Wagner Jakub, Zimmermann Crocomo Paola, Kochman Michał Andrzej, Kubas Adam, Data Przemysław, Lindner Marcin
Institute of Organic Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224, Warsaw, Poland.
Faculty of Chemistry, Silesian University of Technology, M. Strzody 9, 44-100, Gliwice, Poland.
Angew Chem Int Ed Engl. 2022 Jul 4;61(27):e202202232. doi: 10.1002/anie.202202232. Epub 2022 May 5.
Although bowl-shaped N-pyrrolic polycyclic aromatic hydrocarbons (PAHs) can achieve excellent electron-donating ability, their application for optoelectronics is hampered by typically low photoluminescence quantum yields (PLQYs). To address this issue, we report the synthesis and characterization of a series of curved and fully conjugated nitrogen-doped PAHs. Through structural modifications to the electron-accepting moiety, we are able to switch the mechanism of luminescence between thermally activated delayed fluorescence (TADF) and room-temperature phosphorescence (RTP), and to tune the overall PLQY in the range from 9 % to 86 %. As a proof of concept, we constructed solid-state organic light-emitting diode (OLED) devices, which has not been explored to date in the context of concave N-doped systems being TADF/RTP emitters. The best-performing dye, possessing a peripheral trifluoromethyl group adjacent to the phenazine acceptor, exhibits yellow to orange emission with a maximum external quantum efficiency (EQE) of 12 %, which is the highest EQE in a curved D-A embedded N-PAH to date.
尽管碗状的N-吡咯型多环芳烃(PAHs)能够实现优异的给电子能力,但其光致发光量子产率(PLQYs)通常较低,这阻碍了它们在光电子学中的应用。为了解决这个问题,我们报告了一系列弯曲且完全共轭的氮掺杂PAHs的合成与表征。通过对电子接受部分进行结构修饰,我们能够在热激活延迟荧光(TADF)和室温磷光(RTP)之间切换发光机制,并将整体PLQY调节至9%至86%的范围内。作为概念验证,我们构建了固态有机发光二极管(OLED)器件,在凹面氮掺杂体系作为TADF/RTP发射体的背景下,这是迄今为止尚未探索过的。性能最佳的染料,在吩嗪受体附近具有一个外围三氟甲基,呈现出黄色至橙色发射,最大外量子效率(EQE)为12%,这是迄今为止弯曲的D-A嵌入N-PAH中最高的EQE。