介电谱
材料科学
阳极
钛酸锂
电化学
扫描电子显微镜
循环伏安法
尖晶石
锂(药物)
兴奋剂
杂质
分析化学(期刊)
掺杂剂
化学工程
锂离子电池
电极
化学
复合材料
冶金
物理化学
电池(电)
有机化学
医学
功率(物理)
物理
光电子学
量子力学
工程类
内分泌学
作者
Qianyu Zhang,Michael G. Verde,Joon Kyo Seo,Xi Li,Ying Shirley Meng
标识
DOI:10.1016/j.jpowsour.2015.01.124
摘要
Pristine and Gd-doped Li4Ti5O12 (LTO) in the form of Li4−x/3Ti5−2x/3GdxO12 (x = 0.05, 0.10 and 0.15) were prepared by a simple solid-state reaction in air. The structural and electrochemical properties of the as-prepared powders were characterized using X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDS), scanning electron microscopy (SEM), cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS). XRD revealed that only a small amount of the dopant can enter the lattice structure of LTO; excessive addition beyond x = 0.10 resulted in a discrete Gd2O3 impurity phase. The Gd doping did not change the spinel structure and electrochemical reaction process of LTO. The average particle size of as-prepared samples ranged between 0.5 and 1.5 μm. The Gd-doped materials showed much improved rate capability and specific capacity compared with undoped LTO. In particular, Li4−x/3Ti5−2x/3GdxO12 (x = 0.5) exhibited the best rate capability and cycling stability among all samples. Beyond this doping level, however, Gd2O3 impurity phase in the LTO led to adverse electrochemical performance. The rate capability of the anode material made from the modified powder is significantly improved when discharged at high current rates due to the reduced charge transfer resistance and fast lithium insertion/extraction kinetics.
科研通智能强力驱动
Strongly Powered by AbleSci AI