N-Alkyl-N-ethylpyrrolidinium cation-based ionic liquid electrolytes for safer lithium battery systems

TitleN-Alkyl-N-ethylpyrrolidinium cation-based ionic liquid electrolytes for safer lithium battery systems
Publication TypeArticolo su Rivista peer-reviewed
Year of Publication2016
AuthorsMoreno, J.S., Deguchi Y., Panero S., Scrosati B., Ohno H., Simonetti E., and Appetecchi Giovanni Battista
JournalElectrochimica Acta
Volume191
Pagination624-630
ISSN00134686
KeywordsBis(fluorosulfonyl)imide, Bis(trifluoromethane sulfonyl)imide, Electric batteries, Electrochemical stabilities, Electrolytes, Good film forming ability, Ion-transport properties, Ionic liquid electrolytes, Ionic liquids, Ions, Liquids, Lithium, Lithium batteries, Lithium battery system, Lithium compounds, Mixtures, Organic electrolyte, Positive ions, Salts, Secondary batteries
Abstract

The performance of ionic liquid (IL) electrolytes based on N-alkyl-N-ethylpyrrolidinium cations combined with different lithium salts has been used for the design of safer lithium battery systems. These mixtures of ILs, synthesized through an eco-friendly procedure route, and salts were studied and their performance was compared on the basis of anion species. The N-butyl-N-ethylpyrrolidinium bis(fluorosulfonyl)imide/lithium bis(fluorosulfonyl)imide (PYR24FSI-LiFSI) mixture was found to exhibit superior characteristics in terms of ion transport properties even at low temperatures in combination with wide electrochemical stability, feasibility of reversibly plating lithium metal without any reduction of electrolyte and good compatibility with Li anode. These are considered to be due to good film-forming ability of the FSI anion. Conversely, lower thermal stability was also observed. Preliminary tests in lithium/lithium iron phosphate, Li/LiFePO4, half-cells using PYR24FSI-LiFSI as the electrolyte evidenced cycling performance approaching that in organic electrolytes with high capacity retention and efficiency values. © 2016 Elsevier Ltd.

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URLhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84961331541&doi=10.1016%2fj.electacta.2016.01.119&partnerID=40&md5=6f76c33b9890f137a0e15ddd63cc7314
DOI10.1016/j.electacta.2016.01.119