Molecular assembled self-doped polyaniline copolymer ultra-thin films

被引:47
作者
Yang, Chien-Hsin [1 ]
Huang, Liang-Ren
Chih, Yi-Kai
Lin, Wen-Churng
Liu, Feng-Hin
Wang, Tzong-Liu
机构
[1] Natl Univ Kaohsiung, Dept Chem & Mat Engn, Kaohsiung 811, Taiwan
[2] So Taiwan Univ Technol, Dept Chem & Mat Engn, Tainan 710, Taiwan
[3] Natl Cheng Kung Univ, Dept Chem Engn, Tainan 710, Taiwan
[4] Kun Shan Univ, Dept Environm Engn, Tainan 710, Taiwan
[5] Natl United Univ, Dept Chem Engn, Miaoli 360, Taiwan
关键词
self-doped polyaniline (SPANI); molecular self-assembly; ultra-thin film;
D O I
10.1016/j.polymer.2007.04.013
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A self-assembly technique and copolymerization were used to buildup a self-doped polyaniline (SPANI) ultra-thin film on an indium-tin oxide (ITO) substrate. The monomers used were aniline and its derivative MSAN (m-aminobenzenesulfonic acid). Successful MSAN/AN copolymerization and film formation were simultaneously performed in aqueous solution with the addition of oxidant (APS, ammonium persulfate). The film deposition rate of a high AN/MSAN ratio system is generally higher than that of a low AN/MSAN ratio system. Cyclic voltammetry, UV-vis spectroscopy, and oc-step instruments indicate a systematic dependence of the film thickness of these ultra-thin films on the assembly time and temperatures. The Auger depth profile reveals the elemental distribution in these films and exhibits different deposition rates between AN and NISAN. XPS N-1s, spectra also show the variation of the degree of doping. This SPANI film can be used as an electrochromic electrode in a corresponding device. Carboxyl-terminated-butadiene-acrylonitrile (CTBN) blended with LiClO4 was used as a solid polymer electrolyte. A total solid electrochromic device was assembled as ITO/SPANI/LiClO4-CTBN/PEDOT:PSS/ITO, where PEDOT:SS is poly('3,4-ethylenedioxythiophene)/poly(4-styrenesulfonate) as the counter complementary electrode. The device was pale gray at -1.5 V and blue at +1.5 V. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3237 / 3247
页数:11
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