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Direct regeneration has emerged as a pioneering paradigm in green recycling of lithium-ion battery (LIBs) cathode materials, leveraging the inherent atomic and structural advantages of degraded materials. The solution-based regeneration strategy offers significant advantages, particularly in promoting homogeneous lithiation and mitigating the thermal instability of lithium iron phosphate (LFP) materials. However, lithium supplementation for degraded LFP (DLFP) in aqueous solutions is significantly constrained by the narrow electrochemical stability window (ESW) and the limited selection of redox agents. Herein, we propose a promising water-in-salt solution system that enables the spontaneous lithiation of DLFP. This approach not only expands the ESW of the solution but also modifies the lithium solvation structure, facilitating more efficient lithium supplementation. Using the lithium chloride-gallic acid solution as a demonstration, the regenerated cathode materials exhibit excellent electrochemical performance, achieving a specific capacity of 146 mAh g-1 at 1 C with 83% capacity retention after 500 cycles. This research offers critical insights into solution-based lithium supplementation and paves the way for the more efficient recycling of degraded LIBs.
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Jie Tang
Bosi Huang
Xiao Xiao
Journal of the American Chemical Society
Tsinghua University
Tsinghua–Berkeley Shenzhen Institute
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Tang et al. (Thu,) studied this question.
www.synapsesocial.com/papers/69d72a28236f4746d4563be1 — DOI: https://doi.org/10.1021/jacs.5c05384
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