Interfacial engineering of porous SiOx@C composite anodes toward high-performance lithium-ion batteries

被引:25
|
作者
Sun, Lin [1 ,2 ,3 ]
Jiang, Xiaowen [1 ,2 ]
Jin, Zhong [1 ,3 ]
机构
[1] Yancheng Inst Technol, Sch Chem & Chem Engn, Key Lab Adv Technol Environm Protect Jiangsu Prov, Yancheng 224051, Peoples R China
[2] Changzhou Univ, Sch Petrochem Engn, Changzhou 213164, Peoples R China
[3] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Coordinat Chem, MOE Key Lab Mesoscop Chem,Jiangsu Key Lab Adv Orga, Nanjing 210023, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
SiOx anode; Lithium ion battery; Structure regulation; Interfacial design; Full cell; SILICON; CARBON;
D O I
10.1016/j.cej.2023.145960
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
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 atomiclevel 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 SiOxbased anode materials for high-energy-density LIBs.
引用
收藏
页数:9
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