聚吡咯
甲基橙
氯化物
化学
电导率
无机化学
吡咯
盐酸
高分子化学
电化学
有机化学
电极
催化作用
光催化
物理化学
作者
Yu Li,Yanping Wang,Cheng Bian,Jaroslav Stejskal,Yuansuo Zheng,Xinli Jing
标识
DOI:10.1016/j.dyepig.2020.108329
摘要
Abstract Polypyrrole (PPy) synthesized by the oxidation of pyrrole with iron(III) chloride in the presence of sulfonic azo dyes exhibits fascinating nanometer-scale morphology and high conductivity, which are distinctly different from their counterparts prepared without dyes. The present work systematically studied the roles of sulfonic azo dye aggregates formed in acidic medium during the growth of PPy based on structural and elemental analysis. The formation of PPy nanostructures have been investigated by following the pH profile, by adjusting the precipitation rate of dye aggregates and by comparing the molecular structure of three azo dyes, viz. methyl orange, ethyl orange and Orange I. The results showed that the ethyl orange derived aggregates formed in iron(III) chloride solution and in hydrochloric acid solution had exactly the same structure as well as elemental composition. Aggregates derived from methyl orange formed in iron(III) chloride solution involved a trace amount of iron element. Orange I, another azo dye that can induce aggregates rapidly in iron(III) chloride solution, contributed negligibly to both the morphology and conductivity of PPy. The structure-directing effects of methyl orange/iron(III) complexes in directing PPy nanostructures seems to be unique and cannot be simply extended to other azo dyes, probably due to the dye interaction with iron ions.
科研通智能强力驱动
Strongly Powered by AbleSci AI