Glyme electrolytes are prepared by dissolving sodium trifluoromethane sulfonate (NaCF3SO3) either in dimetoxyethane (DME) or in diethyleneglycoledimethylether (DEGDME). The solutions, designed for sodium battery applications, are thermally characterized by TGA and studied in terms of transport properties by combining pulse field gradient nuclear magnetic resonance (PFG NMR) and electrochemical techniques. Both electrolytes reveal suitable characteristics for sodium batteries, such as ion conductivity of about 10−3 S cm−1, sodium transport number of 0.5, a stable stripping-deposition trend, and electrochemical stability windows extending from 0 to 4 V. However, the more volatile DME leads to a higher ion association degree. The suitability of both electrolytes is then verified in sodium-sulfur cells by cyclic voltammetry and galvanostatic test. The measurements confirm the reversibility of the sodium-sulfur process, and reveal the expected trend of the sulfur electrode in sodium cell with average working voltage of about 1.8 V, with a higher polarization and lower capacity for the cell using the DME-based electrolyte. Accordingly, the DEGDME-based solution appears to be more suitable for sodium battery applications.

Characteristics of glyme electrolytes for sodium battery: nuclear magnetic resonance and electrochemical study / Carbone, Lorenzo; Munoz, Stephen; Gobet, Mallory; Devany, Matthew; Greenbaum, Steve; Hassoun, Jusef. - In: ELECTROCHIMICA ACTA. - ISSN 0013-4686. - 231:(2017), pp. 223-229. [10.1016/j.electacta.2017.02.007]

Characteristics of glyme electrolytes for sodium battery: nuclear magnetic resonance and electrochemical study

Carbone, Lorenzo;Hassoun, Jusef
2017

Abstract

Glyme electrolytes are prepared by dissolving sodium trifluoromethane sulfonate (NaCF3SO3) either in dimetoxyethane (DME) or in diethyleneglycoledimethylether (DEGDME). The solutions, designed for sodium battery applications, are thermally characterized by TGA and studied in terms of transport properties by combining pulse field gradient nuclear magnetic resonance (PFG NMR) and electrochemical techniques. Both electrolytes reveal suitable characteristics for sodium batteries, such as ion conductivity of about 10−3 S cm−1, sodium transport number of 0.5, a stable stripping-deposition trend, and electrochemical stability windows extending from 0 to 4 V. However, the more volatile DME leads to a higher ion association degree. The suitability of both electrolytes is then verified in sodium-sulfur cells by cyclic voltammetry and galvanostatic test. The measurements confirm the reversibility of the sodium-sulfur process, and reveal the expected trend of the sulfur electrode in sodium cell with average working voltage of about 1.8 V, with a higher polarization and lower capacity for the cell using the DME-based electrolyte. Accordingly, the DEGDME-based solution appears to be more suitable for sodium battery applications.
diethyleneglycoledimethyleter; dimetoxyethane; electrochemistry; PFG NMR; sodium battery; sodium triflate
01 Pubblicazione su rivista::01a Articolo in rivista
Characteristics of glyme electrolytes for sodium battery: nuclear magnetic resonance and electrochemical study / Carbone, Lorenzo; Munoz, Stephen; Gobet, Mallory; Devany, Matthew; Greenbaum, Steve; Hassoun, Jusef. - In: ELECTROCHIMICA ACTA. - ISSN 0013-4686. - 231:(2017), pp. 223-229. [10.1016/j.electacta.2017.02.007]
File allegati a questo prodotto
File Dimensione Formato  
Carbone_Glyme-electrolytes_2017.pdf

solo gestori archivio

Tipologia: Versione editoriale (versione pubblicata con il layout dell'editore)
Licenza: Tutti i diritti riservati (All rights reserved)
Dimensione 2.07 MB
Formato Adobe PDF
2.07 MB Adobe PDF   Visualizza/Apri   Richiedi una copia

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1043377
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 28
  • ???jsp.display-item.citation.isi??? 28
social impact