Substituent position engineering of diphenylquinoline-based Ir(III) complexes for efficient orange and white PhOLEDs with high color stability/low efficiency roll-off using a solution-processed emission layer

Three new heteroleptic Ir(III) complexes o-LIrpic, m-LIrpic, and p-LIrpic (L = CF(3)DPQ) consisting of 2,4-diphenylquinoline (DPQ) with a - CF3 group at ortho (o)/meta (m)/para (p) positions of the metalated phenyl ring, respectively, as the main ligands were synthesized and used as emitters in phosphorescent organic light-emitting diodes (PhOLEDs). We realized that - CF3 position extremely affects the crucial photophysical and electronic properties such as emission color, photoluminescence quantum yield (PLQY) and energy levels of these Ir(III) complexes resulting in - CF3 position-dependent performance of their PhOLEDs. To verify the effect of - CF3 group position on device performance, three other Ir(III) complexes o-LIrtmd, m-LIrtmd, and p-LIrtmd were synthesized using the same main ligands but a different ancillary ligand. In the two series of Ir(III) complexes, the devices with m-CF3 based complexes are outstanding in performance compared to o-or p-CF3 based ones due to the enhanced PLQY and well suppressed non-radiative deactivations by m-substitution. Finally, the single emission layer solution-processed orange and two-component white PhOLEDs fabricated using m-LIrpic as orange emitter achieved the maximum external quantum efficiency of 17.1% (43.9 cd A(-1)) and 21.1% (48.8 cd A(-1)), respectively, with highly stable color coordinates and low efficiency roll-off. This is the highest efficiency reported to date for solution-processed orange PhOLEDs using a small molecular host with easily accessible emitter.