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Tailoring Crystal Structure and Morphology of LiFePO4/C Cathode Materials Synthesized by Heterogeneous Growth on Nanostructured LiFePO4 Seed Crystals

Authors
Han, DW (Han, Dong-Wook)Ryu, WH (Ryu, Won-Hee)Kim, WK (Kim, Won-Keun)Lim, SJ (Lim, Sung-Jin)Kim, YI (Kim, Yong-Il)Eom, JY (Eom, Ji-Yong)Kwon, HS (Kwon, Hyuk-Sang)
Issue Date
Feb-2013
Publisher
AMER CHEMICAL SOC
Citation
ACS APPLIED MATERIALS INTERFACES, v.5, no.4, pp 1342 - 1347
Pages
6
Journal Title
ACS APPLIED MATERIALS INTERFACES
Volume
5
Number
4
Start Page
1342
End Page
1347
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/147498
DOI
10.1021/am302560m
ISSN
1944-8244
1944-8252
Abstract
Porous and coarse (5-10 mu m) LiFePO4/C composites with excellent electrochemical performance were synthesized by a growth technology using nanostructured (100-200 nm) LiFePO4 as seed crystals for the 2nd crystallization process. The porous and coarse LiFePO4/C presented a high initial discharge capacity (similar to 155 mA h g(-1) at 0.1 C), superior rate-capability (similar to 100 mA h g(-1) at 5 C, similar to 65 % of the discharge capacity at 0.1 C), and excellent cycling performance (similar to 131 mA h g(-1), similar to 98 % of its initial discharge capacity after 100 cycles at 1 C). The improvement in the rate-capability of the LiFePO4/C was attributed to the high reaction area resulted from the pore tunnels formed inside LiFePO4 particles and short Li-ion diffusion length. The improved cycling performance of the LiFePO4/C resulted from the enhanced structural stability against Li-deficient LiFePO4 phase formation after cycling by the expansion of the ID Li-ion diffusion channel in the LiFePO4 crystal structure.
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공과대학 (화공생명공학부)
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