An osmium(II) complex, [-trifluoromethyl-5-(2-pyridyl)-1,2,4-triazole, -diphenyl-phosphan], when doped in a -dicarbazolebiphenyl host as a phosphorescent red emitter in organic light-emitting devices, has the unusual property of resisting concentration quenching and sustaining its external quantum efficiency (EQE) (8%–9%) over a wide range of doping concentration (20%–40%). Single-crystal x-ray diffraction evidence is presented that the difference in doping behaviors can be linked to the octahedral configuration of , which could prevent the undesirable molecular aggregation from occurring at high concentration, thus delaying the onset of quenching. Accordingly, the high doping concentration of leads to a significant suppression of luminescence quenching at high brightness/current and achieves a “flat” EQE versus brightness response owing to the increase in the emission sites in the emission layer.
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We used AC2 to measure the HOMO of the organic materials first. Then we got the energy gap by UV absorption. The LUMO was obtained indirectly from the HOMO and the .