尖晶石
材料科学
阴极
过渡金属
氧化物
同步加速器
八面体
相变
兴奋剂
化学工程
降级(电信)
相(物质)
金属
化学物理
晶体结构
结晶学
光电子学
冶金
化学
物理化学
热力学
计算机科学
电信
工程类
催化作用
物理
有机化学
生物化学
核物理学
作者
Yameng Fan,Emilia Olsson,Bernt Johannessen,Anita M. D’Angelo,Lars Thomsen,Bruce C. C. Cowie,L. A. Smillie,Gemeng Liang,Yaojie Lei,Guyue Bo,Yunlong Zhao,Wei Kong Pang,Qiong Cai,Zaiping Guo
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-01-19
卷期号:9 (2): 487-496
被引量:9
标识
DOI:10.1021/acsenergylett.3c02509
摘要
The irreversible migration of transition metals is a primary issue, resulting in detrimental structural changes and poor battery performance in Li-rich layered oxide (LLO) cathodes. Herein, we propose that manipulating the migration of transition metals between octahedral and tetrahedral sites effectively inhibits undesirable phase transitions by stabilizing the delithiated structure of LLOs at high potential. This is demonstrated by introducing Cr into the Co-free LLO, Li1.2Ni0.2Mn0.6O2. A new spinel-like phase, accompanied by significant lattice variation, was observed in the heavily cycled Co-free LLO at high potential by using operando synchrotron characterizations. Benefiting from a well-maintained solid-solution reaction after long-term cycling, Cr-doped Li1.2Ni0.2Mn0.6O2 delivers up to 99% of its initial discharge capacity after 200 cycles at 1C (∼200 mAh g–1), far surpassing the pristine material (∼74%). The work provides valuable insights into the structural degradation mechanisms of LLOs and underscores the importance of stabilizing the delithiated structure at high potential.
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