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A New Tetracyclic Lactam Building Block for Thick, Broad-Bandgap Photovoltaics

机译:一种新型的四环内酰胺构建基块,用于厚的宽带隙光伏

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摘要

A new tetracyclic lactam building block for polymer semiconductors is reported that was designed to combine the many favorable properties that larger fused and/or amide-containing building blocks can induce, including improved solid-state packing, high charge carrier mobility, and improved charge separation. Copolymeriza-tion with thiophene resulted in a semicrystalline conjugated polymer, PTNT, with a broad bandgap of 2.2 eV. Grazing incidence wide-angle X-ray scattering of PTNT thin films revealed a strong tendency for face-on π-stacking of the polymer backbone, which was retained in PTNT:fullerene blends. Corresponding solar cells featured a high open-circuit voltage of 0.9 V, a fill factor around 0.6, and a power conversion efficiency as high as 5% for >200 nm thick active layers, regardless of variations in blend stoichiometry and nanostructure. Moreover, efficiencies of >4% could be retained when thick active layers of ~400 nm were employed. Overall, these values are the highest reported for a conjugated polymer with such a broad bandgap and are unprecedented in materials for tandem and particularly ternary blend photovoltaics. Hence, the newly developed tetracyclic lactam unit has significant potential as a conjugated building block in future organic electronic materials.
机译:据报道,一种用于聚合物半导体的新型四环内酰胺结构单元被设计为结合较大的稠合和/或含酰胺结构单元可以诱导的许多有利特性,包括改善的固态堆积,高的载流子迁移率和改善的电荷分离。与噻吩共聚得到半结晶共轭聚合物PTNT,其带隙为2.2 eV。掠入入射的PTNT薄膜的广角X射线散射显示出聚合物主链面对π堆叠的强烈趋势,该趋势保留在PTNT:富勒烯共混物中。相应的太阳能电池具有0.9 V的高开路电压,约0.6的填充因数和大于200 nm厚的有源层的功率转换效率高达5%,而不论混合化学计量和纳米结构如何变化。此外,当采用〜400 nm的厚有源层时,可以保持> 4%的效率。总体而言,这些值是具有如此宽禁带宽度的共轭聚合物的最高报告值,在串联和特别是三元混合光伏材料中是前所未有的。因此,新开发的四环内酰胺单元在未来的有机电子材料中作为共轭结构单元具有巨大的潜力。

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  • 来源
    《Journal of the American Chemical Society》 |2014年第33期|11578-11581|共4页
  • 作者单位

    Ian Wark Research Institute, University of South Australia, Adelaide, SA 5095, Australia,Department of Chemical and Biological Engineering, Chalmers University of Technology, 41296 Goeteborg, Sweden;

    Department of Chemical and Biological Engineering, Chalmers University of Technology, 41296 Goeteborg, Sweden;

    Department of Materials Science and Engineering, Stanford University, Stanford, California 94305, United States;

    Department of Physics, Chemistry and Biology, Linkoeping University, 58183 Linkoeping, Sweden;

    Department of Applied Physics, Chalmers University of Technology, 41296 Goeteborg, Sweden;

    Department of Materials Science and Engineering, Stanford University, Stanford, California 94305, United States,Instituto de Fisica de Sao Carlos, Universidade de Sao Paulo, Sao Carlos, SP 13560-970, Brazil;

    Department of Physics, Chemistry and Biology, Linkoeping University, 58183 Linkoeping, Sweden;

    Department of Physics, Wake Forest University, Winston-Salem, North Carolina 27106, United States;

    Department of Chemical and Biological Engineering, Chalmers University of Technology, 41296 Goeteborg, Sweden;

    Department of Chemical and Biological Engineering, Chalmers University of Technology, 41296 Goeteborg, Sweden;

    Department of Applied Physics, Chalmers University of Technology, 41296 Goeteborg, Sweden;

    Department of Physics, Chemistry and Biology, Linkoeping University, 58183 Linkoeping, Sweden;

    Department of Materials Science and Engineering, Stanford University, Stanford, California 94305, United States;

    Department of Chemical and Biological Engineering, Chalmers University of Technology, 41296 Goeteborg, Sweden;

    Ian Wark Research Institute, University of South Australia, Adelaide, SA 5095, Australia,Department of Chemical and Biological Engineering, Chalmers University of Technology, 41296 Goeteborg, Sweden;

  • 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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  • 入库时间 2022-08-18 03:11:11

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