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Spatially inhomogeneous electron state deep in the extreme quantum limit of strontium titanate

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Abstract

When an electronic system is subjected to a sufficiently strong magnetic field that the cyclotron energy is much larger than the Fermi energy, the system enters the extreme quantum limit (EQL) and becomes susceptible to a number of instabilities. Bringing a three-dimensional electronic system deeply into the EQL can be difficult however, since it requires a small Fermi energy, large magnetic field, and low disorder. Here we present an experimental study of the EQL in lightly-doped single crystals of strontium titanate. Our experiments probe deeply into the regime where theory has long predicted an interaction-driven charge density wave or Wigner crystal state. A number of interesting features arise in the transport in this regime, including a striking re-entrant nonlinearity in the current–voltage characteristics. We discuss these features in the context of possible correlated electron states, and present an alternative picture based on magnetic-field induced puddling of electrons.

Introduction

When subjected to a sufficiently strong magnetic field, the bulk properties of an electronic system change dramatically. In particular, a three-dimensional electron gas exhibits very different behaviour when the magnetic field B becomes large enough that the cyclotron energy ħωc=ħeB/m exceeds the Fermi energy EFħ2n2/3/m. (Here, ωc is the cyclotron frequency, ħ is the reduced Planck constant, −e is the electron charge, m is the effective electron mass and n is the electron density.) In this extreme quantum limit (EQL) electron motion in the directions perpendicular to the magnetic field is quantized, and all electrons occupy only the lowest Landau level. Semi-classically, one can visualize the EQL as the state in which electron trajectories are tight spirals along the field direction, with gyration radius that is much shorter than the typical inter-electron spacing.

As a consequence of this quantization by magnetic field, in the EQL the electron kinetic energy retains a dependence only on the momentum parallel to the field, and the Fermi surface takes the form of two parallel rings in momentum space. For a clean, low-temperature electron gas, such a dimensionally reduced dispersion implies a number of potentially competing instabilities, including spin or valley density wave, charge density wave (CDW) and Wigner crystallization1,2,3,4.

Such a high-field situation, however, is difficult to realize experimentally. For a typical metal, for example, the EQL requires fields on the order of 105 T, and is thus relevant only for extreme astrophysical settings2,5. Realization of the EQL in the laboratory requires a material that can exhibit metallic behaviour at very low electron density n.

Doped bulk strontium titanate, SrTiO3 (STO), is such a material. STO, a semiconducting perovskite oxide, has been studied intensively in recent years, with much attention devoted to its potential in thin films and heterostructure devices6,7,8,9,10. But as a bulk material STO has attracted interest for over half a century11,12,13,14,15,16,17,18, largely because of its anomalous dielectric response at low temperature11,14,15. Indeed, STO has a static, long-wavelength dielectric constant ɛ that reaches ≈24,000 at low temperatures (with a weak directional dependence15). One implication of this enormous dielectric constant is that the effective Bohr radius aB=4πɛ0ɛħ2/me2 associated with shallow donor states becomes extremely large: aB≈760 nm. Consequently, in the absence of compensating acceptors, even a very small concentration of electron donors is sufficient to ensure that STO is on the conducting side of the Mott criterion, n1/3aB0.2 (ref. 19). Importantly, as we discuss below, this large dielectric constant also implies a significant robustness against localization by charge disorder.

Crucial to studying the deep EQL is the existence of a strong hierarchy of energy scales:

here, is the effective Rydberg energy and kBT is the thermal energy. The first inequality in equation (1) is equivalent to the large magnetic field condition explained above, while the second set of inequalities guarantees that the electron state deep in the EQL is not destroyed either by thermal excitation or by freezeout of electrons onto donor impurities. While previous high-field studies have managed to approach or even enter the EQL in doped semiconductors, simultaneously achieving both sets of inequalities in equation (1) has been more challenging. For example, studies of the EQL in narrow band gap semiconductors, such as n-type InAs20, InSb20,21,22,23 and HgCdTe22,23, are generally limited to the case where EF and are similar in magnitude. Consequently, in these materials electrons freeze onto donor impurities shortly after the EQL is reached, and achieving a deep-EQL electron state is not possible. Previous high-field studies of STO have also generally failed to satisfy this hierarchy, either because the temperature was too high to satisfy the second inequality24 or because the Fermi energy was too high to satisfy the first25,26.

In this paper we present a clear experimental realization of a deep-EQL state in STO. Using transport measurements at low temperatures and high magnetic fields, we probe deeply into the EQL in a number of low-carrier-density samples. Our samples remain good bulk conductors throughout our measurement conditions, and at large magnetic fields they exhibit a strong, re-entrant nonlinearity in the resistivity. This nonlinearity is discussed in the context of possible correlated electron states, and an alternate picture is presented based on puddling of electrons in disorder potential wells.

Results

Shubnikov-de Haas Oscillations

In our study, we examine millimeter-sized STO single crystals (dimensions: ≈7.5 × 7.5 × 0.5 mm), obtained from CrysTec GmbH. (Crys Tec Gmbh, Köpenicker Str. D-12555, Berlin, Germany. http://www.crystec.de/crystec-d.html. This commercial product is described in this paper in order to specify adequately the experimental procedure. In no case does such identification imply recommendation or endorsement by the National Institute of Standards and Technology, nor does it imply that it is necessarily the best available for the purpose.)

To introduce a finite concentration of conduction-band electrons, the samples were heated within a vacuum chamber following the protocol described in Section IV. This heating process is known to produce oxygen vacancies within the sample volume, which act as electron donors27,28,29,30. (In principle, a single oxygen vacancy acts stoichiometrically as a double-donor, but it is generally accepted that one of the two electron states remains tightly bound to the doubly-charged oxygen ion, so that the vacancy donates only a single electron to the conduction band31,32,33,34.) The heating temperature was varied from one sample to another in order to produce samples with different doping levels. For the samples that are the focus of this study, the resulting carrier densities ranged from (7.7±1.1) × 1015 cm−3 to (1.5±0.2) × 1018 cm−3. (Here and below, all listed values of the experimental uncertainty correspond to 95% confidence intervals.)

Importantly, in addition to the oxygen vacancies, as-grown STO crystals are known to have a significant concentration of additional impurities, mostly Fe and Al, that act as deep acceptors35,36. Indeed, previous studies based on chemical analysis and secondary ion mass spectroscopy29 have shown these impurities to be present at the level of ≈7 × 1017 cm−3. Since this concentration is significantly larger than the measured carrier density n, our samples can be described as almost-completely-compensated semiconductors, for which the number of donors and acceptors are nearly identical and thus the total concentration of charged impurities Ni is much larger than n. This relatively large concentration of impurities is also consistent with the measured zero-field mobility, which suggests an impurity concentration on the order of 1018 cm−3 (as shown in Supplementary Note 1). The consequences of the impurity concentration Nin for transport are discussed in detail below.

As the magnetic field is increased from zero, the longitudinal resistivity exhibits Shubnikov-de Haas (SdH) oscillations, as higher Landau levels are pushed outside the Fermi surface with increasing field (as illustrated in Fig. 1). In particular, the field BN at which the Nth Landau level becomes depopulated follows37

Figure 1: Schematic depiction of the effects of high magnetic field on a clean electron gas.
Figure 1

(a,b) Semi-classical picture of the trajectories of Fermi level electrons, both (a) at zero magnetic field and (b) in the extreme quantum limit. Φ0 is the flux quantum and n is the electron density. (ce) show the evolution of the Fermi surface (blue areas) in a clean system with increasing magnetic field. Grey areas show occupied electron states below the Fermi level. (c) The usual spherical Fermi surface at B=0. (d) In a strong magnetic field, electron states are quantized into Landau cylinders, each with constant magnitude of the squared transverse momentum, . (e) In the extreme quantum limit, all electrons belong to the lowest Landau level.

where Φ0=πħ/e is the flux quantum, and the second equality in equation (2) corresponds to the usual limit of large N. As shown in Fig. 2, the observed oscillations of resistivity are periodic in 1/B, suggesting a single, small electron pocket of Fermi surface38. The position of the final (N=1) oscillation indicates that the EQL is reached at fields B≈10–20 T, varying from sample to sample. Here the field BN is defined experimentally as the position in magnetic field of the Nth local maximum of resistance, counted in order of decreasing magnetic field. The identification of these maxima is facilitated by subtracting a smooth, fourth order polynomial from the ρ versus B curve, as shown in Fig. 2b (see also Supplementary Note 2 and Supplementary Fig. 1). The period of oscillation is also confirmed by the periodicity of the first derivative of ρ versus 1/B (see Fig. 2c). Plotting 1/BN against the Landau index N, as shown in Fig. 2c, indicates unambiguously that each of our samples is well within the EQL at our largest magnetic fields.

Figure 2: Identifying the extreme quantum limit via Shubnikov-de Haas (SdH) oscillations.
Figure 2

(a) The longitudinal resistivity ρxx at T=25 mK for one of our samples is plotted as a function of magnetic field. The arrow indicates the onset of the EQL. (b) The SdH oscillations of resistivity are more easily visible if one subtracts a smooth, fourth-order polynomial from the curve in (a). (c) The index N is plotted against 1/BN. The value of BN can be identified either using the local resistance maxima (filled blue circles) or the local minima of the derivative /dB (open circles). Experimental uncertainty in BN is ≈0.2 T, so that the uncertainty in 1/BN is smaller than the symbol sizes. For the open circles, the plotted value of N is shifted by 1/4. (d) The carrier density nSdH inferred from the SdH period (see equation (2)) is plotted against the measured Hall carrier density nHall. Uncertainty in the value of nHall is about 15%, and is reflected by the size of the symbols, while uncertainty in the value of nSdH is ≈5% except where indicated. Circles correspond to samples for which transport was measured in the 001 direction, while squares indicate measurements in the 111 direction. The arrow indicates the carrier density corresponding to the sample in parts (ac).

One can note that equation (2) assumes that Landau levels are not spin-degenerate. The agreement of this equation with our measurements suggests that this is indeed the case in our samples for all appreciable magnetic fields. This non-degeneracy can be expected if one assumes that the electron g-factor in STO is of order unity. In this case the Zeeman energy is of order 100 μeV per Tesla of field, while the Fermi energy in our samples is in the range 100 to 500 μeV, so that the conduction electrons become completely spin polarized even at relatively high Landau levels.

Using equation (2), the value of the SdH period Δ(1/B) gives a measure of the electron density n. The excellent linear fit to equation (2) indicates that the large-N approximation is appropriate for all N>1. Further, the inferred value of n closely matches the value obtained from Hall effect measurements, as shown in Fig. 2d. (Hall measurements are presented in Supplementary Fig. 2.) The agreement between the two measures of n suggests that electrons are uniformly distributed through the bulk of the STO crystal, since the SdH measurements are sensitive to the average Fermi energy of electrons in the sample, while the Hall effect observes only the thickness-averaged number of carriers. The period of the SdH oscillations is also independent of whether the magnetic field is aligned parallel or perpendicular to the current, as shown in Fig. 3a, which confirms the three-dimensional nature of the electron system. We do, however, observe a noticeable anisotropy in the magnetoresistance (MR) at large fields, as shown in Fig. 3b.

Figure 3: Dependence of the resistivity on field direction.
Figure 3

(a) The resistivity at T=25 mK is shown as a function of magnetic field for both field directions. At large B we observe linear magnetoresistance and a significant anisotropy. (b) The period of the Shubnikov-de Haas oscillations is independent of whether the field is applied in the parallel or perpendicular direction.

Our samples also exhibit a large linear MR in the EQL, as evidenced in Figs 2a and 3b, which show a MR ratio ρ(B=45 T)/ρ(B=0)>100. Such non-saturating, linear MR is commonly associated with semi-classical drift of electron orbits along contours of a disorder potential with a long correlation length21,39,40, or with strong spatial inhomogeneity of the carrier concentration or mobility41,42,43,44. Below we provide an additional comment on these possibilities.

Nonlinear transport

While the Fermi energy of a three-dimensional electron gas is essentially constant at small values of the magnetic field, once the EQL is reached (after the last SdH oscillation) the Fermi energy EF acquires a strong dependence on the field strength. In particular, in the EQL , as constriction of electronic wave functions in the perpendicular directions reduces their quantum overlap and causes the Fermi energy to drop. In our samples, EF is small enough that in the EQL only the lowest t2g band is relevant25,45, and this is consistent with the single frequency observed in the low field SdH measurement. This lowest band has a slight anisotropy of the effective mass25, resulting from the tetragonal distortion of the STO lattice at low temperature, so for the sake of making numerical estimates below we take the effective mass m to be equal to the geometric mean of the three perpendicular masses, which gives m≈1.7m0, where m0 is the bare electron mass.

As the Fermi energy decreases with increasing field, the relative strength of the Coulomb interaction grows, as described by the ratio α=EC/EF, where ECe2kF/4πɛ0ɛ is the typical strength of the Coulomb interaction between neighbouring electrons in the field direction, and EFħ2 is the Fermi energy. Here, is the Fermi wave vector in the field direction, so that one can write . At large α, a clean, low-temperature electron gas becomes unstable with respect to the formation of a CDW or Wigner crystal. In our experiments α is as large as 12, which is two orders of magnitude larger than in previous high-field experiments in STO25,26. At such large values of α, Hartree-Fock calculations predict a CDW gap that exceeds the Fermi energy, indicating a strong instability toward a spatially inhomogeneous phase46,47.

Deep within the EQL, we observe a significant nonlinearity in the current–voltage (IV) characteristics, as illustrated in Fig. 4a. Such nonlinearity typically implies pinning or trapping of carriers by a disorder potential. The observed nonlinearity is also weaker at higher temperatures, while the zero bias resistance is lower, implying weaker pinning as temperature is increased. A careful examination of the power dissipation at low bias confirms that the nonlinearity is not a result of Joule heating, particularly at low bias (see the Methods section IV). We also find it unlikely that the nonlinearity arises from scattering by domain walls separating tetragonal domains, which form below T=105 K as STO undergoes a transition from cubic to tetragonal crystal symmetry11. The nonlinearity that we measure is clearly dependent on the magnetic field strength, while such a domain structure is B-independent. We also observe no sign of any anomalies in the resistivity at T=105 K (see Supplementary Fig. 3).

Figure 4: Nonlinearity of the resistance in the extreme quantum limit.
Figure 4

(a) The differential resistance, dV/dI, is plotted as a function of the source-drain bias current I for different temperatures (different curves on each plot) and for different values of the magnetic field (different plots, each labelled by the corresponding value of B). For each plot, the values of dV/dI are normalized relative to the value at zero bias and T=20 mK. The dotted lines indicate the value of the field relative to the phase of the SdH oscillations, which are shown in (b). (c) The degree of nonlinearity in the IV characteristics is shown to oscillate as a function of B, such that the transport is most nonlinear at maxima of the SdH oscillations, while at minima of the SdH oscillations the nonlinearity essentially disappears. The y axis corresponds to the quantity (dV/dI|I=0−dV/dI|I=300 μA)/(dV/dI|I=0) at T=20 mK, which approximates the slope of the top curves in a.

Strikingly, the observed nonlinearity appears in a re-entrant way at lower magnetic fields, becoming most pronounced at relative resistivity maxima and disappearing at relative resistivity minima. This is illustrated in Fig. 4c. It is worth noting that a similar re-entrant nonlinearity has been observed in both NbSe3 and InAs, although in both cases observations were limited to relatively high Landau levels. In NbSe3 the results were interpreted in terms of CDW physics48, while in InAs it was explained in terms of changes in the effective electron temperature49. A closer analysis of the nonlinearity is presented in Supplementary Note 3 and in Supplementary Figs 4 and 5, including the scaling of the resistivity with bias voltage and magnetic field.

Discussion

Strong nonlinearity in the transport is expected when electrons form a spatially-correlated state, such as a CDW or Wigner crystal, that can be easily pinned by a disorder potential50. Such a spatially inhomogeneous state would also be consistent with the observed anisotropy in conductivity, and, indeed, previous studies of Hg1−xCdxTe have interpreted similar nonlinearity as evidence for a Wigner crystal51. Working against this interpretation, however, is the very small absolute magnitude of the Coulomb interaction strength between individual electrons, owing to the large dielectric constant. Indeed, theoretical estimates of the critical temperature Tc for CDW formation46,47,52 suggest that Tc≈5 mK or lower in our samples, and this is below our lowest measurement temperature of 20 mK. Thus, if the nonlinearity in our measurements indeed arises from a CDW or Wigner crystal phase, then it likely must be understood in combination with structural distortions in the STO lattice53,54 rather than as a simple electronic instability.

The picture of CDW-type order also ignores the role of charged impurities, which can be expected to overwhelm electron–electron interaction effects when the carrier concentration is low. An alternative picture, then, is to assume that the state of the electron system at large B is dictated by fluctuations in the disorder potential. In particular, if one assumes that the impurities are arranged in a spatially uncorrelated way, then random fluctuations in their local density give rise to a disorder potential with relatively large magnitude55,56

In our samples, γ is in the range 10–20 μeV. At B=0, this disorder represents a relatively small perturbation to the electron Fermi level, as illustrated in Fig. 5a. Deep within the EQL, however, the Fermi energy falls dramatically, and one can expect that the electron liquid breaks up into disconnected puddles that are localized in wells of the disorder potential (see Fig. 5b).

Figure 5: Proposed breakup of the electron liquid into puddles at large magnetic field.
Figure 5

(a) At zero magnetic field, the disorder is weak compared to the typical Fermi energy, and so the electron density is nearly uniform spatially. Here, the shaded area represents filled energy levels and the blue line indicates the position of the Fermi level μ. (b) Deep in the extreme quantum limit, the Fermi energy is greatly reduced, and electrons reside in disconnected puddles that are localized in minima of the disorder potential. (c) Evidence for puddling can be seen in the relatively large value of the quantum-limiting field BEQL for samples with low values of the electron density n. Symbols represent measured values of BEQL (with the diamond symbol indicating a measurement in the 111 direction). Experimental uncertainty in BEQL is ≈0.2 T, smaller than the symbol sizes. The solid line shows the predicted value of BEQL for a uniform electron gas, equation (4).

In principle, this puddled state at large B corresponds to an insulator, with a finite activation energy Ea for electron transport that is related to the amplitude of the disorder potential. However, owing to the large dielectric response and the relative ease of percolation between wells of the potential in three dimensions, for our samples the expected value of Ea is relatively small, Ea≈0.15γkB × (15 mK)56,57,58, below our lowest measurement temperatures. In this sense the picture of electron puddles is not inconsistent with the absence of a sharp upturn in the resistivity at large fields. Clear observation of a magnetic field-driven metal-insulator transition in STO may require lower temperatures or samples with lower electron concentration. It is also possible that impurity positions have some degree of spatial correlation59,60,61,62,63, which would further reduce Ea by diminishing the amplitude of disorder potential fluctuations.

Support for the picture of electron puddling at large field can be found by examining the value of the field BEQL at which the system enters the EQL. For a spinless, spatially uniform electron gas,

and one can therefore expect BEQL to decrease with decreasing electron density as BEQLn2/3. We find, however, that BEQL far exceeds this theoretical value for our low-density samples with n1017 cm−3, and appears to saturate at a value on the order of ≈10 T. Indeed, for our lowest-density samples, the disagreement between the observed value of BEQL and the prediction of equation (4) is larger than 3 times, as shown in Fig. 5c. It should be emphasized that this disagreement is much larger than the inaccuracy that results from taking the large N limit in equation (2), which is only ≈30% when applied to N=1.

This discrepancy between the measured and predicted values of BEQL can be explained within the picture of electron puddles, since the typical concentration np of electrons within puddles in the EQL is markedly different from the volume-averaged electron concentration n. Indeed, in the EQL the typical concentration of electrons within puddles takes a value that is independent of the volume-averaged electron concentration55,57:

The value of np is determined by statistical fluctuations of the disorder potential over length scales much shorter than the correlation length of the potential. Such fluctuations are driven by the random influence of the many impurity charges, rather than by the weak nonlinear screening from the sparse electrons, and this leads to the independence of np on n implied by equation (5)55,57.

For our experiments, equation (5) suggests that np is on the order of a few times 1017 cm−3 in the EQL, while the typical puddle radius is 40 nm. One can then arrive at an estimate for BEQL by inserting np from equation (5) into equation (4). This procedure gives BEQL≈10(Φ0/)(Ni)4/9, which for our samples is on the order of 10 T. This is consistent with the observed value in samples with small n1017 cm−3. At larger values of the doping, the carrier concentration n presumably becomes comparable to the total impurity concentration Ni, and the electron gas becomes uniform again so that equation (4) is valid.

One can also rationalize the nonlinearity of the IV characteristics at B>BEQL within the picture of electron puddles. In particular, an applied electric field facilitates the thermal activation of electrons between adjacent puddles by adding a contribution to the potential energy that varies linearly with the electron position. This picture implies a characteristic electric field scale that is consistent with the observed nonlinearity in the EQL (see Supplementary Note 3). The nonlinearity is also identical in both the parallel and perpendicular field directions, which is again consistent with the puddle picture (Supplementary Note 3). Still, the oscillatory behaviour of the nonlinearity presented in Fig. 4 remains a prominent puzzle.

Finally, the picture of electron puddles is also qualitatively consistent with the observed linear MR in the EQL, since it corresponds to a landscape where both the disorder potential and the electron concentration have strong spatial fluctuations with a long correlation length. The observed anisotropy of resistivity is also typical in such situations57,64. (It should be noted, however, that many scenarios for electron transport in the EQL produce significant anisotropy65, and therefore the anisotropy by itself cannot generally be used as a strong diagnostic of the electron state.)

To summarize, this paper has presented a clear experimental demonstration of the EQL in bulk STO across a range of samples. Our experiments probe much more deeply into the EQL than previous studies of STO, and into the regime of small , for which a charge ordering instability has long been predicted to occur for a three-dimensional electron gas. While some of our measurements are consistent with the formation of such a CDW state, including in particular a striking nonlinearity in the IV characteristics, it seems unlikely to us that electron-electron interactions alone are sufficient to induce such a state within the regime of our experiments. Nonetheless, it remains an open question whether a field-induced CDW state can result from the combination of electron interactions and structural distortions in the STO lattice. An alternate explanation for our measurements is that the large-field behaviour is dominated by puddling of electrons in minima of the disorder potential. The observed saturation of the quantum limiting field is apparently consistent with this picture. It may be worth considering, however, whether CDW physics can coexist with an electron-puddled structure. Future studies may provide important additional insight into the electron state in the EQL, particularly if they can complement our transport measurements with thermodynamic probes like capacitance or tunnelling spectroscopy, or with studies of magnetic field-driven structural transitions.

Methods

Sample preparation

The SrTiO3 single crystals studied here were obtained from Crys Tec GmbH. On one side the samples were atomically smooth with regular unit cell high terraces, while the opposite face was unpolished. The (002) peak in all samples in this study had rocking curve full width at half maxima in the range 0.027°<Δω<0.041°. The samples were first cleaned with solvents (including trichloroethylene) to remove any residue or particulate and were then mounted on a stainless steel sample holder. All annealing was carried out using a SiC radiative heater. The samples were annealed in a prep chamber at 400 °C for 30 min to get rid of any adsorbed water or solvents on the holder and substrate. After the pressure of the prep chamber dropped below 4 × 10−6 Pa (3 × 10−8 torr), the sample was cooled down and inserted into the main vacuum chamber, which was typically at a base pressure between 7 × 10−8 Pa and 3 × 10−7 Pa (5 × 10−10 torr and 2 × 10−9 torr). The sample was heated to temperatures between 680 and 850 °C, depending on the doping level desired, at a rate of 30 to 40 °C min−1. The pressure in the chamber near the end of the annealing process was ≈3 × 10−6 Pa (2 × 10−8 torr), comprising mostly H2. Samples were held at the annealing temperature for exactly 60 min, after which time the power to the heater was rapidly reduced and then turned off and the sample was allowed to cool, which took 30 min.

Contacts

The current contacts spanned the full width of the sample (≈0.5 × 7.5 mm), while four voltage contact tabs (with dimensions 1.5 × 1.5 mm) were deposited at the edges of the sample (spaced ≈1.8 mm apart). NiCr (50 nm)/Au (200 nm) contacts were sputtered on the unpolished side of the sample after Ar ion milling only the contact pad area for ≈15 min (400 V, 30 mA, incident at ≈45°). All samples were typically measured within a week of annealing, as the resistivity was found to increase progressively with time.

Transport measurements

Simultaneous measurements of the longitudinal and Hall voltages, Vxx and Vxy, respectively, were carried out in a 5-terminal Hall geometry, as illustrated in Fig. 6. Our measurements used the direct current reversal technique, and the experimental setup was an improved version of the system described in ref. 66.

Figure 6: Schematic of the measurement setup.
Figure 6

A schematic of the sample is shown, showing placement of the contacts and physical dimensions.

Utilized current sources and nanovoltmeters have a built-in option for measurements of differential conductance or differential resistance. Thus, we used the same setup for measurements of differential resistance dVxx/dI in the 4-terminal geometry. (Elsewhere in this article, the notation dV/dI is used in place of dVxx/dI.) The differential resistance at a given bias current, Ibias, was characterized by measuring changes in voltage, dV, associated with small excursions in the current, dI, about the applied bias. During the measurements Ibias was swept through a specified range with a finite step size ΔIbias.

Experiments were performed at several magnet/cryostat configurations available at the National High Magnetic Field Laboratory, and the study was performed in magnetic field as high as 45 T and at temperatures ranging from 20 to 200 mK using dilution cryostats. Care was taken to ensure that our measurements were not affected by Joule heating.

Contact resistance at low temperatures was too low to be measured reliably (1 Ω or lower). Fabrication of contacts with such low resistance was critical for carrying out low-noise voltage measurements at low temperatures, where the samples typically had resistance values in the range 0.1–100 Ω. Furthermore, for measurements in the dilution fridge, the low contact resistances at the current contacts were essential for minimizing heating due to the excitation current.

Heating

To characterize the effects of the excitation current on heating in the sample, and on the value of the measured resistance in our experiments, we measured dV/dI for a range of currents between −300 and +300 μA for several values of the differential current excitation ΔI and the excitation current Ibias. By varying these values at low Ibias we were able to substantially vary the power dissipated in a dV/dI measurement. We observed that for |Ibias|>10 μA the value of dV/dI was independent of the utilized measurement parameters. This is shown for ΔI=2, 5 and 10 μA in Fig. 7. Our estimations show that for Ibias=10 μA and ΔI=2 μA the power dissipated in the sample was about 57 nW, whereas for Ibias=10 μA and ΔI=5 μA this power was about 130 nW. Thus, while corresponding values of the dissipated power differ by more than a factor of 2, the measurements nonetheless produce the same result for the differential resistance. Therefore, at least at low values of the current bias, the change in dV/dI measured as a function of bias (Fig. 4) is not due to heating. The disagreement at zero bias between the curves for ΔI=2, 5 and 10 μA in Fig. 7 can be explained by a coarse graining effect produced by the larger ΔI values near the sharp, cusp-like feature at zero bias. The data for ΔI=2 μA is closest to the intrinsic curve.

Figure 7: Current dependence of the differential resistance.
Figure 7

The differential resistance, measured at temperature 20 mK and magnetic field 45 T, is shown for different values of the excitation current Ibias and the current step size ΔI. (a) Shows the measured differential resistance over a wide range of bias current. (b) Shows the same data plotted very near the point of zero bias. (The rectangle in (a) indicates the approximate range and domain of (b).)

Data availability

The data presented in this study are available from the corresponding authors on request.

Additional information

How to cite this article: Bhattacharya, A. et al. Spatially inhomogeneous electron state deep in the extreme quantum limit of strontium titanate. Nat. Commun. 7, 12974 doi: 10.1038/ncomms12974 (2016).

References

  1. 1.

    & Ground state of an electron gas in a magnetic field. Phys. Rev. 140, A839–A853 (1965).

  2. 2.

    & Electron gas in superstrong magnetic fields: wigner transition. Phys. Rev. Lett. 28, 1077–1079 (1972).

  3. 3.

    & The Wigner transition in a magnetic field. J. Phys. C: Solid State Phys. 8, 2729 (1975).

  4. 4.

    Possible states for a three-dimensional electron gas in a strong magnetic field. Jpn J. Appl. Phys. 26S3, 1913–1919 (1987).

  5. 5.

    Matter in strong magnetic fields. Rev. Mod. Phys. 73, 629–662 (2001).

  6. 6.

    et al. Room-temperature ferroelectricity in strained SrTiO3. Nature 430, 758–761 (2004).

  7. 7.

    & A high-mobility electron gas at the LaAlO3/SrTiO3 heterointerface. Nature 427, 423–426 (2004).

  8. 8.

    , , , & Tunable quasi-two-dimensional electron gases in oxide heterostructures. Science 313, 1942–1945 (2006).

  9. 9.

    et al. Electric field control of the LaAlO3/SrTiO3 interface ground state. Nature 456, 624–627 (2008).

  10. 10.

    et al. Epitaxial SrTiO3 films with electron mobilities exceeding 30,000 cm2 V−1 s−1. Nat. Mater. 9, 482–484 (2010).

  11. 11.

    Lattice dynamics and phase transitions of strontium titanate. Phys. Rev. 134, A981–A997 (1964).

  12. 12.

    Dielectric constant in perovskite type crystals. Phys. Rev. 86, 118–120 (1952).

  13. 13.

    , , , & Shubnikov-de Haas Effect in SrTiO3. Phys. Rev. 158, 775–778 (1967).

  14. 14.

    & Neutron scattering and nature of the soft optical phonon in SrTiO3. J. Phys. Soc. Jpn 26, 396–403 (1969).

  15. 15.

    , & Permittivity of strontium titanate. J. Appl. Phys. 43, 2124–2131 (1972).

  16. 16.

    & Electronic energy bands in strontium titanate. Phys. Rev. 135, A1321–A1325 (1964).

  17. 17.

    et al. Persistent optically induced magnetism in oxygen-deficient strontium titanate. Nat. Mater. 13, 481–487 (2014).

  18. 18.

    , & Superconductivity in Semiconducting SrTiO3. Phys. Rev. Lett. 12, 474–475 (1964).

  19. 19.

    Metal-insulator transition. Rev. Mod. Phys. 40, 677–683 (1968).

  20. 20.

    , , & Magneto-quantum oscillations in the hall constant of three-dimensional metallic semiconductors. J. Phys. Condens. Matter 6, 4289 (1994).

  21. 21.

    , & Quasi-one-dimensional transport in the extreme quantum limit of heavily doped n-InSb. Phys. Rev. B 62, 16645–16652 (2000).

  22. 22.

    , & Magnetic-field-induced localization in narrow-gap semiconductors Hg1−xCdxTe and InSb. Phys. Rev. B 38, 5585–5602 (1988).

  23. 23.

    Possibility of a metal-insulator transition at the Mott critical field in InSb and Hg1−xCdxTe. Phys. Rev. B 40, 8091–8094 (1989).

  24. 24.

    , & Vanishing hall coefficient in the extreme quantum limit in photocarrier-doped SrTiO3. Phys. Rev. Lett. 101, 096601 (2008).

  25. 25.

    et al. Conduction-band edge and Shubnikov-de Haas effect in low-electron-density SrTiO3. Phys. Rev. B 88, 045114 (2013).

  26. 26.

    , , & Fermi surface of the most dilute superconductor. Phys. Rev. X 3, 021002 (2013).

  27. 27.

    , & Comparison of the chemical diffusion of undoped and Nb-doped SrTiO3. J. Phys. Chem. Solids 60, 1835–1844 (1999).

  28. 28.

    , , & Observation of vacancy defect migration in the cation sublattice of complex oxides by 18O tracer experiments. Phys. Rev. Lett. 90, 105901 (2003).

  29. 29.

    , , & Behavior of oxygen vacancies in single-crystal SrTiO3: equilibrium distribution and diffusion kinetics. Phys. Rev. B 85, 174109 (2012).

  30. 30.

    Oxidation kinetics of single-crystal SrTiO3. J. Am. Ceram. Soc. 48, 476–478 (1965).

  31. 31.

    & Defect states induced by oxygen vacancies in cubic SrTiO3: first-principles calculations. J. Phys. Soc. Jpn 79, 114704 (2010).

  32. 32.

    & Electron correlation in oxygen vacancy in SrTiO3. Phys. Rev. Lett. 111, 217601 (2013).

  33. 33.

    , & Magnetism and metal-insulator transition in oxygen-deficient SrTiO3. Phys. Rev. B 92, 115112 (2015).

  34. 34.

    , , & Vacancies and small polarons in SrTiO3. Phys. Rev. B 90, 085202 (2014).

  35. 35.

    & Shared holes trapped by charge defects in SrTiO3. Phys. Rev. B 1, 2799–2810 (1970).

  36. 36.

    & Energy levels of iron and aluminum in SrTiO3. Phys. Rev. B 8, 5847–5854 (1973).

  37. 37.

    Fundamentals of the Theory of Metals Elsevier (1988).

  38. 38.

    , & Scalable T2 resistivity in a small single-component fermi surface. Science 349, 945–948 (2015).

  39. 39.

    Electron transport in the extreme quantum limit in applied magnetic field. Physics-Uspekhi 43, 349 (2000).

  40. 40.

    , & Linear magnetoresistance in metals: guiding center diffusion in a smooth random potential. Phys. Rev. B 92, 180204 (2015).

  41. 41.

    Anomalous plasma resistance in a strong magnetic field. Sov. J. Exp. Theor. Phys. 32, 348 (1971).

  42. 42.

    & Classical magnetotransport of inhomogeneous conductors. Phys. Rev. B 72, 094417 (2005).

  43. 43.

    et al. Linear magnetoresistance due to multiple-electron scattering by low-mobility islands in an inhomogeneous conductor. Nat. Commun. 3, 1097 (2012).

  44. 44.

    et al. Linear magnetoresistance caused by mobility fluctuations in n-Doped Cd3As2. Phys. Rev. Lett. 114, 117201 (2015).

  45. 45.

    & Theory of the SrTiO3 surface state two-dimensional electron gas. Phys. Rev. B 86, 125121 (2012).

  46. 46.

    CDW instability of electron gas in a strong magnetic field. Solid State Commun. 26, 783–786 (1978).

  47. 47.

    Magnetic field induced phase transition of a three-dimensional electron gas. Solid State Commun. 36, 397–401 (1980).

  48. 48.

    , & Nonlinear magnetoresistance and charge-density-wave depinning at liquid-helium temperatures in NbSe3. Phys. Rev. B 35, 4533–4536 (1987).

  49. 49.

    & Low-temperature non-ohmic galvanomagnetic effects in degenerate n-type InAs. Phys. Rev. B 5, 566–579 (1972).

  50. 50.

    Nonlinear and frequency-dependent transport phenomena in low-dimensional conductors. Physica D: Nonlinear Phenomena 8, 1–34 (1983).

  51. 51.

    et al. Evidence for depinning of a Wigner crystal in Hg–Cd–Te. Phys. Rev. B 33, 5082–5085 (1986).

  52. 52.

    & Electron-phonon interactions and charge-density-wave formations in strong magnetic fields. Phys. Rev. B 33, 5461–5464 (1986).

  53. 53.

    & Fermi surface nesting and the origin of charge density waves in metals. Phys. Rev. B 77, 165135 (2008).

  54. 54.

    The phase transition of strontium titanate. Philos. Trans. R. Soc. Lond. A: Math. Phys. Eng. Sci. 354, 2799–2814 (1996).

  55. 55.

    & Localization of electrons in a magnetic field. Sov. J. Exp. Theor. Phys. 37, 1122 (1973).

  56. 56.

    & Electronic Properties of Doped Semiconductors Springer-Verlag (1984) Available from .

  57. 57.

    & Magnetic-field-induced localization of electrons in fluctuation potential wells of impurities. Physica Status Solidi B 157, 17–59 (1990).

  58. 58.

    , & Why is the bulk resistivity of topological insulators so small? Phys. Rev. Lett. 109, 176801 (2012).

  59. 59.

    & Defect association in acceptor-doped SrTiO3: case study for FéTiVö and MńTivö†. Phys. Chem. Chem. Phys. 5, 2297–2303 (2003).

  60. 60.

    , , , & Localized metallic conductivity and self-healing during thermal reduction of SrTiO3. Phys. Rev. Lett. 88, 075508 (2002).

  61. 61.

    et al. Oxygen vacancy clustering and electron localization in oxygen-deficient SrTiO3: LDA+U Study. Phys. Rev. Lett. 98, 115503 (2007).

  62. 62.

    & Structure of transition-metal-oxygen-vacancy pair centers. Phys. Rev. B 19, 109–120 (1979).

  63. 63.

    , & A simulation study of oxygen-vacancy behavior in strontium titanate: beyond nearest-neighbor interactions. J. Phys. Chem. C 118, 15185–15192 (2014).

  64. 64.

    , , , & Magnetic-field-induced localization in InSb and Hg0.79Cd0.21 Te. Phys. Rev. B 32, 6952–6955 (1985).

  65. 65.

    Electron transport phenomena in semiconductors vol. 394, World Scientific (1994).

  66. 66.

    Stand alone experimental setup for dc transport measurements. Rev. Sci. Instrum. 81, 075111 (2010).

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Acknowledgements

Initial measurements of quantum oscillations in reduced STO samples were carried out at the NHMFL in Los Alamos by A.B. with J. Singleton and F. Balakirev. We are grateful to C. Leighton, P.B. Littlewood, A. Lopez-Bezanilla, B.I. Shklovskii and K.V. Reich for helpful discussions. A.B. acknowledges the support of the U.S. Department of Energy (DOE), Office of Science, Basic Energy Sciences (BES), Materials Sciences and Engineering Division. The use of facilities at the Center for Nanoscale Materials, was supported by the U.S. DOE, BES under contract no. DE-AC02-06CH11357. Theory work by BS was initially supported at Argonne National Laboratory by the U.S. Department of Energy, Office of Science, under contract no. DE-AC02-06CH11357; subsequent theory work was supported as part of the MIT Center for Excitonics, an Energy Frontier Research Center funded by the U.S. DOE, Office of Science, BES under Award no. DE-SC0001088. The NHMFL is supported by the NSF Cooperative agreement no. DMR-1157490 and the State of Florida.

Author information

Author notes

    • Guru Khalsa

    Present address: Department of Materials Science and Engineering, Cornell University, 126 Bard Hall, Ithaca, NY 14853-1501

    • Anand Bhattacharya
    •  & Brian Skinner

    These authors contributed equally to this work

Affiliations

  1. Materials Science Division, Argonne National Laboratory, Argonne, Illinois 60439, USA

    • Anand Bhattacharya
    •  & Brian Skinner
  2. Massachusetts Institute of Technology, 77 Mass Ave, Cambridge, Massachusetts 02139, USA

    • Brian Skinner
  3. Center for Nanoscale Science and Technology, National Institute of Standards and Technology, Gaithersburg, Maryland 20899, USA

    • Guru Khalsa
  4. National High Magnetic Field Laboratory, 1800 E. Paul Dirac Dr, Tallahassee, Florida 32310, USA

    • Alexey V. Suslov

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Contributions

A.B. conceived of the experiment and prepared the samples. A.V.S. designed and implemented the experimental setup. Experiments at the NHMFL were performed by A.B. and A.V.S. Theoretical analysis was provided by B.S. and G.K. All authors contributed to writing and editing the manuscript.

Competing interests

The authors declare no competing financial interests.

Corresponding authors

Correspondence to Anand Bhattacharya or Brian Skinner.

Supplementary information

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    Supplementary Information

    Supplementary Figures 1-5, Supplementary Notes 1-3 and Supplementary References

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