Hydrogen-titanate-protected SnO2@C coaxial nanocables as new nanocomposite anode materials for lithium-ion batteries

被引:10
作者
Chen, Zehua [1 ]
Wang, Ting [2 ]
Liu, Yuan [2 ,3 ]
Liu, Yaochun [2 ,4 ]
Yang, Xiaoping [3 ]
机构
[1] Yibin Vocat & Tech Coll, Coll New Energy & Battery, Yibin 644000, Peoples R China
[2] Qingdao Univ, Coll Mat Sci & Engn, Qingdao 266071, Peoples R China
[3] Beijing Univ Chem Technol, State Key Lab Organ Inorgan Composites, Beijing 100029, Peoples R China
[4] Foshan Southern China Inst New Mat, Foshan 528200, Peoples R China
基金
中国国家自然科学基金;
关键词
Core-shell nanoarchitecture; Co-axial nanocable; SnO2; Stable lithium-storage capability; SNO2; STORAGE; ARRAYS;
D O I
10.1016/j.cej.2024.149381
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The core-shell design can effectively overcome the problems of Sn-based anode used in lithium-ion battery by buffering the volume change and stabilizing the electrode/electrolyte interface. The choice of a protective shell with a durable physical structure and chemical stability is thus important for preparing desirable Sn-based anodes. Herein, we introduce hydrogen titanate (HTO) as a new external shell to wrap SnO2@C for targeting the goal. The SnO2@C-HTO core-shell nanocomposite was directly prepared via a facile alkaline hydrothermal method without the need for a secondary coating process. Due to the high specific surface area and twodimensional Li+-diffusion pathways provided by the HTO shells, the SnO2@C-HTO electrode showed stable lithium uptake/release at high rates, i.e., it delivered a reversible capacity of 175 mA h g-1 at a high rate of 5 A g-1 and displayed a long-term operating stability (330 mA h g-1 at 1 A g-1 for 500 cycles). This study offers a broad vision for designing novel Sn-based core-shell nanoarchitectures for safe and reliable lithium-ion batteries with high-energy densities.
引用
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页数:9
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