摘要
The pursuit of narrowband multi-resonance thermally activated delayed fluorescence (MR-TADF) emitters with both high efficiency and color purity remains a critical challenge in the field of organic light-emitting diodes (OLEDs). A novel molecular design paradigm is proposed by hybridizing di-/tri-spiral donors in polycyclic heteroaromatic frameworks. The orthogonal, sterically hindered spiral donors disrupt molecular planarity, which can simultaneously suppress the aggregation-caused quenching and spectral broadening. These emitters exhibit narrowband emission with full-width at half-maximum of 22–24 nm and high photoluminescence quantum yields of ∼100%. The tri-spiral donor configuration further improves horizontal dipole orientation for the enhanced light outcoupling. As a result, the optimal Ts-NBN-based OLED achieves a maximum external quantum efficiency of 39.1% with the CIE y value of 0.70.
| 源语言 | 英语 |
|---|---|
| 期刊论文编号 | e202518014 |
| 期刊 | Angewandte Chemie - International Edition |
| 卷 | 64 |
| 期 | 46 |
| DOI | |
| 出版状态 | 已出版 - 10 11月 2025 |
学术指纹
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