Abstract
Thermally activated delayed fluorescence (TADF) materials have attracted considerable attentions as a new kind of emitters in organic light-emitting diodes. While it is requisite to minimize an energy difference between the lowest excited triplet state (T1) and lowest excited singlet state (S1), so-called ΔEST, a deeper understanding of the emission mechanism is desirable to clarify the comprehensive molecular design. In this paper, we present that the TADF ability and efficiency of (rare-)metal free organic molecules are surely influenced by both the nonradiative decay of T1 and spin-orbit coupling. By investigating a temperature dependent photoluminescence of carbazole benzonitrile derivatives in toluene solutions using a newly developed liquid nitrogen cryostat, we demonstrate the activation of TADF by solvent freezing for room temperature-TADF inactive molecules. Transient photoluminescence measurements of the frozen samples show a significant increase of a lifetime of T1, probing the suppression of nonradiative decay path of T1. A magnitude of the TADF activation by the solvent freezing is closely related to the degree of spin-orbit coupling of the molecules. The present results emphasize the importance of suppression of nonradiative decay of T1 and an increase of spin-orbit coupling together with reducing ΔEST to achieve a high TADF emission efficiency.
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