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首页> 外文期刊>International Journal of Electrochemical Science >Electrochemical Polymerization of Schiff Base Transition Metal Polymer Poly[Ni(Salen)] and Its Electrochemical Performance in Organic Electrolyte
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Electrochemical Polymerization of Schiff Base Transition Metal Polymer Poly[Ni(Salen)] and Its Electrochemical Performance in Organic Electrolyte

机译:席夫碱过渡金属聚合物聚[Ni(Salen)]的电化学聚合及其在有机电解质中的电化学性能

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摘要

Poly[Ni(salen)] films were prepared by electrochemical polymerization with a constant potentialmethod onto a polished Ti substrate in an organic electrolyte system. Fourier transform infraredspectroscopy (FTIR) was used to characterize the specific chemical groups of poly[Ni(salen)] and fieldemission scanning electron microscopy (FESEM) was used to analyze its morphology andmicrostructure. The electrochemical properties of poly[Ni(salen)] were investigated by cyclic-1 voltammetry (CV) and galvanostatic charge-discharge (GCD) in 1 mol L Et3MeNBF4/AN solution.Furthermore, the influence of different polymerization time on the microstructure and electrochemicalperformance were compared. The results showed that the surface coverage of poly[Ni(salen)] on theanode substrate increased as the polymerization time extension, but its electrochemical activity wasgreatly limited. The poly[Ni(salen)] film prepared in the polymerization time of 1000s showed the-1 -1 highest discharge specific capacitance (73.5 Fg ) at a low current density of 0.5 Ag .
机译:聚[Ni(salen)]薄膜是通过以恒定电势方法在有机电解质系统中的抛光Ti衬底上进行电化学聚合制备的。傅里叶变换红外光谱法(FTIR)用于表征聚[Ni(salen)]的特定化学基团,场发射扫描电子显微镜(FESEM)用于分析其形态和微观结构。在1 mol L Et3MeNBF4 / AN溶液中,通过循环1伏安法(CV)和恒电流充放电(GCD)研究了聚[Ni(salen)]的电化学性能。比较电化学性能。结果表明,随着聚合时间的延长,聚[Ni(salen)]在阳极基材上的表面覆盖率增加,但其电化学活性受到很大限制。在1000s聚合时间内制备的聚[Ni(salen)]薄膜在0.5 Ag的低电流密度下显示-1 -1最高放电比电容(73.5 Fg)。

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