4.5 Article

Synthesis of bis(thiophen-2-yl)benzothiadiazole scaffold donor-acceptor polymers: studies of polymerization, electrical, optical, and photovoltaic properties

Journal

POLYMER BULLETIN
Volume 80, Issue 9, Pages 10015-10029

Publisher

SPRINGER
DOI: 10.1007/s00289-022-04535-1

Keywords

Donor-acceptor polymers; Direct C-H arylation polymerization; Optical and electrical properties; Photovoltaic devices

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The facile and efficient synthesis of conjugated donor-acceptor polymers via direct C-H arylation polymerization has received significant interest in the field of organic electronics. In this study, a one-pot synthesis method was used to successfully synthesize a series of bis(thiophen-2-yl)benzothiadiazole-based donor-acceptor polymers. The resulting polymers exhibited excellent solubility and were characterized for their optical and electrochemical properties. Additionally, the polymer films blended with PC71BM showed temperature-dependent absorption for potential photovoltaic applications, with a power conversion efficiency of 3.82%.
Facile and efficient synthesis of conjugated donor-acceptor polymers via direct C-H arylation polymerization has received significant interest in organic electronic applications. We report here a one-pot synthesis of a series of bis(thiophen-2-yl)benzothiadiazole-based donor-acceptor polymers P1-4 via direct C-H arylation polymerization in excellent yield. Two donor moieties [3-hexylthiophene and 1,4-bis(dodecyloxy)benzene], and one acceptor unit 4,7-bis(thiophen-2-yl)benzo[c][1,2,5]thiadiazole were used for direct C-H arylation polymerization. The prowess of the methodology was applied to synthesis of polymer by adding one donor unit followed by a second donor unit after the due course. The resulting polymers are soluble and characterized. Optical and electrochemical properties were carried out by UV-Vis-NIR and cyclic voltammetry, respectively. A temperature-dependent absorption of the polymer films blended with PC71BM was studied for photovoltaic application. Devices were fabricated by solution-processable deposition of active layer and a PCE of 3.82% was achieved.

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