV electron beam. The saturation of the scintillation yield under such excitation conditions has been studied. To explain the results obtained, a model that considers the Auger quenching mechanism was used. The Ce-doped material did not show saturation, whereas a moderate 30% drop of the yield was measured in the Tb-doped sample at the highest excitation beam intensity ~1 A/cm². This put forward a way to exploit the Tb-doped scintillator for indirect β-voltaic batteries.

A method to create compositionally disordered compounds with a high number of cations in the matrices, that utilize the cubic spatial symmetry of the garnet-type crystalline systems is demonstrated. Mixtures of the garnet-type powdered materials solely doped with Ce were used to create atomic compositions of high complexity. Several mixed systems, namely Gd₃Al₂Ga₃O₁₂/(Gd,Y)₃Al₂Ga₃O₁₂, Y₃Al₅O₁₂/Gd₃Al₂Ga₃O₁₂, and Y₃Al₅O₁₂/Y₃Al₂Ga₃O₁₂ were annealed, compacted and sintered in air. The materials were evaluated for structural, luminescence, and scintillation properties. It was demonstrated that the properties of the resulting ceramics are a little dependent on the granularity of powders when the median particle size is below ~5 μm.