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用于磷酸铁锂正极黑粉直接再生的界面金属-溶剂螯合作用

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

作者信息

Li Junfeng, Shi Ruyu, Wang Junxiong, Cao Yang, Ji Haocheng, Tang Jie, Ji Guanjun, Chen Wen, Zhang Mengtian, Xiao Xiao, Zhou Guangmin

机构信息

Shenzhen Geim Graphene Center, Tsinghua-Berkeley Shenzhen Institute & Tsinghua Shenzhen International Graduate School, Tsinghua University, Shenzhen, 518055, China.

出版信息

Adv Mater. 2025 Feb;37(5):e2414235. doi: 10.1002/adma.202414235. Epub 2024 Dec 4.

Abstract

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 LiFePO 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 LiFePO 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 LiFePO cathodes from actual dismantled black mass, thereby accelerating the practical application of battery recycling.

摘要

废旧锂离子电池的直接再生是一种有效回收宝贵资源并造福环境的很有前景的方法。与通常有利于杂质提纯并使结构损伤最小化的受控实验室条件不同,磷酸铁锂正极黑粉面临着重大的界面挑战,包括结构劣化、正极-电解质界面残留物以及储存过程造成的损伤,这些都阻碍了锂的补充和结构再生。在此,引入了一种使用乙酰丙酮锂溶液的金属-溶剂螯合反应,以在环境条件下应对这些挑战。该方法通过Acac阴离子与Fe(III)元素之间的强螯合作用来调节近表面结构,从而有效消除降解的非晶相和残留的氟化合物。通过直接锂连接和减少扩散障碍,重建的表面促进了再嵌锂过程。再生的磷酸铁锂正极在1C下循环400次后容量保持率为88.5%,同时在环境和经济效益方面也优于传统回收方法。这种方法为从实际拆解的黑粉中再生降解的磷酸铁锂正极提供了一种很有前景的解决方案,从而加速了电池回收的实际应用。

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