High-Voltage and Super-Stable Aqueous Sodium-Zinc Hybrid Ion Batteries Enabled by Double Solvation Structures in Concentrated Electrolyte

被引:40
作者
Ao, Huaisheng [1 ]
Zhu, Weiduo [1 ]
Liu, Mengke [1 ]
Zhang, Wanqun [1 ]
Hou, Zhiguo [1 ]
Wu, Xiaojun [1 ]
Zhu, Yongchun [1 ]
Qian, Yitai [1 ]
机构
[1] Univ Sci & Technol China, Sch Chem & Mat Sci, Hefei Natl Lab Phys Sci Microscale, 96 Jinzhai Rd, Hefei 230026, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
aqueous sodium-zinc ion batteries; co-insertion/extraction mechanism; concentrated aqueous electrolytes; solvation structures; ELECTRICAL ENERGY-STORAGE; WATER; HEXACYANOFERRATE; INTERCALATION; CHALLENGES; ANODE;
D O I
10.1002/smtd.202100418
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Aqueous sodium-zinc hybrid ion batteries are attracting extensive attention due to high energy density, low cost, and environmental friendliness. Unfortunately, there are still some drawbacks associated with the low voltage and cycle performance degradation that limit their practical application. Here, a concentrated aqueous electrolyte with solvation-modulated Zn2+ is reported that reduces the hydrogen evolution reaction on the surface of Zn metal, avoiding the generation of ZnO and uneven deposition. Accordingly, the Zn anode exhibits 1600 h Zn plating/stripping and approximate to 99.96% Coulombic efficiency after 700 cycles. In addition, solvation-modulated Na+ promotes the excellent structural stability of zinc hexacyanoferrate (ZnHCF) due to the rhombohedral-rhombohedral rather than rhombohedral-cubic phase transition. A ZnHCF//Zn full cell delivers an average voltage of 1.76 V and 98% capacity retention after 2000 cycles at 5 C rates.
引用
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页数:9
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