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The layered double perovskite microcrystals show excellent stability both under ambient condition and under X-ray irradiation, their luminescent properties and applications in X-ray imaging have been demonstrated. [Display omitted] Metal halide perovskites, as a new class of attractive and potential scintillators, are highly promising in X-ray imaging. However, their application is limited by the sensitivity to moisture and irradiation. To address this issue, we reported a 2D layered double perovskite material Cs 4 Cd 1-x Mn x Bi 2 Cl 12 that exhibits high stability both under ambient condition and under X-ray irradiation. Cs 4 Cd 1-x Mn x Bi 2 Cl 12 demonstrates superior scintillation performance, including excellent X-ray response linearity and a high light yield (∼34,450 photons/MeV). More importantly, the X-ray excited emission intensity maintains 92% and 94% of its original value after stored at ambient condition for over two years and after X-ray irradiation with a total dose of 11.4 Gy, respectively. By mixing with PDMS (polydimethylsiloxane), we have successfully produced a high-quality flexible film that can be bent freely while maintaining its excellent scintillation properties. The scintillating screen exhibits outstanding imaging ability with a spatial resolution of up to 16.7 line pairs per millimeter (lp/mm), also, the superiority of this scintillation screen in flexible X-ray imaging is demonstrated. These results indicate the huge potential of this high-stability double perovskite scintillator in X-ray imaging. [ABSTRACT FROM AUTHOR]

In the present work, the sintering of bismuth germanate through hot pressing and the improvement of scintillator performance were investigated. The linear shrinkage, crystalline structure, microstructure, transparency degree, and radioluminescence (RL) were studied as functions of the sintering pressure. X‐ray diffraction revealed that the samples were predominantly composed of the Bi4Ge3O12 phase, accompanied by small amounts of Bi12GeO20, with concentrations varying according to the sintering parameters. These concentrations were quantified through Rietveld refinement, which also indicated a tendency for the cell parameters to shrink as the sintering pressure increased. The microstructure of the ceramic pellets produced under varying hot‐pressing parameters was investigated using scanning electron microscopy (SEM), revealing that while the grain size was preserved, the porosity and grain boundary thickness were reduced by the hot pressing, forming a quasicontinuum in some areas of the sample. The RL of all the samples exhibited a green color, with a maximum at 540 nm, ascribed to the transitions from the 3P0,1,21P1 excited states to the fundamental 1S0 state of the Bi3+ ions. For samples sintered under a pressure of .18 MPa, the enhancement in the optical transmittance, accompanied by a 61.36% increase in light output at the maximum wavelength, was observed. [ABSTRACT FROM AUTHOR]

Ce3+-doped lithium alumino-silicate (Li-Al-Si) scintillating glass was prepared using a melting method and crystallized via heat treatment. X-ray diffraction and transmission electron microscopy confirmed the presence of nanocrystals in the materials. Radioluminescence spectra, obtained by X-ray excitation, and luminescence spectra, obtained by 338 nm excitation, showed that the luminescence intensity increased after crystallization. The glass was combined with pure silica as the inner cladding to fabricate a hybrid fiber core using a melt-in-tube technique. The composition of the fiber core was examined using an electron probe microanalyzer. The glass fiber produced strong blue luminescence under UV excitation. After a micro-crystallizing heat treatment of the hybrid fiber at 850 °C in a reducing atmosphere, a Ce3+-doped lithium alumino-silicate glass–ceramic scintillating hybrid fiber was obtained. The nanocrystal structure of the fiber core was examined using micro-Raman spectroscopy. Excitation and luminescence spectra of the hybrid fiber before and after micro-crystallization were measured using microspectrofluorimetry. The results demonstrated that the fiber remained luminous after micro-crystallization. Hence, this work provides a new way to prepare scintillating glass–ceramic hybrid fibers for neutron detection. [ABSTRACT FROM AUTHOR]

Most single-photon emission computed tomography (SPECT) scanners employ a gamma camera with a large scintillator crystal and 50–100 large photomultiplier tubes (PMTs). In the past, we proposed that the weight, size and cost of a scanner could be reduced by replacing the PMTs with large-area silicon photomultiplier (SiPM) pixels in which commercial SiPMs are summed to reduce the number of readout channels. We studied the feasibility of that solution with a small homemade camera, but the question on how it could be implemented in a large camera remained open. In this work, we try to answer this question by performing Geant4 simulations of a full-body SPECT camera. We studied how the pixel size, shape and noise could affect its energy and spatial resolution. Our results suggest that it would be possible to obtain an intrinsic spatial resolution of a few mm FWHM and an energy resolution at 140 keV close to 10%, even if using pixels more than 20 times larger than standard commercial SiPMs of 6 × 6 mm 2 . We have also found that if SiPMs are distributed following a honeycomb structure, the spatial resolution is significantly better than if using square pixels distributed in a square grid. [ABSTRACT FROM AUTHOR]

The zero-dimensional copper halide perovskite Cs 3 Cu 2 I 5 displays extraordinary luminescence and scintillation characteristics, and high-quality crystals are extremely desirable for exploring the commercial applications. Currently, the most critical issue in the solution growth of Cs 3 Cu 2 I 5 crystals is the easy oxidation of halides, which significantly hinders the optimization of crystal qualities. The hypophosphorous acid (H 3 PO 2) has been applied to inhibit the oxidation, nevertheless, the related mechanism is elusive and has been largely ignored. Herein, Cs 3 Cu 2 I 5 crystals have been grown from N, N-Dimethylformamide (DMF) solvent by the antisolvent vapor-assisted crystallization (AVC) method. It is verified that H 3 PO 2 effectively prevents the oxidation of Cs 3 Cu 2 I 5 by rapidly reducing Cu2+ and I 3 −, maintaining the stability of the precursor solution and continuously suppressing oxidation during the whole growth process. Meanwhile, by increasing the acidity of the solution, H 3 PO 2 dissolve precursor colloids and efficiently enhance the solubility of halides. Thus, the addition of H 3 PO 2 favors the rapid growth of centimeter-sized Cs 3 Cu 2 I 5 crystals with well-defined crystallographic planes within several days. As excellent gamma ray scintillator, the crystal exhibits high light yield of 38000 photons/MeV, with energy resolution of 5.6 % under 662 keV radiation from a 137Cs source. This work deeply elucidates new insight into the critical effect of H 3 PO 2 in the DMF based solution crystal growth, facilitating the preparation of large-size and high-performance copper halide perovskite crystals. [ABSTRACT FROM AUTHOR]

High-performance and low-cost metal halide perovskite scintillator materials have important applications in X-ray detection and imaging. However, large-sized perovskite scintillator panel with high transmittance, low toxicity and long-term stability is still lacking. Herein, Eu2+ doped cesium alkaline earth chloride nanocrystals (Eu2+: CsCaCl 3 , Eu2+: CsSrCl 3 , and Eu2+: Cs 2 BaCl 4 NCs) embedded in glasses through conventional melt-quenching and subsequent heat-treatment were developed. These NCs doped glasses exhibited highly efficient and narrowband photoluminescence in blue region. Benefitting from the large X-ray absorption coefficient and high photoluminescence quantum yied, these Eu2+: CsCaCl 3 NCs doped glass scintillator shows light yield of ∼9300 photons/MeV, detection limit of ∼213.8 μGy/s, and spatial resolution of 30.0 lp/mm. These results demonstrated that glasses containing Eu2+ doped cesium alkaline earth chloride nanocrystals are promising for X-ray detection and imaging. [ABSTRACT FROM AUTHOR]

In time-of-flight positron emission tomography (TOF-PET), a coincidence time resolution (CTR) below 100 ps reduces the angular coverage requirements and, thus, the geometric constraints of the scanner design. Among other possibilities, this opens the possibility of using flat-panel PET detectors. Such a design would be more cost-accessible and compact and allow for a higher degree of modularity than a conventional ring scanner. However, achieving adequate CTR is a considerable challenge and requires improvements at every level of detection. Based on recent results in the ongoing development of optimised TOF-PET photodetectors and electronics, we expect that within a few years, a CTR of about 75 ps will be be achievable at the system level. In this work, flat-panel scanners with four panels and various design parameters were simulated, assessed and compared to a reference scanner based on the Siemens Biograph Vision using NEMA NU 2-2018 metrics. Point sources were also simulated, and a method for evaluating spatial resolution that is more appropriate for flat-panel geometry is presented. We also studied the effects of crystal readout strategies, comparing single-crystal and module readout levels. The results demonstrate that with a CTR below 100 ps, a flat-panel scanner can achieve image quality comparable to that of a reference clinical scanner, with considerable savings in scintillator material. [ABSTRACT FROM AUTHOR]

Ultra‐high‐speed synchrotron‐based hard X‐ray (i.e. above 10 keV) imaging is gaining a growing interest in a number of scientific domains for tracking non‐repeatable dynamic phenomena at spatio‐temporal microscales. This work describes an optimized indirect X‐ray imaging microscope designed to achieve high performance at micrometre pixel size and megahertz acquisition speed. The entire detector optical arrangement has an improved sensitivity within the near‐ultraviolet (NUV) part of the emitted spectrum (i.e. 310–430 nm wavelength). When combined with a single‐crystal fast‐decay scintillator, such as LYSO:Ce (Lu2−xYxSiO5:Ce), it exploits the potential of the NUV light‐emitting scintillators. The indirect arrangement of the detector makes it suitable for high‐dose applications that require high‐energy illumination. This allows for synchrotron single‐bunch hard X‐ray imaging to be performed with improved true spatial resolution, as herein exemplified through pulsed wire explosion and superheated near‐nozzle gasoline injection experiments at a pixel size of 3.2 µm, acquisition rates up to 1.4 MHz and effective exposure time down to 60 ps. [ABSTRACT FROM AUTHOR]

X-ray excited radioluminescence was demonstrated in Pr-doped lithium niobate polycrystalline samples with varying lithium-to-niobium ratios (R LN). The samples' phase structures, excitation and emission spectra, and radioluminescence were experimentally analyzed to investigate the tuning effects of R LN. Theoretical calculations based on Density Functional Theory (DFT) were conducted to elucidate the underlying mechanisms, and thermoluminescence curves were measured to verify the predictions of the theoretical analysis. We suggest that both photoluminescence and radioluminescence properties can be effectively tailored by adjusting the crystal structure, as well as the depth and density of electron traps within the LiNbO 3 :Pr matrix through R LN modulation. This research contributes to the development and practical implementation of scintillation materials derived from rare-earth-doped lithium niobate. [ABSTRACT FROM AUTHOR]

Objective: Positron Emission Tomography (PET) is a well-known imaging technology for the diagnosis, treatment, and monitoring of several diseases. Most PET scanners use a Ring-Shaped Detector Configuration (RSDC), which helps obtain homogeneous image quality but are restricted to an invariable Field-of-View (FOV), scarce spatial resolution, and low sensitivity. Alternatively, few PET systems use Open Detector Configurations (ODC) to permit an accessible FOV adaptable to different target sizes, thus optimizing sensitivity. Yet, to compensate the lack of angular coverage in ODC-PET, developing a detector with high-timing performance is mandatory to enable Time-of-Flight (TOF) techniques during reconstruction. The main goal of this work is to provide a proof of concept PET scanner appropriate for constructing the new generation of ODC-PET suitable for biopsy guidance and clinical intervention during acquisition. The designed detector has to be compact and robust, and its requirements in terms of performance are spatial and time resolutions < 2 mm and < 200 ps, respectively. Methods: The present work includes a simulation study of an ODC-PET based on 2-panels with variable distance. The image quality (IQ) and Derenzo phantoms have been simulated and evaluated. The phantom simulations have also been performed using a ring-shaped PET for comparison purposes of the ODC approach with conventional systems. Then, an experimental evaluation of a prototype detector that has been designed following the simulation results is presented. This study focused on tuning the ASIC parameters and evaluating the scintillator surface treatment (ESR and TiO2), and configuration that yields the best Coincidence Time Resolution (CTR). Moreover, the scalability of the prototype to a module of 64 × 64mm2 and its preliminary evaluation regarding pixel identification are provided. Results: The simulation results reported sensitivity (%) values at the center of the FOV of 1.96, 1.63, and 1.18 for panel distances of 200, 250, and 300 mm, respectively. The IQ reconstructed image reported good uniformity (87%) and optimal CRC values, and the Derenzo phantom reconstruction suggests a system resolution of 1.6–2 mm. The experimental results demonstrate that using TiO2 coating yielded better detector performance than ESR. Acquired data was filtered by applying an energy window of ± 30% at the photopeak level. After filtering, best CTR of 230 ± 2 ps was achieved for an 8 × 8 LYSO pixel block with 2 × 2 × 12mm3 each. The detector performance remained constant after scaling-up the prototype to a module of 64 × 64mm2, and the flood map demonstrates the module's capabilities to distinguish the small pixels; thus, a spatial resolution < 2 mm (pixel size) is achieved. Conclusions: The simulated results of this biplanar scanner show high performance in terms of image quality and sensitivity. These results are comparable to state-of-the-art PET technology and, demonstrate that including TOF information minimizes the image artifacts due to the lack of angular projections. The experimental results concluded that using TiO2 coating provide the best performance. The results suggest that this scanner may be suitable for organ study, breast, prostate, or cardiac applications, with good uniformity and CRC. [ABSTRACT FROM AUTHOR]

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). [ABSTRACT FROM AUTHOR]

The study of scintillation-causing ionospheric irregularities is important to mitigate their effects on satellite communications. It is also important due to the spatial and temporal variability of these irregularities, given that their characteristics differ from one region to another. This study investigates the spatial and temporal characteristics of L1 amplitude scintillation-causing ionospheric irregularities over the Eastern Arabian Peninsula during the ascending phase of solar cycle 25 (years 2020–2023). The temporal occurrences of weak and strong scintillation were separated by sunset, with weak scintillation observed predominantly pre-sunset during the winter solstice and strong scintillation observed mainly post-sunset during the autumnal equinox. Strong scintillation was much more pronounced in 2023 compared to the other three years, indicating a strong influence of solar activity. Spatially, weak-scintillation-causing irregularities exhibited a wide distribution in azimuth and elevation, while strong-scintillation-causing irregularities were concentrated southwards. The combined analysis of S4 and rate of total electron content index (ROTI) suggested that small-scale ionospheric irregularities were present in both pre- and post-sunset periods, while large-scale irregularities were only seen during the post-sunset period. Furthermore, the presence of southward traveling ionospheric disturbances (TIDs) during the 2023 autumnal equinox was confirmed with the total electron content anomaly (Δ TEC), while the Ionospheric Bubble Index (IBI) provided by the Swarm mission was unable to confirm the presence of equatorial plasma bubbles during the same period. Observations from the FORMOSAT-7/COSMIC-2 mission indicated that strong-scintillation-causing irregularities were more prevalent under the F2-layer peak, while the weak-scintillation-causing irregularities were mostly observed at the E-layer, F2-layer, and above the F2-layer. This study aims to contribute insights into the behavior of scintillation-causing ionospheric irregularities in the region, with implications for future research during the peak of the 25th solar cycle. [ABSTRACT FROM AUTHOR]

The prevalent use of unsustainable polymers in current X‐ray scintillators poses a significant environmental concern. The advancement of biodegradable X‐ray scintillators holds promise in mitigating escalating environmental issues tied to electronic or medical waste and carbon footprints. Herein, a biodegradable and flexible X‐ray scintillation film is presented employing lead‐free 0D Cs3Cu2I5 perovskite nanoparticles integrated into densified‐delignified wood (Cs3Cu2I5@D‐Wood). The Cs3Cu2I5@D‐Wood film demonstrates precise and detailed X‐ray imaging capabilities, achieving a high spatial resolution of 10 line pairs per millimeter (lp·mm−1). To minimize the environmental impact associated with disposal, metal and halide ions (e.g., Cs+, Cu+, I−) from Cs3Cu2I5@D‐Wood can be easily retrieved by a simple solvent extraction process. The approach showcases the potential of biodegradable wood‐based X‐ray scintillation screens as alternatives to conventional, plastic‐based screens. This offers a significant contribution to environmental sustainability by reducing electronic or medical waste. [ABSTRACT FROM AUTHOR]

The aim of this study was to experimentally assess the luminescence efficiency of a cerium fluoride (CeF3) inorganic scintillator in crystal form as a possible alternative to high-luminescence but hygroscopic cerium bromide (CeBr3). The experiments were performed under typical diagnostic radiology X-rays (50–140 kVp). Parameters such as the crystal's absolute luminescence efficiency (AE) and the spectral matching with a series of optical detectors were examined. The replacement of bromine with fluorine appeared to drastically reduce the AE of CeF3 compared to CeBr3 and other commercially available inorganic scintillators such as bismuth germanate (Bi4Ge3O12-BGO). CeF3 reaches a maximum luminescence efficiency value of only 0.8334 efficiency units (EUs) at 140 kVp, whereas the corresponding values for CeBr3 and BGO were 29.49 and 3.41, respectively. Furthermore, the emission maximum (at around 313 nm) moved towards the lower part of the visible spectrum, making CeF3 suitable for spectral coupling with various photocathodes and photomultipliers applied in nuclear medicine detectors, but completely unsuitable for spectral matching with CCDs and CMOS. The obtained luminescence efficiency results denote that CeF3 cannot be applied in medical imaging applications covering the range 50–140 kVp; however, examination of its luminescence output in the nuclear medicine energy range (~70 to 511 keV) could reveal possible applicability in these modalities. [ABSTRACT FROM AUTHOR]

Neutrons are widely used in national defense, security, and medical health fields. It is critical to realize neutron detection with high efficiency. The most popular neutron detection scintillators such as lithium glass and 6LiF/ZnS:Ag screen exhibit insurmountable limitations: the former usually has relatively rather low light yield and latter is opaque. In this research, we report the successful construction of the novel full inorganic composite scintillators by low temperature co‐firing technology. The composite scintillator is derived from the ZnS:Ag and borate glass matrix, and it shows better transparency compared with the standard 6LiF/ZnS:Ag screen. It exhibits excellent scintillation properties with the X‐ray induced emission intensity of these composite scintillators reaching approximately 2.46 times of the standard Bi4Ge3O12 (BGO) crystal. The light output under thermal neutron excitation can reach 75 000 photons/neutron. In addition, it presents excellent neutron detection performance with natural abundance of 10B isotope. Our research findings can serve as a valuable reference for the advancement of robust neutron detection materials, particularly in the domain of ZnS:Ag‐based full inorganic scintillator for neutron detection. [ABSTRACT FROM AUTHOR]

The ability to distinguish multiple forms of plutonium from one another, such as oxide and metal, is paramount in areas of nuclear nonproliferation and international safeguards. In its metal form, plutonium can be readily used in a nuclear weapon, while oxide forms are associated with nuclear reactor fuel. Oxide-based plutonium forms emit neutrons with an energy spectrum that is significantly different from the fission neutrons that are emitted from plutonium metal. Organic scintillation detectors output pulses that are proportional to the neutron energy deposited, and therefore present a means of distinguishing these plutonium forms based on their energy spectra. In this work, metal and oxide forms of plutonium were measured using a handheld detection system based on an organic glass scintillator. Monte Carlo modeling of these experiments was performed to provide insight into the origin of the features in the observed light output spectra. Through analysis of multiple regions of these spectra, in a matter of minutes we were able to unambiguously discriminate oxide and metal plutonium forms from one another and from a plutonium-beryllium neutron source, which was considered for comparison because these sources are commonly used in industrial applications. The ability to discriminate weapons-usable material from nuclear reactor fuel has applications in nuclear treaty verification and safeguards. [ABSTRACT FROM AUTHOR]

Background: The application of semi-conductor detectors such as cadmium–zinc–telluride (CZT) in nuclear medicine improves extrinsic energy resolution and count sensitivity due to the direct conversion of gamma photons into electric signals. A 3D-ring pixelated CZT system named StarGuide was recently developed and implemented by GE HealthCare for SPECT acquisition. The system consists of 12 detector columns with seven modules of 16 × 16 CZT pixelated crystals, each with an integrated parallel-hole tungsten collimator. The axial coverage is 27.5 cm. The detector thickness is 7.25 mm, which allows acquisitions in the energy range [40–279] keV. Since there is currently no performance characterization specific to 3D-ring CZT SPECT systems, the National Electrical Manufacturers Association (NEMA) NU 1-2018 clinical standard can be tailored to these cameras. The aim of this study was to evaluate the performance of the SPECT/CT StarGuide system according to the NEMA NU 1-2018 clinical standard specifically adapted to characterize the new 3D-ring CZT. Results: Due to the integrated collimator, the system geometry and the pixelated nature of the detector, some NEMA tests have been adapted to the features of the system. The extrinsic measured energy resolution was about 5–6% for the tested isotopes (99mTc, 123I and 57Co); the maximum count rate was 760 kcps and the observed count rate at 20% loss was 917 kcps. The system spatial resolution in air extrapolated at 10 cm with 99mTc was 7.2 mm, while the SPECT spatial resolutions with scatter were 4.2, 3.7 and 3.6 mm in a central, radial and tangential direction respectively. Single head sensitivity value for 99mTc was 97 cps/MBq; with 12 detector columns, the system volumetric sensitivity reached 520 kcps MBq−1 cc−1. Conclusions: The performance tests of the StarGuide can be performed according to the NEMA NU 1-2018 standard with some adaptations. The system has shown promising results, particularly in terms of energy resolution, spatial resolution and volumetric sensitivity, potentially leading to higher quality clinical images. [ABSTRACT FROM AUTHOR]

Silicon photomultipliers (SiPMs) are solid-state single-photon-sensitive detectors that show excellent performance in a wide range of applications. In FBK (Trento, Italy), we developed a position-sensitive SiPM technology, called "linearly graded" (LG-SiPM), which is based on an avalanche-current weighted-partitioning approach. It shows position reconstruction resolution below 250 μm on an 8 × 8 mm2 device area with four readout channels and minimal distortions. A recent development in terms of LG-SIPM is a larger chip version (10 × 10 mm2) based on FBK NUV-HD technology (near-ultraviolet sensitive), with a peak photon detection efficiency at 420 nm. Such a large-area detector with position sensitivity is very interesting in applications like MR-compatible PET, high-energy physics experiments, and readout of time-projection chambers, gamma and beta cameras, or scintillating fibers, with a reduced number of channels. These SiPMs were characterized in terms of noise, photon detection efficiency, and position resolution. We also developed tiles of 2 × 2 and 3 × 3 LG-SiPMs, reaching very large sensitive areas of 20 × 20 mm2 and 30 × 30 mm2. We implemented a "smart-channel" configuration, which allowed us to have just six output channels for the 2 × 2 elements and eight channels for the 3 × 3 element tiles, preserving a position resolution below 0.5 mm. These kinds of detectors provide a great advantage in compact and low-power applications by maintaining position sensitivity over large areas with a small number of channels. [ABSTRACT FROM AUTHOR]

We report the photon (PL), electron (CL) and X-ray (XEL) induced luminescence characteristics of high aspect ratio ultra-long (~ 50 µm) ZnO nanorods (NRs) and discuss the potential for fast X-ray detection based on the consistent and efficient visible emission (~ 580 nm) from ZnO NRs. Nanostructured ZnO scintillators were rearranged to form a vertically well-aligned NR design in order to help light absorption and coupling resulting in luminescent and fast scintillation properties. The design of the nanorod array combines the key advantages of a low-cost growth technique together with environmentally friendly and widely available materials. A low temperature hydrothermal method was adopted to grow ZnO NRs in one cycle growth and their structural, optical and X-ray scintillation properties were investigated. The relatively short (~ 10 µm) ZnO NRs emitting in the near-band-edge region were found to be almost insensitive to X-rays. On the other hand, the higher XEL response of long ZnO NRs, which is a key parameter for evaluation of materials to be used as scintillators for high quality X-ray detection and imaging, along with a decay time response in the order of ns confirmed promising scintillation properties for fast and high-resolution X-ray detector applications. [ABSTRACT FROM AUTHOR]

The high durability under harsh environment including high temperature, high humidity, and high radiation is required for scintillators used for decommissioning of nuclear facilities and radiation monitoring in nuclear fusion reactors. α‐SiAlON ceramics are highly potential for such scintillators because of their thermal and mechanical durability and luminescence corresponding to doped rare‐earth ion. In this study, scintillation properties of transparent Lu‐α‐SiAlON:Ce3+ ceramics were investigated for the first time. Lu‐α‐SiAlON:Ce3+ showed the scintillation responses to α‐rays and X‐rays. The α‐rays‐induced scintillation decay curve consists of two components whose decay time are 48 and 652 ns. The faster decay component most presumably results from 4f‐5d transition of Ce3+, whereas the origin of the slower one is unclear but may be defects in α‐SiAlON. The light yield of the Lu‐α‐SiAlON:Ce3+ ceramics was 1300 photons 5.5 MeV−1. [ABSTRACT FROM AUTHOR]

The GNSS-based bistatic SAR (GNSS-BSAR) system has emerged as a hotspot due to its low power consumption, nice concealment, and worldwide reach. However, the weak landing power density of the GNSS signal often necessitates prolonged integration to achieve an adequate signal-to-noise ratio (SNR). In this case, the effects of the receiver's time-frequency errors and atmospheric disturbances are significant and cannot be ignored. Therefore, we propose an ionospheric scintillation compensation-based imaging scheme for dual-channel GNSS-BSAR system. This strategy first extracts the reference phase, which contains the ionospheric phase scintillation and other errors. Subsequently, the azimuth phase of the target is divided into difference phase and reference phase. We apply the two-step phase compensation to eliminate Doppler phase errors, thus achieving precise focusing of SAR images. Three sets of experiments using the GPS L5 signal as the illuminator were conducted, coherently processing a 1.5 km by 0.8 km scene about 300 s. The comparative results show that the proposed method exhibited better focusing performance, avoiding the practical challenges encountered by traditional autofocus algorithms. Additionally, ionospheric phase scintillation extracted at different times of the day suggest diurnal variations, preliminary illustrating the potential of this technology for ionospheric-related studies. [ABSTRACT FROM AUTHOR]

The interaction between free electrons and optical fields constitutes a unique platform to investigate ultrafast processes in matter and explore fundamental quantum phenomena. Specifically, optically modulated electrons in ultrafast electron microscopy act as noninvasive probes that push space-time-energy resolution to the picometer-attosecond-microelectronvolt range. Electron energies well above the involved photon energies are commonly used, rendering a low electron-light coupling and, thus, only providing limited access to the wealth of quantum nonlinear phenomena underlying the dynamical response of nanostructures. Here, we theoretically investigate electron-light interactions between photons and electrons of comparable energies, revealing quantum and recoil effects that include a nonvanishing coupling of surface-scattered electrons to light plane waves, inelastic electron backscattering from confined optical fields, and strong electron-light coupling under grazing electron diffraction by an illuminated crystal surface. Our exploration of electron-light-matter interactions holds potential for applications in ultrafast electron microscopy. [ABSTRACT FROM AUTHOR]

Thanks to advancements in silicon photomultiplier sensors (SiPMs) and system-on-chip (SoC) technology, our INFN Roma1 group developed ArduSiPM in 2012, the first all-in-one scintillator particle detector in the literature. It used a custom Arduino Due shield to process fast signals, utilizing the Microchip Sam3X8E SoC's internal peripherals to control and acquire SiPM signals. The availability of radiation-tolerant SoCs, combined with the goal of reducing system space and weight, led to the development of an innovative second-generation board, a better-performing device called Cosmo ArduSiPM, suitable for space missions. The architecture of the new detector is based on the Microchip SAMV71 300 MHz, 32-bit ARM® Cortex®-M7 (Microchip Technology Inc., Chandler, AZ, USA). While the analog front-end is essentially identical to the ArduSiPM, it utilizes components with the smallest possible package. The board fits in a CubeSat module. Thanks to the compact design, the board has two independent channels, with a total weight of only 40 grams within a CubeSat form factor. The ArduSiPM architecture is based on a single microcontroller and fast discrete analog electronics. It benefits from the continued development of SoCs related to the IoT (Internet of Things) market. Compared with a system with a custom ASIC, this architecture based on software and SoC capabilities offers considerable advantages in terms of cost and development time. The ability to incorporate new commercial SoCs, continuously emerging from advancements in the aerospace and automotive industries, provides the system with a robust foundation for sustained growth over the years. A detailed characterization of the hardware and the system's response to different photon fluxes is presented in this article. Additionally, coupling the device with a scintillator was tested at the end of this article as a preliminary trial for future measurements, showing potential for further enhancement of the detector's capabilities. [ABSTRACT FROM AUTHOR]

Due to the rapid advancements in medical radiography, nondestructive inspection, and radiation detection, there is an increasing demand for scintillators that offer both cost-effectiveness and high-resolution X-ray imaging. In this study, we have successfully synthesized transparent glass-ceramic scintillator by embedding Tb3+-doped NaLu 2 F 7 nanocrystals in a glass matrix. This scintillator demonstrates excellent spatial resolution of 20 lp/mm in X-ray imaging due to its high transmittance (over 90% at 550 nm) and intense luminescent intensity when excited by X-ray (151% higher than that of the Bi 4 Ge 3 O 12 scintillator). More significantly, the as-synthesized scintillator exhibits exceptional stabilities at high temperature, moisture levels, and moderate radiation exposure. Notably, any decline in performance caused by long-term exposure to high-dose X-ray can be fully recovered through heat treatment at 350 °C for 30 min. These findings highlight the great potential of NaLu 2 F 7 :Tb3+ glass ceramics as suitable options for high-resolution and retrievable X-ray imaging. [ABSTRACT FROM AUTHOR]

The large size (4 cm × 4 cm × 1 cm) Ce3+-doped high gadolinium oxyfluoride glass with density of 5.83 g/cm³ was prepared by the melt quench method at 1220 °C. The glass is colorless and transparent over the visible range. The prolonged decay time under 275 nm UV light demonstrates the energy transfer from Gd3+ ions to Ce3+ ions. The X-ray excited luminescence spectra (XEL) show the emission peak corresponds to the 5d→4f transitions of Ce3+ ion. The integral emission intensity of glass was compared with that of bismuth germanate oxide (BGO) crystals. The scintillation property of glass was studied under the γ -ray from 137Cs source and a clear energy peak was observed with light yield (LY) over 1100 ph/MeV. The scintillation decay time comprises fast and slow components. All results presented in this work indicate the appropriate potential to be high-energy rays detecting material for CEPC. [ABSTRACT FROM AUTHOR]

A series of lead-free Rb2ZrCl6:xTe4+ (x = 0%, 0.1%, 0.5%, 1.0%, 2.0%, 3.0%, 5.0%, 10.0%) perovskite materials were synthesized through a hydrothermal method in this work. The substitution of Te4+ for Zr in Rb2ZrCl6 was investigated to examine the effect of Te4+ doping on the spectral properties of Rb2ZrCl6 and its potential applications. The incorporation of Te4+ induced yellow emission of triplet self-trapped emission (STE). Different luminescence wavelengths were regulated by Te4+ concentration and excitation wavelength, and under a low concentration of Te4+ doping (x ≤ 0.1%), different types of host STE emission and Te4+ triplet state emission could be achieved through various excitation energies. These luminescent properties made it suitable for applications in information encryption. When Te4+ was doped at high concentrations (x ≥ 1%), yellow triplet state emission of Te4+ predominated, resulting in intense yellow emission, which stemmed from strong exciton binding energy and intense electron-phonon coupling. In addition, a Rb2ZrCl6:2%Te4+@RTV scintillating film was fabricated and a spatial resolution of 3.7 lp/mm was achieved, demonstrating the potential applications of Rb2ZrCl6:xTe4+ in nondestructive detection and bioimaging. [ABSTRACT FROM AUTHOR]

In this paper, we present the new multi-wavelength dataset of aerosol extinction profiles, which are retrieved from the averaged transmittance spectra by the Global Ozone Monitoring by Occultation of Stars instrument aboard the Envisat satellite. Using monthly and zonally averaged transmittances as a starting point for the retrievals enables us to improve the signal-to-noise ratio and eliminate possible modulation of transmittance spectra by uncorrected scintillations. The two-step retrieval method is used: the spectral inversion is followed by the vertical inversion. The spectral inversion relies on the removal of contributions from ozone, NO2 , NO3 and Rayleigh scattering from the optical depth spectra for each ray perigee altitude. In the vertical inversion, the profiles of aerosol extinction coefficients at several wavelengths are retrieved from the collection of slant aerosol optical depth profiles. The retrieved aerosol extinction profiles (FMI-GOMOSaero dataset v1) are provided in the altitude range 10–40 km at wavelengths of 400, 440, 452, 470, 500, 525, 550, 672 and 750 nm for the whole GOMOS operating period from August 2002 to March 2012. Extensive intercomparisons of the retrieved FMI-GOMOSaero aerosol profiles with aerosol profile data from other satellite instruments at several wavelengths have been performed. It is found that the average difference between FMI-GOMOSaero and other datasets is within 20 %–40 % in the lower and middle stratosphere, the standard deviation is ∼ 20 %–50 %, and the correlation coefficient of the time series is 0.65–0.85. The created FMI-GOMOSaero dataset can be used in merged datasets of stratospheric aerosols. It might be also used as a priori information for satellite retrievals during 2002–2012. [ABSTRACT FROM AUTHOR]

Upconversion nanoparticles (UCNPs), particularly those that are highly doped, possess outstanding properties and have demonstrated tremendous application potential. However, novel fine-tuning strategies are urgently required to enhance the upconversion luminescence (UCL) performance of UCNPs. In this study, a series of core–multishell UCNPs highly doped with Ho3+ and Yb3+ ions were synthesized via the oleate route. The X-ray diffraction (XRD), transmission electron microscopy (TEM), and UCL spectra and decay times, and pump power dependency of the synthesized UCNPs were used to examine their morphology, size, and the UCL properties. Ce3+ ions were introduced to enhance Ho3+-based red UCL, and their doping strategy was also optimized based on summarized UCL trends and detailed UCL mechanism analysis. NaHoF 4 :Gd3+@NaGdF 4 :Yb3+,Ce3+@NaGdF 4 :Yb3+ UCNPs that had 10 mol% Ce3+ dopants in their middle shells exhibited better UCL properties than the larger traditional NaGdF 4 :Yb3+,Ce3+,Ho3+ UCNPs, probably because of the combined influence of the energy interactions between the Ce3+ ions and surface groups, sensitizing energy enhancement by active shells, and the positive cooperation between the Ce3+ ions and highly-doped core–shell structures. In this study, the phenomenon of UCL decrease resulting from Ce3+ ion doping was explored. Using unique core–multishell structures with highly-doped activators and sensitizers placed within and outside the structures, respectively, the UCL decrease due to Ce3+ ion doping was attributed to a competition for photons. Doping the UCNPs with Ce3+ ions near the UCNP surfaces favors Ho3+-based red UCL. Our study findings can deepen the understanding of the Ho3+-based UCL mechanisms and increase the potential uses of NaHoF 4 materials in photo-induced therapy. When Ce3+ ions are doped near the nanoparticle surface, they might have energy interactions with surface groups to relieve phonon energy shortage and thus enhance the efficiency of cross-relaxation between Ho3+ and Ce3+ ions. [Display omitted] [ABSTRACT FROM AUTHOR]

The phosphor-converted white light-emitting diodes (pc- w LEDs) are current research hotspot. To meet simultaneously the requirements of high chemical/thermal stability and color-rendering index (CRI), low correlated color temperature (CCT) for actual application is still not be perfectly achieved. Herein, we studied for the first time the incorporation of Ce3+ (blue-emitting) and Mn2+ (orange/red emission) into the dibarium magnesium phosphate ceramic (Ba 2 Mg(PO 4) 2 , BMP) for packaging of pc- w LEDs via remote 'capping' approach, which exhibits highly efficient color-tunable photoluminescence (PL) with splendid chemical/thermal stability, single-phase/full-color-PL, efficient energy transfer (ET). To reduce the impact of heterovalent substitution (Ba2+ ← Ce3+), the monovalent (Li+, Na+, K+) ion, respectively tridoped in BMP: Ce/Mn and played both roles as flux and charge compensator, were also studied/compared on the basis of PL efficiency, where Na+ is the most effective because of the lowest electronegativity mismatch between the Ba2+ and Na+. An alkaline-earth-metal-ion blending strategy via partial replacement of Ba2+ with Sr2+ was implemented to further regulate PL and obtain better parameters of CCT/CRI due to the variations of crystal field splitting. The site occupations of Ce/Na/Sr in Ba sites (CN = 8 and 7) and Mn in Mg site (CN = 6) were based on the comparisons of ion radius and confirmed by XRD/Rietveld analyses, where Ce/Na/Sr ions gave priority to occupy the Ba site with CN = 8 due to their much closer ion radius. Altogether, the stably composition-optimized BMP: Ce/Mn/Na/Sr has great potential application as a single-component color-tunable phosphor in n -UV pumped pc- w LEDs. The pc- w LED fabricated via remote 'capping' approach by combination of a n -UV chip with BMP: Ce/Mn/Na/Sr phosphor through Ce to Mn ET with the help of charge compensator of Na and the alkaline-earth-metal-ions blending by Ba/Sr replacement. [Display omitted] • Ce/Sr/Na occupied at Ba sites while Mn sited in Mg sites. • ET occurs efficiently from Ce to Mn. • Na + acts as charge balancer to improve PL efficiency. • Replacing partial Ba by Sr could regulate PL and improve ET efficiency. • pc- w LED via ' n -UV LED + white-emitting BMP: Ce/Mn/Na/Sr' is achieved. [ABSTRACT FROM AUTHOR]

Open Hardware-based microcontrollers, especially the Arduino platform, have become a comparably easy-to-use tool for rapid prototyping and implementing creative solutions. Such devices in combination with dedicated front-end electronics can offer low-cost alternatives for student projects, slow control and independently operating small-scale instrumentation. The capabilities can be extended to data taking and signal analysis at mid-level rates. Two detector realizations are presented, which cover the readouts of proportional counter tubes and of scintillators or wavelength-shifting fibers with silicon photomultipliers (SiPMs). The SiPMTrigger realizes a small-scale design for coincidence readout of SiPMs as a trigger or veto detector. It consists of a custom mixed signal front-end board featuring signal amplification, discrimination and a coincidence unit for rates of up to 200 kHz. The nCatcher transforms an Arduino Nano to a proportional counter readout with pulse shape analysis: time over threshold measurement and a 10-bit analog-to-digital converter for pulse heights. The device is suitable for low-to-medium-rate environments up to 5 kHz, where a good signal-to-noise ratio is crucial. We showcase the monitoring of thermal neutrons. For data taking and slow control, a logger board is presented that features an SD card and GSM/LoRa interface. [ABSTRACT FROM AUTHOR]

• CeBr 3 and NaI (Tl) scintillators characterized with array of Silicon Photomultipliers. • Energy resolution improves with lower shaping time and higher SiPM over-voltage. • Temperature dependency of gain of SiPM array: ∼−0.81 %/°C for overvoltage of 2.5 Volts. • Temperature dependency of light yield for CeBr 3 : ∼−0.27 %/°C for −31 °C to +26 °C. • Temperature dependency of light yield for NaI (Tl): ∼+0.5 %/°C for −31 °C to +26 °C. Interaction of X-rays with a scintillation detector produces optical photons in the visible range. The spectral and spatial information of the X-ray can be derived by detecting these output photons using a Silicon Photomultiplier (SiPM). Two types of detector modules: CeBr 3 and NaI (Tl), coupled with an array of SiPM are presented here, which are being developed for the future space exploration programs. The development of the front end electronics (FEE) for the charge readout from SiPM for X-ray spectrometer application is presented here which is characterized for SiPM's over-voltages and shaping amplifier's time constant. In this article, both the detector modules are subjected to a wide temperature range to establish a relationship of the SiPM's gain, energy resolution and scintillators' output photon yield with ambient temperature. The test results show that energy resolution improves with higher over-voltage of SiPM and also with lower operating temperature. The gain of the SiPM array shows negative temperature dependence of ∼−0.81 %/°C for an over-voltage of 2.5 Volts. To derive the temperature dependency of scintillators' output photons, gain of the SiPM array was made constant by operating it at a fixed over-voltage for a wide temperature range. With the constant gain of SiPM, CeBr 3 scintillator shows negative temperature coefficient of ∼−0.27 %/°C and NaI (Tl) shows positive temperature coefficient of ∼+0.5 %/°C for the light output in the temperature range of −31 °C to +26 °C. [ABSTRACT FROM AUTHOR]

Quasi-zero-dimensional quantum dots (QDs) have garnered significant attention owing to their distinct structural attributes, quantum confinement behaviors, optoelectronic characteristics, etc. Regrettably, their susceptibility to stability poses a challenge. In this context, leveraging rational component regulation and crystallization process optimization strategies, we presented the successful preparation of CdS QDs silicate glass through the amalgamation of melt-quenching and controlled crystallization. The optical and morphological analysis substantiated the accomplishment of in-situ precipitation of CdS QDs within the glass matrix, with grain sizes <20 nm. Integrating CdS QDs into an inorganic glass matrix remarkably augmented its fluorescence thermal stability, enabling the preservation of 85.1 % of the room-temperature luminescent intensity even at an elevated temperature of 150 °C. Moreover, the encapsulated W-LED device by near-UV LED chip, CdS QDs glass, and BaMgAl 10 O 17 :Eu2+ phosphor exhibited a warm white-light emission characterized by suitable chromaticity coordinates (0.3741, 0.3452) and a notably high color rendering index (CRI = 93). Ultimately, the radioluminescence behavior of CdS QDs glass was unveiled by utilizing it as the scintillator wafer in an X-ray imaging system, which clearly demonstrated the structure of spring encapsulated within an opaque capsule. In a nutshell, these demonstrations unequivocally emphasize the substantial potential merits of CdS QDs glass, particularly in the domains of long-term W-LED lighting and X-ray imaging applications. [ABSTRACT FROM AUTHOR]

The overall gain of a scintillation detector is temperature-dependent, leading to a drift in the measured gamma energy spectrum with changes in temperature. To mitigate this effect, a temperature drift correction is essential prior to conducting gamma spectrum analysis. In this study, the detector gain ratio is determined by comparing the positions of the same background peak across different spectra. Subsequently, the original spectrum is adjusted accordingly to obtain a gamma spectrum free from temperature drift. Experimental results demonstrate that after implementing this correction, the relative deviation of the 57Co characteristic peak positions in the gamma spectrum measured by the NaI(Tl) detector is reduced from 18.64% to 0.91%. Furthermore, by performing energy calibration beforehand, the characteristic peak position can be utilized for secondary correction, further minimizing temperature drift. Our findings indicate that the relative deviation of the 22Na characteristic peak positions was reduced, respectively, to 0.51% and 0.46% through secondary correction. This approach, which utilizes the background peak for correction, avoids the need for additional radioactivity or circuitry and effectively mitigates peak drift. Overall, this method holds significant implications for enhancing the accuracy of gamma spectrum analysis. [ABSTRACT FROM AUTHOR]

Autonomous nuclear reactor monitoring is a key aspect of the International Atomic Energy Agency's strategy to ensure nonproliferation treaty compliance. From the rise of small modular reactor technology, decentralized nuclear reactor fleets may strain the capacities of such monitoring and requires new approaches. We demonstrate the superior capabilities of a gamma detection system to monitor the criticality of a zero power nuclear reactor from beyond typical vessel boundaries, offering a powerful alternative to neutron-based systems by providing direct information on fission chain propagation. Using the case example of the research reactor CROCUS, we demonstrate how two bismuth germanate scintillators placed outside the reactor vessel can precisely observe reactor criticality using so called noise methods and provide core status information in seconds. Our results indicate a wide range of applications due to the newly gained geometric flexibility that could find use in fields beyond nuclear safety. [ABSTRACT FROM AUTHOR]

Proton radiography is a promising development in proton therapy, and researchers are currently exploring optimal detector materials to construct proton radiography detector arrays. High-density glass scintillators may improve integrating-mode proton radiography detectors by increasing spatial resolution and decreasing detector thickness. We evaluated several new scintillators, activated with europium or terbium, with proton response measurements and Monte Carlo simulations, characterizing relative luminosity, ionization quenching, and proton radiograph spatial resolution. We applied a correction based on Birks's analytical model for ionization quenching. The data demonstrate increased relative luminosity with increased activation element concentration, and higher relative luminosity for samples activated with europium. An increased glass density enables more compact detector geometries and higher spatial resolution. These findings suggest that a tungsten and gadolinium oxide-based glass activated with 4% europium is an ideal scintillator for testing in a full-size proton radiography detector. [ABSTRACT FROM AUTHOR]

The reduction in the effective dose of evacuated injured persons through contaminated areas of nuclear accidents is an essential emergency services requirement. In this context, there appeared a need to develop a dose-optimised route finding method for firefighting rescue vehicles, which includes the development of a real-time decision support measurement and evaluation system. This determines and visualises the radiation exposure of possible routes in a tested area. The system inside and outside of the vehicle measures the ambient dose equivalent rate, the gamma spectra, and also the airborne radioactive aerosol and iodine levels. The method uses gamma radiation measuring NaI(Tl) scintillation detectors mounted on the outside of the vehicle, to determine the dose rate inside the vehicle using the previously recorded attenuation conversation function, while continuously collecting the air through a filter and using an alpha, beta, and gamma radiation measuring NaI(Tl)+ PVT + ZnS(Ag) scintillator to determine the activity concentration in the air, using these measured values to determine the effective dose for all routes and all kinds of vehicles. The energy-dependent shielding effect of the vehicle, the filtering efficiency of the collective protection equipment, and the vehicle's speed and travel time were taken into account. The results were validated by using gamma point sources with different activity and energy levels. The measurement results under real conditions and available real accident data used in our simulations for three different vehicles and pedestrians proved the applicability of the system. During a nuclear accident based on our model calculations, the inhalation of radioactive aerosols causes a dose almost an order of magnitude higher than the external gamma radiation caused by the fallout contamination. The selection of the appropriate vehicle and its route is determined by the spectrum that can be measured at the accident site but especially by the radioactive aerosol concentration in the air that can be measured in the area. In the case of radiation measuring detectors, the shielding effect of the carrier vehicle must be taken into account, especially in the case of heavy shielding vehicles. The method provides an excellent opportunity to reduce the damage to the health of accident victims and first responders during rescue operations. [ABSTRACT FROM AUTHOR]

In recent years, indirect digital radiography detectors have been actively studied to improve radiographic image performance with low radiation exposure. This study aimed to achieve low-dose radiation imaging with a thick scintillation detector while simultaneously obtaining the resolution of a thin scintillation detector. The proposed method was used to predict the optimal point spread function (PSF) between thin and thick scintillation detectors by considering image quality assessment (IQA). The process of identifying the optimal PSF was performed on each sub-band in the wavelet domain to improve restoration accuracy. In the experiments, the edge preservation index (EPI) values of the non-blind deblurred image with a blurring sigma of σ = 5.13 pixels and the image obtained with optimal parameters from the thick scintillator using the proposed method were approximately 0.62 and 0.76, respectively. The coefficient of variation (COV) values for the two images were approximately 1.02 and 0.63, respectively. The proposed method was validated through simulations and experimental results, and its viability is expected to be verified on various radiological imaging systems. [ABSTRACT FROM AUTHOR]

We explored the nonlinear characteristics of energy resolution (ER) for the sealed NaI (Tl) scintillator detector by using a gamma-ray spectroscopy system and Monte Carlo simulation. Our research focused on the two primary factors of energy resolution including the photomultiplier tube (PMT) voltage and the distance between the gamma-ray sources (137Cs and 60Co) and the scintillator detector. The experimental results showed that energy resolution decreased when the PMT voltage increased, and the energy resolution of NaI (Tl) detectors reached a smaller value (6.92%, 6.76%, and 6.56%), especially with the PMT voltage in the range of 575–595 V. In addition, a suitable distance between the gamma-ray source and the scintillator (5 cm) can also effectively reduce the energy resolution. We established the simulation models of the experimental NaI (Tl) detectors and simulated their energy spectra. The simulation results in the peak area agreed with the experimental results. A possible better PMT voltage choice has been proposed to obtain a smaller energy resolution. [ABSTRACT FROM AUTHOR]

Fast neutron beams (E n > 1 MeV) are of relevance for many scientific and industrial applications. This paper explores fast neutron production using a TANDEM accelerator at the Legnaro National Laboratories, via an energetic ion beam (90 MeV 14 N ) onto a lithium target. The high energy models for nuclear collision of FLUKA foresee large neutron yields for reactions of this kind. The experiment aimed at validating the expected neutron yields from FLUKA simulations, using two separate and independent set-ups: one based on the multi-foil activation technique, and the other on the time of flight technique, by using liquid scintillator detectors. The results of the experiment show clear agreement of the measured spectra with the FLUKA simulations, both in the shape and the magnitude of the neutron flux at the measured positions. The neutron spectrum is centered around the 8 MeV range with mild tails, and a maximum neutron energy spanning up to 50 MeV. These advantageous results provide a starting point in the development of fast neutron beams based on high energy ion beams from medium-sized accelerator facilities. [ABSTRACT FROM AUTHOR]

(1) Background: Generally, in nuclear medicine and nuclear power plants, energy spectrum measurements and radioactive nuclide identification are required for evaluation of strong radiation fields to ensure nuclear safety and security; thereby, damage is prevented to nuclear facilities caused by natural disasters or the criminal smuggling of nuclear materials. High count rates can lead to signal accumulation, negatively affecting the performance of gamma spectrometers, and in severe cases, even damaging the detectors. Higher pulse throughput with better energy resolution is the ultimate goal of a gamma-ray spectrometer. Traditionally, pileup pulses, which cause dead time and affect throughput, are rejected to maintain good energy resolution. (2) Method: In this paper, an ultra-throughput boost (UTB) off-line processing method was used to improve the throughput and reduce the pileup effect of the spectrometer. Firstly, by fitting the impulse signal of the detector, the response matrix was built by the functional model of a dual exponential tail convolved with the Gaussian kernel; then, a quadratic programming method based on a non-negative least squares (NNLS) algorithm was adopted to solve the constrained optimization problem for the inversion. (3) Results: Both the simulated and experimental results of the UTB method show that most of the impulses in the pulse sequence from the scintillator detector were restored to δ-like pulses, and the throughput of the UTB method for the NaI(Tl) spectrometer reached 207 kcps with a resolution of 7.71% @661.7 keV. A reduction was also seen in the high energy pileup phenomenon. (4) Conclusions: We conclude that the UTB method can restore individual and piled-up pulses to δ-like sequences, effectively boosting pulse throughput and suppressing high-energy tailing and sum peaks caused by the pileup effect at the cost of a slight loss in energy resolution. [ABSTRACT FROM AUTHOR]

Ce-doped gadolinium gallium aluminum oxide (Ce: GGAG) precursors were first prepared by the microwave-assisted homogeneous precipitation method (MAHP). Thermal gravity-differential thermal analysis (TG-DTA), X-ray diffraction (XRD), specific surface area analysis (BET) and field emission scanning electron microscopy (FE-SEM) were employed to investigate the crystal structure, phase evolution and morphologies of the Ce: GGAG precursors and powders. The influence of Ga ion concentration in the salt solution on the properties of Ce: GGAG powders was investigated. All the precursors were transformed into single-phase GGAG after being calcined at 950 °C in a furnace for 3 h. Monodispersed Ce: GGAG powders were obtained as the Ga ion concentration was lower than 0.06 mol/L. Single-phase and dense Ce: GGAG ceramics were obtained after sintering at 1600 °C in a flowing oxygen atmosphere for 10 h. Specifically, the Ce: GGAG ceramic reached its maximum density of ~6.68 g/cm3, which was close to its theoretical density of 6.70 g/cm3, and exhibited the highest optical transmittance of 65.2% at 800 nm after hot isostatic pressing sintering (HIP) as the Ga ion concentration was 0.02 mol/L. The decay time and light yield of the GGAG ceramic were 35 ns and 35,000 ± 1250 ph/MeV, respectively, suggesting that Ce: GGAG ceramics prepared using MAHP-synthesized nanopowders are promising for scintillation applications. [ABSTRACT FROM AUTHOR]

(1) Background: High dose gradients and manual steps in brachytherapy treatment procedures can lead to dose errors which make the use of in vivo dosimetry (IVD) highly recommended for verifying brachytherapy treatments. A new procedure was presented to obtain a calibration factor which allows fast and robust calibration of plastic scintillation detector (PSD) probes for the geometry of a compact phantom using Monte Carlo simulations. Additionally, characterization of PSD energy, angular, and temperature dependences was performed. (2) Methods: PENELOPE/PenEasy code was used to obtain the calibration factor. To characterize the energy dependence of the PSD, the signal was measured at different radial and transversal distances. The sensitivity to the angular position was characterized in axial and azimuthal planes. (3) Results: The calibration factor obtained allows for an absorbed dose to water determination in full scatter conditions from ionization measured in a mini polymethylmethacrylate (PMMA) phantom. The energy dependence of the PSD along the radial distances obtained was (2.3 ± 2.1)% (k = 1). The azimuthal angular dependence measured was (2.6 ± 3.4)% (k = 1). The PSD response decreased by (0.19 ± 0.02)%/°C with increasing detector probe temperature. (4) Conclusions: The energy, angular, and temperature dependence of a PSD is compatible with IVD. [ABSTRACT FROM AUTHOR]

A facile and low-cost strategy to fabricate CsPbBr3 single crystals is essential for developing perovskite optoelectronic devices. Herein, we have presented a room temperature anti-solvent precipitate method for growing sub-centimeter-sized CsPbBr3 single crystals. The as-prepared CsPbBr3 single crystal has an orthorhombic structure, and phase transition occurs as the measured temperature increases. The as-grown CsPbBr3 single crystal also shows abundant surface morphologies including footsteps, precipitated crystals, cracks, and pits. Subsequently, a metal–semiconductor–metal (MSM)-structured photodetector was fabricated based on the CsPbBr3 single crystal. Under 525 nm green light illumination, the photodetector exhibits an obvious response and the photocurrent linearly increases with the increase in the light intensity. The rise time of the photodetector increases from 0.82 s to 2.19 s as the light intensity is enhanced from 15 mW/cm2 to 160 mW/cm2, indicating that more time is required to reach to a stable photocurrent. However, the decay time is as fast as ~0.82 ms, irrelevant of the light intensity. The photocurrent, under continuous light illumination, was further studied and this indicates that a stronger light intensity can accelerate the attenuation of the device. [ABSTRACT FROM AUTHOR]

Gamma-ray spectroscopy is an effective technique for radioactive material characterization, routine inventory verification, nuclear safeguards, health physics, and source search scenarios. Gamma-ray spectrometers typically cannot be operated in the immediate vicinity of nuclear reactors due to their high flux fields and their resulting inability to resolve individual pulses. Low-power reactor facilities offer the possibility to study reactor gamma-ray fields, a domain of experiments hitherto poorly explored. In this work, we present gamma-ray spectroscopy experiments performed with various detectors in two reactors: The EPFL zero-power research reactor CROCUS, and the neutron beam facility at the Ohio State University Research Reactor (OSURR). We employed inorganic scintillators (CeBr3), organic scintillators (trans-stilbene and organic glass), and high-purity germanium semiconductors (HPGe) to cover a range of typical—and new—instruments used in gamma-ray spectroscopy. The aim of this study is to provide a guideline for reactor users regarding detector performance, observed responses, and therefore available information in the reactor photon fields up to 2 MeV. The results indicate several future prospects, such as the online (at criticality) monitoring of fission products (like Xe, I, and La), dual-particle sensitive experiments, and code validation opportunities. [ABSTRACT FROM AUTHOR]

Er3+ doped high density germanate glasses with compositions of 50GeO 2 -10BaO–10Al 2 O 3 -15Lu 2 O 3 -(15-x) La 2 O 3 -xEr 2 O 3 (x = 0, 0.1, 0.5, 1.0, 1.5, and 2.0, in mol%) have been prepared by the melt-quenching method. The optical and physical properties of the samples were characterized by differential scanning calorimetry (DSC), density, transmittance spectra, photoluminescence (PL) spectra, and X-ray excited luminescence (XEL) spectra. The densities were in the range from 5.90 to 6.07 g/cm3. The strong green emissions around 552 nm of Er3+ were observed upon the excitations of 378 nm light and the X-ray, and the lifetimes of 552 nm emission were in the range of 20.88–96.47 μs. The results show that Er3+ doped high density germanate glasses could be used as potential scintillators for X-ray CT. [ABSTRACT FROM AUTHOR]

Commercial white light-emitting diodes (WLEDs) usually face problems such as lack of red emission, color difference caused by different degradation rates of multiphase phosphors and the poor thermal stability of the organic encapsulants. The development of new single-phase phosphors and glass can solve these problems well. Sr 3 B 14 O 24 :RE3+ (RE = Ce, Tb, Sm, Eu) phosphors and glass were synthesized by solid-phase method. The obtained Sr 3 B 14 O 24 :RE3+ (RE = Ce, Tb, Sm, Eu) samples showed multicolor emission including blue, green, orange and red, respectively. The optimal excitation wavelength of these samples was located in the blue or ultraviolet (UV) light regions, which were well matched with the blue-violet light chips to manufacture WLEDs. More interestingly, UV absorption was found in Sr 3 B 14 O 24 :Ce3+/4+ glass samples. The doping of dual-valence cerium ions could enhance the shielding performance in the light of inferences drawn from the UV-Vis absorption and transmission spectra of glass samples. By co-doping different concentrations of Cs+ ions in Sr 3 B 14 O 24 :Ce3+/4+ glass samples, the function of near infrared (NIR) shielding was also realized. As a new optical multifunctional material, rare earth doped Sr 3 B 14 O 24 have great potential for application in WLEDs, UV and NIR shielding. [ABSTRACT FROM AUTHOR]

Source localisation and real-time dose verification are at the forefront of medical research in brachytherapy, an oncological radiotherapy procedure based on radioactive sources implanted in the patient body. The ORIGIN project aims to respond to this medical community's need by targeting the development of a multi-point dose mapping system based on fibre sensors integrating a small volume of scintillating material into the tip and interfaced with silicon photomultipliers operated in counting mode. In this paper, a novel method for the selection of the optimal silicon photomultipliers to be used is presented, as well as a laboratory characterisation based on dosimetric figures of merit. More specifically, a technique exploiting the optical cross-talk to maintain the detector linearity in high-rate conditions is demonstrated. Lastly, it is shown that the ORIGIN system complies with the TG43-U1 protocol in high and low dose rate pre-clinical trials with actual brachytherapy sources, an essential requirement for assessing the proposed system as a dosimeter and comparing the performance of the system prototype against the ORIGIN project specifications. [ABSTRACT FROM AUTHOR]