Conventional computer electronics creates a dichotomy between how information is processed and how it is stored. Silicon chips process information by controlling the flow of charge through a network of logic gates. This information is then stored, most commonly, by encoding it in the orientation of magnetic domains of a computer hard disk. The key obstacle to a more intimate integration of magnetic materials into devices and circuit processing information is a lack of efficient means to control their magnetization. This is usually achieved with an external magnetic field or by the injection of spin-polarized currents [1,2,3]. The latter can be significantly enhanced in materials whose ferromagnetic properties are mediated by charge carriers [4]. Among these materials, conductors lacking spatial inversion symmetry couple charge currents to spin by intrinsic spin-orbit (SO) interactions, inducing nonequilibrium spin polarization [5,6,7,8,9,10,11] tunable by local electric fields. Here we show that magnetization of a ferromagnet can be reversibly manipulated by the SO-induced polarization of carrier spins generated by unpolarized currents. Specifically, we demonstrate domain rotation and hysteretic switching of magnetization between two orthogonal easy axes in a model ferromagnetic semiconductor.In crystalline materials with inversion asymmetry, intrinsic spin-orbit interactions (SO) couple the electron spin with its momentumhk. The coupling is given by the Hamiltonian H so =h 2σ · Ω(k), whereh is the Planck's constant andσ is the electron spin operator (for holesσ should be replaced by the total angular momentum J). Electron states with different sign of the spin projection on Ω(k) are split in energy, analogous to the Zeeman splitting in an external magnetic field. In zinc-blende crystals such as GaAs there is a cubic Dresselhaus term[12] Ω D ∝ k 3 , while strain introduces a term Ω ε = C∆ε(k x , −k y , 0) that is linear in k, where ∆ε is the difference between strain in theẑ andx,ŷ directions [13]. In wurzite crystals or in multilayered materials with structural inversion asymmetry there also exists the Rashba term[14] Ω R which has a different symmetry with respect to the direction of k,, whereẑ is along the axis of reduced symmetry. In the presence of an electric field the electrons acquire an average momentumh∆k(E), which leads to the generation of an electric current j =ρ −1 E in the conductor, whereρ is the resistivity tensor. This current defines the preferential axis for spin precession Ω(j) . As a result, a nonequilibrium current-induced spin polarization J E Ω(j) is generated, whose magnitude J E depends on the strength of various mechanisms of momentum scattering and spin relaxation [5,15]. This spin polarization has been measured in non-magnetic semiconductors using optical [7,8,9,11,16] and electron spin resonance [17] techniques. It is convenient to parameterize J E in terms of an effective magnetic field H so . Different contributions to H so have different current dependencies (∝ j or j 3 ), as we...

A rapidly developing field of spintronics is based on the premise that substituting charge with spin as a carrier of information can lead to new devices with lower power consumption, non-volatility and high operational speed. Despite efficient magnetization detection, magnetization manipulation is primarily performed by current-generated local magnetic fields and is very inefficient. Here we report a novel non-volatile hybrid multiferroic memory cell with electrostatic control of magnetization based on strain-coupled GaMnAs ferromagnetic semiconductor and a piezoelectric material. We use the crystalline anisotropy of GaMnAs to store information in the orientation of the magnetization along one of the two easy axes, which is monitored via transverse anisotropic magnetoresistance. The magnetization orientation is switched by applying voltage to the piezoelectric material and tuning magnetic anisotropy of GaMnAs via the resulting stress field.Comment: 4 pages, 5 figure

We report charge-ordered Bi0.4Ca0.6MnO3 thin films with charge-ordering temperature near room temperature, and observation of large photoinduced resistivity changes in these films associated with melting of the charge ordering by visible light. Films grown under small compressive strain exhibit the largest photoinduced resistivity changes. The lifetime of the photoinduced low-resistance state is on the order of half a minute. These photoinduced resistivity changes in thin films of Bi0.4Ca0.6MnO3 make them very promising for photonic device application.

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We report the structural and electronic characterization of the charge order phase in Bi0.4Ca0.6MnO3 films, in which photoinduced resistivity changes have been observed at temperatures approaching room temperature. In all films, lattice distortions associated with the charge order are observed, and both the wavevectors and displacements of the distortions are in the plane of the film. Films under compressive and tensile strain are observed to have different resonant xray scattering characteristics-a result that may shed light on the mechanism responsible for the photosensitivity exhibited by this material.