材料科学
钙钛矿(结构)
离子
灵敏度(控制系统)
降级(电信)
碘化物
检出限
极限(数学)
光电子学
探测器
工作(物理)
锁(火器)
化学物理
锚固
辐射
纳米技术
能量(信号处理)
理论(学习稳定性)
活化能
密度泛函理论
结构稳定性
催化作用
辐照
分子物理学
分析化学(期刊)
作者
Shuhan Lin,Yijun Cao,Haibing Zhao,Hongliang Dai,Yongqin Wang,Duofu Li,Min Zhang,Zhixiang Qiu,Yan Sui
摘要
ABSTRACT Ion migration severely limits the sensitivity and stability of lead‐free perovskite X‐ray detectors. Here, we propose a “dual‐anchor molecular lock” strategy to quench this migration, realized in a new 3D lead‐free iodide double perovskite, (Thiomorpholine) 2 RbBiI 6 , abbreviated as (Thiomor) 2 RbBiI 6 . In this material, the thiomorpholinium cation is immobilized within the inorganic framework through the cooperative action of an Rb–S contact and a directional N–H···I interaction network. This dual‐anchor design yields an ultrahigh ion‐migration activation energy of 729 meV and an exceptionally low dark‐current drift of 1.36 × 10 − 6 nA cm − 1 s − 1 V − 1 . Consequently, single‐crystal detectors achieve a high sensitivity of 1242 µC Gy a i r − 1 cm − 2 and an ultralow detection limit of 2.22 ± 0.31 nGy a i r s − 1 —approximately 2,500 times below the medical diagnostic threshold—alongside negligible degradation during continuous operation, long‐term ambient storage, and repeated X‐ray ON–OFF cycling. This work demonstrates that molecular‐scale cation immobilization via synergistic dual‐anchor host–guest anchoring is a decisive and generalizable design principle for creating drift‐free, ultra‐stable, and high‐performance lead‐free radiation detectors.
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