Citation: HAN Jie, LIANG Qiuju, QU Yi, LIU Jiangang, HAN Yanchun. Morphology Control of Non-fullerene Blend Systems Based on Perylene[J]. Acta Physico-Chimica Sinica, ;2018, 34(4): 391-406. doi: 10.3866/PKU.WHXB201709131 shu

Morphology Control of Non-fullerene Blend Systems Based on Perylene

  • Corresponding author: QU Yi, 2686566673@qq.com LIU Jiangang, niitawh@ciac.ac.cn HAN Yanchun, ychan@ciac.ac.cn
  • Received Date: 11 August 2017
    Revised Date: 7 September 2017
    Accepted Date: 7 September 2017
    Available Online: 13 April 2017

    Fund Project: the National Natural Science Foundation of China 21474113The project was supported by the National Natural Science Foundation of China (51573185, 21334006, 21474113) and the Strategic Priority Research Program of the Chinese Academy of Sciences (XDB12020300)the National Natural Science Foundation of China 21334006the Strategic Priority Research Program of the Chinese Academy of Sciences XDB12020300the National Natural Science Foundation of China 51573185

  • In recent years, the development of perylene diimide derivative (PDI)-based non-fullerene organic solar cells has been extensively studied. These solar cells exhibit unique advantages such as complementary light absorption, tunable energy levels, excellent electron transport properties, and relatively low cost. However, the strong π-π stacking between the PDI molecules tends to induce an uncontrolled phase separation structure, large domain size, and an unmanageable mixed phase, leading to severe geminate and non-geminate recombination and restriction of the final power conversion efficiency of the non-fullerene-based systems. In this work, it was found that one of the most important parameters that helps regulate phase structure is the molecular diffusion rate. By tuning the thermal annealing and liquid-solid phase separation and blend ratio, the phase-separated structure could be adjusted. Further, the domain size of blend systems with different compatibilities was regulated by balancing the π-π and charge transfer interactions. In addition, the amount of the intermixed phase was controlled by tuning the solubility parameter difference (Δδ) between the solvent and the solute.
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