系统间交叉
光子上转换
量子产额
光化学
斯托克斯位移
激发态
化学
光敏剂
荧光
单重态
消灭
近红外光谱
光电子学
材料科学
兴奋剂
原子物理学
物理
光学
量子力学
作者
Jikun Li,Ming‐Yu Zhang,Le Zeng,Ling Huang,Xiaoye Wang
标识
DOI:10.1002/anie.202303093
摘要
Triplet-triplet annihilation upconversion (TTA-UC) with near-infrared (NIR) photosensitizers is highly desirable for a variety of emerging applications. However, the development of NIR-to-blue TTA-UC with a large anti-Stokes shift is extremely challenging because of the energy loss during the intersystem crossing (ISC). Here, we develop the first NIR-absorbing B,N-heteroarene-based sensitizer (BNS) with multi-resonance thermally activated delayed fluorescence (MR-TADF) characters to achieve efficient NIR-to-blue TTA-UC. The small energy gap between the singlet and triplet excited states (0.14 eV) of BNS suppresses the ISC energy loss, and its long-delayed fluorescence lifetime (115 μs) contributes to efficient triplet energy transfer. As a result, the largest anti-Stokes shift (1.03 eV) among all heavy-atom-free NIR-activatable TTA-UC systems is obtained with a high TTA-UC quantum yield of 2.9 % (upper limit 50 %).
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