Enhancing lithium titanate anode performance through surface modification with fluorine and nitrogen co-doped carbon nanotubes

被引:3
|
作者
Lee, Soobeom [1 ]
Kim, Seoyeong [1 ]
Kang, Seo Hui [2 ,3 ]
Roh, Kwang Chul [2 ]
An, Geon-Hyoung [1 ,4 ]
机构
[1] Gyeongsang Natl Univ, Dept Energy Syst Engn, Jinju 52725, South Korea
[2] Korea Inst Ceram Engn & Technol, Energy Storage Mat Ctr, Jinju Si 52851, South Korea
[3] Korea Univ, Dept Mat Sci & Engn, Seoul 136713, South Korea
[4] Gyeongsang Natl Univ, Dept Energy Engn, Jinju 52725, South Korea
关键词
Lithium-ion batteries; Lithium titanate; Carbon nanotubes; Doping; ELECTROCHEMICAL PROPERTIES; LI4TI5O12; ANODE; RATE CAPABILITY; ION BATTERY; MECHANISM; INSERTION; ELECTRODE; GRAPHENE; CATHODE; SITE;
D O I
10.1016/j.jallcom.2024.175768
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this study, we explore the efficacy of fluorine and nitrogen co-doped carbon nanotubes (F@N-CNT) as a novel surface modifier for lithium titanate (LTO) anodes in lithium-ion batteries (LIBs). The integration of F@N-CNT enhances the electrochemical properties of LTO anodes by improving electrical conductivity and facilitating lithium-ion diffusion., Electrodes modified with F@N-CNT exhibited significant improvements in capacity retention, achieving 71 % capacity retention over 200 cycles at 2 C and delivering energy capacities up to 162.9 mAh g- 1 at 0.2 C, with an impressive high-rate performance of 74.8 mAh g- 1 at 30 C. This study demonstrates that F@N-CNT effectively forms a conductive network within the LTO matrix, resulting in superior high-rate performance and stability. It presents a comprehensive analysis of the microstructural changes induced by codoping and elucidates their impact on the electrochemical performance, providing valuable insights into the design of high-performance anodes for future energy storage applications. This approach not only addresses the current limitations of LTO anodes but also introduces a scalable strategy for enhancing the overall functionality of LIBs.
引用
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页数:9
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