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Copper hexacyanoferrate-graphene nanocomposite: synthesis, characterisation and application for the electrocatalytic oxidation and determination of thiosulfate

机译:六氰合铁酸铜-石墨烯纳米复合材料:硫代硫酸盐的电催化氧化和测定的合成,表征及应用

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摘要

Copper hexacyanoferrate-graphene nanocomposite was synthesised by a facile precipitation route. The morphology and structure of the nanocomposite were evaluated by scanning electron microscopy, X-ray diffraction and infrared spectroscopy. A nanocomposite-modified carbon paste electrode was fabricated and its redox behaviour was characterised by means of different electrochemical techniques. The diffusion of the counter cation into the nanocomposite and the charge transfer kinetics across the electrode/electrolyte interface were studied by chronocoulometry and cyclic voltammetry. In the Nyquist diagrams, different time constants related to different physical and electrochemical processes appeared. In these diagrams, percolation of electron in the copper hexacyanoferrate nanoparticles appeared at very high frequencies, and exhibited the feature of a diffusion process with a transmissive boundary condition at the interface of nanocomposite/graphite particles. At medium frequencies, the redox reaction of copper hexacyanoferrate was performed. At very low frequencies, the diffusion of counter cation into the copper hexacyanoferrate nanoparticles dominated. The diffusion coefficients of electron and the counter cation and also the charge transfer rate constant within the nanocomposite were obtained using impedance spectroscopy. The modified electrode showed an efficient electrocatalytic activity toward the electrooxidation of thiosulfate.
机译:通过简便的沉淀途径合成了六氰合铁酸铜-石墨烯纳米复合材料。通过扫描电子显微镜,X射线衍射和红外光谱评价纳米复合材料的形态和结构。制备了一种纳米复合修饰的碳糊电极,并通过不同的电化学技术对其氧化还原行为进行了表征。通过计时库仑法和循环伏安法研究了抗衡阳离子向纳米复合材料中的扩散以及跨电极/电解质界面的电荷转移动力学。在奈奎斯特图中,出现了与不同物理和电化学过程相关的不同时间常数。在这些图中,六氰合铁酸铜纳米颗粒中的电子渗透出现在很高的频率下,并且在纳米复合材料/石墨颗粒的界面处表现出具有透射边界条件的扩散过程。在中等频率下,进行了六氰合铁酸铜的氧化还原反应。在非常低的频率下,抗衡阳离子向六氰合铁酸铜纳米颗粒中的扩散占主导。电子和抗衡阳离子的扩散系数以及在纳米复合材料内的电荷转移速率常数使用阻抗谱法获得。改性电极对硫代硫酸盐的电氧化表现出有效的电催化活性。

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