TY - JOUR
T1 - Investigation of positive electrodes after cycle testing of high-power Li-ion battery cells. I. An approach to the power fading mechanism using XANES
AU - Kobayashi, Hironori
AU - Shikano, Masahiro
AU - Koike, Shinji
AU - Sakaebe, Hikari
AU - Tatsumi, Kuniaki
N1 - Funding Information:
This work was carried out in the “Development of Lithium Battery Technology for Use by Fuel Cell Vehicles” program of the New Energy and Industrial Technology Development Organization (NEDO) with the financial support of the Ministry of Economy, Trade and Industry (METI) and NEDO. The authors would like to thank Mr. Y. Ozaki of Matsushita Battery Industrial for providing the battery cells used in this research. The authors would also like to thank Dr. Y. Kihira of CRIEPI for providing the cells degraded by cycle testing.
PY - 2007/12/6
Y1 - 2007/12/6
N2 - Cylindrical lithium-ion (Li-ion) cells with a nickel-cobalt oxide (LiNi0.73Co0.17Al0.10O2) positive electrode and a non-graphitizable carbon (hard carbon) negative electrode were degraded using cycle tests. The degraded cells were disassembled and examined; most attention was paid to the positive electrodes in order to clarify the origin of the power fade of the cells. X-ray absorption near-edge structure (XANES) analysis demonstrated that the crystal structure of the electrode at the surface changed from rhombohedral to cubic symmetry. Furthermore, a film of lithium carbonate (Li2CO3) covered the surface of the positive electrode after the cycle tests. Using a combination of X-ray photoelectron spectroscopy (XPS), infrared spectroscopy (IR), and glow discharge optical emission spectrometry (GD-OES) measurements, a schematic model of the changes occurring in the surface structure of the positive electrode during the cycle tests was constructed. The appearance of both an electrochemically inactive cubic phase and lithium carbonate films at the surface of the positive electrode are important factors giving rise to power fade of the positive electrode.
AB - Cylindrical lithium-ion (Li-ion) cells with a nickel-cobalt oxide (LiNi0.73Co0.17Al0.10O2) positive electrode and a non-graphitizable carbon (hard carbon) negative electrode were degraded using cycle tests. The degraded cells were disassembled and examined; most attention was paid to the positive electrodes in order to clarify the origin of the power fade of the cells. X-ray absorption near-edge structure (XANES) analysis demonstrated that the crystal structure of the electrode at the surface changed from rhombohedral to cubic symmetry. Furthermore, a film of lithium carbonate (Li2CO3) covered the surface of the positive electrode after the cycle tests. Using a combination of X-ray photoelectron spectroscopy (XPS), infrared spectroscopy (IR), and glow discharge optical emission spectrometry (GD-OES) measurements, a schematic model of the changes occurring in the surface structure of the positive electrode during the cycle tests was constructed. The appearance of both an electrochemically inactive cubic phase and lithium carbonate films at the surface of the positive electrode are important factors giving rise to power fade of the positive electrode.
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U2 - 10.1016/j.jpowsour.2007.06.134
DO - 10.1016/j.jpowsour.2007.06.134
M3 - Article
AN - SCOPUS:36148971190
VL - 174
SP - 380
EP - 386
JO - Journal of Power Sources
JF - Journal of Power Sources
SN - 0378-7753
IS - 2
ER -