尖晶石
材料科学
锂(药物)
兴奋剂
电化学
阴极
离子
化学工程
氧化物
扩散
相(物质)
电极
化学
光电子学
冶金
物理化学
医学
物理
有机化学
工程类
热力学
内分泌学
作者
Xin Feng,Yurui Gao,Liubin Ben,Zhenzhong Yang,Zhaoxiang Wang,Liquan Chen
标识
DOI:10.1016/j.jpowsour.2016.03.101
摘要
Lithium-rich manganese-based layer-structured oxides (xLi2MnO3⋅(1-x)LiNi1/3Co1/3Mn1/3O2) have attracted great attention for their potential applications as cathode materials of high energy-density lithium ion batteries. However, these oxides suffer from inferior cycling and poor rate capability due to presence of the Li2MnO3 phase. Herein, the Li+ ions in the Li-layer of the Li1.2Mn0.54Co0.13Ni0.13O2 (or 0.5Li2MnO3⋅0.5LiNi1/3Co1/3Mn1/3O2) are partially substituted with aliovalent Ti4+ ions to improve its long-term cycling stability and rate performance. The obtained oxide (Li1.2-xTixMn0.54Co0.13Ni0.13O2, x = 2.5%) exhibits an initial capacity of 320 mAh g−1 and a capacity retention of 71% after 300 cycles as well as good rate performance. In addition, although Ti doping cannot prevent the transformation from the layered to the spinel-like phase, it stabilizes the structure of the spinel-like phase below 3.0 V. Based on first-principles calculations and performance evaluation, these improvements are attributed to the Ti-doping induced enhancement in conductivity, diffusion, activation energy of Mn migration and TiO bonding. This novel design may furthermore open a door for the synthesis of lithium-rich materials with high rate performance.
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