Thermally activated delayed fluorescence chiral molecules exhibiting photoinduced radical emission
Abstract
Room-temperature stable, photoinduced radical emission is achieved in chiral D–A–D′ thermally activated delayed fluorescence (TADF) molecules doped in poly(methyl methacrylate) (PMMA). Host–guest interactions suppress non-radiative decay, enhancing TADF and enabling reversible radical emission via an anti-Kasha process from higher excited states (D2/D3). This offers new strategies for photoresponsive materials.

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