Deciphering structural changes in LiNixMnyCozO2 cathodes of Li ion batteries during cycling: Experimental and theoretical investigations

X射线吸收光谱法 插层(化学) 阴极 材料科学 离子 电池(电) 结构变化 分析化学(期刊) 氧化物 电极 化学物理 化学 吸收光谱法 无机化学 物理化学 冶金 热力学 物理 宏观经济学 经济 功率(物理) 有机化学 量子力学 色谱法
作者
N Abharana,Kruti K. Halankar,Velaga Srihari,Brindaban Modak,S. N. Jha,D. Bhattacharyya
出处
期刊:Solid State Ionics [Elsevier BV]
卷期号:398: 116270-116270
标识
DOI:10.1016/j.ssi.2023.116270
摘要

Layered oxide material LiNixMnyCozO2 is emerging out as promising cathode for new generation of Li-ion batteries, especially as power sources for electric vehicles and plug-in hybrid vehicles. In this work, structural and electronic changes occurring in LiNixMnyCozO2 (LNMC) cathode materials during charge/discharge cycle of the battery is studied over a wide composition range using in-situ X-ray diffraction (XRD) and in-situ X-ray absorption spectroscopy (XAS) techniques. While in-situ XRD measurements decipher the overall structural changes during the charging/discharging cycles, in-situ element specific XAS measurements reveal site specific information on electronic and local structural changes. It has been found that for the LNMC samples the major charge compensation at the metal site during charging or Li ion de-intercalation is achieved by oxidation of Ni2+ ions without significant change in the oxidation state of Co or Mn ions. It is also found that local structure around Ni undergoes reversible change during charging and discharging cycles whereas local structure around Co or Mn sites show no significant change. Moreover, it has been found that local structural changes at Ni sites in the samples with higher Ni concentrations are much less compared to that in the samples with lower Ni concentrations during charging/discharging cycles, the result being corroborated by ab-initio theoretical simulations also. This is a new finding and would have significant implications in determining the optimum composition of LNMC electrodes of Li ion batteries for commercial applications.
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