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Synthesis and electrochemical properties of LiV_3O_8 via an improved sol-gel process

机译:改进的溶胶-凝胶法合成LiV_3O_8及其电化学性能

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摘要

LiV_3O_8 cathode material was synthesized via a hydrothermal improved sol-gel process using LiOH, NH4VO3 and oxalic acid as raw materials. The thermal decomposition process of the as-prepared LiV_3O_8 precursor was investigated by thermogravimetric (TG) and differential scanning calorimetry (DSC). The structure, morphology and electrochemical performance of the as-synthesized LiV_3O_8 samples were characterized by X-ray diffraction (XRD), Fourier transform infrared (FT-IR), scanning electron microscopy (SEM) and the galvanostatic charge-discharge test. The effects of synthesis conditions on phases, structure and electrochemical performance of the LiV_3O_8 samples were particularly discussed. Result shows that pure LiV_3O_8 sample can be obtained at 300 °C, which is much lower than that of normal citric assisted sol-gel method. The sample synthesized at 350 °C exhibits the best electrochemical performance, which can present an initial discharge capacity of 301.1 mAh/g at a current density of 50 mA/g and maintain 271.6 mA/g (about 90.2% of its initial value) after 10 cycles.
机译:以LiOH,NH4VO3和草酸为原料,通过水热改良溶胶-凝胶法合成了LiV_3O_8正极材料。通过热重分析(TG)和差示扫描量热法(DSC)研究了制备的LiV_3O_8前体的热分解过程。通过X射线衍射(XRD),傅立叶变换红外光谱(FT-IR),扫描电子显微镜(SEM)和恒电流充放电试验对合成的LiV_3O_8样品的结构,形貌和电化学性能进行了表征。特别讨论了合成条件对LiV_3O_8样品的相,结构和电化学性能的影响。结果表明,在300°C可获得纯LiV_3O_8样品,这远低于普通柠檬酸辅助溶胶-凝胶法。在350°C下合成的样品表现出最佳的电化学性能,在50 mA / g的电流密度下可显示301.1 mAh / g的初始放电容量,并在之后保持271.6 mA / g(约为其初始值的90.2%) 10个周期。

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