{"title":"A sustainable delamination approach for simultaneous separation and leaching of cathodes from end-of-life Li ion batteries","authors":"Pietro Cattaneo , Daniele Callegari , Fiorenza D'Aprile , Eliana Quartarone","doi":"10.1016/j.powera.2025.100181","DOIUrl":null,"url":null,"abstract":"<div><div>The increasing demand for Lithium-ion batteries (LIBs) in several applications has led to a substantial rise in their production, posing risks in the supply of critical raw materials (CRM, e.g.: Li, Ni, Co). Additionally, improper disposal of end-of-life batteries can lead to environmental pollution and loss of technological value stressing the necessity for sustainable recycling. Current methods involve shredding batteries into a black mass, further processed via pyrometallurgy (energy-intensive) and/or hydrometallurgy with inorganic acids (environmentally hazardous) to recover CRMs. A more refined approach to LIBs recycling includes the dismantling and the sorting of their components, allowing for a targeted extraction.</div><div>The spent cathodes recycling process here presented involves the simultaneous delamination from the current collector and the leaching (>95 %) of the cathode active material (CAM) in a citric acid solution, enabling also the recovery of Polyvinylidene fluoride (PVDF) and Carbon filler as unleached residues, which can be used as a composite binder for new electrodes manufacturing. Lastly, metals are recovered with high yields (>85 %) as precursors, used to resynthesise fresh CAM and close the recycling loop. To validate the proposed strategy, the recycled CAM was used in a new cathode manufacturing followed by its functional characterization in a half-cell configuration, achieving high coulombic efficiencies (>99.2 %) and satisfying specific capacities upon cycling (initial capacity: 115 mAh g<sup>−1</sup>).</div></div>","PeriodicalId":34318,"journal":{"name":"Journal of Power Sources Advances","volume":"34 ","pages":"Article 100181"},"PeriodicalIF":5.4000,"publicationDate":"2025-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Power Sources Advances","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666248525000150","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
The increasing demand for Lithium-ion batteries (LIBs) in several applications has led to a substantial rise in their production, posing risks in the supply of critical raw materials (CRM, e.g.: Li, Ni, Co). Additionally, improper disposal of end-of-life batteries can lead to environmental pollution and loss of technological value stressing the necessity for sustainable recycling. Current methods involve shredding batteries into a black mass, further processed via pyrometallurgy (energy-intensive) and/or hydrometallurgy with inorganic acids (environmentally hazardous) to recover CRMs. A more refined approach to LIBs recycling includes the dismantling and the sorting of their components, allowing for a targeted extraction.
The spent cathodes recycling process here presented involves the simultaneous delamination from the current collector and the leaching (>95 %) of the cathode active material (CAM) in a citric acid solution, enabling also the recovery of Polyvinylidene fluoride (PVDF) and Carbon filler as unleached residues, which can be used as a composite binder for new electrodes manufacturing. Lastly, metals are recovered with high yields (>85 %) as precursors, used to resynthesise fresh CAM and close the recycling loop. To validate the proposed strategy, the recycled CAM was used in a new cathode manufacturing followed by its functional characterization in a half-cell configuration, achieving high coulombic efficiencies (>99.2 %) and satisfying specific capacities upon cycling (initial capacity: 115 mAh g−1).