Cascading Energy Transfer for Highly Efficient Deep−Red OLED Emission with Cyclometalated [3+2+1] Iridium Complexes

Abstract

AbstractThe promising cyclometalated iridium (III) complexes have been proved to possess great potential in vacuum−deposited organic light−emitting diodes (OLEDs) applications for full−color displays and white solid−state lighting sources. Herein, based on the unique bidentate ligand of dibenzo[a,c]phenazine (dbpz) group with strong conjugated effect of aromatic rings for red emission, four novel [3+2+1] coordinated iridium (III) emissive materials have been rationally designed and synthesized. The monodentate ligands of −CN and −OCN have been effectively employed to tune the deep−red emission of 628−675 nm with high photoluminescence quantum yields up to 98%. Moreover, all devices displayed deep−red color coordinates ranging from (0.675, 0.325) to (0.716, 0.284), which is close to the standard−red color coordinates of (0.708, 0.292), as recommended by International Telecommunication Union Radiocommunication (ITU−R) BT.2020. The device based on nBuIr(dbpz)CN with an exciplex cohost has exhibited maximum external quantum efficiencies of 20.7% and good stability. With nBuIr(dbpz)CN as an effective sensitizer, the nBuIr(dbpz)OCN based phosphorescent OLED devices have successfully demonstrated cascading energy transfer processes, contributing to pure red emission with maximum luminance as high as 6471 cd m−2. Therefore, this work has been successfully demonstrated rational molecular design strategy of [3+2+1] iridium complexes to obtain highly efficient deep−red electrophosphorescent emission.