Facile synthesis of Na2FexFe1-x(SO4)2(OH)x material as a cathode for sodium-ion batteries

被引:3
作者
Wang, Liang [1 ]
Yan, Chenxing [1 ]
Wang, Zheng [1 ]
Zhuang, Quanchao [1 ]
机构
[1] China Univ Min & Technol, Sch Mat Sci & Engn, Li Ion Batteries Lab, Xuzhou 221116, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Sodium-ion batteries; Sulfate compounds; Electrochemical impedance spectroscopy; PHASE-TRANSFORMATION; ELECTRODE MATERIALS; HOLLOW SPHERES; LITHIUM; NA; NA2+2XFE2-X(SO4)(3); INTERCALATION; COMPOSITE; HOST; LI;
D O I
10.1007/s11581-018-2737-6
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 the present work, a new cathode material of Na2FexFe1-x(SO4)(2)(OH)(x) is synthesized for sodium-ion batteries, and its morphologies and structures are characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). SEM results show that the morphology of Na2FexFe1-x(SO4)(2)(OH)(x) is dumbbell-shaped nanorods with the length of about 1.3m and the width of 0.3-0.4m. The obtained material exhibits the initial reversible capacity that is 106mAhg(-1) and 154mAhg(-1) in the potential range 2.0 similar to 4.2V and 1.5 similar to 4.5V, respectively. After 65cycles, the reversible capacity decreases to 74mAhg(-1) and 115mAhg(-1) with capacity retention of 70% and 74%, respectively, displaying an excellent cycle performance. Furthermore, the first charge process of Na2FexFe1-x(SO4)(2)(OH)(x) electrode is investigated by electrochemical impedance spectroscopy (EIS) at different potentials, and the spectra exhibit four semicircles and a slightly inclined line that appear successively as the frequency decreases, representing the Na-ion migration in solid electrolyte interface film (SEI film), the electronic properties of materials, charge transfer, solid state diffusion, and phase transition. According to the results of equivalent circuit analysis, the change of kinetic parameters for desodiation process of Na2FexFe1-x(SO4)(2)(OH)(x) electrode as a function of potential is discussed in detail.
引用
收藏
页码:2509 / 2518
页数:10
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