| Literature DB >> 31313424 |
Jia-Xiong Chen1,2,3, Wen-Wen Tao1, Wen-Cheng Chen2, Ya-Fang Xiao2, Kai Wang1, Chen Cao2, Jia Yu1, Shengliang Li2, Feng-Xia Geng3, Chihaya Adachi4, Chun-Sing Lee2, Xiao-Hong Zhang1.
Abstract
Developing red thermally activated delayed fluorescence (TADF) emitters, attainable for both high-efficient red organic light-emitting diodes (OLEDs) and non-doped deep red/near-infrared (NIR) OLEDs, is challenging. Now, two red emitters, BPPZ-PXZ and mDPBPZ-PXZ, with twisted donor-acceptor structures were designed and synthesized to study molecular design strategies of high-efficiency red TADF emitters. BPPZ-PXZ employs the strictest molecular restrictions to suppress energy loss and realizes red emission with a photoluminescence quantum yield (ΦPL ) of 100±0.8 % and external quantum efficiency (EQE) of 25.2 % in a doped OLED. Its non-doped OLED has an EQE of 2.5 % owing to unavoidable intermolecular π-π interactions. mDPBPZ-PXZ releases two pyridine substituents from its fused acceptor moiety. Although mDPBPZ-PXZ realizes a lower EQE of 21.7 % in the doped OLED, its non-doped device shows a superior EQE of 5.2 % with a deep red/NIR emission at peak of 680 nm.Entities:
Keywords: OLEDs; molecular design; red/near-IR emission; rigid segments; thermally activated delayed fluorescence
Year: 2019 PMID: 31313424 DOI: 10.1002/anie.201906575
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336