首页> 外文期刊>International journal of hydrogen energy >In situ fabrication of porous festuca, scoparia-like Ni0.3Co2.7O4 nanostructures on Ni-foam: An efficient electrode material for supercapacitor applications
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In situ fabrication of porous festuca, scoparia-like Ni0.3Co2.7O4 nanostructures on Ni-foam: An efficient electrode material for supercapacitor applications

机译:在镍泡沫上原位制备多孔的孔雀石,类似角晶石的Ni0.3Co2.7O4纳米结构:一种用于超级电容器的有效电极材料

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Mixed metal oxides designed by using 3d elements in the Periodic Table are expected to play pivotal role in energy storage. In this work, cetyltrimethyl ammonium bromide (CTAB) assisted hydrothermal homogeneous precipitation method and subsequent calcination are employed to, synthesize festuca scoparia-like Ni0.3Co2.7O4 material and compared it with pristine spinel Co3O4 having ultralayered morphology. The specific capacitance (C-s) value for Co3O4 at 1 A g(-1) current density is 202 F g(-1) which has increased to 396 F g(-1) for Ni0.3Co2.7O4 electrode. Further, we have taken two important factors into consideration in fabrication, (i) facile in situ fabrication method, and (ii) desired composition of the active oxide phase on a porous current collector. We have employed same hydrothermal method to grow Ni0.3Co2.7O4 precursor material in situ on Ni foam without using CTAB, and converted it into oxide by heat treatment. The in situ grown Ni0.3Co2.7O4 on Ni foam electrode shows the highest specific capacitance value of 1423 F g(-1), which is 3.6 times larger than the value obtained using Ni0.3Co2.7O4 coated on Ni foil at 1 A g(-1) current density, and excellent cycling stability up to 4000 cycles. The capacitance loss is only similar to 4% at 16 A g(-1) and at 32 A g(-1). This study confirms the influence of unique features such as current collector, composition, surface area, porosity, and microstructural properties of materials on their electrochemical performance. Copyright (C) 2015, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
机译:通过使用元素周期表中的3d元素设计的混合金属氧化物有望在储能中发挥关键作用。在这项工作中,采用十六烷基三甲基溴化铵(CTAB)辅助的水热均相沉淀法和随后的煅烧方法,合成了景天树状的Ni0.3Co2.7O4材料,并将其与具有超层形态的原始尖晶石Co3O4进行了比较。 Co3O4在1 A g(-1)电流密度下的比电容(C-s)值为202 F g(-1),对于Ni0.3Co2.7O4电极已增加到396 F g(-1)。此外,我们在制造中考虑了两个重要因素,(i)简便的原位制造方法,和(ii)多孔集电器上活性氧化物相的所需组成。我们采用相同的水热方法,在不使用CTAB的情况下在Ni泡沫上原位生长Ni0.3Co2.7O4前体材料,并通过热处理将其转化为氧化物。在Ni泡沫电极上原位生长的Ni0.3Co2.7O4表现出最高的比电容值1423 F g(-1),这比在1 A电流下在Ni箔上涂覆的Ni0.3Co2.7O4所获得的值大3.6倍。 g(-1)的电流密度,以及出色的循环稳定性(高达4000个循环)。电容损耗在16 A g(-1)和32 A g(-1)下仅接近4%。这项研究证实了诸如集电器,组成,表面积,孔隙率和材料的微结构特性等独特特征对其材料电化学性能的影响。 Hydrogen Energy Publications,LLC版权所有(C)2015。由Elsevier Ltd.出版。保留所有权利。

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