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Carbazole-pyrene derivatives for undoped organic light-emitting devices

  • S. L. Lai
  • , Q. X. Tong
  • , M. Y. Chan
  • , T. W. Ng
  • , M. F. Lo
  • , C. C. Ko
  • , S. T. Lee
  • , C. S. Lee

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

Abstract

Two carbazole-pyrene derivatives, namely 3,6-dipyrenyl-9-(4′-tert- butylphenyl) carbazole (BPyC) and 3,6-dipyrenyl-9-(4′-pyrenylphenyl) carbazole (TPyC), have been designed and synthesized for application in organic light-emitting devices (OLEDs). While the two compounds have similar chemical structures and photoluminescent properties, OLEDs based on them show distinct electroluminescence (EL) spectra. The BPyC-based devices show a single peak saturated blue emission with CIE coordinates of (0.15, 0.18); whereas the TPyC-based devices exhibit two emission peaks at blue and yellow hues with CIE coordinates of (0.22, 0.29). The difference in their EL spectra is attributed to the substitution of the t-butyl unit of BPyC with a pyrenyl group to form TPyC, which effectively increases the electron-donating property and results in exciplex formation at its interface with the electron-accepting TPBI. A high external quantum efficiency of 3.11% is achieved in the TPyC-based devices. Influences of chemical structure and fluorescent quantum yield on the efficiency of exciplex emission are discussed. © 2011 Elsevier B.V. All rights reserved.
Original languageEnglish
Pages (from-to)541-546
JournalOrganic Electronics: physics, materials, applications
Volume12
Issue number3
DOIs
Publication statusPublished - Mar 2011

Research Keywords

  • Carbazole
  • Electroluminescence
  • Organic light-emitting diode
  • Pyrene
  • Small-molecule
  • Undoped

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