TY - JOUR
T1 - Weakly solvating aqueous-based electrolyte facilitated by a soft co-solvent for extreme temperature operations of zinc-ion batteries
AU - Zhang, Ruizhi
AU - Pang, Wei Kong
AU - Vongsvivut, Jitraporn (Pimm)
AU - Yuwono, Jodie A.
AU - Li, Guanjie
AU - Lyu, Yanqiu
AU - Fan, Yameng
AU - Zhao, Yunlong
AU - Zhang, Shilin
AU - Mao, Jianfeng
AU - Cai, Qiong
AU - Liu, Sailin
AU - Guo, Zaiping
PY - 2024/7/7
Y1 - 2024/7/7
N2 - 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.
AB - 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.
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U2 - 10.1039/d4ee00942h
DO - 10.1039/d4ee00942h
M3 - RGC 21 - Publication in refereed journal
SN - 1754-5692
VL - 17
SP - 4569
EP - 4581
JO - Energy and Environmental Science
JF - Energy and Environmental Science
IS - 13
ER -