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Scientific Reports logoLink to Scientific Reports
. 2020 Dec 23;10:22374. doi: 10.1038/s41598-020-78584-9

The morphology of VO2/TiO2(001): terraces, facets, and cracks

Jon-Olaf Krisponeit 1,2,, Simon Fischer 1, Sven Esser 3,4, Vasily Moshnyaga 4, Thomas Schmidt 1,2, Louis F J Piper 5, Jan Ingo Flege 6, Jens Falta 1,2
PMCID: PMC7758337  PMID: 33361795

Abstract

Vanadium dioxide (VO2) features a pronounced, thermally-driven metal-to-insulator transition at 340 K. Employing epitaxial stress on rutile TiO2(001) substrates, the transition can be tuned to occur close to room temperature. Striving for applications in oxide-electronic devices, the lateral homogeneity of such samples must be considered as an important prerequisite for efforts towards miniaturization. Moreover, the preparation of smooth surfaces is crucial for vertically stacked devices and, hence, the design of functional interfaces. Here, the surface morphology of VO2/TiO2(001) films was analyzed by low-energy electron microscopy and diffraction as well as scanning probe microscopy. The formation of large terraces could be achieved under temperature-induced annealing, but also the occurrence of facets was observed and characterized. Further, we report on quasi-periodic arrangements of crack defects which evolve due to thermal stress under cooling. While these might impair some applicational endeavours, they may also present crystallographically well-oriented nano-templates of bulk-like properties for advanced approaches.

Subject terms: Surfaces, interfaces and thin films; Structure of solids and liquids

Introduction

Featuring a metal-insulator transition1,2, which ist observed at TMI=340K for bulk samples, vanadium dioxide (VO2) is considered a promising functional material for oxide electronic applications37 and functional coatings8. Thin films offer tunability of the electronic properties of transition metal oxides by substrate-induced biaxial strain9. Indeed, when exposed to coherent epitaxial strain, the transition temperature of VO2 thin films can be altered over a remarkably wide range10,11. VO2(110) films on rutile TiO2(110) substrates have shown elevated transition temperatures close to TMI=400K10,12, due to a tensile in-plane strain of 3.6% along the rutile c-axis, and pseudomorphic growth under strain as large as 8.7% could recently be achieved on RuO2(110) substrates13. By contrast, a tensile stress in the rutile ab-plane as small as 0.8%, as experienced on TiO2(001) substrates, has been shown to inversely cause a reduction of TMI into the vicinity of room temperature, facilitating technological use.

Within the scope of this letter, two essential prerequisites for the successful fabrication of novel oxide electronic devices based on VO2(001) are investigated: (1) The quality and stability of the VO2(001) surface is studied. While previous studies mainly addressed the interface quality between substrate and VO2 films, for instance investigating ion interdiffusion phenomena14 and the formation of misfit dislocations, little is known about the surface of VO2(001). Yet, its thorough understanding and control would be crucial for preparing vertically stacked devices where atomically smooth interfaces are required to ensure well-defined electrical top contacts and to enable fabrication of functional oxide interfaces15. (2) It is well known that VO2 single crystals are prone to cracking when undergoing the transition16,17, as are sufficiently thick VO2(001) films under tensile epitaxial stress18. Although such crack defects must be considered as a severe obstacle for technological use, in this letter we discuss also their applicational potential for self-organized patterning.

Two different types of epitaxial VO2/TiO2(001) films were investigated: First, ultrathin films ( 5–10 nm) have been deposited in an ultrahigh vacuum (UHV) system by reactive molecular beam epitaxy (rMBE). These samples have been morphologically characterized in situ by conventional low-energy electron diffraction (LEED) and scanning tunneling microscopy (STM). While such in situ studies on the rMBE samples provide the highest cleanliness, the small achievable deposition rates hinder the growth of thick films. Therefore, a much thicker film (85nm) was prepared by metal-organic aerosol deposition19 (MAD) ex situ and studied by low-energy electron microscopy (LEEM) and μLEED. For this sample, the larger film thickness suggests that imperfections at the film-to-substrate interface, like Ti interdiffusion14, do not affect the surface morphology. Contrasting the significantly reduced transition known for VO2 thin films on TiO2(001), transport data for the thick film show a transition temperature TMI340K, i.e. close to the bulk value, and a rather broad hysteresis loop (see Supplementary Fig. S1). This indicates a partial and inhomogeneous stress release in the sample, due to, for instance, misfit dislocations. Hence, at room temperature, the rMBE is expected to be in the monoclinic state, whereas the MAD sample must be considered rutile. A comparison of these two sample types additionally allows for excluding effects specific to the chosen growth method.

Because the in situ grown rMBE films showed only diffuse LEED spots at the beginning and STM revealed a grainy morphology (see Supplementary Fig. S2), a short post-annealing at 300C was applied to coalesce the grains and obtain much sharper diffraction patterns. Similarly, the same annealing recipe was used to clean the ex situ MAD films from contaminations and to compensate for an overoxidation suffered from the contact with ambient atmosphere. An extensive description of the experimental techniques and procedures is given at the end of this article.

Results and discussion

Surface morphology

After growth and annealing, both sample types exhibit similar diffraction patterns in LEED. Most importantly, a (1×1) reconstruction, attributed to the desired flat VO2(001) termination20, can be observed regardless of their respective rutile and monoclinic bulk phases at room temperature, as well as for elevated temperatures. Note that for simplicity we here adhere to the rutile crystallographic basis which allows a uniform nomenclature for substrate and film. Exhibiting identical spot positions as for the TiO2(001) substrates, the observed (1×1) indicates pseudomorphic growth of the VO2(001) films.

Ultrathin in situ films

For the rMBE samples, STM images accordingly confirmed the existence of atomically flat terraces, separated by integer steps of the rutile c lattice constant and with typical lateral dimensions of several tens of nm (see Fig. 1a,b). For some areas, even much larger terraces (up to 400nm) were found. A corresponding series of LEED images is given in Fig. 1e–g: In agreement with the STM results, a clear (1×1) reconstruction originating from these terraces could be observed for an electron energy of 44eV (Fig. 1e), approximately matching Bragg’s law for the third order of reflection at 42eV and an out-of-plane lattice constant c0.285nm. In addition to this (1×1) reconstruction, however, also evidence for the formation of surface facets was revealed by LEED spots shifting their position with varying electron energy. Since these facet beams appear rather weak in LEED, and no such facet planes could be directly observed in the STM images, their occurrence is limited to a small fraction of the surface. The MBE samples showed a grainy appearance in STM before annealing (see Supplementary Fig. S2). We therefore attribute the facet reflections to small regions on the original grains which have been already aligned with the energetically favorable facet orientations and which hence have a higher stability against annealing. As indicated in Fig. 1f,g, the facet spots visible at reduced electron energies can be attributed to {10x} and {11y} types of facet planes.

Figure 1.

Figure 1

Surface morphology of VO2 films grown by rMBE and MAD. (a) STM images reveal large (001) terraces on the rMBE films after thermal annealing. (b) The height profile, corresponding to the path highlighted in blue in the image, shows integer atomic steps between the terraces. (c) AFM images of the MAD film exhibit a ripple-like texture. (d) The corresponding height profile depicts a slightly inclined (stepped) (001) surface. (eg) LEED patterns of the rMBE films at different energies show a rutile (1×1) reconstruction (e) but also feature {10x} and {11y} facet reflections (f,g).

Thick ex situ samples

Comparable diffraction patterns have been recorded by μLEED also for the MAD sample. These will be characterized in detail later on, enabling an identification of the dominant facet types. Much sharper diffraction spots have been observed for this sample type due to the significantly higher growth temperature. Yet, this sample may also have suffered from the thermal instability of the unfavorable (001) surface, giving rise to more pronounced facet beams. Such behavior is well known for the closely related case of the rutile TiO2(001) surface, which undergoes a faceting transition for temperatures above 400C21. Indeed, the MAD grown sample revealed a slightly rougher surface in AFM. Apart from crack-like features discussed later in this article, a texture of ripple-like objects is visible (Fig. 1c). The corresponding height profile (Fig. 1d), however, shows these ripples to have inclinations of only approximately 5 with respect to the flat (001) plane. Hence, a stepped (001) termination must still be considered as the dominant surface motif. The orientation of the ripples along <110>-like directions might be understood as the onset of faceting, with step edges aligning to energetically favorable orientations.

To summarize, both sample types exhibit very similar surface morphologies with a coexistence of (001)-terminated regions and several types of facets. Subtle differences in roughness and the ripple-like feature found only for the MAD film are attributed to the considerably different growth temperatures. While the MAD sample shows an advanced faceting due to the thermal instability of the (001) termination, a similar behavior may be expected for MBE samples when grown at higher temperatures as well. The above findings, i.e. the occurrence of a (1×1) reconstruction as well as indications for temperature-induced faceting, agree well with the results reported by Goering et al. for the {001} surfaces of VO2 single crystals20 as well as theoretical studies predicting the (001) surface to be rather unfavorable22. It should also be mentioned that a related formation of {110}-like facets was found on the VO2(100) surface by transmission electron microscopy23. Nonetheless, the fact that even an elevated growth temperature of 560C did not induce a severely faceted surface, unlike it is documented for TiO2, is a promising finding for applicational efforts.

The ideal (001) surface

Before focussing on an identification of the relevant facet types, the desired (001) surface itself should be discussed in more detail. Interestingly, the (1×1) reconstruction was observed below the transition temperature for both sample types while, assuming the monoclinic low-temperature phase VO2 (M1), one could expect a (1×2) periodicity (or an apparent (2×2) in LEED due to averaging of rotational domains). As illustrated in Fig. 2, the flat (001) surface, (201¯) in monoclinic notation, actually possesses a (1×2) larger surface unit mesh with respect to the rutile ab-plane, and hence LEED reflections could also be expected at the half-integer positions with respect to the TiO2(001) pattern. Yet, both the metallic and the insulating phase show the same (1×1) reconstruction instead. Consequently, LEED patterns cannot be considered as a reliable method to track the sample state through the MIT. For an explanation of this behavior, several scenarios may be taken into account: (1) Originating from a rather subtle structural rearrangement, the super-structure reflections may appear too weak to be recorded by LEED. (2) Particularly when grown on TiO2(001) substrates, also a structural deviation from the monoclinic M1 structure may be considered for the low-temperature phase: Qiu et al. have recently obtained evidence for the existence of a “tetragonal-like” structural modification of the low-temperature phase by x-ray diffraction on comparable samples and proposed a structural model which indeed comprises a (1×1) periodicity with respect to the rutile ab-plane25. (3) Finally, recent investigations by Wahila et al. provide experimental and computational evidence that the very surface may actually not even participate in the structural transition at all and prefer to remain rutile regardless23. As this observation appears valid even for VO2 surfaces of distinct orientations it hence may be considered as a generic feature.

Figure 2.

Figure 2

Surface periodicity of the monoclinic (201¯) surface. An enlarged (1×2) periodicity is expected with respect to the rutile (001) surface. Crystallographic (shaded blue) und surface unit cells (yellow) are highlighted in (a) the top view onto the monoclinic (201¯)M/rutile (001)R surface, cross sections of (b) the (010)M/(100)R and (c) the (001)M/(010)R plane illustrate the monoclinic cell dimensions. The dashed rectangles outline a rutile cell. The sketch on the left indicates the respective lines of sight. The crystal structures were visualized by the open source software Vesta 3.4.7 (http://jp-minerals.org/vesta/en/)24.

Determination of facet orientations

When discussing the faceting tendency, a thorough comparison with the closely related and extensively studied case of rutile TiO2 appears conclusive26. For both materials, though nonpolar, the {001} surfaces must be considered as energetically unfavorable due to a large density of broken bonds. Density functional theory confirmed the VO2(001) surface to have the second-highest surface energy among the low-indexed surfaces orientations22. Consequently, a tendency to form facets has been reported for both systems. In early studies on TiO2, the dominant {011} and {114} facets have been identified27,28, several additionally involved facet species, i.e. {023}, {045}, and {111}, were reported later21. As stated above, a related faceting tendency of the VO2(001) termination was briefly documented20 but the facet orientations have not been determined so far.

Therefore, in order to identify the relevant facet types, reciprocal space maps (RSMs) of the MAD sample have been created from a series of μLEED images in the energy range from 6 to 25eV and with the electron beam being restricted to a diameter of 5μm. An exemplary μLEED pattern is given is given in Fig. 3a. RSMs have been generated for the (11¯0) and (010) reciprocal planes, shown in Fig. 3b,d, respectively. Note that these represent all {110} and {100} plane types by crystallographic symmetry.

Figure 3.

Figure 3

Identification of facet types on the 85nm thick VO2 film. (a) Exemplary μLEED pattern recorded at 23eV, the highlighted paths illustrate the orientations of the generated reciprocal space maps. The full LEED stack is provided as Supplementary video 1. (b,d) Facet directions have been identified in the RSMs and corresponding structural models are given in (c,e). The structure models were created by the open source software Vesta 3.4.7 (http://jp-minerals.org/vesta/en/)24.

Reciprocal space map of a (110)-like plane

In the first RSM (Fig. 3b), vertical rods are observed at the (1¯,1¯), (0, 0) and (1, 1) LEED positions, indicating the existence of a flat (001)-oriented surface component. In addition, facet reflections have been observed under angles of approximately 25±1 and 43±2. As illustrated in the morphological model shown in Fig. 3c, the angles agree with the occurrence of facets oriented in the {112} (expected at 24 for bulk VO2) and presumably {332} directions. The {332} facets appear much weaker in the RSM, due to their large inclination, i.e. the smaller illumination density in LEED of the projection of the facets to the (001) direction. As they also show a lack of symmetry, due to spatial aberrations of the electron optics significantly affecting the outer regions of the recorded μLEED patterns, this angle is more difficult to determine and the identification as {332} is considered tentative. For the {112} facets, dominant reflections occur with a spacing of 0.145A˚-1, or 0.69nm in real space. Yet, much weaker, an increased intensity is also observed at the half spacing. These spacings would correspond well with (1×1) or (1×2) terminated facets, respectively, as a periodicity of 0.705nm would be expected for (1×1).

Reciprocal space map of a (100)-like plane

The second RSM (Fig. 3d) shows vertical rods at the (1¯,0), (0, 0) and (1, 0) LEED positions, again corresponding to the flat (001) surface component. However, also rather broad streaks of higher intensity are observed under an angle of approximately 33±1 (indicated in green). These can be regarded as a series of narrower sub-streaks at an angle of 26±1 (marked in orange). The latter can be assigned to facet planes in the (045) direction with their narrow spacing reflecting their large unit mesh. The enhanced intensity along (011) in broad streaks can be understood considering this high-indexed plane as as a regularly stepped (011) plane instead. The measured angles are again in good agreement with the expected inclinations of 32.1 for {011} facets and 26.6 for {045} facets. The spacing of 0.35A˚-1 between the {011} reflections suggests a spatial periodicity of 0.28nm in the facet. Being only about half the surface mesh dimension along the corresponding direction (0.54nm) this may appear contradictory at first sight. However, a glide mirror plane perpendicular to the rutile (011) surface must be taken into account which leads to the observed extinction of every second rod in the RSM. Again, a morphological model is given to illustrate the facet orientations (Fig. 3e).

Hence, alike its well-studied relative, rutile TiO2, the VO2(001) surface is prone to an irreversible formation of facets. Yet, as noted before, it features a higher stability: While TiO2(001) becomes unstable already above 400C21. the stepped (001) surface can be obtained on VO2 samples grown at temperature of at least up to 560C. Beyond this enhanced robustness, which may prove very valuable for applicational purposes, also differences in the preferred facet types exist: As on rutile titania, {045} planes, i.e. stepped {011} facets, have been identified as relevant terminations. However, while rather flat {114} facets are common on TiO2, we report indications for the occurrence of much steeper {112} and, tentatively, {332} terminations on VO2(001).

Strain-induced cracking

Beyond the faceting of the VO2(001) surface, the morphology features also stripe-like patterns that have been revealed by LEEM in the mirror electron microscopy mode for the entire surface of the thick VO2/TiO2(001) film, see Fig. 4a. The emergence of stripe patterns has been reported for various VO2 surfaces before: While (110) surfaces show a reversible formation of stripe patterns consisting of the competing VO2 phases at the MIT2932, particularly VO2/TiO2(001) films can suffer permanent cracking along the <100> directions, especially under the occurrence of large thermal stresses18,31,33. Similar to thin films, even VO2 single crystals often crack when going through the MIT17.

Figure 4.

Figure 4

Cracks formed by strain release under thermal cycling. LEEM/MEM image recorded 1.5eV (a). The fast Fourier transform exhibits corresponding streaks of intensity (b), the maxima in the highlighted profile indicate a quasi-periodic spacing of 250nm (c). The AFM image (d) confirms these lines as topographic cracks and depicts the ripple texture of the stepped (001) surface state as substructure with smaller lateral dimensions.

In thin films, large thermal stresses can arise from the incompatible thermal contractions of the rutile TiO2 substrate and the VO2 film:18 The thermal expansion coefficient of rutile VO2 is slightly higher than that of the substrate, αVO2R>αTiO2. Therefore, beginning at the deposition temperature, tensile thermal stresses successively arise during cooling the sample. At the transition temperature, a drastic increase of the thermal expansion coefficient has been reported34, which is responsible for the observed cracking. In the monoclinic phase, however, αVO2M<αTiO2 and thermal stresses are expected to decrease again under further cooling. Nagashima et al. proposed this mechanism of crack formation to occur when exceeding a critical thickness of tcr15nm18. Interestingly, this characteristic thickness was found to be in very good agreement with values estimated according to fracture mechanics as tcr=0.5(kf/σ)2, where kf denotes the fracture toughness and σ the tensile stress35. These considerations further predict a minimal spacing λ=8t(1-1-tcr/t) between the cracks. Yet, random-like crack distributions have been observed with rather small densities, like 22.000/mm-2 for an exemplary film thickness of 30nm, corresponding to crack spacings on a micron scale instead of the expected value λ76nm. Slightly higher crack densities of random distribution were shown by Paik et al33. Here, we report a significantly higher density and regular distributions for the MAD-grown film, caused by repeated slow cooling cycles down to a temperature of 77K, for resistivity measurements. Note that the lower base temperature achieved in the present study, as explained above, should not lead to higher thermal stresses or, respectively, a smaller tcr than in the previous studies.

The cracks have been found to cover the entire sample surface, visible as an almost periodic, crosshatch-like texture in LEEM (Fig. 4a). Additional AFM measurements topographically verified the lines to be cracks (Fig. 4d). On smaller lateral scale, AFM depicts the rippled surface state described above with dominant features appearing rotated by 45 with respect to the cracks, i.e. being aligned to the rutile <110> directions. The faces of these cracks are oriented perpendicular to the film surface and hence invisible in LEED patterns, in contrast to the aforementioned facets identified above by μLEED. As expected, the facet pattern appears to be interrupted a posteriori by the cracks as it has been formed already during deposition. Finally, it should be noted that samples, for which the formation of facets could be entirely avoided during growth, do show similar facet reflections in LEED after cracking23. Therefore, due to the large crack density, also facets located along the crack edges may have contributed to the RSMs shown above and could significantly enhanced their visibility in comparison to the uncracked rMBE samples.

In order to estimate the typical spacing in between adjacent cracks, a fast Fourier transform of the LEEM image has been evaluated (Fig. 4b). The profile along the highlighted path is shown in Fig. 4c, with maxima at ±4μm-1 corresponding to a crack spacing of 250nm. Much closer to the theoretical minimal value of 67nm for the given film thickness, one now needs to consider a higher level of stress relaxation due to the formed cracks. As stated above, already for the initial sample state the metal-insulator transition occurs close to the bulk transition temperature of 340K, indicating that some epitaxial stress was already released via interfacial defect formation during growth and annealing36. Nonetheless, as-grown samples did not show cracks in AFM (see Supplementary Fig. S3). Hence, considering only a reduced residual stress after annealing may account for the observed larger crack spacing with respect to the theoretical expectations. Although systematic investigations on the dependency of the crack densities on the sample dimensions, strain environments and process parameters are required to fully capture this phenomenon, the present results demonstrate that much higher densities can occur and lead to regular, quasi-periodic arrangements of cracks. Despite the regular appearance of the crack pattern, however, their formation ist still interpreted as an inherently random process: Cracks are assumed to nucleate first at such crystal defects that are located in highly strained sample regions. The propagation of crack lines is terminated at sample imperfections as well, most significantly at pre-existing cracks running in the respective perpendicular orientation. Consequently, the crack lengths are random, with rather long crack lines being created first. As the formation of a crack releases stress from its environment, additional, parallel crack defects will only nucleate beyond a characteristic minimal distance, which subsequently results in the quasi-periodic crack arrangement.

On the one hand, such cracking tendencies must be extensively explored, primarily as they hinder technological approaches to tune the MIT characteristics by epitaxial strain. On the other hand, many investigations on the bulk behavior of VO2 may also benefit from this opportunity to prepare bulk-like specimen by rMBE means that do not fully disintegrate (like single crystals) but still provide a defined crystallographic orientation (unlike powder samples). Beyond that, this behavior may even be exploited in applications as a means for mesoscale self-organized patterning.

Conclusions

We have presented a morphological characterization of VO2/TiO2(001) films. As known for TiO2(001), a faceting tendency has been observed and the dominant facet types have been crystallographically identified. Further, it has been demonstrated that the ideal (001) surface can yet be obtained at moderate temperatures, showing large, atomically flat terraces. LEED investigations showed no fingerprints of the structural transition from rutile to monoclinic symmetry. Finally, a temperature induced cracking due to tensile epitaxial strain was found to form a quasi-periodic pattern of islands that show bulk-like transition properties.

Methods

Two different types of epitaxial VO2/TiO2(001) films were investigated: First, ultrathin films (5-10nm) have been deposited in an ultrahigh vacuum (UHV) system by reactive molecular beam epitaxy (rMBE) with an Epi UNI-Bulb RF plasma source for generating atomic oxygen. This growth recipe was largely inspired by studies using ozone as activated oxygen source33,37. Vanadium was evaporated by electron-beam heating and deposited onto the sample at a substrate temperature of 200C and under permanent atomic oxygen exposure. For this, the plasma source was operated at 350W and with a constant O2 background pressure of 5·10-5mbar. As suggested in preceding growth studies33, deposition was followed by a post-anneal, here to 300C to enable a coalescence of the VO2 grains. The stoichiometry of the samples has been verified by x-ray photoelectron spectroscopy (XPS), showing a separation of 14.3eV between the V1s and O2p peaks, characteristic for the V4+ oxidation state38. No contamination was detected by XPS and a degradation of the surface by exposure to ambient atmosphere can be excluded. The surfaces of these samples have been morphologically characterized in situ by conventional low-energy electron diffraction (LEED) and scanning tunneling microscopy (VT-STM by Omicron).

The thicker film (85nm) was prepared by metal-organic aerosol deposition19 (MAD). As precursor, vanadium acetylacetonate was solved in dimethylformamide, which was then sprayed onto the heated TiO2(001) substrate (560C) under near-ambient oxygen partial pressure. This sample was characterized ex situ by low-energy electron microscopy (LEEM) using an Elmitec LEEM III instrument and atomic force microscopy with an NX10 by Park Systems. Diffraction patterns of confined regions were recorded (μLEED) from an illuminated sample area of 5μm in the LEEM instrument. In comparison to the conventional LEED studies performed in situ on the rMBE samples, the μLEED not only introduces spatial resolution but additionally provides a higher resolution in reciprocal space and a larger dynamic range. A comparison of these two sample types also allows for excluding effects specific to the different growth methods. All corresponding crystal structures shown in this article were drawn using the VESTA software24.

The ultrathin rMBE samples were prepared at rather low temperature (200C), whereas the thicker MAD film was deposited at a substrate temperature of 560C. Due to the lower growth temperature, which ensures a minimization of interdiffusion between film and substrate, a grainy surface was observed by STM for the ultrathin films (see Supplementary Fig. S2) and no LEED pattern could be observed directly after growth. The rMBE sample preparation was hence finalized by a post-annealing step 300C after which clear LEED reflections are visible. As the MAD samples were deposited at a much higher temperature, no additional annealing was required in this case to improve the sample morphology. Nonetheless, only very diffuse diffraction spots were observed after sample transfer. This might be due to contaminations from ambient atmosphere and a sample surface which was overoxidized by air exposure. Therefore, also this sample was annealed at 300C and sharp diffraction patterns could be observed afterwards.

Supplementary information

Supplementary material 1 (544.8KB, pdf)

Acknowledgements

The authors gratefully acknowledge A. Cerreta and H. Schmidt (Park Systems Europe) for the AFM measurements. The work was financially supported by the DFG (Grant Numbers 362536548, 408002857) and the Institutional Strategy of the University of Bremen, funded by the German Excellence Initiative.

Author contributions

The studies were initiated by J.O.K., J.I.F., and J.F. V.M. and S.E. prepared and characterized the MAD film, S.F. and J.O.K. prepared the MBE samples and conducted their characterization by STM and LEED. J.O.K. and S.F. conducted the LEEM and μLEED study of the MAD film and J.O.K. lead the AFM experiments. T.S. and J.O.K. generated and interpreted the RSMs. J.F. and L.P. contributed to the LEED discussion. J.O.K. wrote the manuscript. All authors reviewed the manuscript and provided critical feedback.

Funding

Open Access funding enabled and organized by Projekt DEAL.

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.

Supplementary information

is available for this paper at 10.1038/s41598-020-78584-9.

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