高压固态电池用peo基固态电解质稳定性的再评价

Xinsheng Wu, Jay F. Whitacre
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引用次数: 1

摘要

这项工作表明,当与某些类型的高压阴极材料一起使用时,基于peo的固态电解质材料如何比通常预期的更稳定。在测试电池中使用PEO电解质层和LiNixMnyCozO2或LiCoO2正极材料进行动电位和恒流测试。我们发现基于PEO的固态电池的高压不稳定性受到阴极材料界面不稳定性的深刻影响。具体来说,在PEO电解质的存在下,LiCoO2电极经历了不可逆的氧化过程,最终破碎成小块,从而导致容量的快速不可逆损失。相比之下,我们发现peo基固态电解质可以与高镍含量的正极材料(NCM 811、532和111)稳定循环,电池电位高达4.5 V,与Li/Li+相比,在多次循环中容量下降最小;鉴于可能的PEO/阴极界面稳定性概念,这种意想不到的稳定性程度。
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Reevaluating the stability of the PEO-based solid-state electrolytes for high voltage solid-state batteries
This work shows how PEO-based solid state-electrolyte materials can be more stable than commonly expected when used with some types of high voltage cathode materials. Potentiodynamic and galvanostatic tests were performed in test cells using PEO electrolyte layers with either LiNixMnyCozO2 or LiCoO2 cathode materials. We found that the high voltage instability of PEO-based solid-state cells is profoundly affected by the interfacial instability of the cathode material used Specifically, the in the presence of PEO electrolyte, LiCoO2 electrodes were observed to undergo an irreversible oxidation process where they eventually shattered into small pieces, thus leading to a rapid irreversible loss in capacity. In contrast, we found that the PEO-based solid-state electrolytes could be stably cycled with high-nickel content cathode materials (NCM 811, 532, and 111) stably at a cell potential up to 4.5 V vs. Li/Li+ over many cycles with minimal capacity deterioration; this unexpected degree of stability in light of possible PEO/cathode interfacial stability concepts.
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