纳米尺度
材料科学
氧气
比例(比率)
原子单位
化学工程
纳米技术
化学物理
化学
有机化学
量子力学
物理
工程类
作者
Kei Nakayama,Shunsuke Kobayashi,Ryo Ishikawa,Akihide Kuwabara,Yuichi Ikuhara
标识
DOI:10.1021/acs.chemmater.4c02084
摘要
LiCoO 2 is a widely used cathode material in Li-ion batteries, but its practical capacity is limited to about 60% of its theoretical capacity. This limitation occurs because the reversible capacity significantly decreases when more Li ions are extracted. Substantial delithiation leads to oxygen release, which has been regarded as a major factor contributing to capacity fading. However, the associated microstructural changes are not yet sufficiently understood, impeding a thorough comprehension of LiCoO 2 degradation stages. To investigate the final degradation stage, we used scanning/transmission electron microscopy (S/TEM) to examine the microstructure of LiCoO 2 that had undergone irreversible defect formation due to near-surface complete Li removal by a NO 2 BF 4 oxidizer. Our results reveal several types of structural changes occurring sequentially: oxygen release causes Co migration into Li sites, forming a CoO structure. This leads to nanoscale pore formation and lattice expansion, which introduces misfit dislocations at the interface between CoO and the original layered structure. These dislocations, pores, and CoO formation likely disturb Li ion migration by blocking and distorting their pathways, and reducing the number of available Li sites. Consequently, these changes are identified as atomic and nanoscale degradation factors in LiCoO 2 .
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