| Literature DB >> 34297444 |
Yi-Kuan Chen1, Jayachandran Jayakumar1, Chia-Min Hsieh1, Tien-Lin Wu1,2, Chun-Cheng Liao1, Jayabalan Pandidurai1, Chang-Lun Ko3, Wen-Yi Hung3, Chien-Hong Cheng1,4.
Abstract
Highly efficient thermally activated delayed fluorescence (TADF) molecules are in urgent demand for solid-state lighting and full-color displays. Here, the design and synthesis of three triarylamine-pyridine-carbonitrile-based TADF compounds, TPAPPC, TPAmPPC, and tTPAmPPC, are shown. They exhibit excellent photoluminescence quantum yields of 79-100% with small ΔEST values, fast reverse intersystem crossing (RISC), and high horizontal dipole ratios (Θ// = 86-88%) in the thin films leading to the enhancement of device light outcoupling. Consequently, a green organic light-emitting diode (OLED) based on TPAmPPC shows a high average external quantum efficiency of 38.8 ± 0.6%, a current efficiency of 130.1 ± 2.1 cd A-1 , and a power efficiency of 136.3 ± 2.2 lm W-1 . The highest device efficiency of 39.8% appears to be record-breaking among TADF-based OLEDs to date. In addition, the TPAmPPC-based device shows superior operation lifetime and high-temperature resistance. It is worth noting that the TPA-PPC-based materials have excellent optical properties and the potential for making them strong candidates for TADF practical application.Entities:
Keywords: external quantum efficiency of nearly 40%; molecular orientation; operational stability; organic light-emitting diodes; pyridine-carbonitrile; thermally activated delayed fluorescence; triphenylamine
Year: 2021 PMID: 34297444 DOI: 10.1002/adma.202008032
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849