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Electrochemical behavior of hydroquinone at multi-walled carbon nanotubes and ionic liquid composite film modified electrode

机译:对苯二酚在多壁碳纳米管和离子液体复合膜修饰电极上的电化学行为

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摘要

The electrochemical behavior of hydroquinone (HQ) was studied by cyclic voltammetry at a glassy carbon electrode (GCE) modified by a gel containing multi-walled carbon nanotubes (MWNTs) and room temperature ionic liquid (RTIL) of 1-butyl-3-methylimidazolium hexafluorophosphate (BMIMPF_6). At the modified electrode, HQ showed a pair of quasi-reversible redox peaks. The cathodic peak current value (I_(pc)) of HQ was 9.608×10~(-4)A, which is 43 times larger than the one at the GCE, and 11 times larger than that of I_(pc) at the MWNTs/GCE. Furthermore, the capabilities of electron transfer on these three electrodes were also investigated by electrochemical impedance spectroscopy (EIS), and the similar conclusion as cyclic voltammetry has drawn. Besides, we also characterized the surface morphology of the prepared composite film using the scanning electronic microscopy (SEM). The MWNTs were pulled away from the tangle in RTIL. The solvent effect of RTIL may be the reason of higher adsorption amount.
机译:在含有多壁碳纳米管(MWNTs)和室温离子液体1-丁基-3-甲基咪唑鎓的凝胶修饰的玻碳电极(GCE)上,通过循环伏安法研究了氢醌(HQ)的电化学行为。六氟磷酸盐(BMIMPF_6)。在修饰的电极上,HQ显示出一对准可逆的氧化还原峰。总部的阴极峰值电流值(I_(pc))为9.608×10〜(-4)A,是GCE的阴极峰值电流值的43倍,是MWNT处的I_(pc)值的11倍。 / GCE。此外,还通过电化学阻抗谱(EIS)研究了这三个电极上电子的转移能力,得出了与循环伏安法相似的结论。此外,我们还使用扫描电子显微镜(SEM)对制备的复合膜的表面形貌进行了表征。在RTIL中将MWNT从缠结中拉开。 RTIL的溶剂效应可能是较高吸附量的原因。

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