卤化物
锰
取代基
阳离子聚合
闪烁体
X射线
材料科学
化学
无机化学
光学
高分子化学
物理
有机化学
冶金
探测器
作者
Zijian Zhou,Xue Yu,Rongrong Hu,Guang Yan,Yongjing Deng,Shujuan Liu,Feng Wang,Qiang Zhao
标识
DOI:10.1002/lpor.202500657
摘要
Abstract Organic–inorganic hybrid manganese(II) halide glasses exhibit advantages such as exceptional optical transparency, straightforward preparation processes, and potential for large‐scale production. However, the crystallization phenomenon easily occurring in this glass material can induce a marked reduction in transparency, which significantly compromises its X‐ray imaging performance. Herein, a cationic substituent regulation strategy is developed to improve the glassy stability of manganese(II) halides. By replacing the phenyl group in Ph‐Mn cation with methylcyclohexyl substituent, a novel manganese(II) halide MCy‐Mn is successfully synthesized. Such a substitution strategy can effectively weaken both the cation–anion interactions and π – π stacking interactions within the manganese(II) halide lattice, resulting in a remarkable reduction in melting point (T m ). Moreover, the inherent rigid structure of MCy‐Mn also confers an elevated glass transition temperature (T g ). Consequently, the resultant MCy‐Mn crystal demonstrates a high T g /T m ratio of 0.82. Besides, the fabricated MCy‐Mn scintillation glass exhibits a high spatial resolution of 19.3 lp mm −1 and has successfully achieved 3D X‐ray reconstruction. As anticipated, MCy‐Mn glass exhibits outstanding environmental stability, with no crystallization observed after being exposed to atmospheric conditions for 30 days. This work provides valuable insights for the development of high‐stability metal halide scintillation glasses.
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