钝化
电解质
扩散
兴奋剂
材料科学
电化学
化学工程
储能
氧化还原
氟
氧气
杂质
离子
纳米技术
电极
图层(电子)
化学
光电子学
冶金
热力学
物理化学
功率(物理)
有机化学
工程类
物理
作者
Hai Lei,Xinwei Cui,Zihao Zeng,Chao Zhu,Wei Sun,Jing Wang,Peng Ge
标识
DOI:10.1002/anie.202414918
摘要
As great potential recycling strategy, the direct regeneration of spent LiCoO2 (LCO) is beneficial for lowering environmental pollutions and promoting global sustainability. However, owing to the using of binder and electrolyte, some fluorine impurities would be remained into spent materials. Considering the doping behaviors of F‐elements, their suitable content introducing would facilitate the energy‐storage abilities of regenerated LCO. Herein, through the tailored introduction of F‐elements, spent LCO are successfully regenerated with physical‐chemical evolutions. Benefitting from the existed oxygen vacancies, the diffusion energy‐barrier of F‐elements is reduced from 1.73 eV to 0.61 eV, facilitating the establishment of gradient F‐doped subsurface, along with the formation of rigid CoO5F. Meanwhile, excess F‐elements (1 wt.%, as a threshold) lead to the formation of LiF passivation layer on the surface. Thus, the as‐optimized sample displays a considerable capacity of 154.4 mAh g‐1 even at 5.0 C, with retention rate (88.3%) in 3.0~4.5V. Supported by detailed electrochemical and kinetic analysis, the structural advantages are confirmed to boost the improved redox activity of Co‐ions and the alleviating of irreversible oxygen‐release. Give this, the work is anticipated to reveal the evolutions of regenerated LCO with the introduced F‐elements, whilst providing the practical regeneration strategies toward excellent high‐voltage properties.
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