Abstract
Developing easily accessible deep-red/near-infrared circularly polarized emitters for practical organic light-emitting diodes remains a significant challenge. Here, a practical strategy has been proposed for developing deep-red circularly polarized delayed fluorescent emitters based on a novel chiral acceptor platform. By changing triphenylamine (TPA) substitution position from para to meta, R/S-M-TBBTCN demonstrated thermally activated delayed fluorescence (TADF) properties with a delayed lifetime of 6.6 µs that R/S-P-TBBTCN doesn’t have. Furthermore, R/S-M-TBBTCN showed a 65 nm red-shift in emission and a 10-fold enhancement in asymmetry factor (glum), compared with R/S-P-TBBTCN. The solution-processed nondoped circularly polarized organic light-emitting diodes (CP-OLEDs) based on R-M-TBBTCN display deep-red emission and 2.2% external quantum efficiency. (Figure presented.)
| Original language | English |
|---|---|
| Pages (from-to) | 657-663 |
| Number of pages | 7 |
| Journal | Chemical Research in Chinese Universities |
| Volume | 40 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - Aug 2024 |
Bibliographical note
Publisher Copyright:© Jilin University, The Editorial Department of Chemical Research in Chinese Universities and Springer-Verlag GmbH 2024.
Keywords
- Amplified chirality
- Binaphthol based chiral acceptor
- Deep-red circularly polarized organic light emitting-diode