New TIPS-substituted benzo[1,2-b:4,5-b′]dithiophene-based copolymers for application in polymer solar cells

Chinna Bathula, Chang Eun Song, Sachin Badgujar, Seong Jin Hong, In Nam Kang, Sang Jin Moon, Jaemin Lee, Shinuk Cho, Hong Ku Shim, Sang Kyu Lee

Research output: Contribution to journalArticlepeer-review

45 Scopus citations

Abstract

Novel triisopropylsilylethynyl (TIPS)-substituted benzodithiophene-based copolymers, poly[4,8-bis(triisopropylsilylethynyl)benzo[1,2-b:4,5-b′] dithiophene-2,6-diyl-alt-4,6-(2-ethylhexyl-thieno[3,4-b]thiophene-2-carboxylate) ] (P1), poly[4,8-bis(triisopropylsilylethynyl)benzo[1,2-b:4,5-b′] dithiophene-2,6-diyl-alt-[4,6-{(1-thieno[3,4-b]thiophen-2-yl) -2-ethylhexan-1-one}] (P2), and poly[4,8-bis(triisopropylsilylethynyl)benzo[1,2- b:4,5-b′]dithiophene-2,6-diyl-alt-4,6-(2-ethylhexyl(3-fluorothieno[3,4-b] thiophene)-2-carboxylate)] (P3), were designed and synthesized for use in polymer solar cells (PSCs). We describe the effects of the different acceptor segment side groups on the optical, electrochemical, field-effect hole mobility, and photovoltaic characteristics of the resulting TIPS-based copolymers. The side groups in the copolymers were found to significantly influence the carrier mobilities and photovoltaic properties of the copolymers. The field-effect mobilities of the holes varied from 9 × 10 -5 cm 2 V -1 s -1 in P2 to 3 × 10 -3 cm 2 V -1 s -1 in P1. Under optimized conditions, the TIPS-based polymers showed power conversion efficiencies (PCEs) for the PSCs in the range of 3.16-5.76%. Among the TIPS-based copolymers studied here, P1 showed the best photovoltaic performance, with an open-circuit voltage (V oc) of 0.82 V, a short-circuit current density (J sc) of 12.75 mA cm -2, a fill factor (FF) of 0.55, and a power-conversion efficiency of 5.76% using a P1:PC 71BM blend film as the active layer under AM 1.5G irradiation (100 mW cm -2).

Original languageEnglish
Pages (from-to)22224-22232
Number of pages9
JournalJournal of Materials Chemistry
Volume22
Issue number41
DOIs
StatePublished - 7 Nov 2012

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