Abstract
A bipolar macrospirocyclic trimer based on 4,5-diazafluorene and triphenylamine was prepared as a host for solution-processed blue phosphorescent organic light emitting diodes. The oligomer exhibits a high triplet energy of 2.88 eV, excellent thermal and morphological stability, good film-forming ability and solution processability. A solution-processed phosphorescent device based on FIrpic and the trimer achieved a maximum current efficiency of 10.0 cd A−1 with a low current efficiency roll-off at the practical luminance (9.6, 10.0, 9.4 cd A−1 at 102, 207, 1096 cd m−2, respectively). The oligomer additionally showed excellent chemical compatibility with the common host for solution-processing technology. A blue phosphorescent device using mixed hosts of the trimer/4,4′-cyclohexylidenebis(N,N-bis(4-methyl -phenyl)benzenamine) achieved a low turn-on voltage of 3.0 V, a maximum luminance of 28,368 cd m−2, and a maximum current efficiency of 17.7 cd A−1 (11.9 lm W−1), which is almost three times that of a single 4,4′-cyclohexylidenebis(N,N- bis(4-methylphenyl)benzenamine)-hosted device.
| Original language | English |
|---|---|
| Pages (from-to) | 348-357 |
| Number of pages | 10 |
| Journal | Dyes and Pigments |
| Volume | 134 |
| DOIs | |
| State | Published - 1 Nov 2016 |
| Externally published | Yes |
Keywords
- 4,5-Diazafluorene
- Host
- Oligomer
- Phosphorescent organic light-emitting diodes
- Solution-processable
- Triphenylamine
Fingerprint
Dive into the research topics of 'A bipolar macrospirocyclic oligomer based on triphenylamine and 4,5-diazafluorene as a solution-processable host for blue phosphorescent organic light-emitting diodes'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver