Li4Ti5O12-LiAlO2 Composite as High Performance Anode Material for Lithium-Ion Battery

被引:48
作者
Fang, Zi-Kui [1 ]
Zhu, Yan-Rong [1 ]
Yi, Ting-Feng [1 ]
Xie, Ying [2 ]
机构
[1] Anhui Univ Technol, Sch Chem & Chem Engn, Maanshan 243002, Anhui, Peoples R China
[2] Heilongjiang Univ, Key Lab Funct Inorgan Mat Chem, Minist Educ, Sch Chem & Mat Sci, Harbin 150080, Peoples R China
来源
ACS SUSTAINABLE CHEMISTRY & ENGINEERING | 2016年 / 4卷 / 04期
基金
中国国家自然科学基金;
关键词
Lithium-ion battery; Li4Ti5O12; LiAlO2; Modification; Rate capability; ENHANCED RATE PERFORMANCE; SOL-GEL SYNTHESIS; ELECTROCHEMICAL PERFORMANCE; DOPED LI4TI5O12; HYDROTHERMAL SYNTHESIS; ELECTRODE MATERIALS; FACILE FABRICATION; SPINEL; LIALO2; INSERTION;
D O I
10.1021/acssuschemeng.5b01271
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A facile solid-state method to improve the rate performance of Li4Ti5O12 in lithium-ion batteries by LiAlO2 in situ modification is presented in this work. XRD shows that the LiAlO2 modification does not change the spinet structure of Li4Ti5O12 but forms Al-doped Li4Ti5O12-LiAlO2 composites, and little Al doping decreases the lattice parameter of doped Li4Ti5O12. SEM shows that all samples are composed of 1-2 mu m primary particles with irregular shapes. Raman spectra reveal that the intensity of these lines for Li4Ti5O12-LiAlO2 composites obviously decreases caused by a modification of the LiAlO2 phase. CV and EIS tests indicate that the doping of Al3+ and the combination with in situ generated LiAlO2 on the surface of Li4Ti5O12 are favorable for reducing the electrode polarization and charge-transfer resistance, and then improve the reversibility and lithium ion diffusion coefficient of Li4Ti5O12, resulting in its relatively higher rate capacity. Charge-discharge tests reveals that Li4Ti5O12-LiAlO2 composite (5 wt %) exhibits the highest rate capacity and cycling stability at various rates, which is capable of large-scale applications, such as electric vehicles and hybrid electric vehicles, requiring high energy, long life and excellent safety.
引用
收藏
页码:1994 / 2003
页数:10
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