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Facial-shape controlled precursors for lithium cobalt oxides and the electrochemical performances in lithium ion battery

Authors
Shim, Jae-HyunCho, Sang-WooMissiul, AleksandrJung, Hyun-OkLee, Sanghun
Issue Date
15-Jan-2015
Publisher
ELSEVIER SCIENCE BV
Keywords
Lithium ion battery; Lithium cobalt oxide; Facial-shape; Precursor
Citation
JOURNAL OF POWER SOURCES, v.274, pp.659 - 666
Journal Title
JOURNAL OF POWER SOURCES
Volume
274
Start Page
659
End Page
666
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/10868
DOI
10.1016/j.jpowsour.2014.10.113
ISSN
0378-7753
Abstract
Two types of lithium cobalt oxides (LiCoO2) as cathode materials for lithium ion batteries are synthesized from two cobalt sources of different facial-shapes (octahedral and truncated-octahedral Co3O4) and Li2CO3 using solid state synthesis. From X-ray diffraction and scanning electron microscopy measurements, the reaction mechanism of the formation of LiCoO2 is investigated. It is revealed that LiCoO2 from octahedral Co3O4 with only {111} surfaces grows in one direction whereas the crystal orientation of LiCoO2 from truncated-octahedral CO3O4 with {111} and {100}surfaces is not unique and the spinel intermediates of Li5CO2O4 are formed during synthesis. They show largely unequal rate and cycling performances for lithium ion battery, even though their outer appearances are nearly identical. Almost single-crystalline LiCoO2 from octahedral precursors shows much better electrochemical performances than LiCoO2 from truncated-octahedral precursors as a lithium ion battery cathode. By studying crystal orientation, it is shown that the poor electrochemical performances of LiCoO2 from truncated-octahedral Co3O4 are originated by crystal-mismatch between crystallites. (C) 2014 Elsevier B.V. All rights reserved.
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