A Multifunctional Lithium Amide Salt for Circular Battery Recycling
Abstract Electrolyte instability is an intrinsic issue that curtails the cycle life of lithium-ion batteries in energy storage devices. Residual trace moisture inevitably induces LiPF6 hydrolysis, generating aggressive hydrofluoric acid (HF) during cycling, which degrades the cathode-electrolyte interphase (CEI) and accelerates solvent decomposition, thereby decreasing ionic conductivity and escalating interfacial impedance. Herein, we develop a multifunctional lithium trifluoro-N-methylacetamide (LiTFMA) salt to scavenge residual moisture and HF via a thermodynamic mechanism, thereby rejuvenating the ionic conductivity and lithium-ion transference number of degraded electrolytes. Furthermore, TFMA– anions derive a thin and uniform nitrogen-containing CEI, which renovates degraded interphases and suppresses transition-metal dissolution. Consequently, retired NCM811 electrodes remanufactured with the LiTFMA-regenerated electrolyte deliver a capacity retention exceeding 80% after 300 cycles. This dual-functional strategy upcycles hazardous spent electrolytes into high-performance functional components, establishing a scalable pathway toward a circular battery economy.
Authors
- Siru He
- Xuwen Peng (ORCID: https://orcid.org/0009-0006-1535-5877)
- Yang Lu (ORCID: https://orcid.org/0009-0008-0761-5565)
- Wenhui Hou (ORCID: https://orcid.org/0009-0002-6672-9542)
- Kezhuo Li
- Chaoyue Sun
- Kai Liu (ORCID: https://orcid.org/0000-0003-3362-180X)
- Haiyu Zhou
- Yu Ou
- Gang Su
- Zhi Liu
- Lai Wei
- Xiao Ma
- Jia Zhang
- Changjian Li
- Xuan Song
Institutions
- Ministry of Communications (BR)
- III-N Technology (United States) (US)
- South China University of Technology (CN)
- University of South China (CN)
- Tsinghua University (CN)
Publication Details
- Journal
- ACS Energy Letters
- Published
- 2026-09-10
- DOI
- https://doi.org/10.1021/acsenergylett.6c02134
- Primary Topic
- Advanced Battery Materials and Technologies
- Type
- article
- Field-Weighted Citation Impact
- 0.00