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Electrochemical Propertiesof Na0.66V4O10 Nanostructures asCathode Material in Rechargeable Batteriesfor Energy Storage Applications

机译:电化学性质Na0.66V4O10纳米结构的制备充电电池中的正极材料用于储能应用

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摘要

We report the electrochemical performance of nanostructures of Na0.66V4O10 as cathode material for rechargeable batteries. The Rietveld refinement of room-temperature X-ray diffraction pattern shows the monoclinic phase with C2/m space group. The cyclic voltammetry curves of prepared half-cells exhibit redox peaks at 3.1 and 2.6 V, which are due to two-phase transition reaction between V5+/4+ and can be assigned to the single-step deintercalation/intercalation of Na ion. We observe a good cycling stability with specific discharge capacity (measured vs Na+/Na) between 80 (±2) and 30 (±2) mAh g–1 at current densities of 3 and 50 mA g–1, respectively. The electrochemical performance of Na0.66V4O10 electrode was also tested with Li anode, which showed higher capacity but decayed faster than Na. Using density functional theory, we calculate the Na vacancy formation energies: 3.37 eV in the bulk of the material and 2.52 eV on the (100) surface, which underlines the importance of nanostructures.
机译:我们报告了Na0.66V4O10纳米结构作为可充电电池阴极材料的电化学性能。室温X射线衍射图的Rietveld细化显示具有C2 / m空间群的单斜晶相。制备的半电池的循环伏安曲线在3.1和2.6 V处显示氧化还原峰,这是由于V 5 + / 4 + 之间的两相转变反应引起的,可以归为单步Na离子的去嵌入/嵌入。我们观察到在当前电流为80(±2)mAh至30(±2)mAh g –1 时的比放电容量(相对于Na + / Na的测量值)具有良好的循环稳定性。密度分别为3和50 mA g –1 。还用锂阳极测试了Na0.66V4O10电极的电化学性能,该电极显示出更高的容量,但衰减速度比Na快。使用密度泛函理论,我们计算了Na空位形成能:材料中的3.37 eV和(100)表面上的2.52 eV,这突出了纳米结构的重要性。

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