阳极
材料科学
电解质
锂(药物)
电极
石墨烯
化学工程
电池(电)
储能
纳米技术
化学
医学
物理化学
工程类
内分泌学
功率(物理)
物理
量子力学
作者
Lin‐Bo Huang,Lu Zhao,Zhi-Feng Ma,Xing Zhang,Xu‐Sheng Zhang,Zhuo‐Ya Lu,Ge Li,Xiaoxi Luo,Rui Wen,Sen Xin,Qinghai Meng,Yu‐Guo Guo
标识
DOI:10.1002/anie.202413600
摘要
Achieving high energy density has always been the goal of lithium‐ion batteries (LIBs). SiOx has emerged as a compelling candidate for use as a negative electrode material due to its remarkable capacity. However, the huge volume expansion and the unstable electrode interface during (de)lithiation, hinder its further development. Herein, we report a facile strategy for the synthesis of surface fluorinated SiOx (SiOx@vG‐F), and investigate their influences on battery performance. Systematic experiments investigations indicate that the reaction between Li+ and fluorine groups promotes the in‐situ formation of stable LiF‐rich solid electrolyte interface (SEI) on the surface of SiOx@vG‐F anode, which effectively suppresses the pulverization of microsized SiOx particles during the charge and discharge cycle. As a result, the SiOx@vG‐F enabled a higher capacity retention of 86.4% over 200 cycles at 1.0 C in the SiOx@vG‐F||LiNi0.8Co0.1Mn0.1O2 full cell. This approach will provide insights for the advancement of alternative electrode materials in diverse energy conversion and storage systems.
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