Solvation behavior of carbonate-based electrolytes in sodium ion batteries. Issue 1 (5th December 2016)

• Record Type: Journal Article
• Authors: Cresce, Arthur V.; Russell, Selena M.; Borodin, Oleg; Allen, Joshua A.; Schroeder, Marshall A.; Dai, Michael; Peng, Jing; Gobet, Mallory P.; Greenbaum, Steven G.; Rogers, Reginald E.; Xu, Kang
• Is Part Of: Physical chemistry chemical physics. Volume 19:Issue 1(2017)
• Page Start: 574
• Page End: 586
• Publication Date: 2016-12-05
• Subjects: Chemistry, Physical and theoretical -- Periodicals; 541.3
• DOI: 10.1039/c6cp07215a
• Languages: English
• ISSNs: 1463-9076

Abstract

Abstract : Sodium ion batteries are on the cusp of being a commercially available technology. Abstract : 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, 17 O, 23 Na 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.