Journal
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
Volume 48, Issue 15, Pages 3417-3430Publisher
WILEY
DOI: 10.1002/pola.24127
Keywords
charge transport; electroluminescence; fluorescence; host polymer; organic light-emitting diode
Categories
Funding
- Federal Ministry of Education and Research of Germany [01 BD 0685, 01 BD 0687]
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A series of novel styrene derived monomers with triphenylamine-based units, and their polymers have been synthesized and compared with the well-known structure of polymer of N,N'-bis(3-methylphenyl)-N,N'-diphenylbenzidine with respect to their hole-transporting behavior in phosphorescent polymer light-emitting diodes (PLEDs). A vinyltriphenylamine structure was selected as a basic unit, functionalized at the para positions with the following side groups: diphenylamine, 3-methylphenyl-aniline, 1- and 2-naphthylamine, carbazole, and phenothiazine. The polymers are used in PLEDs as host polymers for blend systems with the following device configuration: glass/indium-tin-oxide/PEDOT:PSS/polymer-blend/CsF/Ca/ Ag. In addition to the hole-transporting host polymer, the polymer blend includes a phosphorescent dopant [Ir(Me-ppy)(3)] and an electron-transporting molecule (2-(4-biphenyl)-5-(4-tert-butylphenyl)-1,3,4-oxadiazole). We demonstrate that two polymers are excellent hole-transporting matrix materials for these blend systems because of their good overall electroluminescent performances and their comparatively high glass transition temperatures. For the carbazole-substituted polymer (T-g = 246 degrees C), a luminous efficiency of 35 cd A(-1) and a brightness of 6700 cd m(-2) at 10 V is accessible. The phenothiazine-functionalized polymer (T-g = 220 degrees C) shows nearly the same outstanding PLED behavior. Hence, both these polymers outperform the well-known polymer of N,N'-bis(3-methylphenyl)-N,N'diphenylbenzidine, showing only a luminous efficiency of 7.9 cd A(-1) and a brightness of 2500 cd m(-2) (10 V). (C) 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 3417-3430, 2010
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