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Photo- and Cathodoluminescence of the Combustion-synthesized Al2O3–TiB2 Composites

Published online by Cambridge University Press:  31 January 2011

Tian D. Xia
Affiliation:
Department of Materials Engineering, Gansu University of Technology, Lanzhou 730050, People's Republic of China
Tian Z. Liu
Affiliation:
Department of Materials Engineering, Gansu University of Technology, Lanzhou 730050, People's Republic of China
Wen J. Zhao
Affiliation:
Department of Materials Engineering, Gansu University of Technology, Lanzhou 730050, People's Republic of China
Zuhair A. Munir
Affiliation:
Department of Chemical Engineering and Materials Science, University of California, Davis, California 95616
Tian M. Wang
Affiliation:
School of Science, Beijing University of Aeronautics and Astronautics, Beijing 100083, People's Republic of China
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Abstract

Al2O3–TiB2 composites were synthesized by the combustion reaction 3TiO2 + 3B2O3 – (10 + x)Al, with x ranging from 0 to 4.71. The products consisted of corundum, TiB2, and a trace of Ti2O3 for the reactions with x = 0 and x = 1.4. However, the products of the reaction with x = 2.96 contained corundum and TiB2 only. For products of samples with x = 0, 1.4, and 2.96, similar room-temperature absorption spectra were observed in the ultraviolet and visible range at wavelengths of 265, 706, and 844 nm. Room-temperature photoluminescence spectra of the composites showed one visible band at about 720 nm. Room-temperature cathodoluminescence (CL) spectra of the composites synthesized by reactions with x = 0 and 1.4 exhibited two visible bands centered at 400 and 710 nm, respectively. From samples synthesized with x = 2.96, another visible band centered at 570 nm was observed in the CL spectrum. Comparing secondary electron images to panchromatic and monochromatic CL images of the composites, it was found that the light-emitting phase is TiB2-containing corundum. The 710-nm band is attributed to the transition between 1T1 (et) and 3T2 (et) excited states, and the 570- and 400-nm bands to the transitions between 3T1 (et) or 3A2 (e2) and 1T1 (et) excited states and 3T1 (t2) ground state of Ti2+ in corundum, respectively.

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Articles
Copyright
Copyright © Materials Research Society 2000

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References

REFERENCES

1.Munir, Z.A., Amer. Ceram. Soc. Bull. 67, 342 (1988).Google Scholar
2.Munir, Z.A. and Anselmi-Tamburini, U., Mater. Sci. Rep. 3, 277 (1989).CrossRefGoogle Scholar
3.Merzhanov, A.G., in Combustion and Plasma Synthesis of High-Temperature Materials, edited by Munir, Z.A. and Holt, J.B. (VCH, New York, 1990), pp. 153.Google Scholar
4.Wang, L.L., Munir, Z.A., and Maximov, Y.M., J. Mater. Sci. 28, 3693 (1993).CrossRefGoogle Scholar
5.Cutler, R.A., Virkar, A.V., and Holt, J.B., Ceram. Eng. Sci. Proc. 6, 715 (1985).CrossRefGoogle Scholar
6.Cutler, R.C., Hurford, A.C., and Virkar, A.V., Mater. Sci. Eng. A 105/106, 183(1988).CrossRefGoogle Scholar
7.Adachi, S., Waada, T., Mihara, T., Miyamoto, Y., and Koizumi, M., J. Am. Ceram. Soc. 73, 1451 (1990).CrossRefGoogle Scholar
8.Rabin, B.H., Korth, G.E., and Williamson, R.L., J. Am. Ceram. Soc. 73, 2156 (1990).CrossRefGoogle Scholar
9.Cutler, R.C., Rigtrup, K.M., and Virkar, A.V., J. Am. Ceram. Soc. 75, 36 (1992).CrossRefGoogle Scholar
10.Choi, Y. and Rhee, S-W., J. Mater. Res. 9, 1761 (1994).CrossRefGoogle Scholar
11.Bowen, C.R. and Derby, B., J. Mater. Sci. 31, 3791 (1996).CrossRefGoogle Scholar
12.Logan, K.V. and Walton, J.D., Ceram. Eng. Sci. Proc. 5, 712 (1984).CrossRefGoogle Scholar
13.Ray, S.P., Metall. Trans. A 23A, 2381 (1992).CrossRefGoogle Scholar
14.Xia, T.D., Munir, Z.A., Tang, Y.L., Zhao, W.J., and Wang, T.M., J. Am. Ceram. Soc. 83, 507 (2000).CrossRefGoogle Scholar
15.Zhang, L.H. and Koka, R.V., Mater. Chem. Phy. 57, 23 (1998).CrossRefGoogle Scholar
16.de Groot, P., Appl. Opt. 37, 6654 (1998).CrossRefGoogle Scholar
17.Xia, T.D., Liu, T.Z., Zhao, W.J., Munir, Z.A., and Wang, T.M. (unpublished).Google Scholar
18.Xia, T.D., Ma, B.Y., Zhao, W.J., Liu, T.Z., and Wang, T.M., J. Mater. Sci. Lett. 18, 1329 (1999).CrossRefGoogle Scholar
19.Xia, T.D., Wang, T.M., Ma, B.Y., Liu, T.Z., and Zhao, W.J., Phys. Status Solidi: A 174, 291 (1999).3.0.CO;2-L>CrossRefGoogle Scholar
20.Greenwood, N.N., in Comprehensive Inorganic Chemistry, edited by Trotman-Dickenson, A.F. (Pergamon, Oxford, United Kingdom, 1973), Vol. 1, pp. 665991.Google Scholar
21.McClure, D.S., J. Chem. Phys. 36, 2757 (1962).CrossRefGoogle Scholar
22.McClure, D.S., J. Chem. Phys. 38, 2289 (1963).CrossRefGoogle Scholar
23.McClure, D.S., in Solid State Physics, 9, edited by Seitz, F. and Turnbull, D. (Academic Press, New York, 1960), pp. 399525.Google Scholar
24.Bersuker, I.B., Electronic Structure and Properties of Transition Metal Compounds: Introduction to the Theory (John Wiley & Sons, New York, 1996), pp. 77–120, 351363.Google Scholar
25.Maiman, T.H., Nature (London) 187, 439 (1960).CrossRefGoogle Scholar
26.Paul, A., J. Mater. Sci. 10, 692 (1975).CrossRefGoogle Scholar
27.Byvik, C.E. and Buoncristiani, A.M., IEEE J. Quant. Elect. QE-21, 1619 (1985).CrossRefGoogle Scholar
28.Powell, R.C., Caslavsky, J.L., Al-Shaieb, Z., and Bowen, J.M., J. Appl. Phys. 58, 2331 (1985).CrossRefGoogle Scholar
29.Kuck, S., Petermann, K., Pohlmann, U., Schonhoff, U., and Huber, G., Appl. Phys. B 58, 153 (1994).CrossRefGoogle Scholar
30.Kuck, S., Hartung, S., Hurling, S., Petermann, K., and Huber, G., Phys. Rev. B 57, 2203 (1998).CrossRefGoogle Scholar
31.Tanabe, Y. and Sugano, S., J. Phys. Soc. Jpn. 9, 766 (1954).CrossRefGoogle Scholar