LiF as a crack/defect healer and structural stabilizer for the spent lithium cobalt oxide

IF 20.2 1区 材料科学 Q1 CHEMISTRY, PHYSICAL Energy Storage Materials Pub Date : 2025-02-01 DOI:10.1016/j.ensm.2025.104006
Yongsheng Ji , Dan Yang , Yan Li , Maxim Avdeev , Wang Hay Kan , Mengyi Liao , Zhenyan Zhang , Weichen Du , Xinpeng Pi , Chaofan Liang , Zhou Fang , Xiaoqun Qi , Lan Xue , Renyuan Zhang , Long Qie , Yunhui Huang
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Abstract

The proliferation of lithium-ion batteries results in a substantial accumulation of spent batteries. Traditional pyrometallurgical and hydrometallurgical processes require significant energy inputs, involve the use of hazardous chemicals, and generate large amounts of pollutants, making them inefficient for the economic or environmental recycling of spent batteries. For the spent lithium cobalt oxide (LCO) cathodes, which lose electrochemical activity due to the structural damage, we demonstrated that LiF could serve as both a crack/defect healer to repair the damaged structure and a structural stabilizer to consolidate the electrode/electrolyte interface and the reversibility of phase transitions. The density functional theory calculations revealed the presence of F atoms in the U-LCO crystal leads to a widened energy separation between the Co 3d and O 2p orbitals, such an alteration effectively suppresses the activity of lattice oxygen and stabilizes the structure of U-LCO. The as-upcycled LCO cathode demonstrates significantly improved stability with an impressive capacity retention of 81.6 % after 260 cycles, surpassing those of the pristine LCO (62.3 %) and normally regenerated LCO (35.6 %). Moreover, the recycling process only involves a solid sintering procedure, leading to a reduced carbon footprint by 73.1 % and 64.1 %, and increased benefits by 62.2 % and 47.7 %, as compared with the pyro and hydro methods, respectively. The as-proposed upcycling strategy provides a practical and efficient solution for the closed-loop development of LCO batteries.

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LiF作为废钴酸锂裂纹/缺陷修复剂和结构稳定剂
锂离子电池的激增导致了废电池的大量积累。传统的火法冶金和湿法冶金工艺需要大量的能源投入,涉及使用危险化学品,并产生大量污染物,使其在经济或环境回收废电池方面效率低下。对于由于结构损伤而失去电化学活性的废锂钴氧化物(LCO)阴极,我们证明了LiF既可以作为裂纹/缺陷修复剂修复受损结构,又可以作为结构稳定剂巩固电极/电解质界面和相变的可逆性。密度泛函理论计算表明,在U-LCO晶体中,F原子的存在导致Co 3d和O 2p轨道之间的能量间隔变宽,这种改变有效地抑制了晶格氧的活性,稳定了U-LCO的结构。升级后的LCO阴极在260次循环后的容量保持率为81.6%,超过了原始LCO(62.3%)和正常再生的LCO(35.6%)。此外,回收过程只涉及固体烧结过程,与热法和水法相比,碳足迹分别减少了73.1%和64.1%,效益分别提高了62.2%和47.7%。提出的升级回收策略为LCO电池的闭环开发提供了一种实用高效的解决方案。
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文献相关原料
公司名称
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阿拉丁
Dimethyl carbonate
阿拉丁
Lithium carbonate
阿拉丁
Lithium fluoride
阿拉丁
N-methyl pyrrolidone
来源期刊
Energy Storage Materials
Energy Storage Materials Materials Science-General Materials Science
CiteScore
33.00
自引率
5.90%
发文量
652
审稿时长
27 days
期刊介绍: Energy Storage Materials is a global interdisciplinary journal dedicated to sharing scientific and technological advancements in materials and devices for advanced energy storage and related energy conversion, such as in metal-O2 batteries. The journal features comprehensive research articles, including full papers and short communications, as well as authoritative feature articles and reviews by leading experts in the field. Energy Storage Materials covers a wide range of topics, including the synthesis, fabrication, structure, properties, performance, and technological applications of energy storage materials. Additionally, the journal explores strategies, policies, and developments in the field of energy storage materials and devices for sustainable energy. Published papers are selected based on their scientific and technological significance, their ability to provide valuable new knowledge, and their relevance to the international research community.
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