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Electropolymerization of ethylene dioxythiophene (EDOT) in micellar aqueous solutions studied by electrochemical quartz crystal microbalance and surface plasmon resonance

机译:电化学石英晶体微天平和表面等离子体共振研究胶束水溶液中乙二氧基噻吩(EDOT)的电聚合

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摘要

Electropolymerization of 3,4-ethylene dioxythiophene (EDOT) on gold electrodes was studied in situ by means of an electrochemical quartz crystal microbalance (EQCM) and by surface plasmon resonance spectroscopy (SPR) using aqueous micellar monomer solutions. Electrodeposition from micellar solutions performed by cyclic voltammetry (CV) displayed an enhanced rate as compared to surfactant concentrations lower than the critical micelle concentration (cmc) or in surfactant-free monomer solutions. EQCM data indicate the occurrence of additional film growth during the reductive scan to large negative potentials which does not occur in electropolymerization experiments using potentiostatic pulses or cyclovoltammetric cycles with less negative potential scans. Our results further suggest that in the case of the anionic surfactant the oxidation potential of the monomer is lowered even at surfactant concentrations below the cmc. AFM investigations show a slightly enhanced roughness of the films obtained from micellar monomer solutions.
机译:通过电化学石英晶体微量天平(EQCM)和表面等离振子共振光谱法(SPR)使用胶束单体水溶液对金电极上的3,4-乙撑二氧噻吩(EDOT)进行电聚合研究。与表面活性剂浓度低于临界胶束浓度(cmc)或在不含表面活性剂的单体溶液中相比,通过循环伏安法(CV)从胶束溶液中进行电沉积显示出更高的速率。 EQCM数据表明,在还原扫描过程中会出现额外的薄膜生长,直至出现较大的负电位,而在使用电位电位较低的恒电位脉冲或循环伏安循环进行电聚合实验的情况下,这不会发生。我们的结果进一步表明,在阴离子表面活性剂的情况下,即使表面活性剂的浓度低于cmc,单体的氧化电势也会降低。原子力显微镜研究表明,从胶束单体溶液获得的薄膜的粗糙度略有提高。

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