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首页> 外文期刊>Electrochimica Acta >Electrodeposited Mn3O4-NiO-Co3O4 as a composite electrode material for electrochemical capacitor
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Electrodeposited Mn3O4-NiO-Co3O4 as a composite electrode material for electrochemical capacitor

机译:电沉积Mn3O4-NiO-Co3O4作为电化学电容器的复合电极材料

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摘要

A simple and easy galvanostatic electrodeposition method is used to synthesise a composite electrode consisting of manganese oxide (Mn3O4), nickel oxide (NiO) and cobalt oxide (Co3O4). The influence of Co3O4 on the morphology of fixed Mn3O4-NiO particles is investigated with a field emission scanning electron microscope (FESEM) and transmission electron microscope (TEM). The nature and elemental of the composite are examined by means of X-ray diffraction (XRD) and energy dispersive X-ray spectroscopy (EDX). The electrochemical performances of an Mn3O4-NiO-Co3O4 nanostructure/SS composite electrode are studied by cyclic voltammetry (CV) and galvanostatic charge-discharge (CD) in various electrolytes, i.e. 0.5 M Na2SO4, 0.5 M KOH, 0.5 M Na2SO4/0.04 M K3Fe(CN)(6) and 0.5 M KOH/0.04 M K3Fe(CN)(6) electrolytes. The composite electrode prepared from 0.15 M Co deposition solution exhibits the optimum specific capacitance of 7404 F g(-1) with high energy and power density of 1028 Wh kg(-1) and 99 kW kg(-1) at 20 A g(-1) in mix KOH/0.04 M K3Fe(CN)(6) electrolyte, respectively. The results show that the incorporation of K3Fe(CN)(6) in KOH electrolyte influences the capacitance of Mn3O4-NiO-Co3O4 composite electrodes. (C) 2015 Elsevier Ltd. All rights reserved.
机译:一种简单且容易的恒电流电沉积方法用于合成由氧化锰(Mn3O4),氧化镍(NiO)和氧化钴(Co3O4)组成的复合电极。用场发射扫描电子显微镜(FESEM)和透射电子显微镜(TEM)研究了Co3O4对固定的Mn3O4-NiO颗粒形貌的影响。通过X射线衍射(XRD)和能量色散X射线光谱(EDX)检查复合材料的性质和元素。通过循环伏安法(CV)和恒电流充放电(CD)在各种电解质(即0.5 M Na2SO4、0.5 M KOH,0.5 M Na2SO4 / 0.04 M)中研究了Mn3O4-NiO-Co3O4纳米结构/ SS复合电极的电化学性能。 K3Fe(CN)(6)和0.5 M KOH / 0.04 M K3Fe(CN)(6)电解质。由0.15 M Co沉积溶液制备的复合电极表现出7404 F g(-1)的最佳比电容,在20 A g()下具有1028 Wh kg(-1)和99 kW kg(-1)的高能量和功率密度。 -1)分别混合KOH / 0.04 M K3Fe(CN)(6)电解质。结果表明,在KOH电解质中掺入K3Fe(CN)(6)影响Mn3O4-NiO-Co3O4复合电极的电容。 (C)2015 Elsevier Ltd.保留所有权利。

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