Hostname: page-component-848d4c4894-jbqgn Total loading time: 0 Render date: 2024-07-04T09:20:35.943Z Has data issue: false hasContentIssue false

Correlation of the Charge Storage and Magnetic Susceptibility of Hydrous RuO2

Published online by Cambridge University Press:  01 February 2011

Karen E. Swider-Lyons
Affiliation:
6171, Naval Research Laboratory Washington, DC 20375USA (email) karen.lyons@nrl.navy.mil
Konrad M. Bussmann
Affiliation:
6340, Naval Research Laboratory Washington, DC 20375USA (email) karen.lyons@nrl.navy.mil
Get access

Abstract

Hydrous RuO2 is a mixed metallic-protonic conductor that is used as a charge storage material in electrochemical capacitors and as an electrocatalyst. Previous structural analysis by Dmowski, et. al. has shown that RuO2 is a composite of ordered RuO2 nanoparticles that are surrounded by hydrous grain boundaries. In this paper, magnetic susceptibility (MS) is used to show that the hydrous RuO2 has both localized and delocalized electrons. The localized electrons are attributed to Ru3+ defects that decrease in concentration with decreasing water content. The delocalized electrons are represented by a temperature independent paramagnetic (TIP) component of the MS. The magnetic data is consistent with a structure having metallic nanoparticles whose electrons become more itinerant with decreasing structural water. We conclude that hydrous RuO2 stores charge analogously to double-layer capacitors in which charge is stored at the interface of the hydrous grain boundaries and the metallic nanoparticles, and that there is effectively no difference in the charge storage mechanisms of hydrous RuO2 and carbon.

Type
Research Article
Copyright
Copyright © Materials Research Society 2005

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

REFERENCES

1. Jow, T. R. and Zheng, J. P., J. Electrochem. Soc. 145, 49 (1998).Google Scholar
2. Zheng, J. P., Cygan, P. J., and Jow, T. R, J. Electrochem. Soc. 142, 2699 (1995).Google Scholar
3. Fletcher, J. M., Gardner, W. E., Greenfield, B. F., Holdoway, M. J. and Rand, M. H., J. Chem. Soc A 653 (1968).Google Scholar
4. Burke, A., J. Power Sources 91, 37 (2000).Google Scholar
5. Swider, K. E., Merzbacher, C. I., Hagans, P. L. and Rolison, D. R., Chem. Mater. 9, 1248 (1997).Google Scholar
6. Trasatti, S. and Lodi, G. in Electrodes of Conductive Metallic Oxides, pt. B, edited by Trasatti, S., (Elsevier, Amsterdam, 1981) Chapter 10.Google Scholar
7. Long, J. W., Swider, K. E., Merzbacher, C. I. and Rolison, D. R., Langmuir 15, 780 (1999).Google Scholar
8. Dmowski, W., Egami, T., Swider-Lyons, K. E., Love, C. T. and Rolison, D. R., J. Phys. Chem. B, 106, 12677 (2002)Google Scholar
9. McKeown, D. A., Hagans, P. L., Carette, L. P. L., Russell, A. E., Swider, K. E. and Rolison, D. R., J. Phys. Chem. B, 103, 4825 (1999).Google Scholar
10. Goodenough, J. B., Prog. Solid State Chem. 5, 145 (1971).Google Scholar
11. Rogers, D. B., Shannon, R. D., Sleight, A. W. and Gillson, J. L., Inorg. Chem. 8, 841 (1969).Google Scholar
12. Cox, P. A., Goodenough, J. B., Tavener, P. J., Telles, D. and Egdell, R. G., J. Solid State Chem. 62, 360 (1986).Google Scholar
13. Butler, S. R. and Gillson, J. L., Mat. Res. Bull. 6, 81 (1971).Google Scholar
14. Conway, B. E., J. Electrochem. Soc. 138, 1539 (1991).Google Scholar
15. Yamada, A. and Goodenough, J. B., J. Electrochem. Soc. 145, 737 (1998).Google Scholar
16. Ardizzone, S., Fregonara, G. and Trasatti, S., Electrochim. Acta 35, 263 (1990).Google Scholar