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通过控制晶体形式中三重态发色团的堆积实现超长有机磷光

Manipulating the Stacking of Triplet Chromophores in the Crystal Form for Ultralong Organic Phosphorescence.

作者信息

Gan Nan, Wang Xuan, Ma Huili, Lv Anqi, Wang He, Wang Qian, Gu Mingxing, Cai Suzhi, Zhang Yanyun, Fu Lishun, Zhang Meng, Dong Chaomin, Yao Wei, Shi Huifang, An Zhongfu, Huang Wei

机构信息

Key Laboratory of Flexible Electronics (KLOFE) & Institute of Advanced Materials (IAM), Nanjing Tech University (NanjingTech), 30 South Puzhu Road, Nanjing, 211816, China.

Institute of Flexible Electronics (IFE), Northwestern Polytechnical University (NPU), 127 West Youyi Road, Xi'an, 710072, China.

出版信息

Angew Chem Int Ed Engl. 2019 Oct 1;58(40):14140-14145. doi: 10.1002/anie.201907572. Epub 2019 Aug 28.

Abstract

Provided here is evidence showing that the stacking between triplet chromophores plays a critical role in ultralong organic phosphorescence (UOP) generation within a crystal. By varying the structure of a functional unit, and different on-off UOP behavior was observed for each structure. Remarkably, 24CPhCz, having the strongest intermolecular interaction between carbazole units exhibited the most impressive UOP with a long lifetime of 1.06 s and a phosphorescence quantum yield of 2.5 %. 34CPhCz showed dual-emission UOP and thermally activated delayed fluorescence (TADF) with a moderately decreased phosphorescence lifetime of 770 ms, while 35CPhCz only displayed TADF owing to the absence of strong electronic coupling between triplet chromophores. This study provides an explanation for UOP generation in crystal and new guidelines for obtaining UOP materials.

摘要

这里提供的证据表明,三重态发色团之间的堆积在晶体中的超长有机磷光(UOP)产生中起着关键作用。通过改变功能单元的结构,每种结构都观察到了不同的开关UOP行为。值得注意的是,咔唑单元之间具有最强分子间相互作用的24CPhCz表现出最令人印象深刻的UOP,其长寿命为1.06 s,磷光量子产率为2.5%。34CPhCz表现出双发射UOP和热激活延迟荧光(TADF),磷光寿命适度降低至770 ms,而35CPhCz由于三重态发色团之间缺乏强电子耦合,仅表现出TADF。这项研究为晶体中UOP的产生提供了解释,并为获得UOP材料提供了新的指导方针。

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