Issue 14, 2013

Synthesis and characterization of a low band gap quinoxaline based D–A copolymer and its application as a donor for bulk heterojunction polymer solar cells

Abstract

A new alternating copolymer P comprising of benzo[1,2-b;4,5,b′]dithiophene (BDT) derivative and 4,9-bis-(5-bromothiophene-2-yl)-6,7-di-(2-ethylhexyl)-[1,2,5]thiadiazolo[3,4-g]quinoxaline (DTQx) derivative electron, donating and electron withdrawing units, respectively, has been synthesized by Stille reaction. The copolymer was characterized by TGA, UV-visible absorption and cyclic voltammetry. The optical band gap of P was calculated from the onset wavelength of absorption to be about 1.38 eV. The copolymer P was used as electron donor along with PC60BM or PC70BM as electron acceptors for the fabrication of bulk heterojunction solar cells with configurations of ITO/PEDOT:PSS/P:PC60BM or PC70BM/Al. The power conversion efficiencies (PCE) of the copolymer solar cells blended with PC60BM and PC70BM as electron acceptors, spin cast from THF solvent, were 2.10% and 3.26%, respectively. The PCE device based on the P:PC70BM blend processed from DIO/THF was enhanced up to 4.47%. After optimizing the device parameters, such as blend ratio of P to PCBM and the choice of processing solvent, power conversion efficiency reaches as high as 5.12% for P:PC70BM blend, when processed from DIO/THF solvent, a blend ratio of 1 : 2 w/w and DMSO doped PEDOT:PSS buffer layer is used.

Graphical abstract: Synthesis and characterization of a low band gap quinoxaline based D–A copolymer and its application as a donor for bulk heterojunction polymer solar cells

Article information

Article type
Paper
Submitted
26 Mar 2013
Accepted
01 May 2013
First published
01 May 2013

Polym. Chem., 2013,4, 4033-4044

Synthesis and characterization of a low band gap quinoxaline based D–A copolymer and its application as a donor for bulk heterojunction polymer solar cells

M. L. Keshtov, D. V. Marochkin, V. S. Kochurov, A. R. Khokhlov, E. N. Koukaras and G. D. Sharma, Polym. Chem., 2013, 4, 4033 DOI: 10.1039/C3PY00391D

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