Abstract

We report an aqueous Zn–V2O5 battery chemistry employing commercial V2O5 cathode, Zn anode, and 3 M Zn(CF3SO3)2 electrolyte. We elucidate the Zn-storage mechanism in the V2O5 cathode to be that hydrated Zn2+ can reversibly (de)intercalate through the layered structure. The function of the co-intercalated H2O is revealed to be shielding the electrostatic interactions between Zn2+ and the host framework, accounting for the enhanced kinetics. In addition, the pristine bulk V2O5 gradually evolves into porous nanosheets upon cycling, providing more active sites for Zn2+ storage and thus rendering an initial capacity increase. As a consequence, a reversible capacity of 470 mAh g–1 at 0.2 A g–1 and a long-term cyclability with 91.1% capacity rentention over 4000 cycles at 5 A g–1 are achieved. The combination of the good battery performance, safety, scalable materials synthesis, and facile cell assembly indicates this aqueous Zn–V2O5 system is promising for stationary grid storage applications.

Keywords

CathodeAqueous solutionAnodeIntercalation (chemistry)Materials scienceChemical engineeringBattery (electricity)Energy storageElectrolyteElectrodeInorganic chemistryChemistryPhysical chemistry

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Year
2018
Type
article
Volume
3
Issue
6
Pages
1366-1372
Citations
989
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Ning Zhang, Yang Dong, Ming Jia et al. (2018). Rechargeable Aqueous Zn–V<sub>2</sub>O<sub>5</sub> Battery with High Energy Density and Long Cycle Life. ACS Energy Letters , 3 (6) , 1366-1372. https://doi.org/10.1021/acsenergylett.8b00565

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DOI
10.1021/acsenergylett.8b00565