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World’s First Observation of Nonequilibrium Phase Transition of Positive Electrode Material for Lithium-Ion Batteries (Press Release)

Release Date
10 Apr, 2013
  • BL28XU (RISING)
- Towards realizing fast-charge and fast–discharge batteries -

Kyoto University

A research group of Kyoto University has clarified the transient state of the phase transition*3 of a positive electrode material used for lithium-ion batteries*2 and the mechanism behind a material that can be used for fast-charge and fast-discharge batteries. This study was part of the RISING Project*1 (project leader, Zempachi Ogumi**, professor) supported by Kyoto University and the New Energy and Industrial Technology Development Organization (NEDO). The group was led by Yuki Orikasa* (assistant professor), Yukinori Koyama** (associate professor), Katsutoshi Fukuda** (associate professor), Hajime Arai** (professor), and Yoshiharu Uchimoto* (professor).

*Graduate School of Human and Environmental Studies
**Office of Society-Academia Collaboration for Innovation

The results of this research were posted online as a Just Accepted Manuscript in Journal of the American Chemical Society on 1 April 2013.

Publication:
"Direct Observation of a Metastable Crystal Phase of LixFePO4 under Electrochemical Phase Transition"
Yuki Orikasa, Takehiro Maeda, Yukinori Koyama, Haruno Murayama, Katsutoshi Fukuda, Hajime Tanida, Hajime Arai, Eiichiro Matsubara, Yoshiharu Uchimoto, and Zempachi Ogumi
Journal of the American Chemical Society, 135 (15) 5497–5500, 2013

<<Figures>>

Fig. 1	Measurement method based on time-resolved X-ray diffraction under operating conditions of lithium-ion battery
Fig. 1 Measurement method based on time-resolved X-ray diffraction
under operating conditions of lithium-ion battery


Fig. 2	Change in X-ray diffraction pattern during fast-charging and fast-discharging reactions of LiFePO4
Fig. 2 Change in X-ray diffraction pattern during fast-charging
and fast-discharging reactions of LiFePO4

(The boxed diffraction pattern is not observed in the steady state and is only observed during the fast reaction.)


Fig. 3	Phase transition path via metastable crystal phase during fast reaction of LixFePO4
Fig. 3 Phase transition path via metastable crystal phase
during fast reaction of LixFePO4


<<Glossary>>
*1 Research and Development Initiative for Scientific Innovation of New Generation Batteries (RISING) project

This project is based at and being carried out by Kyoto University and the National Institute of Advanced Industrial Science and Technology (AIST) Kansai in cooperation with various organizations throughout Japan (12 universities, 4 research institutes, and 13 companies). The aim of this project is to realize innovative rechargeable batteries with an energy density fivefold higher than that of currently available batteries. This project is one of the joint research projects supported by NEDO.

*2 Lithium-ion battery
Lithium-ion batteries are secondary (rechargeable) batteries with a high energy density and have been widely used as the main power sources of mobile electronic devices such as cell phones and laptop PCs. Lithium-ion batteries are mainly composed of a positive electrode, a negative electrode, and an organic electrolyte, and their charging and discharging are based on the movement of lithium ions. Recently, lithium-ion batteries have been applied to electric vehicles and large rechargeable batteries, intensifying the worldwide competition for their research and development.

*3 Phase transition
In lithium-ion batteries, lithium ions move between the positive and negative electrodes during charging and discharging. During these processes, the crystal structures of the positive and negative electrodes change. The phase of the positive electrode material examined in this study, LiFePO4, is separated into LiFePO4 and FePO4 phases during charging and discharging, and the reaction proceeds with changing their proportion. In this study, the phase transition behavior between LiFePO4 and FePO4 was analyzed.



For more information, please contact:
  Prof. Hajime Arai (Office of Society-Academia Collaboration for Innovation, Kyoto University)
    E-mail : mail1

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