有机发光二极管
材料科学
量子效率
分子内力
磷光
光致发光
光电子学
背景(考古学)
分子
电致发光
共轭体系
荧光
磷光有机发光二极管
发光
光化学
纳米技术
聚合物
光学
有机化学
化学
物理
复合材料
古生物学
生物
图层(电子)
作者
Bing Li,Zhan Yang,Wenqi Gong,Xinhui Chen,Duncan W. Bruce,Shengyue Wang,Huili Ma,Yu Liu,Weiguo Zhu,Zhenguo Chi,Yafei Wang
标识
DOI:10.1002/adom.202100180
摘要
Abstract Thermally activated delayed fluorescence (TADF) has been explored actively in luminescent organic materials. Yet, realizing such TADF‐active, multifunctional emitters with high emission efficiency still remains hugely challenging. In this context, a series of twist‐conjugated organic molecules bearing diphenylsulfone and 9,9‐dimethylacridine moieties are designed and prepared, and are found to show, in one molecule, TADF, room‐temperature phosphorescence, triboluminescence, and aggregation‐induced emission enhancement. In addition, remarkably high photoluminescence quantum efficiency, up to ≈100%, is achieved for these novel molecules. Single‐crystal analysis and theoretical calculations reveal that the through‐space charge transfer (TSCT) effect in these molecules is responsible for both the multifunctional emission and high emission efficiency. A maximum external quantum efficiency of 20.1% is achieved, which is among the highest recorded in a solution‐processable device containing TSCT‐based TADF materials. These results illustrate a new approach to achieving highly efficient TADF‐active, multifunctional emitters.
科研通智能强力驱动
Strongly Powered by AbleSci AI