阴极
氧化还原
电化学
材料科学
锂(药物)
动力学
阳离子聚合
氧气
相(物质)
氧化物
离子
无机化学
化学工程
分析化学(期刊)
电极
物理化学
化学
高分子化学
有机化学
内分泌学
物理
冶金
医学
量子力学
工程类
作者
Hung‐Ling Yu,Kassa Belay Ibrahim,Po‐Wei Chi,Yu‐Hsuan Su,Wei‐Tin Chen,Shao‐Chin Tseng,Mau‐Tsu Tang,Chi‐Liang Chen,Horng‐Yi Tang,Chih‐Wen Pao,Kuei‐Hsien Chen,Maw‐Kuen Wu,Heng‐Liang Wu
标识
DOI:10.1002/adfm.202112394
摘要
Abstract Li‐rich layered oxide cathodes with conventional transition metal cation and unique oxygen anion redox reactions deliver high capacities in Li‐ion batteries. However, the oxygen redox process causes the oxygen release, voltage fading/hysteresis, and sluggish electrochemical kinetics, which undermine the performance of these materials. By combining operando quick‐scanning X‐ray absorption spectroscopy with online gas chromatography, the effect of the local electronic structure is elucidated on the reaction mechanism and electrochemical kinetics of Li‐rich cathodes. The local electronic structure of Li‐rich cathodes varies with the excess Li (i.e., Li 2 MnO 3 phase) and Ni contents. Compared to the Li‐rich cathodes with higher amounts of Li 2 MnO 3 phase (high excess lithium content (HLC) cathode), those with lower Li 2 MnO 3 contents (low excess lithium content (LLC) cathode) exhibit reversible anion redox reactions and suppressed voltage hysteresis. The cation oxidation process of LLC cathode is kinetically slower than that of HLC cathode and the cation oxidation potential is shifted, likely due to the local coordination associated with different Li/O ratios. The obtained insights into the effect of local electronic structure on the reaction mechanism and kinetics provide a better understanding and control of Li‐rich cathodes.
科研通智能强力驱动
Strongly Powered by AbleSci AI