Dual Emission and Low-Temperature Afterglow in Xanthone-Dibenzoazepine for High EQE Host–Guest OLEDs with Low-Efficiency Roll-Off

Abstract

Research has been driven to demonstrate organic light-emitting diodes (OLEDs) with high efficiency, and in the quest for new materials, thermally activated delayed fluorescence (TADF) emitters have been employed. Preparation of donor− acceptor (D-A) π-conjugates is a useful guideline for developing TADF emitters. TADF emitters have shown excellent progress and high maximum external quantum efficiency (EQE max ) for OLEDs in the recent past; however, they suffer with substantial roll-off resulting in a decrease in their efficiency. In order to have efficient OLED emitters with less efficiency roll-off, we designed a xanthone-amine derivative with twisted electron-rich dibenzoazepine having limited rotation at the donor−acceptor bond. Xan-Azepine shows solvent polarity-dependent fluorescence in the range of 441− 597 nm having a lifetime below 10 ns. At 77 K in Me-THF, a triplet at 557 nm was observed having a decay lifetime of 0.75 s and an afterglow for about 6 s. In powder, it shows dual emission, i.e., fluorescence (490 and 6 ns) and phosphorescence (530 nm and 192 μs) at ambient conditions. The energy difference between the singlet and triplet energy levels of Xan-Azepine is found to be 0.18 eV in the powder sample. Its blend in 4,4′-bis(Ncarbazolyl)-1,1′-biphenyl (CBP) showed delayed fluorescence with a lifetime of 118 μs at 300 K, while it reduced to 84 μs at 150 K. These observations suggest the TADF nature of Xan-Azepine in its CBP blend. OLED devices of Xan-Azepine showing a turn-on voltage of 2.8 V and a EQE max of 12% were successfully fabricated. In the doped films of Xan-Azepine (5 wt %) with CBP, a maximum luminescence of 5980 Cd/m 2 at a current density of 70 mA/cm 2 was obtained, resulting in devices with low-efficiency roll-off (2.75%).