Samsung Advanced Institute of Technology

Understanding and retardation of materials degradation phenomena in blue phosphorescent organic-light emitting diodes (PhOLEDs) are crucial to replace a fluorescent device with an efficient phosphorescent device in practical applications. Among the organic functional materials in the blue PhOLEDs, the host in the emitting layer is the most populated and fragile region in view of its density of states since singlet, triplet excitons, and polarons are continuously accumulated and consumed during operation. In this work, we presented novel n-type hosts which have thermally activated delayed fluorescence (TADF) features without loss of triplet energy even in the p-n mixed host structure. Both high triplet energy of mixed host and triplet up-conversion of a new n-type host within sub ms range allowed to demonstrate highly efficient and operationally stable blue PhOLEDs. Introducing 3,3-di(9H-carbazol-9-yl)biphenyl and 3-[bis(9H-carbazol-9-yl)-1,3,5-triazin-2-yl]-5-(triphenylsilyl)benzonitrile as a mixed host, blue PhOLEDs exhibited maximum external quantum efficiency of 20.9％, color coordinate of (0.16, 0.29), and device lifetime of 13,573 h at 100 cd m^-2, which was 4.2 times longer than that of state of the art blue device. Furthermore, the optimized blue PhOLEDs demonstrated device lifetime longer than 25,000 h, which is one of the longest device lifetimes of blue PhOLEDs without any sensitization or outcoupling enhancement. This result indicated that triplet exciton recycling via TADF mechanism in the n-type host is one of the effective approaches to enhance the operational stability of blue PhOLEDs.