Facial-shape controlled precursors for lithium cobalt oxides and the electrochemical performances in lithium ion battery
- Authors
- Shim, Jae-Hyun; Cho, Sang-Woo; Missiul, Aleksandr; Jung, Hyun-Ok; Lee, 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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