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Vertically Fluorinated Graphene Encapsulated SiO x Anode for Enhanced Li + Transport and Interfacial Stability in High‐Energy‐Density Lithium Batteries
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,...
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Published in: | Angewandte Chemie 2024-11, Vol.136 (47) |
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container_title | Angewandte Chemie |
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creator | Huang, Lin‐Bo Zhao, Lu Ma, Zhi‐Feng Zhang, Xing Zhang, Xu‐Sheng Lu, Zhuo‐Ya Li, Ge Luo, Xiao‐Xi Wen, Rui Xin, Sen Meng, Qinghai Guo, Yu‐Guo |
description | 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. |
doi_str_mv | 10.1002/ange.202413600 |
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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. 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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. 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title | Vertically Fluorinated Graphene Encapsulated SiO x Anode for Enhanced Li + Transport and Interfacial Stability in High‐Energy‐Density Lithium Batteries |
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