发光
化学
激进的
光致发光
锌
光化学
玻璃化
氯化物
混合材料
热的
磷酸锌
无机化学
未成对电子
热稳定性
量子效率
玻璃化转变
锌化合物
电子
兴奋剂
作者
Zhishan Luo,Jiang Ya,Meiying He,Yawen Li,Yulian Liu,Yi‐Fei Deng,Yi Wei,Laizhi Sui,Yuanzhu Zhang,Zewei Quan
摘要
Persistent radicals, species with unpaired electrons, are pivotal for advanced optical and electrical applications but are challenging to stabilize. Herein, we report a melt-quenching vitrification strategy that stabilizes persistent organic radicals within chiral zero-dimensional hybrid zinc chloride glasses, overcoming their intrinsic instability. These radicals are generated via deprotonation-induced organic cations during the vitrification process and are subsequently trapped within the glassy matrix, where they function as continuous electron donors. Compared to crystalline hybrid zinc chloride counterparts, the radical-containing glasses exhibit attractive luminescent properties: a 25-fold enhancement in long lifetime with ultralong persistent luminescence, a 4-fold increase in photoluminescence quantum yield, exceptional thermal emission stability, pronounced circularly polarized luminescence, and a 4 orders of magnitude enhancement in electrical conductivity. This work establishes melt-quenching vitrification as a novel strategy for stabilizing persistent radical materials with integrated functionalities.
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