1. Introduction
Ultrathin magnetic films and heterostructures possessing perpendicular magnetic anisotropy (PMA) are promising objects for both fundamental studies (formation and evolution of specific domain structure [1,2,3,4,5], thermoactivated domain wall creep [6], Spin Transport [7,8], anomalous Hall effect [7,9], spin pumping [8], and spin-wave dynamics [10]) and applications (high-density magnetic memory devices [11,12], magnetic sensors for medicine [13], and superfast elements for spintronics [14]). The intensive study of magnetic heterostructure properties [1,2,3,4,5,6,7,8,9,10] is aimed at mechanisms of their magnetization reversal and magnetic transport. The goal is to build adequate theoretical models necessary for the design and optimization of magnetic devices [11,12,13,14]. In systems where two ferromagnetic (FM) layers are decoupled by a nonmagnetic (NM) layer, a significant problem is the dependence of magnetization, coercivity, domain wall mobility, and other properties on interlayer exchange interaction J = 2 HJ M b, where HJ is the effective field of the interlayer exchange interaction between FM layers, and M and b are the magnetization and thickness of FM layers [6]. Further, J itself depends on both NM interlayer thickness t and temperature T. A change in these parameters can critically affect the reliability and working characteristics of magnetic devices.
The magnetization reversal in this material is controlled mainly by the nucleation of opposite domains and by the motion of their domain walls (DWs) [1,5]. These domain transformations are well examined in continuous ultrathin Co films with PMA [15,16]. Similar processes in layered structures are more complicated, where two ferromagnetic (FM) layers are separated by a nonmagnetic (NM) layer [17,18,19,20,21]. Kinetics, relaxation of domain structure, and dynamical parameters of such FM/NM/FM heterophase films are strongly affected by interlayer coupling of exchange J [1,2,3,4,5,8] or magnetostatic [22] origin. The trilayer objects provide an opportunity for the detailed study of interlayer coupling, manifesting itself in the magnetization reversal of separate layers and of a whole system. The intrinsic feature of exchange coupling is the dependence of interaction on the nonmagnetic layer thickness. It was shown both theoretically [23,24] and experimentally [25,26] that this dependence is oscillatory. The trilayer Co/Au(111)/Co system with a wedge-shaped gold layer was studied in Ref. [26]. By measuring magnetoresistance and the Kerr rotation, the authors show that the mutual orientation of the magnetic moments varies from parallel to antiparallel depending on Au thickness; that is, interaction can be ferromagnetic or antiferromagnetic. Details of the magnetization reversal were not considered. Inhomogeneous nucleation and domain wall motion in trilayers with exchange and magnetostatic interaction were examined in Co/Pt/Co [1,2,3,4,5] and CoPt/NiO/CoPt [22], respectively.
In many such heterostructures [1,2,3,4,5,6,16,17], the Pt layer thickness utilized in the bottom and top layers would bring Dzyaloshinskii–Moriya interaction (DMI) to the system. The magnetic structures in the FM layer coupled to the Pt layer can arise from interplay with spin stiffness, usual crystallographic anisotropy, and DMI. Due to the Heisenberg-type exchange interaction, the distinct change in magnetization should have a comparatively long scale. As the film is ultrathin, only the in-plane degrees of freedom for such changes exist. Namely, such long-ranged magnetic structures can be found on surfaces around the domain walls of thin magnetic films. Theoretical [27,28] and experimental [1,2,3,4,5,6,29] papers show that DMI in ultrathin films acts only on its domain structure, while it has no influence on the exchange coupling between two FM layers through the NM spacer when the magnetization of the heterostructures is reversed.
The dependence of the DW velocity on the magnetic field in separate or exchange coupled Co films of different thickness was studied both theoretically and experimentally in [2,3,4,5]. The authors observed dynamical coupling of domain walls, which have different mobility in different layers but move together with the same speed in case of ferromagnetic exchange coupling between the layers. In the case of wedge-shaped Co/Pt/Co trilayers [1,5,29], the dependence of J on the interlayer thickness t was obtained from minor hysteresis loops or from magneto-optic Kerr visualization of the domain wall motion. It was found that nucleation and motion of domains are uncorrelated in both layers if the interlayer thickness exceeds some critical value tCR, while the walls move synchronously if the Pt layer is thin. The motion and stabilization of DWs at t > tCR and value of tCR itself depend on the properties of both layers, including coercivity and exchange interaction between the layers [29]. Being sensitive to structural defects and coercivity, DW motion should be strongly affected by temperature in addition to interlayer thickness. Currently, this question is not known in detail. In this paper, we study the dynamical properties of domain walls in wedge-shaped Co/Pt/Co trilayers depending on temperature and interlayer thickness.
2. Experiment
The Pt(10 nm)/Co(0.6 nm)/Pt(t)/Co(0.6 nm)/Pt(3 nm) structure was synthesized at room temperature using DC magnetron sputtering on the oxidized silicon <111> substrate with dimensions of 50 mm × 6 mm, with the long direction being the Pt wedge of 10 nm × 0 nm direction. Sputter deposition was performed at an argon pressure of 1.5 × 10−3 Torr with a base pressure below 2 × 10−7 Torr. Wedge-shaped Pt spacer layers were grown by moving a knife-edge shutter in front of the Co bottom layer during Pt deposition. The sample was cut into 10 pieces and the one with dimensions of 5 mm × 6 mm was used. Thickness of the Pt layer t increases uniformly along the sample from 5 to 6 nm. In order to visualize domain structure and measure intensity of a local polar Kerr effect, we used the polarized microscope POLAM P-312 with the optical cryostat. The hysteresis loops were obtained by measuring the magneto-optic (MO) intensity from local (0.3 × 0.3) mm areas of the sample at the magnetic fields up to ±500 Oe. Domain structure and DW motion were registered by the microscope CD camera and analyzed. To improve the magneto-optic contrast, we registered preliminary images of the saturated sample in the strong positive and negative magnetic field. The average of these two magneto-optic pictures was subtracted from every experimental image of transient domain structure. To minimize influence of domain walls from the adjacent layer, the pulse magnetic field was used [29]. The pulse length was chosen so that the wall in the layer with higher coercivity would have no time to follow the fast wall in the first layer.
3. Results and Discussion
Before any measurements, the sample was subjected to perpendicular permanent magnetic field H = +800 Oe, and both FM layers were magnetized until saturation. A decrease in this field until zero and its following increase with opposite polarity result in the nucleation of new domains and displacement of their boundaries. At one side of the sample where the nonmagnetic Pt layer is thin, the new domains appear coherently in both FM layers (Figure 1a). The motion of domain walls in this area is also simultaneous (Figure 1b). Local magneto-optic hysteresis loops measured via the Kerr effect are sharply rectangular in this area. It confirms the simultaneous motion of DWs in both layers. This picture is also observed at higher values of Pt thickness t until it reaches the critical value tCR = 5.3 nm. For higher t kinetics of the magnetization, reversal is different. The new domains in the two layers arise at different fields (Figure 1c), and the domain walls move almost independently (Figure 1d). This process happens first in one FM layer, and only then the second layer is reversed, too. Despite the thickness of both FM layers being the same, it is possible to determine the reversal order of the magnetization in the top MT and bottom MB layers from the magneto-optic intensity, taking into account its weakening for the bottom layer (see Ref. [29] for details). The analysis of MO data shows that the nucleation and motion of domain walls starts in the top FM layer where the MO signal at the leading wall is stronger. Coercivity values HC1 and HC2 are obtained from the start field for domain walls in the top and bottom layers, respectively. The difference in coercivity allows one to observe the incoherent nucleation of new domains and separated motion of walls in these layers.
The application of a number of magnetic field pulses (±100 Oe, 4 ms) results in the formation of a complicated domain structure (Figure 2a). The mutual orientation of magnetization in the two layers can form four different combinations distinguished by magneto-optic Kerr intensity: (i) all down, (ii) all up, (iii) top layer down, bottom layer up, (iv) top layer up, bottom layer down. Shaking the walls with an ac magnetic field (10 Hz, amplitude close to coercivity) allows one to first reduce the number of walls (Figure 2b) and then to fix the point x0 corresponding to the boundary between the areas with ferromagnetic and antiferromagnetic interlayer interaction (Figure 2c and Figure 3a). The registration of the Kerr intensity along the wedge confirms that for all x > x0, the primary state of the magnetization orientation in both layers is parallel; that is, the interlayer exchange is ferromagnetic.
Figure 4 shows local hysteresis loops obtained at different temperatures. It can be seen that the coercivity of the sample increases at low temperatures. Steps in the loops at high temperature confirm the difference in coercivity between the upper Co layer and the bottom one. At low temperature, these steps are absent, meaning that the walls in both layers move simultaneously. These loops can be used to obtain the coercivity of both layers at different temperatures; however, more detailed information about the interlayer exchange interaction can be extracted from magneto-optic measurements of the wall motion in the external field, as described in the paper.
The kinetics of the magnetization reversal in the top Co layer at t < t0 depend drastically on the interlayer thickness, providing that the magnetization MB of the bottom layer remains constant. If a series of 4 ms magnetic field pulses is applied to the sample, the distance traveling by the domain wall diminishes from pulse to pulse until the wall stops in some equilibrium position x, corresponding to a given field amplitude (Figure 3b). For stronger amplitudes, this position tends to be stabilized at x = xCR (Figure 3c). Figure 4 shows the dependence of the equilibrium position x on the field amplitude after a series of 5 to 9 pulses with a fixed amplitude. When the field amplitude is larger than the coercivity in the bottom layer HC2, the second wall starts to move in the bottom layer, so a pulse duration of 4 ms was chosen to separate the motion of these two walls. In this case, the distance between the two walls is much higher than their thickness, and the motion was considered independent. However, the displacement of the two walls equalizes near the critical thickness. Dependence x(H) is essentially nonlinear tending to saturation at x = xCR. When the wall in the top layer reaches this point, its independent motion ends, and the wall remains at x = xCR at all pulse amplitudes until the second wall in the bottom layer joins it. After that, the two walls travel together according to the field amplitude rise. The observed diminishing of the domain wall displacement with every consequent pulse of magnetic field when the wall moves toward the thinner interlayer side (Figure 5) implies the existence of some effective field HJ(x), which is directed against the applied field and whose value rises with the decrease in t.
Nonlinear x(H) dependence has been observed at low temperature, too. Figure 6 shows the DW displacement as a function of the field at different temperatures. It can be seen that the low-temperature motion of the domain walls starts in the region where the nonmagnetic interlayer is thick, and the x(H) curves shift toward higher fields.
The change in free energy necessary for the displacement of the wall along the x axis can be written as
ΔW(x) = 2(H(x) − HC1 − HJ(x)) MT Y b x,(1)
where b is thickness of the FM layer, and Y is the length of the wall along the y axis. H and HC1 are amplitude of the applied field and the coercivity of the top layer, respectively. When the wall stops reaching position x, ΔW(x) = 0. That means2(H(x) − HC1 − HJ(x)) MT Y b x = 0(2)
orHJ(x) = (H(x) − HC1)(3)
The field HJ(x) is caused by the force exerted by interlayer exchange interaction J(t) to the wall. As the interlayer thickness decreases linearly along x with a factor C = Δt/Δx = 1 nm/5 mm = 0.2 nm/mm where Δt is maximal change in the interlayer thickness and Δx is the sample length, the coordinate x in HJ(x) can be replaced with t, t = tMAX − Cx, tMAX = 6 nm is maximal interlayer thickness. The obtained nonlinear dependence HJ(t) is shown in Figure 7. One can see that effective field HJ(t) grows with the decrease in t, that is, the increase in x. The dependence of electric exchange on the distance between atomic layers was discussed recently in [30].
According to (3), the wall moves when H(x) − HJ(x) > HC1. In the case of H(x) − HJ(x) ≤ HC1, the upper wall should stop, as observed in the experiment. Meanwhile, the bottom wall pursues the first one. The isolated motion besides xCR is strongly damped. Further enhancement of H causes joint motion of the two walls, as observed in [1,5]. Nonlinear HJ(t) dependencies at different temperatures, derived from Figure 6, are shown in Figure 8. Replacing x with t, we obtain the detailed dependence HJ(t, T) for ferromagnetic exchange in the HJ(tCR) > HJ(t) > 0 interval, where tCR corresponds to the xCR. One can see that the effective field HJ(t) becomes larger with the diminishing t (that is, enhancement of x). The results show that the HJ value remains between 0 Oe and 125 Oe, depending on the wall position x along the wedge for the temperature interval 200 K to 300 K. Though the HJ(t) dependence itself varies insignificantly with temperature (namely, weak rise in ΔHJ/Δt with T), the change in the HJ value for fixed interlayer thickness is strong.
The obtained results show that the observed stabilization of the domain wall in the top layer in position xCR where interlayer thickness t= tCR depends on both the effective field HJ and coercivity HC1. To establish the influence of temperature on these values and correlations between HC1 и tCR, we performed measurements on these data from x(H,T) and HJ(t). The minimum values for all graphs in Figure 6 correspond to the start fields of the domain wall, that is, coercivity fields HC1. The maximal values of x(H) correspond to the stabilization points xCR. Taking into account linear dependence t(x), one can obtain the critical thickness tCR at xCR. Figure 9a shows the dependence tCR on temperature T. We see that critical thickness decreases with T approximately linearly. Figure 9b shows dependence HC1(T) determined from measured curves x(H)T in Figure 6. This dependence correlates, in general, with tCR(T); however, the change in coercivity is nonlinear.
Interlayer exchange between the ferromagnetic layers through the nonmagnetic layer depends on the interlayer properties. It has the same origin as the RKKY interaction between magnetic impurities in the nonmagnetic medium [24]. This interaction due to spin-polarized conductive electrons controls the magnetic properties of such multilayers. The RKKY theory predicts [24] that for spacer-layer thicknesses, t, the coupling should be given by a sum of terms in the form
J(t)= Σ(Jα/t2) sin(qαt + φa),(4)
where sum is over all critical points, labeled by α, with critical spanning vector qα, coupling strength, Jα, and phase φa. This results in oscillatory behavior of the J(t) dependence taking both positive and negative values, that is, parallel or antiparallel spin orientation in the ferromagnetic layers. The oscillation period is known well, while the J(t) dependence itself is not studied in detail in the case of ferromagnetic interaction between the layers. Our work presents such information determined experimentally via direct measurement of the effective exchange field with its compensation by the external magnetic field, as described above.Further, the RKKY models predict a specific form of the temperature dependence [23], including an additional factor in the form
(2πkBT t/ħvα)/sinh(2πkBT t/ħvα)(5)
associated with each critical spanning vector. One can see that temperature appears here as a product of interlayer thickness. We studied the dependence of the effective field on thickness, ΔHJ/Δt, at different temperatures (Figure 8). This dependence does not change much at different temperatures, as observed in our experiments.4. Conclusions
We studied the in-field evolution of domain structure in a magnetic trilayer Co/Pt/Co using magneto-optic Kerr microscopy. To find the dependence of the exchange interaction between the Co layers on Pt thickness and temperature, we measured the displacement of the domain wall as a function of the applied magnetic field. This allowed us to determine the exact value of the effective field HJ along the wedge-shaped nonmagnetic interlayer. For the first time in an FM/NM/FM trilayer, the dependence of this value on NM thickness has been measured in a temperature range from 200 to 300 K. The formation of the previously discovered [1,5,29] boundary separating the areas with different patterns of the magnetization reversal was studied experimentally at different temperatures. The nonlinear increase in HJ(t) toward the thinner Pt layer side requires a stronger field to induce the motion of the domain wall in this direction. Separate motion of a domain wall becomes damped, and in a still-stronger field, it is accompanied by the motion of the wall in the second FM layer, as observed in [1,5,29]. Stabilization of the wall at critical thickness of Pt depends on the effective exchange field HJ and coercivity HC1. Measured dependencies of HC1 и tCR on temperature are found to be correlated. As the results obtained using the wedge interlayer samples can be influenced by this shape, we will study the temperature-dependent domain wall mobility in the samples with fixed t in our following publications. The measured J(T) dependencies should help to deduce the adequate theory of interlayer exchange interaction in such trilayers.
The paper was conducted in the frame of the state task of ISSP RAS.
Conceptualization, V.S.G.; methodology, Y.P.K. and V.S.G.; formal analysis, V.S.G.; investigation, I.V.S. and Y.P.K.; data curation, I.V.S. and Y.P.K.; writing—original draft preparation, V.S.G. and O.A.T.; writing—review and editing, V.S.G. and O.A.T.; visualization, O.A.T.; supervision, V.S.G.; project aministration, V.S.G. All authors have read and agreed to the published version of the manuscript.
Not applicable.
Our study is not involving humans or animals.
The data are available from the authors on reasonable demand.
The authors declare no conflict of interest.
Footnotes
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Figure 1. Magneto-optic images of nucleation (a,c) and expansion (b,d) of new domains in the FM layers for (a,b) t < tCR and (c,d) t > tCR. MT and MB are magnetization in top and bottom layers, respectively.
Figure 2. Magneto-optic images of (a) domains after application of series of ±100 Oe, 4 ms magnetic field pulses, (b) domains after action of ac magnetic field (10 Hz) with amplitude close to coercivity, (c) resulting domain wall between the areas with ferromagnetic and antiferromagnetic interlayer exchange coupling (middle position of the wall x0 is marked with a dotted line).
Figure 3. Schematic view of the sample (a) in the initial state after formation (Figure 2c) of the boundary between the area with ferromagnetic and antiferromagnetic interlayer interaction, (b) after displacement of the domain wall in the upper FM layer, and (c) after reaching the position with t = tCR.
Figure 4. Hysteresis loops of the sample at (a) T = 293 K, (b) 250 K and (c) 160 K.
Figure 5. Stabilized position of the domain wall as a function of the magnetic field pulse amplitude, room temperature. Dot line is a guide for eyes.
Figure 6. Dependence of the stabilized position of the domain wall on the field pulse amplitude at temperatures: 1—293 K, 2—260 K, 3—240 K, 4—220 K.
Figure 7. Dependence of effective field HJ on interlayer thickness at room temperature. Dot line is a guide for eyes.
Figure 8. Dependence of effective field HJ on interlayer thickness at temperatures: 1—293 K, 2—260 K, 3—240 K, 4—220 K.
Figure 9. Dependencies of (a) critical interlayer thickness and (b) coercive field in the top FM layer on temperature. Dot line is a guide for eyes.
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Abstract
Domain wall mobility as a function of nonmagnetic interlayer thickness and temperature was studied in ultrathin exchange-coupled ferromagnetic layers using magneto-optic Kerr microscopy. The system under study is a Pt/Co/Pt/Co/Pt heterostructure having perpendicular magnetic anisotropy and a middle Pt layer with spatially variable thickness. The ferromagnetic interaction between the Co layers is observed when the Pt interlayer thickness varies from 5 to 6 nm in a temperature range of 200–300 K. There is a certain interval of Pt layer thickness where domain walls in both ferromagnetic layers move independently. Nonlinear dependence of the domain wall displacement on the applied field was measured. It is shown that an equilibrium position of the relaxed domain wall depends on field, temperature, and the nonmagnetic interlayer thickness. This position is determined by the energy balance: (i) domain wall displacement provided by the applied field, (ii) interlayer exchange interaction in the area swept by the domain wall, and (iii) domain wall coercivity. The mechanism of domain wall stabilization in terms of independent wall motion near critical thickness was considered. It is found that both the coercivity of the Co layer and the critical thickness decrease at higher temperature, while the interlayer exchange constant J is changed weakly.
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