Breaking the lifetime barrier for deep blue phosphorescent OLEDs

Perhaps the single most important problem confronting the development of OLED displays and lighting today is how to achieve sufficiently long triplet-controlled emission device lifetime to prevent rapid color change during operation, while achieving 100% internal emission efficiency. It has been shown1 that bimolecular (e.g. triplet-polaron, triplet-triplet) annihilation provides a source of energy sufficient to destroy the blue triplet chromophore (whether a phosphor or a TADF molecule) or its host. Since that time, many materials, structures and strategies to extend blue emission lifetime based on this understanding have been demonstrated. Furthermore, various molecular fragments have been identified whose presence leads to the observed luminance loss. Unfortunately, a fully satisfactory solution has not been shown where blue triplet emitter lifetime is sufficient to meet the standards of high performance displays, although white OLED illumination sources may now have adequate lifetime to meet industry standards. In this talk I will discuss progress in extending blue phosphorescent OLED (PHOLED) lifetime, and in understanding of the limitations to extending the lifetime of blue triplet emitters. In particular, I will focus on the relationship between radiative state lifetime, exciton density, and the longevity of the PHOLED. I will review efforts that have resulted in increasing the deep blue phosphorescent longevity by at least 14 X via emitter design, polaritons, and optical cavity engineering. Prospects for future advances will be discussed. 1. “Intrinsic luminance loss in phosphorescent small-molecule organic light emitting devices due to bimolecular annihilation reactions”. N.C. Giebink, B.W. D’Andrade, M.S. Weaver, P.B. Mackenzie, J.J. Brown, M.E. Thompson, and S.R. Forrest, J. Appl. Phys., 103, 044509 (2008).