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Amorphous Vanadium Titanates as a Negative Electrode for Lithium-ion Batteriesopen access

Authors
Lee, Jeong BeomChae, Oh. B.Chae, SeulkiRyu, Ji HeonOh, Seung M.
Issue Date
Dec-2016
Publisher
KOREAN ELECTROCHEMISTRY SOC
Keywords
Amorphous metal oxides; Lithium-ion batteries; X-ray absorption fine structure (XAFS); Surface hydroxyl groups; Electrochemistry
Citation
JOURNAL OF ELECTROCHEMICAL SCIENCE AND TECHNOLOGY, v.7, no.4, pp.306 - 315
Journal Title
JOURNAL OF ELECTROCHEMICAL SCIENCE AND TECHNOLOGY
Volume
7
Number
4
Start Page
306
End Page
315
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/87340
DOI
10.5229/JECST.2016.7.4.306
ISSN
2093-8551
Abstract
Amorphous vanadium titanates (aVTOs) are examined for use as a negative electrode in lithium-ion batteries. These amorphous mixed oxides are synthesized in nanosized particles (<100 nm) and flocculated to form secondary particles. The V5+ ions in aVTO are found to occupy tetrahedral sites, whereas the Ti4+ ions show fivefold coordination. Both are uniformly dispersed at the atomic scale in the amorphous oxide matrix, which has abundant structural defects. The first reversible capacity of an aVTO electrode (295 mA h g(-1)) is larger than that observed for a physically mixed electrode (1: 2 aV(2)O(5) | aTiO(2), 245 mA h g(-1)). The discrepancy seems to be due to the unique four-coordinated V5+ ions in aVTO, which either are more electron-accepting or generate more structural defects that serve as Li+ storage sites. Coin-type Li/aVTO cells show a large irreversible capacity in the first cycle. When they are prepared under nitrogen (aVTO-N), the population of surface hydroxyl groups is greatly reduced. These groups irreversibly produce highly resistive inorganic compounds (LiOH and Li2O), leading to increased irreversible capacity and electrode resistance. As a result, the material prepared under nitrogen shows higher Coulombic efficiency and rate capability.
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