Regulating electric double layer in non-fluorinated ether electrolyte enables high-voltage and low-temperature lithium metal batteries

The poor oxidation stability of ether-based solvents has long been a major challenge limiting their practical application. To enhance the oxidative stability of ether-based electrolytes, the physicochemical properties of various glycol dimethyl ethers are screened, and diglyme (G2) is selected as the sole solvent for the electrolyte. Lithium bis(fluorosulfonyl)imide (LiFSI), a highly dissociative salt, is used as the primary salt; while lithium nitrate (LiNO 3 ) and lithium difluorophosphate (LiDFP), which have small ionic sizes and strong binding energies, are added as secondary salts. The resulting electrolyte can modulate the electric double layer structure by NO 3 − and DFP − on the cathode side, leading to an increased Li + concentration that is originally repelled by the cathode. Additionally, the oxidation stability of the electrolyte is improved and the formed electrode-electrolyte interphase is more uniform and stable, thereby enhancing the electrochemical performance of the cells. As a result, cells assembled with a total of 1 M ternary lithium salts in G2 solvent can operate at high voltage of 4.4 ​V. The Li||NCM811 ​cells maintain 80.2% capacity retention after 270 cycles at room temperature, with an average Coulombic efficiency of 99.5%, and exhibit 88.4% capacity retention after 200 cycles at −30 ​°C. Due to the small size and high electronegativity of NO 3 − and DFP − , they exhibit a more rapid response to high-voltage cathode compared to FSI − . Consequently, the electric double layer near the cathode is rich in NO 3 − and DFP − . The Li + coordinate with solvent molecules, effectively reducing the concentration of free solvent and enhancing the electrolyte's oxidative stability. • The ternary salts of LiFSI, LiNO 3 and LiDFP can adjust the electric double layer on the cathode side. • The oxidation stability of the electrolyte was improved and electrode-electrolyte interphase was uniform and stable. • The assembled batteries exhibit excellent high-voltage and low-temperature electrochemical performance.

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Publication Details

Journal
Advanced Powder Materials
Published
2025-04-16
DOI
https://doi.org/10.1016/j.apmate.2025.100296
Citations
10
Primary Topic
Advanced Battery Materials and Technologies
Type
article
Field-Weighted Citation Impact
7.30

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Regulating electric double layer in non-fluorinated ether electrolyte enables high-voltage and low-temperature lithium metal batteries

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article

Regulating electric double layer in non-fluorinated ether electrolyte enables high-voltage and low-temperature lithium metal batteries

Renfei Zhao, Yuanhang Gao, Tao Zhang, Anqiang Pan, Renzhi Ma, Xiaohe Liu, Ning Zhang, Gen Chen, Yuelin Li, Zuosu Qin
article en
10 citations

Abstract

The poor oxidation stability of ether-based solvents has long been a major challenge limiting their practical application. To enhance the oxidative stability of ether-based electrolytes, the physicochemical properties of various glycol dimethyl ethers are screened, and diglyme (G2) is selected as the sole solvent for the electrolyte. Lithium bis(fluorosulfonyl)imide (LiFSI), a highly dissociative salt, is used as the primary salt; while lithium nitrate (LiNO 3 ) and lithium difluorophosphate (LiDFP), which have small ionic sizes and strong binding energies, are added as secondary salts. The resulting electrolyte can modulate the electric double layer structure by NO 3 − and DFP − on the cathode side, leading to an increased Li + concentration that is originally repelled by the cathode. Additionally, the oxidation stability of the electrolyte is improved and the formed electrode-electrolyte interphase is more uniform and stable, thereby enhancing the electrochemical performance of the cells. As a result, cells assembled with a total of 1 M ternary lithium salts in G2 solvent can operate at high voltage of 4.4 ​V. The Li||NCM811 ​cells maintain 80.2% capacity retention after 270 cycles at room temperature, with an average Coulombic efficiency of 99.5%, and exhibit 88.4% capacity retention after 200 cycles at −30 ​°C. Due to the small size and high electronegativity of NO 3 − and DFP − , they exhibit a more rapid response to high-voltage cathode compared to FSI − . Consequently, the electric double layer near the cathode is rich in NO 3 − and DFP − . The Li + coordinate with solvent molecules, effectively reducing the concentration of free solvent and enhancing the electrolyte's oxidative stability. • The ternary salts of LiFSI, LiNO 3 and LiDFP can adjust the electric double layer on the cathode side. • The oxidation stability of the electrolyte was improved and electrode-electrolyte interphase was uniform and stable. • The assembled batteries exhibit excellent high-voltage and low-temperature electrochemical performance.

Advanced Powder MaterialsVol. 4(3)
Central South University (CN), National Institute for Materials Science (JP)
National Natural Science Foundation of China, Key Research and Development Program of Hunan Province of China
Affordable and clean energy
Openalex Percentile: Top 3%
Advanced Battery Materials and Technologies
7.30
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