Synthesis and properties of LiMn2O4 from hydrazine hydrate reduced electrolytic manganese dioxide

被引:11
作者
Guo, Donglei [1 ]
Chang, Zhaorong [1 ]
Li, Bao [1 ]
Tang, Hongwei [1 ]
Yuan, Xiao-Zi [2 ]
Wang, Haijiang [2 ]
机构
[1] Henan Normal Univ, Minist Educ, Key Lab Green Chem Medium & React, Coll Chem & Environm Sci, Xinxiang 453007, Peoples R China
[2] Natl Res Council Canada, Vancouver, BC V6T 1W5, Canada
关键词
Hydrazine hydrate; Manganese dioxide; Lithium ion battery; Cathode material; LITHIUM-ION BATTERIES; CATHODE MATERIAL;
D O I
10.1016/j.ssi.2013.02.009
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
Using N2H4-H2O as reductant gamma-Mn3O4 particles were obtained from the electrolytic manganese dioxide (EMD). Via high temperature solid-phase reactions, spinel lithium manganese oxide (LiMn2O4) was produced using the obtained gamma-Mn3O4 as precursor mixed with LiOH center dot H2O for the lithium ion battery cathodes. Atomic absorption (AAS) shows that after the liquid-phase reduction reaction the impurity ions, such as Na+, K+, Ca2+, and Mg2+, are greatly reduced. X-ray diffraction (XRD) and scanning electron microscopy (SEM) show that gamma-Mn3O4 has high crystallinity and uniform size-distribution. Spinel lithium manganese (LiMn2O4) synthesized by the gamma-Mn3O4 precursor has a high crystallinity and the (111) face grows perfectly with a regular and micron-sized octagonal crystal. The electrochemical tests show that LiMn2O4 synthesized by the gamma-Mn3O4 precursor has greater discharge capacity, better cycle performance, and better high-rate capability compared with LiMn2O4 synthesized by the EMD precursor. Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) indicate that LiMn2O4 synthesized by the gamma-Mn3O4 precursor has a better electrochemical reaction reversibility, greater peak current, higher lithium-ion diffusion coefficient, and lower electrochemical impedance. Furthermore, this synthesis process is simple, of low-cost, and easy for a large-scale production. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:34 / 39
页数:6
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