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Abstract Materials for radiation detection are critically important and urgently demanded in diverse fields, starting from fundamental scientific research to medical diagnostics, homeland security, and environmental monitoring. Low-dimensional halides (LDHs) exhibiting efficient self-trapped exciton (STE) emission with high photoluminescence quantum yield (PLQY) have recently shown a great potential as scintillators. However, an overlooked issue of exciton-exciton interaction in LDHs under ionizing radiation hinders the broadening of its radiation detection applications. Here, we demonstrate an exceptional enhancement of exciton-harvesting efficiency in zero-dimensional (0D) Cs3Cu2I5:Tl halide single crystals by forming strongly localized Tl-bound excitons. Because of the suppression of non-radiative exciton-exciton interaction, an excellent α/β pulse-shape-discrimination (PSD) figure-of-merit (FoM) factor of 2.64, a superior rejection ratio of 10−9, and a high scintillation yield of 26 000 photons MeV−1 under 5.49 MeV α-ray are achieved in Cs3Cu2I5:Tl single crystals, outperforming the commercial ZnS:Ag/PVT composites for charged particle detection applications. Furthermore, a radiation detector prototype based on Cs3Cu2I5:Tl single crystal demonstrates the capability of identifying radioactive 220Rn gas for environmental radiation monitoring applications. We believe that the exciton-harvesting strategy proposed here can greatly boost the applications of LDHs materials.

Pr-doped scintillators are attracting attention because of their potential applications in medical devices. In this study, we focused on Pr-doped (La, Y)2Si2O7 scintillators to grow single crystals by the micro-pulling-down method and to evaluate their optical and scintillation properties. From the powder XRD results, the crystal structure and the space group were identified to be monoclinic and P21/n, respectively. The results of optical and scintillation characterization show that the luminescence from the Pr3+ 5d1–4f transition increases with increasing Pr3+ concentration. The maximum light yield was also obtained for the sample with the highest Pr3+ concentration. The Pr-doped (La, Y)2Si2O7 single crystal shows promising properties for application in radiation detection.

(Gd,Y,Ce)3(YxGa1−x)2GaAl2O12 (GYGAG:Ce) scintillation ceramics with different Y excess, where x = 0.005−0.08, were fabricated by the solid-state reaction method. The effects of stoichiometry on the phase composition, optical quality, and microstructure of GYGAG:Ce ceramics were analyzed. GYGAG:Ce ceramics have a pure garnet phase and obtain good in-line transmittance when x < 0.04, while more Y excess leads to the creation of the secondary phase. The change of x value influences the sintering behavior of the GYGAG:Ce ceramics: The excess of Y works as the self-sintering aid and significantly reduces the sintering temperature of ceramics. When x = 0.01–0.04, the X-ray excited luminescence (XEL) spectra and light yields of GYGAG:Ce ceramics are similar. The fast scintillation decay time and afterglow intensity of GYGAG:Ce ceramics show a slight decrease with increasing x value. Finally, additional 50–500 ppm MgO and 100–500 ppm CaO were introduced to the GYGAG:Ce ceramic with x = 0.04, and both were found to significantly increase the fast scintillation component and reduce the afterglow intensity by two orders of magnitude to 0.01% after X-ray cut-off.

In this study, we propose novel three-layer composite scintillators designed for the simultaneous detection of different ionizing radiation components. These scintillators are based on epitaxial structures of LuAG and YAG garnets, doped with Ce3+ and Sc3+ ions. Samples of these composite scintillators, containing YAG:Ce and LuAG:Ce single crystalline films with different thicknesses and LuAG:Sc single crystal substrates, were grown using the liquid phase epitaxy method from melt solutions based on PbO-B2O3 fluxes. The scintillation properties of the proposed composites, YAG:Ce film/LuAG:Sc film/LuAG:Ce crystal and YAG:Ce film/LuAG:Ce film/LuAG:Sc crystal, were investigated under excitation by radiation with α-particles from a 239Pu source, β-particles from 90Sr sources and γ-rays from a 137Cs source. Considering the properties of the mentioned composite scintillators, special attention was paid to the ability of simultaneous separation of the different components of mixed ionizing radiation containing the mentioned particles and quanta using scintillation decay kinetics. The differences in scintillation decay curves under α- and β-particle and γ-ray excitations were characterized using figure of merit (FOM) values at various scintillation decay intensity levels (1/e, 0.1, 0.05, 0.01).

Halide scintillators have been playing a crucial role in the detection of ionizing radiation since the discovery of scintillation in NaI:Tl in 1948. The discovery of NaI:Tl motivated the research and development (R&D) of halide scintillators, resulting in the development of CsI:Tl, CsI:Na, CaF2:Eu, etc. Later, the R&D shifted toward oxide materials due to their high mechanical and chemical stability, good scintillation properties, and relative ease of bulk single‐crystal growth. However, the development in crystal growth technology allows for the growth of high‐quality single crystals of hygroscopic and mechanically fragile materials including SrI2 and LaBr3. Scintillators based on these materials exhibit excellent performance and push the limits of inorganic scintillators. These results motivate intense research of a large variety of halide‐based scintillators. Moreover, materials based on lead halide perovskites find applications in the fields of photovoltaics, solid‐state lighting, and lasers. The first studies show also the significant potential of lead halide perovskites as ultrafast scintillators in the form of nanocrystals. The purpose of this review is to summarize the R&D in the field of halide scintillators during the last decade and highlight perspectives for future development.

Lutetium oxyorthosilicate Lu2SiO5 (LSO) and pyrosilicate Lu2Si2O7 (LPS) activated by Ce3+ or Pr3+ are known to be effective and fast scintillation materials for the detection of X-rays and γ-rays. Their performances can be further improved by co-doping with aliovalent ions. Herein, we investigate the Ce3+(Pr3+) → Ce4+(Pr4+) conversion and the formation of lattice defects stimulated by co-doping with Ca2+ and Al3+ in LSO and LPS powders prepared by the solid-state reaction process. The materials were studied by electron paramagnetic resonance (EPR), radioluminescence spectroscopy, and thermally stimulated luminescence (TSL), and scintillation decays were measured. EPR measurements of both LSO:Ce and LPS:Ce showed effective Ce3+ → Ce4+ conversions stimulated by Ca2+ co-doping, while the effect of Al3+ co-doping was less effective. In Pr-doped LSO and LPS, a similar Pr3+ → Pr4+ conversion was not detected by EPR, suggesting that the charge compensation of Al3+ and Ca2+ ions is realized via other impurities and/or lattice defects. X-ray irradiation of LPS creates hole centers attributed to a hole trapped in an oxygen ion in the neighborhood of Al3+ and Ca2+. These hole centers contribute to an intense TSL glow peak at 450–470 K. In contrast to LPS, only weak TSL peaks are detected in LSO and no hole centers are visible via EPR. The scintillation decay curves of both LSO and LPS show a bi-exponential decay with fast and slow component decay times of 10–13 ns and 30–36 ns, respectively. The decay time of the fast component shows a small (6–8%) decrease due to co-doping.

The crystals of (Lu,Gd)3(Ga,Al)5O12 multicomponent garnets with high density ρ and effective atomic number Zeff are characterized by high scintillation efficiency and a light yield value up to 50,000 ph/MeV. During recent years, single-crystalline films and composite film/crystal scintillators were developed on the basis of these multicomponent garnets. These film/crystal composites are potentially applicable for particle identification by pulse shape discrimination due to the fact that α-particles excite only the film response, γ-radiation excites only the substrate response, and β-particles excite both to some extent. Here, we present new results regarding scintillating properties of selected (Lu,Gd)3(Ga,Al)5O12:Ce single-crystalline films under excitation by alpha and beta particles and gamma ray photons. We conclude that some of studied compositions are indeed suitable for testing in the proposed application, most notably Lu1.5Gd1.5Al3Ga2O12:Ce film on the GAGG:Ce substrate, exhibiting an α-particle-excited light yield of 1790–2720 ph/MeV and significantly different decay curves excited by α- and γ-radiation.

The paper addresses the development of composite scintillation materials providing simultaneous real-time monitoring of different types of ionizing radiation (α-, β-particles, γ-rays) in mixed fluxes of particles and quanta. The detectors are based on composite heavy oxide scintillators consisting of a thin single-crystalline film and a bulk single-crystal substrate. The film and substrate respond to certain types of ionizing particles, forming together an all-in-one composite scintillator capable of distinguishing the type of radiation through the different time characteristics of the scintillation response. Here, we report the structure, composition, and scintillation properties under different ionizing radiations of (Lu,Gd,Tb)3(Al,Ga)5O12:Ce films deposited using liquid phase epitaxy onto Gd3(Al1−xGax)5O12:Ce (GAGG:Ce) single-crystal substrates. The most promising compositions with the highest light yields and the largest differences in scintillation decay timing under irradiation with α-, β-particles, and γ-rays were selected. Such detectors are promising for environmental security purposes, medical tomography, and other radiation detection applications.

This manuscript summarizes recent results on the development of composite luminescent materials based on the single-crystalline films and single crystals of simple and mixed garnet compounds obtained by the liquid-phase epitaxy growth method. Such composite materials can be applied as scintillating and thermoluminescent (TL) detectors for radiation monitoring of mixed ionization fluxes, as well as scintillation screens in the microimaging techniques. The film and crystal parts of composite detectors were fabricated from efficient scintillation/TL materials based on Ce3+-, Pr3+-, and Sc3+-doped Lu3Al5O12 garnets, as well as Ce3+-doped Gd3−xAxAl5−yGayO12 mixed garnets, where A = Lu or Tb; x = 0–1; y = 2–3 with significantly different scintillation decay or positions of the main peaks in their TL glow curves. This work also summarizes the results of optical study of films, crystals, and epitaxial structures of these garnet compounds using absorption, cathodoluminescence, and photoluminescence. The scintillation and TL properties of the developed materials under α- and β-particles and γ-quanta excitations were studied as well. The most efficient variants of the composite scintillation and TL detectors for monitoring of composition of mixed beams of ionizing radiation were selected based on the results of this complex study.

The sensitization of scintillation was investigated in crosslinked polymeric composite materials loaded with luminescent gold clusters aggregates acting as sensitizers, and with organic dye rhodamine 6G as the emitting species. The evolution in time of the excited states population in the systems is described by a set of coupled rate equations, in which steady state solution allowed obtainment of an expression of the sensitization efficacy as a function of the characteristic parameters of the employed luminescent systems. The results obtained indicate that the realization of sensitizer/emitter scintillating complexes is the strategy that must be pursued to maximize the sensitization effect in composite materials.

CsPbBr3 nanocrystals have been identified as a highly promising material for various optoelectronic applications. However, they tend to coexist with Cs4PbBr6 phase when the reaction conditions are not controlled carefully. It is therefore imperative to understand how the presence of this phase affects the luminescence performance of CsPbBr3 nanocrystals. We synthesized a mixed CsPbBr3-Cs4PbBr6 sample, and compared its photo- and radioluminescence properties, including timing characteristics, to the performance of pure CsPbBr3 nanocrystals. The possibility of energy transfer between the two phases was also explored. We demonstrated that the presence of Cs4PbBr6 causes significant drop in radioluminescence intensity of CsPbBr3 nanocrystals, which can limit possible future applications of Cs4PbBr6-CsPbBr3 mixtures or composites as scintillation detectors.

The scintillation properties of novel type of composite scintillator based on Lu3Al5O12:Pr (LuAG:Pr) single crystalline film (SCF) and LuAG:Sc substrate grown by the liquid-phase epitaxy method are considered in this work. The registration of α-particles and γ-quanta in such types of composites occurs by means of separation of the scintillation decay kinetics of SCF and crystal parts, respectively. Namely, under excitation by α-particles of 241Am (5.5 MeV) source and γ-quanta of 137Cs (662 keV) source, the large differences in the respective scintillation decay kinetics and decay time values tα and tγ are observed for the LuAG:Pr SCF/LuAG:Sc SC composite scintillator with various film thicknesses. Furthermore, the best tγ/tα ratio above 4.5 is achieved for such types of epitaxial structure with SCF and substrate thicknesses of 17 μm and about 0.5 mm, respectively. The development types of composite scintillators can be successfully applied for simultaneous registration of α-particles and γ-quanta in the mixed radiation fluxes.

Recent developments in medical imaging techniques, in particular, those in time-of-flight positron emission tomography put new challenges on scintillating material performance that cannot be fulfilled by conventional scintillators. Bright and ultrafast nanoparticles represent promising candidates to build up an advanced detection system needed. We synthesize colloidal CsPbBr3 nanoplatelets emitting blue light with fast sub-nanosecond decay. We also prepare a nanocomposite material by embedding the nanoplatelets in the polystyrene matrix. We show that blue emission is preserved provided the composite is not exposed to UV/vis light and/or elevated temperatures. Motivated by conflicting information from the literature about the room temperature structure of colloidal CsPbX3 (X = Cl, Br, I) particles, that results being orthorhombic, rather than cubic, we perform ab initio electronic structure calculations of bulk crystals with an orthorhombic structure. We calculate optical properties, as well as exciton diameters and binding energies and compare them to those previously obtained for cubic CsPbX3 crystals.

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.

Bi-doped compounds recently became the subject of an extensive research due to their possible applications as scintillator and phosphor materials. The oxides co-doped with Bi3+ and trivalent rare-earth ions were proposed as prospective phosphors for white light-emitting diodes and quantum cutting down-converting materials applicable for enhancement of silicon solar cells. Luminescence characteristics of different Bi3+-doped materials were found to be strongly different and ascribed to electronic transitions from the excited levels of a Bi3+ ion to its ground state, charge-transfer transitions, Bi3+ dimers or clusters, radiative decay of Bi3+-related localized or trapped excitons, etc. In this review, we compare the characteristics of the Bi3+-related luminescence in various compounds; discuss the possible origin of the corresponding luminescence centers as well as the processes resulting in their luminescence; consider the phenomenological models proposed to describe the excited-state dynamics of the Bi3+-related centers and determine the structure and parameters of their relaxed excited states; address an influence of different interactions (e.g., spin-orbit, electron-phonon, hyperfine) as well as the Bi3+ ion charge and volume compensating defects on the luminescence characteristics. The Bi-related luminescence arising from lower charge states (namely, Bi2+, Bi+, Bi0) is also reviewed.

Erbium-doped active optical fiber was successfully prepared by incorporation of ceramic nanocrystals inside a core of optical fiber. Modified chemical vapor deposition was combined with solution-doping approach to preparing preform. Instead of inorganic salts erbium-doped yttrium-aluminium garnet nanocrystals were used in the solution-doping process. Prepared preform was drawn into single-mode optical fiber with a numerical aperture 0.167. Optical and luminescence properties of the fiber were analyzed. Lasing ability of prepared fiber was proofed in a fiber-ring set-up. Optimal laser properties were achieved for a fiber length of 20~m. The slope efficiency of the fiber-laser was about 15%. Presented method can be simply extended to the deposition of other ceramic nanomaterials.

In the recent successful improvement of scintillation efficiency in Lu3Al5O12:Ce driven by Ga3+ and Gd3+ admixture, the “band-gap engineering” and energy level positioning have been considered the valid strategies so far. This study revealed that this improvement was also associated with the cerium valence instability along with the changes of chemical composition. By utilizing X-ray absorption near edge spectroscopy technique, tuning the Ce3+/Ce4+ ratio by Ga3+ admixture was evidenced, while it was kept nearly stable with the Gd3+ admixture. Ce valence instability and Ce3+/Ce4+ ratio in multicomponent garnets can be driven by the energy separation between 4f ground state of Ce3+ and Fermi level.