Abstract
Abstract A highly luminescent mononuclear Al complex with β-diketone ligands exhibiting superior thermally activated delayed fluorescence (TADF) properties was developed in this work. The complex showed yellow emission with promising photofunctions, including a near-unity photoluminescence quantum yield (PLQY), a rapid radiative decay rate, and a short delayed fluorescence lifetime in the solid state. When applied in a solution-processed organic light-emitting device, an external quantum efficiency (EQE) exceeding 18% and a low turn-on voltage of 2.9 V at 1 cd/m2 were obtained, surpassing those of the corresponding β-diketone ligand. Metal complexation with Al generated unique electronic structures that significantly strengthened the photofunctions of the original β-diketone ligand in the solid state.
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