Abstract
New emitters with deeply red emission and slow efficiency roll-off in non-doped organic light-emitting diodes (OLEDs) are highly expected. In this work, we used our recently developed 2-phenylbenzo[g]furo[2,3-b]-quinoxaline as the acceptor (A) and triphenylamine (TPA) as the donor (D), synthesized a D-A type red emitter, TPA-PFQ. The TPA-PFQ presented a high quantum yields of 88.03% in toluene solution. Using it as emitter, the non-doped OLEDs showed a saturated red emission with a peak of 620 nm and a maximum luminance of 11190 cd m−2. Moreover, the non-doped OLEDs presented a maximum EQE of 2.09% (2.47 cd A-1) at 100 cd m−2, and remained 2.0% (2.40 cd A-1) at 1000 cd m−2, 2.03% (2.49 cd A-1) at 5000 cd m−2, only 2.9% efficiency roll-off with the luminance changed from 100 cd m−2 to 5000 cd m−2. Our experiments demonstrated benzo[g]furo[2,3-b]quinoxaline skeleton could serve as a promising acceptor unit for constructing deep red emitters.
Original language | English |
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Article number | 139199 |
Journal | Chemical Physics Letters |
Volume | 787 |
DOIs | |
State | Published - Jan 2022 |
Keywords
- Benzo[g]furo[2,3-b]-quinoxaline
- Low efficiency roll-off
- Non-doped OLEDs
- Red emitters