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Catalytic production of impurity-free V3.5+ electrolyte for vanadium redox flow batteries

The vanadium redox flow battery is considered one of the most promising candidates for use in large-scale energy storage systems. However, its commercialization has been hindered due to the high manufacturing cost of the vanadium electrolyte, which is currently prepared using a costly electrolysis m...

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Bibliographic Details
Published in:Nature communications 2019-09, Vol.10 (1), p.1-9, Article 4412
Main Authors: Heo, Jiyun, Han, Jae-Yun, Kim, Soohyun, Yuk, Seongmin, Choi, Chanyong, Kim, Riyul, Lee, Ju-Hyuk, Klassen, Andy, Ryi, Shin-Kun, Kim, Hee-Tak
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Language:English
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Summary:The vanadium redox flow battery is considered one of the most promising candidates for use in large-scale energy storage systems. However, its commercialization has been hindered due to the high manufacturing cost of the vanadium electrolyte, which is currently prepared using a costly electrolysis method with limited productivity. In this work, we present a simpler method for chemical production of impurity-free V 3.5+ electrolyte by utilizing formic acid as a reducing agent and Pt/C as a catalyst. With the catalytic reduction of V 4+ electrolyte, a high quality V 3.5+ electrolyte was successfully produced and excellent cell performance was achieved. Based on the result, a prototype catalytic reactor employing Pt/C-decorated carbon felt was designed, and high-speed, continuous production of V 3.5+ electrolyte in this manner was demonstrated with the reactor. This invention offers a simple but practical strategy to reduce the production cost of V 3.5+ electrolyte while retaining quality that is adequate for high-performance operations. The vanadium redox flow battery is promising for commercial applications, but is hampered by high-cost electrolytes that are typically prepared via electrolysis. Here the authors demonstrate cost-effective chemical production of a high-quality vanadium electrolyte using platinum nanoparticles as a catalyst.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-019-12363-7