Diamine-cored tetrastilbene compounds as solution-processable hole transport materials for stable organic light emitting diodes

Abstract

A series of diamine-cored tetrastilbene (DTS) derivatives bearing various aliphatic and aromatic substituents was designed and synthesized for use as solution-processed hole transport layers (HTLs) in organic light emitting diodes (OLEDs). The chemical structures of the DTS derivatives were strategically designed to increase solubility in organic solvents as well as to avoid self-crystallization, and thus ensure a stable morphology under Joule heating while maintaining efficient hole transport capabilities. The five DTS derivatives, composed of different conjugation structures, yielded reasonably good hole transport behavior with a marginal charge carrier mobility of similar to 10(-5) cm(2)V(-1) s(-1), which is similar to that of vacuum-deposited N,N'-bis(1-naphthyl)-N,N'-diphenyl-1,1'biphenyl-4,4'-diarnine (NPB). Due to the high glass transition temperatures of the DTS derivatives, this satisfactory charge transport behavior and smooth surface morphology were conserved up to 180 degrees C. Green OLEDs were prepared using tris-(8-hydroxyquinoline) aluminum (Alq(3)):C545T as the emission layer, and the OLED performances of the solution-processed DTS HTLs and the vacuum-deposited NPB HTL were compared. A high luminance efficiency of 11.5 cd A(-1) was obtained for one solution-processed DTS HTL, which exceeds that of the NPB HTL (10.01 cd A(-1)). Furthermore, the DTS HTLs enabled a stable OLED operation, with double the accelerated half-life of the NPB-based device.