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Protecting benzylic C?H bonds by deuteration doubles the operational lifetime of deep blue Ir-phenylimidazole dopants in phosphorescent OLEDs

Journal
Advanced Optical Materials
Date
2021.05.18
Abstract

Much effort has been dedicated to increase the operational lifetime of blue phosphorescent materials in organic light-emitting diodes (OLEDs), but the reported device lifetimes are still too short for the industrial applications. An attractive method for increasing the lifetime of a given emitter without making any chemical change is exploiting the kinetic isotope effect, where key C?H bonds are deuterated. A computer model identifies that the most vulnerable molecular site in an Ir-phenylimidazole dopant is the benzylic C?H bond and predicted that deuteration may lower the deactivation pathway involving C?H/D cleavage notably. Experiments show that the device lifetime (T70) of a prototype phosphorescent OLED device can be doubled to 355 hours with a maximum external quantum efficiency of 25.1 % at 1000 cd m?2. This is one of the best operational performances of blue phosphorescent OLEDs observed to date in a single stacked cell.

Reference
Adv. Opt. Mater. 2100630 (2021)
DOI
http://dx.doi.org/10.1002/adom.202100630