阴极
材料科学
电解质
溶解
化学工程
电极
相(物质)
曲面重建
同步加速器
纳米技术
曲面(拓扑)
光学
化学
物理
几何学
数学
有机化学
物理化学
工程类
作者
Gang Sun,Changtai Zhao,Fu‐Da Yu,Ruizhi Yu,Jian Wang,Jigang Zhou,Guangjie Shao,Xueliang Sun,Zhen‐Bo Wang
出处
期刊:Nano Energy
[Elsevier BV]
日期:2020-10-08
卷期号:79: 105459-105459
被引量:84
标识
DOI:10.1016/j.nanoen.2020.105459
摘要
The critical challenges hindering the commercialization of Li-rich cathodes are their rapid-decaying capacity and voltage during cycling, originating from the degradation of lattice structure and interface side reaction between electrode and electrolyte. Surface engineering is considered to be an effective strategy to mitigate these disadvantages. Herein, an in-situ self-reconstruction strategy is proposed and developed to simultaneously optimize surface chemical composition and local structure of Li-rich cathodes. Specifically, the multifunction protective layer consisting of cation disorder phase and LiTMPO4-like (TM: Ni, Co, Mn) phase is produced by a simple PH3 gas treatment. LiTMPO4 featuring the ability against high potential is responsible for preventing interface side reaction and further reduce the dissolution of Mn. Both LiTMPO4-like phase and surface cation disorder phase contribute to stabilizing surface oxygen structure and limiting surface O2 release. Compared to the pristine one, better integrity of chemical phases and higher oxidation state of TM cations after long-term cycling are confirmed in the modified sample by synchrotron-based scanning transmission X-ray microscopy, highlighting the key roles of the multifunction protective layer in stabilizing the capacity and voltage during cycling. This surface self-reconstruction strategy provides a new path for guiding the interface design of high energy density cathodes.
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