Abstract
The highest efficiency thermally activated delayed fluorescence (TADF) emitters in OLEDs are mostly based on twisted donor/acceptor (D/A) type organic molecules. Herein, we report the rational molecular design on twisted all ortho-linked carbazole/oxadiazole (Cz/OXD) hybrids with tunable D-A interactions by adjusting the numbers of donor/acceptor units and electron-donating abilities. Singlet-triplet energy bandgaps (ΔEST) are facilely tuned from ∼0.4, 0.15 to ∼0 eV in D-A, D-A-D to A-D-A type compounds. This variation correlates well with triplet-excited-state frontier orbital spatial separation efficiency. Non-TADF feature with solid state photoluminescence quantum yield (PLQY) < 10% is observed in D-A type 2CzOXD and D-A-D type 4CzOXD. Owing to the extremely low ΔEST for efficient reverse intersystem crossing, strong TADF with PLQY of 71%–92% is achieved in A-D-A type 4CzDOXD and 4tCzDOXD. High external quantum efficiency from 19.4% to 22.6% is achieved in A-D-A typed 4CzDOXD and 4tCzDOXD.
Original language | English |
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Pages (from-to) | 1955-1958 |
Number of pages | 4 |
Journal | Chinese Chemical Letters |
Volume | 30 |
Issue number | 11 |
DOIs | |
State | Published - Nov 2019 |
Keywords
- Carbazole
- Donor-acceptor
- Organic light-emitting diodes
- Oxadiazole
- Thermally activated delayed fluorescence