氧化还原
阴极
化学
无机化学
材料科学
氧化物
化学工程
物理化学
冶金
工程类
作者
Xiaohui Rong,Jue Liu,Enyuan Hu,Yijin Liu,Yi Wang,Jinpeng Wu,Xiqian Yu,Katharine Page,Yong‐Sheng Hu,Wanli Yang,Hong Li,Xiao‐Qing Yang,Liquan Chen,Xuejie Huang
出处
期刊:Joule
[Elsevier BV]
日期:2017-11-01
卷期号:2 (1): 125-140
被引量:429
标识
DOI:10.1016/j.joule.2017.10.008
摘要
Anionic redox reaction (ARR) in lithium- and sodium-ion batteries is under hot discussion, mainly regarding how oxygen anion participates and to what extent oxygen can be reversibly oxidized and reduced. Here, a P3-type Na0.6[Li0.2Mn0.8]O2 with reversible capacity from pure ARR was studied. The interlayer O-O distance (peroxo-like O-O dimer, 2.506(3) Å), associated with oxidization of oxygen anions, was directly detected by using a neutron total scattering technique. Different from Li2RuO3 or Li2IrO3 with strong metal-oxygen (M-O) bonding, for P3-type Na0.6[Li0.2Mn0.8]O2 with relatively weak Mn-O covalent bonding, crystal structure factors might play an even more important role in stabilizing the oxidized species, as both Li and Mn ions are immobile in the structure and thus may inhibit the irreversible transformation of the oxidized species to O2 gas.
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