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Structural Modification of V2O5 as High-Performance Aqueous Zinc-Ion Battery Cathode.

Authors :
Boya Tang
Jiang Zhou
Guozhao Fang
Shan Guo
Xun Guo
Lutong Shan
Yan Tang
Shuquan Liang
Source :
Journal of The Electrochemical Society; 2019, Vol. 166 Issue 4, pA480-A486, 7p
Publication Year :
2019

Abstract

We report theNH<subscript>4</subscript><superscript>+</superscript> intercalated V<subscript>2</subscript>O<subscript>5</subscript>, i.e. (NH<subscript>4</subscript>)<subscript>2</subscript>V<subscript>10</subscript>O<subscript>25</subscript>•8H<subscript>2</subscript>O, with excellent electrochemical performance as cathode in aqueous zinc-ion battery (ZIBs), as compared to V<subscript>2</subscript>O<subscript>5</subscript>, Na<subscript>5</subscript>V<subscript>12</subscript>O<subscript>32</subscript> and K<subscript>2</subscript>V<subscript>8</subscript>O<subscript>21</subscript>. This work reveals that the ionic conductivity of Zn<superscript>2+</superscript> can be enhanced by introducing cations into the V2O5 framework and the vanadium oxygen structural units will be rearranged. Compared to a single layer of vanadium pentoxide consisting solely of VO5 units, the electrochemical performance of the structural units rearranged vanadates shows a significant improvement. As a result, the obtained (NH<subscript>4</subscript>)<subscript>2</subscript>V<subscript>10</subscript>O<subscript>25</subscript>•8H<subscript>2</subscript>O delivers high discharge capacity (376 mA h g<superscript>-1</superscript> at 0.5 A g<superscript>-1</superscript>), superior rate capability up to 10 A g<superscript>-1</superscript>, excellent cycling stability (a capacity retention over 93% for 1000 cycles) and high energy density (341 Wh kg<superscript>-1</superscript>). [ABSTRACT FROM AUTHOR]

Subjects

Subjects :
CATHODES
AQUEOUS solutions

Details

Language :
English
ISSN :
00134651
Volume :
166
Issue :
4
Database :
Supplemental Index
Journal :
Journal of The Electrochemical Society
Publication Type :
Academic Journal
Accession number :
135363941
Full Text :
https://doi.org/10.1149/2.0081904jes