Abstract

Host materials play an important role in the development of phosphorescent and thermally activated delayed fluorescence (TADF) organic light emitting diodes (OLEDs). Herein, a universal bipolar host material TPA-(PyF)3 based on triphenylamine and pyridine was designed and synthesized through a simple Friedel-Crafts reaction with a high yield of 83.5%. TPA-(PyF)3 possesses a high triplet energy level of 2.83 eV, excellent thermal and morphological stability, and good solution processability. Using TPA-(PyF)3 as a host material, solution-processed OLEDs with a simple single emitting layer were fabricated. Blue phosphorescent OLEDs based on bis((3,5-difluorophenyl)-pyridine) iridium picolinate (FIrpic) show a maximum current efficiency of 18.5 cd A−1 and a maximum brightness of 13,838 cd m−2, with a low current efficiency roll-off of 9.7% at the practical brightness of 100–1000 cd m−2. Green TADF OLEDs using TPA-(PyF)3 as the host and 2,4,5,6-tetrakis(carbazol-9-yl)-1,3-dicyano-benzene (4CzIPN) as the emitter with the same structure of the phosphorescent OLEDs exhibit a maximum current efficiency of 12.7 cd A−1, compared with 10.2 cd A−1 of the control device based on the common host material of 2,6-bis(3-(9H-carbazol-9-yl)phenyl)pyridine (26DCzPPy). This study demonstrates the effective utilization of TPA-(PyF)3 as a universal bipolar host for both phosphorescent and TADF OLEDs.

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