A bipolar macrospirocyclic oligomer based on triphenylamine and 4,5-diazafluorene as a solution-processable host for blue phosphorescent organic light-emitting diodes

Nengquan Li, Zhaokang Fan, Huiru Zhao, Yiwu Quan, Qingmin Chen, Shanghui Ye, Shuhua Li, Quli Fan, Wei Huang

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

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 languageEnglish
Pages (from-to)348-357
Number of pages10
JournalDyes and Pigments
Volume134
DOIs
StatePublished - 1 Nov 2016
Externally publishedYes

Keywords

  • 4,5-Diazafluorene
  • Host
  • Oligomer
  • Phosphorescent organic light-emitting diodes
  • Solution-processable
  • Triphenylamine

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