X射线光电子能谱
氧化还原
自行车
阴极
相(物质)
材料科学
固溶体
钌
高原(数学)
电压
分析化学(期刊)
结晶学
化学
化学工程
物理化学
冶金
电气工程
催化作用
考古
生物化学
有机化学
历史
色谱法
数学分析
数学
工程类
作者
M. Sathiya,K. Ramesha,Gwenaëlle Rousse,Dominique Foix,D. Gonbeau,A. S. Prakash,Marie‐Liesse Doublet,K. Hemalatha,Jean‐Marie Tarascon
摘要
Understanding the origin of the high capacity displayed by Li2MnO3–LiMO2 (M = Ni, Co) composites is essential for improving their cycling and rate capability performances. To address this issue, the Li2Ru1–yMnyO3 series between the iso-structural layered end-members Li2MnO3 and Li2RuO3 was investigated. A complete solid solution was found, with the 0.4 ≤ y ≤ 0.6 members showing sustainable reversible capacities exceeding 220 mAh·g–1 centered around 3.6 V vs Li+/Li. The voltage–composition profiles display a plateau on the first charge as compared to an S-type curve on subsequent discharge which is maintained on the following charges/discharges, with therefore a lowering of the average voltage. We show this profile to evolve upon long cycling due to a structural phase transition as deduced from XRD measurements. Finally we demonstrate, via XPS measurements, the oxidation and reduction of ruthenium (Ru5+/Ru4+) during cycling together with a partial activity of the Mn4+/Mn3+ redox couple. Moreover, we provide direct evidence for the reversibility of the O2– → O– anionic process upon cycling, hence accounting for the high capacity displayed by these materials. This work, by capturing the main redox processes pertaining to these materials, should facilitate their development.
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