Abstract
In this work, we designed and investigated two TADF molecules, AcCN and PxCN, introducing donor moieties into the 3,5-position of 4-pyridinecarbonitrile acceptor core. These D‒A‒D type compounds exhibit effective utilization of triplet excitons through a reverse intersystem crossing (RISC) process with relatively small singlet-triplet energy splitting (ΔEST) values less than 0.1 eV. With their high PL quantum yield (ΦPL) and sufficient rate constant for RISC process (kRISC), organic light-emitting diodes (OLEDs) employing AcCN and PxCN as emitters achieve a maximum external quantum efficiency (ηext) of 20.6% and 15.5%, respectively, with green emissions.
Original language | English |
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Article number | 107775 |
Journal | Dyes and Pigments |
Volume | 171 |
DOIs | |
State | Published - Dec 2019 |
Keywords
- Organic light-emitting diodes (OLEDs)
- Ortho-substitution
- Pyridinecarbonitrile derivatives
- Thermally activated delayed fluorescence (TADF)