氧化还原
阴极
法拉第效率
过渡金属
相变
材料科学
离子
相(物质)
化学
化学物理
化学工程
纳米技术
无机化学
电化学
电极
催化作用
物理化学
热力学
有机化学
物理
工程类
作者
Xiaohui Rong,Enyuan Hu,Yaxiang Lu,Fanqi Meng,Chenglong Zhao,Xuelong Wang,Qinghua Zhang,Xiqian Yu,Lin Gu,Yong‐Sheng Hu,Hong Li,Xuejie Huang,Xiao‐Qing Yang,Claude Delmas,Liquan Chen
出处
期刊:Joule
[Elsevier]
日期:2018-11-13
卷期号:3 (2): 503-517
被引量:310
标识
DOI:10.1016/j.joule.2018.10.022
摘要
Layered metal oxides have attracted widespread attention as cathodes for Na-ion batteries (NIBs) because of easy synthesis, high specific capacity, and high energy density. However, most reported layered oxides suffer from complex phase transitions upon a large amount of Na deintercalation. Here we report a P2-type Na0.72[Li0.24Mn0.76]O2, exhibiting exceptionally high initial charge capacity of ∼210 mAh/g (0.72 Na) based on a pure anionic redox reaction (ARR). Surprisingly, global P2 structure can be maintained with minimal volume change (1.35%) upon complete removal of Na+ ions. This is due to the reduced Coulombic repulsion associated with ARR and consequent suppression of the phase transition as observed in other P2 materials. Here we reveal for the first time that ARR has the functionality of stabilizing the structure, in addition to its role in increasing its already known capacity. This would pave the way for the further improvement of high-energy-density NIBs.
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