Electropolymerization of EDOT in an anionic surfactant-stabilized hydrophobic ionic liquid-based microemulsion

IF 3 3区 化学 Q3 CHEMISTRY, PHYSICAL
Na Gao and Xirong Huang
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引用次数: 2

Abstract

Here, an anionic surfactant [AOT]? (bis-(2-ethylhexyl) sulfosuccinate)-stabilized H2O/[Omim][PF6] (1-octyl-3-methylimidazolium hexafluorophosphate) microemulsion has been tested for the first time as a medium for the electropolymerization of 3,4-ethylenedioxythiophene (EDOT). To formulate AOT-stabilized [Omim][PF6]-based microemulsions of different water contents, the phase triangle was determined at 35 °C. Measurements of the conductivities of the microemulsions, their solubilization capacities toward EDOT and their catalytic effects on EDOT electrooxidation show that the present [AOT]?-stabilized ionic liquid microemulsion is a good medium for EDOT electropolymerization. Studies on the process of the electropolymerization of EDOT in this [Omim][PF6]-based microemulsion indicate that the water content (i.e., microstructure) of the microemulsion medium is an important factor affecting the onset potential and the deposition rate of the PEDOT. The morphology and the doping level of the as-prepared PEDOT are also found to be correlated with the water content of the ionic liquid microemulsion. The microemulsion with higher water content results in a PEDOT with better electroactivity and higher doping levels. FTIR spectra and XPS analysis show that the PEDOT electrosynthesized in the microemulsion is co-doped by both [AOT]? and [PF6]?. Compared with the neat [Omim][PF6], the use of the ionic liquid microemulsions can reduce not only the consumption of the expensive ionic liquid, but also the onset potential for the electrooxidation of EDOT. Moreover, by tuning the water content of the medium, the electropolymerization of PEDOT and its electrochemical properties could be regulated accordingly. Under the identical deposited charge, the PEDOT originated from the high water content microemulsion (50% H2O μE) has a higher specific capacitance (124 F g?1) than that from neat [Omim][PF6] (117 F g?1). It follows that the present ionic liquid microemulsion is a good medium for EDOT electropolymerization. The present study opens up a new route for the green and low-cost electrochemical preparation of high-performance PEDOT.

Abstract Image

阴离子表面活性剂稳定疏水离子液体微乳液中EDOT的电聚合
阴离子表面活性剂[AOT]?首次用(双-(2-乙基己基)琥珀酸磺基)稳定的水/[Omim][PF6](1-辛基-3-甲基咪唑六氟磷酸)微乳液作为电聚合3,4-乙烯二氧噻吩(EDOT)的介质进行了试验。为了制备不同含水量的aot稳定[Omim][PF6]基微乳,在35℃下测定相三角形。对微乳的电导率、对EDOT的增溶能力以及对EDOT电氧化的催化作用的测量表明,[AOT]?-稳定离子液体微乳液是EDOT电聚合的良好介质。对该[Omim][PF6]基微乳液中EDOT电聚合过程的研究表明,微乳液介质的含水量(即微观结构)是影响PEDOT起始电位和沉积速率的重要因素。制备的PEDOT的形貌和掺杂水平也与离子液体微乳液的含水量有关。微乳液含水量越高,PEDOT的电活性越好,掺杂水平越高。FTIR光谱和XPS分析表明,微乳液中电合成的PEDOT是由[AOT]?和[PF6] ?。与纯[Omim][PF6]相比,使用离子液体微乳不仅可以减少昂贵的离子液体的消耗,而且可以降低EDOT的电氧化起始电位。此外,通过调节介质的含水量,可以调节PEDOT的电聚合及其电化学性能。在相同电荷沉积条件下,高含水量微乳液(50% H2O μE)制备的PEDOT比电容(124 F g?1)高于纯[Omim][PF6] (117 F g?1)制备的PEDOT。由此可见,离子液体微乳液是一种良好的EDOT电聚合介质。本研究为高性能PEDOT的绿色低成本电化学制备开辟了一条新途径。
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来源期刊
Physical Chemistry Chemical Physics
Physical Chemistry Chemical Physics 化学-物理:原子、分子和化学物理
CiteScore
5.50
自引率
9.10%
发文量
2675
审稿时长
2.0 months
期刊介绍: Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.
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