Affiliation:
1. College of Environment and Materials Engineering Yantai University Yantai 264005 China
2. Key Laboratory for Palygorskite Science and Applied Technology of Jiangsu Province Huaiyin Institute of Technology Huai'an 223003 China
3. Department of Materials Science and Engineering Shanghai University Shanghai 200444 China
4. Key Laboratory of Comprehensive and Highly Efficient Utilization of Salt Lake Resources Qinghai Institute of Salt Lakes Chinese Academy of Sciences Xining 810008 China
Abstract
AbstractAs one of promising candidates for large‐scale energy‐storage systems, Zn‐I2 aqueous battery exhibits multifaceted advantages including low cost, high energy/powder density, and intrinsic operational safety, but also suffers from fast self‐discharge and short cycle/shelf lifespan associating with I3− shuttle, Zn dendrite growth, and corrosion. In this paper, the battery's self‐discharge rate is successfully suppressed down to an unprecedent level of 17.1% after an ultralong shelf‐time of 1 000 h (i.e., 82.9% capacity retention after 41 days open‐circuit storage), by means of manipulating solvation structures of traditional ZnSO4 electrolyte via simply adjusting electrolyte concentration. Better yet, the optimized 2.7 m ZnSO4 electrolyte further prolongs the cycle lifespan of the battery up to >10 000 and 43 000 cycles at current density of 1 and 5 A g−1, respectively, thanks to the synthetic benefits from reduced free water content, modified solvation structure and lowered I2 dissolution in the electrolyte. With both long lifespan and ultralow self‐discharge, this reliable and affordable Zn‐I2 battery may provide a feasible alternative to the centuries‐old lead‐acid battery.
Funder
National Natural Science Foundation of China
Shanghai Municipal Education Commission
Chinese Academy of Sciences
Natural Science Foundation of Shandong Province
Subject
Biomaterials,Biotechnology,General Materials Science,General Chemistry
Cited by
12 articles.
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