Issue 6, 2024

Evaluating the synthesis of Mg[Al(hfip)4]2 electrolyte for Mg rechargeable batteries: purity, electrochemical performance and costs

Abstract

Enhancing the performance of electrolytes stands as one of the key challenges for moving toward practical applications of Mg batteries. Within this work, we investigate different synthesis procedures for the state-of-the-art MgAlhfip electrolyte. The results show that the purity and electrochemical performance of MgAlhfip electrolytes depend on whether they are synthesized from organometallic or inorganic reagents. Additionally, electrolyte properties vary depending on the electrolyte preparation method, either in situ electrolyte formation or salt isolation. To improve electrolyte performance, we explore two approaches: additional salt isolation steps and the use of a scavenging additive. Salt precipitation results in a modest improvement in the coulombic efficiency of Mg plating/stripping, while a scavenging additive significantly reduces overpotentials and enhances coulombic efficiency, especially in electrolytes synthesized from inorganic reagents. Finally, investigated syntheses are evaluated in terms of their practical applicability through procedure complexity and costs of used chemicals. Based on this, we propose a synthesis procedure that strikes a balance between the electrochemical performance of Mg electrolyte and its costs.

Graphical abstract: Evaluating the synthesis of Mg[Al(hfip)4]2 electrolyte for Mg rechargeable batteries: purity, electrochemical performance and costs

Supplementary files

Article information

Article type
Paper
Submitted
19 Oct 2023
Accepted
30 Dec 2023
First published
03 Jan 2024
This article is Open Access
Creative Commons BY license

J. Mater. Chem. A, 2024,12, 3386-3397

Evaluating the synthesis of Mg[Al(hfip)4]2 electrolyte for Mg rechargeable batteries: purity, electrochemical performance and costs

T. Pavčnik, J. Imperl, M. Kolar, R. Dominko and J. Bitenc, J. Mater. Chem. A, 2024, 12, 3386 DOI: 10.1039/D3TA06378J

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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