Abstract
Magnetic domain memory (MDM) is the ability exhibited by certain magnetic materials to reproduce the exact same nanoscale magnetic domain pattern, even after it has been completely erased by an external magnetic field. In this chapter, we review the various circumstances under which this unusual phenomenon occurs. We explain how partial MDM was first observed in rough Co/Pt multilayers with perpendicular magnetization as a result of structural defects. We then show how 100 % MDM was achieved, even in smooth ferromagnetic films, by coupling Co/Pd multilayers to an antiferromagnetic IrMn template via exchange interactions. We describe how high MDM, extending throughout nearly the entirety of the magnetization process, is obtained when zero-field-cooling the material below its blocking temperature where exchange couplings occur. We also review the persistence of MDM through field cycling and while warming the material all the way up to the blocking temperature. Additionally, we discuss the spatial dependence of MDM, highlighting intriguing oscillatory behaviors suggesting magnetic correlations and rotational symmetries at the nanoscopic scales. Finally, we review the dependence of MDM on cooling conditions, revealing how MDM can be fully controlled, turned on and off, by adjusting the magnitude of the cooling field.
Keywords
- magnetic domains
- ferromagnetic films
- perpendicular magnetic anisotropy
- magnetic domain memory
- defect-induced memory
- exchange-coupling induced memory
“
1. Introduction to the principles of MDM
1.1. Magnetic domain patterns in ferromagnetic films
Ferromagnetic materials are typically composed of magnetic domains. A magnetic domain is a region where the magnetic moments carried by individual atoms, i.e., the atomic spins, align in the same direction due to exchange couplings, as illustrated in Figure 1a. Rather than forming one giant macroscopic magnetic domain, the material often breaks down into a multitude of microscopic domains of different orientations, as illustrated in Figure 1b. At the delimitation between one magnetic domain and a neighboring one, a coherent rotation of the atomic spins occurs. The delimitating region, called domain wall, may be small in respect to the domain size. Domain sizes typically range from 1 to 100 μm in bulk ferromagnetic materials, and from 100 nm to 1 μm in thin ferromagnetic films [1, 2, 3].
In a ferromagnetic material, the microscopic magnetic domains of various magnetization directions arrange in specific ways that minimize the competing magnetic energies present in the system. The three dimensional sum of the magnetic moments carried by the individual domains produces, at the macroscopic scale, a net magnetization
Thin ferromagnetic films have been extensively studied during the past decades, in particular because of the variety of magnetic domain patterns they exhibit [4, 5, 6, 7, 8]. Depending on the composition, the crystallographic structure and the thickness of the film, the magnetization may point in-plane or out-of-plane. The magnetic domains may take various shapes, from round bubbles to elongated, almost infinite, stripes. Some thin film materials exhibit complex formations such as vortices [9, 10, 11] and skyrmions [12, 13], illustrated in Figure 1c, d, which have instigated a renewed interest in the recent years because of their potential applications in magnetic memory technologies and spintronics [14, 15].
1.2. The case of thin films with perpendicular magnetic anisotropy
Thin ferromagnetic films with perpendicular magnetic anisotropy (PMA) [16] exhibit a particularly rich set of magnetic domain patterns. In PMA films, the domain magnetization points mostly out-of-plane, thus producing high demagnetization fields and leading to the formation of regular domain patterns and magnetic textures [17, 18, 19, 20, 21]. PMA films have attracted an accrued attention in the years 2000–2010s because the perpendicular magnetization has enabled significant domain size reductions, in comparison to the in-plane magnetic films, thus benefiting the magnetic recording industry. State-of-the-art ultra-high density magnetic recording technologies utilizes granular PMA thin film media, where magnetic domain sizes are as small as 20–50 nm [22].
In smooth PMA films, magnetic domains take a variety of shapes and they form patterns of various topologies. Such variety of shapes and topologies is for example observed in [Co/Pt]N multilayers where the thickness of Co typically varies between 5 and 50 Å, the thickness of the Pt layer is around 7 Å, and the number of repeat around N = 50. In these multilayers, the PMA is primarily achieved by exploiting the surface anisotropy created by the layering between the Co and the Pt layers, and the high number of repeats, as well as the magneto-crystalline anisotropy produced by the crystallographic texturing [23, 24, 25, 26].
The magnetic domain topologies observed in these Co/Pt multilayers vary from bubble domain patterns to pure maze patterns formed of long interlaced striped domains, as shown in Figure 2. Both patterns in Figure 2 are observed at remanence, where the external field is
1.3. Magnetic domain memory
Magnetic domain memory (MDM) is the tendency for magnetic domains to retrieve the same exact same pattern after the pattern has been erased by a saturating magnetic field. When MDM occurs, not only the magnetic domains retrieve the same type of shape and size, but their distribution in space, or topology, is similar. MDM may be total, in which case the domain topology is identical; or MDM may be partial, in which case the domain pattern is similar, with some topological differences.
Ferromagnetic films usually do not exhibit any MDM. Like in the Co/Pt multilayers previously mentioned, the domain pattern at a given field point
MDM has been so far only observed in specific thin ferromagnetic films that have specific structural or magnetic properties. As explained in the following sections, MDM has first been discovered in rough Co/Pt films, due to the presence of defects, acting as pinning sites for the domain nucleation. In that case, the observed defect-induced MDM is partial and only occurs in the nucleation phase of the magnetization cycle. We will see how MDM can however be maximized by exploiting magnetic exchange between the ferromagnetic (F) layer and an antiferromagnetic (AF) layer. This has been successfully achieved in [Co/Pd] IrMn films where F Co/Pd multilayers are sandwiched in between AF IrMn layers. The film is field-cooled (FC) down below its blocking temperature, to allow exchange couplings to occur. Under these conditions, the magnetic domain pattern imprinted in the IrMn layer plays the role of a magnetic template. In this case, the observed exchange-bias induced MDM reaches 100% throughout a large portion of the magnetization process.
2. Probing MDM
2.1. Real space imaging
Magnetic domain patterns may be directly measured via Magnetic Force Microscopy (MFM), as seen in Figures 2 and 3. The MFM technique allows the visualization of magnetic domains by probing the out-of-plane magnetic stray fields emanating from the surface of the film. With a spatial resolution down to about 20–25 nm, MFM allows the detection of individual magnetic domains in thin PMA ferromagnetic films, as these domains are typically 50–200 nm wide.
The investigation of MDM may be possible via MFM under certain experimental conditions. In 2003, Kappenberger et al. [29] showed in their study of CoO/[Co/Pt] multilayers via MFM that the specific magnetic domain pattern initially observed in a particular region of the film was fully recovered after magnetically saturating the material, as seen in Figure 4. In this experiment, the material was zero-field-cooled (ZFC) down to 7.5 K and then imaged at 7.5 K while applying a large magnetic field up to 7 T. The initial striped domain pattern observed in the Co/Pt layer immediately after ZFC was completely erased under application of magnetic field, but it was fully retrieved when the magnetic field was decreased back to near coercive point
Such experiment requires very sophisticated MFM instrumentation, with cryogenic and in-situ magnetic field capabilities. Only very few MFM instruments in the world allow such extreme temperature and field environments. Because of the difficulty to measure MFM images at low temperature and under high in-situ magnetic field, the study of MDM via MFM is somewhat limited in practice. The magnetization of the MFM tip may reverse while the in-situ magnetic field is being varied. Also the maximum possible value for the magnetic field may be smaller than the value required to saturate the material, making the collection of MFM images throughout the entire magnetization loop impossible. Lastly, MFM images are typically micrometric, covering a few microns of the film, and a handful of magnetic domains, thus providing a localized view only.
2.2. Coherent x-ray resonant magnetic scattering
Complementary to MFM, the technique of coherent x-ray magnetic scattering [30, 31] is a powerful tool to study MDM. Under coherent illumination, the material produces a speckled scattering pattern that is a unique fingerprint of the charge and magnetic configuration of the material [32, 33], as illustrated in Figure 5. Because x-rays are insensitive to magnetic fields, an in-situ magnetic field of any value and any direction can be applied to the material while collecting the x-ray scattering signal. This allows the study of MDM throughout the entire magnetization process. Also, if mounted on a cryogenic holder, the material can be cooled down under various field cooling conditions, and x-ray scattering can be measured at low temperature. Lastly, the region illuminated by the x-rays is set by the size of the spatial filter used to obtain transverse coherence. The illumination spot size, typically in the order of 20–50 μm, allows covering a relatively large number of magnetic domains, thus providing useful statistical information [34].
A magneto-optical contrast can be obtained by finely tuning the x-ray energy to specific resonance edges associated to the magnetic elements present in the material. This technique, called x-ray resonant magnetic scattering (XRMS), offers chemical selectivity [35, 36, 37]. Typical resonant edges used in XRMS are the L2 and L3 edges which correspond to the excitation of electrons from the (2p) to the (3d) electronic bands in transition metals. For iron (Fe), the L2,3 edges are at around 708 and 720 eV, respectively. For cobalt (Co), the L2,3 edges are at around 778 and 791 eV, respectively. At these energies (soft x-rays), the x-ray wavelength is around 1–2 nm, thus allowing the probing of magnetic structures in ferromagnetic films, with spatial resolutions down to few nanometers.
By collecting XRMS patterns at various magnetic field values, one can follow the evolution of the magnetic configuration of the material throughout the magnetization process. An example of such experiment is shown in Figure 6, where XRMS patterns collected on the descending branch of the magnetization loop are compared to MFM images at nearly same field values. At saturation, no magnetic domain exists so the XRMS pattern has no magnetic signal, only a pure charge background. Shortly after nucleation, sparse domains have nucleated and started to expand, leading to a diffuse disk around the center of the XRMS pattern. As the domain propagation progresses, interlaced domains of opposite directions fill the entire space, leading to a ring-like XRMS pattern. The radius of the ring relates to the magnetic period existing in the material at that stage [38].
Combining coherent x-rays with XRMS, the technique of
2.3. Speckle cross-correlation metrology
To evaluate MDM via CXRMS, speckle patterns collected at different field values are compared. This comparison is typically done via cross-correlation [39, 40]. In the cross-correlation process, the intensity in the two images is compared pixel by pixel. In practice, this done by multiplying the intensity of two image, pixel by pixel, while one image is spatially shifted in respect to the other one. Mathematically, this operation may be written as follows:
where
To quantify MDM, the intensity in the cross-correlation pattern
The coefficient
2.4. Mapping MDM
MDM can be evaluated in a number of different ways. The most straightforward way to evaluate MDM is to compare magnetic speckle patterns measured at the same point
A more complete exploration of MDM may be performed by cross-correlating two speckle images
More subtle measurements of MDM may exploit the spatial information contained in the CXRMS patterns. Instead of computing the cross-correlation on the entire image, the correlation is computed on specific portions of the image. One can for example look at the dependence on the scattering vector
3. Defect-induced MDM
3.1. First observations in Co/Pt thin films
The first studies of MDM via x-ray speckle correlation metrology were carried out on [Co/Pt] multilayered thin films by Pierce et al. [39] in 2003. These multilayers, made of 50 repeats of a Co/Pt bilayers, where the Co thickness is 0.4 nm, the Pt thickness is 0.7 nm, exhibit perpendicular anisotropy, leading to the formation of microscopic striped domain patterns.
These magnetic correlation studies demonstrated the occurrence of microscopic magnetic return-point-memory (RPM) when these films exhibited some interfacial roughness. It was found that smooth films with no roughness did not produce any RPM. However, films with large roughness produced significant RPM in the nucleation region of the magnetization process. It was established that the observed microscopic magnetic memory was induced by the presence of defects in the film, playing the role of anchors for magnetic domains to nucleate. This phenomenon is referred to as ‘defect-induced’ or ‘disorder-induced’ MDM [41, 42].
In Figure 10, magnetic domain configurations are shown for different film roughnesses. When the film is smooth (grown under 3 mT of Ar pressure), a typical interlaced stripe domain pattern occurs. When the film is rough (grown under 12 mT of Ar pressure), the magnetic domain pattern becomes fuzzy and the magnetic periodicity is somewhat lost. The associated XRMS scattering profile shows a well-defined peak for the 3 mT film, but a weaken peak for the 12 mT film.
In these studies, microscopic magnetic correlations were evaluated while cycling the magnetic field throughout minor loops and major loops. In particular RPM and CPM were measured at various field values along the ascending and the descending branches of the major magnetization loop. These measurements were carried out on films with various roughnesses.
3.2. RPM and CPM dependence on magnetic field
RPM and CPM were evaluated on the [Co(0.4 nm)/Pt(0.7 nm)]50 multilayers at different points throughout the ascending and descending branches of the major loop after cycling the field multiple times. Co/Pt multilayers with significant interfacial roughness exhibited non-zero RPM and CPM, as illustrated in Figure 11a. It was found that CPM was systematically lower than RPM. This suggested that disorder has a component that breaks spin reversal symmetry. It was also found that both RPM and CPM exhibited the same trend: their value was larger at nucleation (
3.3. Dependence on roughness
As expected, the observed defect-induced MDM depended on the amount of interfacial roughness exhibited by the [Co(0.4 nm)/Pt(0.7 nm)]50 multilayers. If the film was relatively smooth, no memory was found. If, on the contrary, the film was rough enough, some RPM and CPM would be detected. The dependence of MDM with interfacial roughness is illustrated in Figure 11b, where RPM and CPM are measured at the coercive point. For roughness below 0.5 nm or so, no RPM and no CPM was observed. When the roughness exceeded 0.5 nm, both RPM and CPM quickly increased and started to plateau at around 0.7 nm of roughness, reaching about 40% for CPM and 50% for RPM. This behavior, measured at room temperature was, to some extent, reproduced by nonzero-temperature numerical simulations based on Ising models [41, 42].
The observation of microscopic magnetic memory induced by defects in [Co/Pt] multilayered thin films opened the door to new perspectives and led to further questions, both on the fundamental and applied levels. In particular, the observed CPM and RPM were somewhat limited in magnitude, not exceeding 50–60% in best cases, and also they occurred in a limited region of the magnetization process, namely the nucleation region. Would there be ways, in some materials, to increase MDM to higher values and to extend it to a wider region of the magnetization loop?
4. Exchange-bias induced MDM
In an attempt to increase the amount of MDM initially observed in rough ferromagnetic materials came the idea of incorporating exchange couplings in the film by interlaying the ferromagnetic (F) layer with an antiferromagnetic (AF) layer that would play the role of a magnetic template.
This was successfully achieved by combining a F Co/Pd multilayer with an AF IrMn layer [44]. After cooling the material below its blocking temperature
If the material is cooled down under a non-zero field, the EC interactions produce a net exchange bias (EB) in the magnetization loop. However, because the origin of MDM is microscopic, high MDM can be observed even when zero-field cooling the material (in the absence of field), in which case not net bias exists.
4.1. First MDM observations in [Co/Pd]IrMn multilayers
The first observations of EC induced MDM were reported by Chesnel et al. [44] in 2008, in [Co/Pd]/IrMn multilayers. It was found that when zero-field-cooled (ZFC), the material exhibited high MDM. The magnetic correlations reached high values throughout a wide range of field values.
The material consisted of an interlay of F [Co(0.4 nm)/Pd (0.7 nm)]12 multilayers with AF layers made of IrMn (2.4 nm) alloy, repeated 4 times. This film exhibited PMA, leading to the formation of serpentine magnetic domains that were about 150–200 nm wide, as seen in Figure 12a.
To enhance the exchange couplings between the [Co/Pd] and the IrMn layers, the film was first demagnetized at high temperature and was then cooled down below its blocking temperature,
4.2. Dependence on magnetic field throughout magnetization loop
The MDM observed in the ZFC [Co/Pd]/IrMn film shows an interesting behavior, which drastically differs from the behavior observed in rough Co/Pt films. Figure 12c shows the amount RPM measured in [Co/Pd]/IrMn at 20 K after ZFC and its dependence on magnetic field throughout the ascending branch magnetization loop. Unlike for rough Co/Pt films, RPM is low at nucleation. However, as the magnetic field increases, RPM rapidly increases when the field approaches the remanent coercive point
4.3. Cross-field MDM maps
In addition to measuring RPM, cross-field magnetic correlations were further carried out throughout the entire magnetization loop. Speckle patterns collected along the ascending branch and along the descending branch of the magnetization loop were cross-correlated. Resulting correlation maps
4.4. Imprinting of a magnetic template via field cooling
The drastic behavioral differences between the MDM observed in ZFC [Co/Pd]/IrMn films and the MDM observed in rough Co/Pt films arise from the different microscopic magnetic interactions. In one case, MDM is induced by defects or disorder. In the other case, MDM is induced by exchange couplings. In this later case, MDM exits even in the absence of defects, that is, in smooth films. In the absence of defects, MDM is low at nucleation, as observed in Figure 12, because domains nucleate at random locations in the film. The reason for high MDM to occur at higher field values is the presence of a magnetic template imprinted in the AF layer during the cooling.
In the specific material, the magnetic pattern gets imprinted from the F Co/Pd layer into the AF IrMn layer through exchange couplings via interfacial uncompensated spins. In ZFC state, the imprinted pattern is typically formed of interlaced magnetic domains with opposite magnetization, pointing perpendicular to the material, either out-of-plane or into the plane, as illustrated in Figure 14a, b. The area covered by one magnetization direction nearly equals the area covered by the other magnetization direction. When, in the ZFC state, the external magnetic field is cycled, the magnetic domains in the F layer successively nucleate, propagate, expand and eventually collapse at saturation. However, due to the frozen underlying magnetic pattern in the AF layer, the domain formation process in the F layer is not random (as it would be for a single smooth F layer). The domain formation process is highly guided by exchange coupling interactions with the underlying frozen template, so that when the remanent coercive point is reached, the domain pattern exactly matches the imprinted one [38, 44].
Guided by the exchange interactions with the magnetic template imprinted in the AF layer, the magnetic domain formation and reversal in the F layer is deterministic. The magnetic domains in the F layer always form in a way to match the underlying template. Consequently, high MDM occurs from about the remanent coercive point
5. Persistence of MDM through field cycling
When MDM is observed, a question that arises is if the memory persists through multiple field cycles. This question was investigated both in disorder-induced MDM and in exchange-bias induced MDM. In both cases, the magnetic correlations persisted through field cycling.
5.1. Field cycling dependence measurements
In the ergodic assumption, the measured correlation, which is an average over a statistical ensemble of microscopic magnetic domains, is expected to be the same than the time averaged magnetic correlation one would measure at any given location of the material. Because the area of the material probed by the x-rays typically includes thousands of magnetic domains and the system is at equilibrium, the ergodic assumption applies. It is therefore expected that the magnetic correlation measured between two magnetic states separated by a given number of cycles should not change in time.
For statistical purposes, correlation coefficients measured at the same number of separating loops but at different times have been averaged. For example, if speckle patterns were collected throughout five subsequent field cycles, the correlation coefficients between cycles 1 & 2, cycles 2 &3, cycles 3 & 4 and cycles 4 & 5 were all averaged, producing an average correlation coefficient corresponding to one separating cycle. Similar averages were applied for two separating cycles (averaging cycles 1 & 3, 2 & 4 and 3 & 5), three separating cycles, etc. Ultimately, the average correlation coefficient
5.2. Dependence of MDM on number of field cycles
RPM and CPM correlations in [Co/Pd] multilayers and in [Co/Pd]/IrMn films were measured throughout many field cycles. In Figure 15a, the average RPM measured in Co/Pt films after 1 and after 11 cycles is plotted against the field
6. Spatial dependence of EC-induced MDM
The MDM results previously discussed in this chapter were obtained by cross-correlating entire speckle patterns altogether. The associated correlation numbers provided an ensemble average microscopic information, but no spatial dependency was probed. Spatial information is however included in the 2D speckle patterns which are being correlated for the estimation of MDM. This spatial information can be exploited to extract information about possible spatial dependency in MDM. Interesting oscillatory spatial dependence was found in the MDM exhibited by [Co/Pd]IrMn multilayers.
6.1. Exploring spatial dependence
Each 2D speckle pattern, such as the one in Figure 7, represents the intensity of the x-rays coherently scattered by the material. Because the scattering process involves an inversion from the real space to the scattering space, the spatial scale on the speckle images is an inverse of a distance. A common quantity to locate positions in the speckle patterns is the scattering vector
Most scattering patterns observed when probing magnetic domain patterns in PMA films show a ring. The presence of the ring reveals a magnetic periodicity in the domain pattern with an isotropic arrangement (no preferred direction). The radius
By cross-correlating selected regions of the scattering speckle pattern rather than the entire pattern, one obtains spatially dependent correlation numbers. This is useful to detect any spatial correlation features occurring at the nanoscale. For instance, magnetic domains patterns may correlate well at the short scale (100–500 nm), but not correlate so well in the long range (1 μm and above) or vice versa.
6.2. Space-field maps of MDM
To study the spatial behavior of MDM, in particular its dependence on
Because speckle patterns are collected at specific points in field
6.3. Oscillatory behavior of MDM in [Co/Pd] IrMn
The spatial and field dependence of MDM was explored in [Co/Pd] IrMn films [46]. The films were ZFC below the blocking temperature. Speckle patterns were collected at low temperature, throughout the magnetization cycle and several subsequent loops. Ring selective cross-correlations were carried out. The resulting
The oscillation observed in the
6.4. Azimuthal angular dependence
Since the speckle patterns used for the evaluation of MDM are 2D images, one can explore the spatial dependence of MDM in at least two directions. In addition to probing the dependence on the scattering vector
7. Dependence of EC-induced MDM on temperature
The results discussed in the previous sections show the occurrence of MDM via exchange bias when the film is cooled down to low temperatures, well below the blocking temperature TB. Most of the measurements were performed at around 20 K after ZFC cooling the material. A question that arises next is if the EC-induced MDM depends on temperature and how it behaves at the phase transition near TB. These questions were investigated in exchange biased [Co/Pd]IrMn films [38].
7.1. Probing temperature dependence in zero-field-cooled (ZFC) state
To probe the temperature dependence of MDM, the [Co/Pd]/IrMn films were first heated up to around 400 K, well above the blocking temperature
7.2. Persistence of MDM through warming up
The correlation maps in Figure 18a show the occurrence of high MDM extending throughout a wide region of the magnetization loop at all temperatures below
The temperature dependence of MDM may be compared to the temperature dependence of the magnetization loop. The shape of the magnetization loop in the ZFC state, as seen in Figure 18b is symmetrical, centered about the origin. The loop has an hourglass-like shape; it is narrow at the center and opens up at the extremities, due to the presence of exchange couplings. When increasing the temperature from the ZFC state, the overall shape of the magnetization loop remains the same, but the magnitude of the opening, or hysteresis, progressively decreases. Despite the changes observed in the magnetization loop while warming the film up from the ZFC state, MDM remains strong and extended at all temperatures below
7.3. Disappearance of MDM above the blocking temperature
When the temperature is increased above
The persistence of high MDM throughout warming, at all temperatures below
8. Optimizing EC-induced MDM by adjusting field cooling conditions
All the studies of EC-induced MDM discussed in the previous sections were carried out on zero-field-cooled [Co/Pd]/IrMn films. Next question is what happens if the film is now field-cooled (FC), i.e., cooled in the presence of a magnetic film. Will MDM remain as high in the FC state as it is in the ZFC state?
This question was investigated by studying the magnetic correlations after cooling the [Co/Pd]/IrMn films under various cooling field conditions. The resulting correlation maps showed drastic changes as a function of the magnitude of the cooling field [33]. The result of this study is summarized in Figure 19. Magnetic correlations were measured in [Co/Pd]/IrMn films after field cooling the material under magnetic field of various magnitudes
8.1. Dependence of MDM on cooling field magnitude
When the magnitude
When
When
When
8.2. Shaping MDM by adjusting cooling field conditions
In the ZFC state, the magnetic domain template imprinted in the AF layer is formed of long interlaced stripes with about the same amount of domains of opposite magnetizations (about a 50% up: 50% down split). The imprinted domain pattern constitutes a template for the domain reversal in the F layer. Because of exchange couplings occurring between the Co spins in the F layer and the uncompensated interfacial Mn spins in the AF layer, the domains form in a way to match the underlying template. The matching occurs rapidly when approaching the coercive point (where the up-down magnetization split is exactly 50–50%). The matching persists at higher field values, all the way up to near saturation. This is possible because, even though the magnetic domains of opposite magnetization expand and shrink, the specific topology of the domain pattern still matches the underlying template, as illustrated in Figure 20.
In the FC states, the magnetic domain template imprinted in the film has an unbalance of up and down domains, and the net magnetization is non-zero. However, if the magnitude
If the magnitude
These results demonstrate the possibility to induce and control nanoscale MDM in exchange biased films by adjusting the field cooling conditions. High, up to 100% MDM, extending throughout the entirety of the magnetization loop can be achieved by cooled under no field or relatively low field values. However, MDM can be almost eliminated, by cooling the material under high magnetic field, approaching saturation and higher.
9. Conclusion
Magnetic domain memory (MDM) is an unusual property exhibited by certain ferromagnetic films, where the microscopic magnetic domains tend to reproduce the same topological pattern after it has been erased by an external magnetic field. In most ferromagnetic materials, MDM does not occur. When an external magnetic field is applied and cycled, microscopic magnetic domains form and propagate throughout the material in non-deterministic ways. However, it has been found that some ferromagnetic thin films with perpendicular magnetic anisotropy (PMA) do show significant MDM under certain structural and magnetic conditions. One structural condition is the presence of defects. When rough enough, thin Co/Pt multilayers with PMA, exhibits partial MDM occurring in the nucleation phase of the magnetization process. This disorder-induced MDM is caused by the presence of microscopic structural defects, playing the role of pinning sites for the domain nucleation. Another way to induce MDM and to maximize it, even in smooth films, is incorporating magnetic exchange couplings (EC) between a PMA ferromagnetic (F) film and an underlying antiferromagnetic (AF) film. This has been achieved by combining F [Co/Pd] multilayers with AF IrMn layers. After demagnetizing the material and zero-field-cooling it below its blocking temperature, high MDM up to 100% was observed throughout almost the entirety of the magnetization process. This high MDM is induced by EC interactions between the Co spins in the F layer and the interfacial uncompensated spin in the IrMn layer. When the material is cooled down below its blocking temperature, a specific magnetic domain pattern gets imprinted into the AF layer. When the field is cycled at low temperature, the frozen imprinted AF pattern then plays the role of a template for the domain formation in the F layer. The resulting high MDM extends throughout a wide range of field values, from the coercive point to nearly saturation. This EC-induced MDM persists through field cycling and through warming the material all the way up the blocking temperature, above which MDM vanishes. Additionally, it was found that the amount of EC-induced MDM can be varied by adjusting the magnitude of the field applied during the cooling. If the material is cooled under no field or moderate field, MDM reaches high values up to 100% throughout most of the magnetization process. If, however, the material is cooled under a nearly saturating field, MDM vanishes, except at the nucleation and saturation extremities of the magnetization cycle.
These observations of MDM in certain PMA ferromagnetic films opens the door to more investigations. A particular question is if there are other ways to induce and control MDM in a material. It has been recently found that EC-induced MDM may be affected by light, such as x-rays. If the material is illuminated by too intense x-rays, the film may lose its EC properties and MDM may vanish. This finding, which resonates with the emergent all-optical magnetic switching phenomena observations [48, 49, 50], suggest that EC-induced MDM could be controlled by light illumination. Ultimately, the ability to induce and control MDM in PMA ferromagnetic film, either by structural disorder, or by exchange couplings and light illumination, may offer a tremendous potential for improving technological applications in the field of magnetic recording and spintronics.
References
- 1.
Néel L. Les lois de l’aimantation et de la subdivision en domaines élémentaires d’un monocristal de fer. Journal de Physique et Le Radium. 1944; 5 :241 - 2.
Kittel C. Theory of the Structure of Ferromagnetic Domains in Films and Small Particles. Physics Review. 1946; 70 :965 - 3.
Kittel C. Physical theory of ferromagnetic domains. Reviews of Modern Physics. 1949; 21 :541 - 4.
Fowler Jr CA. Fryer EM. Magnetic domains of thin films of Nickel-Iron. Physics Review. 1955; 100 :746 - 5.
Williams HJ, Sherwood RC. Magnetic domains in thin films. Journal of Applied Physics. 1957; 28 :548 - 6.
Chapman JN. The investigation of magnetic domain structures in thin foils by electron microscopy. Journal of Physics D: Applied Physics. 1984; 17 :623 - 7.
Allenspach R, Stampanoni M, Bischof A. Magnetic domains in thin epitaxial Co/Au(111) films. Physical Review Letters. 1990; 65 :3344 - 8.
Lecoeur P, et al. Magnetic domain structures of LaSrMnO3 thin films with different morphologies. Journal of Applied Physics. 1997; 82 :3934 - 9.
Vedmedenko EY, Ghazali A, Levy J-CS. Magnetic vortices in ultrathin films. Physical Review B. 1999; 59 :3329 - 10.
Wachowiak A, et al. Direct observation of internal spin structure of magnetic vortex cores. Science. 2002; 298 :577 - 11.
Shigeto K, Okuno T, Mibu K, Ono TS. Magnetic force microscopy observation of antivortex core with perpendicular magnetization in patterned thin film or permalloy. Applied Physics Letters. 2002; 80 :4190 - 12.
Yu XZ, et al. Near room- temperature formation of a skyrmion crystal in thin-films of the helimagnet FeGe. Nature Materials. 2011; 10 :106 - 13.
Wilson MN, et al. Extended elliptic skyrmion gratings in epitaxial MnSi thin films. Physical Review B. 2012; 86 :144420 - 14.
Fert A, Cros V, Sampaio J. Skyrmions on the track. Nature Nanotechnology. 2013; 8 :152 - 15.
Jiang W, et al. Blowing magnetic skyrmion bubbles. Science. 2015; 349 :283 - 16.
Johnson MT, Bloemen PJH, den Broeder FJA, de Vriest JJ. Magnetic anisotropy in metallic multilayers. Reports on Progress in Physics. 1996; 59 : 1409 - 17.
Gehanno V, Samson Y, Marty A, Gilles B, Chamberod A. Magnetic susceptibility and magnetic domain configuration as a function of the layer thickness in epitaxial FePd (001) thin films ordered in the L10 structure. Journal of Magnetism and Magnetic Materials. 1997; 172 :26 - 18.
Gehanno V, Marty A, Gilles B, Samson Y. Magnetic domains in epitaxial ordered FePd (001) thin films with perpendicular magnetic anisotropy. Physical Review B. 1997; 55 :12554 - 19.
Thiele J-U, Folks L, Toney MF, Weller DK. Perpendicular magnetic anisotropy and magnetic domain structure in sputtered epitaxial FePt (001) L10 films. Journal of Applied Physics. 1998; 84 :5686 - 20.
Hellwig O, Denbeaux GP, Kortright JB, Fullerton EE. X-ray studies of aligned magnetic stripe domains in perpendicular multilayers. Physica B. 2003; 336 :136 - 21.
Hellwig O, Berger A, Kortright JB, Fullerton EE. Domain structure and magnetization reversal of antiferromagnetically coupled perpendicular anisotropy films. Journal of Magnetism and Magnetic Materials. 2007; 319 :13 - 22.
Richter HJ, Harkness IV SD. Media for magnetic recording beyond 100 Gbit/in.2. MRS Bulletin. 2006; 31 :384 - 23.
Chappert C, Renard D, Beauvillain P, Renard JP, Seiden J. Ferromagnetism in very thin films of Nickel and Cobalt. Journal of Magnetism and Magnetic Materials. 1986; 54 :795 - 24.
Carcia PF. Perpendicular magnetic anisotropy in Pd/Co and Pt/Co thin-film layered structures. Journal of Applied Physics. 1988; 63 :5066 - 25.
Lin CJ, Gorman GL, Lee CH, Farrow RFC, Marinero EE, do HV, Notarys H, Chien CJ. Magnetic and structural properties of Co/Pt multilayers. Journal of Magnetism and Magnetic Materials. 1991; 93 :194 - 26.
Winkler G, Kobs A, Chuvilin A, Lott D, Schreyer A, Oepen HP. On the variation of magnetic anisotropy in Co/Pt(111) on silicon oxide. Journal of Applied Physics. 2015; 117 :105306 - 27.
Chesnel K, Westover AS, Cardon KH, Dodson B, Healey M, et al. Topological bubble stripe phase transition in remanent magnetic domain patterns in Co/Pt thin films and its dependence with Co thickness. to appear - 28.
Westover AS, Chesnel K, Hatch K, Salter P, Hellwig O. Enhancement of magnetic domain topologies in Co/Pt thin films by fine tuning the magnetic field path throughout the hysteresis loop. Journal of Magnetism and Magnetic Materials. 2016; 399 :164 - 29.
Kappenberger P, Martin S, Pellmont Y, Hug HJ, Kortright JB, Hellwig O, Fullerton EE. Direct imaging and determination of the uncompensated spin density in exchange-biased CoO/ (CoPt) multilayers. Physical Review Letters. 2003; 91 :267202 - 30.
Chesnel K, Belakhovsky M, Livet F, Collins SP, van der Laan G, Dhesi SS, Attané JP, Marty A. Soft x-ray magnetic speckles from a nanostructured FePd wire. Physical Review B. 2002; 66 :172404 - 31.
Chesnel K, Belakhovsky M, van der Laan G, Livet F, Marty A, Beutier G, Collins SP, Haznar A. Tracking the local reversal processes in nanostructures by magnetic speckles. Physical Review B. 2004; 70 :180402(R) - 32.
Eisebitt S, Luning J, Schlotter WF, Lorgen M, Hellwig O, Eberhardt W, Stohr J. Lensless imaging of magnetic nanostructures by x-ray spectro-holography. Nature. 2004; 432 :885 - 33.
Chesnel K, Safsten A, Rytting M, Fullerton EE. Shaping nanoscale magnetic domain memory in exchange-coupling ferromagnets by field cooling. Nature Communications. 2016; 7 :11648 - 34.
Chesnel K, Turner JJ, Pfeifer M, Kevan SD. Probing complex materials with coherent soft x-rays. Applied Physics A: Materials Science & Processing. 2008; 92 :431 - 35.
de Bergevin F, Brunel M. Diffraction of x-rays by magnetic materials. I. General formulae and measurements on ferro- and ferrimagnetic compounds. Acta Cryst. 1981; A37 : 314 - 36.
Hannon JP, Trammell GT, Blume M. D, Gibbs. X-ray resonance exchange scattering. Physical Review Letters. 1988; 61 :1245 - 37.
Kortright JB, Awschalom DD, Stohr J, Bader SD, Idzerda YU, Parkin SSP, Schuller I, Siegmann H-C. Research frontiers in magnetic materials at soft x-ray synchrotron radiation facilities. Journal of Magnetism and Magnetic Materials. 1999; 207 :7 - 38.
Chesnel K, Wilcken B, Rytting M, Kevan SD, Fullerton EE. Field mapping and temperature dependence of magnetic domain memory induced by exchange couplings. New Journal of Physics. 2013; 15 :023016 - 39.
Pierce MS, Moore RG, Sorensen LB, Kevan SD, Hellwig O, Fullerton EE, Kortright JB. Quasistatic x-ray speckle metrology of microscopic magnetic return-point memory. Physical Review Letters. 2003; 90 :175502 - 40.
Chesnel K, Nelson J, Wilcken B, Kevan SD. Mapping spatial and field dependence of magnetic domain memory by soft x-ray speckle metrology. Journal of Synchrotron Radiation. 2012; 19 :293 - 41.
Pierce MS, Buechler CR, Sorensen LB, Turner JJ, Kevan SD, Jagla EA, Deutsch JM, Mai T, Narayan O, Davies JE, liu K, Dunn JH, Chesnel KM, Kortright JB, Hellwig O, Fullerton EE. Disorder-induced microscopic magnetic memory. Physical Review Letters. 2005; 94 :017202 - 42.
Pierce MS, Buechler CR, Sorensen LB, Kevan SD, Jagla EA, Deutsch JM, Mai T, Narayan O, Davies JE, Liu K, Zimanyi GT, Katzgraber HG, Hellwig O, Fullerton EE, Fischer P, Kortright JB. Disorder-induced magnetic memory: experiments and theories. Physical Review B. 2007; 75 :144406 - 43.
Seu KA, Su R, Roy S, Parks D, Shipton E, Fullerton EE, Kevan SD. Microscopic return point memory in Co/Pd multilayer films. New Journal of Physics. 2010; 12 :035009 - 44.
Chesnel K, Fullerton EE, Carey MJ, Kortright JB, Kevan SD. Magnetic memory in ferromagnetic thin films via exchange coupling. Physical Review B. 2008; 78 :132409 - 45.
Nelson J, Wilcken B, Chesnel K. Persistence of magnetic domain memory through field cycling in exchange bias thin films. Journal of the Utah Academy of Sciences, Arts & Letters. 2010; 87 :267 - 46.
Chesnel K, Nelson JA, Kevan SD, Carey MJ, Fullerton EE. Oscillating spatial dependence of domain memory in ferromagnetic films mapped via x-ray speckle correlation. Physical Review B. 2011; 83 :054436 - 47.
Su R, Seu KA, Parks D, Kan JJ, Fullerton EE, Roy S, Kevan SD. Emergent rotational symmetries in disordered magnetic domain patterns. Physical Review Letters. 2011; 107 :257204 - 48.
Stanciu CD, Hansteen F, Kimel AV, Kirilyuk A, Tsukamoto A, Itoh A, Rasing T. All-optical magnetic recording with circularly polarized light. Physical Review Letters. 2007; 99 :047601 - 49.
Mangin S, Gottwald M, C-H Lambert, Steil D, Uhlir V, Pang L, Hehn M, Alebrand S, Cinchetti M, Malinowski G, Fainman Y, Aeschlimann M, Fullerton EE. Engineered materials for all-optical helicity-dependent magnetic switching. Nature Materials. 2014; 13 :286 - 50.
Shcherbakov M, Vabishchevich PP, Shorokhov AS, Chong KE, Choi D-Y, Staude I, Miroshnichenko AE, Neshev DN, Fedyanin AA, Kivshar YS. Ultrafast all-optical switching with magnetic resonances in nonlinear dielectric nanostructures. Nano Letters. 2015; 15 :6985