High Performance of Pb-doped Li4Ti5O12 as an Anode Material for Lithium Ion Batteries

被引:12
|
作者
Ding, Keqiang [1 ]
Wei, Binjuan [1 ]
Zhang, Yan [1 ]
Li, Chenxue [1 ]
Shi, Xiaomi [1 ]
Pan, Junqing [2 ]
机构
[1] Hebei Normal Univ, Coll Chem & Mat Sci, Shijiazhuang 050024, Hebei, Peoples R China
[2] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Li4Ti5O12; lead acetate; Pb doping; anode materials; lithium ion batteries; ELECTROCHEMICAL PERFORMANCE; TITANATE LI4TI5O12; RATE CAPABILITY; NANOPARTICLES; CAPACITY;
D O I
10.20964/2017.09.40
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
For the first time, Pb-doped Li4Ti5O12 (Pb-LTO) was prepared by a solution-drying-calcination (SDC) method in which lead acetate was employed as a dopant. In the present work, the effect of Pb to Ti atomic ratio on the physicochemical properties as well as the electrochemical performance of the synthesized materials was systematically investigated. X-ray diffraction (XRD), scanning electron microscopy (SEM), cyclic voltammometry (CV), electrochemical impedance spectroscopy (EIS) and galvanostatic charge-discharge test were mainly used to examine the as-prepared samples. XRD results not only effectively demonstrated the formation of Li4Ti5O12 but also indicated that the crystallinities of the resultant samples were closely related to the Pb to Ti atomic ratio used. Also, SEM images indicated that relatively regular particles with an average size of 0.5 mu m could be prepared when the Pb to Ti atomic ratio was 0.01 (sample b). The results of electrochemical measurements indicated that the initial discharge capacity of sample b was as high as 185 mAh g(-1) at 0.2C rate and sample b could show a high specific capacity of 169 mAh g(-1) after 20 cycles at 0.2 C rate. Using a very cheaper dopant of lead acetate to prepare the high performance Pb-doped LTO was the main contribution of this preliminary work, which was believed to be very beneficial to the further commercialization of LTO.
引用
收藏
页码:8381 / 8398
页数:18
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