TY - JOUR
T1 - Irreversible phase transition between LiFePO4 and FePO4 during high-rate charge-discharge reaction by operando X-ray diffraction
AU - Takahashi, Ikuma
AU - Mori, Takuya
AU - Yoshinari, Takahiro
AU - Orikasa, Yuki
AU - Koyama, Yukinori
AU - Murayama, Haruno
AU - Fukuda, Katsutoshi
AU - Hatano, Masaharu
AU - Arai, Hajime
AU - Uchimoto, Yoshiharu
AU - Terai, Takayuki
N1 - Funding Information:
This work was partly supported by the Research and Development Initiative for Scientific Innovation of New Generation Batteries (RISING) project under the auspices of New Energy and Industrial Technology Department Organization (NEDO (Japan)). The synchrotron radiation experiments were performed with the approval of the Japan Synchrotron Radiation Research Institute (JASRI) (Proposal No. 2012A7601, 2012B7601, 2013A7601, 2013B7601, 2014A7601, 2014B7601).
Publisher Copyright:
© 2016 Elsevier B.V. All rights reserved.
PY - 2016/3/31
Y1 - 2016/3/31
N2 - LiFePO4 is a practically used cathode material for lithium-ion batteries due to a high theoretical capacity, high cycle capability and the high-rate performance. The metastable LixFePO4 (LxFP) phase with an intermediate composition appears in the non-equilibrium state at high-rate condition. However, the formation process of the metastable LxFP phase and its impact to the electrochemical property are still unclear. In order to elucidate these points, we directly observed the phase transition behavior by applying operando XRD during 10C charge-discharge. LxFP phase does not form in charge reaction but preferentially forms in discharge reaction. The phase transition from LxFP to Li-rich phase is less likely to proceed in the end of discharge reaction. The asymmetric phase transition between LiFePO4 and FePO4 results in decreasing the discharge capacity and increasing the irreversible capacity at high-rate conditions.
AB - LiFePO4 is a practically used cathode material for lithium-ion batteries due to a high theoretical capacity, high cycle capability and the high-rate performance. The metastable LixFePO4 (LxFP) phase with an intermediate composition appears in the non-equilibrium state at high-rate condition. However, the formation process of the metastable LxFP phase and its impact to the electrochemical property are still unclear. In order to elucidate these points, we directly observed the phase transition behavior by applying operando XRD during 10C charge-discharge. LxFP phase does not form in charge reaction but preferentially forms in discharge reaction. The phase transition from LxFP to Li-rich phase is less likely to proceed in the end of discharge reaction. The asymmetric phase transition between LiFePO4 and FePO4 results in decreasing the discharge capacity and increasing the irreversible capacity at high-rate conditions.
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U2 - 10.1016/j.jpowsour.2016.01.077
DO - 10.1016/j.jpowsour.2016.01.077
M3 - Article
AN - SCOPUS:84957078076
SN - 0378-7753
VL - 309
SP - 122
EP - 126
JO - Journal of Power Sources
JF - Journal of Power Sources
ER -