分子内力
材料科学
有机发光二极管
激发态
接受者
芴
荧光
化学物理
激子
分子工程
二极管
分子
电荷(物理)
准分子
光电子学
光化学
纳米技术
原子物理学
聚合物
光学
物理
化学
立体化学
凝聚态物理
图层(电子)
复合材料
量子力学
作者
Rui‐hong Liu,Meng‐Tian Li,Yue‐Jian Yang,Shi‐Jie Ge,Zhi‐Hao Qu,Ziqi Feng,Yu Wang,Zhanshuang Yu,Dong‐Ying Zhou,Cheng Zhong,Liang‐Sheng Liao,Zuo‐Quan Jiang
标识
DOI:10.1002/adma.202415951
摘要
Intramolecular through-space charge-transfer (TSCT) excited states have emerged as promising candidates for thermally activated delayed fluorescence (TADF) emitters. This study addresses the challenges in tuning excited state dynamics through conformational engineering, which significantly impacts exciton utilization. An effective strategy is presented to enhance the performance of TSCT-TADF molecules by restricting the lateral rocking of the spiro unit via immobilizing groups, which indirectly adjusts the conformations of the donor and acceptor subunits. This approach is successfully illustrated with two TSCT-TADF emitters, 8PhDM-B and 8PyDM-B, featuring sterical aryl phenyl and pyridine substitutions at the C8 site of a rigid spiro-fluorene bridge. Organic light-emitting diodes (OLEDs) utilizing these emitters demonstrated impressive maximum external quantum efficiencies of 33.1% and 31.0%, respectively. The findings underscore the importance of the rocking confined strategy in refining excited state dynamics, thereby providing valuable insights for the design of highly efficient OLED emitters.
科研通智能强力驱动
Strongly Powered by AbleSci AI