阳离子聚合
氧化还原
化学
锂(药物)
无机化学
氧气
萤石
阴极
电化学
半反应
氧化物
电极
有机化学
物理化学
医学
内分泌学
作者
Chun Zhan,Zhenpeng Yao,Jun Lü,Lu Ma,V.A. Maroni,Liang Li,Eungje Lee,Ekin Esen,Tianpin Wu,Jianguo Wen,Yang Ren,Christopher S. Johnson,Michael M. Thackeray,Maria K. Y. Chan,Chris Wolverton,Khalil Amine
出处
期刊:Nature Energy
[Springer Nature]
日期:2017-12-01
卷期号:2 (12): 963-971
被引量:162
标识
DOI:10.1038/s41560-017-0043-6
摘要
Anionic redox reactions in cathodes of lithium-ion batteries are allowing opportunities to double or even triple the energy density. However, it is still challenging to develop a cathode, especially with Earth-abundant elements, that enables anionic redox activity for real-world applications, primarily due to limited strategies to intercept the oxygenates from further irreversible oxidation to O2 gas. Here we report simultaneous iron and oxygen redox activity in a Li-rich anti-fluorite Li5FeO4 electrode. During the removal of the first two Li ions, the oxidation potential of O2− is lowered to approximately 3.5 V versus Li+/Li0, at which potential the cationic oxidation occurs concurrently. These anionic and cationic redox reactions show high reversibility without any obvious O2 gas release. Moreover, this study provides an insightful guide to designing high-capacity cathodes with reversible oxygen redox activity by simply introducing oxygen ions that are exclusively coordinated by Li+. It is challenging to exploit anionic redox activity to boost performance of battery electrodes, especially for anti-fluorite structures. Here the authors report simultaneous anionic and cationic redox in Li5FeO4, which enables its high capacity and eliminates the undesired oxygen gas release.
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