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

dc.authoridertan, salih/0000-0001-8852-1879
dc.authorscopusid57195338830
dc.authorscopusid54782763000
dc.authorscopusid57194534079
dc.authorscopusid55240269100
dc.authorscopusid57195338554
dc.authorscopusid55925768200
dc.authorwosidErtan, Salih/M-6370-2013
dc.authorwosidÖzkut, Merve İçli/AAD-7011-2019
dc.authorwosidCihaner, Atilla/AAC-9468-2021
dc.contributor.authorErtan, Salih
dc.contributor.authorCihaner, Atilla
dc.contributor.authorGokce, Gurcan
dc.contributor.authorErtan, Salih
dc.contributor.authorTutuncu, Esra
dc.contributor.authorCihaner, Atilla
dc.contributor.otherChemical Engineering
dc.date.accessioned2024-07-05T15:29:14Z
dc.date.available2024-07-05T15:29:14Z
dc.date.issued2017
dc.departmentAtılım Universityen_US
dc.department-temp[Abdulrazzaq, Mohammed; Ertan, Salih; Cihaner, Atilla] Atilim Univ, Dept Chem Engn & Appl Chem, Atilim Optoelect Mat & Solar Energy Lab ATOMSEL, TR-06836 Ankara, Turkey; [Ozkut, Merve Icli; Gokce, Gurcan; Tutuncu, Esra] Yuzuncu Yil Univ, Fac Engn & Architecture, Dept Chem Engn, TR-65080 Van, Turkeyen_US
dc.descriptionertan, salih/0000-0001-8852-1879en_US
dc.description.abstractA 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.en_US
dc.description.sponsorshipAtilim University [ATU-BAP-A-1314-01]; Yuzuncu Yil University [2015-MIM-B112]en_US
dc.description.sponsorshipThe authors thank Atilim University (ATU-BAP-A-1314-01) and Yuzuncu Yil University (2015-MIM-B112) for their financial supports.en_US
dc.identifier.citation11
dc.identifier.doi10.1016/j.electacta.2017.08.007
dc.identifier.endpage197en_US
dc.identifier.issn0013-4686
dc.identifier.issn1873-3859
dc.identifier.scopus2-s2.0-85027282628
dc.identifier.startpage189en_US
dc.identifier.urihttps://doi.org/10.1016/j.electacta.2017.08.007
dc.identifier.urihttps://hdl.handle.net/20.500.14411/2896
dc.identifier.volume249en_US
dc.identifier.wosWOS:000410675100022
dc.identifier.wosqualityQ2
dc.language.isoenen_US
dc.publisherPergamon-elsevier Science Ltden_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectElectropolymerizationen_US
dc.subjectElectrochromicen_US
dc.subjectAmbipolaren_US
dc.subjectDonor-Acceptor-Donoren_US
dc.subjectSelenopheneen_US
dc.subjectBenzobis(thiadiazole)en_US
dc.titleA Low Band Gap Polymer Based on Selenophene and Benzobis (thiadiazole)en_US
dc.typeArticleen_US
dspace.entity.typePublication
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