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Direct comparison of ARPES, STM, and quantum oscillation data for band structure determination in Sr2RhO4

Abstract

Discrepancies in the low-energy quasiparticle dispersion extracted from angle-resolved photoemission, scanning tunneling spectroscopy, and quantum oscillation data are common and have long haunted the field of quantum matter physics. Here, we directly test the consistency of results from these three techniques by comparing data from the correlated metal Sr2RhO4. Using established schemes for the interpretation of the experimental data, we find good agreement for the Fermi surface topography and carrier effective masses. Hence, the apparent absence of such an agreement in other quantum materials, including the cuprates, suggests that the electronic states in these materials are of different, non-Fermi liquid-like nature. Finally, we discuss the potential and challenges in extracting carrier lifetimes from photoemission and quasiparticle interference data.

Introduction

Strongly correlated electrons are at the root of some of the most mysterious quantum materials, including unconventional superconductors, strange metals, and heavy fermion materials1,2,3,4,5. Most of the exotic phases of electronic matter in these systems emerge from collective behavior of the electrons. A universally accepted understanding of these systems is still lacking, and requires close cooperation between scientists using different theoretical and experimental methods. From the experimental side, many insights to date have come from spectroscopic techniques that probe the band structure and many-body renormalizations of electrons close to the Fermi level, including angle-resolved photoemission (ARPES), scanning tunneling microscopy (STM), and quantum oscillations (QO), which are the focus of this article.

In the most widely used interpretations, spectroscopic-imaging STM (SI-STM) and ARPES probe the spectral function in real and reciprocal space6,7,8,9,10. Quantum oscillations probe the Fermi surface area and the k-averaged cyclotron mass which can in turn be related to the pole of the spectral function at energies close to the Fermi level11. There should thus be well-defined relations between the quantities measured by these three techniques12.

Surprisingly though, several apparent contradictions between results based on these techniques can be found in the literature. Such contradictions can involve very fundamental properties of the electronic structure: for example, quantum oscillation studies on underdoped cuprate high-temperature superconductors claim the existence of Fermi surface pockets while STM and ARPES reported disconnected Fermi arcs13,14. Similarly, the strength of gap inhomogeneities seen by STM in several unconventional superconductors appears to be inconsistent with gap broadening in ARPES spectra that average over large areas. These and other discrepancies between results of different techniques have previously been discussed in cuprate superconductors15,16,17,18, heavy fermion systems19, and topological insulators20. However, it often remains unknown if these apparent differences are a consequence of some inherent limitations of the techniques or if they are due to challenges of data interpretation, also connected to the exotic non-Fermi-liquid nature of some of these systems. Given this lack of understanding, discrepancies are frequently attributed to the use of samples grown in different research laboratories or are ignored because of a lack of trust in one of the techniques.

With this article, we aim to test the consistency of data from ARPES, STM, and QO experiments by making an unbiased comparison on the same correlated electron material. The ideal candidate for such a comparison should be a quasi-two-dimensional (2D) metal in which electron correlations still play an important role, but without the mysteries associated with materials like unconventional superconductors. Ideally it should further be structurally similar to the cuprates, ruthenates, and iridates. Such a material could then act as a representative for the wider class of transition metal oxides, but in contrast to cuprates, ruthenates and iridates is well understood and simple enough that it can clearly be described within Fermi liquid theory. With this in mind, we chose Sr2RhO4, a layered perovskite that fulfills the conditions above.

Results & discussions

ARPES and QPI Fermi surface

In Figs 1 and 2, we compare Fermi surface data from the three techniques. Consistent with previous reports11,21,22, the ARPES k-space map (Fig. 1a) shows two nearly circular contours that are backfolded to form three pockets; a hole-like α pocket centered at Γ, a lens-shaped electron pocket at M (βM) and a square-shaped hole pocket at X (βX). The backfolding is of structural origin and arises from a staggered rotation of the RhO6 octahedra around the c-axis, which doubles the in-plane unit cell. Hybridization with eg states pushes the xy band of Sr2RhO4 below the chemical potential, leaving a Fermi surface with out-of-plane xz/yz character, containing three electrons per Rh site11,22,23. Despite the quasi-1D hopping associated with the out-of-plane orbitals, the Fermi surface is nearly isotropic. This change arises from a strong level repulsion of states that would be degenerate in the absence of spin–orbit coupling24,25. The marked anticrossing can be attributed to an enhancement of spin–orbit splittings in the presence of electronic correlations25,26,27.

Figure 1b, c shows an STM topography and a constant energy conductance layer, where spatial modulations attributed to quasiparticle interference are neatly resolved. The few atomic defects in the field of view clearly act as scattering centers for quasiparticles, creating the interfering standing wave patterns. The Fourier transform of the normalized conductance layer at the Fermi level E = 0 meV is shown in Fig. 1d. To mitigate the set-up effect, we take the Fourier transform not of the conductance layers dI/dV(r,eV), but of the normalized conductance data, dI/dV(r,eV)/(I(r,eV)/V), where I(r,eV) is the tunneling current and V is the bias voltage (see discussion in the methods and Supplementary Fig. 1)28,29,30,31,32. For the β band, we directly observe the STM ‘Fermi surface’ with wave-vector q = 2kF. More generally, we expect to observe features corresponding to scattering vectors q that connect points of high spectral weight in momentum space. For the present case, we can readily connect these q vectors with the Fermi surface measurement from ARPES. Interestingly, different scattering processes have different strengths. While some scattering processes are very clear, others are less visible or completely absent. Varying intensities or absences of scattering processes have been observed in other materials33,34,35 and can stem from the differences in the scattering process. For example, different QPI scattering intensities are expected from magnetic versus potential scattering or from broad coulombic potentials versus localized impurity potentials36,37,38,39,40. In principle, theoretical tools exist to predict QPI intensities based on both the electronic structure of the material and the nature of the scattering potential36,37,38,39,40. A comparison with such QPI simulations could allow us to learn more about the defect states in Sr2RhO4.

In Fig. 1e, we use the Fourier transform of the SI-STM data discussed above to reconstruct the entire FS of Sr2RhO4 from the QPI pattern. To this end, we first extract peaks in the data by fitting the intensity profiles in radial cuts (see Supplementary Fig. 2). We then obtain the fundamental β band in k-space by rescaling the q vectors by a factor of two. The backfolded β bands are obtained by translating the fundamental band by reciprocal lattice vectors determined from the STM topography. The α band is reconstructed by subtracting the interband vector qα–β from the intraband scattering qβ–β. In Fig. 1e, we display in blue the data points derived in this way, and in gray the direct interband scattering vectors qα–β that we used for the derivation. The identification of the gray scattering vectors as qα–β is corroborated by the Fermi velocity we obtain for this vector (see below). The direct comparison of these contours with the ARPES Fermi surface shows good agreement for all Fermi surface pockets, as further illustrated in Supplementary Fig. 3.

Shubnikov–de Haas Oscillations

Next, we use QO to find the Fermi surface areas and quasiparticle masses. The inset of Fig. 2a shows a trace of quantum oscillations in the magnetoresistance at 0.1 K (Shubnikov–de Haas (SdH) oscillations). To extract Fermi surface information from the quantum oscillations measurement, we analyze the frequency components plotted in Fig. 2a. Seven closely spaced peaks are resolved, corresponding to seven frequencies between 0.9 and 1.3 kT. This might be surprising at first, as from our previous analysis we expect only three distinct Fermi surface pockets. We attribute the higher number of QO frequencies to two effects. Firstly, the finite interlayer hopping implies that the Fermi surface of Sr2RhO4 is quasi-cylindrical, and thus has multiple extremal orbits per sheet. The characteristic signature of such a remnant 3D Fermi surface warping is an overall 1/cos(θ) field angle dependence of the frequencies (consistent with quasi-2D electronic structure) with small splittings that disappear for certain angles, as observed in Fig. 2b. The quasi-2D nature of the quasiparticle band structure is confirmed directly by photon-energy-dependent ARPES measurements (Fig. 2c) probing the Fermi surface along kz. Secondly, the ARPES measurements resolve a small splitting in the β-band along ГM. This small degeneracy lifting can be attributed to the doubling of the unit cell along the c-axis and is reproduced by LDA + U + SO band structure calculations25. Hence, there are four primary frequencies up to the measured out-of-plane angle of 40°. We can then use multiple facts to constrain the band assignments: (i), Following ARPES and STM data, the extremal orbit areas increase in size from the α (hole), βM (electron), and βX (hole). (ii), The total electron count should be three electrons per Rh atom. (iii), The experimental specific heat γ can be calculated in the 2D approximation from:

$$\gamma = \left( {\pi N_{\mathrm{A}}k_{\mathrm{B}}^2a^2} \right)\left( {3\hbar ^2} \right)^{ - 1}\left( {m_{\upalpha} + 2m_{{\upbeta {\mathrm{M}}}} + m_{{\upbeta {\mathrm{X}}}}} \right)$$
(1)

where NA is Avogadro’s number, kB is Boltzmann’s constant, a is the tetragonal lattice parameter (3.857 Å), and ħ is Planck’s constant. (iv), Following the ARPES data, the βM band should be split leading to two frequencies.

Combining these conditions, we draw the conclusion that α corresponds to the lowest frequency (0.93 kT, corresponding to 1.934 electron/Rh, see methods), βM to the two middle frequencies (average 1.068 kT, 0.152 electrons/Rh), and βX to the highest frequency (1.288 kT, 0.908 electrons/Rh). The calculated $$\gamma = 17.4 \pm 0.8$$ mJ/Rh mol K2 then agrees with the directly observed value of 17.7 ± 0.7 mJ/Rh mol K2 22, and the total electron count is 2.994 electrons per Rh. A quantitative comparison of the Fermi surface volumes extracted from ARPES, QO, and STM based on this assignment can be found in Table 1. QO amplitudes also yield the Dingle temperatures (1.5 K for the α pocket,1.5 K for the βM pocket, and 1.9 K for the βX pocket), which can be related to the mean free path of the electrons. We refer to the literature for a detailed discussion on the challenges of such an interpretation41.

Quasiparticle dispersion

We now turn our attention to the low-energy dispersion. In Fig. 3, we show constant energy layers for selected energy levels and the energy–momentum dispersion along the two high-symmetry directions for both ARPES and SI-STM. These data confirm that βM is an electron pocket while α and βX are hole-like. The ARPES data also reproduce the splitting of the β band along ΓM observed in Fig. 2. The STM dispersion plots show several features that are not observed by ARPES. These can all be assigned to different β–β intraband and α–β interband scattering vectors translated by reciprocal lattice vectors. The q vector which is most clearly resolved by STM along both high-symmetry directions arises from β–β intraband scattering. Comparing its dispersion with the β-band measured by ARPES, we find quantitative agreement along ΓX, where both techniques lead to measured Fermi velocities vF = 0.55 eVÅ. Along ΓM, where band structure calculations find a small splitting in the Fermi surface, our ARPES data resolves both bands and shows that they have slightly different dispersion with Fermi velocities of 0.57 and 0.77eVÅ, respectively, compared to vF = 0.70 eVÅ extracted from the STM dispersion. The lack of a noticeable splitting in the STM dispersion cannot be explained by insufficient momentum resolution, suggesting that it is due to a vanishing STM matrix element for one of the bands.

In order to extend this comparison to QO, we look at the quasiparticle cyclotron masses m*. These masses can be deduced for individual Fermi surface pockets from the temperature dependence of the quantum oscillation amplitudes using the Lifshitz–Kosevich formula (Supplementary Fig. 4). For a 2D Fermi surface, they can also be calculated without any approximations from the full mapping of the low-energy quasiparticle band structure obtained by STM and ARPES, using $$m^ \ast = \frac{{\hbar ^2}}{{2{\uppi}}}\frac{{{\mathrm{d}}A_{{\mathrm{FS}}}}}{{{\mathrm{d}}E}}$$ (2) where AFS is the Fermi surface volume. To this end, we extract the areas of the pockets not only at the Fermi energy, but at a few constant energy layers within a small window. The linear fits of these areas shown in Fig. 4 yield the effective masses of the different pockets. We note that the slope dAFS/dE decreases strongly near the chemical potential in the ARPES data while no such effect is observed in STM. This change of slope is a known artifact arising from the combination of a Fermi cutoff and finite energy resolution. For the quantification of m*, we thus exclude a narrow energy range around EF from the ARPES data. Table 1 shows the values of the effective masses obtained by STM, ARPES, and QO measurements. Knowledge of m* and the Fermi surface area also allows a sheet-averaged Fermi velocity to be calculated from QO data as vF = ħ(A/π)1/2/m* (3). These values are also shown in Table 1 for comparison with STM and ARPES.

Finally, we discuss the extraction of peak widths in the ARPES and STM data, which can in principle be related to quasiparticle lifetimes. Here, the two techniques face rather different challenges. In simple systems, like Sr2RhO4 studied here, the measured photoemission intensity appears to represent the spectral function. For a sufficiently linear band, the imaginary part of the self-energy (which is equal to half the inverse lifetime in a Fermi liquid) can thus be obtained from the width Wk of the momentum distribution curves (MDC) as Σ”(k, ω) = Wk (ω) v(ω)/2 (4), where v(ω) is the slope of the dispersion at the same energy. In practice, the main difficulty is the treatment of the effective resolution of ARPES measurement. ARPES peak widths measured at state-of-the-art instruments are rarely limited by the instrumental energy and momentum resolution but contain a variety of other contributions that are notoriously hard to quantify. These include in particular broadening from the finite integration over perpendicular momenta, structural mosaicity in the probed area and the often-unknown quality of the surface. Additional broadening can occur from work function inhomogeneities of and around the sample which cause uncontrolled electric fields that degrade the resolution of the electron optics. Finally, in an energy range of ~ dE/2, where dE is the effective energy resolution, the MDC peak position starts to deviate noticeably from the intrinsic quasiparticle pole, which prohibits a model-free analysis of very low-energy dispersions and self-energies. STM does not suffer from these experimental difficulties. However, it is not always clear to what extent the tunneling spectra reflect A(r, ω). In particular the so-called set-up effect, the dependence of the tunneling spectra on the lateral variation of the tip–sample distance, which itself is defined by the set-up current and voltage, can cause complications. In many cases, the set-up effect can be mitigated by taking ratios between different quantities as we do here, but then the interpretation of the resulting data is less straight forward. In addition, analyzing self-energies from STM data can be complicated when different q vectors overlap, especially for complex Fermi surfaces. We also note that a unique reconstruction of the spectral function from STM data is not always possible. Perhaps most importantly, one has to consider the scattering mechanism, which can strongly influence line-shapes and linewidths36,37,38,39,40. For this reason, only few attempts have been made to extract lifetimes from STM data42,43,44,45.

Despite these difficulties, an analysis of the MDC’s along the ΓX direction shown in Fig. 5a–c clearly shows an energy dependence of the quasiparticle lifetime in fair agreement with the expectations for a Fermi liquid-like metal. In a Fermi liquid, we expect the imaginary part of the self-energy to be a quadratic function at low energy, Σ”(ω) = 2 (5), where A is a material specific prefactor. To compare our results with the expectation, we plot the linewidths and self-energies extracted from ARPES and STM data as a function of energy in Fig. 5d, e (for a comparison of the individual ARPES and STM spectral lines, see Supplementary Fig. 6). Indeed, our results are consistent with a quadratic dependence on energy. Further, the absolute scale of the measured self-energy is of the same order than what is obtained for Sr2RhO4 with dynamical mean field theory (DMFT)46,47 calculated for a generic two-dimensional Fermi liquid using the random phase approximation48,49,50,51. We note that the agreement holds for an energy range that is a significant fraction of the Fermi energy, which is roughly 400 meV for the β band when defined in the parabolic band approximation as EF = ħ2AFS/2πm (6). This is encouraging for further lifetime investigations: given a good understanding of both the resolution for ARPES and the scattering process for STM, both techniques have the potential to bring insight into energy- and momentum-dependent correlation effects in electronic matter of quantum materials.

We show SI-STM results of Sr2RhO4 and extract its Fermi surface and low-energy dispersion, and present a quantitative comparison of the STM quasiparticle interference data with ARPES and QOs. Our data here reveals the previously unknown band structure above the Fermi level, and quasiparticle lifetimes for Sr2RhO4. We show that Fermi surface volumes agree among the three techniques within ~1% of an electron for all pockets, while quasiparticle masses exhibit a relative variation of ~30%. We consider these values to be characteristic for the precision that can realistically be obtained in favorable cases with these three techniques, and therefore conclude that for the oxide Sr2RhO4, STM, ARPES, and QO can extract the same information regarding Fermi surface and low-energy dispersion. The relevance of our study goes beyond Sr2RhO4: our data suggest that apparent disagreements in the literature on cuprates do not arise from the intrinsic structural complexity of oxides but are likely a consequence of our limited understanding of materials with non-Fermi liquid electronic states and the applications of the techniques to such samples, especially ones with significant spatial inhomogeneity.

Methods

Sample preparation

Our single-crystal samples were grown in a Crystal Systems four mirror image furnace using a flux feeding floating zone method. Dried SrCO3 and Rh2O3 (3 N) were ground together in a 1:0.575 ratio, pelletised, and calcined at 1000 °C in flowing O2 atmosphere for 24 h. Rods were hydrostatically pressed using the usual methods and sintered at 1100 °C for 2 h in flowing O2. The growth conditions in the image furnace were 100% O2 gas at 10 bar pressure, growth speed of 10 mmhr−1 and a counter rotation of 30 rpm. Subsequently, the crystals were annealed 1150 °C under flowing oxygen for 2 weeks, as described elsewhere22.

The surfaces studied by STM and ARPES have been obtained by cleavage in ultra-high vacuum.

Quantum oscillations

Quantum oscillations measure low-energy characteristics of the electron fluid in an applied magnetic field. The oscillations, caused by the Landau quantization from the magnetic field, give precise information on the size of the Fermi pockets and the effective masses of the electrons. Quantum oscillations are a true bulk probe that is generally not influenced by surface effects but they are very sensitive to disorder in the crystals and require high-quality samples to be observed. Furthermore, they also require high magnetic field and low temperatures to suppress the quasiparticle–quasiparticle scattering and the interpretation is not always simple as little information is given about the loci, shape, and type (electron or hole) of the Fermi pockets. When a strong magnetic field B is applied to the sample, the Landau quantization of quasiparticle orbits leads to an oscillation of the density of states at the Fermi level, periodic in reciprocal field. These oscillations are reflected in most of the physical properties; in the case of magnetoresistance they are called Shubnikov–de Haas (SdH) oscillations41,52. By analyzing the frequency f (in Tesla) of the oscillations across an inverse field range, the number and sizes of the Fermi surface pockets can be obtained. Moreover, the effective masses for the various pockets can be deduced from the temperature dependence of the oscillation amplitude (Fig. S4) via the Lifshitz–Kosevich formula, although, we note that the data analysis can be non-standard when measuring across a broad magnetic field range (for a comprehensive discussion see ref. 22). The QO amplitudes also contain the Dingle temperature. These can be used to find mean free paths of 500 Å for the α pocket, 714 Å for the βM pocket, and 481 Å for the βX pocket.

Quantum oscillation data was acquired using a standard four probe technique in a dilution refrigerator (current I = 300 μA) for temperatures between 0.1 and 1.0 K and magnetic fields between 7 and 15 T. Low contact-resistance electrical connections were made to the crystals using gold wire (25 micron) and Dupont 6838 high-temperature curing paint (annealed at 470 °C under O2). The current was applied in the ab plane (the two-dimensional morphology of the crystals allowed for easy identification of the crystallographic ab plane and c-axis). In the dilution refrigerator the samples were mounted on an in situ single-axis rotator for the angular quantum oscillation study. Three crystals were measured from the same batch, with consistent results.

ARPES

ARPES measures single particle excitations directly in momentum space. The most commonly used expression for the photocurrent I(k, ω) is:

$$I_{{\mathrm{ARPES}}} = I_0\left| {M_{f,i}} \right|^2f\left( \omega \right)A\left( {{\mathbf{k}},\omega } \right) \ast R\left( {\delta {\mathbf{k}},\;\delta \omega } \right)$$
(7)

where $$M_{f,i}$$ represents the photoemission matrix elements, A(k, ω) is the spectral function, and $$f\left( \omega \right)$$ the Fermi function10. The expression for the intrinsic photocurrent is then convolved with the experimental momentum and energy resolution R$$\left( {\delta {\mathbf{k}},\;\delta \omega } \right)$$. Besides experimental difficulties, complications can arise from the interference of photocurrents from different emission sites and/or from different terms in the light-matter interaction Hamiltonian. Expressing the photocurrent in terms of the spectral function further relies on the sudden approximation, i.e., the assumption that the photoexcitation is instantaneous and that there is no interaction between photoelectron and the sample during the photoemission process10. This approximation is well tested down to much lower photon energies than used in the present work.

The ARPES experiments reported in this paper have been performed at beamline I05 of Diamond Light source using photon energies in the range of 20–80 eV53. Energy and momentum resolutions were set to ~5 meV / 0.008 Å−1, except for the data shown in Fig. 2c where the resolution varied with photon energy and thus with kz. All data were acquired at T ~ 8 K.

STM

STM measures the tunneling current generated between an atomically sharp tip and a conducting sample when a voltage V is applied between the two. By scanning the tip over the sample surface, STM directly delivers real-space information with atomic resolution54. The tunneling current I is directly proportional to the integrated local density of states (LDOS) of quasiparticles, which in the formalism of many-body physics can be defined via the local spectral function $$A\left( {\omega ,{\boldsymbol{r}}} \right) = \mathop {\sum}\nolimits_{\boldsymbol{k}} {A\left( {{\boldsymbol{k}},\omega ;{\boldsymbol{r}}} \right)}$$. The local spectral function of the sample can be accessed for both occupied and unoccupied states by measuring the local differential conductance52:

$$\frac{{{\mathrm{d}}I}}{{{\mathrm{d}}V}}\left( {eV,\;{\mathbf{r}}} \right) = \frac{{4{\uppi}e^2}}{\hbar }\left| {t\left( {\mathbf{r}} \right)} \right|^2\;A_{\mathrm{T}}A_{\mathrm{S}}\left( {\omega = eV,\;{\mathbf{r}}} \right)$$
(8)

where $$A_{{\mathrm{S}},{\mathrm{T}}}$$ are the spectral functions of sample and tip, respectively, and where we approximated the Fermi–Dirac distribution as a step function. $$\left| {t({\mathbf{r}})} \right|^2$$ represents the position-dependent tunneling matrix element that contains the exponential dependence on tip–sample distance. Usually, the spectral function of the tip, AT is designed to be constant, and the momentum dependence of the tunneling matrix elements is ignored.

When measuring in spectroscopic-imaging mode (SI-STM), for each pixel on a chosen field of view a $${\mathrm{d}}I/{\mathrm{d}}V$$ spectrum is acquired at the tip–sample distance determined locally by the set-up conditions $$\left( {V_{\mathrm{S}},\;I_{\mathrm{S}}} \right)$$. The result of such a measurement is a three-dimensional dataset representing the local density of states as function of position and energy.

Because we determine the tip–sample distance at each point by the set-up conditions, the effect of the matrix element (assuming it is energy independent) is canceled. However, the procedure does bring in an extra denominator: $$\frac{{{\mathrm{d}}I}}{{{\mathrm{d}}V}}\left( {eV,\;{\mathbf{r}}} \right) = \frac{{I_{\mathrm{S}}A_{\mathrm{S}}\left( {eV,\;{\mathbf{r}}} \right)}}{{{\int \nolimits_0^{eV_{\mathrm{s}}}} A\left( {E,\;{\mathbf{r}}} \right){\mathrm{d}}E}}$$ (9). The procedure can thus introduce additional artifacts into the measured differential conductance $${\mathrm{d}}I/{\mathrm{d}}V$$28, the so-called set-up effect.

A common way to reduce this effect is to choose set-up conditions far away from the Fermi level such that inhomogeneities in the integrated density of states average out; however, this is not always experimentally possible. Other methods include the use of the ratio between quantities with positive and negative bias55, or the division of the differential conductance by the total conductance $$({\mathrm{d}}I/{\mathrm{d}}V)/(I/V)$$28,29,30 – the approach that we also use in this paper. See Fig. 5b, c and Supplementary Figs 1 and 6 for comparisons. The current I is the measured current at that particular location and bias V, which means it is small but generally non-zero at the Fermi level. The voltage V is a value set in the experiment, implying for the Fermi level that the data would be multiplied by 0 in the normalization. To circumvent this, we manually add a 10 uV (negligible to the energy scale set by temperature) offset in data processing.

The STM experiments reported in this paper have been performed with an ultra-high vacuum, home-built STM with exceptional stability, described elsewhere56. All data was taken at a base temperature of 4.2 K. Measurements are performed with a chemically etched tungsten tip that is prepared by field emission on a gold surface before measuring Sr2RhO4.

Data availability

The data used in this paper is available at https://doi.org/10.26037/yareta:upufx3qatvbsldxstyz6tezszi.

Code availability

The code used in this work are available from the corresponding author upon reasonable request.

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Acknowledgements

This work was supported by the UK-EPSRC under grant EP/G007357/1, by the Swiss National Science Foundation (SNSF) under grants 200020_165791 and 200020_184998, by the Max Planck Society, by the European Research Council (ERC StG SpinMelt), and by the Netherlands Organization for Scientific Research (NWO) under grants 680–47–536 and FOM-167. We acknowledge Diamond Light Source for time on beamline I05 under proposals no. SI13398 and SI5282.

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I.B., W.T., and A.T. performed STM experiments; A.T. and S.R. performed ARPES experiments; R.P. performed QO experiments and fabricated samples. All authors participated in discussion, data analysis, and interpretation.

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Correspondence to A. P. Mackenzie, F. Baumberger or M. P. Allan.

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Battisti, I., Tromp, W.O., Riccò, S. et al. Direct comparison of ARPES, STM, and quantum oscillation data for band structure determination in Sr2RhO4. npj Quantum Mater. 5, 91 (2020). https://doi.org/10.1038/s41535-020-00292-4