A Low Band Gap Polymer Based on Selenophene and Benzobis (thiadiazole)

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Date

2017

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Pergamon-elsevier Science Ltd

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Chemical Engineering
(2010)
Established in 2010, and aiming to train the students with the capacity to meet the demands of the 21st Century, the Chemical Engineering Department provides a sound chemistry background through intense coursework and laboratory practices, along with fundamental courses such as Physics and Mathematics within the freshman and sophomore years, following preparatory English courses.In the final two years of the program, engineering courses are offered with laboratory practice and state-of-the-art simulation programs, combining theory with practice.

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Abstract

A new derivative of benzobis(thiadiazole) based donor-acceptor-donor type monomers, namely 4,7-di (selenophen-2-yl)benzo[1,2-c;4,5-c']bis[1,2,5]thiadiazole (SeBTSe), was synthesized and its polymerization was carried out successfully via electrochemical polymerization in an electrolyte solution of 0.1 M tetrabutylammonium hexafluorophosphate dissolved in dichloromethane. The monomer SeBTSe is a deep red chromophore and it has four redox states: one oxidation, one neutral and two reduction states. The electrochemical behaviour of the corresponding polymer called PSeBTSe was studied by cyclic and differential pulse voltammetry. There is a good agreement between electrochemical (0.62-0.66 eV) and optical (0.63 eV) bandgaps of the polymer. Like the monomer, the ambipolar polymer has four redox states and electrochromic properties: gray beige at neutral state, smoky azurite at oxidized state, beige at first reduced state and dark beige at second reduced state. (C) 2017 Elsevier Ltd. All rights reserved.

Description

ertan, salih/0000-0001-8852-1879

Keywords

Electropolymerization, Electrochromic, Ambipolar, Donor-Acceptor-Donor, Selenophene, Benzobis(thiadiazole)

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Citation

11

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Volume

249

Issue

Start Page

189

End Page

197

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