Yang Minlang, Park In Seob, Yasuda Takuma
INAMORI Frontier Research Center (IFRC), Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395, Japan.
Department of Applied Chemistry, Graduate School of Engineering, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395, Japan.
J Am Chem Soc. 2020 Nov 18;142(46):19468-19472. doi: 10.1021/jacs.0c10081. Epub 2020 Nov 5.
Herein, we demonstrate that the strategic implementation of electron-accepting tricoordinate boron and electron-donating carbazole subunits into polycyclic aromatic hydrocarbons (PAHs) produces a family of attractive full-color luminophores that can emit narrowband and efficient thermally activated delayed fluorescence (TADF). A versatile modular design for these boron- and carbazole-embedded PAHs can facilitate the systematic modulation of their photophysical and optoelectronic properties. Organic light-emitting diodes that utilize these PAHs as TADF emitters demonstrate narrowband electroluminescence from blue to red, achieving high maximum external quantum efficiencies of 29.3%, 31.8%, and 22.0% for blue, green, and red, respectively.
在此,我们证明,将电子接受性三配位硼和电子供体咔唑亚基策略性地引入多环芳烃(PAHs)中,可产生一系列引人注目的全色发光体,它们能够发出窄带且高效的热激活延迟荧光(TADF)。这些嵌入硼和咔唑的PAHs的通用模块化设计有助于系统地调节其光物理和光电性质。利用这些PAHs作为TADF发射体的有机发光二极管表现出从蓝色到红色的窄带电致发光,蓝色、绿色和红色的最大外量子效率分别达到29.3%、31.8%和22.0%的高水平。