氧化还原
材料科学
阴极
氧化物
扫描透射电子显微镜
化学工程
密度泛函理论
过渡金属
氧气
透射电子显微镜
无机化学
化学物理
纳米技术
冶金
物理化学
催化作用
化学
计算化学
有机化学
工程类
生物化学
作者
Shuwei Li,Zepeng Liu,Lu Yang,Xi Shen,Qiuyan Liu,Zhiwei Hu,Qingyu Kong,Jun Ma,Jiedong Li,Hong‐Ji Lin,Chien‐Te Chen,Xuefeng Wang,Richeng Yu,Zhaoxiang Wang,Liquan Chen
出处
期刊:Nano Energy
[Elsevier BV]
日期:2022-05-04
卷期号:98: 107335-107335
被引量:80
标识
DOI:10.1016/j.nanoen.2022.107335
摘要
The Ni-rich layer-structured oxide is one of the most promising candidate cathode materials for the high energy-density Li-ion batteries. However, the commercial applications of these materials are hindered with drawbacks such as structural instability and poor cycling performance at high potentials. Herein, we comprehensively studied the oxygen redox reaction and the structural reversibility of LiNi0.83Co0.12Mn0.05O2 at deep delithiation using the synchrotron X-ray absorption spectroscopy, scanning transmission electron microscopy and density functional theory calculations. The oxygen redox occurs due to the cation mixing upon delithiation in this material though there are no Li-O-Li configurations in its pristine form. The formation of the I41 structure was attributed to the migration of the transition metals in the deeply delithiated material, extending the route of the phase transformation from the layered to the rock-salt structure. These findings are helpful to enrich the understanding of the origin of the oxygen redox and reveal its impact on the structural transformations in the Ni-rich layered oxides. These will spur new strategies to enhance the performance of the cathode materials for the next-generation Li-ion batteries.
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