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Recent experiments indicate that films of V1-xCrxO2 may be obtained which retain the tetragonal rutile phase to low temperature. In order to better understand this system we have calculated its electronic structure using density functional theory in the generalized gradient approximation and density functional theory with empirical on-site Coulomb correlations (LDA+U). Within these approximations we find that the ground state of rutile phase V1-xCrxO2 is quite simple. Both V and Cr are in the +4 state, implying that the V and Cr ions have moments of 1μB and 2μB, respectively. Similar to CrO2, V1-xCrxO2 is predicted to be ferromagnetic and half-metallic. Our results appear to be consistent with the experimental observations that VO2 is paramagnetic and metallic for temperatures above 340 K where it is stable. It is not clear, however, that these results are completely consistent with recent experimental observations of ferromagnetism at low temperature in V1-xCrxO2 for x=0.1 and x=0.2. [ABSTRACT FROM AUTHOR]

We present tight-binding calculations of the spin torque in noncollinear magnetic tunnel junctions based on the nonequilibrium Green functions approach. We have calculated the spin torque via the effective local magnetic moment approach and the divergence of the spin current. We show that both methods are equivalent, i.e., the absorption of the spin current at the interface is equivalent to the exchange interaction between the electron spins and the local magnetization. The transverse components of the spin torque parallel and perpendicular to the interface oscillate with different phase and decay in the ferromagnetic layer (FM) as a function of the distance from the interface. The period of oscillations is inversely proportional to the difference between the Fermi momentum of the majority and minority electrons. The phase difference between the two transverse components of the spin torque is due to the precession of the electron spins around the exchange field in the FM layer. In the absence of applied bias and for a relatively thin barrier, the component of the spin torque perpendicular to the interface is nonzero due to the exchange coupling between the FM layers across the barrier. [ABSTRACT FROM AUTHOR]

The so-called zigzag edge of graphenes theoretically has localized electrons due to the presence of flat energy bands near the Fermi level. The localized electron spins are strongly polarized, resulting in ferromagnetism. We fabricate graphenes with honeycomb-like arrays of hydrogen-terminated and low-defect hexagonal nanopores by a nonlithographic method using nanoporous alumina templates. We report large-magnitude room-temperature ferromagnetism caused by electron spins localizing at the zigzag nanopore edges. This promises to be a realization of rare-element free, controllable, transparent, flexible, and mono-atomic layer magnets and novel spintronic devices. [ABSTRACT FROM AUTHOR]

Recent experiments indicate that films of V1-xCrxO2 may be obtained which retain the tetragonal rutile phase to low temperature. In order to better understand this system we have calculated its electronic structure using density functional theory in the generalized gradient approximation and density functional theory with empirical on-site Coulomb correlations (LDA+U). Within these approximations we find that the ground state of rutile phase V1-xCrxO2 is quite simple. Both V and Cr are in the +4 state, implying that the V and Cr ions have moments of 1μB and 2μB, respectively. Similar to CrO2, V1-xCrxO2 is predicted to be ferromagnetic and half-metallic. Our results appear to be consistent with the experimental observations that VO2 is paramagnetic and metallic for temperatures above 340 K where it is stable. It is not clear, however, that these results are completely consistent with recent experimental observations of ferromagnetism at low temperature in V1-xCrxO2 for x=0.1 and x=0.2. [ABSTRACT FROM AUTHOR]