The lattice sites, valence states, resulting magnetic behaviour and spin-lattice relaxation of Fe ions in GaN and AlN were investigated by emission Mössbauer spectroscopy following the implantation of radioactive 57Mn+ ions at ISOLDE/CERN. Angle dependent measurements performed at room temperature on the 14.4 keV ?-rays from the 57Fe Mössbauer state (populated from the 57Mn ?- decay) reveal that the majority of the Fe ions are in the 2+ valence state nearly substituting the Ga and Al cations, and/or associated with vacancy type defects. Emission Mössbauer spectroscopy experiments conducted over a temperature range of 100-800 K show the presence of magnetically split sextets in the "wings" of the spectra for both materials. The temperature dependence of the sextets relates these spectral features to paramagnetic Fe3+ with rather slow spin-lattice relaxation rates which follow a T2 temperature dependence characteristic of a two-phonon Raman process.
Lattice sites, charge states and spin-lattice relaxation of Fe ions in 57Mn+ implanted GaN and AlN
Mantovan R;
2016
Abstract
The lattice sites, valence states, resulting magnetic behaviour and spin-lattice relaxation of Fe ions in GaN and AlN were investigated by emission Mössbauer spectroscopy following the implantation of radioactive 57Mn+ ions at ISOLDE/CERN. Angle dependent measurements performed at room temperature on the 14.4 keV ?-rays from the 57Fe Mössbauer state (populated from the 57Mn ?- decay) reveal that the majority of the Fe ions are in the 2+ valence state nearly substituting the Ga and Al cations, and/or associated with vacancy type defects. Emission Mössbauer spectroscopy experiments conducted over a temperature range of 100-800 K show the presence of magnetically split sextets in the "wings" of the spectra for both materials. The temperature dependence of the sextets relates these spectral features to paramagnetic Fe3+ with rather slow spin-lattice relaxation rates which follow a T2 temperature dependence characteristic of a two-phonon Raman process.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.