首页> 外文期刊>RSC Advances >Improvement in interlayer structure of p-i-n-type organic solar cells with the use of fullerene-linked tetrabenzoporphyrin as additive
【24h】

Improvement in interlayer structure of p-i-n-type organic solar cells with the use of fullerene-linked tetrabenzoporphyrin as additive

机译:用富勒烯连接的四苯并卟啉作为添加剂的富勒烯连接的四苯并卟啉的层间结构改善P-I-N型有机太阳能电池

获取原文
获取原文并翻译 | 示例
           

摘要

The additive effect on small-molecule-based p-i-n-type devices has been little investigated so far. We focus on the improvement of the miscibility of tetrabenzoporphyrin (BP) and [6,6]-phenyl-C-61-butyric acid methyl ester (PC61BM) blend film by addition of fullerene-linked tetrabenzoporphyrin (BP-C-60) as an additive to the interlayer (i-layer). BP is one of the most promising p-type organic semiconductors, and BP films can be prepared readily by heating as-cast films of the precursor (a bicyclo[2.2.2]octadiene-fused porphyrin; CP), that results in changes from amorphous CP films to polycrystalline BP films. Because of the high crystallinity of BP, large BP grains on the scale of tens to hundreds of nanometers are generated in blend films of BP and PC61BM during film fabrication. We found that the addition of BP-C-60 as an additive (3, 5, 7, and 10 wt%) to the i-layer composed of BP and PC61BM improves the miscibility of BP and PC61BM. The power conversion efficiency of p-i-n-type organic solar cells consisting of a blend film of BP and PC61BM (i-layer) sandwiched by BP (p-layer) and PC61BM (n-layer) improved by up to 50% as compared to that of a control device after the addition of BP-C-60 to the i-layer. The film morphology was investigated using atomic force microscopy, fluorescence microspectroscopy, two-dimensional grazing-incident wide-angle X-ray diffraction measurements, and scanning electron microscopy. Interacting with both BP and PC61BM, the addition of BP-C-60 led to changes in the grain size as well as an increase in the size of the BP/PC61BM interface and hence effective charge separation in the p-i-n device. This morphological improvement is attributable to the ability of BP-C-60, which exhibits the characteristics of both BP and C-60, to promote the compatibility of BP and PC61BM. This study is a significant step towards the development of high-performance p-i-n-type solar cells and should pave the way for the fabrication of high-performance bulk-heterojunction layers in solution-processed organic photovoltaic devices.
机译:到目前为止,基于小分子的P-I-N型器件的添加剂效果几乎没有研究。我们专注于通过加入富勒烯连接的四苯并卟啉(BP-C-60)的富勒烯连接的四苯基卟啉(BP)和[6,6] - 苯基-C-61-丁酸甲酯(PC61BM)共混膜的溶解质的改善。中间层(I层)的添加剂。 BP是最有前途的p型有机半导体之一,并且通过在前体的浇铸膜(双环[2.2.2]八烯稠合的卟啉; CP)的浇铸薄膜,可以容易地制备BP膜,从而导致来自的变化非晶CP膜到多晶BP薄膜。由于BP的高结晶度,在薄膜制造期间,在BP和PC61BM的共混膜中产生大量的大BP晶粒。我们发现,将BP-C-60添加到由BP和PC61BM组成的I层的添加剂(3,5,7和10wt%)提高了BP和PC61BM的混溶性。由BP(P型)和PC61BM(N层)夹在一起的BP和PC61BM(I层)的共混膜组成的销型有机太阳能电池的功率转换效率,相比,高达50%在向I层加入BP-C-60后的控制装置的内容。使用原子力显微镜,荧光微四射光学,二维放牧入射的广角X射线X射线衍射测量和扫描电子显微镜研究,研究了薄膜形态。与BP和PC61BM相互作用,添加BP-C-60导致晶粒尺寸的变化以及BP / PC61BM界面的大小的增加,因此在P-I-N设备中的有效电荷分离。这种形态改善可归因于BP-C-60的能力,它表现出BP和C-60的特征,促进BP和PC61BM的相容性。该研究是促进高性能P-I-N型太阳能电池的显着步骤,并且应该为溶液加工有机光伏器件中的高性能散装 - 异质结层铺平道路。

著录项

  • 来源
    《RSC Advances》 |2018年第61期|共9页
  • 作者单位

    Nara Inst Sci &

    Technol Grad Sch Sci &

    Technol Div Mat Sci 8916-5 Takayama Cho Ikoma Nara 6300192 Japan;

    Nara Inst Sci &

    Technol Grad Sch Sci &

    Technol Div Mat Sci 8916-5 Takayama Cho Ikoma Nara 6300192 Japan;

    Kwansei Gakuin Univ Dept Appl Chem &

    Environm 2-1 Gakuen Sanda Hyogo 6691337 Japan;

    Japan Synchrotron Radiat Res Inst 1-1-1 Kouto Sayo Hyogo 6795198 Japan;

    Kwansei Gakuin Univ Dept Appl Chem &

    Environm 2-1 Gakuen Sanda Hyogo 6691337 Japan;

    Nara Inst Sci &

    Technol Grad Sch Sci &

    Technol Div Mat Sci 8916-5 Takayama Cho Ikoma Nara 6300192 Japan;

    Nara Inst Sci &

    Technol Grad Sch Sci &

    Technol Div Mat Sci 8916-5 Takayama Cho Ikoma Nara 6300192 Japan;

    Nara Inst Sci &

    Technol Grad Sch Sci &

    Technol Div Mat Sci 8916-5 Takayama Cho Ikoma Nara 6300192 Japan;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号