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Lithium metal batteries promise higher energy densities than current lithium-ion batteries but require novel electrolytes to extend their cycle life. Fluorinated solvents help stabilize the solid electrolyte interphase (SEI) with lithium metal, but are believed to have weaker solvation ability compared to their nonfluorinated counterparts and are deemed ‘poorer electrolytes’. In this work, we synthesize tris(2-fluoroethyl) borate (TFEB) as a new fluorinated borate ester solvent and show that TFEB unexpectedly has higher lithium salt solubility than its nonfluorinated counterpart (triethyl borate). Through experiments and simulations, we show that the partially fluorinated –CH2F group acts as the primary coordination site that promotes lithium salt dissolution. TFEB electrolyte has a higher lithium transference number and better rate capability compared to methoxy polyethyleneglycol borate esters reported in the literature. In addition, TFEB supports compact lithium deposition morphology, high lithium metal Coulombic efficiency, and stable cycling of lithium metal/LiFePO4 cells. This work ushers in a new electrolyte design paradigm where partially fluorinated moieties enable salt dissolution and can serve as primary ion coordination sites for next-generation electrolytes.
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Probing the Influence of Steric Hindrance in Nonfluorinated Ether Electrolytes for Lithium Metal Batteries
Lithium metal batteries (LMBs), especially “anode-free“ LMBs, promise much higher energy density than current lithium-ion batteries but suffer from poor capacity retention. While novel electrolytes have been designed to extend cycle life in anode free LMBs, most of them contain a high fraction of fluorinated solvents or diluents that may cause environmental concerns. Herein, we report the design and synthesis of a group of nonfluorinated ether solvents (termed xME solvents). By substituting the methyl terminal group of 1,2-dimethoxy ethane (DME) with different alkyl groups, the solvation power of xME solvents was tuned to be weaker, leading to more ion pairing in electrolyte solvation structure. In anode free type Cu/LiFePO4(Cu/LFP) cells, xME electrolytes in general show better capacity retention than DME-based electrolyte. Some xME electrolytes also show better oxidative stability than DME against aluminum and LiNi0.8Mn0.1Co0.1O2(NMC811) electrodes. While the general improvement in LMB cycle life and oxidative stability can be attributed to more ion pairing, the local variation within xME electrolytes indicates other factors are also important. Our work proposes a molecular design strategy to fine-tune ion solvation structure of nonfluorinated ether electrolytes for LMBs.
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- PAR ID:
- 10565608
- Publisher / Repository:
- Journal of Electrochemical Society
- Date Published:
- Journal Name:
- Journal of The Electrochemical Society
- Volume:
- 171
- Issue:
- 12
- ISSN:
- 0013-4651
- Page Range / eLocation ID:
- 120536
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript
- Journal Article:
- https://doi.org/10.1149/1945-7111/ad9cca
