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Understanding How Processing Additives Tune the Nanoscale Morphology of High Efficiency Organic Photovoltaic Blends: From Casting Solution to Spun-Cast Thin Film

机译:了解加工添加剂如何调整高效有机光伏混合物的纳米级形态:从浇铸溶液到纺铸薄膜

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摘要

Adding a small amount of a processing additive to the casting solution of photoactive organic blends has been demonstrated to be an effective method for achieving improved power conversion efficiency (PCE) in organic photo-voltaics (OPVs). However, an understanding of the nano-structural evolution occurring in the transformation from casting solution to thin photoactive films is still lacking. In this report, the effects of the processing additive dii-odooctane (DIO) on the morphology of the established blend of PBDTTT-C-T polymer and the fullerene derivative PC_(71)BM used for OPVs are investigated, starting in the casting solution and tracing the effects in spun-cast thin films by using neutron/X-ray scattering, neutron reflectometry, and other characterization techniques. The results reveal that DIO has no observable effect on the structures of PBDTTT-C-T and PC_(71)BM in solution; however, in the spun-cast films, it significantly promotes their molecular ordering and phase segregation, resulting in improved PCE. Thermodynamic analysis based on Flory-Huggins theory provides a rationale for the effects of DIO on different characteristics of phase segregation due to changes in concentration resulting from evaporation of the solvent and additive during film formation. Such information may help improve the rational design of ternary blends to more consistently achieve improved PCE for OPVs.
机译:已证明向光敏有机共混物的浇铸溶液中添加少量加工助剂是实现有机光伏(OPV)中改进的功率转换效率(PCE)的有效方法。然而,仍然缺乏对从流延溶液到薄光敏膜的转变中发生的纳米结构演变的理解。在这份报告中,研究了加工添加剂二碘-辛辛烷(DIO)对已建立的PBDTTT-CT聚合物与用于OPV的富勒烯衍生物PC_(71)BM的共混物形态的影响,从浇铸溶液开始并进行了追踪通过使用中子/ X射线散射,中子反射测量法和其他表征技术,对喷铸薄膜的影响。结果表明,DIO对溶液中PBDTTT-C-T和PC_(71)BM的结构无明显影响。然而,在纺丝薄膜中,它显着促进了它们的分子有序化和相分离,从而改善了PCE。基于Flory-Huggins理论的热力学分析为DIO对相分离不同特性的影响提供了理论依据,这是由于成膜过程中溶剂和添加剂的蒸发导致浓度变化所致。此类信息可能有助于改善三元混合物的合理设计,从而更一致地实现OPV的PCE改善。

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  • 来源
    《Advanced Functional Materials》 |2014年第42期|6647-6657|共11页
  • 作者单位

    Center for Nanophase Materials Sciences Oak Ridge National Laboratory Oak Ridge, TN 37831, USA;

    Center for Nanophase Materials Sciences Oak Ridge National Laboratory Oak Ridge, TN 37831, USA,Neutron Scattering Science Divisions Oak Ridge National Laboratory Oak Ridge, TN 37831, USA;

    Center for Nanophase Materials Sciences Oak Ridge National Laboratory Oak Ridge, TN 37831, USA,Computer Science and Mathematics Division Oak Ridge National Laboratory Oak Ridge, TN 37831, USA;

    Center for Nanophase Materials Sciences Oak Ridge National Laboratory Oak Ridge, TN 37831, USA;

    Neutron Scattering Science Divisions Oak Ridge National Laboratory Oak Ridge, TN 37831, USA;

    Department of Electrical Engineering and Computer Science University of Tennessee Knoxville, TN 37996, USA;

    Material Sciences Division Argonne National Laboratory Argonne, Illinois 60439, USA;

    Institute of Chemistry Chinese Academy of Sciences Beijing 10080, China;

    Neutron Scattering Science Divisions Oak Ridge National Laboratory Oak Ridge, TN 37831, USA;

    Neutron Scattering Science Divisions Oak Ridge National Laboratory Oak Ridge, TN 37831, USA;

    Center for Nanophase Materials Sciences Oak Ridge National Laboratory Oak Ridge, TN 37831, USA;

    Center for Nanophase Materials Sciences Oak Ridge National Laboratory Oak Ridge, TN 37831, USA;

    Center for Nanophase Materials Sciences Oak Ridge National Laboratory Oak Ridge, TN 37831, USA,Computer Science and Mathematics Division Oak Ridge National Laboratory Oak Ridge, TN 37831, USA;

    Center for Nanophase Materials Sciences Oak Ridge National Laboratory Oak Ridge, TN 37831, USA;

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