三联烯
光致发光
分子内力
材料科学
荧光
热稳定性
光化学
兴奋剂
激子
接受者
化学
化学物理
光电子学
纳米技术
物理
光学
立体化学
有机化学
量子力学
凝聚态物理
作者
Yangyang Huang,Donghai Zhang,Xiaodong Tao,Zhuangzhuang Wei,Shanshan Jiang,Lingyi Meng,Mingxue Yang,Xu‐Lin Chen,Can‐Zhong Lu
标识
DOI:10.1016/j.dyepig.2022.110397
摘要
Thermally activated delayed fluorescence (TADF) materials with through-space charge transfer (TSCT) have recently attracted extensive attention. However, how to rationally design high-performance TSCT-TADF emitters with small ΔEST, high photoluminescence quantum yields (PLQYs) and high stability remains challenging. Herein, two triptycene-derived TADF molecules bearing ortho-donor (D)-acceptor (A) conformations are designed and characterized. These emitters exhibit unique V-shaped face-to-face D-A alignments with significant intramolecular D-A interactions, which mediate TSCT between the D and A moieties in addition to the through-bond charge transfer (TBCT) and facilitate realizing small ΔEST and high efficiencies. Meanwhile, the rigid 3D triptycene scaffold endows the emitters with excellent thermal stability and high film-formation quality. These TADF emitters exhibit small ΔEST of 6.7 and 10.8 meV and high photoluminescence quantum yields of 0.80 and 0.40 in doped films, respectively. The doped OLEDs employing these emitters achieve high external quantum efficiencies up to 20.5%.
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