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Scale-up Chemical Synthesis of Thermally-activated Delayed Fluorescence Emitters Based on the Dibenzothiophene-S,S-Dioxide Core
Published on: October 24, 2017
Thermally Activated Delayed Fluorescence in Commercially Available Materials for Solution-Process Exciplex OLEDs
Zong-Liang Tseng1,2, Wei-Lun Huang1,2, Tzu-Hung Yeh2
1Department of Electronic Engineering, Ming Chi University of Technology, New Taipei City 243303, Taiwan.
Abstract:
Organic light-emitting diodes (OLEDs) have developed rapidly in recent years. Thermally activated delayed fluorescent (TADF) molecules open a path to increase exciton collection efficiency from 25% to 100%, and the solution process provides an alternative technology to achieve lower cost OLEDs more easily. To develop commercial materials as exciplex hosts for high-performance and solution-processed OLEDs, we attempted to use 4,4'-cyclohexylidenebis[N,N-bis(4-methylphenyl)benzenamine (TAPC), poly(9-vinylcarbazole) (PVK), N,N'-Di(1-naphthyl)-N,N'-diphenyl-(1,1'-biphenyl)-4,4'-diamine (NPB), and poly(N,N'-bis-4-butylphenyl-N,N'-bisphenyl)benzidine (Poly-TPD) as the donors and 2,4,6-tris[3-(diphenylphosphinyl)phenyl]-1,3,5-triazine (POT2T) as the acceptor to obtain the TADF effect. All donors and the acceptor were purchased from chemical suppliers. Our work shows that excellent TADF properties and high-efficiency exciplex OLEDs with low turn-on voltage and high luminance can be achieved with a simple combination of commercial materials.
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