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

被引:43
|
作者
Zhang, Ruizhi [1 ,2 ,3 ]
Pang, Wei Kong [2 ]
Vongsvivut, Jitraporn [4 ]
Yuwono, Jodie A. [1 ]
Li, Guanjie [1 ]
Lyu, Yanqiu [1 ]
Fan, Yameng [2 ]
Zhao, Yunlong [5 ]
Zhang, Shilin [1 ]
Mao, Jianfeng [1 ]
Cai, Qiong [3 ]
Liu, Sailin [1 ]
Guo, Zaiping [1 ]
机构
[1] Univ Adelaide, Sch Chem Engn, Adelaide, SA 5005, Australia
[2] Univ Wollongong, Inst Superconducting & Elect Mat, Wollongong, NSW 2500, Australia
[3] Univ Surrey, Sch Chem & Chem Engn, Guildford GU2 7XH, Surrey, England
[4] Australian Nucl Sci & Technol Org, Australian Synchrotron, Clayton, Vic 3168, Australia
[5] Imperial Coll London, Dyson Sch Design Engn, London SW7 2BX, England
基金
澳大利亚研究理事会;
关键词
CATHODE; GROWTH; DESIGN; OXIDE;
D O I
10.1039/d4ee00942h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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 degrees C to 60 degrees C). The Zn//KV12O30-y<middle dot>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 degrees C and 86.5% for 1200 cycles (5.0 A g-1) at 60 degrees C, respectively. This work optimizes interface chemistry and temperature adaptability of AZIBs, offering guidance for designing weakly solvating aqueous-based electrolytes towards practical application. The weakly solvating electrolyte achieves optimized interface chemistry and good temperature adaptability for aqueous zinc ion batteries.
引用
收藏
页码:4569 / 4581
页数:13
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