X射线光电子能谱
材料科学
氧气
阴极
氟
锂(药物)
离子
降级(电信)
电子能量损失谱
离子键合
化学工程
表面改性
透射电子显微镜
空位缺陷
扫描透射电子显微镜
扫描电子显微镜
表层
图层(电子)
纳米技术
化学
结晶学
复合材料
物理化学
有机化学
冶金
医学
电信
计算机科学
工程类
内分泌学
作者
Aierxiding Abulikemu,Toshiyuki Matsunaga,Xian Shi,Mukesh Kumar,Neha Thakur,Tsuyoshi Takami,Kentaro Yamamoto,Tomoki Uchiyama,Toshiki Watanabe,Miki Inada,Yoshiharu Uchimoto
标识
DOI:10.1021/acsami.3c11511
摘要
Layered-type Li-rich cathode materials have attracted significant attention for next-generation Li-ion batteries, but the advantage of their high capacity is eclipsed by their poor reversibility upon cycling. Irreversible oxygen redox activity and surface degradation have been deemed as the root cause and direct cause for their poor performance, respectively. We attempted to suppress surface degradation by inserting fluoride ions up to some depth on the surface. By fluorination with NH4HF2 after introducing a significant amount of oxygen vacancies in layered Li1.2Ni0.2Co0.2Mn0.4O2 by using CaH2 as a reducing agent, the reversible capacity reached 268 mAh/g, and the capacity retention after 100 cycles was about 99%. The scanning transmission electron microscopy-electron energy loss spectroscopy (STEM-EELS) technique revealed that, in contrast to directly fluorinated samples, our materials exhibit deeper fluorine signals besides surface signals, and hard X-ray photoelectron spectroscopy (HAXPES) patterns show ionic and covalent fluorine coordination. These results indicate that the combination of oxygen deficiency introduction and surface fluorination allows some F- ions to occupy near-surface oxygen vacancy sites rather than forming only a LiF layer on the surface, suggesting a new strategy to modify cathode materials for lithium-ion batteries.
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