Phenoxazines having various electron acceptor or donor fragments as new host materials for green phosphorescent OLEDs

We report on the synthesis and characterization of a new series of phenoxazine-based compounds as potential host materials of phosphorescent OLEDs. The derivatives are thermally stable materials as it was demonstrated by thermogravimetric analysis. Electron photoemission spectra of thin layers of th...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Dyes and pigments 2020-01, Vol.172, p.107839, Article 107839
Hauptverfasser: Tavgeniene, Daiva, Blazevicius, Dovydas, Eidimtas, Marius, Krucaite, Gintare, Zhang, Baohua, Sutkuviene, Simona, Grigalevicius, Saulius
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:We report on the synthesis and characterization of a new series of phenoxazine-based compounds as potential host materials of phosphorescent OLEDs. The derivatives are thermally stable materials as it was demonstrated by thermogravimetric analysis. Electron photoemission spectra of thin layers of the materials show ionization potentials in the range of 5.24–5.56 eV. Some of the developed materials formed homogenous amorphous layers with high glass transition temperatures and were used as hosts for bis[2-(2-pyridinyl-N)phenyl-C](acetylacetonato)iridium(III), Ir(ppy)2(acac), guest in green phosphorescent organic light-emitting diodes. Results indicated that a device with 3-[bis(9-ethylcarbazol-3-yl)methyl)-10-hexylphenoxazine host exhibited superior performance with external quantum efficiency exceeding 5.9%, maximum current efficiency of 18.3 cd/A, maximum brightness of 5366 cd/m2 and low turn on voltage of 3.1 V. •Phenoxazines with electron donating or accepting fragments were synthesized.•The compounds were tested as host materials in phosphorescent OLEDs.•Green device demonstrated maximum current efficiency exceeding 18.3 cd/A.
ISSN:0143-7208
1873-3743
DOI:10.1016/j.dyepig.2019.107839