磷光
系统间交叉
分子间力
激发态
光化学
卤素
化学物理
分子
磷光有机发光二极管
Atom(片上系统)
量子效率
化学
大气温度范围
材料科学
光电子学
原子物理学
荧光
有机化学
热力学
光学
单重态
计算机科学
嵌入式系统
烷基
物理
作者
Zhiyong Yang,Zhu Mao,Xuepeng Zhang,Depei Ou,Yingxiao Mu,Yi Zhang,Cunyuan Zhao,Siwei Liu,Zhenguo Chi,Jiarui Xu,Yuan‐Chun Wu,Po‐Yen Lu,Alan Lien,Martin R. Bryce
标识
DOI:10.1002/ange.201509224
摘要
Abstract Although persistent room‐temperature phosphorescence (RTP) emission has been observed for a few pure crystalline organic molecules, there is no consistent mechanism and no universal design strategy for organic persistent RTP (pRTP) materials. A new mechanism for pRTP is presented, based on combining the advantages of different excited‐state configurations in coupled intermolecular units, which may be applicable to a wide range of organic molecules. By following this mechanism, we have developed a successful design strategy to obtain bright pRTP by utilizing a heavy halogen atom to further increase the intersystem crossing rate of the coupled units. RTP with a remarkably long lifetime of 0.28 s and a very high quantum efficiency of 5 % was thus obtained under ambient conditions. This strategy represents an important step in the understanding of organic pRTP emission.
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