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| Hauptseite > Publikationsdatenbank > Interfacial Potentiodynamics of “Water-in-Salt” Electrolytes in Aqueous Lithium-Ion Batteries Using Nonlinear Spectroscopy and Molecular Simulations |
| Hauptseite > Publikationsdatenbank > Interfacial Potentiodynamics of “Water-in-Salt” Electrolytes in Aqueous Lithium-Ion Batteries Using Nonlinear Spectroscopy and Molecular Simulations |
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| Hybrid-OA | 0.00 | 0.00 | EUR | (Publish and Read) | ZB | |
| Sum | 0.00 | 0.00 | EUR | |||
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| Journal Article | FZJ-2025-01924 |
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2024
Soc.
Washington, DC
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Please use a persistent id in citations: doi:10.1021/acs.jpcc.4c04982 doi:10.34734/FZJ-2025-01924
Abstract: The molecular arrangement of the electrode/electrolyte interface is crucial for enlarging the electrochemical stability of “water-in-salt” electrolytes in aqueous lithium-ion batteries. Using in situ vibrational sum-frequency generation (SFG) spectroscopy and molecular dynamics (MD) simulations, we investigated the interfacial structure and molecular orientation of water molecules and anions of a LiTFSI-based “water-in-salt” electrolyte as a function of electrode potential. Shifting the electrode potential from positive to negative values induces significant interfacial changes in the structure of the electrolyte species, transitioning from anion surface excess to a water-rich interface. Furthermore, TFSI anions undergo a conformational change from cis to trans at the interface at positive electrode potentials. The results of comprehensive MD simulations support the experimental observations, demonstrating a potentiodynamic change in the number densities of water molecules, TFSI anions, and Li-ions at the interface accompanied by increasing dihedral angles of TFSI anions at higher positive electrode potentials.
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