Abstract
FeSn is a topological kagome ferromagnet that possesses numerous Weyl points close to the Fermi energy, which can manifest various unique transport phenomena such as chiral anomaly, anomalous Hall effect, and giant magnetoresistance. However, the magnetodynamic properties of FeSn have not yet been explored. Here, we report, for the first time, the measurements of the intrinsic Gilbert damping constant (), and the effective spin mixing conductance (g) of Pt/FeSn bilayers for FeSn thicknesses down to 2 nm, for which is , and g is . The films have a high saturation magnetization, , and large anomalous Hall coefficient, . The large values of g, together with the topological properties of FeSn, make FeSn/Pt bilayers useful heterostructures for the study of topological spintronic devices.
Subject terms: Magnetic properties and materials, Electronic properties and materials, Spintronics
Introduction
The existence of strong electronic correlations, band topology, spin-orbit coupling, and magnetism in topological quantum materials holds great promise for future memory applications1–7. Weyl semimetals belong to a class of topological materials distinguished by the absence of either the crystal’s inversion symmetry or the time-reversal symmetry8. In Weyl semimetals, the opposite chirality of Weyl nodes can result in a non-trivial Berry phase9–12, which can influence the magneto-transport properties such as the anomalous Hall effect (AHE)13–18 and the anomalous Nernst effect (ANE)19–21. Recently, the kagome ferromagnet FeSn, belonging to the FeSn-family (m : n = 1:1, 3:2, 5:3), has emerged as a novel topological quantum material for spintronic devices, thanks to its rich non-trivial magnetic and topological properties22–24. FeSn, with a high Curie temperature K25, which makes its Weyl nodes stable at room temperature26, has significant potential for applications in spintronics27, magnetic sensors28, and other areas of advanced electronics29,30. FeSn possesses several other promising features, such as a large AHE17. It is also predicted that FeSn can exhibit a fractional quantum Hall effect even at room temperature31. At temperature ( K), the FeSn shows the transition of spin re-orientation from the c-axis to the ab-plane25,32,33. Another interesting feature of FeSn is the presence of a dispersionless flat band ( eV below fermi level), and it is formed due to the destructive interference of the electron wavefunctions34. Furthermore, both numerical and experimental studies show the formation of magnetic skyrmions in FeSn, which is stabilized without requiring Dzyaloshinskii-Moriya interaction30.
As shown in Fig. 1a, the FeSn crystal structure consists of the repeated stacking of two FeSn kagome lattices and one Sn stanene lattice. In our previous study35, we investigated the impact of platinum (Pt) seed layer on the polycrystalline growth of ferromagnetic FeSn thin films on complementary metal-oxide-semiconductor (CMOS)-compatible Si-based substrates, which are extremely useful for low-dissipation devices for industrial applications36,37. Furthermore, Lyalin et al. showed efficient spin-orbit torque effects in an epitaxial FeSn(0001)/Pt(111) bilayer system27 deposited using molecular beam epitaxy. However, the sputtered growth of ultrathin FeSn films ( nm) and the characterization of their magneto-transport and magneto-dynamic properties have not yet been investigated, which is essential for the generation of pure spin current in such quantum material-based magnetic heterostructures.
Figure 1.
(a) Schematic of the unit cell of ferromagnet FeSn, where grey and green symbols denoting the tin (Sn) and iron (Fe) atoms, respectively. (b) Glancing incidence (GI) X-ray diffraction (XRD) spectra were obtained for the various thicknesses () of polycrystalline FeSn. The inset represents the schematic of Ta/Pt/FeSn/AlO thin film stack. (c) Atomic force microscopy surface morphology of 2 nm-thick-FeSn for a scan area of .
In this work, we demonstrate sputter growth of high-quality polycrystalline FeSn ultrathin films with very low interfacial/surface roughness ( nm), using a Ta/Pt seed layer on Si/SiO substrates. Through magnetization and transport measurements, we show a large saturation magnetization, , and a large anomalous Hall coefficient, . Using broadband ferromagnetic resonance (FMR) measurements, we, for the first time, also extract the intrinsic Gilbert damping constant (), and the effective spin mixing conductance (g), for FeSn thickness down to 2 nm, finding values of , and g. The large values of g make Pt an excellent spin current source for using FeSn thin films in topological materials-based spintronic applications.
Results and discussion
Structural analysis
The inset of Fig. 1b shows a schematic of the Ta/Pt/FeSn/AlO thin film stack. First, a 1.5 nm-thin Ta seed layer was used to increase the adhesion between the Pt and the Si-SiO substrate. The 5 nm-thick Pt seed layer was used both to promote the growth of the ferromagnetic phase of FeSn27,35 and to act as a spin sink and future source of spin currents, which will be discussed later. Fig. 1b shows the grazing incidence X-ray diffraction (GI-XRD) measurements performed for Si-SiO/Ta(1.5 nm)/Pt(5 nm)/FeSn/AlO(3 nm) with an incidence angle 1 to characterize the structural properties. We observed a strong Bragg peak at 2, corresponding to the (002)-reflection of FeSn for all thicknesses, indicating the formation of a [002]-oriented polycrystalline FeSn ferromagnetic phase28,35. The thickness, density, and roughness of these FeSn thin films were obtained by fitting X-ray reflectivity (XRR) measurements [supplementary, Fig. S1d] with the recursive theory of Parratt38. We found average interfacial roughness ( nm) for all the films, which indicates a smooth interface between each layer. AFM measurements also confirmed these roughness numbers. Figure 1c shows a AFM image of a 2 nm thick FeSn film, yielding a root mean square roughness () of about 0.3 nm, indicating a very smooth surface quality. The AFM is b e l o w 0.6 nm for all other thicknesses. The thickness dependence of surface/interfacial roughness in these films is plotted in supplementary Fig. S1 and summarized in Table S1.
It is noteworthy that the measured roughness is substantially lower than the best literature values of about 0.8 nm39. The interfacial roughness plays a crucial role in the transfer of spin current in ferromagnet/heavy metal (FM/HM) heterostructures, where a large interfacial roughness or disorder can reduce the spin current via spin memory loss40,41. Therefore, high-quality ultra-thin films with low roughness are highly desirable.
Magnetization and transport measurements
Figure 2a shows the magnetization (M) versus the in-plane external magnetic field (H) for a 5 nm FeSn film. The high = 620 emu/cm and low 20 Oe confirm a soft ferromagnetic nature of the polycrystalline FeSn films. The is comparable to that reported for epitaxial FeSn films21,39 and bulk single crystals16.
Figure 2.
(a) In-plane magnetic hysteresis measurements (M-H) for 5 nm ultra-thin FeSn film, inset represents the corresponding zoom scan. (b) The transverse Hall resistivity () versus magnetic field for 5 nm ultra-thin FeSn film when the external field is swept perpendicular to the film plane. The data in the inset with the open symbols indicates the measured , which includes the resistivity contribution from the seed layer, while the data in the main panel with the closed symbol indicates the after correction for the resistivity of the seed layer in the Ta/Pt/FeSn/AlO film stack. The black dashed arrow indicates the anomalous Hall resistivity () for only FeSn. (c) The variation of longitudinal resistivity for 5 nm ultra-thin FeSn film when the external field is applied perpendicular to the film plane, inset represents the magnetoresistance (MR) calculated using . All measurements are performed at room temperature.
In contrast to our earlier work on thicker FeSn films35, additional care must be taken when extracting the longitudinal () and transverse () resistivities as the current distribution through the Ta/Pt seed layer must be considered. The total longitudinal resistivity of the entire film stack is found to be . We also measured of only the seed layer Ta/Pt, in control samples without FeSn, and found it to be , which corresponds to the longitudinal conductivity, . Using the parallel resistance model, the value for only the FeSn layer can be obtained using the following expression21:
| 1 |
Here, , and t represent the thickness of the layer, seed (Ta/Pt) layer, and Ta/Pt/ layer, respectively. Using Eq. (1), is found to be , which is comparable to that of epitaxial thin films ()21 and slightly higher than the bulk value of single crystals ()16.
In Fig. 2b and c, room temperature Hall and longitudinal measurements were performed using a direct current ( mA) flowing parallel to the film plane while sweeping the external magnetic field ( kOe) perpendicular to the film plane. To avoid voltage probe misalignment, we use the formulae (H) = [ () ()]/2 and (H) = [ () ()]/2, to extract the longitudinal resistivity () and Hall resistivity (), respectively. To determine the , we use , where the first term represents the ordinary Hall resistivity (), and the second term represents the anomalous Hall resistivity (). and represent the coefficients of ordinary and anomalous Hall resistivity, respectively42. is found to be , from which we determine the value of the charge carrier density at 300 K in Ta/Pt/FeSn(5 nm)/AlO. The positive sign of indicates that hole-like charge carriers dominate in Ta/Pt/FeSn(5 nm)/AlO films, which is in agreement with previous reports39. Furthermore, we determine the carrier mobility at 300 K, which is two orders of magnitude larger than earlier reported values [ for FeSn(10 nm)]39. The large might be due to the low effective mass of the hole carriers in the FeSn(5 nm) film, similar to the reported mobility for Weyl semimetal NbP ( at 300 K)43. In the inset of Fig. 2b, the measured transverse resistivity of the complete film stack Ta/Pt/FeSn(5 nm)/AlO is shown. Using a linear fit (black line) to in the saturation region (), and extrapolating to the y-axis, for the Ta/Pt/FeSn/AlO films stack is found to be . To determine the value of for the FeSn layer from the measured data for the complete film stack of Ta/Pt/FeSn/AlO, we use the expression21:
| 2 |
As shown in Fig. 2b, the value of of only the FeSn layer (denoted by a black dashed arrow) is extracted from the saturation region of and found to be . This value for polycrystalline FeSn ultrathin film is comparable to the epitaxial FeSn thin film reported by D. Khadka et al.21. Using from SQUID measurements, we also determine the coefficient () of the anomalous Hall resistivity for Ta/Pt/FeSn(5 nm)/AlO film. The value of for Ta/Pt/FeSn(5 nm)/AlO film is found to be at 300 K, which is comparable to our previous report on polycrystalline FeSn thin films35 and two orders higher than conventional ferromagnets (Ni & Fe)44,45. Moreover, we determine the value of the anomalous Hall conductivity () using the equation: . The value of is found to be at 300 K. A large value of and in FeSnfilm indicates an intrinsic band structure (Berry curvature) origin of the AHE16,17,35. These results indicate that the intrinsic transport properties, such as a large value of and a significant , remain intact even for ultra-low thicknesses of FeSn films. In Fig. 2c, we have also plotted the variation of longitudinal resistivity () versus external magnetic field for 5 nm ultra-thin FeSn film. The inset of Fig. 2c represents the corresponding magnetoresistance (MR) of Ta/Pt/FeSn(5 nm)/AlO film. A negative change in MR in our thin films is caused due to the suppression of magnon at room temperature (300 K), consistent with the previous report on single crystal FeSn16,22.
Ferromagnetic resonance measurement
Figure 3a represents the schematic of a co-planar waveguide (CPW) based FMR setup with the film placed on top of it. Here, H is the external magnetic field swept parallel to the film plane and perpendicular to the rf excitation field (). The FMR setup details can be found in the Methods section. Fig. 3b shows FMR measurements for a Ta/Pt/FeSn(5 nm)/AlO thin film. The frequency (f) dependent FMR spectra are shown at an interval of 2 GHz. The solid black lines are fits to derivatives of symmetric and asymmetric Lorentzian functions46–49. From these fits, we extract the resonance field () and linewidth () in the frequency range GHz. The variation of f is plotted as a function of in Fig. 4a for all FeSn thicknesses, and then fitted to the Kittel formula50:
| 3 |
Figure 3.
(a) The schematic of CPW-based FMR setup, inset shows the zoom image of the sample placed on top of CPW sweeping the external magnetic field H parallel to the film plane. (b) The frequency dependence of this FMR spectrum (open triangles) was obtained for FeSn(5 nm) and fitted (solid black line) with the sum of the derivative of the Lorentzian function.
Figure 4.
(a) Frequency (f) plotted as a function of resonance field and fitted with Kittel Eq. (3). (b) The dependence of uniaxial anisotropy field over the thickness of FeSn film, the dotted line represents the average value of . (c) The extracted value of is plotted over the inverse thickness () of the ferromagnet and fitted with Eq. (4). (d) The variation of linewidth with frequency (f) and fitted with linewidth Eq. (5). (e) The variation of inhomogeneous linewidth plotted over the thickness of FeSn film. (f) Effective damping constant () as a function of inverse thickness () of ferromagnet together with the fit using Eq. (6). Here, the solid symbols and solid lines represent the experimental data and fit, respectively.
Here, is the gyromagnetic ratio. , , and are the resonance field, uniaxial anisotropy field, and the effective saturation magnetization of the ferromagnet. Using the value of 27 and fitting with Eq. (3) we extracted and for different thickness of FeSn [Fig. 4b and c]. In Fig. 4b, the average value of for FeSn(2-7 nm) films is found to be around 130 Oe. Furthermore, the uniaxial anisotropy constant () of FeSn film is determine by: . The value of is found to be , which is one order lower than bulk single crystal51. In Fig. 4c, the behavior of over the thickness of FeSn is plotted and fitted with the equation;
| 4 |
Here, is the permeability constant of free space. and are the saturation magnetization and surface anisotropy constant, respectively. From the fitting, the values of and are found to be and , respectively. It is noteworthy that we found a good agreement between the values of obtained from the FMR technique and the SQUID data.
The versus f for all the thicknesses is plotted (solid open symbol) in Fig. 4(d) and fitted with the expression52–55:
| 5 |
Here, the first term, denotes the inhomogeneous broadening, which largely depends on the quality of the sample. The second term indicates the effective damping (). In Fig. 4d, from fits of versus f with the Eq. (5) for various thicknesses, we extracted and . The value of the inhomogeneous broadening, is found to be less than 40 Oe for all films [as shown in Fig. 4e]. Here, we found a monotonic increase in for the thickness of ferromagnet FeSn. Figure 4f shows the value of with the inverse of ferromagnetic thickness (). The behavior was fitted with56,57:
| 6 |
where represent the intrinsic Gilbert damping constant of the ferromagnet FeSn, while and g represent the effective spin mixing conductance of Pt/FeSn system. From the fitting, we found to be around and g to be . The depends on both spin-orbit coupling as well as the phase lag between the distortions of the Fermi surface and the precessing magnetization. The intrinsic mechanism of Gilbert damping is commonly ascribed to spin-orbit coupling through two potential mechanisms: interband and intraband scattering58,59. In the interband scattering mechanism, the magnetization dynamics can generate electron-hole pairs across different bands. This leads to a Gilbert damping effect that scales with the resistivity60,61. Conversely, in the intraband scattering scenario, electron-hole pairs are generated within the same electronic band, resulting in a Gilbert damping effect that scales with the conductivity62,63. Our value of is relatively larger compared to transition metal thin films, and since the resistivity of FeSn is found to be larger, we speculate that the mechanism of intrinsic damping in our polycrystalline FeSn films is “resistivity-like”. However, more studies (e.g., temperature dependence) are needed to determine the mechanism of intrinsic damping in FeSn. The order of g for FeSn/Pt is almost comparable to other Pt-based FM heterostructures48,64,65, indicating that ferromagnet FeSn can also be used as an effective spin current source. Hence, a large value of spin mixing conductance in FeSn/Pt bilayer system, together with its exotic magneto-transport properties, can be beneficial for memory-based device applications.
Conclusion
In summary, we demonstrate the growth of ultra-thin polycrystalline phase of FeSn films with varying thicknesses (2-7 nm). The XRD, XRR, and AFM results show high-quality films with low surface/interfacial roughness. The magneto-static and magneto-transport results suggest the formation of the ferromagnetic phase and the intrinsic AHE nature of FeSn films, respectively. Here, we report the first measurements of the intrinsic Gilbert damping constant (), and effective spin mixing conductance (g) in FeSn films. The extracted value of , and g is found to be , and , respectively. A large value of g obtained from FMR measurements suggest ferromagnet FeSn can also be a potential material to generate pure spin current. These results promote the inexpensive and widely used sputter material growth of such quantum materials.
Methods
Sample preparation
The ultrathin films of FeSn with varying thicknesses (t = 2, 3, 5, and 7) on Si-SiO substrate were deposited using RF magnetron sputtering35 at room temperature. An optimized low growth rate of 0.2 was used for better control over the ultra-low thickness of FeSn films. The base pressure of the sputtering chamber was better than 6.7 mbar, while the working pressure was maintained at 2.7 mbar. These thin films were post-annealed in-situ at C for 1 hour to improve the crystallinity. A 3 nm aluminum (Al) layer was capped on all films to protect these samples from oxidation.
Sample characterization
The structural properties of these films were analyzed with the help of the X-ray diffraction (XRD) technique using a PANalytical X’Pert diffractometer with Cu- radiation (). The elemental and compositional analyses of these films were determined with the help of the electronic probe microscopy analysis (EPMA) technique. We determine the composition of Fe and Sn to be 61 at.% and 39 at.% in all the samples. The average surface roughness and topography of these films were obtained using the atomic force microscopy (AFM) technique in tapping mode (Asylum Research, MFP-3D system). The thickness, roughness, and density of these FeSn films were measured using the X-ray reflectivity (XRR) measurement technique. The static magnetization measurements were carried out using the magnetic property magnetic system (MPMS) with a superconducting quantum interference device (SQUID) using Quantum Design Inc. The magneto-transport properties were measured using the physical property measurement system (PPMS) technique from Quantum Design Inc. (Evercool-II). We employed four-terminal sensing techniques: linear contact geometry for determining longitudinal resistivity and Hall contact geometry for the transverse resistivity. One pair of contact electrodes is used to supply the DC current in the sample, while the other pair of contact electrodes perpendicular (parallel) to the current direction is used for sensing the transverse (longitudinal) voltage. The magneto-dynamic measurements are performed using NanOsc PhaseFMR-40 FMR setup in the 4-20 GHz frequency range. The instrument used field modulation (AC field of 1 Oe peak to peak) for a higher signal-to-noise ratio (using Helmholtz coils with 490 Hz reference frequency). The measurements are performed with an RF power of 12.5-17.6 dBm (varying for different frequency ranges).
Supplementary Information
Acknowledgements
The partial support from the Science & Engineering Research Board [SERB File no. CRG/2022/002821], the Ministry of Human Resource Development under the IMPRINT program [Grant no: 7519 and 7058], the Department of Science and Technology under the Nanomission program [Grant no: ], the Department of Electronics and Information Technology (DeitY), Joint Advanced Technology Centre at IIT Delhi, and the Grand Challenge project supported by IIT Delhi are gratefully acknowledged. KIAK acknowledges support from the University Grants Commission (UGC), India. This work was also partially supported by the Horizon 2020 research and innovation program No. 835068 “TOPSPIN” and the Swedish Research Council (VR Grant No. 2016-05980).
Author contributions
P.K.M. and J.Å. proposed the experiment and provided the experiment facilities. K.I.A.K. executed the project and grew the samples. K.I.A.K. and R.S.Y. performed the structural, magnetization, and magneto-transport measurements. A.K. and P.G. performed the spin-dynamic measurement. All authors helped in data analysis, co-wrote, and revised the manuscript.
Funding
Open access funding provided by University of Gothenburg.
Data availability
The datasets used and analysed during the current study available from the corresponding author on reasonable request.
Competing interests
The authors declare no competing interests.
Footnotes
Publisher's note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Contributor Information
Johan Åkerman, Email: johan.akerman@physics.gu.se.
Pranaba Kishor Muduli, Email: muduli@physics.iitd.ac.in.
Supplementary Information
The online version contains supplementary material available at 10.1038/s41598-024-53621-z.
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Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
The datasets used and analysed during the current study available from the corresponding author on reasonable request.




