Theoretical calculation demonstrates high luminescence in organic semiconductors, suggesting efficient material design techniques.
Combining high mobility and high‐efficiency luminescence in one material is challenging because of their contradictory design principles. Here, under the three‐state exciton model, a molecular descriptor is proposed to quantitatively design materials with balanced luminescence and mobility in aggregated states, where a large would promise high crystalline photoluminescence quantum yield (PLQY) with small J (excitonic coupling) and significant and (hole and electron transfer integrals) would indicate high mobility. Through theoretical calculation and experimental validation, it is found that the asymmetric anthracene derivatives are quite effective in simultaneously achieving high mobility and high PLQY. Following the asymmetric guideline, the newly developed compounds, 2‐phenyl vinyl anthracene (2‐PhVA) and 6‐(2‐(anthracene‐2‐yl)vinyl)benzo[b]thiophene (6‐BTVA) demonstrate high values alongside excellent performance: 2‐PhVA exhibits a PLQY of 81.5% and a maximum hole mobility of 10.0 cm 2 V −1 s −1 , and 6‐BTVA shows a PLQY of 30.9% with a maximum mobility of 9.3 cm 2 V −1 s −1 . The above results demonstrate the validation of the descriptor and the asymmetric strategy in further developing high‐mobility light‐emitting aggregated materials.
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Sun et al. (2025) studied this question.
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