Imaging Science and Photochemistry ›› 2017, Vol. 35 ›› Issue (5): 736-748.DOI: 10.7517/j.issn.1674-0475.2017.04.034

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Synthesis and Properties of 4,4'-Spiro-bi[cyclopenta[2,1-b;3,4-b']dithiophene]Cored 1,8-Naphthalimide Derivatives for Organic Solar Cells

ZHANG Jiabin1,2, MA Yuchao2, YI Jinduo2, DOU Junyan2, WANG Hongyu1, MA Changqi2   

  1. 1. Department of Chemistry, College of Science, Shanghai University, Shanghai 200444, P. R. China;
    2. Printable Electronics Research Center, Suzhou Institute of Nano-Tech and Nano-Bionics(SINANO), Chinese Academy of Sciences, Suzhou 215123, Jiangsu, P. R. China
  • Received:2017-05-27 Revised:2017-06-12 Online:2017-09-15 Published:2017-09-15

Abstract:

With the rapid development of high performance non-fullerene electron acceptor, the power conversion efficiency of polymer solar cells increased dramatically in the last few years, among which structurally non-planar electron acceptors play a very important role. In this paper, a new family non-fullerene electron acceptor based on 1,8-naphthalimide unit with cyclopenta[2,1-b;3,4-b']dithiophene(CPDT-(NMI)2), 4,4'-spiro-bi[cyclopenta[2,1-b;3,4-b']dithiophene](SCPDT-(NMI)4) or 4-H-cyclopenta-[2,1-b;3,4-b']dithiophene-4-one (CPDT-O-(NMI)2) core were synthesized. The absorption and fluorescence spectra, as well as the electrochemical properties of these compounds were characterized. Results showed that SCPDT-(NMI)4 showed a blue-shifted absorption compared to that of CPDT-(NMI)2, which is ascribed to the twisted molecular structure of CPDT-(NMI)2 for its high steric hindrance. While CPDT-O-(NMI)2 showed two absorption bands with peaking wavelength at 420 nm and 550 nm, which is quite different to that of SCPDT-(NMI)4 and CPDT-(NMI)2. Solid state absorption spectra confirm that SCPDT-(NMI)4 and CPDT-(NMI)2 showed low intermolecular interaction, which could be attributed to the non-planar molecular structure of these two compounds as well. Fluorescence of the SCPDT-(NMI)4 film was found to be red-shifted 11 nm over CPDT-(NMI)2, which is ascribed to the spiro-conjugation effect of SCPDT-(NMI)4 in excited state. Cyclic voltammetry results demonstrated that LUMO energy levels of these compounds are around -3.5 to -3.8 eV, making them suitable electron acceptor in polymer solar cells. Polymer solar cell using PBDB-T as the electron donor and SCPDT-(NMI)4 as the electron acceptor showed a high power conversion efficiency of 1.16%, which is much higher than that of CPDT-(NMI)2 (0.11%). Fluorescence of the blended films confirmed that photon induced electron transfer between PBDB-T and NMIs is not completed, which is believed to be one of the main reason for the low device performance.

Key words: organic solar cells, non-fullerene electron acceptor, photosensitive materials, spiro conjugation