Impact of residuals on recovered nickel-rich LiNi1-x-yMnxCoyO2 cathodes for direct recycling and reuse
At present, industrial-scale recycling of lithium-ion batteries typically involves rather energy-intensive processes and toxic solvents to recover, in particular, the metallic elements from the positive electrode active material. These recovered metals subsequently serve as precursors for the synthesis of new electrode materials. One approach to reduce the energy and cost needed is the direct recycling of the electrode active materials. Herein, two recovery methods, namely thermal and solvent-based recovery, are investigated for single-crystalline Ni-rich LiNi 1-x-y Mn x Co y O 2 (NMC) high-energy cathodes. The NMC obtained via the thermal recovery method exhibits poor performance due to the generation of HF and the degradation of the material. In contrast, the NMC obtained via the solvent-based method, utilizing dimethyl sulfoxide as a non-toxic solvent, demonstrates superior performance, with a reduction in capacity of only 1.5 % compared to pristine NMC. This comparative analysis highlights the critical role of the separation procedure and, particularly, the detrimental effect of any remaining fluorinated binder. • Systematic investigation of thermal and solvent-based direct recovery of scrap NMC. • Near-complete removal of the binder and carbon via solvent-based recovery. • Maintenance of the original structure and performance after recovery. • Removal of PVdF residues is a critical parameter for follow-up thermal treatments.
Authors
- Mehrdad Talebi
- J. Kim
- Markus Binder (ORCID: https://orcid.org/0000-0002-6374-3931)
- Dominic Bresser
- Thomas Diemant
Institutions
- Karlsruhe Institute of Technology (DE)
- Universität Ulm (DE)
- Cheongju University (KR)
- Helmholtz-Institute Ulm (DE)
- Technische Hochschule Ulm (DE)
Publication Details
- Journal
- Journal of Power Sources Advances
- Published
- 2026-01-01
- DOI
- https://doi.org/10.1016/j.powera.2025.100200
- Primary Topic
- Extraction and Separation Processes
- Type
- article
- Field-Weighted Citation Impact
- 0.00