Lithium silicate-lithium phosphate (xLi4SiO4-(1-x)Li3PO4) coating on lithium nickel manganese oxide (LiNi0.7Mn0.3O2) with a layered structure

被引:8
作者
Kim, Dong-jin [1 ]
Ko, Hyoung Shin [2 ]
Lee, Jae-won [3 ]
机构
[1] Dankook Univ, Dept Mat Sci Engn, Cheonan 330714, South Korea
[2] POSCO ESM, Gumi 703853, South Korea
[3] Dankook Univ, Dept Energy Engn, Cheonan 330714, South Korea
关键词
Lithium-ion battery; Coating; Lithium silicate; Lithium phosphate; Rate capability; SOL-GEL METHOD; CATHODE MATERIAL; ION BATTERIES; ELECTROCHEMICAL PERFORMANCE; LICOO2; ELECTRODES; AL2O3; GITT; EIS;
D O I
10.1016/j.ssi.2015.06.025
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
Solid solution of lithium silicate and lithium phosphate (xLi(4)SiO(4-)(1 - x)Li3PO4, LSP) is coated on LiNi0.7Mn0.3O2 using the reaction between the residual lithium compounds (Li2CO3 and LiOH) on the surface of LiNi0.7Mn0.3O2 particles and the sol prepared from tetraethyl orthosilicate (TEOS) and anhydrous phosphoric acid. The physical properties of the samples are analyzed by powder X-ray diffraction (PXRD), scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS). Electrochemical analyses, such as cyclic voltammetry (CV), galvanostatic intermittent titration technique (GITT) and galvanostatic cycling, are carried out for the samples. As a result, LSP-coating is found to be effective for improving the rate capability of LiNi0.7Mn0.3O2 as a cathode material for lithium-ion batteries. The specific capacity of the LSP-coated sample retains 58% at high current density of 7 C-rate (vs. 0.5 C-rate) while the bare sample shows only 44% capacity retention. Higher Li+-chemical diffusion coefficient and fast charge transfer process at the interface of the LSP-coated sample estimated by GITT and CV analyses are believed to be the reasons for the better rate capability. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:239 / 244
页数:6
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