Abstract
Using one waste to upgrade another through a simple process is a promising strategy for the circular economy. Herein, spent batteries are upgraded using per- and polyfluoroalkyl substances (PFAS) via a one-pot mechanochemical route without involving any solvents, gases, byproducts, or heating. A facile ball-milling process drives the cleavage of strong C─F bonds in PFAS while simultaneously enabling the selective fluoridation of inactive FePO4 in spent lithium-iron phosphate (LFP-Spe). The newly formed FeF2, together with the unreacted lithium-iron phosphate (LFP), delivers an impressive capacity of 307.3 mAh g−1 at 1C, far exceeding the theoretical capacity of LFP (169.8 mAh g−1, 1 e) and surpassing the one-electron theoretical capacity of FeF2 (285 mAh g−1). Meanwhile, carbon derived from PFAS forms an in situ conductive coating on the composite surface, which enables the cathode to retain 92.7% of its initial capacity after 1000 cycles at 5C. Additionally, mechanochemically activated carbon appears to provide a reducing environment and to participate in partial interfacial coupling with phosphate-containing species. This work shows that solid‑state nanoarchitectonics can serve as a promising route to construct functional electrode architectures directly from multiple wastes, offering a new upcycling direction that turns different wastes into wealth.
| Original language | English |
|---|---|
| Journal | Advanced Energy Materials |
| DOIs | |
| State | Accepted/In press - 2026 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
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SDG 8 Decent Work and Economic Growth
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SDG 12 Responsible Consumption and Production
Keywords
- PFAS
- green synthesis
- mechanochemistry
- nanocomposites
- spent battery
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