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A Novel Method to Synthesize Blue-Luminescent Doped GaN Powders

Published online by Cambridge University Press:  01 February 2011

R. Garcia
Affiliation:
Department of Physics and Astronomy, Arizona State University, Tempe, AZ 85281-1504
A. Thomas
Affiliation:
Rogers Corporation, Durel Division, Chandler, AZ 85224-6155
A. Bell
Affiliation:
Department of Physics and Astronomy, Arizona State University, Tempe, AZ 85281-1504
F. A. Ponce
Affiliation:
Department of Physics and Astronomy, Arizona State University, Tempe, AZ 85281-1504
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Abstract

A new method to synthesize highly luminescent GaN:Mg powders has been developed. This method has a high control over the concentration of magnesium in the final product. The method consists of reacting a high purity (99.999 %) galliummagnesium alloy with ultra-high purity ammonia in a horizontal quartz tube reactor at high temperatures for several hours. Electron microscopy showed that the light-gray powders produced by this method consist of at least two different shaped crystallites; large columnar crystals sized around 10 μm and small platelets crystals between 1 and 2 μm. X-ray diffraction showed that those crystallites have a well defined wurtzite structure. Room temperature photoluminescence (PL) and cathodoluminescence (CL) showed a high intensity blue emission around 2.94 eV (422 nm). At helium temperature the well known Mg-related donor-acceptor pair band was observed at 3.25 eV (380 nm) by PL and CL.

Type
Research Article
Copyright
Copyright © Materials Research Society 2005

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References

1 Ponce, F. A. and Bour, D. P., Nature (London) 386, 351 (1997).Google Scholar
2 Nakamura, S., Science 281, 956 (1998).Google Scholar
3 Srite, S. and Morkoc, H., J. Vac. Sci. Technol. B10, 12371262 (1992).Google Scholar
4 Stekle, A. J and Zavada, J. M., MRS Bull. 24, 3338 (1999).Google Scholar
5 Lee, S. H., Nahm, K. S., Suh, E.-K. and Hong, M. H., Phys. Stat. Sol., 288, 371373 (2001).Google Scholar
6 Massalski, T. B., Okamoto, H., Subramanian, P. R., Kacprzak, L., “Binary Alloy Phase Diagrams,” ed. Massalki, T. B., Okamoto, H., Subramanian, P. R. and Kacprzak, L., pp.18221823 (1990).Google Scholar
7 García, R., Hirata, G. A., Farías, M. H. and McKittrick, J., Materials Science and Engineering (B): Solid State Materials for Advanced Technology, B90, 712 (2002).Google Scholar
8 Kim, W., Botchkarev, A. E., Salvator, A., Popovici, G., Tang, H. and Morkoc, H., J. Appl. Phys., 82, 219226 (1997).Google Scholar
9 Monemar, B., J. Phys.: Condens. Matter, 13, 70117026 (2001).Google Scholar
10 Albrecht, M., Christiansen, S., Salviati, G., Zanotti-Fregonara, C., Rebane, Y. T., Shreter, Y. G., Mayer, M., Pelzmann, A., Kamp, M., Ebeling, K. J., Bremser, M. D., Davis, R. F., and Strunk, H. P., Mat. Res. Soc. Symp. Proc. Vol., 468, 293298 (1997).Google Scholar
11 Dingle, R. and Ilegems, M., Solid State Communications, 9, 175180 (1971).Google Scholar