Sorry, you need to enable JavaScript to visit this website.

Molecular environment and enhanced diffusivity of Li+ ions in lithium-salt-doped ionic liquid electrolytes

TitoloMolecular environment and enhanced diffusivity of Li+ ions in lithium-salt-doped ionic liquid electrolytes
Tipo di pubblicazioneArticolo su Rivista peer-reviewed
Anno di Pubblicazione2011
AutoriCastiglione, F., Ragg E., Mele A., Appetecchi Giovanni Battista, Montanino M., and Passerini S.
RivistaJournal of Physical Chemistry Letters
Volume2
Paginazione153-157
ISSN19487185
Parole chiaveActivation energy, Brownian motion, Brownian movement, Coordination shells, Data support, diffusion, Diffusivities, Electrolytes, Heteronuclear, Ionic liquid electrolytes, Ionic liquids, Ions, Li-ion batteries, Lithium, Lithium salts, Molar ratio, Molecular environment, NMR diffusion, Self-diffusion coefficients, Temperature measurement
Abstract

Lithium salts dissolved in ionic liquids (ILs) are interesting alternatives to the commonly used electrolytes for Li-ion batteries. In this study, the solution of Li [bis-(trifluoromethanesulfonyl)imide] (LiTFSI) in N-butyl-N-methylpyrrolidinium TFSI (PYR14TFSI) ionic liquid in the 0.1:0.9 molar ratio is studied by heteronuclear NOE and NMR diffusion measurements. The main purpose is to spot on the interions organization and mobility. NOE data support the existence of strongly coordinated Li+ species, whereas variable temperature measurements of the self-diffusion coefficients D show large, selective, and unexpected enhancement of Li + mobility with T. The measured activation energy for Li+ diffusion is significantly larger than those of TFSI- and PYR 14 +. These findings can be related to the mechanism of Li+ diffusion in ILs based on disruption formation of the coordination shells of Li+ with TFSI anions rather than on the Brownian motion of the whole Li+ coordinated species. © 2011 American Chemical Society.

Note

cited By 61

URLhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-79952919712&doi=10.1021%2fjz101516c&partnerID=40&md5=820e7edd7f04b4e032c6d18523558588
DOI10.1021/jz101516c
Citation KeyCastiglione2011153