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首页> 外文期刊>Organic Electronics >Effects of fullerene solubility on the crystallization of poly(3-hexylthiophene) and performance of photovoltaic devices
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Effects of fullerene solubility on the crystallization of poly(3-hexylthiophene) and performance of photovoltaic devices

机译:富勒烯溶解度对聚(3-己基噻吩)结晶和光伏器件性能的影响

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摘要

The substantial crystallization suppression of poly(3-hexylthiophene) (P3HT) in the untreated P3HT:C60 composite film prepared from o-dichlorobenzene (ODCB) solution has been revealed. Besides, the effective conjugation length of P3HT in this composite has been nearly maintained to that in the solution. The different crystallization behaviors of P3HT in its composites with C60 and [6,6]-phenyl C_(61) butyric acid methyl ester (PCBM) are mainly attributed to the relative solubility of C60 and PCBM with respect to P3HT in ODCB. The solution to overcome this disadvantage of chain conformation and crystallinity of P3HT in the composite with C60 is thus proposed and finalized by resorting to the addition of low volatile solvent with much higher solubility of C60 than P3HT into the main solvent used, so as P3HT can crystallize before C60 forms crystallites in the solution. The feasibility of this approach has been proven by the improved efficiency of devices based on composites of P3HT and the low cost C60 without resorting to post-treatments. Our results demonstrated in this study could further benefit development of new electron acceptor materials, particularly based on fullerenes and their derivatives, by considering the role of the new materials in determining the crystallization of the other components involved in the composite film.
机译:已经揭示了在由邻二氯苯(ODCB)溶液制备的未处理的P3HT:C60复合膜中,聚(3-己基噻吩)(P3HT)的基本结晶抑制作用。此外,该复合物中P3HT的有效结合长度几乎保持在溶液中。 P3HT在其与C60和[6,6]-苯基C_(61)丁酸甲酯(PCBM)的复合物中的不同结晶行为主要归因于C60和PCBM相对于P3HT在ODCB中的相对溶解度。因此,提出了克服C3复合材料中P3HT的链构象和结晶性这一缺点的解决方案,并通过向所用的主要溶剂中添加了比C3HT溶解度高得多的C60溶解度的低挥发性溶剂来最终确定P3HT可以C60在溶液中形成微晶之前先结晶。这种方法的可行性已通过基于P3HT复合材料的设备效率的提高和低成本C60的改进而无需进行后处理,从而得到证明。通过考虑新材料在确定复合膜中涉及的其他组分的结晶中的作用,我们的研究结果表明,新材料尤其是基于富勒烯及其衍生物的电子受体材料的开发将进一步受益。

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  • 来源
    《Organic Electronics》 |2009年第7期|1334-1344|共11页
  • 作者单位

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

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

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

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

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

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    polymer solar cells; fullerene; solubility; poly(3-hexylthiophene); crystallinity;

    机译:聚合物太阳能电池;富勒烯溶解度聚(3-己基噻吩);结晶度;

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