Sodium ion batteries are on the cusp of being a commercially available technology. Compared to lithium ion batteries, sodium ion batteries can potentially offer an attractive dollar-per-kilowatt-hour value, though at the penalty of reduced energy density. As a materials system, sodium ion batteries present a unique opportunity to apply lessons learned in the study of electrolytes for lithium ion batteries; specifically, the behavior of the sodium ion in an organic carbonate solution and the relationship of ion solvation with electrode surface passivation. In this work the Li⁺ and Na⁺-based solvates were characterized using electrospray mass spectrometry, infrared and Raman spectroscopy, ¹⁷O, ²³Na and pulse field gradient double-stimulated-echo pulse sequence nuclear magnetic resonance (NMR), and conductivity measurements. Spectroscopic evidence demonstrate that the Li⁺ and Na⁺ cations share a number of similar ion-solvent interaction trends, such as a preference in the gas and liquid phase for a solvation shell rich in cyclic carbonates over linear carbonates and fluorinated carbonates. However, quite different IR spectra due to the PF₆^- anion interactions with the Na⁺ and Li⁺ cations were observed and were rationalized with the help of density functional theory (DFT) calculations that were also used to examine the relative free energies of solvates using cluster - continuum models. Ion-solvent distances for Na⁺ were longer than Li⁺, and Na⁺ had a greater tendency towards forming contact pairs compared to Li⁺ in linear carbonate solvents. In tests of hard carbon Na-ion batteries, performance was not well correlated to Na⁺ solvent preference, leading to the possibility that Na⁺ solvent preference may play a reduced role in the passivation of anode surfaces and overall Na-ion battery performance.

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