PACS 72.25. Mk, 75.50.Gg We analyze the spin-controlled charge transfer through a heterostructure consisting of one octahedral and one tetrahedral iron -oxygen ionic clusters, which are site-coupled, sharing an oxygen ion. A number of charge carriers can be manipulated by valence-uncompensated doping. The electron-energy structure of the clusters and that of the heterostructure are found on the basis of the Anderson model. Current -voltage (I-V) characteristics, derived from the Landauer-like formula, turn out to be highly sensitive to the position of the Fermi level. We also calculated the magnetoresistance for the heterostructure with different orientations of the magnetic field. The result confirmed the empirical data for Ca : YIG, which indicate strong anisotropy of the magnetoresistance.
A microscopic model of the heterostructure and its magnetic propertiesIron-oxygen garnets, doped with divalent calcium ions (Ca:YIG) which donate compensating holes, offer a rare opportunity to produce semiconducting materials with permanent magnetic moments and a controlled number of the charge carriers [1]. Divalent diamagnetic ions substitute diamagnetic yttrium, which indirectly tailors also the magnitude and orientation of permanent magnetic moments attached to the clusters, while leaving magnetic cations unchanged. In our analysis, special attention will be focused on a role which the oxygen ions play in the charge transfer. One of our objectives is to show that the process is due to the p-d hybridization and can occur mostly via the oxygen ions. This suggestion remains in good agreement with the empirical data, and, it is confirmed by our previous theoretical results [2]. The heterostructure is attached to two reservoirs of the electrons. A control of the number of the charge carriers in the clusters can be maintained by assuming different positions of the Fermi level. We assume that all five 3d orbital states of Fe 3+ are occupied and, according to the Hund's rule, their respective spins are along the same direction. Thus, at either iron site, the angular momentum L is zero, whereas the net spin S is equal to 5 2 S = / . In case of O 2-, all six 2p spin-orbital states are occupied, and both the resultant orbital angular momentum and the resultant spin are equal to zero. In terms of orbital holes we start with vacuum at O 2-and five holes at each iron site. The available empirical data indicate that the charge transport in Ca:YIG is of the p-type. The Coulomb repulsion at the iron sites is limited to the strongest one between electrons in the same orbital eigen-states with mutually opposite spins. The on-site Coulomb repulsion, however, is neglected at the oxygen sites.