A detailed analytical and numerical study of the spin wave modes of two nanopillar spin torque nano-oscillators coupled by magnetostatic interactions is presented under the macrospin approximation. Results show that the normal modes of the system oscillate with the magnetizations in-phase or anti-phase in both disks. The frequencies and critical current densities necessary to induce auto-oscillations of the spin wave modes of the coupled system depend on the relative position of the nanopillars and the applied magnetic field. If the oscillators are identical, these modes are degenerate at a certain relative position of the nanopillars, while if the oscillators are non-identical, such degeneracy is removed. Then, we can conclude that the magnetostatic coupling between two spin transfer torque nano-oscillators is a powerful mechanism to control the spin wave modes of these systems.

During the last two decades, the study of spin transfer torque nano-oscillators (STNOs) has received quite a bit of attention due to their potential applications in wireless telecommunication technology, in the implementation of magnetic field sensors, and in several other radio frequency (RF) nano-scale devices.1–4 A frequently addressed STNO is a nanopillar, typically composed of two ferromagnetic layers separated by a non-magnetic spacer. The ferromagnetic layers are known as the fixed and the free layer, since their magnetizations are mainly fixed or free to move in response to external stimulus. When a current is injected into the system, the electron spins get polarized in the direction of the magnetization of the fixed layer and then exert a torque on the magnetization of the free layer. This spin transfer torque has an anti-damping effect that can generate an auto-oscillatory regime in the normal modes of the free layer.5,6 The minimum dc current density necessary to observe these oscillations is called the critical current density.

Due to their properties, such structures are proposed as a model-system to emulate neurons and synapses through their nonlinear dynamics.7–9 Currently, coupled oscillator networks are candidates for the realization of associative memories, in which a recognition is obtained when this network converges to a synchronized state.10–12 This synchronization may be obtained through the interaction between the STNOs, as through electrical connections,13–15 emission of spin waves,16,17 or by magnetostatic interactions.18–21 Some studies have addressed the magnetostatic coupling between nano-oscillators; however, most of them consider a vortex state as the equilibrium magnetization configuration19,22,23 instead of a uniform state of the magnetization.21,24 In particular, Chen et al.21 developed an interesting work determining the critical current needed for synchronizing two nano-oscillators considering that the same or different currents are applied to both oscillators. A similar study was done by Zhang et al.,24 who determined the different degrees of synchronization that two nano-oscillators show in the presence of different external magnetic fields and injected currents to each STNO.

Despite the advances made by these authors, an open question is the role played by the STNO’s relative locations when the equilibrium magnetizations are fixed by an external magnetic field applied along a particular direction. In these systems, the magnetostatic interaction plays a significant role because the relative position of the nano-oscillators can favor the parallel or antiparallel magnetization alignment. An example of this can be seen in the studies of the interaction between two magnetic nanotubes25 or two rough slabs,26 in which the magnetic interaction energy changes sign depending on the relative positions between the samples.

Thus, in this work, we study the uniform normal modes of two STNOs located in the same plane, coupled by the magnetostatic interaction, as a function of their relative position. Using a standard Hamiltonian formalism,27–29 we determined the spin wave modes of the coupled disks in the macrospin approximation. We found that there are two uniform modes, with the magnetic moments oscillating in-phase or anti-phase, respectively. The frequencies of the modes depend on the relative positions of the two nanopillars and the applied magnetic field. We also obtained the critical current density needed to induce self-oscillations for identical and different STNOs.

This paper is organized as follows: in Sec. II, we describe the model and formalism used to determine the spin wave modes and the critical current densities; in Sec. III, we present and discuss our results; and finally, in Sec. IV, we present our conclusions.

Our model system consists of two nanopillar devices of circular cross sections, with radii R1 and R2. Each nanopillar is composed of two ferromagnetic layers separated by a non-magnetic metallic spacer. We define S as the shortest distance between the surfaces of the nanopillars, i.e., they have a center to center distance D=R1+R2+S. The unit vector along the direction that connects nanopillars 1 and 2 is n^, as illustrated in Fig. 1. There is an external magnetic field applied to the system, H=Hxx^. We consider that the free layers, located in the same plane, are disks of soft ferromagnets with a saturation magnetization Ms and a very small thickness L, as shown in Fig. 1. Both free layers are magnetized in plane along the direction of the applied field, i.e., the x-direction. In addition, the same current density J=Jz^ is injected to each nanopillar. Both nanopillars are coupled through magnetostatic interactions (see  Appendix A for details). In this work, we focus our attention on the magnetostatic interaction between the free layers, and we vary the angle θ between n^ and x^, i.e., cos(θ)=n^x^. Also, the magnetostatic interaction between the fixed and free layers slightly modifies the eigenfrequencies and critical current of the system, as is discussed in Appendix A 3.

FIG. 1.

Spatial configuration of the nanopillars and magnetic field, all in the same plane.

FIG. 1.

Spatial configuration of the nanopillars and magnetic field, all in the same plane.

Close modal

To find the normal modes and critical current densities of our system as a function of the magnetostatic interaction between the free layers, we analyze the magnetization dynamics of them by means of the Landau-Lifshitz-Slonczewski (LLS) equation4 using the Hamiltonian formalism.27–29 We use the macrospin approximation,30,31 that is, we assume that the magnetizations of the free layers are uniform.

The magnetizations of the free layers are free to move in response to the external current applied to the system, and their dynamics can be obtained through the LLS equation4 given by

(1)

where mk=Mk/Ms is the normalized magnetization of the k free layer, with k={1,2} and Ms the saturation magnetization. Time is normalized through τ=|γ|4πMst, where |γ|=1.76107Oe1s1 is the absolute value of the gyromagnetic ratio. The normalized effective field is heff,k=Heff,k/(4πMs), α is a dimensionless quantity and corresponds to the damping parameter, J represents the current density applied on each free layer, p^ the spin polarization direction, and β=2πϵ/[(4πMs)2eL] is the spin transfer torque parameter,27 with ϵ the polarization factor that varies between 0 and 1 and e the magnitude of the electron charge.

To study the dynamics of our system, we introduce new variables ak and ak through a classical Holstein-Primakoff transformation,32,33 which are related with the magnetization components through

(2a)
(2b)
(2c)

where super-indices x, y, and z represent the components of the magnetization in the corresponding directions and k identifies free layer 1 or 2. The variable ak is the complex conjugate of ak. These new variables represent perturbations around the equilibrium magnetization, which is in plane. Through this change of variables, the LLS equations for the magnetizations mk are transformed, to linear order, into the following equations29,34,35

(3)

where Vk is the volume of the k free layer and Utot=Etot/4πMs2 is the normalized total energy of the system defined as

(4)

In this expression, UZ, UD, and UI are the normalized Zeeman, self demagnetizing, and magnetostatic interaction energies, respectively. The expressions for these energies, as a function of ak and ak, are found in  Appendix B (see Sec. B 1 for UZ, Sec. B 2 for UD, and Sec. B 3 for UI). We do not include an exchange term because we assume that the magnetizations are uniform.

In this subsection, we develop the methodology to obtain the normal mode frequencies and the critical current densities of our system. We start with a well known result for an isolated nanopillar. After that, we introduce the magnetostatic coupling between the free layers.

In an isolated nanopillar with free layer magnetized in plane and from Eq. (3), we obtain

(5)

where Ak=hx+hkd/2 and Bk=hkd/2. The expressions hx=Hx/(4πMs) and hkd are the magnitudes of the normalized external magnetic field and the normalized demagnetizing factor in the z direction, respectively [see Eq. (B7) for hkd]. The normalized demagnetizing field points along the z-axis with hkd=hkdmkzz^, where the demagnetization factor hkd depends on the geometrical parameters of the disk, i.e., the thickness L and the radius Rk. To obtain the normal modes of an isolated nanopillar, we diagonalize the set of Eq. (5) through the change of variables32 

(6)

with λk=(Ak+ωk)/(2ωk), μk=(Akωk)/(2ωk), and ωk the normalized angular frequency. Finally, Eq. (5) and its conjugate are equivalent to

(7)

and its complex conjugate equation. The solution of Eq. (7) corresponds to a damped oscillator, bk(τ)=bk0e(iωk+γk)τ, in which34,36

(8a)
(8b)

The constant bk0 represents the initial condition at τ=0 and γk corresponds to the effective dissipation constant. In this expression, γk depends on the current density, J. To obtain the critical current density necessary to induce auto-oscillation of the magnetization, the effective dissipation must be zero. With this condition, the critical current density of the isolated macrospin mode is34,36

(9)

If we now include the magnetostatic interaction between the free layers, Eq. (3) for ak and ak and their conjugates become

(10)

where a=(a1,a1,a2,a2) and M=[(1iαI)M+iβJI]. The elements of the I matrix are Iij=δij(1)i+1, with I the identity matrix and

(11)

Here,

The quantities gx, gy, and gz are related to the magnetostatic interaction between the free layers and are derived in  Appendix B [see Eqs. (B13a)–(B13d)]. To obtain the normal modes and the critical current densities of the coupled nanopillars, we need to diagonalize the M matrix. In this step, we write M=PDP1, where the P matrix is related to the eigenstates of the system and the D diagonal matrix is related to the eigenvalues of the system. Then, we introduce a new change of variables a=Pb, with b=(bip,bip,bap,bap), where the subscripts ip and ap represent in-phase and anti-phase, respectively. In this way, we obtain

(12)

where the diagonal elements of D are D11=ωip+iγip, D22=D11, D33=ωap+iγap, and D44=D33. The quantities ωip, ωap, γip, and γap are real numbers. ωip and ωap represent the normalized oscillation frequencies (angular), and γip and γap represent the effective damping, as we can see from the solutions of Eq. (12):

(13a)
(13b)

Initial conditions at τ=0 are given by bip0 and bap0. The above solutions show that the normal modes oscillate in-phase or anti-phase, with the eigenvectors given by P. The in-phase mode is characterized by the y^ and z^ components of the magnetization having the same sign in both nanopillars. On the other hand, the anti-phase mode is characterized by opposite signs for these components of the magnetization, i.e., sgn(m1y)=sgn(m2y) and sgn(m1z)=sgn(m2z), as shown in Fig. 2. In both modes, we have sgn(m1x)=sgn(m2x) when the amplitudes of the spin waves are small. These modes are also called binding and anti-binding modes37 or optical and acoustic modes38 and have been observed by ferromagnetic resonance force microscopy.39 

FIG. 2.

Qualitative representation of the normal modes of two coupled nano-oscillators, at θ=0, with the same dimensions.

FIG. 2.

Qualitative representation of the normal modes of two coupled nano-oscillators, at θ=0, with the same dimensions.

Close modal

From Eq. (10), it is possible to obtain analytical expressions for the eigenfrequencies, by diagonalizing the matrix M when the system is free of dissipation and spin transfer torque, i.e., α=0 and J=0 or M=M. In this case, the angular eigenfrequencies are

(14)

where

(15)
(16)

It is important to note that the frequencies ω± are functions of θ. It is possible to identify a particular angle, θ1, such that for θ<θ1, ω+=ωip and ω=ωap, and for θ>θ1, ω+=ωap and ω=ωip. To determine θ1, it is necessary to interpret the eigenvectors that can be numerically obtained.

Finally, to obtain the critical current densities, we solved numerically Eq. (10) including dissipation and spin transfer torque. Then, the critical current densities, JipC and JapC, can be obtained imposing γip=0 and γap=0, respectively.

We consider two permalloy free layers defined by magnetic parameters Ms=860 kA/m and A=1.3×1011 J/m. To solve the LLS equation, we used a damping parameter α=0.01 and a polarization factor ϵ0.11. In all the cases, we considered an applied magnetic field with magnitude |H|=1 kOe. With these parameters, we addressed two cases, identical and non-identical nano-oscillators, where the shortest distance between them is S=10 nm (see  Appendix C for other values of S). Both free layers have the same thickness, L=5 nm.

In this section, we find the frequencies and critical current densities for two identical free layers of radius R=50 nm, with demagnetizing factors h1d=h2d=hd, and normalized applied magnetic field hx. In the absence of dissipation and spin transfer torque, we obtained an analytical expression for the angular eigenfrequencies from Eq. (14):

(17a)
(17b)

where gx, gy, and gz were already introduced after Eq. (11) [see Eqs. (B13a)–(B14c)]. According to Eq. (8a), the eigenfrequency for an isolated nanopillar is ωk=hx(hx+hkd). By comparing this with Eqs. (17a) and (17b), we identify effective applied fields hx±=hx+(gx±gy) and effective demagnetizing factors hd±=hd±(gzgy). In this way, we write Eqs. (17a) and (17b) as

(18a)
(18b)

Figure 3 illustrates the frequencies fip=2|γ|Msωip and fap=2|γ|Msωap, obtained from Eqs. (18a) and (18b) for different θ values, for R=50 nm and D=110 nm. In addition, the frequency of an isolated disk, f0=2|γ|Msω0, is also depicted. We observe that for θ=0, the lower frequency mode is the anti-phase one, while for θ=π/2, the lower frequency mode is the in-phase one. Also, there is a degeneracy in the frequency at θ1, i.e., fap=fip. This angle can be obtained through the condition

(19)

and for the parameters previously mentioned θ10.6 rad. This behavior can be understood through the analysis of the surface magnetic charges of the free layers. In Fig. 4, we show a schematic representation of these magnetic charges. Figures 4(a) and 4(c) represent the in-phase modes at θ=0 and θ=π/2, respectively. Figures 4(b) and 4(d) represent the anti-phase modes at θ=0 and θ=π/2, respectively. At θ=0, we observe that the distance between the positive charge of the free layer 1 and the negative charge of the free layer 2 is smaller in the anti-phase mode. For this reason, when θ=0, we may argue that the lower frequency mode is the anti-phase one. On the contrary, when θ=π/2, we observe that this distance is smaller in the in-phase mode, and then we may argue that the lower frequency mode is the in-phase one.

FIG. 3.

Frequencies of the in-phase (fip) and anti-phase (fap) modes as a function of θ for identical nano-oscillators with a radius of 50 nm and at a distance D=110 nm apart. In addition, f0 represents the frequency of an isolated nano-oscillator.

FIG. 3.

Frequencies of the in-phase (fip) and anti-phase (fap) modes as a function of θ for identical nano-oscillators with a radius of 50 nm and at a distance D=110 nm apart. In addition, f0 represents the frequency of an isolated nano-oscillator.

Close modal
FIG. 4.

Magnetic charges at the surfaces of two free layers. The center column represents the in-phase mode and the right column represents the anti-phase mode. The center rod represents the configurations with θ=0 and the bottom rod represents the configurations with θ=π/2.

FIG. 4.

Magnetic charges at the surfaces of two free layers. The center column represents the in-phase mode and the right column represents the anti-phase mode. The center rod represents the configurations with θ=0 and the bottom rod represents the configurations with θ=π/2.

Close modal

In addition, from Fig. 3, we observe that the changes in frequency with angle for the in-phase mode is larger than the equivalent variation for the anti-phase mode. To explain qualitatively this behavior, first, we calculate the difference of the expected value of the total energy between θ=0° and θ=90°, for the in-phase and anti-phase modes, in the absence of dissipation and spin transfer torque (γip=γap=0). Then, we compare these differences between the two modes. To calculate the difference between the expected value of the total energy between θ=0° and θ=90° for one mode, it is necessary to calculate only the expected value of the magnetostatic interaction energy. It is because the Zeeman and the self-magnetostatic energies are the same if we consider the same oscillation amplitude for both angles. The magnetostatic interaction energy [see Eq. (B15)], normalized by the volume V=πR2L of a disk is

(20)

(we neglected terms that couple mx and my that produce a small effect on the linear spin wave modes). We write the magnetizations of the free layers as a function of the normal modes, and we calculate the time average of the normalized magnetostatic energy over a period of oscillation, uIip(θ) and uIap(θ), for the in-phase and anti-phase modes, respectively:

(21)
(22)

In these calculations, we only consider a time average over the interaction energy of the perturbations around the equilibrium magnetization of the system (there is a time invariant interaction energy associated with the equilibrium magnetizations that depends on the relative positions but that is independent of the modes involved). Then, we consider the interaction energy to second order, written with respect to bip and bip, or to bap and bap. In this context, the results obtained from Eqs. (21) and (22) are proportional to |bip0|2 or |bap0|2, and they are time invariant in an oscillation period. For the in-phase mode, we obtain |uIip(π/2)uIip(0)|/|bip0|20.021 and for the anti-phase mode |uIap(π/2)uIap(0)|/|bap0|20.001. Since it is possible to relate the variations of the mode interaction energies with frequency variations, one may conclude that the anti-phase frequency exhibits smaller changes than the in-phase frequency as a function of θ, which corresponds to what is illustrated in Fig. 3.

Finally, we analyze the critical current densities of both normal modes. According to Eq. (9), the critical current density of an isolated free layer is JkC=α(hx+hkd/2)/β. Using this expression and replacing the applied field by the effective applied fields, hx±=hx+(gx±gy), and the demagnetizing factor by the effective demagnetizing factors hd±=hd±(gzgy), the critical current densities obtained for the two modes when the free layers are coupled through the magnetostatic interaction are J±C=α(hx±+hd±/2)/β, i.e., the critical current densities for the in-phase and the anti-phase modes would be

(23a)
(23b)

In addition to this analysis, we have computed the critical current densities numerically by diagonalizing M in Eq. (10). We verified that both procedures deliver the same results. The critical current densities are plotted in Fig. 5 as a function of θ. In this figure, it is shown an angle, θ2, at which both critical current densities are the same, i.e., JipC=JapC. Then, by using Eqs. (23a) and (23b), we have the condition gy(θ2)+gz=0. For our parameters, θ21.03 rad. For θ<θ2, the lower critical current density corresponds to the anti-phase mode, while for θ>θ2, it corresponds to the in-phase mode. Therefore, there is a region between θ1 and θ2 in which the lowest critical current density corresponds to the normal mode of the highest frequency, i.e., the anti-phase mode. In the same way, for this region, the highest critical current density corresponds to the normal mode of the lowest frequency, i.e., the in-phase mode. This behavior occurs because the effective dissipation for the in-phase mode, γip=α(hx+hd/2)βJ, and the anti-phase mode, γap=α(hx++hd+/2)βJ, is not proportional to the frequencies, as shown from Eqs. (18a) and (18b).

FIG. 5.

Critical current densities, for two identical nano-oscillators with R=50 nm, of the anti-phase (JapC) and the in-phase (JipC) modes, as a function of θ. J0C represents the critical current density of an isolated nano-oscillator.

FIG. 5.

Critical current densities, for two identical nano-oscillators with R=50 nm, of the anti-phase (JapC) and the in-phase (JipC) modes, as a function of θ. J0C represents the critical current density of an isolated nano-oscillator.

Close modal

It is interesting to note that there is a region in which the critical current densities of both modes are lower than the critical current density of an isolated free layer represented by J0C. This region, shown in Fig. 5, corresponds to θθ2.

In this section, we find the frequencies and critical current densities for two non-identical oscillators with R2R1, and therefore, h1dh2d. We considered an applied magnetic field Hx that normalized by 4πMs defines hx. In the absence of dissipation and spin transfer torque, the frequencies are given by Eq. (14). Figure 6 illustrates these frequencies as a function of θ. We consider two cases: for the first one, we used R1=50 nm and R2=48 nm [see Fig. 6(a)]. For the second case, we used R1=50 nm and R2=40 nm [see Fig. 6(b)].

FIG. 6.

Frequencies of the in phase (fip) and anti phase (fap) modes as a function of θ for two non-identical nano-oscillators. f1 represents the frequency of the isolated nanopillar 1 and f2 represents the frequency of the isolated nanopillar 2. The geometrical parameters are (a) R1=50 nm and R2=48 nm and (b) R1=50 nm and R2=40 nm. (c) Zoom of Fig. 6(a).

FIG. 6.

Frequencies of the in phase (fip) and anti phase (fap) modes as a function of θ for two non-identical nano-oscillators. f1 represents the frequency of the isolated nanopillar 1 and f2 represents the frequency of the isolated nanopillar 2. The geometrical parameters are (a) R1=50 nm and R2=48 nm and (b) R1=50 nm and R2=40 nm. (c) Zoom of Fig. 6(a).

Close modal

In Figs. 6(a) and 6(b), the horizontal lines illustrate the frequencies of the isolated free layers, denoted f1 and f2, and the vertical line shows the transition between the different modes at the angle θ1. Below θ1, the frequency of the in-phase mode is higher than the frequency of the anti-phase mode, but above θ1, the opposite occurs. This behavior can be understood from Fig. 4, as occurs for identical oscillators. A difference between identical and non-identical oscillators is the split of frequencies, δf=|fipfap| for non-identical oscillators at θ=θ1. This split of frequencies increases as the difference between R1 and R2 increases. For example, we have δf0.01 GHz for R2=48 nm, see Fig. 6(c), while δf0.06 GHz for R2=40 nm, see Fig. 6(b). This split of frequencies can be understood from Eq. (14). When we have identical oscillators, the expression inside the root (δ2Δ+Δ) in Eq. (14) is zero at θ=θ1, then ω+=ω. On the contrary, (δ2Δ+Δ) is different from zero when we have non-identical oscillators (different demagnetization and magnetostatic fields); therefore, there is a split in the frequencies at θ=θ1. To understand the transition between the two modes shown in Figs. 6(a) and 6(b), we run simulations for the magnetization given by Eq. (1) for different θ. We consider two non-identical nano-oscillators with R1=50 nm, R2=40 nm, and S=10 nm. The objective was to compare these results with our analytical and numerical results and to confirm the validity of our model.

Figure 7 illustrates the y-component of the magnetization dynamics of the two oscillators, m1y and m2y, as a function of time, where the time T is much larger than the transient time. The applied current densities are higher than the minimum critical current density, and then, we observe oscillations of the magnetization associated with the mode of lowest frequency. In Fig. 7(a), for θ=0° and J=5.61×107 A/cm2, the oscillations correspond to the anti-phase mode. In Fig. 7(b), for θ=37° and J=5.56×107 A/cm2, the oscillations still correspond to the anti-phase mode. In Fig. 7(c), for θ=39° and J=5.56×107 A/cm2, the oscillations now represent an in-phase mode. Finally, in Fig. 7(d), for θ=90° and J=5.48×107 A/cm2, the oscillations describe an in-phase mode. We observe that the amplitude of the oscillator 2 is always bigger than the oscillation amplitude of the oscillator 1, but the difference of amplitudes increases for angles near to 37° and 39°, where the amplitude of the oscillator 1 tends to zero. We conclude that there is a continuous transition from the anti-phase mode to the in-phase mode for an angle between 37° and 39°. At the specific angle of transition, θ1, the amplitude of the oscillator 1 is zero when the applied current density is equal to the critical current density. This behavior is qualitatively consistent with our previous results; however, there is a quantitative difference in the angle of transition, given that our analytical calculations predict θ134.55°. The difference appears because in our analytical calculations, for simplicity, we consider that the equilibrium magnetization is in the x-direction, i.e., we consider that gxy=0 [see  Appendix B, specifically Sec. 3]. In addition, we analyze the Fourier spectrum of the signal m1y. We observe that the peaks of the signal are: f8.63 GHz for θ=0°, f8.51 GHz for θ=37°, f8.50 GHz for θ=39°, and f7.88 GHz for θ=90°. This behavior is consistent with Fig. 6(b), where the frequency decreases as θ increases.

FIG. 7.

Numerical integration of Eq. (1) for two non-identical oscillators with R1=50 nm and R2=40 nm. Magnetizations m1y and m2y as a function of time for (a) θ=0° and J=5.61×107 A/cm2; (b) θ=37° and J=5.56×107 A/cm2; (c) θ=39° and J=5.56×107 A/cm2; and (d) θ=90° and J=5.48×107 A/cm2.

FIG. 7.

Numerical integration of Eq. (1) for two non-identical oscillators with R1=50 nm and R2=40 nm. Magnetizations m1y and m2y as a function of time for (a) θ=0° and J=5.61×107 A/cm2; (b) θ=37° and J=5.56×107 A/cm2; (c) θ=39° and J=5.56×107 A/cm2; and (d) θ=90° and J=5.48×107 A/cm2.

Close modal

Finally, Fig. 8 illustrates the critical current densities for the in-phase and anti-phase modes as a function of θ. These current densities are obtained from numerical calculations. The behavior illustrated in Fig. 8(a) is similar to the one exhibit for identical oscillators shown in Fig. 5, but in the region closer to θ1, the critical current densities change abruptly their slopes. At θ1, one of the amplitudes of the magnetization oscillation is zero, that is, there is a steady state with a saturated magnetization in one direction. This magnetization (from free layer i) exerts a magnetic field in the x-direction on the other free layer (free layer j) equal to (Ri/Rj)gx [see Eq. (B12)], and then

(24)
(25)

The difference between both critical currents at θ1 is

(26)

This quantity increases as the difference between the radius of the free layers increases.

FIG. 8.

Critical current densities of the anti-phase (JapC) and the in-phase (JipC) modes as a function of θ for two non-identical nano-oscillators. J1C represents the critical current density of the isolated nanopillar 1 and J2C represents the critical current density of the isolated nanopillar 2. (a) R1=50 nm and R2=48 nm. (b) R1=50 nm and R2=40 nm. (c) Zoom of Fig. 8(a).

FIG. 8.

Critical current densities of the anti-phase (JapC) and the in-phase (JipC) modes as a function of θ for two non-identical nano-oscillators. J1C represents the critical current density of the isolated nanopillar 1 and J2C represents the critical current density of the isolated nanopillar 2. (a) R1=50 nm and R2=48 nm. (b) R1=50 nm and R2=40 nm. (c) Zoom of Fig. 8(a).

Close modal

In summary, by means of analytical and numerical calculations, we studied the normal modes of two free layers coupled through magnetostatic interactions. Two cases were considered, identical and non-identical free layers. We focused on the eigenfrequencies of the in-phase and anti-phase modes as well as on the critical current densities necessary to induce self-oscillations of the magnetization. Both the eigenfrequencies and the critical current densities were studied as a function of the relative position between the nanopillars.

While the frequency of the magnetization oscillation of the anti-phase mode is almost constant as a function of the relative position of the nanopillars, in the in-phase mode, such frequency changes with this position. This behavior is explained analyzing the time average of the normalized magnetostatic energy over a period of oscillation for the in-phase and anti-phase modes. In addition, for identical oscillators, both modes are degenerate at a particular position, while for non-identical nanopillars, the difference in the geometry induces a split in the frequencies that removes the degeneracy. This split increases with the difference between the radius of both STNOs.

We also observe that the coupling of two identical nanopillars generates a decrease of the critical current densities of both modes for some positions, as compared to an isolated nanopillar. For non-identical oscillators, there exists a particular relative position at which the critical current densities of both modes behave quite sensitively. This behavior is explained through an analysis of the amplitude of the oscillation of the magnetization in both free layers. Therefore, by changing the relative position of two STNOs, it is possible to control their normal modes and critical current. In consequence, relative position is a powerful element and can be used for the design and control of STNOs for associative memory.

The authors thank A. O. León for fruitful discussions and acknowledge financial support in Chile from FONDECYT (Nos. 1161018, 1160198, and 1170781), Financiamiento Basal para Centros Científicos y Tecnológicos de Excelencia (No. FB 0807), and AFOSR Neuromorphics Inspired Science (No. FA9550-16-1-0384). D.M.-A. acknowledges financial support in Chile from CONICYT, Postdoctorado FONDECYT 2018, folio 3180416.

The magnetostatic field produced by the i fixed layer can be calculated through the magnetostatic potential Φifix, and then the demagnetizing field can be obtained through the relation Hifix=Φifix. The magnetostatic potential is given by

(A1)

where σifix=n^iM(xi)=ρ^iMsx^=Mscos(ϕi) is the effective surface magnetic charge density on the surface of the disk i. We consider that fixed and free layers are made of the same material and that they are magnetized along the x-direction. The fixed layer i has a thickness Lfix and a radius Ri. The demagnetizing potential can be written as

(A2)

where Jm(kρ) are the Bessel functions of the first kind. Calculating the integrals, the magnetostatic potential of the i fixed layer, for z>Lfix, is

(A3)

Finally, the magnetostatic field can be written as

(A4)

1. Magnetostatic interaction between the free and fixed layers of the same nanopillar

In this section, we consider the magnetostatic interaction between the fixed and free layers of the same nanopillar. The average of the magnetostatic field produced by the fixed layer in the volume of the i free layer is

(A5)

where Ls is the thickness of the non-magnetic spacer. When integrating in the ϕ coordinate, only the x-component of the field remains. This field, normalized by 4πMs, is

(A6)

where g1(q,Ri)=(1eqLfix/Ri)(1eqL/Ri)eqLs/Ri. In particular, if we consider R1=R2=50 nm, Lfix=5 nm, L=5 nm, and Ls=10 nm, we obtain hiifix0.02x^, which is approximately 20% of the applied field. The effect of this interaction is to decrease both the eigenfrequencies and the critical current densities.35 

2. Magnetostatic interaction between the free layer and the fixed layer of different nanopillars

In this section, we consider the magnetostatic interaction between a fixed layer and a free layer of a different nanopillar. Coordinates ρ and ϕ in Eq. (A3) are related to the center of the i fixed layer. In order to relate these coordinates to the polar coordinates of the j free layer, we write

(A7)

where the new coordinates ρ and ϕ are related to the center of the j free layer. The next step is to average the magnetostatic field produced by the fixed layer in the volume of the j free layer, i.e.,

(A8)

where Ls is the thickness of the non-magnetic spacer. The normalized magnetostatic field can then be written as

(A9)

with

(10a)
(10b)
(10c)

where g2(q)=(1eqLfix/D)(1eqL/D)eqLs/D. In particular, if we consider R1=R2=50 nm, Lfix=5 nm, L=5 nm, Ls=10 nm, and D=110 nm, we obtain k10.0060, k20.0027, and k30.0028. With these parameters, the maximum values of the field for each axis are in the x-axis hijfixV0.0060, in the y-axis hijfixV0.0044, and in the z-axis hijfixV0.0028. These values represent less than 6% of the applied field, and then in a first approximation, we neglect this interaction.

3. Effect of the magnetostatic interaction between the free and fixed layers

In this section, we discuss the effect of the magnetostatic interaction between the free and the fixed layers in the eigenfrequencies of the coupled free layers. In summary, the fixed layers exert an external field on the free layers. These fields have a component in all the directions. The components of the fields in the y^ and z^ directions just change the direction of the equilibrium magnetization, but it is negligible for the range of parameters we have considered here. In relation to the fields in the x^ direction, they change the eigenfrequencies and the critical current densities of the spin waves. We can identified an effective applied field in every disk as

(A11)
(A12)

where hiifixV is the magnetic field of the fixed layer i in the free layer i and hijfixV is the magnetic field of the fixed layer i in the free layer j. With these new fields, we observe that some of the elements of the matrix M in Eq. (11) change. Then, M11=h1x+h1d/2+(R2/R1)gx(θ) and M21=h2x+h2d/2+(R1/R2)gx(θ). In consequence, the eigenfrequencies and critical current densities are modified.

In this section, we obtain the expressions for the total normalized free energy in the macrospin approximation given by

(B1)

where WZ and WD represent the Zeeman and the self-magnetostatic energy densities of the two free layers, respectively, and WI is the magnetostatic interaction energy density between the free layers. Next, we show the expressions for the different contributions to the energy.

1. Zeeman energy

The Zeeman energy of the two nanopillars UZ, normalized by 4πMs2, is given by

(B2)

where we have neglected the constant terms. hx=Hx/(4πMs) is the normalized applied magnetic field, and V1 and V2 are the volumes of disks 1 and 2, respectively.

2. Self-magnetostatic energy

To obtain the self-magnetostatic energy, we need to calculate the magnetostatic potential Φ given by

(B3)

where σj=n^Mj is the effective magnetic charge density of all surfaces, top, bottom, and side, of disk j. The Green’s function can be written in cylindrical coordinates as

(B4)

Then, the demagnetizing field is calculated through the relation HjD=Φj, and the normalized demagnetizing energy can be written as

(B5)

where HjD/(4πMs)=hjdmjzz^, i.e., hjd is a normalized demagnetizing factor in the z direction. Finally, the normalized demagnetizing energy is

(B6)

with

(B7)

Figure 9 illustrates the normalized demagnetizing factor given by Eq. (B7), hkd, as a function of the radius Rk for L=5 nm. We observe that as Rk becomes extremely large, the value of hkd approaches 1.

FIG. 9.

Normalized demagnetizing factor, hkd, as a function of the radius Rk for L=5 nm.

FIG. 9.

Normalized demagnetizing factor, hkd, as a function of the radius Rk for L=5 nm.

Close modal

3. Magnetostatic interaction energy

The normalized interaction energy between the two free layers can be written as

(B8)

where the magnetostatic fields are obtained through the relation HjI=Φj. The contribution from the bottom and top surfaces to the magnetostatic potential is

(B9)

and the contribution from the side surface of the disk to the magnetostatic potential is

(B10)

In the same way as in  Appendix A, we relate the coordinates of free layer j (ρ and ϕ) with the coordinates of the free layer l (ρ and ϕ) through Eq. (A7). Finally, the magnetostatic field is

(B11)

Then, the normalized magnetostatic field can be written as

(B12)

with

(B13a)
(B13b)
(B13c)
(B13d)

and

(B14a)
(B14a)
(B14a)

where r1=R1/D, r2=R2/D, and l=L/D. Figure 10(a) illustrates the parameters gx, gy, gxy, and gz as a function of θ for S=10 nm, L=5 nm, and R1=R2=50 nm. Figure 10(b) illustrates the parameters K1, K2, and K3, as a function of S for L=5 nm and R1=R2=50 nm. We observe that as S increases, these quantities approach 0. Figure 10(c) illustrates the parameters K1, K2, and K3, as a function of R for L=5 nm and a center to center distance D=400 nm. We observe that as R increases, these quantities also increase.

FIG. 10.

Interaction parameters as a function of the geometry. (a) gx, gy, gxy, and gz as a function of θ for R1=R2=50 nm and S=10 nm. (b) K1, K2, and K3 as a function of S for R1=R2=50 nm. (c) K1, K2, and K3 as a function of R for D=400 nm.

FIG. 10.

Interaction parameters as a function of the geometry. (a) gx, gy, gxy, and gz as a function of θ for R1=R2=50 nm and S=10 nm. (b) K1, K2, and K3 as a function of S for R1=R2=50 nm. (c) K1, K2, and K3 as a function of R for D=400 nm.

Close modal

Finally, the normalized interaction energy is

(B15)

In Eq. (B15), we have neglected the terms proportional to m1xm2y and m2xm1y because they are of first order and greater than second order. The first order only modifies the equilibrium of the magnetization, but its effect is negligible for the range of parameters we have considered here. The terms larger than second order do not modify the spin waves and they are only relevant for nonlinear studies.

In this section, we show the effect of the distance between the free layers on the eigenfrequencies and critical current densities. Figure 11 illustrates the frequencies of the in-phase and anti-phase modes for θ=0° (a) and θ=90° (b), and Fig. 12 illustrates the critical current densities for θ=0° (a) and θ=90° (b). Both figures evidence that the frequencies and the critical current densities of both modes reach the values for an isolated free layer as S increases.

FIG. 11.

Frequencies of the in phase (fip) and anti phase (fap) modes as a function of the distance S between two identical nano-oscillators with R=50 nm for (a) θ=0° and (b) θ=90°. The frequency of an isolated nanopillar is represented by f0.

FIG. 11.

Frequencies of the in phase (fip) and anti phase (fap) modes as a function of the distance S between two identical nano-oscillators with R=50 nm for (a) θ=0° and (b) θ=90°. The frequency of an isolated nanopillar is represented by f0.

Close modal
FIG. 12.

Critical current densities of the in phase (JipC) and anti phase (JapC) modes as a function of the distance S between two identical nano-oscillators with R=50 nm for (a) θ=0° and (b) θ=90°. The critical current density of an isolated nanopillar is represented by J0C.

FIG. 12.

Critical current densities of the in phase (JipC) and anti phase (JapC) modes as a function of the distance S between two identical nano-oscillators with R=50 nm for (a) θ=0° and (b) θ=90°. The critical current density of an isolated nanopillar is represented by J0C.

Close modal
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