NiS@CeO2球形纳米薄片的电化学性能增强

Indumati D. Yadav , Dineshkumar Yadav , Aleem Ansari , Shyamalava Mazumdar , Shivram S. Garje
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摘要

本文报道了以氢氧化铈为原料,以肉桂醛缩硫脲配合物(单源分子前体)和CeO2纳米颗粒为原料,采用溶剂热法制备了裸氧化铈纳米颗粒和NiS@CeO2纳米复合材料(NC),乙二醇为封盖剂。利用粉末x射线衍射、傅里叶变换红外光谱、扫描电镜、高分辨率透射电镜和能量色散x射线技术对这些材料进行了表征。通过XRD计算得到复合纳米颗粒的晶粒尺寸为17.99 nm。透射电镜显示NiS@CeO2纳米复合材料呈球形,平均粒径小于10 nm。采用循环伏安法、恒流充放电法和电化学阻抗法对CeO2裸电极和NiS@CeO2 NC电极的电化学性能进行了评价。电化学测量结果表明,在电流密度为1 A g−1时,NiS@CeO2 NC电极的电容值(707.84 F g−1)明显高于裸CeO2电极(80.91 F g−1)。这可归因于纳米复合材料的协同效应。在2 A g−1电流密度下,经过6000次充放电循环后,NiS@CeO2 NC电极的循环稳定性为98.41 %。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhanced electrochemical properties of NiS@CeO2 spherical nanoflakes
Herein we report synthesis of bare cerium oxide nanoparticles from cerium hydroxide and NiS@CeO2 nanocomposite (NC) from nickel cinnamaldehyde thiosemicarbazone complex (single source molecular precursor) and CeO2 nanoparticles by solvothermal method using ethylene glycol as a capping agent. These materials were characterized using powder X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, high resolution transmission electron microscopy and energy dispersive X-ray techniques. The crystallite size of the composite nanoparticles calculated using XRD is 17.99 nm. TEM shows spherical shape morphology of NiS@CeO2 nanocomposite with average particle size less than 10 nm. Electrochemical properties of bare CeO2 and NiS@CeO2 NC electrodes were evaluated by cyclic voltammetry, galvanostatic charge/discharge and electrochemical impedance spectroscopy. The electrochemical measurements show that the capacitance value of NiS@CeO2 NC electrode is significantly higher (707.84 F g−1) compared to bare CeO2 electrode (80.91 F g−1) at current density 1 A g−1. This can be attributed to synergistic effect in nanocomposite. The cycle stability of NiS@CeO2 NC electrode was found to be 98.41 % even after 6000 charge–discharge cycles at 2 A g−1 current density.
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