A High Efficiency Organic Solar Cell Enabled by Strong Intramolecular Electron Push-Pull Effect of Non-Fullerene Acceptor
Wanning Li a, Long Ye b, Sunsun Li a, Huifeng Yao a, Harald Ade b, Jianhui Hou a
a Institute of Chemistry, Chinese Academy of Sciences (ICCAS), China
b North Carolina State University, Partners Way, 911, Raleigh, United States
International Conference on Hybrid and Organic Photovoltaics
Proceedings of International Conference on Hybrid and Organic Photovoltaics (HOPV18)
Benidorm, Spain, 2018 May 28th - 31st
Organizers: Emilio Palomares and Rene Janssen
Poster, Wanning Li, 115
Publication date: 21st February 2018

Molecular design has played a critical role in advancing photovoltaic properties of the non-fullerene (NF) acceptors.[1-3] In the various types of NF acceptors, the materials with a so-called A(acceptor)-D(donor)-A(acceptor) structure, in which electron-rich central unit is end-capped by two electron-deficient segments and hence intramolecular electron push-pull effect can be formed, has exhibited promising photovoltaic properties. Besides broadening of the absorption spectrum, modulating molecular energy levels and other well-studied properties,[4-7] a stronger intramolecular electron push-pull effect also affords other advantages in NF acceptors. A strong push-pull effect improves the dipole moment of the wings in IT-4F over IT-M, resulting 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 (OSCs). Above all, a power conversion efficiency of 13.7% is recorded in PBDB-TF: IT-4F-based devices.

References

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