Purification–lithiation collaborative regeneration of mixed graphite/LiFePO 4 : building 2D Li + -diffusion channels towards enhanced energy-storage capabilities
Direct regeneration of LiFePO 4 (LFP), as a promising short-process recycling method, has attracted considerable attention. However, spent materials in industry mainly arise from large-scale mechanical dismantling, which is composed of spent graphite, whereas retired graphite constitutes 30% of mixe...
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Veröffentlicht in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2024-10, Vol.12 (40), p.27712-27723 |
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Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Direct regeneration of LiFePO 4 (LFP), as a promising short-process recycling method, has attracted considerable attention. However, spent materials in industry mainly arise from large-scale mechanical dismantling, which is composed of spent graphite, whereas retired graphite constitutes 30% of mixed materials. Owing to the high oxidation temperature of graphite, a relatively high sintering temperature is selected for graphite removal. However, over-calcined LFP pre-oxidized precursors lead to low recovery of the spent phase. Herein, a purification–lithiation collaborative regeneration method is proposed for preparing precursors with high purity. Assisted by a “tailored” reductive carbon, the crystalline phase was recovered. As a Li-storage cathode, the optimized samples displayed an initial capacity of 133.0 mA h g −1 at 1.0C. Even at a current density of 5.0C, optimized samples showed 112.5 mA h g −1 with 100% capacity retention ratio after 500 cycles. Supported by detailed physical–chemical analysis, the rationally introduced Li–Fe anti-sites could induce the construction of two-dimensional Li-diffusion channels, along with enhanced Li-diffusion behaviors. This work is expected to provide guidance of the direct regeneration process of LFP samples with graphite impurities. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/D4TA04717F |