Interfacial Metal-Solvent Chelation for Direct Regeneration of LiFePO4 Cathode Black Mass

被引:1
作者
Li, Junfeng [1 ,2 ]
Shi, Ruyu [1 ,2 ]
Wang, Junxiong [1 ,2 ]
Cao, Yang [1 ,2 ]
Ji, Haocheng [1 ,2 ]
Tang, Jie [1 ,2 ]
Ji, Guanjun [1 ,2 ]
Chen, Wen [1 ,2 ]
Zhang, Mengtian [1 ,2 ]
Xiao, Xiao [1 ,2 ]
Zhou, Guangmin [1 ,2 ]
机构
[1] Tsinghua Univ, Tsinghua Berkeley Shenzhen Inst, Shenzhen Geim Graphene Ctr, Shenzhen 518055, Peoples R China
[2] Tsinghua Univ, Tsinghua Shenzhen Int Grad Sch, Shenzhen 518055, Peoples R China
基金
中国国家自然科学基金;
关键词
chelation reaction; direct regeneration; spent LiFePO4 cathode black mass; surface reconstruction; LITHIUM-ION BATTERIES; IRON PHOSPHATE BATTERIES; RECOVERY; EFFICIENT; COBALT; ACID;
D O I
10.1002/adma.202414235
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Direct regeneration of spent lithium-ion batteries presents a promising approach to effectively reuse valuable resources and benefit the environment. Unlike controlled laboratory conditions that commonly facilitate impurity purification and minimize structural damage, the LiFePO4 cathode black mass faces significant interfacial challenges, including structure deterioration, cathode-electrolyte interphase residues, and damage from storage procedures, which hinder lithium replenishment and structure regeneration. Here, a metal-solvent chelation reaction using a lithium acetylacetonate solution is introduced to address these challenges under ambient conditions. This method regulates the near-surface structure through strong chelation between Acac(-) anions and Fe (III) elements, thus effectively eliminating the degraded amorphous phase and residual fluorine compounds. By direct lithium connection and reducing diffusion barriers, the reconstructed surface facilitates the re-lithiation process. The regenerated LiFePO4 cathodes demonstrate a capacity retention of 88.5% after 400 cycles at 1 C, while also outperforming traditional recycling methods in terms of environmental and economic benefits. This approach provides a promising solution for regenerating degraded LiFePO4 cathodes from actual dismantled black mass, thereby accelerating the practical application of battery recycling.
引用
收藏
页数:13
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