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

Ruizhi Zhang, Wei Kong Pang, Jitraporn (Pimm) Vongsvivut, Jodie A. Yuwono, Guanjie Li, Yanqiu Lyu, Yameng Fan, Yunlong Zhao, Shilin Zhang, Jianfeng Mao, Qiong Cai*, Sailin Liu*, Zaiping Guo*

*Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

127 Citations (Scopus)

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. © 2024 The Royal Society of Chemistry.
Original languageEnglish
Pages (from-to)4569-4581
JournalEnergy and Environmental Science
Volume17
Issue number13
Online published21 May 2024
DOIs
Publication statusPublished - 7 Jul 2024
Externally publishedYes

Funding

This work was financially supported by Australian Research Council Discovery Projects (DP200101862, FL210100050), and grants for observations on the Australian Synchrotron infrared Microspectroscopy beamline (M18527, M18890, M19576), and an Australian Institute of Nuclear Science and Engineering \u2013 Early Career Researcher Grant (AINSE-ECRG) (S.L Liu). The authors gratefully acknowledge the Electron Microscopy Centre at the University of Wollongong for XPS test. The English editing of this manuscript by Dr Tania Silver is also greatly appreciated.

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