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Tailoring optoelectronic properties of thieno[3,2-b]thiophene comprising homopolymers via electron acceptor moieties: thienopyrrolodione, 2,1,3-benzoselenadiazole, isoindigo
Date
2020-09-15
Author
Göker, Seza
Sarigül, Hatice
Toppare, Levent Kamil
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In this work, thieno[3,2-b]thiophene based homopolymers, namely poly(5,6-bis(octyloxy)-4,7-bis(thieno[3,2-b] thiophen-2-yl)benzo[c][1,2,5]selenadiazole; PBSeThTh), poly(5-(2-ethylhexyl)-1,3-bis(thieno[3,2-b]thiophen-2-yl)4H-thieno[3,4-c]pyrrole-4,6(5H)-dione; PTPDThTh) and poly((E)-6,6 '-bis(thieno[3,2-b]thiophen-2-yl)-1,1 ' diundecyl-[3,3 '-biindolinylidene]-2,2 '-dione; PIIDThTh), were obtained potentiodynamically to tailor optoelectronic properties via altering electron acceptor moieties which were 5,6-bis(octyloxy)benzo[c][1,2,5]selenadiazole 5-(2ethylhexyl)-4H-thieno[3,4-c]pyrrole-4,6(5H)-dione (TPD) and (E)-1,1 '-diundecyl-[3,3 '-biindolinylidene]-2,2 '-dione (IID). The polymers were characterized cyclic voltammetry and spectroelectrochemistry studies. All polymers reveal ambipolar and multichromic characteristics with broad spectral absorptions, low-lying highest occupied molecular orbital (-5.69 eV, -5.59 eV, -5.60 eV), and as well as low band gap ranging from 1.58 eV to 1.86 eV. Isoindigo comprising polymer resulted in the lowest optical band gap which was 1.16 eV due to a red shift in the absorption most probably due to richer electron density and strong inter-chain interactions, structural planarity. (C) 2020 Published by Elsevier B.V.
Subject Keywords
Analytical Chemistry
,
Electrochemistry
,
General Chemical Engineering
URI
https://hdl.handle.net/11511/56639
Journal
Journal of Electroanalytical Chemistry
DOI
https://doi.org/10.1016/j.jelechem.2020.114372
Collections
Department of Chemistry, Article
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S. Göker, H. Sarigül, and L. K. Toppare, “Tailoring optoelectronic properties of thieno[3,2-b]thiophene comprising homopolymers via electron acceptor moieties: thienopyrrolodione, 2,1,3-benzoselenadiazole, isoindigo,”
Journal of Electroanalytical Chemistry
, pp. 0–0, 2020, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/56639.