Theoretical predictions of room-temperature ferromagnetism in Mn-doped GaN and other wide band gap semiconductors suggest that these materials might be useful for spintronic applications. In this short review, we summarize recent observations on the gap states of GaN : Mn, which make it impossible that the two main prerequisites of these predictions can be fulfilled at the same time, which are (1) a large concentration of localized Mn 2þ spins coexisting with (2) a high density of free holes in the valence band. Such conditions have been observed in only a few materials like e.g. GaAs : Mn. More typically, transition-metal impurities act as traps for free carriers, thus pinning the Fermi level in the semiconductor band gap far from the valence or conduction band. Alternatively to ferromagnetism mediated by free carriers, the interactions between bound magnetic polarons and the double-exchange mechanism have been suggested to possibly lead to ferromagnetism in GaN : Mn. Because of the energy position and the character of its gap states, Mn seems to be rather unsuitable for these two mechanisms. Better candidates would be GaN : Fe : Mg for a system of magnetic polarons, and GaN : Cr for a double-exchange ferromagnet. Because of its short-range nature, the double-exchange interaction requires rather concentrated alloys and does not offer significant advantages of GaN : Mn over the established ferromagnetic materials. However, microscopic ferromagnetic inclusions observed in many SQUID measurements of GaN : Mn could possibly help to achieve spin injection in nitride semiconductors.
Prerequisites for carrier-mediated ferromagnetismParticularly high Curie temperatures T c have recently been predicted for GaN and other wide band gap semiconductors upon heavy Mn doping [1,2]. Because of the large potential of room-temperature ferromagnetic semiconductors in spintronic devices [3,4], this perspective has triggered significant research activities [5][6][7][8][9][10][11][12][13][14]. According to [1], the magnetic ordering in dilute magnetic semiconductors results from the exchange interaction between localized magnetic spins and delocalized carriers. In particular, the extended wavefunctions of free or weakly bound holes enable a long-range magnetic ordering, which should be adjustable by charge control, e.g. via external gates [15,16], even for low Mn concentrations up to high temperatures. The highest Curie temperatures with T c ! 300 K according to a mean-field Zener model are expected for a d 5 configuration (as found e.g. for Mn 2þ ) and valence-band holes as carriers mediating the magnetic coupling. In GaAs:Mn, the pd exchange energy N 0 b is typically about 1 eV, where N 0 is the concentration of cation sites and b the pd exchange integral between the mostly p-like valence-band states and the mostly d-like Mn 2þ orbitals. It is