原子单位
材料科学
相(物质)
容量损失
钴
位错
降级(电信)
化学物理
粒子(生态学)
化学
电极
复合材料
地质学
物理化学
冶金
电解质
海洋学
物理
电信
有机化学
量子力学
计算机科学
作者
Chunyang Wang,Rui Zhang,Kim Kisslinger,Huolin L. Xin
出处
期刊:Nano Letters
[American Chemical Society]
日期:2021-04-06
卷期号:21 (8): 3657-3663
被引量:40
标识
DOI:10.1021/acs.nanolett.1c00862
摘要
LiNiO2 and cobalt-free ultrahigh-Ni content cathodes suffer from rapid capacity loss and severe chemomechanical degradation, especially when operated at high voltages. Here, by cycling LiNiO2 up to 4.7 V, we report the atomic-scale observation of O1 faulted phase-induced deactivation of LiNiO2. We find that, although a thin layer of the O3 phase forms on the particle surface by reversible O3 → O1 transformation during discharge, the bulk interior still maintains the O1 faulted phase, leading to rapid capacity loss of LiNiO2. Moreover, the atomic configuration of the O1/O3 interface is investigated comprehensively. We reveal that the misfit along the c axes of the O1 and O3 phases results in the formation of misfit dislocations, whereby cation mixing is promoted at the dislocation cores. A transition zone with continuous shear along the a–b plane is uncovered between the O1 and O3 phases for the first time. Besides, severe oxygen loss-induced pore formation and concurrent rock salt transformation are also identified.
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