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Synthesis of Hybrid Electroactive Materials by Low-Potential Electropolymerization of Gold Nanoparticles Capped with Tailored EDOT-Thiophene Precursor Units

机译:用定制的EDOT-噻吩前体单元封端金纳米粒子的低电位电聚合制备混合电活性材料

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摘要

The synthesis of gold nanoparticles (GNPs) capped with alkanethiols with terminal bithiophenic polymerizable groups, consisting of 3,4-ethylenedioxythiophene (EDOT) and 3-alkylsulfanylthiophene, is described. Transmission electron microscopy (TEM) and light diffusion show that these stabilized GNPs have an average size of 2–3 nm with low polydispersity. The electrochemical behavior of C10S-Au is investigated in dichloromethane in the presence of Bu4NPF6. The results show that these capped GNPs undergo straightforward and efficient electropolymerization under potentiodynamic or potentiostatic conditions. TEM images show that the electrodeposited films of the composite material present a very homogeneous structure, in which the size of the GNPs incorporated into the polythiophene matrix is unchanged. Results of cyclic voltammetry and spectroelectrochemistry obtained on polymer films deposited on platinum electrodes and transparent indium tin oxide electrodes, respectively, show that the reversible charging–discharging process and electrochromic behavior typical of poly(thiophenes) are preserved in the hybrid electroactive material.
机译:描述了金纳米颗粒(GNPs)的合成,该纳米颗粒被链烷硫醇封端,链烷硫醇具有由3,4-亚乙二氧基噻吩(EDOT)和3-烷基硫烷基噻吩组成的末端联噻吩可聚合基团。透射电子显微镜(TEM)和光扩散表明,这些稳定的GNP的平均尺寸为2-3nm,且多分散性较低。在Bu4NPF6存在下,在二氯甲烷中研究了C10S-Au的电化学行为。结果表明,这些加帽的GNP在电位动力学或恒电位条件下进行了直接有效的电聚合。 TEM图像显示复合材料的电沉积膜具有非常均匀的结构,其中并入聚噻吩基质中的GNP的尺寸未改变。分别在沉积在铂电极和透明铟锡氧化物电极上的聚合物膜上获得的循环伏安法和光谱电化学结果表明,杂化电活性材料中保留了聚噻吩特有的可逆充放电过程和电致变色行为。

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