阳极
材料科学
锂(药物)
电极
石墨烯
能量密度
化学工程
纳米技术
工程物理
化学
医学
物理
工程类
内分泌学
物理化学
作者
Lin‐Bo Huang,Lu Zhao,Z.Y. Ma,Xing Zhang,Xusheng Zhang,Zhuo‐Ya Lu,Ge Li,Xiaoxi Luo,Rui Wen,Sen Xin,Qinghai Meng,Yu‐Guo Guo,Yu‐Guo Guo
出处
期刊:Angewandte Chemie
[Wiley]
日期:2024-08-13
卷期号:63 (47): e202413600-e202413600
被引量:21
标识
DOI:10.1002/anie.202413600
摘要
Abstract Achieving high energy density has always been the goal of lithium‐ion batteries (LIBs). SiO x 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 SiO x (SiO x @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 SiO x @vG−F anode, which effectively suppresses the pulverization of microsized SiO x particles during the charge and discharge cycle. As a result, the SiO x @vG−F enabled a higher capacity retention of 86.4 % over 200 cycles at 1.0 C in the SiO x @vG−F||LiNi 0.8 Co 0.1 Mn 0.1 O 2 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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