材料科学
尖晶石
表层
化学工程
离子键合
离子
相(物质)
石墨
图层(电子)
氧化还原
纳米技术
复合材料
冶金
化学
有机化学
工程类
作者
Wangyang Ding,Hengyu Ren,Zijian Li,Mingjie Shang,Yongli Song,Wenguang Zhao,Liang Chang,Tianlu Pang,Shenyang Xu,Haocong Yi,Lin Zhou,Hai Lin,Qinghe Zhao,Feng Pan
标识
DOI:10.1002/aenm.202303926
摘要
Abstract Recently, the rock‐salt (RS) phases are utilized to enhance the surface stability of LiCoO 2 (LCO), however, the optimization mechanism still remains vague. Herein, the structure stability of LCO is successfully enhanced via constructing a tough surface RS layer (≈5 nm), namely, the RS‐LCO. This surface RS layer plays a significant role on capturing the migrated lattice O ions upon charging, leading to the progressive phase transition from an inert RS phase to an ionic conductive spinel phase in the surface, and suppresses the bulk H1‐3 separation beyond 4.6 V. As a result, not only the oxygen redox induced side reactions are greatly reduced, but also the Li + ‐ion's transport is significantly promoted. The RS‐LCO/Li cells show a remarkable cycle stability with 89.7% capacity retention after 1000 cycles in 3–4.6 V at current of 1 C (1 C = 200 mA g −1 ), and 81.2% capacity retention after 400 cycles in 3–4.65 V at 1 C. Besides, the RS‐LCO/graphite cells show nearly no capacity decay in 600 cycles in 3–4.55 V at 1 C. This work provides a new insight to understand the role of surface RS phase layer on developing the advanced LCO.
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