材料科学
阴极
镍
电解质
锂(药物)
过渡金属
化学工程
氧化镍
电化学
氧化物
非阻塞I/O
锰
冶金
电极
物理化学
医学
生物化学
工程类
内分泌学
催化作用
化学
作者
Yan Li,Rui Xu,Yang Ren,Jun Lü,Huiming Wu,Lifen Wang,Dean J. Miller,Yang‐Kook Sun,Khalil Amine,Zonghai Chen
出处
期刊:Nano Energy
[Elsevier]
日期:2015-07-29
卷期号:19: 522-531
被引量:69
标识
DOI:10.1016/j.nanoen.2015.07.019
摘要
Nickel-rich metal oxides have been widely pursued as promising cathode materials for high energy-density lithium-ion batteries. Nickel-rich lithium transition metal oxides can deliver a high specific capacity during cycling, but can react with non-aqueous electrolytes. In this work, we have employed a full concentration gradient (FCG) design to provide a nickel-rich core to deliver high capacity and a manganese-rich outer layer to provide enhanced stability and cycle life. In situ high-energy X-ray diffraction was utilized to study the structural evolution of oxides during the solid-state synthesis of FCG lithium transition metal oxide with a nominal composition of LiNi0.6Mn0.2Co0.2O2. We found that both the pre-heating step and the sintering temperature were critical in controlling phase separation of the transition metal oxides and minimizing the content of Li2CO3 and NiO, both of which deteriorate the electrochemical performance of the final material. The insights revealed in this work can also be utilized for the design of other nickel-rich high energy-density cathode materials.
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