Affiliation:
1. School of Physics and Electronics Hunan University Changsha 410082 P. R. China
2. Department of Physics and Astronomy Clemson Nanomaterials Institute Clemson University Clemson SC 29634 USA
3. School of Materials Science and Engineering Central South University Changsha 410083 P. R. China
4. State Key Laboratory of Optoelectronic Materials and Technologies School of Materials Science and Engineering Sun Yat‐sen (Zhongshan) University Guangzhou 510275 P. R. China
5. State Key Laboratory of Advanced Design and Manufacturing for Vehicle Body Hunan University Changsha 410082 P. R. China
Abstract
AbstractAqueous electrolytes are highly important for batteries due to their sustainability, greenness, and low cost. However, the free water molecules react violently with alkali metals, rendering the high‐capacity of alkali‐metal anodes unusable. Here, water molecules are confined in a carcerand‐like network to build quasi‐solid aqueous electrolytes (QAEs) with reduced water molecules' freedom and matched with the low‐cost chloride salts. The formed QAEs possess substantially different properties than liquid water molecules, including stable operation with alkali‐metal anodes without gas evolution. Specifically, the alkali‐metal anodes can directly cycle in a water‐based environment with suppressed growth of dendrites, electrode dissolution, and polysulfide shuttle. Li‐metal symmetric cells achieved long‐term cycling over 7000 h (and over 5000/4000 h for Na/K symmetric cells), and all the Cu‐based alkali‐metal cells exhibited a Coulombic efficiency of over 99%. Full metal batteries, such as Li||S batteries, attained high Coulombic efficiency, long life (over 4000 cycles), and unprecedented energy density among water‐based rechargeable batteries.
Funder
National Natural Science Foundation of China
Subject
Mechanical Engineering,Mechanics of Materials,General Materials Science
Cited by
51 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献