首页> 外文期刊>Electrochimica Acta >In situ scanning tunneling microscopy imaging of electropolymerized poly(3,4-ethylenedioxythiophene) on an iodine-modified Au(111) single crystal electrode
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In situ scanning tunneling microscopy imaging of electropolymerized poly(3,4-ethylenedioxythiophene) on an iodine-modified Au(111) single crystal electrode

机译:碘修饰的Au(111)单晶电极上电聚合的聚(3,4-乙撑二氧噻吩)的原位扫描隧道显微镜成像

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摘要

The electrochemical polymerization of 3,4-ethylenedioxythiophene (EDOT) on an iodine-modified Au(111) single crystal electrode in aqueous 0.10 M HClO_4 was investigated by cyclic voltammetry (CV) and electrochemical scanning tunneling microscopy (EC-STM). The cyclic voltammetric and EC-STM data revealed the stability of the iodine adlayer provided a suitable potential range for EDOT electropolymerization was controlled at 1.20 V (vs. the reversible hydrogen electrode). EC-STM was used to examine the formation of the PEDOT adlayer on the iodine-modified Au(111) electrode. In situ electropolymerization of EDOT was carried out by slowly increasing the electrode potential to 1.20V. This process resulted in the formation of single molecular chains of PEDOT with a diameter of 0.90nm and lengths of 5-7 nm. Higher resolution STM images further revealed PEDOT nanostructures with bent polymer backbones at angles of 105°, 144° and 180°. The growth of PEDOT multi-layers was observed when the potential was held for a longer time.
机译:通过循环伏安法(CV)和电化学扫描隧道显微镜(EC-STM)研究了3,4-乙撑二氧噻吩(EDOT)在碘改性的Au(111)单晶电极上在0.10 M HClO_4水溶液中的电化学聚合。循环伏安法和EC-STM数据显示,如果将EDOT电聚合的合适电势范围控制在1.20 V(相对于可逆氢电极),则碘吸附层的稳定性。 EC-STM用于检查碘修饰的Au(111)电极上PEDOT附加层的形成。 EDOT的原位电聚合是通过将电极电位缓慢增加到1.20V来进行的。该过程导致形成直径为0.90nm,长度为5-7nm的PEDOT单分子链。更高分辨率的STM图像进一步揭示了PEDOT纳米结构,其中聚合物主链的弯曲角度为105°,144°和180°。当电位保持较长时间时,观察到PEDOT多层膜的生长。

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