Issue 7, 2020, Issue in Progress

Redox-active glyme–Li tetrahalogenoferrate(iii) solvate ionic liquids for semi-liquid lithium secondary batteries

Abstract

Solvate ionic liquids (SILs), comprising long-lived, Li solvate cations and counter anions, serve as highly Li-ion-conductive and non-flammable electrolytes for use in lithium secondary batteries. In this work, we synthesized a series of novel redox-active glyme(oligoether)–Li salt-based SILs, consisting of a symmetric ([Li(G3)]+) or asymmetric ([Li(G3Bu)]+) triglyme–Li salt complex and redox-active tetrahalogenoferrate ([FeX] (X = Br4, Cl3Br, Cl4)), for use as the catholyte in semi-liquid lithium secondary batteries. The successful formation of stable molten complexes of [Li(G3/G3Bu)][FeX] was confirmed by Raman spectroscopy and thermogravimetry. The melting point (Tm) depended on both the molecular weights of the complex anions and the structures of the complex cations. [Li(G3)][FeCl4] comprised complex cations with a symmetric structure, and the smallest complex anions showed the lowest Tm of 28.2 °C. The redox properties of the [FeX]/[FeX]2− couple strongly suggested the suitability of [Li(G3/G3Bu)][FeX] as a catholyte. The discharge capacities of semi-liquid lithium secondary batteries utilizing the [Li(G3/G3Bu)][FeX] catholyte depended on the structure of the SILs, and the cell with [Li(G3)][FeCl4] showed the highest capacity with relatively good capacity retention. This study confirmed the feasibility of the glyme-based redox-active SILs as catholytes for scalable redox-flow type batteries.

Graphical abstract: Redox-active glyme–Li tetrahalogenoferrate(iii) solvate ionic liquids for semi-liquid lithium secondary batteries

Supplementary files

Article information

Article type
Paper
Submitted
04 Dec 2019
Accepted
17 Jan 2020
First published
24 Jan 2020
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2020,10, 4129-4136

Redox-active glyme–Li tetrahalogenoferrate(III) solvate ionic liquids for semi-liquid lithium secondary batteries

Y. Kemmizaki, Y. Katayama, H. Tsutsumi and K. Ueno, RSC Adv., 2020, 10, 4129 DOI: 10.1039/C9RA10149G

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