窄带
有机发光二极管
方向(向量空间)
偶极子
光电子学
量子效率
材料科学
量子
物理
光学
纳米技术
量子力学
几何学
数学
图层(电子)
作者
Kaiyuan Zhang,Xingdong Wang,Mengyu Wang,Shumeng Wang,Lixiang Wang
标识
DOI:10.1002/ange.202423812
摘要
The multiple resonance thermally activated delayed fluorescence (MR‐TADF) device has drawn great attention due to their outstanding efficiency and color purity. However, the efficiency of solution‐processed MR‐TADF devices is still far behind their vacuum‐deposited counterparts, due to the uncontrollable horizontal emitting dipole orientation for emitters during solution process, resulting in low light out‐coupling efficiency. Here, we proposed a new strategy namely electrostatic interaction between a dendritic host with high positive electrostatic potential (ESP) and dendritic emitter with multiple negative ESP sites, which could induce high horizontal dipole ratio (ΘII) up to 83.0% in solution‐processed films. For this couple, the largest plane of dendritic host tends to anchor on the substrate, and thus the strong positive electrostatic site mainly lies at the exposed tetraphenylsilicon, which could electrostatically attract the multiple negative electrostatic sites of the dendritic emitter, realizing horizontal dipole orientation. Moreover, the highly twisted structure of dendritic host and dendron encapsulation of emitter could effectively suppress aggregation, leading a high photoluminescence quantum yield of 98.6%. As a result, the solution‐processed blue MR‐TADF devices exhibit a record‐break external quantum efficiency of 35.3%, as well as narrow bandwidth of 17 nm and pure blue color with CIE coordinates of (0.137, 0.176).
科研通智能强力驱动
Strongly Powered by AbleSci AI