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Synthesis and Characterization of Solution-Processible Donor-Acceptor Electrochromic Conjugated Copolymers Based on Quinoxalino[2',3':9,10]phenanthro[4,5-abc]phenazine As the Acceptor Unit

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Publisher MDPI
Date 2023 Feb 28
PMID 36850223
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Abstract

Donor-acceptor (D-A) type conjugated polymers are of high interest in the field of electrochromism. In this study, three novel conjugated copolymers (PBPE-1, PBPE-2 and PBPE-3) based on quinoxalino[2',3':9,10]phenanthro[4,5-abc]phenazine (A) as the acceptor unit and 4,8-bis((2-octyldodecyl)oxy)benzo[1,2-b:4,5-b']dithiophene (D1) and 3,3-didecyl-3,4-dihydro-2-thieno[3,4-b][1,4]dioxepine (ProDOT-decyl, D2) as the donor units with different donor-to-acceptor ratios were successfully synthesized through Stille coupling polymerization. The polymers were then characterized by cyclic voltammetry (CV), fourier transform infrared (FT-IR) spectoscopy, X-ray photoelectron spectroscopy (XPS), spectroelectrochemistry, thermogravimetry (TG), electrochromic switching and colorimetry. Optical band gap values were calculated as 1.99 eV, 2.02 eV and 2.03 eV, respectively. The three copolymers have good solubility, distinct redox peaks, wide absorption spectra, good thermal stabilities, bright color changes and significant electrochromic switching properties. Compared to the other two copolymers, the PBPE-3 film exhibited high coloration efficiency values of 513 cm·C at 504 nm and 475 cm·C at 1500 nm. The films have the advantage of exhibiting cathodic and anodic coloration.

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References
1.
An L, Huang Y, Wang X, Liang Z, Li J, Tong J . Fluorination Effect for Highly Conjugated Alternating Copolymers Involving Thienylenevinylene-Thiophene-Flanked Benzodithiophene and Benzothiadiazole Subunits in Photovoltaic Application. Polymers (Basel). 2020; 12(3). PMC: 7254375. DOI: 10.3390/polym12030504. View

2.
Park J, Cho K, Rhee Y . Mechanism of Ir(ppy) Guest Exciton Formation with the Exciplex-Forming TCTA:TPBI Cohost within a Phosphorescent Organic Light-Emitting Diode Environment. Int J Mol Sci. 2022; 23(11). PMC: 9180450. DOI: 10.3390/ijms23115940. View

3.
Cataldo F . On the Optical Activity of Poly(L-Lactic Acid) (PLLA) Oligomers and Polymer: Detection of Multiple Cotton Effect on Thin PLLA Solid Film Loaded with Two Dyes. Int J Mol Sci. 2020; 22(1). PMC: 7792576. DOI: 10.3390/ijms22010008. View

4.
Beaujuge P, Reynolds J . Color control in pi-conjugated organic polymers for use in electrochromic devices. Chem Rev. 2010; 110(1):268-320. DOI: 10.1021/cr900129a. View

5.
Wang X, Wang Z, Li M, Tu L, Wang K, Xiao D . A New Dibenzoquinoxalineimide-Based Wide-Bandgap Polymer Donor for Polymer Solar Cells. Polymers (Basel). 2022; 14(17). PMC: 9460915. DOI: 10.3390/polym14173590. View