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Design and modification of three-component randomly incorporated copolymers for high performance organic photovoltaic applications

In this study we report the molecular design, synthesis, characterization, and photovoltaic properties of a series of diketopyrrolopyrrole (DPP) and dithienothiophene (DTT) based donor-acceptor random copolymers. The six random copolymers are obtained via Stille coupling polymerization using various...

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Bibliographic Details
Published in:Polymer chemistry 2013-01, Vol.4 (3), p.84-811
Main Authors: Li, Jun, Ong, Kok-Haw, Sonar, Prashant, Lim, Siew-Lay, Ng, Ging-Meng, Wong, Hoi-Ka, Tan, Huei-Shuan, Chen, Zhi-Kuan
Format: Article
Language:English
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Summary:In this study we report the molecular design, synthesis, characterization, and photovoltaic properties of a series of diketopyrrolopyrrole (DPP) and dithienothiophene (DTT) based donor-acceptor random copolymers. The six random copolymers are obtained via Stille coupling polymerization using various concentration ratios of donor to acceptor in the conjugated backbone. Bis(trimethylstannyl)thiophene was used as the bridge block to link randomly with the two comonomers 5-(bromothien-2-yl)-2,5-dialkylpyrrolo[3,4- c ]pyrrole-1,4-dione and 2,6-dibromo-3,5-dipentadecyl-dithieno[3,2- b ;2′,3′- d ]thiophene. The optical properties of these copolymers clearly reveal a change in the absorption band through optimization of the donor-acceptor ratio in the backbone. Additionally, the solution processability of the copolymers is modified through the attachment of different bulky alkyl chains to the lactam N-atoms of the DPP moiety. Applications of the polymers as light-harvesting and electron-donating materials in solar cells, in conjunction with PCBM as acceptor, show power conversion efficiencies (PCEs) of up to 5.02%. Molecular design, synthesis, and characterization of a series of diketopyrrolopyrrole and dithienothiophene based donor-acceptor random copolymers are discussed; power conversion efficiencies up to 5.02% are obtained by using these polymers.
ISSN:1759-9954
1759-9962
DOI:10.1039/c2py20763j