X-ray Imaging Applications Research Articles

A study of structural effects on the focusing and imaging performance of hard X-rays with 20-30 nm zone plates.

Hard X-ray microscopes with 20-30 nm spatial resolution ranges are an advanced tool for the inspection of materials at the nanoscale. However, the limited efficiency of the focusing optics, for example, a Fresnel zone plate (ZP) lens, can significantly reduce the power of a nanoprobe. Despite several reports on ZP lenses that focus hard X-rays with 20 nm resolution -mainly constructed by zone-doubling techniques -a systematic investigation into the limiting factors has not been reported. We report the structural effects on the focusing and imaging efficiency of 20-30 nm-resolution ZPs, employing a modified beam-propagation method. The zone width and the duty cycle (zone width/ring pitch) were optimized to achieve maximum efficiency, and a comparative analysis of the zone materials was conducted. The optimized zone structures were used in the fabrication of Pt-hydrogen silsesquioxane (HSQ) ZPs. The highest focusing efficiency of the Pt-HSQ-ZP with a resolution of 30 nm was 10% at 7 keV and >5% in the range 6-10 keV, whereas the highest efficiency of the Pt-HSQ-ZP with a resolution of 20 nm was realized at 7 keV with an efficiency of 7.6%. Optical characterization conducted at X-ray beamlines demonstrated significant enhancement of the focusing and imaging efficiency in a broader range of hard X-rays from 5 keV to 10 keV, demonstrating the potential application in hard X-ray focusing and imaging.

In Situ Crystal Growth and Fusing-Confined Engineering of Quasi-Monocrystalline Perovskite Thick Junctions for X-ray Detection and Imaging.

Metal halide perovskites exhibit great promise for utilization in X-ray detection owing to their excellent optoelectronic properties and high X-ray attenuation capabilities. However, fabricating large-area thick films for high-performance perovskite X-ray detection remains challenging. This study develops an in situ crystal growth and fusing-confined approach to prepare high-quality, large-scale perovskite quasi-monocrystalline thick junctions. The perovskite crystals are grown in situ using a highly concentrated perovskite colloidal solution in 2-methoxyethanol. Introducing methylammonium chloride enhances grain reorganization during in situ growth and fusing-confined processes, effectively reducing grain boundaries and surface defects. This allows for the preparation of quasi-monocrystalline thick junctions of large grains (>100 μm) with high crystallinity, uniform orientation, and vertical penetration across the film thickness. Additionally, the carrier mobility and lifetime of the thick junctions are significantly enhanced. The optimized MAPbI3 detectors demonstrate an X-ray sensitivity of 2.6 × 104 μC Gyair-1 cm-2 and an exceptionally low detection limit of 1 nGyair s-1. Furthermore, inspired by a honeycomb structure, these detectors realize X-ray imaging in 64 × 64 pixels through a pixelated separation design, effectively reducing the charge-sharing effect. This study offers valuable insights into the preparation of large-scale perovskite quasi-monocrystalline thick junctions for highly sensitive X-ray detection and imaging applications.

Reversible Interconversion between Ag2 and Ag6 Clusters and Their Responsive Optical Properties.

The exploration of structural interconversion in clusters triggered by external stimuli has attracted significant interest due to its potential to elucidate structure-property relationships of metal clusters. In this study, two types of silver clusters, Ag2 and Ag6, are synthesized. Interestingly, the clusters exhibit reversible transformations in response to changes in the solvent conditions. The structures and optical properties of these clusters are thoroughly characterized using techniques such as mass spectrometry, single-crystal X-ray diffraction, photoluminescence, and radioluminescence spectroscopy. While both Ag2 and Ag6 display excellent photoluminescence properties, Ag2 demonstrates superior performance in X-ray radioluminescence compared to Ag6. Flexible scintillator films fabricated from Ag2 clusters exhibit outstanding X-ray imaging capabilities, achieving a spatial resolution of 15.0 lp/mm and an impressive detection limit for an X-ray dose of 0.58 μGy s-1. This detection limit is nearly 10 times lower than the typical dose rate used in X-ray diagnostics (5.5 μGy s-1). This work introduces a novel approach for designing thiol-free silver clusters capable of solvent-dependent reversible interconversion, offering new insights into the development of silver clusters for advanced X-ray imaging applications.

Green massive mechanical synthesis of highly efficient Zn-Doped Cs3Cu2I5 for LED and X-ray imaging applications

As a new generation of environmentally friendly halide materials, Cs3Cu2I5 shows up the promising application in scintillation, LED, and photoelectric detection fields. However, liquid phase methods cannot produce Cs3Cu2I5 on a large scale, and the preparation process is accompanied by serious pollution. Although the ball milling method can solve the problems caused by the liquid phase synthesis method, the Cs3Cu2I5 obtained has many surface defects and low luminescence efficiency. In this work, a strategy of doping-assisted ball-milling synthesis using ZnI2 is proposed. Similar to the chemical preparation of Cs3Cu2I5, the iodine-rich environment during the modified ball milling process can also play a role in repairing surface defects. And it has been demonstrated through experiments and first principles calculations that the distortion of [Cu2I5]3- under ground/excited state can be adjusted through doping Zn into the Cu1 site, the formation barrier of self-trapped excitons is reduced, and the luminous efficiency of Cs3Cu2I5 is significantly improved. Subsequently, using the simple hot-pressing method, the representative Cs3Cu2I5:1.0Zn sample was combined with commercially available polypropylene to fabricate Cs3Cu2I5:1.0Zn@PP film. Finally, the potential applications of the newly-developed film in portable and customizable WLED and scintillation fields were explored.

Development and performance evaluation of a thin GAGG:Ce scintillator plate for high resolution synchrotron radiation X-ray imaging

Scintillator-based X-ray imaging detectors are pivotal in numerous scientific and practical domains, including medical imaging, food and device inspection, and security monitoring. Recent advancements have spurred interest in 4D X-ray imaging using synchrotron radiation, necessitating higher temporal resolutions. Consequently, this places stringent demands on X-ray detector technology, especially when X-ray energy exceeds 20 keV. The selection of a suitable scintillator material is crucial for achieving optimal timing resolution, yet it poses a significant challenge in dynamic X-ray imaging. This study delves into the optimization of scintillator properties and their impact on spatial resolution and light output, elucidating the performance of Ce-doped Gd3Ga3Al2O12 (GAGG:Ce) scintillators for X-ray imaging applications. We developed a micro X-ray imaging detector using a 100 μm-thick GAGG:Ce scintillator plate and conducted X-ray imaging tests at the Aichi SR facility. The results demonstrated that the resolution, quantified as the chart slit width at a contrast transfer function (CTF) value of 10%, reached 2 ∼ 3 μm with a 4× lens, 0.52 μm± 0.03 μm with a 20× lens, and 0.42 μm± 0.01 μm with a 40× lens. Although the results of this study did not achieve a spatial resolution nearing the effective pixel size of the 40× lens, the text also elucidates the underlying reasons for this limitation. Furthermore, we compared the X-ray sensitivity of our GAGG:Ce scintillator plate with that of a commercial LuAG:Ce scintillator, revealing an approximately 1.5-fold increase in light output. As a demonstration, transmission images of dried small fish were captured using the GAGG:Ce scintillator plate and the developed X-ray imaging system. These findings highlight the potential of the X-ray imaging detector devised in this study for future generations of X-ray imaging applications.

Tb-doped borosilicate glass scintillators with high thermal stability for high-resolution X-ray imaging

Scintillators with high thermal stability and excellent spatial resolution are desirable for X-ray imaging applications in harsh environments. Here, Tb3+-doped borosilicate glass scintillators were prepared using conventional melt-quenching method. The optimized Tb3+-doped borosilicate glass (G-15Tb) scintillator exhibited a significantly higher X-ray excited luminescence intensity (147 % of Bi4Ge3O12). Furthermore, it possessed a remarkable imaging spatial resolution of 20 lp/mm, surpassing the standard requirement for X-ray imaging and medical computed tomography scans (2 lp/mm). Moreover, the X-ray excited luminescence intensity of G-15Tb glass sample remained unchanged even after being submerged in water for 30 days, indicating exceptional water resistance. Additionally, the integral intensity of photoluminescence at 573 K is 96.7 % of its initial value. Most importantly, the G-15Tb glass scintillator remains high-quality X-ray images even at elevated operating temperatures. Therefore, the Tb3+-doped borosilicate glass scintillator holds immense potential for high-resolution X-ray imaging in harsh environments.

3D printed microcrystalline CsI:Tl composite scintillating thin films for X-ray imaging

The utilization of additive manufacturing techniques, especially Digital Light Printing (DLP), in fabricating CsI:Tl scintillator films demonstrates considerable potential for streamlining the production of scintillators tailored for X-ray imaging applications. This research focuses on the fabrication of CsI:Tl-based composite plastic scintillator thin films. In this study, circular films measuring 1-inch in diameter and 0.1 mm & 0.2 mm in thickness are being produced and tested for gamma photon counts under alpha and gamma radiation. To establish the stopping power range of the films, a Monte Carlo based GEANT4 simulation has been carried out. Additionally, investigations into their suitability for X-ray imaging applications are being conducted, revealing the spatial resolution of the films (0.2 and 0.1 mm) between 100 and 130 μm and 1.26 lp/mm with a contrast range of 4.0–12.3 %. The observed decrease in spatial resolution and contrast for the 0.2 mm thick film is attributed to the thickness increase exacerbating the scattering phenomenon while simultaneously enhancing the X-ray stopping power. This highlights the significance of inherent trade-off between maximizing spatial resolution and compromising light yield of 0.1 mm films compared to the 0.2 mm thick film. By utilizing 3D printing, this approach offers a cost-effective and time-efficient method for producing thin-film scintillators with enhanced flexibility and customization options compared to conventional methods.

Tb3+-doped a zero-dimensional all-inorganic metal halide perovskite scintillator Cs2ScCl5·H2O for X-ray imaging

All-inorganic zero-dimensional (0D) metal halide perovskite materials have been widely studied in solid-state lighting due to their unique optical properties. However, there are few researchs on their potential applications in X-ray imaging. Herein, we synthesized an all-inorganic 0D metal halide perovskite scintillator, Cs2ScCl5·H2O:Tb3+, was prepared by using a hydrothermal method. Upon 240 nm excitation, the emission spectrum of Cs2ScCl5·H2O:Tb3+ is primarily composed of characteristic emissions from Tb3+, with the strongest emission peak at 548 nm. Additionally, under X-ray excitation, it exhibits blue light showing an intense emission band centered at 425 nm due to self-trapped (STE) emission, and a rather weaker green emission caused by energy transfer from STE emission to Tb3+ ions. Based on this, a flexible film prepared by using the as-obtained scintillator Cs2ScCl5·H2O:Tb3+ demonstrates real-time X-ray imaging with a resolution of 9.5 lp mm−1. These results suggest the potential application prospect of Cs2ScCl5·H2O:Tb3+ in X-ray detection and imaging.

Ca co-doped CsI(Tl) crystal scintillator for γ- and X-ray detecting applications

The vertical Bridgman method is used for the growth of single-doped CsI(Tl) and CsI(Tl:Ca) crystals, which has been evaluated for feasible applications in X-ray imaging and radiation detection. The powder XRD technique study reveals a single-crystalline phase of the grown crystal. The emission spectra show a broad emission band with a maximum of 540 nm under X-ray excitation, along with the characteristic emissions that arose from the Tl+ intra-center transition. The scintillation qualities of the grown crystal were studied via the pulse height spectra, scintillation light yield, energy resolution, and scintillation decay time. Pulse shape discrimination (PSD) was investigated under γ-rays and α-particles excitation sources. Moreover, the X-ray imaging application was investigated by an X-ray synchrotron at the Synchrotron Light Research Institute to study the performance of the grown crystal. These preliminary investigations suggest that the grown CsI(Tl:Ca) crystal can be one of the promising crystals for γ- and X-ray detecting applications.

Characterization of a new low-dose and low-energy Gafchromic film LD-V1.

To characterize the dose-response, energy dependence, postexposure changes, orientation dependence, and spatial capabilities of LD-V1, a new low-dose Gafchromic film for low-energy x-ray dosimetry. A single sheet of LD-V1 Gafchromic film was cut into 15 × 20mm2 rectangles with a notch to track orientation. Eight different doses between 5 and 320mGy were delivered by an MXR-160/22 x-ray tube using x-ray beams of 90, 100, and 120kVp filtered with 3mm of Al and 2mm of Ti. The 120kVp films were scanned at 1, 1.5, 2, 3, 12, 24, 48, 72, and 168h postexposure in portrait orientation and additionally scanned in landscape orientation at 24h. The 90 and 100kVp films were scanned at 24h postexposure in portrait orientation. Lastly, a 20 × 200mm2 strip of film was irradiated using a thin-slit imaging collimator and scanned 24h postexposure to test the film performance in an x-ray imaging application. Of the three color channels, the red channel was found to produce a dose-response curve with a large range of net optical density (netOD) values across the considered dose range. A prominent energy dependence was discovered, resulting in dose discrepancies on the scale of 17mGy between 90 and 120kVp for a dose of 80mGy. The measured postexposure changes suggest that the calibration irradiation-to-scan time should be longer than 12h with a±4h scanning time window for dose errors of<0.5%. An average dose difference of 3.4% was found between the two scanning orientations. Lastly, noise of 4% was measured in the thin slit collimator film for a dose of 30mGy. We have characterized the LD-V1 film for low-energy, low-dose x-ray dosimetry. Energy, scan-time, and orientation dependencies should be considered when using this film.

High transparency Ce3+-doped oxyfluoride glass scintillator for X-ray imaging and γ-ray detection

High transparency Ce3+-doped dense gadolinium aluminum borosilicate (GSx) glass scintillator was synthesized in reducing atmosphere by melt-quenching process. The transmittance of the glasses exceeds 80%, and the light attenuation length is between 5-20 cm within the range of 400–600 nm. GSx glass shows an photoluminescence (PL) in range of 350–550 nm, with the strongest emission peak around 420 nm. The PL decay time of GSx glasses is around 37 ns, with a maximum PL quantum yield of 44.05%. The integrated X-ray excited luminescence (XEL) intensity of GSS glass is 52.5% compared with BGO crystal. For X-ray imaging, GSL glass based imaging system shows a high spatial resolution of 9 lp/mm, which is comparable to CsI:Tl X-ray detectors. Under γ-ray, the highest light yield of GSS glass is 1235 ph/MeV with an energy resolution of 24.0% at 662 keV, close to that of BSO crystal. The scintillation decay time of GSx glasses is consisted of fast (∼100 ns) and slow (∼560 ns) components. In thermally stimulated luminescence (TSL), GSS glass exhibits a strong TSL peak at approximately 440 K, with low intensity shoulders at about 520 K, implying different types of defects and traps. Therefore, GSx glass has promising prospects for X-ray imaging and high-energy physics applications.

Development of a flat jet delivery system for soft X-ray spectroscopy at MAX IV.

One of the most challenging aspects of X-ray research is the delivery of liquid sample flows into the soft X-ray beam. Currently, cylindrical microjets are the most commonly used sample injection systems for soft X-ray liquid spectroscopy. However, they suffer from several drawbacks, such as complicated geometry due to their curved surface. In this study, we propose a novel 3D-printed nozzle design by introducing microscopic flat sheet jets that provide micrometre-thick liquid sheets with high stability, intending to make this technology more widely available to users. Our research is a collaboration between the EuXFEL and MAX IV research facilities. This collaboration aims to develop and refine a 3D-printed flat sheet nozzle design and a versatile jetting platform that is compatible with multiple endstations and measurement techniques. Our flat sheet jet platform improves the stability of the jet and increases its surface area, enabling more precise scanning and differential measurements in X-ray absorption, scattering, and imaging applications. Here, we demonstrate the performance of this new arrangement for a flat sheet jet setup with X-ray photoelectron spectroscopy, photoelectron angular distribution, and soft X-ray absorption spectroscopy experiments performed at the photoemission endstation of the FlexPES beamline at MAX IV Laboratory in Lund, Sweden.

Solution processed high aspect ratio ultra-long vertically well-aligned ZnO nano scintillators for potential X-ray imaging applications

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.

Radiation-tolerant dose sensor based on undoped amorphous silicon

Single-crystal silicon diodes are replacing gas-filled dose-rate meters because they are batch-processable, mechanically robust, compact, and operable at low voltages. However, they are prone to radiation damage in high dose fields. Hydrogenated amorphous silicon (a-Si:H) provides the manufacturing and operational benefits of silicon while adding inherent radiation hardness because of its wider bandgap and disordered microstructure. Previously, sensors with tens of micrometers thick a-Si have been investigated for direct dose sensing in x-ray imaging applications. However, the limited charge carrier lifetimes of the medium can reduce the charge collection efficiency and thereby the sensitivity. If a higher density, higher Z active media is coupled to thin amorphous silicon active layers, then an additional indirect component can be added to this direct signal to exhibit ∼15 μGy/s dose-rate sensitivities at zero and low-bias (<0.5 V) operation. Here we show that thin (150, 300, 450 nm) a-Si:H optical sensors can produce external quantum efficiencies above 40% and internal quantum efficiencies that exceed 70 % over a broad band from 380 nm to 650 nm, resulting in dose-rate sensitivity even at 0 V. When the charge-collecting electrodes abutting the a-Si:H serve the dual purpose as reflective layers in a lossy Fabry-Perot cavity, then internal quantum efficiencies greater than 83 % can be realized in a 30 nm thick layer at 410 nm. Cobalt-60 gamma-ray irradiation to 100 kGy (air) shows no radiation-induced degradation for even the thicker 300 nm sample; rather, a radiation hardening effect is observed as evinced in reduced dark current.

Dimethylamine Copper(I) Halide Single Crystals: Structure, Physical Properties, and Scintillation Performance.

Hybrid copper(I) halides have garnered a significant amount of attention as potential substitutes in luminescence and scintillation applications. Herein, we report the discovery and crystal growth of new zero-dimensional compounds, (C2H8N)3Cu2I5 and (C2H8N)4Cu2Br6. The bromide and iodide have a triclinic structure with space group P1̅ and an orthorhombic structure with space group Pnma, respectively. (C2H8N)3Cu2I5 exhibits cyan emission peaking at 504 nm with a photoluminescence quantum yield (PLQY) of 34.79%, while (C2H8N)4Cu2Br6 shows yellowish-green emission peaking at 537 nm with a PLQY of 38.45%. The temperature-dependent photoluminescence data of both compounds were fitted to theoretical models, revealing that nonradiative intermediate states significantly affect thermal quenching and antiquenching. Electron-phonon interactions, the origin of emission line width broadening and peak shifting, were also investigated via fittings. The scintillation properties of (C2H8N)3Cu2I5 were evaluated, and an X-ray imaging device was successfully fabricated using (C2H8N)3Cu2I5. This work demonstrates the potentiality of copper halides in lighting and X-ray imaging applications.

Thermal stability and flexible X-Ray scintillation screen through in-situ assembling Cs3Cu2Cl5 nanocrystals in polymer matrix

Copper-based halides have emerged as promising scintillator materials for X-ray imaging, attributed to their favorable photophysical characteristics, such as negligible self-absorption, high light output, and fast decay. Within this category of materials, Cs3Cu2Cl5 composite polymer scintillator films stand out, delivering excellent performance as flexible X-ray detector screens. However, severe scattering and light degradation induced by the inevitable agglomeration during recombination restricted the application in high-resolution and flexible X-ray imaging. In this study, a Cs3Cu2Cl5@PMMA film prepared by in-situ growth strategy is successfully developed, which represents uniform area, adjustable flexibility and excellent scintillation performance. The prepared large-area film exhibits green emission at 527 nm, with a high light yield, low detection limit and excellent spatial resolution. Meanwhile, the Cs3Cu2Cl5@PMMA film exhibits a remarkable degree of flexibility, enabling imaging applications on non-planar surfaces. Furthermore, it also demonstrates excellent resistance to high temperature environment, maintaining its high-quality imaging performance at 403 K.

Highly Emissive Lanthanide-Based 0D Metal Halide Nanocrystals for Efficient Ultraviolet Photodetector.

Recently, lanthanide-based 0D metal halides have attracted considerable attention for their applications in X-ray imaging, light-emitting diodes (LEDs), sensors, and photodetectors. Herein, lead-free 0D gadolinium-alloyed cesium cerium chloride (Gd3+-alloyed Cs3CeCl6) nanocrystals (NCs) are introduced as promising materials for optoelectronic application owing to their unique optical properties. The incorporation of Gd3+ in Cs3CeCl6 (CCC) NCs is proposed to increase the photoluminescence quantum yield (PLQY) from 57% to 96%, along with significantly enhanced phase and chemical stability. The structural analysis is performed by density functional theory (DFT) to confirm the effect of Gd3+ in Cs3Ce1- xGdxCl6 (CCGC) alloy system. Moreover, the CCGC NCs are applied as the active layer in UVPDs with different Gd3+ concentration. The excellent device performance is shown at 20% of Gd3+ in CCGC NCs with high detectivity (7.938 × 1011 Jones) and responsivity (0.195 A W-1) at -0.1V at 310nm. This study paves the way for the development of lanthanide-based metal halide NCs for next-generation UVPDs and other optoelectronic applications.

Bivalent metal ion co-doped methylammonium lead tribromide perovskite nanocrystal scintillator for X-ray imaging

Perovskite scintillators with low cost, easy preparation, environmental stability, and high-resolution have become candidates for X-ray imaging applications. Here, based on the calculation results of surface formation energy (Ef) and vacancy defect energy (Evac), a series of co-doped perovskite nanocrystals (NCs) with photoluminescence high quantum yield (PLQY) and fast luminescence decay time had been prepared by doping several bivalent metal ions into the B-site of methylammonium lead tribromide (MAPbBr3). In addition, the scintillator with flexibility was prepared using poly(vinylidene fluoride-hexafluoropropylene) (PVDF-HFP) as the carrier, showing excellent stability and scintillation performance, with a light yield of 21,200 photons/MeV, imaging resolution reached 11.7 lp/mm, and low detection limits of 462 nGyair s−1. Finally, we demonstrated the scintillator characteristic with high-quality imaging results and excellent tolerance under high dose rate X-ray (25 mGy s−1). Therefore, the combination of co-doped nanocrystals with excellent optical properties and PVDF-HFP further paves the way for the development of a scintillator.

Narrowband room temperature phosphorescence of closed-loop molecules through the multiple resonance effect

Luminescent materials with narrowband emission show great potential for diverse applications in optoelectronics. Purely organic phosphors with room-temperature phosphorescence (RTP) have made significant success in rationally manipulating quantum efficiency, lifetimes, and colour gamut in the past years, but there is limited attention on the purity of the RTP colours. Herein we report a series of closed-loop molecules with narrowband phosphorescence by multiple resonance effect, which significantly improves the colour purity of RTP. Phosphors show narrowband phosphorescence with full width at half maxima (FWHM) of 30 nm after doping into a rigid benzophenone matrix under ambient conditions, of which the RTP efficiency reaches 51.8%. At 77 K, the FWHM of phosphorescence is only 11 nm. Meanwhile, the colour of narrowband RTP can be tuned from sky blue to green with the modification of methyl groups. Additionally, the potential applications in X-ray imaging and display are demonstrated. This work not only outlines a design principle for developing narrowband RTP materials but also makes a major step forward extending the potential applications of narrowband luminescent materials in optoelectronics.

Luminescence properties of Tb3+ -doped sodium phosphate glasses for green laser and X-ray imaging application

Tb3+ doped sodium-gadolinium-aluminum-phosphate glass samples (PGNA) with chemical compositions 30Na2CO3:8Gd2O3:5Al2O3:(57- x)P2O5: x Tb4O7 (where x=0, 0.25, 0.5, 1.0, 2.0, 3.0, 4.0, and 5 mol. %) were manufactured by using adopting the conventional melt quenching technique. The PXRD study of the prepared samples was used to confirm the amorphous structure. FE-SEM, EDS, and FTIR studies were carried out to analyze the elemental and structural characteristics of synthesized glasses. The X-ray induced luminescence spectra were obtained at room temperature and the emission peak at 311 nm corresponding to Gd3+ transition was observed decreasing with the increase of Tb4O7 concentrations, while emission peak intensities corresponding to Tb3+ electronic transitions increased with the concentrations of Tb4O7. The results from the photoluminescence (PL) studies in the UV–Vis–NIR region showed the glasses emitting intense green light with the highest peak at 544 nm under excitations at 220, 272, and 311 nm. The PL emission intensities were found reasonably high under characteristic excitations of both Gd3+ and Tb3+, peaking at 380, 414, 437, 489, 544, 584, and 623 nm, which corresponding to 5D3→7F6,5D3→7F5, 5D3→7F4, 5D4→7F6, 5D4→7F5, 5D4→7F5, 5D4→7F4, 5D4→7F3 transitions, respectively. The decay time of Tb3+ ions has been observed to decrease when the concentration of Tb4O7 increases. The energy transfer from Gd3+ to Tb3+ was found increased with increasing of Tb3+ concentrations. The CIE 1931 chromaticity coordinates of Tb doped PGNA glasses were found to be in the green range, indicating a strong potential for green laser application. The results from X-ray imaging showed that Tb-doped glass scintillators promise of efficient and low-cost solution for X-ray imaging applications.