Letter | Published:

Direct evidence of ferromagnetism in a quantum anomalous Hall system

Nature Physicsvolume 14pages791795 (2018) | Download Citation


Quantum anomalous Hall (QAH) systems are of great fundamental interest and potential application because of their dissipationless conduction without the need for an external magnetic field1,2,3,4,5,6,7,8,9. The QAH effect has been realized in magnetically doped topological insulator thin films10,11,12,13,14. However, full quantization requires extremely low temperature (T < 50 mK) in the earliest works, athough it has been significantly improved by modulation doping or co-doping of magnetic elements15,16. Improved ferromagnetism has been shown in these thin films, yet direct evidence of long-range ferromagnetic order is lacking. Herein, we present direct visualization of long-range ferromagnetic order in thin films of Cr and V co-doped (Bi,Sb)2Te3 using low-temperature magnetic force microscopy with in situ transport. The magnetization reversal process reveals typical ferromagnetic domain behaviour—that is, domain nucleation and possibly domain wall propagation—in contrast to much weaker magnetic signals observed in the endmembers, possibly due to superparamagnetic behaviour17,18,19. The observed long-range ferromagnetic order resolves one of the major challenges in QAH systems, and paves the way towards high-temperature dissipationless conduction by exploring magnetic topological insulators.


Dissipationless conduction is technologically appealing because of a wide range of potential applications. There are two ways to achieve dissipationless conduction in condensed matter systems—through superconductivity and through topological chiral edge states. For this reason, high-temperature superconductivity has been extensively investigated for decades20,21,22,23. Dissipationless conduction due to chiral edge states is realized in the quantum Hall effect (QHE), which requires low temperature and an external magnetic field. The closely related phenomenon, the quantum anomalous Hall effect (QAHE), however, does not require an external magnetic field. The realization of the QAHE requires the breaking of time-reversal symmetry and a topologically nontrivial band structure with the Fermi level inside the bandgap. There have been a number of theoretical proposals1,2,3,4,5,6,7,8,9, and eventually it was realized experimentally in magnetically doped three-dimensional topological insulator thin films10,11,12,24. Here the ferromagnetism, induced by doping magnetic elements, breaks time-reversal symmetry, and opens a mass gap at the Dirac point of the topological surface states. By tuning the Fermi level inside the mass gap, the magnetic topological insulator thin film is equivalent to two copies of half-integer QHE systems25. Quantized Hall conduction was first observed at ultralow temperature (~30 mK) in Cr-doped BixSb2−xTe3 (BST) thin films synthesized by molecular beam epitaxy (MBE)10. This observation was soon confirmed by other groups11,12,13,14. Later, a robust QAHE with higher precision in quantization was observed in a V-doped BST thin film, which is a harder ferromagnet with a greater coercive field (Hc) and a higher Curie temperature (TC) with the same doping level24. Nevertheless, ultralow temperature (T < 50 mK) is needed to achieve full quantization. Therefore, it is imperative to understand the origin of the requirement for ultralow temperature for full quantization.

Magnetic inhomogeneity has been proposed to be one of the main factors that limit the QAH temperature. Disordered ferromagnetic or superparamagnetic behaviour and electronic inhomogeneity have been reported in Cr-doped BST thin films17,18,19,26. Since the mass gap is proportional to the strength of the exchange interaction, the reduced QAH temperature is probably limited by the regions with the weakest exchange17,18. Although modulation doping of Cr was shown to improve the quantization temperature in penta-layer thin films15, it is unclear whether it reduces magnetic inhomogeneity. On the other hand, recent angle-resolved photoemission spectroscopy (ARPES) studies of V-doped BST thin films suggest that the valance band maximum (VBM) is above the Dirac point27. Therefore, an ultralow temperature is needed to localize the bulk states near the Dirac point along with sufficient disorder28. These mechanisms for lowering the quantization temperature indicate that Cr and V co-doping could be a viable way to reduce magnetic inhomogeneity while enhancing the mobility gap of localized states. Empirically, alloy doping is commonly known as an effective route to improve ferromagnetic order in a diluted magnetic semiconductor29,30.

Indeed, an increased QAH temperature was observed in Cr- and V-doped BST thin films16. At the optimal Cr/V ratio, full quantization was achieved at 300 mK, an order of magnitude higher than the endmembers with single dopants16. The Hall hysteresis loop is more square-like, suggesting a sharper magnetization reversal (that is, reduced magnetic inhomogeneity). Furthermore, the temperature dependence of the anomalous Hall resistance is more mean-field-like. These observations indicate improved ferromagnetism in Cr/V co-doped topological insulator thin films. However, direct microscopic evidence of long-range ferromagnetic ordering is still lacking. Note that the intrinsic anomalous Hall effect is determined by the Berry phase of the occupied bands, which is independent of the magnitude of the magnetization31. In this letter, we report a systematic study of Cr/V co-doped BST thin films using magnetic force microscopy (MFM). Our MFM results reveal clear ferromagnetic domain behaviour of the magnetization reversal process in the optimally doped BST thin films, confirming long-range ferromagnetic ordering in this QAH system, presumably via the Van Vleck mechanism5. Furthermore, the ferromagnetism of co-doped thin films is robust against a significant change in the bulk charge carrier density, although the exchange interaction is enhanced by hole-doping. This indicates a significant contribution from the Ruderman–Kittel–Kasuya–Yosida (RKKY) exchange coupling32,33. The direct evidence of long-range ferromagnetic order eases concerns about the fragility of the QAHE due to magnetic inhomogeneity, alleviating the need for ultralow temperature to achieve full quantization. Our results should encourage further exploration of the QAHE and related phenomena in magnetically doped topological materials for dissipationless conduction at elevated temperature.

Figure 1a shows a schematic of the Hall bar device of the magnetic topological insulator thin films fabricated for MFM and in situ transport measurements. Three (CryV1−y)0.19(BixSb1−x)1.81Te3 films (y = 0, 0.16, 1, respectively, and x ≈ 0.4) are fabricated into the Hall bar devices. All MFM data presented here were taken at 5 K. As shown in Fig. 1b, the y = 0.16 film is the optimized sample (TC ≈ 28 K) with the best ferromagnetic behaviour (sharpest reversal) and the highest Hall conductance (at 1.5 K). In addition, the temperature dependence of the Hall resistance is more mean-field-like, indicating robust ferromagnetism16. The longitudinal resistance starts to decrease immediately below TC, indicating that the sample enters the QAH regime as soon as the long-range ferromagnetic order forms (see Supplementary Fig. 1). The endmember (y = 0 or 1), however, enters the QAH regime at a much lower temperature. A gate voltage (Vg) was applied to the back of the SrTiO3(111) (STO) substrate to tune the Fermi level. At 1.5 K, the Hall resistance reaches 0.95h/e2 (where h is Planck’s constant and e is the electronic charge) at \({V}_{{\rm{g}}}^{0}\) (Supplementary Fig. 1). Such a quantization level was achieved only below 50 mK in single Cr- or V-doped thin films10,11,12,24.

Fig. 1: Schematic of the in situ transport set-up and the Cr concentration (y) dependence of σxy and Hc/FWHMMR.
Fig. 1

a, Schematic of the Hall bar device for MFM and in situ transport measurements. The 5 quintuple layers (QLs) Cr/V co-doped BST thin film was grown on a STO(111) substrate using MBE, followed by deposition of a 15 nm layer of Au film. Both the Au film and the magnetic tip were grounded to eliminate any electrostatic interactions between them. A back-gate voltage Vg was applied to the bottom electrode to tune the charge carrier density. The Hall resistance ρyx and longitudinal resistance ρxx were obtained by measuring Vyx and Vxx. b, Cr concentration (y) dependence of the zero magnetic field Hall conductance σxy (blue) and the ratio of coercivity (Hc) to the full-width at half-maximum (FWHM) of the magnetoresistance (MR) at 1.5 K.

Figure 2a,h shows MFM images and in situ transport data (ρxx and ρyx) of the optimally doped film (y = 0.16) at \({V}_{{\rm{g}}}^{0}\) 10 V at various magnetic fields. The ρyx(H) loop shows a saturation ~0.5h/e2 with a coercive field Hc ~ 0.26 T. The magnetization reversal process from downward (red) to upward (blue) magnetized states is illustrated in the MFM images. The downward saturated state has very weak magnetic contrast with a small positive field (+0.05 T), indicating the single-domain state persists at a small reversed field, showing compelling evidence of robust ferromagnetism. The observed stable single-domain state, with little relaxation, is in sharp contrast to the superparamagnetic behaviour previously reported in Cr-doped BST films, where significant relaxation was already observed at small magnetic fields17. (See Supplementary Fig. 1 for transport results.) At 0.15 T, up domains start to nucleate, represented by light blue regions. As the field increases further, the up domains expand and the down domains shrink. At the coercive field Hc where ρyx = 0 and ρxx peaks at ~ 0.8h/e2, equally populated up and down domains were observed, confirming the zero-magnetization state (M = 0). For H ≥ 0.35 T, no red regions are visible in the MFM images, indicating the system is in a saturated (single domain) state. The MFM observation of ferromagnetic domain behaviour is in excellent agreement with the in situ transport data, suggesting the local observation is representative of the global (bulk) properties. Note that the Hall data at 1.5 K and 5 K show similar square-like hysteresis loops, indicating no qualitative difference between these two temperatures. Furthermore, a higher coercive field and sharper reversal observed at the lower temperature suggest better ferromagnetism. Therefore, the observed ferromagnetic behaviour is expected to persist at the lower temperature, where full quantization was observed on the same sample16.

Fig. 2: The magnetization reversal process at 5 K at the neutral point \({{\bf{\it V}}}_{{\bf{g}}}^{{\bf{0}}}\).
Fig. 2

a, Left column: stack of MFM images from 0.05 T to 0.35 T to illustrate domain evolution. Right column: differential images by taking the difference between adjacent MFM images. Different colours represent local magnetization reversed at different magnetic fields. bg, Images of the reversed areas at various fields by combining the differential images, which illustrate domain nucleation and possible domain wall propagation. Dashed squares label nucleation sites and solid circles label possible domain wall propagation. h, Top: in situ transport data (ρxx) at \({V}_{{\rm{g}}}^{0}\) 10 V. Middle: H-dependence of normalized magnetization M/Ms, estimated from domain population, is consistent with the anomalous Hall loop (ρyx). Bottom: H-dependence of the domain contrast (δfrms), which peaks at Hc. The MFM images show ferromagnetic domain behaviour during the magnetization reversal from 0.15 T to 0.35 T, consistent with transport data.

The ferromagnetic domain behaviour can be further illustrated using the difference between the MFM images of adjacent fields, as shown in Fig. 2a. The locations where the changes in MFM signal are above the noise level (~ 2 mHz) are defined as the newly reversed regions. They are marked in different colours for each field value, which are shown in the right column of Fig. 2a. The unchanged areas are marked in white. In Fig. 2b–g, these differential images are stacked together to show the spatial correlations of magnetization reversal events so as to differentiate isolated domain nucleation from domain expansion (see Supplementary Fig. 5 for the complete data set). For example, as shown in Fig. 2c, some of the newly reversed regions (yellow) at 0.2 T have no correlation with previously reversed regions (red). These regions, labelled by dashed squares, are isolated nucleation sites. The other yellow regions, labelled by solid circles, have some overlap with the red regions, probably due to tilted domain walls. This behaviour is consistent with domain growth via either domain wall propagation or domain-wall-induced nucleation. The domain behaviour is distinctively different from the superparamagnetic behaviour of random switching events in a previous report17.

In addition to direct visualization of ferromagnetic domain behaviour, MFM data can also be used to extract the hysteresis loop of the normalized magnetization (M/Ms, where Ms is the saturated magnetization), which is estimated from the populations of up and down domains34. As shown in Fig. 2h, the M/Ms(H) curve agrees quantitatively with the ρyx(H) loop. The agreement between local (domain population) and global (ρyx) measurements demonstrates that our MFM results are representative of the bulk magnetic properties. Consistently, the domain contrast, estimated by the root-mean-square value of the MFM signal (δfrms), peaks at Hc when up and down domains are equally populated. The observed domain behaviour provides unambiguous evidence of long-range ferromagnetic order in the optimally Cr/V co-doped BST thin films. In contrast, MFM measurements on single-doped BST films do not reveal clear ferromagnetic behaviour (see Supplementary Figs. 2 and 3 for MFM results of endmembers.) Therefore, our MFM data provide direct evidence that long-range ferromagnetic order is essential for the enhancement of the QAH temperature16.

Long-range ferromagnetic order is one of the key ingredients of the QAHE. Yu et al. proposed a Van Vleck mechanism in magnetically doped topological insulators, where the exchange interaction between local moments is mediated by band electrons with significant Van Vleck susceptibility5,35. Therefore, the Van Vleck mechanism is independent of the bulk carrier density. However, other studies indicate that an RKKY-type exchange plays a significant role when bulk or surface carriers are present36,37,38,39. To shed light on the exchange mechanisms, we investigate the bulk carrier dependence of the ferromagnetism by applying a gate voltage. Similar to the neutral point \({V}_{{\rm{g}}}^{0}\) case, both electron-doped (300 V) and hole-doped (−300 V) states show typical ferromagnetic domain behaviour, confirming that long-range ferromagnetic order is robust against tuning the Fermi level near the neutral point (see Supplementary Figs. 6 and 7), supporting the presence of a Van Vleck mechanism. Figure 3a–c shows the MFM images at Hc and the nucleation maps at the three gate voltages. Comparing the three multi-domain states, hole-doping results in a larger domain size, fewer nucleation sites, and stronger domain contrast, whereas electron-doping results in an opposite trend. Consistently, Hc is enhanced (suppressed) by hole-(electron-)doping, as shown in the ρyx(H) loops in Fig. 3d. On the other hand, both hole- and electron-doping away from the neutral point suppress the AHE. Note that the domain contrast of the multi-domain state is proportional to the saturated magnetization40. The enhanced domain contrast at Hc indicates an increase in saturated magnetization with hole-doping. Compared to the local magnetic moment density, the gate-induced charge carrier density is negligible (see Supplementary Information section D for an estimation), so the saturated magnetization at zero temperature Ms(0) is independent of the gate voltage. Therefore, the enhancement of the magnetization at 5 K indicates a decrease in the reduced temperature T/TC (that is, an increase of TC, due to enhanced exchange coupling in the hole-doped films). This is also consistent with a higher Hc and fewer nucleation sites in the hole-doped state, suggesting the presence of the RKKY mechanism. Therefore, the gating dependence of the MFM results indicates that both the Van Vleck and the RKKY mechanisms are present in magnetically doped topological insulators. Interestingly, some nucleation sites (labelled by black circles) are independent of the gate voltage, so they are probably caused by neutral defects or imperfections that are insensitive to charge carriers. On the other hand, there are nucleation sites that do depend on the gate voltage, which indicates that they might be related to charged defects.

Fig. 3: Gate dependence of ferromagnetic behaviour.
Fig. 3

ac, MFM images around the coercive field (top) and nucleation-site (bottom) maps, at Vg = 300 V, 10 V and −300 V, respectively. Larger domain size and stronger domain contrast were observed for Vg = −300 V (hole-doping). Black circles label some of the common nucleation sites at three different Vg values. d, Hall resistance (top) and MFM domain contrast (δfrms) (bottom) as a function of magnetic field at three different Vg values. The values of Hc deduced from the two panels are consistent with each other, as Hc1 ≈ 0.21 T (Vg = 300 V), Hc2 ≈ 0.26 T (\({V}_{{\rm{g}}}^{0}\) = 10 V), Hc3 ≈ 0.33 T (Vg = −300 V).

The Vg-dependences of ρyx and Hc are summarized in Fig. 4a. The ρyx(Vg) curve was measured at zero magnetic field with slowly ramping of Vg from −300 V to +300 V after the film was saturated at high magnetic field. The ρyx(Vg) curve shows a peak at \({V}_{{\rm{g}}}^{0}\) ≈ 10 V, the charge neutral point. This result agrees well with the saturation state resistance from hysteresis loop measurements (red stars), indicating the single-domain state at zero magnetic field is robust against tuning the bulk carrier density (that is, robust ferromagnetism). In contrast to the monotonic gate dependence of the coercive field Hc, ρyx shows a non-monotonic behaviour, consistent with the proximity of the Dirac point to the VBM in BST, as shown in Fig. 4b (refs 10,16,24). The hole-doping will not only enhance the exchange interaction via an RKKY-type exchange mechanism, but will also significantly enhance dissipation, thus reducing ρyx. On the other hand, electron-doping pushes the Fermi level up above the VBM, but presumably below the conduction band minimum (CBM). Therefore, electron-doping probably induces surface state carriers with only slightly enhanced dissipation. Previous ARPES studies of V-doped BST film suggest that the Dirac point is below the VBM, so the mass gap overlaps with bulk states27. In contrast, transport studies indicate the Dirac point is above the VBM for Cr-doped BST films10,16. Therefore, it is possible that Cr-doping in co-doping samples slightly lowers the VBM so that it is easier to localize the bulk states inside the mass gap (see Supplementary Fig. 9). Alternatively, Cr/V co-doping might significantly enhance the scattering of bulk carriers, resulting in enhanced localization of the in-gap bulk states. Further studies on the impact of dopants on magnetic exchange and transport are needed to understand the mechanism behind the enhanced QAHE temperature in co-doped samples. The observed robust ferromagnetism resolves one of the major concerns in magnetically doped topological insulators, and opens a door to the exploration of high-temperature dissipationless conduction with magnetic topological materials.

Fig. 4: Gate dependence of ρyx and Hc and schematic band structure.
Fig. 4

a, ρyx and Hc versus Vg. Red stars are the zero-field ρyx from hysteresis loops at −300 V, 10 V and 300 V. b, Schematic picture of the band structure of the Cr/V co-doped BST film. The Dirac point of the surface state is close to the VBM.


Sample preparation

Epitaxial thin film Cr/V co-doped BST films capped with 2 nm Al were grown on a heat-treated SrTiO3(111) (STO) substrate by co-evaporation in a MBE system. The nominal thickness of the film is 5 QLs. The film was scratched by hand into a Hall bar shape connected with a large square-like area for MFM measurements. An approximately 15 nm Au film layer was deposited on the square area to eliminate electrostatic interactions between the sample and the magnetic tip.

MFM measurement and in situ transport measurement

The MFM experiments were carried out in an in-house-built cryogenic atomic force microscope (AFM) using commercial piezoresistive cantilevers (spring constant k ≈ 3 N m−1, resonant frequency f0 ≈ 42 kHz). This AFM is interfaced with a Nanonis SPM Controller (SPECS) and a commercial phase-lock loop (SPECS)34,41. The tips for the MFM were prepared by depositing a nominally 100 nm Co film onto bare tips using e-beam evaporation. MFM images were taken in a constant-height mode with the scanning plane ~ 40 nm above the sample surface. To avoid the relaxation effect (domain wall creeping) near Hc and to minimize the stray field effect of the MFM tips, all MFM images were taken at a low magnetic field of approximately 0.05 T after the magnetic field was ramped to the desired values. The MFM signal, the change of cantilever resonant frequency, is proportional to the out-of-plane stray field gradient42. Electrostatic interaction was minimized by nulling the tip–surface contact potential difference. Blue (red) regions in the MFM images represent up (down) ferromagnetic domains, where magnetizations are parallel(anti-parallel) with respect to the positive external field.

The magnetic topological insulator films were fabricated into Hall bar devices. The Hall resistance and longitudinal resistance were measured by standard lock-in techniques with an alternating current of 5 μA modulated at 314 Hz.

Data availability

The data that support the plots within this paper and other findings of this study are available from the corresponding author upon reasonable request.

Additional information

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We thank C. Chang for helpful discussions and P. Sass for proofreading the manuscript. This work at Rutgers is supported by the Office of Basic Energy Sciences, Division of Materials Sciences and Engineering, US Department of Energy under Award numbers DE-SC0008147 and DE-SC0018153. The work at Tsinghua University is supported by the National Natural Science Foundation of China and the Ministry of Science and Technology of China.

Author information


  1. Department of Physics and Astronomy, Rutgers University, Piscataway, NJ, USA

    • Wenbo Wang
    •  & Weida Wu
  2. State Key Laboratory of Low Dimensional Quantum Physics, Department of Physics, Tsinghua University, Beijing, China

    • Yunbo Ou
    • , Chang Liu
    • , Yayu Wang
    • , Ke He
    •  & Qi-Kun Xue
  3. Collaborative Innovation Center of Quantum Matter, Beijing, China

    • Yayu Wang
    • , Ke He
    •  & Qi-Kun Xue


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W.Wu, K.H. and Y.W. conceived the project. W.Wu and W.Wa designed the MFM experiment. W.Wa performed MFM experiments with in situ transport measurements, and analysed the data. Y.O. synthesized the MBE films under the supervision of K.H. and Q.X. C.L. and Y.W. carried out transport characterization of the films. W.Wu and W.Wa wrote the manuscript with inputs from all authors.

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The authors declare no competing interests.

Corresponding author

Correspondence to Weida Wu.

Supplementary information

  1. Supplementary information

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