Entanglement of the spin–orbit and magnetic order in multiferroic materials bears a strong potential for engineering novel electronic and spintronic devices. Here, we explore the electron and spin structure of ferroelectric α-GeTe thin films doped with ferromagnetic Mn impurities to achieve its multiferroic functionality. We use bulk-sensitive soft-X-ray angle-resolved photoemission spectroscopy (SX-ARPES) to follow hybridization of the GeTe valence band with the Mn dopants. We observe a gradual opening of the Zeeman gap in the bulk Rashba bands around the Dirac point with increase of the Mn concentration, indicative of the ferromagnetic order, at persistent Rashba splitting. Furthermore, subtle details regarding the spin–orbit and magnetic order entanglement are deduced from spin-resolved ARPES measurements. We identify antiparallel orientation of the ferroelectric and ferromagnetic polarization, and altering of the Rashba-type spin helicity by magnetic switching. Our experimental results are supported by first-principles calculations of the electron and spin structure.
The interplay between electronic eigenstates, spin and orbital degrees of freedom, combined with fundamental breaking of symmetries is currently one of the most exciting fields of research. It not only forms the basis for giant magnetoresistance1, spin-torque manipulation of magnetic domains2 and the use of Rashba effects for spin manipulation3, but has also lead to outstanding recent discoveries of new quantum phases such as topological insulators4, Weyl semimetals5 and Majorana fermions6. While already each of these topics has initiated new research fields, the combination of several of these effects in a single material opens up a new realm of opportunities. For example, superconductors with sizable Rashba spin splitting and ferromagnetic (FM) order would unite all ingredients for formation and manipulation of so-called anyons, generalizing the concept of Majorana fermions7. Multiferroics, such as Ge1−xMnxTe (ref. 8), fulfil these requirements providing unusual physical properties9,10,11 due to the coexistence and coupling between FM and ferroelectric (FE) order in one and the same system. Here we show that multiferroic Ge1−xMnxTe inherits from its parent FE α-GeTe compound a giant Rashba splitting of three-dimensional (3D) bulk states12,13,14, which competes with the Zeeman spin splitting induced by the magnetic exchange interactions. The collinear alignment of FE and FM polarization leads to an opening of a tunable Zeeman gap of up to 100 meV around the Dirac point of the Rashba bands, coupled with a change in spin texture by entanglement of magnetic and spin–orbit order. Through applications of magnetic fields, we demonstrate manipulation of spin-texture by spin-resolved photoemission experiments, which is also expected for electric fields based on the multiferroic coupling. The control of spin helicity of the bands and its locking to FM and FE order opens fascinating new avenues for highly multifunctional multiferroic Rashba devices suited for reprogrammable logic and/or non-volatile memory applications.
Similar to how the magnetic moment of an unpaired electron strongly enhances the exchange interaction, the local spin–orbit interaction is greatly enhanced by broken inversion symmetry. The larger the symmetry breaking, the larger the Rashba spin splitting becomes15,16,17. This is exemplified by the giant spin splitting observed for the polar semiconductor BiTeI (refs 18, 19), the polar surface of SrTiO3 (ref. 20), as well as for high-Z surface alloys21,22. In FE materials, the inversion symmetry is naturally broken by the FE polarization produced by the relative anion/cation displacements in the crystal lattice. Thus, the spin splitting in ferroelectric Rashba semiconductors (FERS) can assume exceedingly high values. α-GeTe exhibits record splitting values12,13,14,23 due to the very large rhombohedral lattice distortion providing cation/anion displacements as large as 10% of the (111) lattice plane spacing (Fig. 1a). The spin splitting of its bulk bands is intimately linked to the FE polarization, meaning that it can be switched and controlled by reversing the FE polarization direction12. Doping of GeTe with Mn maintains the rhombohedral lattice distortion and FE in Ge1−xMnxTe up to Mn concentrations as high as 30% (ref. 8). At the same time, the Mn spins couple to each other via free carrier mediated RKKY (Ruderman-Kittel-Kasuya-Yosida) exchange interactions. As a result, FM ordering as in (GaMn)As (ref. 24) occurs, which turns Ge1−xMnxTe into a multiferroic Rashba semiconductor (MUFERS) that combines both FE and FM properties as shown by Fig. 1e,f, respectively. In fact, multiferroic Ge1−xMnxTe features one of the highest FM Curie temperatures8,25 and highest reported magnetic moments amongst diluted ferromagnetic semiconductors (FMS)26.
FM ordering and FE symmetry breaking both lead to a spin splitting of the electronic band structure. For FMS, the spontaneous magnetization leads to a vertical Zeeman splitting of the bands (Fig. 1b), whereas for FERS the electric polarization induces a Rashba splitting in the k|| direction (Fig. 1c). In MUFERS both effects are entangled with each other, modifying the spin texture and band dispersions (Fig. 1d). For a basic discussion, we consider a simplified Rashba–Zeeman (RZ) model based on a two-dimensional (2D) free-electron approximation (RZ gas) in which the energy eigenvalues E±(k) of the Rashba split bands in the presence of magnetic order are given by
where E0 is the energy of the band edge, m* the effective electron mass, αR the k-linear Rashba coupling constant and ΔZ the momentum-independent Zeeman gap near . In principle, any orientation of the magnetization opens a gap near (Fig. 1d). Considering the momentum-dependent expected values of the spin components in all directions, however, only systems with magnetization parallel to the inversion symmetry breaking direction can reorient the spin of the Rashba electrons and open a gap in all k|| directions as illustrated by Fig. 1g and Supplementary Fig. 1 (Supplementary Note 1.1). Due to coupling between the easy axis of magnetization and the rhombohedral lattice distortion, (111) Ge1−xMnxTe films fulfil these criteria8 because the electric polarization and magnetic moments are colinear and perpendicular to the surface (Fig. 1e,f). Since the helicity of the Rashba effect is locked to the FE moments13,14,27, multiferroic switching is expected to entangle with the spin helicity as sketched in Fig. 1g,h.
For a systematic spectroscopic study of the RZ effect in this multiferroic system, we have prepared epitaxial Ge1−xMnxTe films with various Mn content up to 13% (xMn=0.03, 0.054, 0.08 and 0.13, see ‘Methods’ section). We use SX-ARPES to elucidate the local electronic structure of the Mn ions and RZ splitting with 3D k-space resolution, and spin-resolved ARPES (SARPES) in the ultraviolet photon energy range to explore the corresponding changes in the spin textures in this multiferroic material (see ‘Methods’ section). Figure 2 summarizes our SX-ARPES data obtained with photon energies from 340 to 800 eV. A fundamental advantage of this energy range28 is an increase of the photoelectron escape depth and thus of the intrinsic definition of the ARPES experiments in surface-perpendicular momentum k⊥ (ref. 29) crucial for observation of the inherently 3D electronic structure of Ge1−xMnxTe. This is illustrated in Fig. 2a by showing the dispersive spectral weight at the Fermi level (EF) and at a binding energy of 700 meV as a function of k⊥ varied through photon energy. This map, that is similar for all samples except for an increase of the spectral broadening with increasing x, readily identifies the Z-points in the 3D Brillouin zone where the Rashba splitting is most pronounced14. Measured in the Z-point at hν=480 eV, where the spectral intensity is maximal, the ARPES spectral weight along the A–Z–A direction is shown in Fig. 2b. This map clearly shows the pair of Rashba split bands in the vicinity of the Z-point consistent with the theoretical expectation (Fig. 2c). Another virtue of SX-ARPES is its chemical specificity achieved with resonant photoemission. The corresponding data measured at the Mn L-edge as indicated by the X-ray absorption (Fig. 2d) demonstrates that the Mn 3d states hybridize into the GeTe host states through the whole valence band, in particular into the Rashba bands below the Zeeman gap (see Supplementary Fig. 3 in Supplementary Note 2). In particular, we note the absence of any impurity states in the vicinity of EF which might otherwise interfere with the RZ splitting in this region.
Our further discussions of the Zeeman gap opening is based on Fig. 2f, which presents the experimental band structure along A–Z–A in vicinity of the Z-point, measured through the whole sample series. To elucidate the correlation between Rashba splitting and Zeeman gap, and its dependence on Mn doping, we compare in Fig. 3 the zoom-in band maps around the Z point near EF (dashed rectangle in Fig. 2b) with ab initio calculations. As detailed in Supplementary Fig. 4, careful experimental alignment is needed for the quantitative assessment of the Zeeman gap. To derive the competing Rashba and Zeeman terms αR and ΔZ for different Mn concentrations, both theoretical and experimental data in Fig. 3 are fitted with the simplified RZ gas model described above (red–blue lines). Due to the simplicity of the free electron model that neglects both third order corrections in momentum, and the strong band non-parabolicity of the IV–VI compounds, the fit does not reproduce the actual dispersions but it is accurate for small momenta and yields direct values for both αR (±7%) and ΔZ (±10 meV), listed in Supplementary Table 1. More accurate fits based on a massive Dirac fermion seen in light-blue are listed in Supplementary Table 2 and discussed in Supplementary Note 1.2. As fitted results from both models are consistent (Supplementary Fig. 2), we discuss next the Mn-concentration dependence of the αR and ΔZ based on the simplified model.
We observe both in experiment and theory that a Zeeman gap, absent in α-GeTe, appears and widens with increasing Mn concentration, that is, increasing film magnetization. This is clear-cut evidence that the Zeeman gap opening of the Rashba bands is induced by the FM order of the multiferroic system. To the best of our knowledge, this is the first experimental confirmation of the opening of a Zeeman gap at the Dirac point in a bulk system with strong FM order. In magnetically doped topological insulators such results are still being debated due to the lack of measurements justifying the FM ordering of the dilute dopants at the ARPES measurement conditions30,31,32. Plotting in the lower right panels of Fig. 3a,b, the resulting values for αR and ΔZ as a function of Mn content reveals that the Zeeman gap reaches remarkably high values around 100 meV for xMn>10%. Furthermore, the progression of the Zeeman gap is accompanied by a decrease of the Rashba splitting in both fitting models. The microscopic origin of this trend is that higher Mn doping reduces the rhombohedral distortion of the Ge1−xMnxTe lattice8. This, in turn, reduces the FE polarization (cf. Fig. 1a) and thus, the strength of the Rashba coupling constant. For the host α-GeTe(111) we find that αR is as high as 4.3 eVÅ, which is in excellent agreement with theoretical predictions by Picozzi23. We also note that since the experimental Zeeman gap appears to saturate for xMn around 10%, our conjecture is that higher Mn doping might lead to Mn-phase segregation in the undoped host GeTe lattice25,33 and that at high xMn antiferromagnetic coupling between neighbouring Mn atoms reduces the average FM moment per Mn atom34.
A particularly interesting feature for device applications is the fact that with increasing Mn doping the Zeeman gap shifts towards EF. This will reduce the bias voltage needed to move EF inside this gap and create a single spin polarized Fermi surface reminiscent of an ideal topological insulator4. In contrast to the 2D surface state of a topological insulator, however, Ge1−xMnxTe has a 3D Fermi surface, which in the absence of FM order takes the form of a spin polarized spindle torus19,35. The constant energy surface shows a strong hexagonal warping which becomes three-fold away from the Γ and Z points, in accordance with the crystal symmetry. In Fig. 3c the 3D Fermi surfaces of Ge1−xMnxTe are shown for three different chemical potentials, taking into account both the deviation from an ideal torus due to the warping and the opening of a Zeeman gap. For μ>ΔZ the gap opening does not influence the Fermi surface, and for μ<−ΔZ the gap is only visible for a limited k⊥ range because of the dispersion to higher binding energy away from Z. For μ=0, however, the chemical potential is within the Zeeman gap and the 3D Fermi surface obtains a non-trivial spin texture due to the presence of only one single non-degenerate Fermi sheet. The exact consequences of this configuration require further study, but in both one-dimensional and 2D equivalents this leads to a template for the formation of Majorana fermions.
Spin-resolved ARPES measurements
We now turn to spin-resolved information achieved with ultraviolet-SARPES to show that Ge1−xMnxTe still retains the Rashba-type spin splitting from the host GeTe (Supplementary Fig. 5), but exhibits an out-of-plane spin reorientation due to FM ordering. According to previous studies, α-GeTe already exhibits a complex surface electronic structure where surface states coexist with a variety of bulk-derived states13,14. For Ge1−xMnxTe, the data measuring the in-plane spin polarization shown in Supplementary Fig. 6 indicate opposite spin helicity of the bulk states above and below the Zeeman gap as sketched Fig. 1g. Thus, the in-plane spin polarization is similar as for α-GeTe above and below the Dirac point14.
To resolve the question of how the presence of FM order affects the Ge1−xMnxTe spin texture, Fig. 4a presents Pz calculations for four different Mn concentrations based on the one-step photoemission approach (see ‘Methods’ section). Clearly, FM ordering leads to a progressive Pz spin reorientation with increasing Mn concentration. In particular, the characteristic Pz hexagonal warping typical for GeTe is smeared out at (Supplementary Fig. 7). The theoretical and experimental Pz spinors are visualized in Fig. 4c,d as spin-resolved energy distribution curves measured across the Zeeman gap at normal emission. Apart from difference in amplitude due to inelastic scattering effects, our experimental data and the theoretical results represented by Fig. 4c inset consistently reproduce the characteristic Pz spin reorientation wiggle across the Zeeman gap induced by spontaneous FM order.
The virtue of MUFERS obviously lies in the ample possibilities for spin manipulation using electrical as well as magnetic fields or by combination of both (Fig. 1). The latter is demonstrated by Fig. 4d, where we present and compare the Pz spin texture measured before and after magnetization reversal, that is, after switching the magnetization between the  and  directions with magnetic fields ±B applied perpendicular to the sample. After application of B along , the Pz polarization is significantly enhanced, meaning that the intrinsic FM order is into the sample. After switching the magnetization in the opposite  direction, the Pz spin-texture reverts, which clearly confirms the entanglement of the spin-splitting as sketched in Fig. 1g,h. To demonstrate the Pz spin reorientation around , the SARPES data in Fig. 4d was measured for finite momenta indicated by the vertical dashed line in Fig. 4b. The data shows exactly the same Pz modulation as in normal emission, which is in sharp contrast to pure α-GeTe where the out-of-plane spin texture is dominated by warping and photoemission effects14 (Supplementary Fig. 7). According to Fig. 1f, for Ge0.87Mn0.13Te magnetic field strengths of less than 1,000 Gauss are sufficient for this reversal process, but the actually required switching field depends also on temperature and Mn concentration8.
The coupling between the FM and FE order implies that also the Rashba-like spin texture is influenced by the magnetic field switching. Due to the intricate mixture of states with both bulk derived and surface character at finite momenta14, measurements of this change are rather complex with currently available experimental techniques. However, as shown in Supplementary Fig. 8, the canted Rashba-type spin texture allows us to indirectly also verify this aspect of the MUFERS.
In a broader perspective, our work introduces a paradigm of MUFERS, which generalizes and expands the concept of FERS and FMS. The unveiled RZ splitting has far reaching consequences both for fundamental physics and device applications. From a theoretical point of view, the Zeeman gap of MUFERS may give rise to excitations with the characteristics of localized Majorana fermions. In terms of applications, adding magnetism to FE FERS opens additional degrees of freedom and allows to strongly enhance the fidelity of spin control through additional Larmor precession of spins injected in field effect spin transistors. Spin control in such devices can be attained through electric or magnetic means, as well as by combinations of both. This vastly enhances the functionality of MUFERS devices beyond that of FM or FE systems only36. Thus, our results will pave the way for a new field of MUFERS systems, bringing new multifunctional assets for spintronic device applications.
Sample preparation method
Experiments were performed on 200 nm thick Ge1−xMnxTe films grown by molecular beam epitaxy on BaF2(111) substrates8,25,37. A protective stack of amorphous Te- and Se-capping layers with a total thickness of 20 nm was used to avoid surface oxidation and degradation. It was completely removed in the ultrahigh ARPES vacuum chamber by annealing the samples for 30–45 min at 250 °C. Comparison of SX-ARPES spectra measured through the protective Te/Se stack and on the uncapped samples evidenced that the annealing did not change the Ge1−xMnxTe bulk electronic structure but only unleashed the otherwise suppressed surface states.
The bulk-sensitive SX-ARPES experiments have been carried out at the SX-ARPES endstation38 of the high-brilliance ADvanced RESonance Spectroscopies beamline at the Swiss Light Source synchrotron radiation facility, Paul Scherrer Institute, Switzerland, using p-polarized soft-X-ray photons in the energy range 300–800 eV. The slit of the hemispherical photoelectron analyser PHOIBOS-150 was oriented in the scattering plane including the incident photons and detected photoelectrons. The combined (beamline and analyser) energy resolution was 80 meV, and analyser angular resolution 0.07°. The experiments were carried out at low temperature of 12 K to quench the thermal effects destroying the coherent k-resolved spectral component at high photon energies39. The complementary SARPES experiments were performed at the COPHEE end-station of the Surfaces and Interfaces Spectroscopy beamline at SLS using p-polarized photons in the energy range 20–25 eV. The Omicron EA 125 hemispherical energy analyser was equipped with two orthogonally mounted classical Mott detectors40. The whole set-up allows simultaneous measurements of all three spatial components of the spin-polarization vector for each point of the band structure. The SARPES data were measured with the sample azimuths Z–U or Z–A aligned perpendicular to the scattering plane. The SARPES error bars indicated in figures are given by 1/(S), where S is the detector Sherman function (0.08 at COPHEE) and N is the detector count rate. The angular and combined energy resolution were 1° and 60 meV, respectively. In spin-integrated mode these resolutions were set to 0.5° and 20 meV. SARPES data from magnetized samples were measured at Soleil CASSIOPÉE beamline where S=0.12. All data were taken at 20–30 K. The experimental results in the main text were reproduced on fourteen samples with individual annealing preparation over different experimental runs. The magnetic properties were measured using a superconducting quantum interference device (SQUID) in vibrating sample magnetometry mode. Magnetic hysteresis loops were recorded at 5 K with the applied field directed perpendicular to the sample plane. The piezo-force microscopy was performed at the NanoXAS endstation at the SLS using plain platinum tip at room temperature.
First principles calculations
The ab-initio calculations are based on the multiple scattering approach (Korringa–Kohn–Rostoker (KKR) method) and density functional theory41. Spin–orbit coupling has been naturally included by use of a fully relativistic four-component scheme. As a first step of our investigations we performed self-consistent calculations for 3D bulk as well as 2D semi-infinite surface of Ge1−xMnxTe within the screened Korringa–Kohn–Rostoker formalism41. The corresponding ground state band structures are presented in terms of Bloch spectral functions. The self-consistent results served as an input for our spectroscopic investigations. The ARPES calculations were performed in the framework of the fully relativistic one-step model of photoemission42 in its spin-density matrix formulation, which accounts properly for the complete spin-polarization vector, in particular for Rashba systems like GeTe. Together with a realistic model for the surface barrier potential, the one-step calculations were decisive to substantiate the Ge1−xMnxTe spectral features on both qualitative and quantitative levels. Ground state, as well as one-step calculations of substitutionally disordered Ge1−xMnxTe has been described by means of coherent potential approximation alloy theory. For simplicity the ground state calculations in Fig. 3b were based on the GeTe lattice structure12 with added Mn substitutional doping on Ge sites, being the primary reason for the difference in the strength of the Rashba splitting α between theory and experiment reported in Fig. 3.
The data that support the findings of this study are available on request from the corresponding author.
How to cite this article: Krempaský, J. et al. Entanglement and manipulation of the magnetic and spin–orbit order in multiferroic Rashba semiconductors. Nat. Commun. 7, 13071 doi: 10.1038/ncomms13071 (2016).
Chappert, C., Fert, A. & Nguyen Van Dau, F. The emergence of spin electronics in data storage. Nat. Mater. 6, 813–823 (2007).
Mihai Miron, I. et al. Current-driven spin torque induced by the Rashba effect in a ferromagnetic metal layer. Nat. Mater. 9, 230–234 (2010).
Bychkov, Y. A. & Rashba, E. I. Oscillatory effects and the magnetic susceptibility of carriers in inversion layers. J. Phys. C 17, 6039–6045 (1984).
Hasan, M. Z. & Kane, C. L. Colloquium: topological insulators. Rev. Mod. Phys. 82, 3045–3067 (2010).
Murakami, S. Phase transition between the quantum spin Hall and insulator phases in 3D: emergence of a topological gapless phase. New J. Phys. 9, 356 (2007).
Mourik, V. et al. Signatures of majorana fermions in hybrid superconductor–semiconductor nanowire devices. Science 336, 1003–1007 (2012).
Beenakker, C. W. J. Search for majorana fermions in superconductors. Annu. Rev. Condens. Matter Phys. 4, 113–136 (2013).
Przybylińska, H. et al. Magnetic-field-induced ferroelectric polarization reversal in the multiferroic Ge1−xMnxTe semiconductor. Phys. Rev. Lett. 112, 047202 (2014).
Eerenstein, W., Mathur, N. D. & Scott, J. F. Multiferroic and magnetoelectric materials. Nature 442, 759–765 (2006).
Ramesh, R. & Spaldin, N. A. Multiferroics: progress and prospects in thin films. Nat. Mater. 6, 21–29 (2007).
Tokura, Y. & Seki, S. Multiferroics with spiral spin orders. Adv. Mater. 22, 1554–1565 (2010).
Di Sante, D., Barone, P., Bertacco, R. & Picozzi, S. Electric control of the giant Rashba effect in bulk GeTe. Adv. Mater. 25, 509–513 (2013).
Liebmann, M. et al. Giant Rashba-type spin splitting in ferroelectric GeTe(111). Adv. Mater. 28, 560–565 (2016).
Krempaský, J. et al. Giant Rashba splitting of bulk states in the ferroelectric αGeTe (111) semiconductor. Preprint at https://arxiv.org/abs/1503.05004v1 (2015).
Bihlmayer, G., Koroteev, Y., Echenique, P. M., Chulkov, E. V. & Blügel, S. The Rashba-effect at metallic surfaces. Surf. Sci. 600, 3888–3891 (2006).
Dil, J. H. Spin and angle resolved photoemission on non-magnetic low-dimensional systems. J. Phys.: Condens. Matter 21, 403001 22pp. (2009).
Slomski, B., Landolt, G., Bihlmayer, G., Osterwalder, J. & Dil, J. H. Tuning of the Rashba effect in Pb quantum well states via a variable Schottky barrier. Sci. Rep. 3, 1963 (2013).
Ishizaka, K. et al. Giant Rashba-type spin splitting in bulk BiTeI. Nat. Mater. 10, 521–526 (2011).
Landolt, G. et al. Disentanglement of surface and bulk Rashba spin splittings in noncentrosymmetric BiTeI. Phys. Rev. Lett. 109, 116403 (2012).
Santander-Syro, A. F. et al. Giant spin splitting of the two-dimensional electron gas at the surface of SrTiO3 . Nat. Mater. 13, 1085–1090 (2014).
Ast, C. R. et al. Giant spin splitting through surface alloying. Phys. Rev. Lett. 98, 186807 (2007).
Gierz, I. et al. Structural influence on the Rashba-type spin splitting in surface alloys. Phys. Rev. B 81, 245430 (2010).
Picozzi, S. Ferroelectric Rashba semiconductors as a novel class of multifunctional materials. Front. Phys. 2, 10 (2014).
Kobayashi, M. et al. Unveiling the impurity band induced ferromagnetism in the magnetic semiconductor (Ga,Mn)As. Phys. Rev. B 89, 205204 (2014).
Lechner, R. T. et al. Phase separation and exchange biasing in the ferromagnetic IV–VI semiconductor Ge1−xMnxTe. Appl. Phys. Lett. 97, 023101 (2010).
Fukuma, Y. et al. Carrier-induced ferromagnetism in Ge0.92Mn0.08Te epilayers with a Curie temperature up to 190 K. Appl. Phys. Lett. 93, 252502 (2008).
Elmers, H. J. et al. Spin mapping of surface and bulk Rashba states in ferroelectric αGeTe (111) films. Preprint at http://arxiv.org/abs/1512.01363v1 (2015).
Strocov, V. N. et al. Soft-X-ray ARPES at the Swiss light source: from 3D materials to buried interfaces and impurities. Synchrotron Radiat. News 27, 31–40 (2014).
Strocov, V. N. Intrinsic accuracy in 3-dimensional photoemission band mapping. J. Electron Spectrosc. Relat. Phenom. 130, 65–80 (2003).
Chen, Y. L. et al. Massive dirac fermion on the surface of a magnetically doped topological insulator. Science 329, 659–662 (2010).
Xu, S.-Y. et al. Hedgehog spin texture and Berry’s phase tuning in a magnetic topological insulator. Nat. Phys. 8, 616–622 (2012).
Sanchez-Barriga, J. et al. Nonmagnetic band gap at the Dirac point of the magnetic topological insulator (Bi1−xMnx)2Se3 . Nat. Commun. 7, 10559 (2016).
Sato, K., Fukushima, T. & Katayama-Yoshida, H. Ferromagnetism and spinodal decomposition in dilute magnetic nitride semiconductors. J. Phys.: Condens. Matter 19, 365212 (2007).
Fukushima, T. et al. First principles studies of GeTe based dilute magnetic semiconductors. J. Phys.: Condens. Matter 27, 015501 (2015).
Landolt, G. et al. Direct measurement of the bulk spin structure of noncentrosymmetric BiTeCl. Phys. Rev. B 91, 081201 (2015).
Rinaldi, C. et al. Evidence for spin to charge conversion in GeTe(111). APL Mater. 4, 032501 (2016).
Hassan, M. et al. Molecular beam epitaxy of single phase gemnte with high ferromagnetic transition temperature. J. Cryst. Growth 323, 363–367 (2011)) Proceedings of the 16th International Conference on Molecular Beam Epitaxy (ICMBE).
Strocov, V. N. et al. Soft-X-ray ARPES facility at the ADRESS beamline of the SLS: concepts, technical realisation and scientific applications. J. Synchrotron Radiat. 3, 631–643 (2014).
Braun, J. et al. Exploring the xps limit in soft and hard x-ray angle-resolved photoemission using a temperature-dependent one-step theory. Phys. Rev. B 88, 205409 (2013).
Hoesch, M. et al. Spin-polarized Fermi surface mapping. J. Electron Spectrosc. Relat. Phenom. 124, 263–279 (2002).
Ebert, H., Ködderitzsch, D. & Minár, J. Calculating condensed matter properties using the KKR-Green’s function method-recent developments and applications. Rep. Prog. Phys. 74, (2011).
Braun, J. & Donath, M. Theory of photoemission from surfaces. J. Phys.: Condens. Matter 16, 2539–2555 (2004).
This work was supported by the Swiss National Science Foundation Project No. PP00P2_1447421 and n.200021 146890. Financial support from the German funding agency DFG (SPP1666) and the German ministry BMBF (05K13WMA) is also gratefully acknowledged (H.V., H.E., J.B. and J.M.) G.S. and V.V.V. acknowledge support from the Austrian Science Funds (SFB-025, IRON). Financial support from the priority programme SPP 1666 of the Deutsche Forschungsgemeinschaft (Grant No. EB154/26-1) is gratefully acknowledged (H.V., H.E., J.B. and J.M.). J.M. acknowledges CENTEM PLUS (LO1402) project. F.B. and P.W. acknowledge the European Community's Seventh Framework Programme (FP7/2007–2013) under the grant agreement n.290605 (PSI-FELLOW/COFUND). P.W. acknowledges the technical support from N. Bingham and A. K. Suszka.
The authors declare no competing financial interests.
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Krempaský, J., Muff, S., Bisti, F. et al. Entanglement and manipulation of the magnetic and spin–orbit order in multiferroic Rashba semiconductors. Nat Commun 7, 13071 (2016). https://doi.org/10.1038/ncomms13071
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