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Multi-scale ordering in highly stretchable polymer semiconducting films

机译:高伸缩性聚合物半导体薄膜的多尺度有序化

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摘要

Stretchable semiconducting polymers have been developed as a key component to enable skin-like wearable electronics, but their electrical performance must be improved to enable more advanced functionalities. Here, we report a solution processing approach that can achieve multi-scale ordering and alignment of conjugated polymers in stretchable semiconductors to substantially improve their charge carrier mobility. Using solution shearing with a patterned microtrench coating blade, macroscale alignment of conjugated-polymer nanostructures was achieved along the charge transport direction. In conjunction, the nanoscale spatial confinement aligns chain conformation and promotes short-range p-p ordering, substantially reducing the energetic barrier for charge carrier transport. As a result, the mobilities of stretchable conjugated-polymer films have been enhanced up to threefold and maintained under a strain up to 100%. This method may also serve as the basis for large-area manufacturing of stretchable semiconducting films, as demonstrated by the roll-to-roll coating of metre-scale films.
机译:可拉伸的半导体聚合物已被开发为实现皮肤般可穿戴电子设备的关键部件,但必须改善其电性能以实现更高级的功能。在这里,我们报告了一种解决方案处理方法,该方法可以实现可伸缩半导体中共轭聚合物的多尺度排序和排列,从而显着提高其电荷载流子迁移率。使用带图案的微沟槽涂层刀片进行溶液剪切,共轭聚合物纳米结构沿电荷传输方向进行了大规模对准。结合起来,纳米级空间限制使链构象对齐并促进短程p-p有序化,从而大大降低了电荷载流子传输的能垒。结果,可拉伸的共轭聚合物薄膜的迁移率提高了三倍,并保持在高达100%的应变下。这种方法还可以作为可拉伸半导体薄膜大面积生产的基础,如米级薄膜的卷对卷涂布所证明的。

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  • 来源
    《Nature Materials》 |2019年第6期|594-601|共8页
  • 作者单位

    Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA|Argonne Natl Lab, Nanosci & Technol Div, Lemont, IL USA;

    Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA;

    Stanford Univ, Dept Elect Engn, Stanford, CA 94305 USA;

    Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA;

    Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA;

    Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA;

    Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA|Univ Chicago, Inst Mol Engn, Chicago, IL 60637 USA;

    Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA|Katholieke Univ Leuven, Dept Mat Engn, Leuven, Belgium;

    Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA|SLAC Natl Accelerator Lab, Stanford Synchrotron Radiat Lightsource, Menlo Pk, CA USA|Univ Southern Mississippi, Sch Polymer Sci & Engn, Hattiesburg, MS 39406 USA;

    Nanjing Univ, Sch Chem & Chem Engn, Dept Polymer Sci & Engn, State Key Lab Coordinat Chem, Nanjing, Jiangsu, Peoples R China;

    Nanjing Univ, Sch Chem & Chem Engn, Dept Polymer Sci & Engn, State Key Lab Coordinat Chem, Nanjing, Jiangsu, Peoples R China;

    Gyeongsang Natl Univ, Dept Chem, Jinju, South Korea|Gyeongsang Natl Univ, RINS, Jinju, South Korea;

    Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA;

    Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA;

    Stanford Univ, Dept Mat Sci & Engn, Stanford, CA 94305 USA;

    Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA;

    Stanford Univ, Dept Elect Engn, Stanford, CA 94305 USA;

    Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA|Asahi Kasei Corp, Corp Res & Dev, Performance Mat Technol Ctr, Fuji, Shizuoka, Japan;

    Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA;

    Hong Kong Univ Sci & Technol, Dept Chem, Chinese Natl Engn Res Ctr Tissue Restorat & Recon, Kowloon, Hong Kong, Peoples R China|Hong Kong Univ Sci & Technol, Hong Kong Branch, Chinese Natl Engn Res Ctr Tissue Restorat & Recon, Kowloon, Hong Kong, Peoples R China;

    Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA|Samsung Adv Inst Technol, Mat Res Ctr, Suwon, Gyeonggi Do, South Korea;

    Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA;

    Stanford Univ, Dept Elect Engn, Stanford, CA 94305 USA;

    Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA;

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