Weakly solvating aqueous-based electrolyte facilitated by a soft co-solvent for extreme temperature operations of zinc-ion batteries

Publication Name

Energy and Environmental Science

Abstract

The aqueous zinc-ion battery (AZIB) is a promising option for grid-scale energy storage, but it faces challenges from parasitic water-related reactions and limited operational temperature range. Replacing H2O molecules in the solvation sheath of Zn2+ with strongly solvating co-solvents can effectively suppress water-related side reactions. However, the excessive Zn2+-co-solvent interaction can cause a large activation energy of desolvation (Ea) and the decomposition of the co-solvent may introduce non-ionic conductive solid electrolyte interphase (SEI) species. Hence, we propose a weakly solvating electrolyte that adopts diethylene glycol dimethyl ether (G2) as a soft co-solvent. The G2 has a moderate Gutmann donor number (19 kcal mol−1) and a low dielectric constant (7.4), which reduces the presence of water in the solvation sheath and enhances Zn2+-anion interaction. This electrolyte achieves an optimal Ea and a robust anion-derived SEI (ZnS-ZnSO3-ZnF2) on the zinc anode, allowing highly reversible Zn plating/stripping for over 7500 hours. The strong G2-H2O interaction enables G2 to bind free H2O and reconstruct the hydrogen bond network, which prevents water decomposition and widens the electrolyte's operational temperature range (−60 °C to 60 °C). The Zn//KV12O30−y·nH2O (KVOH) full battery delivers a high-capacity retention of 91.2% following 8000 cycles at 5.0 A g−1 at room temperature. It also achieves capacity retention of 82.9% over 4000 cycles (0.1 A g−1) at −45 °C and 86.5% for 1200 cycles (5.0 A g−1) at 60 °C, respectively. This work optimizes interface chemistry and temperature adaptability of AZIBs, offering guidance for designing weakly solvating aqueous-based electrolytes towards practical application.

Open Access Status

This publication is not available as open access

Funding Number

M19576

Funding Sponsor

Australian Institute of Nuclear Science and Engineering

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Link to publisher version (DOI)

http://dx.doi.org/10.1039/d4ee00942h