Abstract
Realizing high efficiency deep blue emission with a Commission international de I'Eclairage (CIE) coordinate of CIEy < 0.08 is still a big challenge. In this contribution, three molecules, named TTT-TPA-R (R = H, OMe, tBu), using tris(triazolo)triazine (TTT) as the acceptor and triphenylamine derivatives (TPA-R, R = H, OMe, and tBu) as the donor are prepared and characterized. All these emitters show deep/pure blue emission between 420 and 470 nm in the PMMA film, concomitant with the excellent emission efficiency of 80–100%. Both experimental and calculated methods demonstrate that these emitters exhibit a clearly hybridized local and charge-transfer excited state and can harvest both singlet and triplet excitons via reverse intersystem crossing process from the high-lying triplet to singlet states. Therefore, the solution processable deep blue organic light-emitting diodes (OLEDs) achieve a maximum external quantum efficiency (EQEmax) of 10.5% which is the recorded value for the solution processable deep blue OLED based on the “hot exciton” mechanism. Using TTT-TPA-H as the host material, solution-processed phosphorescent OLED based on PO-01 presents the EQEmax of 20.2%. These results pave a novel avenue for designing highly efficient deep blue emitter in solution processable OLED.
| Original language | English |
|---|---|
| Article number | 2113183 |
| Journal | Advanced Functional Materials |
| Volume | 32 |
| Issue number | 20 |
| DOIs | |
| State | Published - 13 May 2022 |
Keywords
- deep blue emitter
- hot excitons
- reverse intersystem crossing process
- solution-processable OLED
- tris(triazolo)triazine
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