| Literature DB >> 35441761 |
Ling Zhou1, Fan Ni2, Nan Li3, Kai Wang3, Guohua Xie1, Chuluo Yang1,4.
Abstract
Purely organic emitters have shown great potential but still suffer from low efficiency in near-infrared organic light-emitting diodes (NIR-OLEDs) due to the intensive non-radiative recombination. In this contribution, two pairs of thermally activated delayed fluorescence (TADF) enantiomers (R/S-DOBP and R/S-HDOBP) with tetracoordinate boron geometries were designed and synthesized. The TADF emitters simultaneously showed aggregation-induced emission, circularly polarized luminescence, high-contrast mechanochromism, and piezochromism behaviors. More importantly, R/S-DOBP and R/S-HDOBP revealed high photoluminescence quantum yields and efficient reverse intersystem crossing in neat films. The nondoped solution-processed OLEDs based on these unique emitters revealed the NIR emission (peaking at 716 nm) with a maximum external quantum efficiency of 1.9 % and high exciton utilization efficiency of 86 %, which represent one of the best solution-processed nondoped NIR-OLEDs.Entities:
Keywords: Aggregation-Induced Emission; Circularly Polarized Luminescence; Organic Electronics; Organic Light-Emitting Devices; Organic Semiconductors; Sensitizers
Year: 2022 PMID: 35441761 DOI: 10.1002/anie.202203844
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336