The introduction of silver into the samarium-containing silica glasses prepared by the original solgel method leads to the formation of complex optical centers involving samarium ions and simple and/or complex silver ions. These centers are characterized by the effective sensitization of Sm³⁺ luminescence by Ag⁺, (Ag₂)⁺, and (Ag⁺)₂ ions according to the exchange mechanism for, at least, Sm³⁺-Ag⁺ centers. The formation of Sm-Ag centers is accompanied by an increase in the concentration of nonbridging oxygen ions, which prevent the reduction of silver ions by hydrogen. Silver nanoparticles formed in small amounts upon this reduction are effective quenchers of luminescence from the corresponding excited states of Sm³⁺ ions.

Polycrystalline europium huntite EuAl₃(BO₃)₄ has been prepared by solid-phase synthesis. The spectral and kinetic characteristics of its luminescence under the excitation by a xenon lamp, single laser pulse, and electron beam have been studied. It has been established that the laser excitation of the polycrystalline samples in the ⁷ F ₀ →⁵ L ₆ transition of Eu³⁺ ions with the power density P ≥ 5 × 10⁷ W/cm² leads to the structure rearrangement of the optical centers, which is accompanied by an increase in the probability of the radiation transitions of the activator. The stimulated radiation of the main type of Eu³⁺ centers in the ⁵ D ₀→⁷ F ₁, ⁷ F ₂, and ⁷ F ₄ transitions has been obtained under the excitation by the electron beam with an energy of 200 keV and a duration of 2 ns.

The spectroscopic behavior of Sm3+ ions is investigated in monoactivated and coactivated (with cerium) glasses obtained by the direct sol-gel-glass transition. It is shown that the majority of the Sm3

Two series of (Gd, Y, Yb)₃Al₂Ga₃O₁₂ quintuple compounds with a garnet structure and solely doped with Ce and Tb were prepared in the form of ceramics by sintering in oxygen at 1600 °C for two hours and studied for the interaction of activator ions with ytterbium ions entering the matrix. It was shown that the photoluminescence and scintillation of Ce³⁺ ions are completely suppressed, predominantly by tunneling ionization through the charge transfer state (CTS) of the Ce⁴⁺-Yb²⁺ ions. The photoluminescence of Tb³⁺ ions is quenched in the presence of ytterbium, but not completely due to the poor resonance conditions of Tb³⁺ intraconfiguration transitions and the CTS of the single Yb³⁺ and the CTS of Ce⁴⁺-Yb²⁺ ions. The scintillation in the visible range of both Ce³⁺- and Tb³⁺-doped samples is intensely quenched as well, which indicates strong competition from Yb³⁺ ions to activators in interaction with the Gd substrate.

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.