In this study, Ce3+-doped Lu3Al5O12 garnet (LuAG) crystal detectors, with a density of ρ = 6 g/cm3 and an effective atomic number Zeff = 62, are proposed as promising materials for radiotherapy applications. This type of detector demonstrates excellent uniformity of structural and optical properties, high thermoluminescence (TL) light yield, optimal position of main TL glow peaks at temperatures around 245-295 °C, and high radiation stability. The set of TL detectors made from LuAG:Ce single crystal was used to evaluate the uniformity of dose and energy spectra of X-ray radiation from a clinical accelerator with 6 MV and 15 MV beams at the Department of Medical Physics, Oncology Center in Bydgoszcz, Poland, and γ-rays from a 60Co source at the National Institute of Oncology in Warsaw. The LuAG:Ce crystal detectors demonstrated highly promising results for registering X-ray radiation from accelerators with both 6 MV and 15 MV electron beams, as well as γ-rays from a 60Co source with energies of 1.17 and 1.33 MeV.

CaB2O4 nanorods doped with different concentrations of Cu were prepared by using co-precipitation method. The recorded Thermoluminescence (TL) and Optically stimulated luminescence (OSL) of CaB2O4:Cu samples for different concentrations of Cu irradiated with 6 Gy of X-Ray shows that 0.05 at.wt% of Cu concentrations have higher sensitivity. The TL and OSL kinetic parameters of glow curves were evaluated using \"tgcd\" and conventional fitting methods. The TL glow curve of the CaB2O4:Cu have three individual glow peaks with maximum peak temperatures at 404.50, 453.04 and 484.02 K respectively. The OSL glow curves of the CaB2O4:Cu nanoparticles follow non-first order kinetics which can be fitted with the sum of two first order decay curves.

Any experimental Thermoluminescent (TL) glow-peak contains the activation energy information of its corresponding energy level within the band gap in insulating materials. The theory of peak shape methods (PSM) correlates the macroscopic geometrical characteristics of a single TL peak with activation energy of the level responsible for the TL peak by assuming that the area under a TL peak can be approximated by the area of a triangle. In this way the geometrical characteristics becomes the measure of the activation energy. In the present work new PSM expressions are derived, which are not empirical as the existing ones but are based of the physical model of one trap one recombination (OTOR) center. Three cases are considered. (I) Delocalized OTOR for re-trapping probability smaller than the recombination probability. (II) Delocalized OTOR for re-trapping probability greater than recombination probability. (III) Localized transitions OTOR model. The system of differential equations of each case model were solved analytically using the Lambert W function (or equivalently the Wright ω function). Then the resulted analytical expressions of TL intensity as a function of temperature were used to derive new PSM. The new PSM from all cases are formally exactly the same, having, however, strong differentiation in their coefficients. The functionality of the new expressions is tested and its comparison with pre-existing PSM is performed.

This research aims to study the effects of ultraviolet C (UVC) radiation on low-density polyethylene (LDPE) food packaging. Main objectives include evaluating LDPE degradation and detecting UVC radiation using thermoluminescent dosimeters (TLDs) placed under LDPE samples. Results confirm accurate UVC detection after one hour of exposure, providing a useful tool for optimize food treatment procedures. ATR-FTIR spectroscopy analysis revealed subtle alterations (<8 % transmittance relative) in UVC-irradiated LDPE samples, including possible CH breakage (2910 and 2848 cm-1) and potential CC bond vibrations (1470 cm-1), among others. However, observed variations may stem from LDPE properties rather than entirely from UVC radiation. A comparative study of UVC-induced thermoluminescence (TL) emissions provided insights into various TLDs materials. TL kinetic analysis, using computerised glow curve deconvolution (CGCD) method, unveiled trap charge activation due to UVC exposure, including partial ionization, bleaching effect and photo-transfer (PTTL) processes. LDPE samples amplified UVC-TL responses, revealing intensity differences between the TLDs attributed to the PTTL process, accentuated by the lack of an annealing treatment. Additionally, chemical composition of the TL detectors such as, type, concentration, number, oxidation states and ionic radii of their dopants may influence UVC-TL response. Consequently, TL intensity ratios follow as: GR-200 (LiF: Mg, Cu, P) > TLD-100 (LiF: Ti, Mg) > TLD-400 (CaF2: Mn) > TLD-200 (CaF2: Dy). Thus, GR-200 detects ionizing radiation but cannot distinguish between ionizing and non-ionizing UVC radiation, while TLD-100 has limited effectiveness as a UVC radiation detector. In contrast, TLD-400 is suitable for detecting UVC radiation and TLD-200 emerges as the most favorable UVC detector, showing consistent response levels and minimal PTTL effect placed under the LDPE samples without the need of a thermal annealing treatment that makes the TLD-200 to be reusable in a low-cost measurement protocol.

Considering the low-level dose detection requirement for neutron and γ radiation in cancer therapy, synthesis and exploratory studies have been performed on a newly developed phosphor LiAlO2:Gd. Our results reveal that the presence of both Li and Gd makes it sensitive to both gamma and thermal neutrons. The applicability of LiAlO2:Gd for beta, gamma, and neutrons in both thermally stimulated and optically stimulated modes has been verified by extensive experiments followed by kinetic parametric evaluation with theoretical calculations. The current work confirms that LiAlO2:Gd is a highly sensitive phosphor with a minimum detectable dose of 5.7 μSv for gamma and 92 μSv for themral neutrons. The phosphor is found to show very high sensitivity at low energy and dose. Its ability for detection and discrimination of both gamma and thermal neutrons makes it a potential material to be used in medical dosimetry.

In the present study, the synthesis of BaSrSiO4 co-doped Yb3+ and Nd3+ nanophosphors (NPs) was successfully achieved through the conventional sol-gel method, as confirmed by X-ray diffraction and SEM analysis, verifying the formation of pure NPs. The FTIR and Raman spectra analysis confirm the formation of silicates, as different modes and vibrations of Si-O and Si-O-Si were seen at 800-1000 cm-1. The energy transfer (ET) mechanism between Nd3+ and Yb3+ ions was seen as the emission spectra showed a rise in intensity of one over another. PLE emission spectra showed transitions at 2F7/2-2F5/2 for Yb3+ and from 4F3/2 to (4I9/2, 4I11/2, and 4I13/2) for Nd3+ when excited at 785 nm. All the samples record low activation energy, which shows that the rate of reaction will be higher in all the samples, and it will be highest for 1 mol% Nd3+ and 1 mol% Yb3+. An increasing value of τ was seen with increasing Yb3+ concentration, which confirms the increase in the population of trap centers. The positron annihilation lifetime (PAL) curve showed that 1 mol% Yb3+ and 2 mol Nd3+ have single vacancies or shallower positron traps, whereas 3 mol% Yb3+ and 2 mol% Nd3+ have larger defects like surface oxygen vacancy clusters. The other two samples have balance vacancies, which makes them best for thermometry applications. The fluorescence intensity ratio (FIR) was calculated to get sensitivity for thermometry application. 2.13% K-1 sensitivity achieved at 303-333 K temperature.

Aluminum garnets display exceptional adaptability in incorporating mismatching elements, thereby facilitating the synthesis of novel materials with tailored properties. This study explored Ce3+-doped Tb3Al5-xScxO12 crystals (where x ranges from 0.5 to 3.0), revealing a novel approach to control luminescence and photoconversion through atomic size mismatch engineering. Raman spectroscopy confirmed the coexistence of garnet and perovskite phases, with Sc substitution significantly influencing the garnet lattice and induced A1g mode softening up to Sc concentration x = 2.0. The Sc atoms controlled sub-eutectic inclusion formation, creating efficient light scattering centers and unveiling a compositional threshold for octahedral site saturation. This modulation enabled the control of energy transfer dynamics between Ce3+ and Tb3+ ions, enhancing luminescence and mitigating quenching. The Sc admixing process regulated luminous efficacy (LE), color rendering index (CRI), and correlated color temperature (CCT), with adjustments in CRI from 68 to 84 and CCT from 3545 K to 12,958 K. The Ce3+-doped Tb3Al5-xScxO12 crystal (where x = 2.0) achieved the highest LE of 114.6 lm/W and emitted light at a CCT of 4942 K, similar to daylight white. This approach enables the design and development of functional materials with tailored optical properties applicable to lighting technology, persistent phosphors, scintillators, and storage phosphors.

Zinc polycarboxylate cement is one of the few dental materials that demonstrate true adhesion to tooth structure. It is suitable for use in living organisms without causing harm. Its strong adhesion to teeth and low level of irritancy are two important parameters for the dental applications. In this study, the dosimetry properties of zinc polycarboxylate cement using thermoluminescence (TL) method were investigated and determined the effectiveness of its use as a good dosimeter. According to the results of this study, the sample shows a good TL properties with three main peaks found around 140°C, 220°C and 330°C. It has a wide linear dose response between 72 Gy and 2.3 kGy and good reusability of the TL peak found at 330°C. Unfortunately, the TL peak intensity values are rapidly faded within a short waiting time interval. Zinc polycarboxylate cement, which is frequently used in dental crowns, can be used as a retrospective dosimeter for measuring the amount of radiation in space studies and nuclear accidents due to its wide linear dose-response curve in the high dose region.

In the present work, glass samples in the (100 - x)B2O3-xLi2O binary system, with x varying from 30 to 50 mol%, were prepared using the conventional melting and moulding method, with the main objective of evaluating the thermoluminescence response when exposing these materials to ultraviolet (UV) radiation. Complementary analysis based on density, optical absorption on the UV-visible region (UV-vis absorbance), Fourier transform infrared spectroscopy on the medium region, X-ray diffraction, and differential thermal analysis measurements were performed. Thermoluminescence measurements of vitreous samples showed glow curves with at least one peak with a maximum temperature of ~170°C after exposure to UV radiation in the temperature range 50-250°C. Samples were also exposed to beta radiation in the temperature range 25-275°C, also showing single peaks with a maximum temperature of ~150°C.

Samples of ZrO2 ceramics with different concentrations of impurity titanium ions were synthesized by mixing zirconium and titanium oxide powders in different mass ratios. The X-ray diffraction analysis was used to determine the phase composition, lattice parameters, and crystallite size of the ceramics with varying dopant concentrations. Upon irradiation of the samples with 220 MeV Xe ions to a fluence of 1010 ions/cm2, a decrease in the intensity of the pulsed cathodoluminescence band at 2.5 eV was observed. Additionally, ion irradiation resulted in the emergence of a new thermoluminescence peak at 450-650 K attributed to radiation-induced traps of charge carriers. Further analysis revealed that the thermoluminescence curves of samples irradiated with electrons and ions comprise a superposition of several elementary peaks. Notably, a complex non-monotonic dependence of cathodo- and thermoluminescence intensity on titanium concentration was observed, suggesting the influence of concentration quenching and the presence of tunneling transitions.