4.8 Article

Structure evolution and energy storage mechanism of Zn3V3O8 spinel in aqueous zinc batteries

Journal

NANOSCALE
Volume 13, Issue 34, Pages 14408-14416

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1nr02347k

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Funding

  1. Stable Support Funding for Universities in Shenzhen [GXWD20201231165807007, 20200807111854001]

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By adjusting the electrolyte concentration and cell voltage range, the electrochemical performance of Zn3V3O8 can be improved, leading to capacity activation and stable cycling performance. The energy storage mechanism in the nano-crystalline spinel involves the co-intercalation of zinc ions and protons with water.
Spinel-type materials are promising for the cathodes in rechargeable aqueous zinc batteries. Herein, Zn3V3O8 is synthesized via a simple solid-state reaction method. By tuning the Zn(CF3SO3)(2) concentration in electrolytes and the cell voltage ranges, improved electrochemical performance of Zn3V3O8 can be achieved. The optimized test conditions give rise to progressive structure evolution from bulk to nano-crystalline spinel, which leads to capacity activation in the first few cycles and stable cycling performance afterward. Furthermore, the energy storage mechanism in this nano-crystalline spinel is interpreted as the co-intercalation of zinc ions and protons with some water. This work provides a new viewpoint of the structure evolution and correlated energy storage mechanism in spinel-type host materials, which would benefit the design and development of next-generation batteries.

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