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A triazoloquinoxaline and benzodithiophene bearing low band gap copolymer for electrochromic and organic photovoltaic applications
Date
2017-06-01
Author
HACIOGLU, Serife O.
UNLU, Naime A.
AKTAS, Ece
HIZALAN, Gonul
Yildiz, Esra D.
Çırpan, Ali
Toppare, Levent Kamil
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A new triazoloquinoxaline and benzodithiophene based copolymer was synthesized to investigate its electro-chemical, optical and photovoltaic behaviors. According to the polymer design, combination of two acceptor units (benzotriazole and quinoxaline) which contribute imine bonds to the structure and a triazoloquinoxaline unit for enhancing electron accepting ability was pursued. As a result of electrochemical studies, the copolymer PTQBDT has a low lying HOMO energy level as - 5.23 eV which increases the chemical stability of the resulting polymer and leads to a higher V-oc. In addition, the copolymer has an ambipolar character with two well-defined redox couples in the n-doped state and multichromic behavior. In the context of optical studies, PTQBDT has wide absorption range in the visible region with a tail in the NIR region, which yields a low band gap of 1.20 eV. Organic photovoltaic devices were designed using PTQBDT (the electron donor) and PC71BM (the electron acceptor) for the preliminary studies. The resulting device exhibits a power conversion efficiency of 2.0% with a current density of 8.07 mA cm(-2), an open-circuit voltage of 0.45 V, and a fill factor of 55%. The carrier mobility of the PTQBDT was calculated as 3.00 x 10(-3) cm(2) V-1 S-1 via space-charge-limited current (SCLC) method.
Subject Keywords
Conjugated polymers
,
Triazoloquinoxaline
,
Benzodithiophene
,
Organic solar cell
,
Organic solar cell
,
Copolymer
URI
https://hdl.handle.net/11511/35454
Journal
SYNTHETIC METALS
DOI
https://doi.org/10.1016/j.synthmet.2017.04.017
Collections
Department of Chemistry, Article
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S. O. HACIOGLU et al., “A triazoloquinoxaline and benzodithiophene bearing low band gap copolymer for electrochromic and organic photovoltaic applications,”
SYNTHETIC METALS
, pp. 111–119, 2017, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/35454.