Synthesis of polycrystalline K0.25V2O5 nanoparticles as cathode for aqueous zinc-ion battery
Polycrystalline K0.25V2O5 nanoparticles have been synthesized and evaluated as cathode for aqueous zinc-ion batteries, which demonstrates excellent Zn2+ storage capability. As elucidated, a high capacity of 306 mA h g−1, excellent rate capability of 5 A g−1 and long-term cyclic stability up to 500 c...
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Published in | Journal of alloys and compounds Vol. 801; pp. 82 - 89 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Lausanne
Elsevier B.V
15.09.2019
Elsevier BV |
Subjects | |
Online Access | Get full text |
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Summary: | Polycrystalline K0.25V2O5 nanoparticles have been synthesized and evaluated as cathode for aqueous zinc-ion batteries, which demonstrates excellent Zn2+ storage capability. As elucidated, a high capacity of 306 mA h g−1, excellent rate capability of 5 A g−1 and long-term cyclic stability up to 500 cycles at 2 A g−1 are achieved. The effect of the K+ ions and the role of morphology for K0.25V2O5 cathode were also discussed in this work. CV measurements at different rates demonstrate that partial surface-controlled capacitive behavior contributes to the capacity of polycrystalline K0.25V2O5 nanoparticles. The zinc storage mechanism is investigated, which demonstrates as a highly reversible intercalation-type cathode for K0.25V2O5 with unique three-dimensional tunnel structure.
We have synthesized and employed the polycrystal K0.25V2O5 nanoparticles as cathode for aqueous zinc-ion batteries, which demonstrates excellent Zn2+ storage capability. [Display omitted]
•Polycrystalline K0.25V2O5 nanoparticles are evaluated as cathode for aqueous ZIBs.•K0.25V2O5 demonstrates a highly reversible intercalation storage mechanism.•The K0.25V2O5 exhibits superior Zn2+ storage capability, e.g. long-term cyclic stability. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 |
ISSN: | 0925-8388 1873-4669 |
DOI: | 10.1016/j.jallcom.2019.06.084 |