Aqueous electrosynthesis of an electrochromic material based water-soluble EDOT-MeNH2 hydrochloride

被引:7
|
作者
Sun, Hui [1 ]
Zhang, Long [2 ]
Dong, Liqi [1 ]
Zhu, Xiaofei [1 ]
Ming, Shouli [1 ]
Zhang, Youshan [1 ]
Xing, Huakun [1 ]
Duan, Xuemin [1 ]
Xu, Jingkun [1 ]
机构
[1] Jiangxi Sci & Technol Normal Univ, Sch Pharm, Nanchang 330013, Peoples R China
[2] Univ Wollongong, Intelligent Polymer Res Inst, Wollongong, NSW 2522, Australia
基金
中国国家自然科学基金;
关键词
Conducting polymer; Aqueous solution; Electrochemical polymerization; PEDOT derivative; Electrochromic; ELECTROCHEMICAL POLYMERIZATION; FUNCTIONALIZED PEDOT; MICELLAR-SOLUTION; POLYMERS; 3,4-ETHYLENEDIOXYTHIOPHENE; ELECTROPOLYMERIZATION; FILMS; POLY(3,4-ETHYLENEDIOXYTHIOPHENE); TRANSPORT; ELECTRON;
D O I
10.1016/j.synthmet.2015.11.019
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
2'-Aminomethyl-3,4-ethylenedioxythiophene (EDOT-MeNH2) showed unsatisfactory results when its polymerization occurred in organic solvent in our previous report. Therefore, a water-soluble EDOT derivative was designed by using hydrochloric modified EDOT-MeNH2 (EDOT-MeNH2 center dot HCl) and electropolymerized in aqueous solution to form the corresponding polymer with excellent electrochromic properties. Moreover, the polymer was systematically explored, including electrochemical, optical properties and structure characterization. Cyclic voltammetry showed low oxidation potential of EDOT-MeNH2 center dot HCl (0.85 V) in aqueous solution, leading to the facile electrodeposition of uniform the polymer film with outstanding electroactivity. Compared with poly(2'-aminomethyl-3,4-ethylenedioxythiophene) (PEDOT-MeNH2), poly(2'-aminomethyl-3,4-ethylenedioxythiophene salt) (PEDOT-MeNH(3)(+)A(-)) revealed higher efficiencies (156 cm(2) C-1), lower bandgap (1.68 eV), and faster response time (1.4s). Satisfactory results implied that salinization can not only change the polymerization system, but also adjust the optical absorption, thereby increase the electrochromic properties. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:147 / 154
页数:8
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