A High‐Efficiency Organic Solar Cell Enabled by the Strong Intramolecular Electron Push–Pull Effect of the Nonfullerene Acceptor

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  • Wanning Li
    State Key Laboratory of Polymer Physics and Chemistry Institute of Chemistry Chinese Academy of Sciences Beijing 100190 P. R. China
  • Long Ye
    Department of Physics and Organic and Carbon Electronics Lab (ORaCEL) North Carolina State University Raleigh NC 27695 USA
  • Sunsun Li
    State Key Laboratory of Polymer Physics and Chemistry Institute of Chemistry Chinese Academy of Sciences Beijing 100190 P. R. China
  • Huifeng Yao
    State Key Laboratory of Polymer Physics and Chemistry Institute of Chemistry Chinese Academy of Sciences Beijing 100190 P. R. China
  • Harald Ade
    Department of Physics and Organic and Carbon Electronics Lab (ORaCEL) North Carolina State University Raleigh NC 27695 USA
  • Jianhui Hou
    State Key Laboratory of Polymer Physics and Chemistry Institute of Chemistry Chinese Academy of Sciences Beijing 100190 P. R. China

書誌事項

公開日
2018-03-13
権利情報
  • http://onlinelibrary.wiley.com/termsAndConditions#am
  • http://onlinelibrary.wiley.com/termsAndConditions#vor
DOI
  • 10.1002/adma.201707170
公開者
Wiley

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説明

<jats:title>Abstract</jats:title><jats:p>Besides broadening of the absorption spectrum, modulating molecular energy levels, and other well‐studied properties, a stronger intramolecular electron push–pull effect also affords other advantages in nonfullerene acceptors. A strong push–pull effect improves the dipole moment of the wings in IT‐4F over IT‐M and results in a lower miscibility than IT‐M when blended with PBDB‐TF. This feature leads to higher domain purity in the PBDB‐TF:IT‐4F blend and makes a contribution to the better photovoltaic performance. Moreover, the strong push–pull effect also decreases the vibrational relaxation, which makes IT‐4F more promising than IT‐M in reducing the energetic loss of organic solar cells. Above all, a power conversion efficiency of 13.7% is recorded in PBDB‐TF:IT‐4F‐based devices.</jats:p>

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