首页> 外文期刊>Journal of the American Chemical Society >Aromatic Extension at 2,6-Positions of Anthracene toward an Elegant Strategy for Organic Semiconductors with Efficient Charge Transport and Strong Solid State Emission
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Aromatic Extension at 2,6-Positions of Anthracene toward an Elegant Strategy for Organic Semiconductors with Efficient Charge Transport and Strong Solid State Emission

机译:蒽在2,6-位置的芳香延伸,实现了一种具有高效电荷传输和强固态发射的有机半导体优雅策略

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摘要

Organic semiconductors integrating excellent charge transport with efficient solid emission are very challenging to be attained in the construction of light-emitting transistors and even for realization of electrically pumped organic lasers. Herein, we introduce naphthyl units at 2,6-positions of anthracene to achieve 2,6-di(2-naphthyl)anthracene (dNaAnt), which adopts J-aggregated mode in the solid state as a balanced strategy for excellent charge transporting and efficient solid state emission. Single crystal field-effect transistors show mobility up to 12.3 cm~2·V~(-1)·s~(-1) and a photoluminescence quantum yield of 29.2% was obtained for dNaAnt crystals. Furthermore, organic light-emitting transistors (OLETs) based on dNaAnt single crystals distribute outstanding balanced ambipolar charge transporting property = 1.10 cm2-V~(-1)·s~(-1), μ_e = 0.87 cm~2·V~(-1)·s~(-1)) and spatially controllable emission, which is one of the best performances for OLETs.
机译:在发光晶体管的构造中甚至对于实现电泵浦有机激光器而言,要实现将优异的电荷传输与有效的固体发射相结合的有机半导体是非常具有挑战性的。在这里,我们在蒽的2,6-位引入萘基单元以实现2,6-二(2-萘基)蒽(dNaAnt),其采用固态的J聚集模式作为平衡策略,从而实现了出色的电荷传输和有效的固态发射。单晶场效应晶体管的迁移率高达12.3 cm〜2·V〜(-1)·s〜(-1),dNaAnt晶体的光致发光量子产率为29.2%。此外,基于dNaAnt单晶的有机发光晶体管(OLET)具有出色的平衡双极性电荷传输特性= 1.10 cm2-V〜(-1)·s〜(-1),μ_e= 0.87 cm〜2·V〜( -1)·s〜(-1))和空间可控的发射,这是OLET的最佳性能之一。

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  • 来源
    《Journal of the American Chemical Society》 |2017年第48期|17261-17264|共4页
  • 作者单位

    Beijing National Laboratory for Molecular Science, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China ,University of Chinese Academy of Sciences, Beijing 100190, China;

    Beijing National Laboratory for Molecular Science, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China ,University of Chinese Academy of Sciences, Beijing 100190, China;

    Beijing National Laboratory for Molecular Science, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China;

    State Key Laboratory of Polymer, Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China;

    State Key Laboratory of Polymer, Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China;

    Beijing National Laboratory for Molecular Science, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China;

    Tianjin Key Laboratory of Molecular Optoelectronic Sciences, Department of Chemistry, School of Science, Tianjin University and Collaborative Innovation Center of Chemical Science and Engineering, Tianjin 300072, China;

    Beijing National Laboratory for Molecular Science, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China;

    Beijing National Laboratory for Molecular Science, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China ,Tianjin Key Laboratory of Molecular Optoelectronic Sciences, Department of Chemistry, School of Science, Tianjin University and Collaborative Innovation Center of Chemical Science and Engineering, Tianjin 300072, China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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