氧化还原
化学
氧气
过渡金属
阳离子聚合
析氧
催化作用
电化学
无机化学
物理化学
电极
高分子化学
生物化学
有机化学
作者
Zengqing Zhuo,Kehua Dai,Jinpeng Wu,Liang Zhang,Nobumichi Tamura,Yi‐De Chuang,Jun Feng,Jinghua Guo,Zhi‐Xun Shen,Gao Liu,Feng Pan,Wanli Yang
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2021-09-03
卷期号:6 (10): 3417-3424
被引量:50
标识
DOI:10.1021/acsenergylett.1c01101
摘要
Li2MO3 (M = transition metal) systems are parent compounds of Li-rich materials and widely considered to offer oxygen redox for high-energy batteries. However, recent clarifications have revealed that, among the three representative Li2MO3 (M = Mn, Ru, Ir) compounds, no reversible oxygen redox takes place in the Mn and Ir systems. Here, we reevaluate the redox reactions in Li2RuO3 through advanced spectroscopy, which shows both Ru redox and highly reversible O redox (96% initial-cycle reversibility, 80% retained after 10 cycles, and 77% after 50 cycles). This is in sharp contrast with the Li2MnO3 and Li2IrO3 systems and concludes the three distinct oxygen behaviors in the Li2MO3 systems during charging: (i) only irreversible oxygen oxidation in Li2MnO3; (ii) reversible Ru and O redox in Li2RuO3; (iii) only cationic redox in Li2IrO3. This work suggests the critical role of transition metals and their coupling to oxygen for maintaining reversible oxygen redox activities for high-energy batteries.
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