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Employment of SnO2:F@Ni3Sn2/Ni nanoclusters composites as an anode material for lithium-ion batteries

Authors
Kim, Min KyuKim, A-YoungWoo, Jae YoungLim, Jong ChooJeon, Bup JuLee, Joong Kee
Issue Date
25-Sep-2016
Publisher
ELSEVIER SCIENCE SA
Keywords
Intermetallics; Transition metal alloys and compounds; Energy storage materials; Solid state reactions; Electrochemical reactions
Citation
JOURNAL OF ALLOYS AND COMPOUNDS, v.680, pp 744 - 751
Pages
8
Indexed
SCI
SCIE
SCOPUS
Journal Title
JOURNAL OF ALLOYS AND COMPOUNDS
Volume
680
Start Page
744
End Page
751
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/15016
DOI
10.1016/j.jallcom.2016.04.174
ISSN
0925-8388
1873-4669
Abstract
Surface modification of SnO2:F particles which obtained from a large-scale electron cyclotron resonance metal organic chemical vapor deposition system was carried out by two consecutive processes: electroless plating processing and annealing. First, Ni film on the SnO2:F and Ni nanoclusters were observed after Ni electrodes plating; the film on the SnO2:F was then converted to Ni3Sn2 after annealing at 800 degrees C under an argon atmosphere. A Ni3Sn2 bimetallic structure formed instead of Ni0 during the annealing process because of the presence of carbon impurities in SnO2:F. The surface-modified Ni3Sn2-covered SnO2:F with Ni nanoclusters (SnO2:F@Ni3Sn2/Ni-nc) was employed as an anode material for lithium-ion batteries. The inactive Ni in Ni3Sn2 acts as a buffer matrix against the Sn active material during the charge-discharge reactions, enhancing the electrochemical performance. The Ni nanoclusters in SnO2:F@Ni3Sn2/Ni-nc perform dual functions: they not only improve the conductivity as the contacting media, but also increase the initial columbic efficiency by the decomposition of Li2O-an electrochemically irreversible material. An outstanding reversible capacity of 600.69 mA h g(-1) and a coulombic efficiency of 99.23% for SnO2:F@Ni3Sn2/Ni-nc were observed at the 350th cycle under 200 mA g(-1) in the our experimental range. (C) 2016 Elsevier B.V. All rights reserved.
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