蒽
材料科学
有机发光二极管
系统间交叉
激子
激发态
光致发光
电致发光
单重态
超快激光光谱学
单重态裂变
光电子学
化学物理
光化学
纳米技术
原子物理学
凝聚态物理
光谱学
物理
图层(电子)
化学
量子力学
作者
Shu Xiao,Xianfeng Qiao,Chengwei Lin,Yuanzhao Li,Shian Ying,Jianwen Qin,Runda Guo,Lei Wang,Yuguang Ma,Dongge Ma
标识
DOI:10.1002/adfm.202207123
摘要
Abstract It is well‐known that the electrically generated excitons can perform the spin evolution between high‐lying excited states, providing an efficient way to utilize triplet excitons in organic light‐emitting diodes (OLEDs). Anthracene families offer an opportunity to deeply investigate the processes of triplet excitons on high‐lying excited states in detail. Here, a simplified model is proposed to study the exciton dynamics in anthracene derivatives‐based devices. The mechanism on the processes of high‐energy level intersystem crossing in anthracene derivatives is well revealed by theoretical calculation, transient electroluminescence, transient photoluminescence, and transient absorption spectrum measurements. Besides, doping strategy is proposed to suppress the exciton loss channel for improving the efficiency of devices. The studies establish an in situ method to evaluate the apparent singlet exciton formation ratio in devices due to the exciton evolution between high‐lying excited states and offer some clues to further utilize these triplet excitons, thus improving the efficiency of the resulting fluorescence OLEDs in the future.
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