Zhen Xu, Ling-qian Kong, Jinsheng Zhao
Feb 5, 2016
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Influential Citations
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Journal
Chinese Journal of Polymer Science
Abstract
Two novel decyloxyphenylquinoxaline-based donor-acceptor (D-A) electroactive monomers bearing dialkoxythiophene as the donor unit are synthesized using Stille coupling reaction. The corresponding polymers, poly[2,3-bis(4-decyloxyphenyl)-5,8-bis(3,4-dimethoxylthiophen-2-yl)quinoxaline] (P1) and poly[2,3-bis(4-decyloxyphenyl)-5,8-bis(2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl)quinoxaline] (P2), are directly deposited onto the working electrode surface by electropolymerization. All materials were characterized by nuclear magnetic resonance (NMR), mass spectrometry (MS), scanning electron microscopy (SEM), cyclic voltammetry (CV), ultraviolet-visible absorption spectrometry (UV-Vis) and spectro-electrochemical measurements. Electrochemical studies demonstrate that both polymers are capable of showing both reasonable n- and p-doping processes, and advanced long-term switching stabilities. 3,4-Ethylenedioxythiophene substituted for 3,4-dimethoxythiophene as a donor unit, which enhances the conjugated double-bond character of the conducting polymer, thus leading to a lower electronic band-gap. Likewise, the neutral state color of the synthesized polymer tuned from blue to blue-green corresponding to the red shift of the maximum absorption wavelengths in the visible region. In addition, kinetics study of P1 revealed 42% (595 nm), 30% (839 nm) and 69% (1500 nm) transmittance changes (ΔT%), while P2 exhibited 32% (740 nm), 71% (2000 nm) at the dominant wavelengths. It was also observed that both films could switch quickly between the neutral state and oxidation state, with the response time less than 1 s both in visible and near infrared regions.