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从废旧锂离子电池阴极中选择性提取关键金属:阳离子-阴离子配位和反溶剂结晶

Selective Extraction of Critical Metals from Spent Li-Ion Battery Cathode: Cation-Anion Coordination and Anti-Solvent Crystallization.

作者信息

Lyu Yanqiu, Yuwono Jodie A, Fan Yameng, Li Jingxi, Wang Jingxiu, Zeng Rong, Davey Kenneth, Mao Jianfeng, Zhang Chaofeng, Guo Zaiping

机构信息

School of Chemical Engineering, The University of Adelaide, Adelaide, South Australia, 5005, Australia.

Faculty of Engineering, Institute for Superconducting & Electronic Materials, University of Wollongong, Wollongong, New South Wales, 2522, Australia.

出版信息

Adv Mater. 2024 Jun;36(24):e2312551. doi: 10.1002/adma.202312551. Epub 2024 Mar 26.

Abstract

Owing to continuing global use of lithium-ion batteries (LIBs), in particular in electric vehicles (EVs), there is a need for sustainable recycling of spent LIBs. Deep eutectic solvents (DESs) are reported as "green solvents" for low-cost and sustainable recycling. However, the lack of understanding of the coordination mechanisms between DESs and transition metals (Ni, Mn and Co) and Li makes selective separation of transition metals with similar physicochemical properties practically difficult. Here, it is found that the transition metals and Li have a different stable coordination structure with the different anions in DES during leaching. Further, based on the different solubility of these coordination structures in anti-solvent (acetone), a leaching and separation process system is designed, which enables high selective recovery of transition metals and Li from spent cathode LiNiCoMnO (NCM111), with recovery of acetone. Recovery of spent LiCoO (LCO) cathode is also evidenced and a significant selective recovery for Co and Li is established, together with recovery and reuse of acetone and DES. It is concluded that the tuning of cation-anion coordination structure and anti-solvent crystallization are practical for selective recovery of critical metal resources in the spent LIBs recycling.

摘要

由于锂离子电池(LIBs)在全球范围内持续使用,特别是在电动汽车(EVs)中,因此需要对废旧LIBs进行可持续回收利用。据报道,深共晶溶剂(DESs)作为“绿色溶剂”可实现低成本且可持续的回收利用。然而,由于对DESs与过渡金属(镍、锰和钴)以及锂之间的配位机制缺乏了解,使得实际中难以对具有相似物理化学性质的过渡金属进行选择性分离。在此,研究发现过渡金属和锂在浸出过程中与DES中的不同阴离子具有不同的稳定配位结构。此外,基于这些配位结构在反溶剂(丙酮)中的不同溶解度,设计了一种浸出和分离工艺系统,该系统能够从废旧正极LiNiCoMnO(NCM111)中高选择性地回收过渡金属和锂,并回收丙酮。废旧LiCoO(LCO)正极的回收也得到了证实,实现了对钴和锂的显著选择性回收,同时实现了丙酮和DES的回收与再利用。研究得出结论,阳离子 - 阴离子配位结构的调控和反溶剂结晶对于废旧LIBs回收中关键金属资源的选择性回收具有实际意义。

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