磷光
材料科学
钋
聚合物
量子产额
相(物质)
反离子
分子工程
聚乙烯醇
纳米团簇
混溶性
溴化物
化学工程
聚芴
兴奋剂
纳米技术
鏻盐
光化学
灵活的显示器
烷基
溶解
产量(工程)
聚丙烯酰胺
智能聚合物
卤化物
分子印迹聚合物
智能材料
旋节分解
系统间交叉
作者
Jiangang Li,Jing Zhang,Yuyang Ju,Zijian Zhou,Shu-Juan Liu,Yun Ma,Zhao Qiang
标识
DOI:10.1002/adom.202502364
摘要
Abstract The development of doped organic room‑temperature phosphorescent (RTP) polymers is hampered by the physicochemical incompatibility between hydrophilic hosts such as polyvinyl alcohol (PVA) and conventional hydrophobic phosphors. This mismatch triggers severe phase separation and lowers RTP performance. A molecular engineering strategy that addresses this challenge by introducing intrinsically water‑soluble phosphonium salt emitters is presented. The design combines a bromide counterion that enhances intersystem crossing with a bulky alkyl chain that suppresses aggregation‑induced quenching, while also guaranteeing seamless miscibility with PVA. This approach eliminates phase separation and yields highly efficient, full‑color RTP in doped films, with emissions tunable from 427 to 619 nm. The best performer shows an ultralong lifetime of 2.18 s and a quantum yield of 11.63%. Building on these properties, the versatility of the material in two key applications is demonstrated, namely high‑performance flexible displays and high‑resolution X‑ray imaging with a spatial resolution of 11.51 lp mm −1 .
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