氧化还原
锂(药物)
阴极
氧气
阳离子聚合
材料科学
降级(电信)
化学物理
化学工程
化学
计算机科学
物理化学
高分子化学
内分泌学
工程类
医学
电信
有机化学
冶金
作者
Ho‐Young Jang,Donggun Eum,Jiung Cho,Jun Lim,Ye‐Ji Lee,Jun‐Hyuk Song,Hyeokjun Park,Byunghoon Kim,Dohoon Kim,Sung‐Pyo Cho,Sugeun Jo,Jaehoon Heo,Sunyoung Lee,Jongwoo Lim,Kisuk Kang
标识
DOI:10.1038/s41467-024-45490-x
摘要
Abstract O2-type lithium-rich layered oxides, known for mitigating irreversible transition metal migration and voltage decay, provide suitable framework for exploring the inherent properties of oxygen redox. Here, we present a series of O2-type lithium-rich layered oxides exhibiting minimal structural disordering and stable voltage retention even with high anionic redox participation based on the nominal composition. Notably, we observe a distinct asymmetric lattice breathing phenomenon within the layered framework driven by excessive oxygen redox, which includes substantial particle-level mechanical stress and the microcracks formation during cycling. This chemo-mechanical degradation can be effectively mitigated by balancing the anionic and cationic redox capabilities, securing both high discharge voltage (~ 3.43 V vs . Li/Li + ) and capacity (~ 200 mAh g −1 ) over extended cycles. The observed correlation between the oxygen redox capability and the structural evolution of the layered framework suggests the distinct intrinsic capacity fading mechanism that differs from the previously proposed voltage fading mode.
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