阳极
锂(药物)
复合数
材料科学
多孔性
离子
化学工程
复合材料
化学
电极
工程类
有机化学
物理化学
医学
内分泌学
作者
Lin Sun,Xiaowen Jiang,Zhong Jin
标识
DOI:10.1016/j.cej.2023.145960
摘要
SiOx@C anodes have been regarded as one of the most attractive candidates for next-generation high-capacity lithium-ion batteries (LIBs). However, the uneven thickness and lack of continuity in the carbon coating have led to a decrease in capacity, lifespan, and coulombic efficiency. Thus, there is a pressing need to address the atomic-level construction of the Si/C interface. In this study, we present a simple interfacial engineering approach to achieve an in-situ compact carbon layer on porous SiOx@C (pSiOx@C) anodes through low-temperature zinc thermal reduction. Following prelithiation, the pSiOx@C anode demonstrates excellent performance, including a high initial Coulombic efficiency (93.4%), a reversible capacity exceeding 900 mAh/g, long-term cycling stability (1300 charge/discharge cycles at 0.3 A/g) and remarkable rate capability. Furthermore, when coupled with the LiCoO2 (LCO) cathode, the pSiOx@C//LCO full cell exhibits superior Li-ion storage performance, achieving a high reversible capacity of 147 mAh/g at 0.2 A/g. This work provides valuable insights into the design of SiOx-based anode materials for high-energy–density LIBs.
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