Fundamentals Spin-dependent scattering (DOS) in magnetic and non-magnetic metals. 1: the structure of two ferromagnetic and one non-magnetic layers (arrows indicate the direction of magnetization). 2: splitting of DOS for electrons with different spin directions for each layer (arrows indicate the spin direction). F:
Fermi level. The magnetic moment is antiparallel to the direction of total spin at the Fermi level. In magnetically ordered materials, the electrical resistance is crucially affected by scattering of electrons on the magnetic sublattice of the crystal, which is formed by crystallographically equivalent atoms with nonzero magnetic moments. Scattering depends on the relative orientations of the electron spins and those magnetic moments: it is weakest when they are parallel and strongest when they are antiparallel; it is relatively strong in the paramagnetic state, in which the magnetic moments of the atoms have random orientations. For good conductors such as gold or copper, the
Fermi level lies within the
sp band, and the
d band is completely filled. In ferromagnets, the dependence of electron-atom scattering on the orientation of their magnetic moments is related to the filling of the band responsible for the magnetic properties of the metal, e.g., 3
d band for
iron,
nickel or
cobalt. The
d band of ferromagnets is split, as it contains a different number of electrons with spins directed up and down. Therefore, the density of electronic states at the Fermi level is also different for spins pointing in opposite directions. The Fermi level for majority-spin electrons is located within the
sp band, and their transport is similar in ferromagnets and non-magnetic metals. For minority-spin electrons the
sp and
d bands are hybridized, and the Fermi level lies within the
d band. The hybridized
spd band has a high density of states, which results in stronger scattering and thus shorter
mean free path λ for minority-spin than majority-spin electrons. In cobalt-doped nickel, the ratio λ↑/λ↓ can reach 20. According to the
Drude theory, the conductivity is proportional to λ, which ranges from several to several tens of nanometers in thin metal films. Electrons "remember" the direction of spin within the so-called spin relaxation length (or
spin diffusion length), which can significantly exceed the mean free path. Spin-dependent transport refers to the dependence of electrical conductivity on the spin direction of the charge carriers. In ferromagnets, it occurs due to electron transitions between the unsplit 4
s and split 3
d bands. In some materials, the interaction between electrons and atoms is the weakest when their magnetic moments are antiparallel rather than parallel. A combination of both types of materials can result in a so-called inverse GMR effect.
CIP and CPP geometries s in the reading head of a sensor in the CIP (left) and CPP (right) geometries. Red: leads providing current to the sensor, green and yellow: ferromagnetic and non-magnetic layers. V: potential difference.
Electric current can be passed through magnetic superlattices in two ways. In the current in plane (CIP) geometry, the current flows along the layers, and the electrodes are located on one side of the structure. In the current perpendicular to plane (CPP) configuration, the current is passed perpendicular to the layers, and the electrodes are located on different sides of the superlattice. The CPP geometry results in more than twice higher GMR, but is more difficult to realize in practice than the CIP configuration.
Carrier transport through a magnetic superlattice Magnetic ordering differs in superlattices with ferromagnetic and antiferromagnetic interaction between the layers. In the former case, the magnetization directions are the same in different ferromagnetic layers in the absence of applied magnetic field, whereas in the latter case, opposite directions alternate in the multilayer. Electrons traveling through the ferromagnetic superlattice interact with it much weaker when their spin directions are opposite to the magnetization of the lattice than when they are parallel to it. Such anisotropy is not observed for the antiferromagnetic superlattice; as a result, it scatters electrons stronger than the ferromagnetic superlattice and exhibits a higher electrical resistance. Applications of the GMR effect require dynamic switching between the parallel and antiparallel magnetization of the layers in a superlattice. In first approximation, the energy density of the interaction between two ferromagnetic layers separated by a non-magnetic layer is proportional to the scalar product of their magnetizations: : w = - J (\mathbf M_1 \cdot \mathbf M_2). The coefficient
J is an oscillatory function of the thickness of the non-magnetic layer ds; therefore
J can change its magnitude and sign. If the ds value corresponds to the antiparallel state then an external field can switch the superlattice from the antiparallel state (high resistance) to the parallel state (low resistance). The total resistance of the structure can be written as : R = R_0 + \Delta R \sin^2 \frac{\theta}{2}, where R0 is the resistance of ferromagnetic superlattice, ΔR is the GMR increment and θ is the angle between the magnetizations of adjacent layers.
Mathematical description The GMR phenomenon can be described using two spin-related conductivity channels corresponding to the conduction of electrons, for which the resistance is minimum or maximum. The relation between them is often defined in terms of the coefficient of the spin anisotropy β. This coefficient can be defined using the minimum and maximum of the specific electrical resistivity ρF± for the spin-polarized current in the form : \rho_{F\pm}=\frac{2\rho_F}{1\pm\beta}, where
ρF is the average resistivity of the ferromagnet.
Resistor model for CIP and CPP structures If scattering of charge carriers at the interface between the ferromagnetic and non-magnetic metal is small, and the direction of the electron spins persists long enough, it is convenient to consider a model in which the total resistance of the sample is a combination of the resistances of the magnetic and non-magnetic layers. In this model, there are two conduction channels for electrons with various spin directions relative to the magnetization of the layers. Therefore, the
equivalent circuit of the GMR structure consists of two parallel connections corresponding to each of the channels. In this case, the GMR can be expressed as : \delta_H = \frac{\Delta R}{R}=\frac{R_{\uparrow\downarrow}-R_{\uparrow\uparrow}}{R_{\uparrow\uparrow}}=\frac{(\rho_{F+}-\rho_{F-})^2}{(2\rho_{F+}+\chi\rho_N)(2\rho_{F-}+\chi\rho_N)}. Here the subscript of R denote collinear and oppositely oriented magnetization in layers,
χ = b/a is the thickness ratio of the magnetic and non-magnetic layers, and ρN is the resistivity of non-magnetic metal. This expression is applicable for both CIP and CPP structures. Under the condition \chi\rho_N \ll \rho_{F\pm} this relationship can be simplified using the coefficient of the spin asymmetry : \delta_H = \frac{\beta^2}{1-\beta^2}. Such a device, with resistance depending on the orientation of electron spin, is called a
spin valve. It is "open", if the magnetizations of its layers are parallel, and "closed" otherwise.
Valet-Fert model In 1993, Thierry Valet and Albert Fert presented a model for the giant magnetoresistance in the CPP geometry, based on the Boltzmann equations. In this model the
chemical potential inside the magnetic layer is split into two functions, corresponding to electrons with spins parallel and antiparallel to the magnetization of the layer. If the non-magnetic layer is sufficiently thin then in the external field E0 the amendments to the
electrochemical potential and the field inside the sample will take the form : \Delta\mu = \frac{\beta}{1-\beta^2}eE_0\ell_se^{z/\ell_s}, : \Delta E = \frac{\beta^2}{1-\beta^2}eE_0\ell_se^{z/\ell_s}, where
ℓs is the average length of spin relaxation, and the z coordinate is measured from the boundary between the magnetic and non-magnetic layers (z AS or by the so-called interface resistance (inherent to the boundary between a ferromagnet and non-magnetic material) : R_i= \frac{\beta(\mu_{\uparrow\downarrow}-\mu_{\uparrow\uparrow})}{2ej} = \frac{\beta^2\ell_{sN}\rho_N}{1+(1-\beta^2)\ell_{sN}\rho_N/(\ell_{sF}\rho_F)}, where
j is current density in the sample,
ℓsN and
ℓsF are the length of the spin relaxation in a non-magnetic and magnetic materials, respectively. ==Device preparation==