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POSS-Derived Synthesis and Full Life Structural Analysis of Si@C as Anode Material in Lithium Ion Battery

机译:基于POSS的锂离子电池负极材料Si @ C的合成及全寿命结构分析

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摘要

Polyhedral oligomeric silsesquioxane (POSS)-derived Si@C anode material is prepared by the copolymerization of octavinyl-polyhedral oligomeric silsesquioxane (octavinyl-POSS) and styrene. Octavinyl-polyhedral oligomeric silsesquioxane has an inorganic core (-Si8O12) and an organic vinyl shell. Carbonization of the core-shell structured organic-inorganic hybrid precursor results in the formation of carbon protected Si-based anode material applicable for lithium ion battery. The initial discharge capacity of the battery based on the as-obtained Si@C material Si reaches 1500 mAh g−1. After 550 charge-discharge cycles, a high capacity of 1430 mAh g−1 was maintained. A combined XRD, XPS and TEM analysis was performed to investigate the variation of the discharge performance during the cycling experiments. The results show that the decrease in discharge capacity in the first few cycles is related to the formation of solid electrolyte interphase (SEI). The subsequent rise in the capacity can be ascribed to the gradual morphology evolution of the anode material and the loss of capacity after long-term cycles is due to the structural pulverization of silicon within the electrode. Our results not only show the high potential of the novel electrode material but also provide insight into the dynamic features of the material during battery cycling, which is useful for the future design of high-performance electrode material.
机译:多面体低聚倍半硅氧烷(POSS)衍生的Si @ C阳极材料是通过八乙烯基-多面体低聚倍半硅氧烷(octavinyl-POSS)和苯乙烯的共聚制备的。八乙烯基多面体低聚倍半硅氧烷具有无机核(-Si8O12)和有机乙烯基壳。核-壳结构的有机-无机杂化前体的碳化导致形成适用于锂离子电池的碳保护的硅基负极材料。基于所获得的Si @ C材料Si的电池的初始放电容量达到1500mAh g -1 。在550次充放电循环后,维持了1430mAh g -1 的高容量。结合XRD,XPS和TEM分析来研究循环实验过程中放电性能的变化。结果表明,在前几个循环中放电容量的下降与固体电解质中间相(SEI)的形成有关。容量的随后增加可归因于阳极材料的逐渐形态演变,并且长期循环后容量的损失归因于电极内硅的结构粉碎。我们的结果不仅显示了新型电极材料的高潜力,而且还提供了在电池循环期间该材料动态特性的见识,这对于高性能电极材料的未来设计很有用。

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