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Blue aggregation-induced emission bipolar materials consisting of diphenylsulfone or benzophenone core and triphenylethene-carbazole fragments for highly efficient OLEDs.
- Source :
-
Dyes & Pigments . Sep2024, Vol. 228, pN.PAG-N.PAG. 1p. - Publication Year :
- 2024
-
Abstract
- Bipolar derivatives having aggregation-induced emission (AIE) properties were synthesized in reactions of 4,4′-difluorobenzophenone, 4-fluorophenyl-phenylsulfone or bis(4-fluorophenyl)sulfone with prepared key starting materials: 1,1,2-triphenyl-2-(9H-carbazol-2-yl)ethylene or 1-(9H-carbazol-2-yl)-4-(1,2,2-triphenylethenyl)benzene. The objective materials have shown high thermal stabilities and can form amorphous layers having high glass transition temperatures in the region of 110–173 °C. The photoluminescence spectra of the prepared derivatives registered using tetrahydrofuran-water solutions demonstrated strong blue emissions, confirming their AIE property. Thin films of the compounds were tested in multilayer organic light-emitting diodes. The device using bis(4-{2-[4-(1,1,2-triphenylethylenyl)phenyl]carbazol-9-yl}phenyl)sulfone emitter (EM3) outperformed the other devices, achieving a peak efficiencies of 3.4 % (5.6 cd/A and 4.7 lm/W) with maximum luminance of about 11000 cd/m2. However OLED using 4-{2-[4-(1,1,2-triphenylethylenyl)phenyl]carbazol-9-yl}phenyl-phenylsulfone (EM2) as emitter demonstrated higher efficiency at higher luminance values. The maximum efficiencies of the device were obtained at a luminance value of about 100 cd/m2 and were recorded as 3.2 % (5.2 cd/A and 4.1 lm/W) with luminance of 17515 cd/m2. • Bipolar derivatives having aggregation-induced emission (AIE) properties were synthesized. • The compounds have shown high thermal stabilities. • The materials can form amorphous layers having high glass transition temperatures. • Thin films of the compounds were tested in multilayer organic light-emitting diodes. • Peak efficiencies of 3.4 % (5.6 cd/A and 4.7 lm/W) were registered for one device. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 01437208
- Volume :
- 228
- Database :
- Academic Search Index
- Journal :
- Dyes & Pigments
- Publication Type :
- Academic Journal
- Accession number :
- 177866673
- Full Text :
- https://doi.org/10.1016/j.dyepig.2024.112231