材料科学
阴极
兴奋剂
氧化物
锂(药物)
锰
离子
氧化还原
氧气
化学物理
无机化学
分析化学(期刊)
物理化学
冶金
光电子学
色谱法
有机化学
化学
内分泌学
医学
作者
Panawan Vanaphuti,Jianming Bai,Lu Ma,Steven N. Ehrlich,Kim Kisslinger,Feng Wang,Yan Wang
标识
DOI:10.1016/j.ensm.2020.08.003
摘要
Regardless of the prevailing capacity and energy density of lithium, manganese-rich layered oxide (LMR-NMC) cathodes, continuous decay of voltage and overall energy density during cycling hinders this material from commercialization in Li-ion batteries. Although significant work focuses on single doping of Na and F, analysis in portraying the benefit of these ions in diminishing the structural distortion during activation cycle is in doubt. Herein, the effects of co-doping Na and F into the LMR-NMC structure in stabilizing the structure and mitigating oxygen loss during the first cycle are closely examined via in situ x-ray measurements. Na and F co-doping shows a 30% lower degree of Li+/Ni2+ mixing in the Li layer (C2/m structure), 50% reduced Debye-Waller factor of Mn-O bonding, increase reversible TM migration, and faster Li diffusion relative to the pristine material. Due to the utilization of Ni redox chemistry below 4.4 V, less oxygen redox is required for charge compensation at high voltage. This study offers the first instance to quantitatively evaluate the effects of co-doping Na and F in LMR-NMC cathode in order to minimize voltage degradation by altering the local ordering of O3-type structure, which may rationalize strategies to overcome the issues of the material.
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