Microstructure and Spectroscopy of Lu2O3:Eu Prepared Using Various Synthesis Techniques

Article Preview

Abstract:

Nanocrystalline powders of Lu2O3:Eu with activator content varying between 0.2%-10% were prepared using four different methods of synthesis. The products differed in their microstructure and crystallites sizes. Combustion of Lu(NO3)3 with urea produced strongly agglomerated material, most probably with significantly non-uniform distribution of the Eu3+ dopant. Replacing urea with glycine for the combustion produced only slightly agglomerated, voluminous, fluffy powder. Applying the Pechini technique resulted in significantly agglomerated powder while the homogeneous precipitation of Lu(OH)3 with urea at 90 °C and its subsequent decomposition to Lu2O3 at 650 °C resulted in a powder of perfectly spherical particles with a uniform size of about 130 nm with very low agglomeration. The efficiency of X-ray excited luminescence of our nanocrystalline Lu2O3:5%Eu was compared to that of the commercial microcrystalline Gd2O2S:Eu. It was found that the commercial phosphor performed four times more efficiently than our nanocrystalline powder. We consider this to be rather encouraging as the fabrication of our powder is not optimized yet. It seems that Lu2O3:Eu, even in nanocrystalline form, can perform much more efficiently which would make it a promising X-ray phosphor.

You might also be interested in these eBooks

Info:

Periodical:

Solid State Phenomena (Volumes 99-100)

Pages:

25-30

Citation:

Online since:

July 2004

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2004 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

[1] A. Lempicki, A. J. Wojtowicz, and C. Brecher, Inorganic Scintillators in: Wide-Gap Luminescent Materials: Theory and Applications, ed. S. R. Rotman (1996) Kluwer Academic Publishers, Norwell, MA), p.235.

DOI: 10.1007/978-1-4615-4100-4_5

Google Scholar

[2] E. Zych, D. Hreniak, and W. Stręk, , J. Alloys Compd. Vol. 341(1-2) (2002), p.385.

Google Scholar

[3] A. Lempicki, C. Brecher, P. Szupryczynski, H. Lingertat, V. V. Nagarkar, S. V. Tipnis, and S. R. Miller, Nucl. Instrum. Meth. A Vol. 488 (2002), p.579.

DOI: 10.1109/nssmic.2001.1008426

Google Scholar

[4] R. D. Shannon, Acta Cystallogr A. Vol. 32 (1976), p.751.

Google Scholar

[5] S. E. Derenzo, W. W. Moses, R. H. Huesman, and T. F. Budinger, ed. K. Uemura, N. A. Lassen, T. Jones, Elsevier Science Publishers, Amsterdam, (1993), p.25.

Google Scholar

[6] S. E. Derenzo, W. W. Moses, M. J. Weber, and A. C. West, Mater. Res. Soc. Symp. Proc. Vol. 348 (1994), p.39.

Google Scholar

[7] W. W. Mosses, in SCINT99 Proceedings of the International Conference on Inorganic Scintillators and Their Applications, ed. V. Mikhailin, Russia, (1999), p.11.

Google Scholar

[8] A. Saiki, N. Ishizawa, N. Mizutani, and M. Kato, Acta Crystallogr. B Vol. 40 (1984), p.76.

Google Scholar

[9] FIZ Karlsruhe & Gmelin Inst., ICSD Collection Code No. 40471 (1990), release 99/1.

Google Scholar

[10] D. Godlinski, M. Kuntz, and G. Grathwohl, J. Am. Ceram., Soc. Vol. 85(10) (2002), p.2449.

Google Scholar

[11] R. Apetz, and M. P. B van Bruggen, J. Am. Ceram. Soc. Vol. 86(3) (2003), p.480.

Google Scholar

[12] E. Zych, A. Meijerink, and C. de Mello Donega, J. Phys.: Condens. Matter. Vol. 15 (2003), p.5145.

Google Scholar

[13] E. Zych, J. Trojan-Piegza, H. Hreniak, and W. Stręk, J. Appl. Phys. vol 94(3) (2003) p.1318.

Google Scholar

[14] M. P. Pechini, US Patent 3 330 697, 11 July (1967).

Google Scholar

[15] E. Zych, J. Phys.: Condens. Matter, 14 (2002), p.5637.

Google Scholar