Electrochemical copolymerization of aniline with m-aminophenol and novel electrical properties of the copolymer in the wide pH range

被引:45
作者
Zhang, Jing [1 ]
Shan, Dan [1 ]
Mu, Shaolin [1 ]
机构
[1] Yangzhou Univ, Dept Chem, Yangzhou 225002, Peoples R China
基金
中国国家自然科学基金;
关键词
electrochemical copolymerization; aniline and m-aminophenol; IR spectra; pH dependence; impedance measurements; conductivity;
D O I
10.1016/j.electacta.2005.12.005
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
A copolymer, poly(aniline-co-m-aminophenol), has been synthesized using repeated potential cycling. The monomer concentration ratio, acid concentration and applied potential strongly affect the copolymerization rate and the properties of the copolymer. The optimum conditions for the copolymerization are that the scan potential range is controlled between -0.10 and 0.95 V (vs.SCE), and a solution consists of 0.34M aniline, 0.012 M m-aminophenol and 2 M H2SO4. The IR spectra of the copolymers demonstrate that the m-aminophenol units are included in the copolymer chains. The cyclic voltammograms of the copolymers in 0.3 M Na2SO4 solution with various pH values were performed at the potential ranges from -0.20 to 0.80 V and at a scan rate of 60 mV s(-1). The results indicate that the copolymer still hold 41.7% of the electrochemical activity when the copolymer electrode was transferred from a solution of pH 5.0 to a solution of pH 11.0 in the potential range of -0.20 to 0.80 V. An impedance plot of the copolymer in a solution with pH 12.0 and at 0.40 V is constructed of a semicircle and a Warburg line with a slope of 1. This means that the electrode reaction of the copolymer at pH 12.0 is also under mass transfer control. The conductivity of the copolymer prepared under the optimum conditions is 1.42 S cm(-1), and slightly depends on the pH value. Thus, the pH dependence of the electrical properties of the copolymer is improved compared with poly(aniline-co-o-aniinophenol), and is much better than that of the parent polyaniline. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4262 / 4270
页数:9
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