Abstract

Si anode is considered to be one of the most promising candidates for the next-generation lithium-ion batteries (LIBs). However, the severe volume variation of Si (> 300%) during the lithiation/delithiation process results in unstable interface and thus contributes to poor cycling stability. Moreover, the relatively low conductivity derived from the semiconductor nature of Si leads to inferior rate performance. Herein, Li2SiO3 layer with fast lithium-ions transport capability and high mechanical property was formed on Si surface in an in-situ electrochemical method. The relationships between the valence of SiOx and LixSiOy constituents were readily studied. Fortunately, the as-prepared Si@ES-LSO showed great potential to mitigate the expansion and high lithium-ions diffusion coefficient. When employed as anode materials for LIBs, the modified Si anode delivered a specific capacity of 2074.8 mAh g−1 at 1000 mA g−1 with a retention ratio of 98.9% after 100 cycles, demonstrating superior electrochemical performance. This work provides a facial and efficient strategy for the roadmap of Si anode application.

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