United States

In the race for the miniaturization of electronic devices, modern science reached the ultimate level of monoatomic layers. Whereas, magnetic tunnel junctions with perpendicular magnetic anisotropy reached the limit of about twenty atomic monolayers [1]. In our work, we systematically study the magnetic anisotropy of Fe and FeCo thin films of size from one to twenty atomic monolayers.&lt;br/&gt;&lt;br/&gt;Theoretical studies are based on calculations using the full-potential local-orbital electronic structure code FPLO [2] and generalized gradient approximation (GGA). The chemical disorder in FeCo layers was modeled using virtual crystal approximation (VCA). A set of layers with different thicknesses formed based on the bcc structure was subjected to full geometry optimization. The set of equilibrium structures was then recalculated using a fully relativistic approach for two orthogonal magnetization directions (in-plane and out-of-plane). The results of calculations allow the interpretation of parallel experimental studies in which FeCo layers on Au substrate are analyzed.&lt;br/&gt;&lt;br/&gt;The result of ab-initio calculations is a series of dependences of structural and magnetic parameters on layer thickness. Fig. 1 shows an example of the dependence of the optimized lattice constant on the Fe layer thickness. For few-atom-thick Fe layers there is a large reduction of the lattice parameter with respect to the value for bulk bcc Fe, to which the parameters determined for thicker layers converge. Fig. 2 presents the dependence of the magnetocrystalline anisotropy energy (MAE) on the Fe layer thickness. Positive values denote perpendicular magnetic anisotropy, negative values denote anisotropy in-plane. The calculated value of MAE for Fe monolayer equal to 0.58 meV/atom is in good agreement with the previous GGA result equal to 0.50 meV/atom [3]. These results were compared with measurements of the ratio of orbital to spin magnetic moment using VNA-FMR. We found that the contribution of surface anisotropy to the effective anisotropy is strong enough to overcome the shape anisotropy in Au/CoFe/Au systems.

![](https://assets.underline.io/uploads/markdown_image/1/image/0cc0613d2960ba04eae25216e4150cf3.jpg)

Fig.1 Dependence of the lattice parameter on the Fe layer thickness.


![](https://assets.underline.io/uploads/markdown_image/1/image/05159cf1c9b8516a3e45b8cc11e76092.jpg)

Fig.2 Dependence of MAE on Fe layer thickness.

2022 Joint MMM-INTERMAG

Magnetocrystalline Anisotropy of Fe and FeCo Thin Films

The 65th Annual Conference on Magnetism and Magnetic Materials (MMM 2020) was held in a virtual form. The COVID-19 pandemic, with its associated uncertainty about international travel and the ability to gather in large groups, meant that the Steering Committee decided to cancel the face-to-face meeting that had been planned in Palm Beach, Florida November 2-6, 2020.

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MMM 2020

In the race for the miniaturization of electronic devices, modern science reached the ultimate level of monoatomic layers. Whereas, magnetic tunnel junctions with perpendicular magnetic anisotropy reached the limit of about twenty atomic monolayers [1]. In our work, we systematically study the magnetic anisotropy of Fe and FeCo thin films of size from one to twenty atomic monolayers. Theoretical studies are based on calculations using the full-potential local-orbital electronic structure code FPLO [2] and generalized gradient approximation (GGA). The chemical disorder in FeCo layers was modeled using virtual crystal approximation (VCA). A set of layers with different thicknesses formed based on the bcc structure was subjected to full geometry optimization. The set of equilibrium structures was then recalculated using a fully relativistic approach for two orthogonal magnetization directions (in-plane and out-of-plane). The results of calculations allow the interpretation of parallel experimental studies in which FeCo layers on Au substrate are analyzed. The result of ab-initio calculations is a series of dependences of structural and magnetic parameters on layer thickness. Fig. 1 shows an example of the dependence of the optimized lattice constant on the Fe layer thickness. For few-atom-thick Fe layers there is a large reduction of the lattice parameter with respect to the value for bulk bcc Fe, to which the parameters determined for thicker layers converge. Fig. 2 presents the dependence of the magnetocrystalline anisotropy energy (MAE) on the Fe layer thickness. Positive values denote perpendicular magnetic anisotropy, negative values denote anisotropy in-plane. The calculated value of MAE for Fe monolayer equal to 0.58 meV/atom is in good agreement with the previous GGA result equal to 0.50 meV/atom [3]. These results were compared with measurements of the ratio of orbital to spin magnetic moment using VNA-FMR. We found that the contribution of surface anisotropy to the effective anisotropy is strong enough to overcome the shape anisotropy in Au/CoFe/Au systems.

![](https://assets.underline.io/uploads/markdown_image/1/image/0cc0613d2960ba04eae25216e4150cf3.jpg)

Fig.1 Dependence of the lattice parameter on the Fe layer thickness.


![](https://assets.underline.io/uploads/markdown_image/1/image/05159cf1c9b8516a3e45b8cc11e76092.jpg)

Fig.2 Dependence of MAE on Fe layer thickness.

technical paper

The 15th Joint MMM-INTERMAG Conference (2022 Joint) is sponsored jointly by AIP Publishing and the IEEE Magnetics Society. Members of the international scientific and engineering communities interested in recent developments in fundamental and applied magnetism are invited to attend and contribute to the technical sessions. The technical program will include invited and contributed papers in oral and poster sessions, invited symposia, a plenary session, and an evening session, with about 1500 presentations overall. This Conference provides an outstanding opportunity for worldwide participants to meet their colleagues and collaborators and discuss developments in all areas of magnetism research.

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Ensemble magnetization of magnetic nanoparticles (NPs) has a sensitive dependence on the structural arrangement of particles. To better understand the correlation between spatial positions of NPs and ensemble magnetization, an experimental system is needed where particle position can be adjusted while simultaneously probing nanoscale magnetization. Here, we describe experiments using polarization analyzed small angle neutron scattering (PASANS) to study the change in magnetic correlations of ~7 nm iron oxide (Fe3O4) NPs embedded in stretched silicone rubber. PASANS is a powerful tool for mapping both the inter- and intra- particle magnetization of NPs on length scales ranging from 0.1 – 100 nm. The magnetic NP polymer gel, or magnetogel, can be stretched on the neutron beamline during an experiment. The macroscopic stretching is accompanied by nanoscale deformations, where polymer chains move to accommodate a new equilibrium configuration. NPs embedded in the gel change their configuration as a function of applied stress, providing a method to adjust the average center-to-center spacing between particles. The scattering data from the unstretched gel in a 1 T applied magnetic field can be modelled by 7.4 nm iron oxide NPs assembled in a hard sphere packing with 30% volume fraction. When the sample is stretched 3x its original size in a direction parallel to the applied field, the morphology changes dramatically. Specifically, the data can be described using a cluster model where NP dimers have emerged (Figures 1a and 1b). Stretching causes the particles to morph from semi-close packed, but individual, 7.4 nm diameter NPs into dimer-like clusters that are 15 nm long, as viewed perpendicular to the applied field (Figures 2a and 2b). These PASANS experiments clearly demonstrate that stretching the magnetogel modulates the structural characteristics of magnetic NPs in a pronounced, controllable manner.

![](https://assets.underline.io/uploads/markdown_image/1/image/39e948b29d4a9faea0cd8a27867ee2bb.jpg)

Fig. 1: Magnetic scattering from (a) unstretched and (b) 3x stretched gel in a 1 T field. The data set in (a) is fit to a hard sphere-like packing and (b) is fit to a model containing dimers

![](https://assets.underline.io/uploads/markdown_image/1/image/5b350fa63e4727cecd3c135d0fb252f5.jpg)

Fig. 2: Schematic showing rearrangement of NPs in (a) unstretched and (b) 3x stretched configurations.

Magnetic Correlations of Iron Oxide Nanoparticles as Probed by PASANS in Stretched Magnetogel Composites

The utilization of magnetic torques at the nano and microscale induced via an externally applied magnetic field is of particular interest for applications such as micromixing [1] and mechanical cancer cell destruction [2]. Over the past several years, synthetic antiferromagnetic (SAF) nanoplatelets with perpendicular magnetic anisotropy (PMA) have been identified as one of the most promising vehicles due to their high tunability, easy-axis/hard-plane PMA efficiently transferring the full magnetic torque to their environment [3]. However, the fabrication of these nanoplatelets, especially in the submicron regime with a high yield is still a challenge and efficient characterization methods of the magnetic properties and mechanical behavior in a fluid environment are still lacking. In this work, we present a novel fabrication method based on substrate conformal imprint lithography (SCIL) [4] and discuss the size effect on the magnetic properties. The basic thin film stack is shown in the insert of Fig. 1. Platelets with 1.89 ± 0.02 µm dimeter (Fig. 1) and 102 ± 1 nm diameter were successfully produced with a yield of ~108 and ~ 1010 particles per 2 inch wafer. MOKE and SQUID were used to measure the hysteresis loop. A dramatically increase of the coercivity (Hc) after patterning is observed (see Fig. 2) rendering the particles ferromagnetic at zero applied field destroying their favorable properties. To define where the increase comes from, a systematic size study is conducted on PMA-SAF nanoplatelets fabricated through electron beam lithography (EBL). We find that Hc and its distribution increase with decreasing size (see Fig. 2). A model based on local anisotropy distribution and thermal activation was established to fit the data [5]. The fit can accurately describe the Hc behavior giving insight on how to engineer the particles. In this talk we will discuss the physics, our current methods to circumvent the Hc issue and give an outlook on single-platelet mechanical behavior characterization methods [6].

![](https://assets.underline.io/uploads/markdown_image/1/image/1f533b6fc3b9014d316dd90edc92ea86.jpg)

![](https://assets.underline.io/uploads/markdown_image/1/image/cd16737989cc4310aba5cad6a49c1556.jpg)

Substrate Conformal Imprint Lithography Defined Synthetic Antiferromagnetic Nanoplatelets for Torque Related Applications

Substrate Conformal Imprint Lithography Defined Synthetic Antiferromagnetic Nanoplatelets for Torque Related Applications

The structural inversion symmetry plays an important role in low-dimensional nanomagnets, due to its strong influence on magnetic and electrical properties. It can lead to the appearance of chiral effects, such as the topological Hall effect [1], or to the formation of chiral noncollinear magnetic textures, as skyrmions [2] and chiral domain walls (DWs) [3]. These chiral structures are envisioned to be the key components for realizing novel concepts for magnonics [4], antiferromagnetic spintronics [5], spin-orbitronics [6], and oxitronics [7]. The main magnetic interaction being responsible for the stabilization of chiral magnetic textures is the intrinsic Dzyaloshinskii-Moriya interaction (DMI) [8,9]. It originate in certain magnetic crystals in which the unit cell lacks inversion symmetry, such as the gyrotropic magnetic crystals, or appear typically in ultrathin films or bilayers due to the inversion symmetry breaking on the film interface [3]. At present, tailoring of DMI is done by optimizing materials, either doping a bulk single crystal or adjusting interface properties of thin films and multilayers. A viable alternative to the conventional material screening approach can be the exploration of the interplay between geometry and topology. This interplay is of fundamental interest throughout many disciplines in condensed matter physics, including thin layers of superconductors [10] and superfluids [11], nematic liquid crystals [12], cell membranes [13], semiconductors [14]. In the emergent field of curvilinear magnetism chiral effects are associated to the geometrically broken inversion symmetries [15]. Those appear in curvilinear architectures of even conventional materials. There are numerous exciting theoretical predictions of exchange- and magnetostatically-driven curvature effects, which do not rely on any specific modification of the intrinsic magnetic properties, but allow to create non-collinear magnetic textures in a controlled manner by tailoring local curvatures and shapes [16,17]. Until now the predicted chiral effects due to curvatures remained a neat theoretical abstraction. Recently, we provided the very first experimental confirmation of the existence of the curvature-induced chiral interaction with exchange origin in a conventional soft ferromagnetic material. It is experimentally explored the theoretical predictions, that the magnetisation reversal of flat parabolic stripes shows a two step process [18,19]. At the first switching event, a domain wall pinned by the curvature induced exchange-driven DMI is expelled leading to a magnetisation state homogeneous along the parabola's long axis. Measuring the depinning field enables to quantify the effective exchange-driven DMI interaction constant. The magnitude of the effect can be tuned by the parabola's curvature. It is found that the strength of the exchange-induced DMI interaction for the experimentally realised geometries is remarkably strong, namely ~0.4 mJ/m2, compared the surface induced DMI. The presented study legitimates the predictive power of full-scale micromagnetic simulations to design the properties of ferromagnets through their geometry, thus stabilising chiral textures. We explore these curvilinear magnetic thin films for the realization of novel artificial magnetoelectric materials based on curvilinear helimagnets embedded in piezoelectric matrix [20], to enable the geometrical tuning of the magnetochirality in curvilinear 1D architectures [21], tailoring of magnetic states in flat nanospirals [22] and as components of shapeable magnetoelectronics for interactive wearables [23].

Local and Non-local Curvature-induced Chiral Effects in Nanomagnetism

In-depth investigation of structural and magnetic property correlation in technologically important heavy metal/ferromagnet/oxide heterostructures are crucial for the development of spintronics based devices [1]. In recent times, in Ta/CoFeB/TaOx heterostructures, zero-field magnetization switching, reasonably large Dzyaloshinskii-Moriya interaction, and stabilization of skyrmions have been reported [2-4]. Here, we study the change in magnetic and structural properties of sputter deposited (1 nm) Ta/(1.5 nm) CoFeB/(0.5 nm) TaOx heterostructures induced by post-deposition annealing at 300 °C. Both as-deposited and annealed film stacks possess in-plane magnetic anisotropy and we observe nearly two times increase in the saturation magnetization (Ms) of annealed film stack (~ 800 emu/cc) in comparison to the as-deposited one (~ 400 emu/cc). The surface topography study suggests reduced surface roughness for the annealed film stack as compared to the as-deposited stack. Using, x-ray photoelectron spectroscopy we analyze the B 1s, Ta 4f and Fe 2p spectra for both as-deposited and annealed heterostructures. Interestingly, the analysis of Ta spectra revealed that B has intermixed with Ta layers in the annealed stack, thus forming new chemical states such as TaB and TaOB (cf. Fig.1). Boron 1s peak analysis suggests that the annealing causes B diffusion out of the CoFeB layer and subsequent exposure to the atmosphere results in the formation of BOx. Analysis of Fe 2p spectra in the annealed stack shows an additional signature of metallic Fe0 2p1/2 peak, which likely plays a critical role in enhancing the Ms (cf. Fig.2). These XPS results are crucial in thorough understanding of the mechanism that governs Ms and ultimately, spin-orbit coupling induced effects in ferromagnetic thin film heterostructures.

![](https://assets.underline.io/uploads/markdown_image/1/image/a5c66219d056c0e02fc86687536ed4ca.jpg)

Fig. 1. XPS spectra of Ta 4f core levels of as-deposited and annealed films. The binding energy shift in the annealed spectra are due to formation of new chemical state such as TaB.


![](https://assets.underline.io/uploads/markdown_image/1/image/92c1c60f482d4ee564ad597e655c00b7.jpg)

Fig. 2. XPS spectra of Fe 2p core levels of as-deposited and annealed films. An additional peak Fe0 2p1/2 is observed in the annealed film stack.

Study of As-deposited and Annealed Ta/CoFeB/TaOx Heterostructures Using X-Ray Photoelectron Spectroscopy

The meta-magnetic phase transition of equiatomic FeRh allows the 3 temperature model of phase transitions to be probed as it undergoes: (i) a lattice expansion, (ii) an antiferromagnetic (AF) to ferromagnetic (FM) transition [1], and (iii) a change in electronic structure. A spin canting model has been used to describe a spin re-orientation pathway [2], where a feedback loop with induced Rh moments promotes FM order. To investigate such behaviour, a probe of the AF spins is required [3]. In general, the zero-stray field of anti-ferromagnetic materials means that it is hard to detect and perform such measurements. Here, we demonstrate a probe of long-range AF order using non-resonant x-ray scattering. The G2-type order of FeRh in the AF state provides a probe of AF order using ‘magnetic’ Bragg peaks [4]. We demonstrate that these peaks can be measured using x-rays at energies below the Fe K edge. Due to the low efficiency of the magnetic scattering in this material, we describe a grazing incidence geometry to optimise the intensity (see Fig. 1). Based on Scherrer analysis we estimate a coherence length of 40-80 nm, smaller than previous reports in XMLD experiments [5], indicating we are limited by structural defects. The temperature dependent behaviour of the AF order shows an inverse correlation to the emergence of FM moment as seen in Fig. 2. The AF-FM transition as determined by the ordering appears later indicating a mixed phase [6]. Long-range AF order appears to persist when FM moment is already established. Time resolved experiments based on this technique may determine the existence of a meta-stable AF state on time scales where the FM band structure has already formed [7]. It has been shown that the lattice expansion occurs in ≈ 30 ps [8], but it is not known how the long range AF order evolves on such timescales. X-ray diffraction can therefore be used to ascertain if how and if the AF structure is related to lattice expansion occurring at the phase transition.

![](https://assets.underline.io/uploads/markdown_image/1/image/a76ec58a6231ba98b20b00b66541e5c6.jpg)

Dependence of the (3/2,1/2,1/2) peak intensity upon grazing incidence angle (E=4.95 keV)

![](https://assets.underline.io/uploads/markdown_image/1/image/7d4ef6a766865d9d74ecbbf6cb3bfec2.jpg)

The inverse correlation between the intensity of the FeRh (1/2, 3/2, 1/2) magnetic peak, and the saturation moment of the FeRh film

X-ray investigation of long-range antiferromagnetic ordering in FeRh

Flexibility for interface engineering, and access to all-optical switching of the magnetization, make synthetic ferrimagnets (SFiMs) an interesting candidate for advanced spintronic devices like racetrack memory [1,2]. However, the absence of compensation at room temperature (RT) in Co/Gd bilayers has hampered the efficiency with which their magnetic order can be manipulated, as the highest efficiency of spin-orbit torques and current induced domain wall motion (CIDWM) are generally achieved under compensation [3,4]. In order to combine the favourable properties of SFiMs with compensation at RT, Co/Gd/Co/Gd quadlayer structures are investigated. We present a systematic study of the conditions for magnetization compensation and perpendicular magnetic anisotropy (PMA) in Co/Gd/Co/Gd quadlayers. These conditions were investigated on a sample with the middle Co and Gd films wedged orthogonally with respect to each other, as shown in Fig. 1a. By scanning the polar magneto-optical Kerr effect (MOKE), a magnetostatic phase diagram like in Fig. 1b can be obtained. Three regimes are distinguished: In-plane magnetization (teal), and out-of-plane (OOP) Co (red) and Gd (blue) dominated. The boundaries between these regimes provide valuable insight into the balance between shape anisotropy and PMA, and the conditions for compensation. A simple model based on partial intermixing at Co/Gd interfaces has been developed which explains the experiments well, and provides a tool to qualitatively and quantitatively understand these phase diagrams. This work provides a simple framework to experimentally characterise, and describe basic magnetostatic properties in these promising heterostructures. The compensated SFiMs investigated in this research, carry the promise of breaking the elusive 1000 m/s barrier for CIDWM, and exhibiting ultrafast exchange-driven dynamics, both relevant properties for future spintronic devices.

![](https://assets.underline.io/uploads/markdown_image/1/image/97d2d2073b964b56a371f90f9d4c02dc.jpg)

Characterization of double wedge Co(0.65)/Gd(0-3)/Co(0-2)/Gd(1.5) SFiMs. a): Schematic of wedge orientations in the multilayer. b): Magnetostatic phase diagram measured with polar MOKE. Yellow dashed line indicates compensation at RT. Green lines indicate a toy model fit to the boundaries between the three regimes.

Tuning Room Temperature Compensation in Synthetic Co/Gd Ferrimagnetic Quadlayers for Advanced Spintronics Devices

Metallic ferrimagnets consisting of rare earth (RE) / transition metal (TM) alloys exhibit an intriguing magnetic compensation of the RE/TM magnetic sublattices as a function of composition and temperature. We are developing compositionally modulated RE/TM alloy films that exploit the large change in TMagComp as the RE content is varied. We grow Fe1-xGdx films where the Gd content x is modulated throughout the depth of the film and key question in such structures is the interface length between two Fe1-xGdx layers with different Gd content; this will establish the minimum modulation length of RE/TM structures with varying composition. We examine a series of bilayer structures [Si/ SiO2(3nm)/Ta(10nm)/Fe1-xGdx(50nm)/ Fe1-yGdy(50nm)/ Ta(8nm)] where the Gd content (x or y) is varied. To investigate the magnetic profile of these films, we utilize polarized neutron reflectometry (PNR) as a function of temperature. PNR is an ideal technique to examine these structures as it probes the magnetization parallel to the field as a function of depth and the magnetic scattering length density (mSLD) is modified significantly as the temperature is tuned through TMagComp of a particular layer. We examine samples where TMagComp of a particular layer is &gt; 300 K, ~100 K and ~50 K. A sample that has TMagComp &gt;300K and ~100K for the bottom and top layers respectively exhibits strong modifications to the spin asymmetry [SA: (↑↑- ↓↓)/(↑↑+↓↓)] of the PNR. The SA develops a pronounced dip at Q~0.045 Å-1 and reduced broadening of the peak at Q~0.28 Å-1 as the temperature decreases (Fig 1). Similar variations to the SA are observed in samples with different compensation temperatures. To extract the magnetic behavior of the samples while emphasizing the interfacial region, we fit the mSLD for each temperature while keeping the structural properties the same. The fitting suggests that the evolution of the magnetic interface is nontrivial.

![](https://assets.underline.io/uploads/markdown_image/1/image/44fb4812d3585f892c0995ff14de1a9a.jpg)

1-A: High field (1 T) magnetometry vs. temperature for a magnetic bilayer. PNR measurements performed at selected temperatures, denoted by stars, across the complicated temperature profile. 1-B: Spin Asymmetry for the bi-layer samples performed at the 5 temperatures from 1-a.

Modified Magnetic Interface in Compositionally Modulated Ferrimagnetic Fe1-xGdx Multilayers

Exchange springs are versatile systems in which domain walls can be tailored by the different magnetic properties of exchange coupled layers such as in ferrimagnetic GdCo/GdCo’ multilayers [1]. We present here an experimental study by soft X-ray magnetic vector tomography [2] of Gd12Co88/Nd17Co83/Gd24Co76 multilayers with weak stripe domains (induced by NdCo) and in which the competition between exchange and magnetostatic coupling can be tuned by the composition of the ferrimagnetic GdCo layers (as sketched in Fig. 1) [3]. The 3D analysis of the vector magnetic configuration of the Gd sublattice m(Gd) in a demagnetized state shows a complex configuration that includes stripe domains with a distorted closure domain structure across the thickness, exchange spring walls with out-of-plane magnetization reversal and modulated ripple patterns (Fig. 2). An analytical model, proposed to describe global coupling across the exchange spring boundary between NdCo and GdCo layers, shows that the strength of effective interlayer coupling can be finely tuned playing with the averaging of lateral and in-depth competing interactions so that it can be externally adjusted by magnetic history. Work supported by Spanish MICINN under grant PID2019-104604RB/AEI/10.13039/501100011033.

![](https://assets.underline.io/uploads/markdown_image/1/image/6887055ecf6e425f078f1db90e0ff8e4.jpg)

Fig. 1 Sketch of GdCo/NdCo/GdCo' ferrimagnetic multilayer with competing interactions. Exchange at the interface favors parallel alignment of M(Co) in all the layers. However, at top layer Gd24Co76 layer, net magnetization is aligned with M(Gd) and antiparallel with M(Co). Magnetostatic interactions, represented by an effective stray field εHd, favor an antiparallel alignment of M(Co) at both sides of the interface. These competing interactions create an exchange spring near the top of the multilayer.

![](https://assets.underline.io/uploads/markdown_image/1/image/ee173d4a2dd2f9bc12ca1560245e6d9e.jpg)

Fig 2. Tomographic reconstruction of m(Gd) (my contrast): At top Gd24Co76, there is a ripple pattern around easy anisotropy axis; At bottom Gd12Co88, there is a distorted closure domain structure. Across the thickness, closure vortex cores are arranged in a zig-zag. Sketch shows the exchange spring between stripe domains at NdCo/GdCo layers and in-plane domain with ripple at top Gd24Co76 layer.

Adjustable exchange springs in ferrimagnetic multilayers with stripe domain patterns visualized by X-ray vector tomography

Interfacial phenomena in magnetic thin film systems are key to future spintronic applications. For materials close to the Stoner criterion, such as Pt, electronic hybridisation at the interface with a magnetic material results in a proximity induced moment (PIM), with debate ongoing regarding the role of the induced moment with regards to interfacial spin transport [1,2]. Recently, rare-earth:transition metal (RE:TM) ferrimagnetic alloys have shown promise in spintronic applications, due to the net zero magnetisation at the compensation point of the two competing magnetic sub-lattices. This compensation, which occurs as a function of both temperature and alloy composition, enhances domain wall motion [3], thermal switching [4] and leads to vanishing skyrmion Hall angles [5]. However, in multilayered systems, it has not been experimentally shown whether the induced moment in a Pt at the interface with a RE:TM ferrimagnet will align with the net moment, or one of the magnetic sublattices. Here we present the results of a recently published study [6] investigating the magnetic moments in ferrimagnetic / Pt systems, using Co77Gd23 and (Co50Fe50)77Gd23 ferrimagnetic alloys to vary the dominant magnetic sublattice. Temperature dependent SQUID measurements, combined with element specific resonant x-ray measurements at the APS, Argonne Lab on the Pt and Gd L3 edges, allowed for the determination of the alignment of the Gd moments and induced Pt moments on either side of the compensation transition. In both cases, the PIM was found to be parallel to the TM sublattice rather than the RE or the net moment. Our results highlight the prominence of the d−d mediated interactions between the Pt and the constituents of the ferrimagnetic RE:TM alloys over the net macroscopic moment.

![](https://assets.underline.io/uploads/markdown_image/1/image/4ff3a1ca1079ff9c262e75f9fde1108a.jpg)

Fig 1: Element specific hysteresis loops taken at the Pt and Gd L3 edges for CoGd/Pt (Gd dominated) and CoFeGd/Pt (CoFe dominated)

Proximity induced magnetism in Pt layered with rare-earth:transition metal ferrimagnetic alloys

Combining perpendicular magnetic anisotropy (PMA) with half-metallicity (HM) in thin-film geometry may provide additional functionalities for spintronic devices. However, such combination may be a challenging task, since HM is usually destroyed in thin-film geometry (e.g., due to the emergence of surface states), while PMA is most pronounced in reduced geometry, because of the contribution from surface anisotropy. Here, we explore the nature of PMA in thin-film full Heusler alloy Co2MnSi. This material is one of the first compounds for which half-metallic electronic structure was experimentally confirmed. In addition, it has been reported that this alloy may exhibit PMA in thin-film geometry. Here, by analyzing site-projected magnetocrystalline anisotropy energy (MAE), we confirm that both PMA and surface half-metallicity are very sensitive to the termination surface and mechanical strain. In particular, while MnSi-termination under compressive strain may retain both 100% spin-polarization and out-of-plane magnetization orientation, Co-termination has a detrimental impact on both. These results may serve as a guide for practical nano-device applications in the field of spintronics. This research is supported by the National Science Foundation (NSF) under Grant Numbers 2003828 and 2003856 via DMR and EPSCoR.

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