p-doping of GaN by MOVPE


S. Haffouz, B. Beaumont, M. Leroux, M. Laugt, P. Lorenzini, Pierre GIBART
Centre de Recherche sur l'Hétéroépitaxie et ses Applications, CRHEA-CNRS

L.G.Hubert-Pfalzgraf
Laboratoire de Chimie Moléculaire,Faculté des Sciences, Nice, France

This article was received on Wednesday, July 2, 1997 and accepted on Tuesday, September 16, 1997.

Abstract

Mg has been widely used as p-doping species despite its intrinsic difficulties. It is nowadays well established that during the growth process of Mg doped GaN, atomic H is generated from the decomposition of NH3 and Mg-H complexes are formed in the layer. This has been for instance shown by the occurrence of LO mode in IR absorption, and by the observation of the Mg-H local vibration modes. This H passivation limits the electrical activity of Mg, therefore an activation process is required to get full activation of the Mg atoms. In the present study, bismethylcyclopentadienyl magnesium [(MeCp)2Mg] was used as precursor. However, this precursor reacts in the gas phase with NH3 to produce tiny solid particles as evidenced by a very bright diffuse emission visible along the laser beam used for reflectometry measurements. This simplest obvious product would be [(MeCp)Mg(NH2)]m (m>=2). To limit this drawback, Ga and Mg precursor lines have been separated. With proper in situ heat treatment, doping densities up to 1.5x1018 cm-3 have been obtained. PL spectra of lightly Mg doped samples (1016 cm-3) are dominated by shallow donor-acceptor pairs whereas for higher doping densities ( 1018 cm-3), the luminescence is dominated by a broad band in the 2.7-2.9 eV range. GaN LEDs were fabricated from Si doped (n-type) and Mg-doped (p-type) GaN, these LEDs emit in the blue-UV range.

Outline

  • Introduction 
  • Experimental : growth of Mg-doped GaN
  • Chemistry
  • Photoluminescence
  • LED's fabrication
  • Acknowledgments
  • Linked Pages

    Cite this article as: MRS Internet J. Nitride Semicond. Res. 2, 37(1997).

    last updated Thursday, November 2, 2000 5:40:40 PM.

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