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Nucleation and Growth of Porous MnO2 Coatings Prepared on Nickel Foam and Evaluation of Their Electrochemical Performance

机译:镍泡沫制备的多孔MnO2涂层的形核和生长及其电化学性能评价

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摘要

Porous MnO2 was uniformly electrodeposited on nickel foam in MnSO4 solution, which was applied as the electrode of supercapacitors. The nucleation/growth mechanisms of porous MnO2 were investigated firstly. Then two kinds of electrochemical measuring technologies, corresponding to the cycle voltammetry (CV) and galvanostatic charge-discharge, were adopted to assess the electrochemical performance of MnO2 electrodes. The results demonstrated that the deposition of MnO2 on nickel foam included four stages. Prior to the deposition, an extremely short incubation period of about 2 s was observed (the first stage). Then the exposed nickel foam was instantly covered by a large number of MnO2 crystal nuclei and crystal nuclei connected with each other in a very short time of about 3 s (the second stage). Nucleation predominated in the second stage. The sharply rise of current was caused by the increase in substrate surface area which due to nucleation of MnO2. Grain boundaries grew preferentially due to their high energy, accompanied with a honeycomb-like structure with the higher surface area was formed. However, accompanied with the electrochemical reactions gradually diffusion-controlled, the current presented the decline trend with increasing the time (the third stage). When the electrochemical reactions were completely diffusion-controlled, the porous MnO2 coating with an approximately constant surface area was formed (the fourth stage). MnO2 coatings deposited for different time (30, 60, 120, 300 s) exhibited a similar specific capacitance (CV: about 224 F/g; galvanostatic charge-discharge: about 264 F/g). Comparatively speaking, the value of MnO2 deposited for 600 s was highest (CV: 270 F/g; galvanostatic charge-discharge: 400 F/g).
机译:多孔MnO2在MnSO4溶液中均匀地电沉积在泡沫镍上,用作超级电容器的电极。首先研究了多孔MnO2的成核/生长机理。然后采用循环伏安法和恒电流充放电两种电化学测量技术对MnO2电极的电化学性能进行评估。结果表明,MnO2在泡沫镍上的沉积包括四个阶段。在沉积之前,观察到非常短的约2 s的孵育时间(第一阶段)。然后,在大约3 s的极短时间内,暴露的镍泡沫立即被大量相互连接的MnO2晶核和晶核覆盖(第二阶段)。在第二阶段,成核作用占主导。电流的急剧上升是由于MnO2成核导致的基板表面积的增加而引起的。晶界由于其高能量而优先增长,并伴随着具有较高表面积的蜂窝状结构的形成。然而,随着电化学反应逐渐扩散控制,电流随着时间的增加呈现下降趋势(第三阶段)。当电化学反应被完全扩散控制时,形成具有近似恒定表面积的多孔MnO 2涂层(第四阶段)。在不同时间(30、60、120、300 s)沉积的MnO2涂层表现出相似的比电容(CV:约224 F / g;恒电流充放电:约264 F / g)。相对而言,在600 s内沉积的MnO2值最高(CV:270 F / g;恒电流充放电:400 F / g)。

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