4.3 Article

A new benzo[1,2-b:4,5-b′]difuran-based copolymer for efficient polymer solar cells

Journal

JOURNAL OF MATERIALS CHEMISTRY
Volume 22, Issue 34, Pages 17724-17731

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c2jm32843g

Keywords

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Funding

  1. NSFC [51173206, 21161160443]
  2. National High Technology Research and Development Program [2011AA050523]
  3. Natural Science Foundation of Hunan Province, China [11JJ4010]
  4. China Postdoctoral Science Foundation [20110490150]
  5. Fundamental Research Funds for the Central Universities [2010QZZD0112]

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A new donor-acceptor type copolymer, namely poly{4,8-bis(2-ethylhexyloxy)benzo[1,2-b:3,4-b']difuran-alt-6-octylnaphtho[2,3-c]thiophene-4,9-dione} (PBDFNTDO) was synthesized by a Stille coupling reaction and characterized by H-1 NMR, GPC, TGA, UV-Vis absorption spectroscopy and cyclic voltammetry. PBDFNTDO is readily soluble in common organic solvents with a number-average molecular weight (M-n) of 10.7 kDa mol(-1) and a polydispersity index of 1.71. TGA analysis shows the copolymer exhibits good thermal stability with 5% weight loss at a temperature of 341 degrees C. PBDFNTDO possesses a broad absorption band at 300-750 nm with an optical bandgap of 1.65 eV. Cyclic voltammetry gives HOMO and LUMO energy levels of -5.33 eV and -3.40 eV, respectively. The hole mobility of PBDFNTDO:PC71BM (1 : 1.5, w/w) reaches up to 5.0 x 10(-3) cm(2) V-1 s(-1) by the space-charge-limited current (SCLC) method. A polymer solar cell with the configuration of ITO/PEDOT:PSS/PBDFNTDO:PC71BM (1 : 1.5, w/w)/Ca/Al demonstrates a promising power conversion efficiency of 4.71% under the illumination of AM 1.5 G, 100 mW cm(-2).

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