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首页> 外文期刊>Advanced Functional Materials >Tunable Crystallinity in Regioregular Poly(3-Hexylthiophene) Thin Films and Its Impact on Field Effect Mobility
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Tunable Crystallinity in Regioregular Poly(3-Hexylthiophene) Thin Films and Its Impact on Field Effect Mobility

机译:区域规则的聚(3-己基噻吩)薄膜的可调节结晶度及其对场效应迁移率的影响

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摘要

The properties of poly(alkylthiophenes) in solution are found to have a profound impact on the self assembly process and thus the microstructural and electrical properties of the resultant thin films. Ordered supramolecular precursors can be formed in regioregular poly(3-hexylthiophene) (P3HT) solutions through the application of low intensity ultrasound. These precursors survive the casting process, resulting in a dramatic increase in the degree of crystallinity of the thin films obtained by spin coating. The crystallinity of the films is tunable, with a continuous evolution of mesoscale structures observed as a function of ultrasonic irradiation time. The photophysical properties of P3HT in solution as well in the solid state suggest that the application of ultrasound leads to a /r stacking induced molecular aggregation resulting in field effect mobilities as high as 0.03 cm2 V"1 s~ A multiphase morphology, comprising short quasi-ordered and larger, ordered nanofibrils embedded in a disordered amorphous phase is formed as a result of irradiation for at least 1 min. Two distinct regions of charge transport are identified, characterized by an initial sharp increase in the field effect mobility by two orders of magnitude due to an increase in crystallinity up to the percolation limit, followed by a gradual saturation where the mobility becomes independent of the thin film microstructure.
机译:发现溶液中聚(烷基噻吩)的性质对自组装过程具有深远影响,因此对所得薄膜的微观结构和电学性质具有深远的影响。通过应用低强度超声,可以在区域规则的聚(3-己基噻吩)(P3HT)溶液中形成有序的超分子前体。这些前体在流延过程中幸存下来,从而导致通过旋涂获得的薄膜的结晶度显着提高。膜的结晶度是可调的,观察到的中尺度结构的连续演变是超声照射时间的函数。 P3HT在溶液中以及在固态时的光物理性质表明,超声的应用导致/ r堆积诱导的分子聚集,从而导致场效应迁移率高达0.03 cm2 V“ 1 s〜。多相形态,包括短准辐照至少1分钟形成了排列在无序非晶相中的有序和更大,有序的纳米原纤维,鉴定出两个不同的电荷传输区域,其特征是场效应迁移率最初急剧增加了两个数量级。由于结晶度增加到渗滤极限而导致的最大强度,然后逐渐饱和,其中迁移率变得与薄膜微结构无关。

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  • 来源
    《Advanced Functional Materials》 |2011年第14期|p.2652-2659|共8页
  • 作者单位

    School of Chemical and Biomolecular Engineering Georgia Institute of Technology Atlanta, GA 30332, USA;

    School of Materials Science and Engineering Georgia Institute of Technology Atlanta, GA 30332, USA;

    School of Chemistry and Biochemistry Georgia Institute of Technology Atlanta, GA 30332, USA,DuPont Central Research and Development, Experimental Station, Wilmington, DE 19880, USA;

    School of Chemistry and Biochemistry Georgia Institute of Technology Atlanta, GA 30332, USA;

    School of Chemical and Biomolecular Engineering Georgia Institute of Technology Atlanta, GA 30332, USA,School of Materials Science and Engineering Georgia Institute of Technology Atlanta, GA 30332, USA,School of Chemistry and Biochemistry Georgia Institute of Technology Atlanta, GA 30332, USA;

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