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Abstract
Optics Physical Sciences Science & Technology
Bilayered vanadium oxide, delta-V2O5.nH(2)O, is a promising electrode material for Na-ion batteries due to its large interlayer spacing, 11.5 angstrom, that allows for insertion of many charge-carrying ions. Previously, delta-V2O5.nH(2)O electrodes have shown high capacities in Na-ion batteries1-3. However, capacity fade is common when synthesized via cost effective, sol-gel routes. Poor cycling stability is attributed to the loss of V-O layers stacking order upon cycling1. Therefore, methods to improve the structural stability of the delta-V2O5.nH(2)O phase are necessary for its utilization as Na-ion cathodes.
A synthesis approach known as chemical pre-intercalation allows for the insertion of inorganic cations into the structure of electrode materials prior to electrochemical cycling. Previously, we have demonstrated that chemical pre-intercalation of Na-ions into the bilayered phase results in high initial capacities above 350 mAh g(-1) in Na-ion cells(3). In this study, we focus on the incorporation of low-temperature annealing to increase structural and electrochemical stability of the bilayered phase in Na-ion batteries. We demonstrate that annealing can lead to increased crystallinity leading to increased cycling stability. This result shows how synthesis approaches affect the structure of the bilayered vanadium oxide phase and can lead to increased electrochemical stability in Na-ion cells.
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Details
Title
Effect of Annealing on Electrochemical Stability of Chemically Preintercalated Bilayered Vanadium Oxide Cathodes in Batteries
Creators
Mallory Clites - Drexel University
Ryan Andris - Drexel University
Phillip Ridley - Drexel University
Ekaterina A. Pomerantseva - Drexel University
Contributors
N P Kobayashi (Editor)
A A Talin (Editor)
A V Davydov (Editor)
Publication Details
LOW-DIMENSIONAL MATERIALS AND DEVICES 2019, v 11085, pp 110850Q-110850Q-10
Series
Proceedings of SPIE
Publisher
Spie-Int Soc Optical Engineering
Number of pages
10
Grant note
DMR-1609272 / National Science Foundation; National Science Foundation (NSF)
Resource Type
Conference proceeding
Language
English
Academic Unit
Materials Science and Engineering
Web of Science ID
WOS:000502318700005
Scopus ID
2-s2.0-85073878502
Other Identifier
991020785739904721
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