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Toward Commercialization of the Beta-Alumina Family of Ionic Conductors

Published online by Cambridge University Press:  31 January 2011

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The beta-alumina family of materials has played a central role in the field of solid-state ionics. β- and β-alumina have been a principal theme in the field ever since Yao and Kummer reported the extraordinarily high conductivity for sodium β-alumina. The material “came of age” at a time when there was great interest in the science and technology of highconductivity solid electrolytes. A previous MRS Bulletin review introduced this broad family of materials, examining the range of compositions and the two major structures. The beta-alumina family emerged as almost an ideal system in which to explore structure-property relations, as its unusual structure is responsible for its remarkable ion-transport properties. Although the initial interest in this material, and the one which endures to this day, is its rapid sodium-ion transport, the rich ion-exchange chemistry added a dimension to this material that few inorganic systems can match, let alone exceed. β-alumina, in particular, is an almost universal solid electrolyte for cations. It constitutes a broad family of solid electrolytes whose properties are dependent upon the nature of the ion inserted into the conduction plane. As a result, the β-aluminas have served as model systems for a wide range of studies: proton transport and mixed-ion diffusion, order-disorder reactions, and superlattice phenomena. Moreover, these β-alumina compositions demonstrated that fast-ion transport was not limited to a few monovalentions, but could be extended to divalent and even trivalent cations. With the latter materials, the interest was not necessarily ion transport, but optical properties instead. The presence of trivalent cations in this unusual structure, coupled with the ability to control the chemistry of the local environment, enabled the β-aluminas to exhibit a number of novel optical properties.

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Research Article
Copyright
Copyright © Materials Research Society 2000

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References

1.Yao, Y.F.Y. and Kummer, J.T., J. Inorg. Nucl. Chem. 29 (1967) p. 2453.Google Scholar
2.Dunn, B., Farrington, G.C., and Thomas, J.O., MRS Bull. XIV (9) (1989) p. 22.Google Scholar
3.Farrington, G.C. and Briant, J.L., Science 204 (1979) p. 1371.CrossRefGoogle Scholar
4.Bates, J.B., Wang, J.C., and Dudney, N.J., Phys. Today (July 1982) p. 46.CrossRefGoogle Scholar
5.Stevens, R. and Binner, J.G.P., J. Mater. Sci. 19 (1984) p. 695.CrossRefGoogle Scholar
6.Simkin, D.J., J. Phys. Chem. Solids 52 (1991) p. 175.CrossRefGoogle Scholar
7.Rankin, G.A. and Merwin, H.E., J. Am. Chem. Soc. 38 (1916) p. 568.CrossRefGoogle Scholar
8.Boilot, J.P., Collin, G., Ph. Colomban, and Comes, R., Phys. Rev. B: Condens. Matter 22 (1980) p. 5912.CrossRefGoogle Scholar
9.Wang, B., Bates, J.B., Hart, F.X., Sales, B.C., Zuhr, R.A., and Robertson, J.D., J. Electrochem. Soc. 143 (1996) p. 3203.CrossRefGoogle Scholar
10.Tan, A., Kuo, C.K., and Nicholson, P.S., Solid State Ionics 67 (1993) p. 131.CrossRefGoogle Scholar
11.Kuo, C.K. and Nicholson, P.S., Solid State Ionics 67 (1993) p. 157.CrossRefGoogle Scholar
12.Kuo, C.K. and Nicholson, P.S., Solid State Ionics 82 (1995) p. 173.CrossRefGoogle Scholar
13.Prakash, O., Khare, R., Kuo, C.K., and Nicholson, P.S., Solid State Ionics 98 (1997) p. 113.CrossRefGoogle Scholar
14.Shimizu, Y., Kuo, C.K., and Nicholson, P.S., Solid State Ionics 110 (1998) p. 69.CrossRefGoogle Scholar
15.Neiman, A. and Gorodetskaya, I., Solid State Ionics 106 (1998) p. 309.CrossRefGoogle Scholar
16.Galloway, R.C., J. Electrochem. Soc. 134 (1987) p. 1.CrossRefGoogle Scholar
17.Wedlake, R.J., Coetzer, J., and Vlok, I.L., J. Power Sources 12 (1988) p. 563.Google Scholar
18.Sudworth, J.L., J. Power Sources 51 (1994) p. 105.CrossRefGoogle Scholar
19.Bugden, W.G. and Duncan, J.H., Sci. Ceram. 9 (1977) p. 348.Google Scholar
20.Jones, I.W. and Miles, L.J., Proc. Br. Ceram. Soc. 19 (1971) p. 161.Google Scholar
21.Tan, S.R. and May, G.J., Sci. Ceram. 9 (1977) p. 103.Google Scholar
22.Duncan, J.H. and Bugden, W.G., Proc. Br. Ceram. Soc. 31 (1981) p. 221.Google Scholar
23.Duncan, J.H., Barrow, P., Van Zyl, A., and Kingon, A., U.S. Patent No. 4,732,741 (1986).Google Scholar
24.Yasui, I. and Doremus, R.H., J. Electrochem. Soc. 125 (1978) p. 1007.CrossRefGoogle Scholar
25.Sieh, M.Y.H. and DeJonghe, L.C., J. Am. Ceram. Soc. 61 (1978) p. 185.Google Scholar
26.Miller, M.L., McEntire, B., Miller, G.R., and Gordon, R.S., Am. Ceram. Soc. Bull. 58 (1979) p. 522.Google Scholar
27.Armstrong, R.D., Dickenson, T., and Turner, J., Electrochim. Acta 19 (1974) p. 187.CrossRefGoogle Scholar
28.Tennenhouse, G.J., Ku, R.C., Richman, R.H., and Whalen, T.J., Am. Ceram. Soc. Bull. 54 (1979) p. 246.Google Scholar