【摘 要】
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Thermally activated delayed fluorescence (TADF) molecules have attracted great attention as high efficient lumines-cent materials.Most of TADF molecules possess small energy gap between the first singlet excited state (S1) and the first triplet excited st
【机 构】
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Shandong Key Laboratory of Medical Physics and Image Processing & Shandong Provincial Engineering an
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Thermally activated delayed fluorescence (TADF) molecules have attracted great attention as high efficient lumines-cent materials.Most of TADF molecules possess small energy gap between the first singlet excited state (S1) and the first triplet excited state (T1) to favor the up-conversion from T1 to S1.In this paper,a new TADF generation mechanism is re-vealed based on theoretical simulation.By systematic study of the light-emitting properties of SOBF-OMe in both toluene and in aggregation state,we find that the single SOBF-OMe could not realize TADF emission due to large energy gap as well as small up-conversion rates between S1 and T1.Through analysis of dimers,we find that dimers with intermolecular hydrogen bond (H-bond) are responsible for the generation of TADF,since smaller energy gap between S1 and T1 is found and the emission wavelength is in good agreement with experimental counterpart.The emission properties of SOBF-H are also studied for comparison,which reflect the important role of H-bond.Our theoretical results agree ith experimental results well and confirm the mechanism of H-bond induced TADF.
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