4.2 Article

Synthesis and Characterization of Thermally Crosslinkable Hole-Transporting Polymers for PLEDs

Journal

JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
Volume 51, Issue 23, Pages 5111-5117

Publisher

WILEY-BLACKWELL
DOI: 10.1002/pola.26943

Keywords

charge transport; conjugated polymers; functionalization of polymers; heteroatom-containing polymers; light-emitting diodes (LED)

Funding

  1. Industrial Strategic Technology Development Program (Development of Fundamental Technologies for Flexible Combined-Function Organic Electronic Device) [KI002104]
  2. Ministry of Knowledge Economy (MKE, Korea)
  3. Korea Evaluation Institute of Industrial Technology (KEIT) [KI002104] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Two new thermally crosslinkable hole-transporting polymers, X-PTPA and X-PCz, were synthesized via Yamamoto coupling reactions. The number-averaged molecular weights (M-n) of X-PTPA and X-PCz were found to be 45,000 and 48,000, respectively, and therewith, polydispersity indices were of 1.8 and 1.7, respectively. Thermally crosslinked X-PTPA and X-PCz exhibit excellent solvent resistance and stable optoelectronic properties. The UV-visible maximum absorption peaks of X-PTPA and X-PCz in the thin film state are at 389 and 322 nm, respectively. The HOMO levels of X-PTPA and X-PCz are estimated to be -5.27 and -5.39 eV, respectively. Multilayered devices (ITO/crosslinked X-PTPA or X-PCz/SY-PPV/LiF/Al) were fabricated with SY (SuperYellow) as the emitting layer. The maximum efficiency of the multilayered device with a crosslinked X-PTPA layer is approximately three times higher than that of the device without a crosslinked X-PTPA layer and much higher than that of the crosslinked X-PCz device. This result can be explained by the observations that crosslinked X-PTPA produces increased electron accumulation within the emitter, SY, and also efficient exciton formation due to improved charge balance. (c) 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013, 51, 5111-5117

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