X-ray Imaging Applications Research Articles

Novel Tb3+ doped borophosphate glass scintillator for X-ray imaging

In this study, we introduce an efficient green-emitting material made from Tb3+ doped borophosphate scintillating glass for X-ray imaging. An influence of Tb2O3 concentration on the physical, optical, luminescent, and scintillation properties of glasses were investigated. The glass density and refractive index increase, while the molar volume and Tb3+ inter-ionic distance decreases with Tb2O3 addition. These glasses absorb the photons in range of UV, Vis, and NIR. The excitations by UV and X-ray on glasses causes the strong green emission centered around 545 nm by the 5D4 → 7F5 transition of Tb3+. The energy transfer from Gd3+ to Tb3+ was occurred in this emission. The glass doped with 4 mol% of Tb2O3 demonstrates the highest emission intensity at 545 nm due to the concentration quenching. The decay time of glasses are in few milliseconds. The integral X-ray scintillation efficiency of 4 mol% doped glass is 52% compared to that of BGO crystal. Additionally, this glass was proceeded in the X-ray imaging and yielded the image with satisfied resolution, characteristics and MTF values, compared to that obtained from YAG:Ce crystal. The developed glass has a potential for X-ray imaging applications, especially in the medical imaging, flaw detection, and security inspection.

Practical Multi-Mesh Registration for Few-View Poly-Chromatic X-Ray Inspection

Accurate 3D mesh registration is essential in many industrial applications of X-ray imaging, as it allows quality assessment and inspection of manufactured objects. Conventional methods rely mainly on time-consuming and expensive X-ray computed tomography (X-CT) or ancillary camera systems. Instead, we propose a novel approach for efficient 3D multi-mesh registration in few-view industrial X-ray imaging scenarios. Our approach harnesses the capabilities of CAD-ASTRA, an X-ray mesh projector, compatible with the ASTRA toolbox and popular GPU libraries such as CuPy and PyTorch, for the simulation of X-ray projec tions from a known object surface mesh. As a differentiable program, CAD-ASTRA allows iterative improvement of the objects’ position in space by back-propagation of a differentiable measure of the projection error. The potential of this approach is demonstrated through tests on simultaneous multiple object registration in a poly-chromatic imaging, even in cases where the spectral characteristics of the imaging system are unknown. Results from a diverse set of real experiments highlight the efficacy of mesh registration, achieving successful registrations even when only two projections at a 10∘\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$^\\circ $$\\end{document} angle relative to the scanning system center are available. The mesh projector facilitates resource-efficient registration in industrial applications with few viewpoints, thereby reducing the demand for resources and eliminating the need for X-CT reconstruction.

Insights into luminescence and energy transfer processes in Ce3+- and Tb3+ co-doped (Gd, Y)3Al2Ga3O12 garnet single crystals

Driven by the pursuit of optimizing the luminescent properties of garnet-based single crystals for X-ray imaging applications, this work reports on the successful synthesis and in-depth characterization of GYAGG crystals doped with Ce³⁺ or Tb³⁺ ions, and doubly-doped with both of them. Micro-pulling down synthesis yielded crystals with a single cubic phase confirmed by X-ray diffraction. Photoluminescence (PL) and radioluminescence (RL) measurements on Ce³⁺,Tb³⁺ co-doped GYAGG revealed bidirectional energy transfer processes. Characteristic broadband 5d1→4f emission of Ce³⁺ centers peaking at 530 nm and narrow 4f→4f emission lines of Tb³⁺ ions starting from 5D4 level within 480–630 nm were observed. At higher doping levels, cross-relaxation in Tb³⁺ pairs resulted depleted 5D3 state and only the emission from 5D4 one was observed in the spectra. Analysis of PL decay characteristics corroborated the spectral observations, confirming progressively decreasing Ce³⁺ decay time (down to 40 ns at 15 % Tb3+) due to enhanced Ce³⁺→Tb³⁺ energy transfer. Similarly, the Tb³⁺ decay time accelerated by more than 60 % after the Ce³⁺ co-doping. Notably, co-doping with 0.5 % Ce³⁺ and 10–15 % Tb³⁺ doubled the luminescence intensity of RL spectra compared to 0.5 % Ce³⁺-doping alone, attributed to the increased density of emitting centers.

Sensitive and Low-Noise Perovskite Nanocrystal-Organic Bulk Heterostructure X-ray Detectors Enabled by Sodium Bromide-Assisted In Situ Reparation.

Perovskite nanocrystals (PNCs) offer unique advantages in large-area and thick-film deposition for X-ray detection applications due to the decoupling of the crystallization of perovskite from film formation, as well as their low-temperature and scalable deposition methods. However, the partial detachment of long-chain ligands in PNCs during the purification process would lead to the exposure of surface defects, making it challenging to ensure efficient charge carrier extraction and stable X-ray detection. In this study, we propose a beneficial strategy that involves the in situ reparation of these exposed defects with sodium bromide (NaBr) during the purification process to construct CsPbBr3 PNC-organic bulk heterostructure X-ray detectors. The NaBr-passivated PNCs exhibit stronger photoluminescence intensity and lower trap density in films compared to those of the control samples, confirming the effective passivation of halide vacancy defects. Furthermore, the NiOx hole transport layer with remarkable electron blocking capability is introduced to further suppress the dark current of the devices. Consequently, the optimal devices exhibit a large sensitivity of 4237 μC Gyair-1 cm-2 and a low dark current density of 10 nA cm-2, as well as improved operational stability, which allows for high-contrast and low-dose X-ray imaging applications.

Eu2+ doped cesium alkaline earth chloride nanocrystals in glass for X-ray imaging

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+: CsCaCl3, Eu2+: CsSrCl3, and Eu2+: Cs2BaCl4 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+: CsCaCl3 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.

Cs2NaGdCl6:Tb3+─A Highly Luminescent Rare-Earth Double Perovskite Scintillator for Low-Dose X-ray Detection and Imaging.

Rare-earth-based double perovskite (DP) X-ray scintillators have gained significant importance with low detection limits in medical imaging and radiation detection owing to their high light yield (LY) and remarkable spatial resolution. Herein, we report the synthesis of 3D double perovskite (DP) crystals, namely, Cs2NaGdCl6 and Tb3+-Cs2NaGdCl6 using hydrothermal reaction. Cs2NaGdCl6 DP single crystals exhibited a blue self-trapped exciton (STE) emission at 470 nm under ultraviolet (265 nm) excitation with a photoluminescence quantum yield (PLQY) of 8.4%. Introducing Tb3+ ions into Cs2NaGdCl6 has resulted in quenching of STE emission and enhancing green emission at 549 nm attributed to the 5D4 → 7F5 transition of Tb3+, suggesting efficient energy transfer (ET) from STE to Tb3+. This ET process is evidenced by the appearance of Tb3+ bands in the excitation spectra of the host, the shortening of the STE lifetimes in the presence of Tb3+ ions, and the enhancement of PLQY (72.6%). Furthermore, Cs2NaGdCl6:5%Tb3+ films of various thicknesses (0.1-0.6 mm) were synthesized and their X-ray scintillating performance has been examined. The Cs2NaGdCl6:5%Tb3+ film with 0.4 mm thickness has exhibited an excellent linear response to the X-ray dose rate with a low detection limit of 41.32 nGyair s-1, an LY of 39,100 photons MeV-1, and excellent radiation stability. Benefiting from the strong X-ray excited luminescence (XEL) of Cs2NaGdCl6:5%Tb3+, we developed a Cs2NaGdCl6:5%Tb3+ X-ray scintillator screen with a least thickness (0.1 mm), exhibiting remarkable imaging ability with a spatial resolution of 10.75 lp mm-1. These results suggest that Cs2NaGdCl6:Tb3+ can be a potential candidate for low-dose and X-ray imaging applications.

Layered Chalcogenide Scintillators Enabled by Reversible Hydrous-Induced Phase Transformation for High-Resolution X-ray Imaging.

Scintillation materials have been widely used in various fields, such as medical diagnosis and industrial detection. Chalcogenides have the potential to become a new generation of high-performance scintillation materials due to their high effective atomic number and good resistance to radiation damage. However, research on their application in radiation detection is currently very scarce. Herein, single crystals of rare earth ion-doped ternary chalcogenides NaGaS2/Eu were grown by a high-temperature solid-phase method. It exhibits unique characteristics of structure transformation by absorbing water molecules from the air. To maintain the anhydrous phase of the material, we have used a strategy of organic-inorganic composites of epoxy resin and NaGaS2/Eu to prepare devices for radiation detection and discuss the irradiation luminescence properties of the two phases. The anhydrous phase of NaGaS2/Eu demonstrates excellent sensitivity to X-rays, with a low detection limit of 250 nGy s-1, which is approximately 1/22 of the medical imaging dose. Additionally, composite flexible films were prepared, which exhibited excellent performance in X-ray imaging. These films enable clear observation of a wide range of objects with a high spatial resolution of up to 13.2 line pairs per millimeter (lp mm-1), indicating that chalcogenide holds promising prospects in the realm of X-ray imaging applications.

Colloidal Synthesis of Hollow Double Perovskite Nanocrystals and Their Applications in X-ray Imaging.

Rare earth-based halide double perovskites are regarded as an emerging class of X-ray scintillation materials. However, the majority of related scintillator applications are still focused on single crystal and powder systems; the application of nanocrystal (NC) scintillators is rarely reported. Here, we present the synthesis of high-purity Cs2NaTbCl6 NCs by an improved hot-injection method. Interestingly, hollow Cs2NaTbCl6 NCs are observed, the monitoring of the growth process indicates that micrometer-sized NaCl is the initial product, and then the NaCl would convert into Cs2NaTbCl6 NCs through the diffusion of Cs+ and Tb3+ into NaCl lattice, and the faster outward diffusion of Na+ results in the formation of hollow NCs. The double perovskite NCs exhibit green light emission, and the photoluminescence intensity can be significantly enhanced through Ce3+ doping. In particular, the Cs2NaTbCl6:5%Ce3+ scintillator exhibits a linear response and a low detection limit of 79.09 nGy/s when exposed to X-rays. Furthermore, a flexible scintillator film for X-ray imaging is prepared by mixing NCs with polymer, showing a high spatial resolution imaging capability of 10 lp/mm. This work provides a new strategy for hollow perovskite NCs and may shed light on the synthesis of related hollow NCs and their applications in X-ray detection.

Preparing the In-doped lead-free Cs3Cu2I5 perovskite scintillator by a co-firing technique for its application in high-resolution X-ray imaging

The perovskite scintillators have been extensively studied recently for their merits of tunable emission spectra and simple preparation processes. However, the practical applications of perovskite scintillator-based X-ray image sensor are still impeded by inadequate radioluminescence, poor environmental stability, and low imaging resolution. Herein, we demonstrate a scalable co-firing method to fabricate high-quality lead-free Cs3Cu2I5 perovskite scintillator and an Indium (In)-doping strategy is introduced to enhance its radioluminescence performance at the same time. The In-doped Cs3Cu2I5 obtains a high PLQY of 77.9% and a relative light output of 53372 ph/MeV, which are 0.34 and 1.08 times higher than those of the undoped counterpart, respectively. The X-ray detection limit of the In:Cs3Cu2I5 can reach 150.55 nGyair/s, 36.53 times lower than the requirement for X-ray medical diagnosis. The synthesized scintillator also shows superior stability under continuous high dose X-ray irradiation of 6800 μGyair/s for 120 minutes, maintaining 95% of its initial radioluminescence intensity. Furthermore, a large-area (300 cm2) flexible perovskite scintillator film is prepared, which owns a much competitive resolution of 10 lp/mm and less distortion in X-ray imaging. This work provides a practical path for the wide application of perovskite scintillator in the field of X-ray detection and imaging in near future.

Inorganic metal oxide material BaSiO3:Eu2+ for convenient 3D X-ray imaging

X-ray storage phosphors are found wide-ranging applications in medical diagnosis, nondestructive testing and X-ray imaging. However, designing X-ray storage phosphors with high electron storage capacity still poses a daunting challenge. In this study, we designed a fluorescent powder based on Eu2+-doped BaSiO3, demonstrating excellent optical information storage characteristic. Under high-energy X-ray filling, shallow traps exhibit low electron capacity and only produce weak afterglow, which greatly helps to minimize the impact of afterglow on the image quality during X-ray imaging. In addition, the deep traps at 1.01 eV filled with high-energy X-ray allow the material to store information for a long time. The crystal structure, photoluminescence (PL) and thermoluminescence (TL) spectra were studied systematically. The electron trapping properties of the material were analyzed using TL spectroscopy. Finally, we fabricated a flexible film with phosphors, the flexible film has been utilized to demonstrate high-quality real-time X-ray imaging and achieve time-delayed X-ray imaging of curved objects, such as flexible circuit boards.

Development of a toroidal soft x-ray imaging system and application for investigating three-dimensional plasma on J-TEXT

A toroidal soft x-ray imaging (T-SXRI) system has been developed to investigate three-dimensional (3D) plasma physics on J-TEXT. This T-SXRI system consists of three sets of SXR arrays. Two sets are newly developed and located on the vacuum chamber wall at toroidal positions of ° and °, respectively, while one set was established previously at °. Each set of SXR arrays consists of three arrays viewing the plasma poloidally, and hence can be used separately to obtain SXR images via the tomographic method. The sawtooth precursor oscillations are measured by T-SXRI, and the corresponding images of perturbative SXR signals are successfully reconstructed at these three toroidal positions, hence providing measurement of the 3D structure of precursor oscillations. The observed 3D structure is consistent with the helical structure of the m/n = 1/1 mode. The experimental observation confirms that the T-SXRI system is able to observe 3D structures in the J-TEXT plasma.

Fabrication of large-area photonic crystal-modified X-ray scintillator imager for optical coding imaging.

The limited pattern area of periodic nanostructures limits the development of practical devices. This study introduces an X-ray interference lithography (XIL) stitching technique to fabricate a large-area (1.5 cm × 1.5 cm) two-dimensional photonic crystal (PhC) on the YAG: Ce scintillator, which functions as an encoder in a high numerical aperture optical encoding imaging system to effectively capture high-frequency information. An X-ray imaging experiment revealed a substantial 7.64 dB improvement in the signal-to-noise ratio (SNR) across a large field of view (2.6 mm × 2.6 mm) and achieved comparable or superior image quality with half the exposure dose. These findings have significant implications for advancing practical applications of X-ray imaging.

Charge carrier trapping management in Bi3+ and lanthanides doped Li(Sc,Lu)GeO4 for x-ray imaging, anti-counterfeiting, and force recording

Discovering energy storage materials with rationally controlled trapping and de-trapping of electrons and holes upon x-rays, UV-light, or mechanical force stimulation is challenging. Such materials enable promising applications in various fields, for instance in multimode anti-counterfeiting, x-ray imaging, and non-real-time force recording. In this work, photoluminescence spectroscopy, the refined chemical shift model, and thermoluminescence studies will be combined to establish the vacuum referred binding energy (VRBE) diagrams for the LiSc1−xLuxGeO4 family of compounds containing the energy level locations of Bi2+, Bi3+, and the lanthanides. The established VRBE diagrams are used to rationally develop Bi3+ and lanthanides doped LiSc1−xLuxGeO4 storage phosphors and to understand trapping and de-trapping processes of charge carriers with various physical excitation means. The thermoluminescence intensity of x-ray irradiated LiSc0.25Lu0.75GeO4:0.001Bi3+,0.001Eu3+ is about two times higher than that of the state-of-the-art x-ray storage phosphor BaFBr(I):Eu2+. Particularly, a force induced charge carrier storage phenomenon appears in Eu3+ co-doped LiSc1−xLuxGeO4. Proof-of-concept non-real-time force recording, anti-counterfeiting, and x-ray imaging applications will be demonstrated. This work not only deepens our understanding of the capturing and de-trapping processes of electrons and holes with various physical excitation sources, but can also trigger scientists to rationally discover new storage phosphors by exploiting the VRBEs of bismuth and lanthanide levels.

Numerical modeling of defects induced dark current in halide perovskite X-ray detectors

Metal halide perovskites have been widely used in x-ray detection due to their outstanding optoelectronic properties. However, the dark current of perovskite x-ray detectors is not appreciably low for integration on thin-film transistors pixel circuits and thus limits their applications in X-ray imaging. Based on numerical models, we investigate the correlation between the dark current and defects of perovskite x-ray detectors. The deep-level defects are the major factor to induce dark current, which has a proportional relation to the defect density. Compared to deep-level defects, the dark current induced by shallow-level defects depends on both of defect energy level and defect density. At last, simulation results present a guidance to engineer defects with suitable values of density and energy level, which yields desirably low dark current. This work provides implications and theoretical guidance for the optimization of defects in halide perovskites, which is believed to assist the further development of x-ray detectors with a low dark current density.

Ce3+-doped oxyfluoride glass scintillator: optimized radioluminescence and application in X-ray imaging

Glass scintillators have attracted increasing attention for X-ray imaging because of their low cost, easy manufacturing, superb transparency, and uniformity. In this paper, oxyfluoride glass scintillators doped with Ce3+ were developed through the utilization of carbon as a reducing agent. All oxyfluoride glasses exhibit exceptional transmittance (surpassing 90% @ 550 nm). The optimal glass prepared with carbon presents excellent integrated X-ray excited luminescence (XEL) intensity. It is about 86% of that of Bi4Ge3O12, which is 2.1 times of that of glass prepared without carbon. And the spatial resolution of optimal glass for X-ray imaging can reach 18 lp·mm−1. Notably, the integrated XEL intensity of optimal sample is comparable to the best Ce3+-doped glass materials and its spatial resolution exceeds that of Ce3+-doped glass ceramics. The aforementioned results demonstrate the possible utility of Ce3+-doped glass scintillators in the field of X-ray imaging applications.

Near-Unity Green Luminescent Hybrid Manganese Halides as X-ray Scintillators.

The increasing demands in optoelectronic applications have driven the advancement of organic-inorganic hybrid metal halides (OIMHs), owing to their exceptional optical and scintillation properties. Among them, zero-dimensional (0D) low-toxic manganese-based scintillators have garnered significant interest due to their exceptional optical transparency and elevated photoluminescence quantum yields (PLQYs), making them promising for colorful light-emitting diodes and X-ray imaging applications. In this study, two OIMH single crystals of (Br-PrTPP)2MnBr4 (Br-PrTPP = (3-bromopropyl) triphenylphosphonium) and (Br-BuTPP)2MnBr4 (Br-BuTPP = (4-bromobutyl) triphenylphosphonium) were prepared via a facile saturated crystallization method. Benefiting from the tetrahedrally coordinated [MnBr4]2- polyhedron, both of them exhibited strong green emissions peaked at 517 nm owing to the d-d electron transition of Mn2+ with near-unity PLQYs of 99.33 and 86.85%, respectively. Moreover, benefiting from the high optical transparencies and remarkable luminescence properties, these manganese halides also exhibit excellent radioluminescent performance with the highest light yield of up to 68,000 photons MeV-1, negligible afterglow (0.4 ms), and linear response to X-ray dose rate with the lowest detection limit of 45 nGyair s-1. In X-ray imaging, the flexible film made by the composite of (Br-PrTPP)2MnBr4 and PDMS shows an ultrahigh spatial resolution of 12.78 lp mm-1, which provides a potential visualization tool for X-ray radiography.

Luminescent CdS quantum dot-embedded glass for W-LED lighting and X-ray imaging

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 BaMgAl10O17: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.

Transparent and Planar Cs3Cu2Cl5 Crystals for Micrometer-Resolution X-ray Imaging Screen.

Copper-based (I) halide perovskites have emerged as a promising candidate for scintillation screens in X-ray inspection and imaging areas due to their solution processability and high light yield. Here, a centimeter-sized Cs3Cu2Cl5 single crystal was grown by a slow-cooling method. The planar orientation was controlled in a space-confined chamber, generating a planar crystal which is readily used for a scintillation screen without any further shaping. The crystal exhibited a unity photoluminescence quantum yield and superior scintillation performance. The Cs3Cu2Cl5 single crystal exhibited a high light yield up to 95,000 photons/MeV, which enabled an X-ray detector of a detection limit down to 2.7 μGyair/s. The homemade imager demonstrated a spatial resolution of 105 lp/mm, representing an unprecedented micrometer resolution in laboratory. Importantly, the stability of Cs3Cu2Cl5 was significantly improved by a new surface passivation procedure, whereby the passivated crystal reserved its phase after 6 months' storage in a vial. This work introduced a new solution-based synthetic method for two-dimensional scintillating crystals, opening many avenues to high-performance X-ray imaging applications.

InCl3-Assisted Surface Defects Restoring to Enhance Lead-Free Cs2ZrCl6 Nanocrystals for X-Ray Imaging and Blue LED Applications.

As one type of recent emerging lead-free perovskites, Cs2ZrCl6 nanocrystals are widely concerned, benefiting from the eminent designability, high X-ray cutoff efficiency, and favorable stability. Improving the luminescence performance of Cs2ZrCl6 nanocrystals has great importance to cater for practical applications. In view of the surface defects frequently formed by the liquid phase method, the particle morphology and surface quality of this material are expected to be regulated if certain intervention is made in the synthesis process. In the work, differing from normal cell lattice modulation based on the ion doping, the grain size and surface morphology of Cs2ZrCl6 nanocrystals are optimized via adding a certain amount of InCl3 to the synthetic solution. The surface defects are restored to inhibit the defect-induced non-radiative transition, resulting in the improvement of the luminescence properties. Moreover, a flexible Cs2ZrCl6@polydimethylsiloxane film with excellent heat, water, and bending resistance and a light-emitting diode (LED) device are fabricated, exhibiting excellent application potential for X-ray imaging and blue LED.

Yellow-emissive organic copper(i) halide single crystals with [Cu4I4] cubane unit as efficient X-ray scintillators

The (4-bzpy)4Cu4I4 compound exhibits excellent X-ray scintillation properties with a high light yield and great potential in X-ray imaging applications.