期刊
JOULE
卷 2, 期 7, 页码 1287-1296出版社
CELL PRESS
DOI: 10.1016/j.joule.2018.04.008
关键词
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资金
- TomKat Center for Sustainable Energy
- Anthropocene Institute
- State Grid Corporation of China
- NSF Graduate Research Fellowship through Stanford Energy 3.0 Corporate Affiliate Program
- Stanford Graduate Fellowship through Stanford Energy 3.0 Corporate Affiliate Program
- NSF Graduate Research Fellowship
- Stanford Interdisciplinary Graduate Fellowship
- National Science Foundation [ECCS-1542152]
- Basic Science Research Program through the National Research Foundation of Korea - Ministry of Education [2017R1D1A1B03035336, 2017R1A4A1015022]
Flow batteries are a compelling grid-scale energy storage technology because the stored energy is decoupled from the system power. Aqueous redox flow batteries (RFBs), however, are limited by low open-circuit voltages (OCVs). Replacing the aqueous negative electrolyte (negolyte) with liquid alkali metals-of which Na-K, a room-temperature liquid metal alloy, is attractive-would increase the OCV considerably. However, a suitable solid electrolyte has not been reported for Na-K. Here we show that K-beta ''-alumina is a selective and robust K+ ion conductor in contact with Na-K, to which it is stable with minimal exchange of Na. We report the cycling of cells with OCVs of 3.1-3.4 V employing aqueous and nonaqueous positive electrolytes (posolytes), and power density tests showing promising maximum power densities of 65 mW cm(-2) at 22 degrees C and >100 mW cm(-2) at 57 degrees C, ohmically limited by 330-mu m K-beta ''-alumina membranes. Further development of Na-K vertical bar K-beta ''-alumina batteries could unlock cost-effective energy storage.
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