发光
磷光
材料科学
共聚物
光化学
掺杂剂
激发态
离子键合
持续发光
聚合物
红外线的
荧光
兴奋剂
化学
光电子学
光学
有机化学
原子物理学
离子
热释光
复合材料
物理
作者
Zesen Lin,Maosheng Li,Rengo Yoshioka,Ryoko Oyama,Ryota Kabe
标识
DOI:10.1002/anie.202314500
摘要
Organic materials exhibiting long-lasting emission in the near infrared are expected to have applications in bio-imaging and other areas. Although room temperature phosphorescence and thermally activated delayed fluorescence display long-lived emission of approximately one minute, organic long-persistent luminescence (OLPL) systems with a similar emission mechanism to inorganic persistent emitters can emit for several hours at room temperature. In particular OLPL with a hole-diffusion mechanism can function even in the presence of oxygen. However, ionic materials lack long-term stability in neutral organic host owing to aggregation and phase separation. In this study, we synthesized polymers with stable near-infrared persistent luminescence at room temperature via the copolymerization of electron donors and acceptors. The copolymers exhibit long-persistent luminescence (LPL) at temperatures below the glass transition temperature and can be excited by approximately the entire range of visible light. LPL properties and spectra can be controlled by the dopant.
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