Journal article
Recyclable Li‐Metal Battery Electrolytes via In Situ Cyclic Carbonate Polymerization
- Abstract:
- Enabling recycling and improving performance are key challenges for next‐generation electrolytes for rechargeable batteries. Here, an equilibrium polymerization: trimethylene carbonate (TMC) ring‐opening polymerization, in the presence of lithium difluoro(oxalato)borate salt, is utilized to form an electrolyte in situ during coin cell fabrication for lithium batteries. This process creates a semi‐solid poly(trimethylene carbonate) electrolyte with high ambient ionic conductivity (0.52 mS cm−1), thermal stability (Td, 5% = 160 °C), and oxidative stability up to 4.7 V. Using this electrolyte with commercial lithium iron phosphate cathodes, results in 97% capacity retention after 350 cycles at 2C, achieving theoretical capacities of 170 mAh g−1 at 0.1C. The cells retain excellent performance at high current densities (86 mAh g−1 at 4C). Post‐use, the polymer can be separated from the salt and selectively recycled to pure starting monomer (TMC) through a solid‐state chemical recycling process. The recycled monomer, when repolymerized to reform the polycarbonate electrolyte, yields cells with performance identical to the original. The exploitation of polymerization‐depolymerization equilibria offers a useful strategy for enhancing battery performance, ensuring effective material recycling, and advancing a circular economy.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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(Preview, Version of record, pdf, 1.7MB, Terms of use)
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- Publisher copy:
- 10.1002/advs.202504206
Authors
- Publisher:
- Wiley
- Journal:
- Advanced Science More from this journal
- Volume:
- 12
- Issue:
- 32
- Article number:
- e04206
- Publication date:
- 2025-06-09
- DOI:
- EISSN:
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2198-3844
- ISSN:
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2198-3844
- Language:
-
English
- Keywords:
- Pubs id:
-
2129209
- Local pid:
-
pubs:2129209
- Source identifiers:
-
3013643
- Deposit date:
-
2025-06-10
- ARK identifier:
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Terms of use
- Copyright date:
- 2025
- Licence:
- CC Attribution (CC BY)
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