堆积
有机发光二极管
化学
分子间力
位阻效应
半最大全宽
共发射极
光电子学
分子
量子效率
三联烯
二极管
放松(心理学)
兴奋剂
包络线(雷达)
分子物理学
甲苯
电致发光
超分子化学
光化学
二苯并呋喃
分子工程
Atom(片上系统)
发光二极管
窄带
光谱宽度
作者
Kai Wu,Jingjun Yang,Ruiqi Sun,Jingwen Xu,Zujin Zhao,Ming‐Yu Teng
摘要
Carbonyl‐nitrogen (CO‐N) multiresonance (MR) materials have emerged as promising candidates for ultra‐high‐definition displays due to their high color purity, but they often suffer from severe spectral broadening in organic light‐emitting diodes (OLEDs), which hinders the construction of wide‐color‐gamut displays. Herein, we report a novel molecule QA‐TP constructed by integrating bulky steric triptycene substituents into the CO‐N‐based trans‐quinacridone skeleton. The rigid 3D structure of QA‐TP can not only suppress molecular structural relaxation but also effectively restrict intermolecular stacking in the aggregated state, resulting in pure green emission with a narrow full width at half maximum (FWHM) value of 21 nm in toluene and 27 nm in doped film, both superior to the counterpart molecule QA‐4Ph. Furthermore, hyperfluorescent OLED based on QA‐TP emitter exhibits a satisfactory external quantum efficiency of 16.7% and a narrow FWHM of 27 nm, with CIE coordinates of (0.27, 0.66). These results verify the feasibility of directly incorporating rigid steric substituents into CO‐N MR skeletons for developing narrowband emitters as well as OLEDs.
科研通智能强力驱动
Strongly Powered by AbleSci AI