材料科学
阴极
氧化物
化学物理
中尺度气象学
价(化学)
微晶
格子(音乐)
电化学
纳米技术
电极
化学
地质学
冶金
物理
有机化学
物理化学
气候学
声学
作者
Zhichen Xue,Feixiang Wu,Mingyuan Ge,Xiaojing Huang,Yong S. Chu,P. Pianetta,Yijin Liu
出处
期刊:eScience
[Elsevier BV]
日期:2024-02-28
卷期号:4 (4): 100251-100251
被引量:44
标识
DOI:10.1016/j.esci.2024.100251
摘要
Single-crystalline layered oxide materials for lithium-ion batteries are featured by their excellent capacity retention over their polycrystalline counterparts, making them sought-after cathode candidates. Their capacity degradation, however, becomes more severe under high-voltage cycling, hindering many high-energy applications. It is long speculated that the interplay among composition heterogeneity, lattice deformation, and redox stratification could be a driving force for the performance decay. The underlying mechanism, however, is not well-understood. In this study, we use X-ray microscopy to systematically examine single-crystalline NMC particles at the mesoscale. This technique allows us to capture detailed signals of diffraction, spectroscopy, and fluorescence, offering spatially resolved multimodal insights. Focusing on early high-voltage charging cycles, we uncover heterogeneities in valence states and lattice structures that are inherent rather than caused by electrochemical abuse. These heterogeneities are closely associated with compositional variations within individual particles. Our findings provide useful insights for refining material synthesis and processing for enhanced battery longevity and efficiency.
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