淡出
晶间腐蚀
容量损失
材料科学
衰退
电极
开裂
微晶
电池(电)
动力学
阳极
化学工程
复合材料
阴极
冶金
微观结构
化学
热力学
电信
计算机科学
物理
功率(物理)
解码方法
物理化学
量子力学
工程类
操作系统
作者
Hao Liu,Mark Wolfman,Khim Karki,Young‐Sang Yu,Eric A. Stach,Jordi Cabana,Karena W. Chapman,Peter J. Chupas
出处
期刊:Nano Letters
[American Chemical Society]
日期:2017-05-26
卷期号:17 (6): 3452-3457
被引量:418
标识
DOI:10.1021/acs.nanolett.7b00379
摘要
Capacity fading has limited commercial layered Li-ion battery electrodes to <70% of their theoretical capacity. Higher capacities can be achieved initially by charging to higher voltages, however, these gains are eroded by a faster fade in capacity. Increasing lifetimes and reversible capacity are contingent on identifying the origin of this capacity fade to inform electrode design and synthesis. We used operando X-ray diffraction to observe how the lithiation-delithiation reactions within a LiNi0.8Co0.15Al0.05O2 (NCA) electrode change after capacity fade following months of slow charge-discharge. The changes in the reactions that underpin energy storage after long-term cycling directly correlate to the capacity loss; heterogeneous reaction kinetics observed during extended cycles quantitatively account for the capacity loss. This reaction heterogeneity is ultimately attributed to intergranular fracturing that degrades the connectivity of subsurface grains within the polycrystalline NCA aggregate.
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