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Na Insertion Mechanisms in Vanadium Oxide Nanotubes for Na-Ion Batteries

机译:钒离子纳米管中钠离子电池中的钠插入机理

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In this study, we successfully synthesized lamellar-structured Ni0.1VOx NTs by a microwave-assisted hydrothermal method and cation exchange reaction. High initial discharge capacity and 100% efficiency were obtained when the Ni0.1VOx NTs cathode was used as a cathode material for the Na battery. The intercalation mechanism and capacity fading effect were investigated in detail both experimentally using Transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR) and X-ray photoelectron spectroscopy (XPS) analyses and theoretically using the ab initio simulation method. During the intercalation of Na+ into VOx NT structures, TEM, XRD, FT-IR, and XPS data revealed the cointercalation of the solvent, resulting in the expansion of the interlayer spacing and carbon and oxygen adsorption. The experimental and simulation results suggest that solvent molecules coordinated the Na insertion mechanisms into the amine interlayer during discharging. These understandings of the Na intercalation mechanism in materials based on Ni0.1VOx NTs would be useful to design more stable and high-performance VOx-based electrodes for Na battery applications.
机译:在这项研究中,我们成功地通过微波辅助水热法和阳离子交换反应合成了层状结构的Ni0.1VOx NTs。当将Ni0.1VOx NTs阴极用作Na电池的阴极材料时,可获得高的初始放电容量和100%的效率。使用透射电子显微镜(TEM),X射线衍射(XRD),傅里叶变换红外光谱(FT-IR)和X射线光电子能谱(XPS)进行了实验,详细研究了插层机理和容量衰减效果使用从头算模拟方法。在将Na +嵌入VOx NT结构期间,TEM,XRD,FT-IR和XPS数据显示溶剂共嵌入,从而导致层间距的扩大以及碳和氧的吸附。实验和模拟结果表明,溶剂分子在放电过程中协调了Na插入胺中间层的机理。对基于Ni0.1VOx NTs的材料中的Na嵌入机理的这些理解对于设计用于Na电池应用的更稳定和高性能的基于VOx的电极非常有用。

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