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乙醇对双核酞菁钴掺杂聚苯胺膜修饰电极特性的影响
引用本文:曹勇,郭黎平,安敏,朱连德,崔秀君.乙醇对双核酞菁钴掺杂聚苯胺膜修饰电极特性的影响[J].分析化学,2006,34(4):469-473.
作者姓名:曹勇  郭黎平  安敏  朱连德  崔秀君
作者单位:东北师范大学化学学院,长春,130024;东北师范大学化学学院,长春,130024;东北师范大学化学学院,长春,130024;东北师范大学化学学院,长春,130024;东北师范大学化学学院,长春,130024
基金项目:中国科学院长春应用化学研究所电分析化学国家重点实验室资助项目(SKLEAC2004-1)
摘    要:研究了乙醇对双核酞菁钴(b i-CoPc)掺杂聚苯胺(PAn)膜修饰电极特性的影响。用循环伏安法(CV)考察了乙醇浓度不同时,玻碳电极(GC)上双核酞菁钴掺杂聚苯胺的电聚合过程,用紫外-可见吸收光谱(UV-V is)、红外光谱(FTIR)和扫描电子显微镜(SEM)表征了在氧化铟锡玻璃(ITO)电极上b i-CoPc掺杂的PAn膜,研究了乙醇对膜以及该膜修饰电极对溶液中分子氧电催化性能的影响。结果表明,乙醇对苯胺的电聚合有促进作用,有助于增加b i-CoPc掺杂量,膜的光谱特性发生变化,表面形貌更加均匀。乙醇存在下制备的修饰电极对溶液中分子氧的电催化活性明显提高。当乙醇含量为10%时,制备的电极催化能力最强。

关 键 词:聚苯胺  双核酞菁钴  乙醇  修饰电极
收稿时间:06 30 2005 12:00AM
修稿时间:2005-06-302005-08-29

Effect of Ethanol on Properties of Polyaniline Modified Electrode Doped with Planar Binuclear Cobalt Phthalocyanine
Cao Yong,Guo Liping,An Min,Zhu Liande,Cui Xiujun.Effect of Ethanol on Properties of Polyaniline Modified Electrode Doped with Planar Binuclear Cobalt Phthalocyanine[J].Chinese Journal of Analytical Chemistry,2006,34(4):469-473.
Authors:Cao Yong  Guo Liping  An Min  Zhu Liande  Cui Xiujun
Institution:Faculty of Chemistry, Northeast Normal University , Changchun 130024
Abstract:The electropolymerization of polyaniline(PAn) film in the presence of planar binuclear cobalt phthalocyanine(bi-CoPc) on different concentration of ethanol on glassy carbon electrode was examined by cyclic voltammetry(CV).The effects of ethanol on properties of films on indium-tin oxide(ITO) glass were investigated by CV,ultraviole-visible spectroscopy,Fourier transform infrared spectroscopy and scanning(electron) microscope.The results show that in the presence of(10%) ethanol which the electropolymerization rate was(enhanced),and the doping amount of bi-CoPc was increased,leads to finer structure of PAn film.It is found that the electrocatalytic activity of bi-CoPc-PAn modified electrodes towards oxygen reduction is higher in the presence of 10% ethanol than that of its absence.
Keywords:Polyaniline  binuclear cobalt phthalocyanine  ethanol  modified electrode  
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