Abstract

AbstractWe report photoluminescence quenching studies on model DCJTB‐doped Alq3 electroluminescent devices. The spectroscopy versus doping density suggests that solvatochromic effects are minor but that energy transfer plays a large role. Quenching of DCJTB fluorescence is due to Förster energy transfer to DCJTB cations, and measurements of the bleaching recovery dynamics show that charge extraction from ionized DCJTB sites is slow and consistent with biexponential kinetics. Temperature‐dependent studies find effective activation barriers for detrapping that are too small to be consistent with simple HOMO offsets between host and dopant.

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