Semi-liquid configuration of sulfur cell is proposed as simple strategy to develop high-energy lithium battery. Two solutions of Li2S8 in diethylene glycol dimethyl ether (DEGDME), containing either lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) or lithium trifluoromethansulfonate (LiCF3SO3) and lithium nitrate (LiNO3), are studied as catholytes for Li/S cells exploiting the polysulfides electrochemical reaction at about 2.2 V vs. Li+/Li. X-ray photoelectron spectroscopy (XPS) and thermal analyses, respectively, reveal composition and high-temperature stability of the catholyte solutions. Ad hoc study conducted by impedance spectroscopy, voltammetry, and galvanostatic techniques suggests well suitable characteristics in terms of Li+-transport ability, electrochemical stability window, and electrode/electrolyte interphase features. Cells with sulfur loading ranging from about 3 to 6 mg cm−2 into the solution are successfully studied with remarkable performances in terms of current rates, efficiency and cycle life. Hence, the lithium cells based on the catholyte deliver maximum capacity of the order of 1100 mAh gS−1 at C/10 rate and stable capacity of about 800 mAh gS−1 at C/3 rate with Coulombic efficiency exceeding 99%. Therefore, the catholyte solutions studied herein are considered as a very promising candidates for high-energy storage in next generation systems, such as the intriguing hybrid and electric vehicles.

High capacity semi-liquid lithium sulfur cells with enhanced reversibility for application in new-generation energy storage systems

Di Lecce, Daniele
Primo
;
Marangon, Vittorio
Secondo
;
Hassoun, Jusef
Ultimo
2019

Abstract

Semi-liquid configuration of sulfur cell is proposed as simple strategy to develop high-energy lithium battery. Two solutions of Li2S8 in diethylene glycol dimethyl ether (DEGDME), containing either lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) or lithium trifluoromethansulfonate (LiCF3SO3) and lithium nitrate (LiNO3), are studied as catholytes for Li/S cells exploiting the polysulfides electrochemical reaction at about 2.2 V vs. Li+/Li. X-ray photoelectron spectroscopy (XPS) and thermal analyses, respectively, reveal composition and high-temperature stability of the catholyte solutions. Ad hoc study conducted by impedance spectroscopy, voltammetry, and galvanostatic techniques suggests well suitable characteristics in terms of Li+-transport ability, electrochemical stability window, and electrode/electrolyte interphase features. Cells with sulfur loading ranging from about 3 to 6 mg cm−2 into the solution are successfully studied with remarkable performances in terms of current rates, efficiency and cycle life. Hence, the lithium cells based on the catholyte deliver maximum capacity of the order of 1100 mAh gS−1 at C/10 rate and stable capacity of about 800 mAh gS−1 at C/3 rate with Coulombic efficiency exceeding 99%. Therefore, the catholyte solutions studied herein are considered as a very promising candidates for high-energy storage in next generation systems, such as the intriguing hybrid and electric vehicles.
2019
Di Lecce, Daniele; Marangon, Vittorio; Benítez, Almudena; Caballero, Álvaro; Morales, Julián; Rodríguez-Castellón, Enrique; Hassoun, Jusef
File in questo prodotto:
File Dimensione Formato  
03 2019 J Pow Sources High-capacity semi liquid sulfur cell.pdf

solo gestori archivio

Descrizione: versione editoriale
Tipologia: Full text (versione editoriale)
Licenza: NON PUBBLICO - Accesso privato/ristretto
Dimensione 1.99 MB
Formato Adobe PDF
1.99 MB Adobe PDF   Visualizza/Apri   Richiedi una copia
Di Lecce_High capacity semi-liquid lithium sulfur cells AAM.pdf

accesso aperto

Descrizione: post print
Tipologia: Post-print
Licenza: Creative commons
Dimensione 1.69 MB
Formato Adobe PDF
1.69 MB Adobe PDF Visualizza/Apri

I documenti in SFERA 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/11392/2398303
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 22
  • ???jsp.display-item.citation.isi??? 22
social impact