Hostname: page-component-586b7cd67f-r5fsc Total loading time: 0 Render date: 2024-11-23T16:03:45.641Z Has data issue: false hasContentIssue false

Impact of Surface Chemistry on the Electrochemical Performance of LiCoO2

Published online by Cambridge University Press:  26 February 2011

Nathalie Pereira
Affiliation:
[email protected], Rutgers, The State University of New Jersey, Energy Storage Research Group, Department of Materials Science and Engineering, 671 US Highway 1, North Brunswick, NJ, 08902, United States
Jafar Al-Sharab
Affiliation:
[email protected], Rutgers, The State University of New Jersey, Department of Materials Science and Engineering, North Brunswick, NJ, 08902, United States
Frederic Cosandey
Affiliation:
[email protected], Rutgers, The State University of New Jersey, Department of Materials Science and Engineering, North Brunswick, NJ, 08902, United States
Fadwa Badway
Affiliation:
[email protected], Rutgers, The State University of New Jersey, Energy Storage Research Group, Department of Materials Science and Engineering, 671 US Highway 1, North Brunswick, NJ, 08902, United States
Glenn Amatucci
Affiliation:
[email protected], Rutgers, The State University of New Jersey, Energy Storage Research Group, Department of Materials Science and Engineering, 671 US Highway 1, North Brunswick, NJ, 08902, United States
Get access

Abstract

For almost a decade there have been spurious reports that high specific capacity LiCoO2 can be stabilized through modification of the synthesis protocol, however no basis for this improvement was ever proven. In this study, high specific capacity (190 mAh/g) LiCoO2 with good cycling stability was successfully fabricated in this study with the purpose to identify the basis for, and reproduce the high specific capacity. Extensive physical and electrochemical characterization confirmed the improvement was directly related to the surface chemistry as opposed to bulk modification of the crystal chemistry. In particular, high resolution transmission electron microscopy confirmed the thermodynamic growth of a distinct surface phase of 5-10nm on the best materials. In contrast to extrinsically deposited surface coating, the intrinsic approach enabled a one step synthesis and modification using intrinsic constituents to result in a 5-10nm uniform coating of a cubic cobaltite based on fundamental phase stabilities as dictated by the phase diagram of the Li-Co-O system.

Type
Research Article
Copyright
Copyright © Materials Research Society 2007

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1. Ohzuku, T., Ueda, A., Solid State Ionics, 69 (1994) 201211.Google Scholar
2. Ohzuku, T., Ueda, A., J. Electrochem. Soc., 141 (1994) 29722977.Google Scholar
3. Amatucci, G. G., Tarascon, J. M., Klein, L. C., Solid State Ionics, 83 (1996) 167173.Google Scholar
4. Aurbach, D., Markovsky, B., Levi, M. D., Cohen, Y. S., Kim, H. J., Schmidt, M., Electrochim. Acta, 47 (2002) 42914306.Google Scholar
5. Wang, Z., Liu, L., Chen, L., Huang, X., Solid State Ionics, 148 (2002) 335342.Google Scholar
6. Amatucci, G. G., Tarascon, J. M., U.S. Pat. #5,693,435.Google Scholar
7. Chen, Z., Dahn, J. R., Electrochem. Solid-State Lett., 6 (2003) A221–A224.Google Scholar
8. Pereira, N., Matthias, C., Bell, K., Badway, F., Plitz, I., Al-Sharab, J., Cosandey, F., Shah, P., Isaacs, N., Amatucci, G. G., J. Electrochem. Soc., 152 (2005) A114–A125.Google Scholar
9. Johnston, W. D., Heikes, R. R. and Sestrich, D., Phys. Chem. Solids, 7 (1958) 113.Google Scholar
10. Moore, R. J. and White, J., J. Mater. Sci., 9 (1974) 14011408.Google Scholar