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Reactivity of Carbonaceous Anodes Used in Lithium-ion Batteries, Part I: Correlation of Structural Parameters and Reactivity

Published online by Cambridge University Press:  10 February 2011

G. A. Nazri
Affiliation:
University of Michigan, Department of Chemistry, Ann Arbor, Michigan 48109
B. Yebka
Affiliation:
University of Michigan, Department of Chemistry, Ann Arbor, Michigan 48109
M. Nazri
Affiliation:
University of Michigan, Department of Chemistry, Ann Arbor, Michigan 48109
D. Curtis
Affiliation:
University of Michigan, Department of Chemistry, Ann Arbor, Michigan 48109
K. Kinoshita
Affiliation:
Lawrence Berkeley National Laboratory, 1 Cyclotron Rd, Building 90, CA, Berkeley 94720
Dave Derwin
Affiliation:
Superior Graphite Company, 6540 S. Laramie Ave, Bedford Park, I1 60638
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Abstract

Carbonaceous anodes are the most practical elecrode for application in lithium-ion battery, mainly due to their low cost, flexibility for modification to achieve high energy capacity and high rate capability, abundance and environmentally uniquencess. Despite superior advantages of carbonaceous anodes vs other alternative anode and metallic lithium, there is considerable reactivity of lithiated graphite with organic electrolytes, which is a major safety concern. In this work, we report the nature of gaceous species generated on various carbonaceous anodes during initial charge-discharge cycling. The correlation between structural parameters of carbonaceous materials and their irreversible capacity loss have been investigated. Structural parameters have been studied using x-ray diffraction, Raman spectroscopy, and scanning and transmission electron microscopy. We have found a direct correlation between crystal morphology, degree of disorder, degree of graphitisation and the irreversible capacity loss. There is also a direct correlation between the irrversible capacity loss and the volume of gas generated during initial charge- disharge cycling. Results also show the importance of removing adsorbed and trapped gases in addition to removal of bonded impurities, such as functional groups from carbonaceous electrode before fabrication of batteries.

Particular attention is given on thermal analysis for different graphite compounds and the influence of different parameters and conditions: nature of graphite in term of specific surface area, degree of graphitization and the length of microcristallites, degree of intercalation, nature of electrolytes on irreversible capacity loss and volume of gases generated during the initial charge-discharge cycles.

Type
Research Article
Copyright
Copyright © Materials Research Society 1999

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References

REFERENCES

[1] Nagaura, T. and Tozawa, K., Progress in Batteries and Solar Cells, Vol. 9, 209, (1990).Google Scholar
[2] Yamaki, J., IEE, J., Japan, 117, 167, (1997).Google Scholar
[3] Zhou, P., Papanek, P., Bindra, C., Lee, R., Fisher, J.E., J. of Power Sources, 68, 296 (1997).Google Scholar
[4] Novak, P., Scheifele, W., Winter, M., Haas, O., J. Power Sources, 68, 267, (1997).Google Scholar
[5] Armstrong, A.R. and Bruce, P., Nature, 381, 499 (1996).Google Scholar
[6] Dahn, J.R., Phys. Rev. B44, 9170 (1991).Google Scholar
[7] Fong, R., Sacken, U.V., Dahn, J.R., J. Electrochem. Soc., 137, 2009 (1990).Google Scholar
[8] Zheng, T., Reimers, J.N. and Dahn, J.R., Phys. Rev. B51, 734 (1995).Google Scholar
[9] Takami, N., Satoh, T. Ohsaki and Kanda, M., Electrochim. Acta, 42, 2537 (1997).Google Scholar
[10] Nazri, G.A., Yebka, B. to be published.Google Scholar
[11] Takamura, T., Awano, H., Ura, T., Ikezawa, T., Anal. Sc. Technol. 8, 583 (1995).Google Scholar
[12] Chusid, O., Ein-Eli, Y., Aurbach, D., Babi, M., and Carmeli, Y., J. Power Sources, 43–44, 47 (1993).Google Scholar
[13] Tuinsta, F. and Koenig, J.L., J. Chem. Phys. 53, 1126 (1970).Google Scholar
[14] Shi, H., Barker, J., Saidi, M.Y., Koksbang, R., Morris, L., J. of Power Sources 68, 291 (1997)Google Scholar
[15] Dey, A.N. and Sullivan, B.P., J. Electrochem. Soc. 117, 222 (1970)Google Scholar
[16] Shu, Z.X., Mcmillan, R.S., and Murray, J.J., J. Eclectrochem. Soc. 140, 922 (1993).Google Scholar
[17] Wilkinson, D.P. & Dahn, J.R., U.S. Pat.5,130,211 (1992)Google Scholar
[18] Boem, H.P., Adv. Catal., 16, 179 (1966).Google Scholar