{"title":"Application of high thermal stability inorganic scintillator material Ba1.31Ca0.69SiO4:Eu2+,Dy3+ in X-ray imaging","authors":"Kuo Shen , Yahong Jin , Yanmei Li , Yihua Hu","doi":"10.1016/j.jlumin.2025.121097","DOIUrl":null,"url":null,"abstract":"<div><div>Inorganic scintillator materials have garnered widespread attention due to their applications in high-energy X-ray detection and imaging. However, developing materials that possess both high thermal stability and the capability to provide high-resolution X-ray imaging remains a significant challenge in this field. This article reports the synthesis of Ba<sub>1.31</sub>Ca<sub>0.69</sub>SiO<sub>4</sub> inorganic scintillator materials doped with Eu<sup>2+</sup> and Dy<sup>3+</sup> through a high-temperature solid-phase method. Their structure, photoluminescent properties under visible light and X-ray excitation, and thermoluminescence characteristics were thoroughly characterized. Experimental results indicate that the material's traps were enriched through the aliovalent substitution of Dy<sup>3+</sup>, enhancing the afterglow at room temperature. Under 350 nm excitation, the material demonstrated excellent thermal stability (maintaining 90% of its intensity at 150 °C compared to 30 °C) and a high quantum efficiency (IQE = 96.64 %). Furthermore, under X-ray excitation, the material exhibits a high electron storage capacity, which can be read out under near-infrared light at 870 nm, and can be rapidly erased under heating conditions or under visible light at 470 nm. Finally, we prepared flexible films using the phosphor, demonstrating a spatial resolution of 11.9 lp/mm<sup>−1</sup> under X-rays, as well as showcasing the real-time and delayed imaging capabilities of the flexible film under X-ray exposure.</div></div>","PeriodicalId":16159,"journal":{"name":"Journal of Luminescence","volume":"280 ","pages":"Article 121097"},"PeriodicalIF":3.3000,"publicationDate":"2025-01-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Luminescence","FirstCategoryId":"101","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0022231325000377","RegionNum":3,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"OPTICS","Score":null,"Total":0}
引用次数: 0
Abstract
Inorganic scintillator materials have garnered widespread attention due to their applications in high-energy X-ray detection and imaging. However, developing materials that possess both high thermal stability and the capability to provide high-resolution X-ray imaging remains a significant challenge in this field. This article reports the synthesis of Ba1.31Ca0.69SiO4 inorganic scintillator materials doped with Eu2+ and Dy3+ through a high-temperature solid-phase method. Their structure, photoluminescent properties under visible light and X-ray excitation, and thermoluminescence characteristics were thoroughly characterized. Experimental results indicate that the material's traps were enriched through the aliovalent substitution of Dy3+, enhancing the afterglow at room temperature. Under 350 nm excitation, the material demonstrated excellent thermal stability (maintaining 90% of its intensity at 150 °C compared to 30 °C) and a high quantum efficiency (IQE = 96.64 %). Furthermore, under X-ray excitation, the material exhibits a high electron storage capacity, which can be read out under near-infrared light at 870 nm, and can be rapidly erased under heating conditions or under visible light at 470 nm. Finally, we prepared flexible films using the phosphor, demonstrating a spatial resolution of 11.9 lp/mm−1 under X-rays, as well as showcasing the real-time and delayed imaging capabilities of the flexible film under X-ray exposure.
期刊介绍:
The purpose of the Journal of Luminescence is to provide a means of communication between scientists in different disciplines who share a common interest in the electronic excited states of molecular, ionic and covalent systems, whether crystalline, amorphous, or liquid.
We invite original papers and reviews on such subjects as: exciton and polariton dynamics, dynamics of localized excited states, energy and charge transport in ordered and disordered systems, radiative and non-radiative recombination, relaxation processes, vibronic interactions in electronic excited states, photochemistry in condensed systems, excited state resonance, double resonance, spin dynamics, selective excitation spectroscopy, hole burning, coherent processes in excited states, (e.g. coherent optical transients, photon echoes, transient gratings), multiphoton processes, optical bistability, photochromism, and new techniques for the study of excited states. This list is not intended to be exhaustive. Papers in the traditional areas of optical spectroscopy (absorption, MCD, luminescence, Raman scattering) are welcome. Papers on applications (phosphors, scintillators, electro- and cathodo-luminescence, radiography, bioimaging, solar energy, energy conversion, etc.) are also welcome if they present results of scientific, rather than only technological interest. However, papers containing purely theoretical results, not related to phenomena in the excited states, as well as papers using luminescence spectroscopy to perform routine analytical chemistry or biochemistry procedures, are outside the scope of the journal. Some exceptions will be possible at the discretion of the editors.