P. R. P. R. Shalom, Vaishnavi Sreekala Kumari Gopakumar, A. M. Aravind, Xavier T. Suryabai
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引用次数: 0
摘要
本研究通过微波辅助共沉淀法成功合成了尖晶石镍锰氧化物,随后在 500°C 煅烧。通过 X 射线衍射(XRD)和傅立叶变换红外光谱(FT-IR)对镍锰氧化物的晶体结构和官能团的存在进行了表征。场发射扫描电子显微镜(FE SEM)对表面形貌进行了检测。通过 BET 分析,计算出介孔 NMO 纳米粒子的表面积和平均孔径分别为 10.513 m2g-1 和 8.55nm。通过循环伏安法(CV)和电化学阻抗光谱法(EIS)分析了该材料作为超级电容器电极材料的电化学性能。在 5mV/s 的扫描速率下,随着浓度从 IM KOH 增加到 6M KOH,NMO 电极的比电容从 290.56 F/g 增加到 751.57F/g。这些结果表明尖晶石镍锰酸锂有望成为高性能储能应用的候选材料。
Microwave assisted synthesis of NiMn2O4 as electrode material for supercapacitor applications
In this work, spinel NiMn2O4 was successfully synthesized through microwave assisted co-precipitation method and followed by calcination at 500°C. The crystal structure and the presence of functional groups in NiMn2O4 were characterized through X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FT-IR). The surface morphology was examined by field emission scanning electron microscopy (FE SEM). From the BET analysis surface area and average pore diameter of the mesoporous NMO nanoparticles are calculated to be 10.513 m2g-1and 8.55nm. The electrochemical performance of material as electrode material for supercapacitor applications was analysed by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The specific capacitance of the NMO electrode increased from 290.56 F/g to 751.57F/g with increase concentration from IM KOH to 6M KOH at scan rate of 5mV/s. These results indicate spinel NiMn2O4 as a promising candidate for high performance energy storage applications.