The mechanism of lithium intercalation in graphite film electrodes in aprotic media .2. Potentiostatic intermittent titration and in situ XRD studies of the solid-state ionic diffusion
被引:201
作者:
Levi, MD
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BAR ILAN UNIV,DEPT CHEM,IL-52900 RAMAT GAN,ISRAELBAR ILAN UNIV,DEPT CHEM,IL-52900 RAMAT GAN,ISRAEL
Levi, MD
[1
]
Levi, EA
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BAR ILAN UNIV,DEPT CHEM,IL-52900 RAMAT GAN,ISRAELBAR ILAN UNIV,DEPT CHEM,IL-52900 RAMAT GAN,ISRAEL
Levi, EA
[1
]
Aurbach, D
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BAR ILAN UNIV,DEPT CHEM,IL-52900 RAMAT GAN,ISRAELBAR ILAN UNIV,DEPT CHEM,IL-52900 RAMAT GAN,ISRAEL
Aurbach, D
[1
]
机构:
[1] BAR ILAN UNIV,DEPT CHEM,IL-52900 RAMAT GAN,ISRAEL
来源:
JOURNAL OF ELECTROANALYTICAL CHEMISTRY
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1997年
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421卷
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1-2期
The potentiostatic intermittent titration technique (PITT) and in situ XRD have been used to measure the dependence of the diffusion coefficient D-o of lithium ions in graphite on the intercalation level X. Thin graphite electrodes provide an excellent opportunity to obtain highly-resolved data (with respect to X). A non-monotonic peak-shape dependence of log D-o vs. X has been observed, which correlates well with the corresponding dependence of the XRD peak intensity and the cyclic voltammetric peaks. The results thus obtained have been explained tentatively within a framework similar to the Daumas and Herold cluster model for the staged phase transition. Problems connected with the determination of the true values of D-o for porous electrodes are also discussed.