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Nature Communications logoLink to Nature Communications
. 2019 Dec 2;10:5487. doi: 10.1038/s41467-019-13421-w

Magnetic field-tuned Fermi liquid in a Kondo insulator

Satya K Kushwaha 1,2, Mun K Chan 1, Joonbum Park 1, S M Thomas 2, Eric D Bauer 2, J D Thompson 2, F Ronning 2, Priscila F S Rosa 2, Neil Harrison 1,
PMCID: PMC6889157  PMID: 31792205

Abstract

Kondo insulators are expected to transform into metals under a sufficiently strong magnetic field. The closure of the insulating gap stems from the coupling of a magnetic field to the electron spin, yet the required strength of the magnetic field–typically of order 100 T–means that very little is known about this insulator-metal transition. Here we show that Ce3Bi4Pd3, owing to its fortuitously small gap, provides an ideal Kondo insulator for this investigation. A metallic Fermi liquid state is established above a critical magnetic field of only Bc 11 T. A peak in the strength of electronic correlations near Bc, which is evident in transport and susceptibility measurements, suggests that Ce3Bi4Pd3 may exhibit quantum criticality analogous to that reported in Kondo insulators under pressure. Metamagnetism and the breakdown of the Kondo coupling are also discussed.

Subject terms: Phase transitions and critical phenomena, Topological insulators, Electronic properties and materials


The interaction of localized and conduction electrons in some heavy fermion materials is believed to give rise to a Kondo insulating state. Kushwaha et al. present evidence that Ce3Bi4Pd3 is a Kondo insulator with a gap small enough to be driven into a Fermi liquid phase with accessible magnetic fields.

Introduction

Kondo insulators are a class of quantum materials in which the coupling between conduction electrons and nearly localized f-electrons may lead to properties that are distinct from those of conventional band insulators13. Remarkable properties of current interest include topologically protected surface states that are predicted46 and reportedly confirmed by experiments712, and reports of magnetic quantum oscillations originating from the insulating bulk1316. The very same magnetic field that produces quantum oscillations also couples to the f-electron magnetic moments, driving the Kondo insulator inexorably towards a metallic state17,18. The required magnetic fields in excess of 100 T17,19 have, however, proven to be prohibitive for a complete characterization of the metallic ground state.

Thermodynamic experiments have thus far provided evidence for the presence of electronic correlations in Kondo insulators at high-magnetic fields. Quantum oscillation experiments, for example, have found moderately heavy masses within the insulating phase in strong magnetic fields15. Furthermore, heat capacity experiments have shown that the electronic contribution undergoes an abrupt increase with increasing magnetic field20,21: in one case20 the increase occurs within the insulating phase, suggesting the presence of in-gap states22, whereas in another, it coincides21 with the onset of an upturn in the magnetic susceptibility18,19 and reports of metallic behavior7,18. An unambiguous signature of metallic behavior, such as electrical resistivity that increases with increasing temperature at accessible magnetic fields, has yet to be reported.

We show here that insulating Ce3Bi4Pd3, once polished to remove surface contamination, exhibits properties consistent with it being a reduced gap variant of its sister Kondo insulator Ce3Bi4Pt322,23, which is also a topological Kondo insulator candidate4,24,25. The atypically small magnetic field of Bc 11 T required to overcome the Kondo gap of insulating Ce3Bi4Pd3 (see Fig. 1), makes this material26 ideal for investigating the metallization of a Kondo insulator in strong magnetic fields. We find a magnetic field-induced metallic state exhibiting an electrical resistivity that varies as T2 at low temperatures (where T is the temperature), thereby revealing a Fermi liquid ground state in the high-magnetic field metallic phase. We also identify a magnetic field-tuned collapse of the Fermi liquid temperature scale TFL near Bc, indicating that Ce3Bi4Pd3 may exhibit a magnetic field-tuned quantum critical point analogous to that observed in SmB6 as a function of pressure2731. The origin of the collapsing Fermi liquid temperature scale in Ce3Bi4Pd3 is revealed by susceptibility measurements, which find a peak as a function of magnetic field at Bc that can be traced back to a broad maximum in the susceptibility as a function of temperature at TM in weak magnetic fields. This maximum implies the formation of Kondo singlets at a temperature TK=cTM (where 3 <c< 4)20, yielding 15 <TK< 20 K. A gradual evolution of the susceptibility from a crossover along the temperature axis to a sharper peak along the magnetic field axis at Bc is therefore unveiled.

Fig. 1.

Fig. 1

Magnetic field versus temperature phase diagram of Ce3Bi4Pd3. TM indicates the peak in the susceptibility (χ) obtained from χ versus T (triangles) and B (stars) from Fig. 6. Here, Bc=B(TM0) is indicated by a green circle. Also shown is the temperature TFL (circles) above which the resistivity departs from ρxx=ρ0+AT2 (i.e., Fermi liquid) behavior. Shaded regions and lines are drawn as guides to the eye. The gray dashed line shows where the derivative ρxxT=0 (plus symbols from sample A in static fields, × symbols from sample A in pulsed fields and asterisk symbols from sample B in static fields; see Methods). To the left of this line ρxxT<0, indicative of insulating behavior, while to the right of this line ρxxT>0, indicative of metallic behavior. The right-hand-axis indicates the magnetic field-dependence of the A coefficient (squares), with the values for B 20 T corresponding to the average of samples A and B in Fig. 5. Error bars represent the standard error.

Results

Evidence for a small gap Kondo insulator

Typical signatures of a Kondo insulating state include an electrical resistivity that exhibits a thermally activated insulating ρxxT<0 behavior (where ρxx is the electrical resistivity) over a wide range of temperatures and a Curie–Weiss behavior in the magnetic susceptibility at high temperatures that crosses over via a maximum in the susceptibility into a Kondo gapped state at low temperatures1,3,22,3235. Zero magnetic field electrical resistivity and magnetic susceptibility measurements reveal Ce3Bi4Pd3 to exhibit such signatures (see Figs. 1 and 2 and Supplementary Fig. 1), but with a Kondo temperature scale that is significantly reduced relative to those found in the archetypal Kondo insulators SmB6 and Ce3Bi4Pt3. Typical Kondo insulators have Kondo gaps of several millielectronvolts, accompanied by inverse residual resistivity ratios in the range 102<RRRR1< 105 and maxima in the magnetic susceptibility and heat capacity20,36 in the range of temperatures 10 K TM 100 K. Ce3Bi4Pd3, however, appears to have a significantly smaller Kondo gap, accompanied by an inverse residual resistivity ratio of only RRRR1~ 5 (see Fig. 2a) and maxima in the susceptibility (see Fig. 2b) and heat capacity (see Fig. 3) at TM 5 K. A possible explanation for the smaller Kondo gap in Ce3Bi4Pd3 compared to its sister compound Ce3Bi4Pt3 is the reduction in the strength of the hybridization identified in electronic structure calculations37.

Fig. 2.

Fig. 2

Sample characterization. a Comparison of ρxx versus T at B=0 for two Ce3Bi4Pd3 samples (labeled A and B) with Ce3Bi4Pt3 (sample D). The inset graph shows Arrhenius plots. Whereas Ce3Bi4Pt3 exhibits activated (ρxx~eΔkBT) behavior for 5 T 30 K, Ce3Bi4Pd3 appears to exhibit such behavior over a range 6 T   35 K (with a smaller slope) that lies outside the fitting range, suggesting that Δ cannot be estimated reliably from ρxx in the case of Ce3Bi4Pd3. The shallow slope and departure from activated behavior at low T is suggestive of a temperature-dependent scattering rate or residual in-gap states associated either with bulk defects, inclusions of other phases or the sample surface (see Methods). Also shown is a schematic of the crystal structure (see Methods). b Susceptibility χ versus T for Ce3Bi4Pd3 (at B= 0.1 and 5 T in gray and blue, respectively) compared with that for Ce3Bi4Pt3 (at B= 0.1 T) from ref. 35, with TM indicating the maxima. The inset shows 1χ versus T for Ce3Bi4Pd3, evidencing Curie–Weiss behavior (indicated by red dashed fitted line) over a broad range of T and a Curie constant C 0.8 mol Ce per emu K.

Fig. 3.

Fig. 3

Specific heat data. Low-temperature heat capacity divided by temperature, CT, plotted versus logarithmically scaled T (symbols). Solid lines represent fits in which the Kondo gap is modeled using the Schotte–Schotte model (see Methods). A full fit is initially made only for B=0 (purple line). On extending to fit to CT for B= 4, 7, and 9 T (light blue, green and yellow lines), only the Zeeman splitting ±12geffμBB is allowed to vary (where μB is the Bohr magneton). The inset shows the locations of the Zeeman-split Lorentzians used in the Schotte–Schotte model (see Methods).

The small size of the Kondo gap in Ce3Bi4Pd3 in Fig. 2a gives rise to a shallow slope of the resistivity Arrhenius plot in Fig. 2a (see Supplementary Fig. 2 for the magnetic field B-dependence), which therefore has a strong likelihood of being affected by the presence of in-gap states and changes in the transport scattering rate with temperature. To obtain an estimate of the Kondo gap that is less dependent on the scattering rate, we turn to the approximately activated behavior observed in Hall effect measurements38 (see Fig. 4a), whereupon we obtain Δ= 1.8 ± 0.5 meV ( 21 K). This value is quantitatively consistent with estimates obtained from modeling the heat capacity and susceptibility (see below). An important factor in being able to extract the carrier density is that ρxy (shown in Fig. 4a) is linear in B at low B. We therefore find that ΔkBTK, which is quantitatively consistent with the hybridized many-body band picture4. The activated behavior can also be approximately rescaled against that measured in Ce3Bi4Pt3 (see inset of Fig. 4a)39—the only significant difference being that Ce3Bi4Pd3 has a several times smaller gap and a higher concentration of in-gap states, n0* (corresponding to 0.2% holes per Ce), than Ce3Bi4Pt3. Consistent with Ce3Bi4Pd3 having a several times smaller gap, the insulating state is found to be suppressed by magnetic fields that are several times weaker in strength than those required in Ce3Bi4Pt3 (see Fig. 4b).

Fig. 4.

Fig. 4

Magnetic field-dependent electrical transport measurements. a The Hall resistivity ρxy of Ce3Bi4Pd3 plotted versus B measured at several temperatures. The inset shows the carrier density n* (green circles) plotted versus T for Ce3Bi4Pd3 at B= 2 T (left-hand and bottom axes), estimated using n*Beρxy (not corrected for the anomalous Hall component), with the magenta line representing a fit to n*=n0*+n1*exp(ΔkBT), where n0*= 0.2 ×1026 m–3, and n1*= 3.7 ×1026 m–3 and Δ= 1.8 ± 0.5 meV. The residual value of n0* (equivalent to 2% of the Brillouin zone or ~0.2% per Ce) is smaller than the concentration of uncompensated Ce moments and magnetic impurities inferred from the susceptibility (see Methods), suggesting that the latter contribute only partly to the residual in-gap states. For comparison, the dotted line shows n* plotted versus T for Ce3Bi4Pt3 at B= 5 T (right-hand and top axes) from ref. 39. b Measured magnetoresistivity ρxx of Ce3Bi4Pd3 sample A (for B100) at different temperatures (as indicated in different colors) plotted versus B. For comparison, the inset shows the magnetoresistance of Ce3Bi4Pt3 at different temperatures.

The atypically small Kondo gap and finite concentration of in-gap states in Ce3Bi4Pd3 imply that this system lies closer to the insulator-metal threshold40 than archetypal Kondo insulators, leaving open the possibility that its Kondo insulating behavior is tuned by impurities and defects, as has been found to be the case in CeNiSn41,42. Although subsequent samples of CeNiSn prepared with fewer impurities were found to exhibit increased metallic behavior, the opposite has thus far been found in Ce3Bi4Pd340,43. Further, in nominally pure CeNiSn, a residual carrier density quantitatively similar to n0* in the inset to Fig. 4a yields a coherent metallic state with an a-axis resistivity of between 20 and 50 μΩcm or less42,44, whereas this same value of residual carrier density in Ce3Bi4Pd3 yields an insulating behavior with an electrical resistivity that is 20 to 50 times higher. Indications are therefore that the residual carriers in Ce3Bi4Pd3 are incoherent or extrinsic in contrast to CeNiSn (see Methods). Here, we consistently prepare samples of Ce3Bi4Pd3 with insulating behavior at B=0 (two examples of which are shown in Fig. 2) by polishing away surface oxidation (see Methods) and by avoiding superconducting binaries inherent to the flux technique used to grow these materials (see Supplementary Fig. 3). All samples prepared in such a manner have a thermally activated carrier density at low-magnetic fields (see Fig. 4a) of similar magnitude to that in Ce3Bi4Pt3, and have an electrical resistivity that increases with decreasing T for all T 250 K (see Fig. 2a), which includes the absence of saturating behavior at low temperatures (see Methods and Supplementary Fig. 4)45. The above observations are consistent with the finding made by way of electronic structure calculations performed in the non-interacting limit (in which the f-electrons are regarded as itinerant) that Ce3Bi4Pt3 and Ce3Bi4Pd3 both similarly exhibit a charge gap37,46, with the robustness of the Kondo gap being largely contingent upon the strength of TK.

Magnetic field-induced metallization

Metallization of the Kondo insulating Ce3Bi4Pd3 samples beyond Bc 11 T (in the limit T0) is evidenced in Figs. 1, 4b and 5 by the crossover from insulating behavior for B<Bc to metallic behavior for B>Bc. We identify metallic behavior as an electrical resistivity having a value that decreases with decreasing temperature in the limit T 0 (i.e., ρxxT>0). Further evidence for the transition or crossover from insulating to metallic behavior with the closure of the Kondo insulating gap in Ce3Bi4Pd3 is provided by Hall effect measurements at high-magnetic fields. The Hall resistivity ρxy begins to drop on the approach to Bc, which indicates an increase in carrier density in advance of the closing of the Kondo gap, likely caused by thermal excitations of carriers across the reduced gap. The nonlinearity of ρxy above Bc indicates the presence of multiple bands and a possible anomalous Hall contribution from skew scattering47 (see Methods). In the absence of a dominant anomalous Hall component from skew scattering, the positive Hall coefficient implies either that the hole carriers have numerical supremacy over electron carriers, as would be expected on the basis of band structure calculations37, or that the hole carriers are of higher mobility38.

Fig. 5.

Fig. 5

Temperature-dependent electrical resistivity measurements of Ce3Bi4Pd3. a Electrical resistivity ρxx versus T at various values of the magnetic field (as indicated) extracted from Fig. 4a. Connecting lines are a guide to the eye. b ρxx versus T2 at various values of the magnetic field (as indicated) extracted from Fig. 4a. c ρxx versus T for the same sample measured at various steady static magnetic fields (as indicated). d The same ρxx as in c versus T2. e and f Same as for c and d but measured on a different sample (as indicated). Dashed lines indicate the linearity in T2 while arrows indicate TFL (the temperature above which ρxx appears to deviate from T2 behavior). The slopes of the lines versus T2 provide an estimate of A (plotted in Fig. 1). A small departure from T2 behavior in the limit T20 is sample-dependent, suggesting it to be of extrinsic origin.

Fermi liquid behavior

On entering the high-magnetic field regime, we find the low-temperature electrical resistivity to display the Fermi liquid form ρxx=ρ0+AT2, where ρ0 is a constant and A is a coefficient proportional to the square of the quasiparticle effective mass. The quadratic-in-temperature form is demonstrated by plotting the electrical resistivity versus T2 in Fig. 5, yielding linear behavior at the lowest temperatures. The Fermi liquid temperature scale TFL, which we define as the point beyond which the resistivity is observed to exhibit a downward curvature from T2 behavior on increasing the temperature, is found to collapse on approaching Bc in Fig. 1. At the same time, A is observed to undergo a steep upturn on approaching Bc from high-magnetic fields in Fig. 1. Both the upturn in A and collapse of TFL are indicative of a collapsing Fermi liquid energy scale in the vicinity of Bc, which is one of the primary signatures of quantum criticality in Fermi liquid systems48,49. However, rather than peaking precisely at Bc, A is observed to peak at B 15 T. This is a likely consequence of the metallic contribution to the conductivity vanishing due to the collapse of the sizes of the Fermi surface pockets in the limit BBc. Other possible factors include sample inhomogeneities causing Bc to be non-uniform throughout the sample or an anisotropic gap causing the gap closure field to be momentum-space-dependent.

Magnetic susceptibility measurements

Thermodynamic evidence linking Bc to the breakdown of the Kondo coupling accompanying the closing of the gap is provided by measurements of magnetization and magnetic susceptibility in Fig. 6. A strong argument for the reduction in Kondo screening is provided by the approach of the magnetization towards saturation in the inset to Fig. 6a, which is indicative of a state in which the f-electron moments are to a large extent polarized and subject to reduced fluctuations. More directly, we find the insulator-to-metal transition or crossover near Bc to be accompanied by a low-temperature peak in the magnetic susceptibility χ in Fig. 6a, which we trace back to the peak in χ at TM along the temperature axis. On performing magnetic susceptibility measurements over a range of temperatures and magnetic fields, we construct a pseudo phase boundary from the locus of the peak that continuously connects Bc with TM within the B,T plane (see Fig. 1), revealing that Bc=B(TM0). In the low-magnetic field limit, the broadness of the peak is indicative of a crossover, yet it becomes increasingly sharp on increasing the magnetic field and reducing the temperature.

Fig. 6.

Fig. 6

Magnetization and susceptibility measurements of Ce3Bi4Pd3. a Magnetic susceptibility χ=MB versus B of Ce3Bi4Pd3 (for B100) at different temperatures (as indicated; see Methods). Vertical bars indicate the T-dependent maximum. The inset shows the magnetization M versus B. b χ versus T at different static magnetic fields (as indicated), with vertical bars indicating the maxima in the temperature dependence. Note that at B= 2 T, a shoulder rather than a peak is observed due to a low T contribution from magnetic impurities (or defects) at low B and T (see Methods). A similar low T contribution is observed in Ce3Bi4Pt3 in Fig. 2b, although, in that case, it is farther from TM.

Specific heat measurements

Further thermodynamic evidence for the magnetic field-induced closing of the Kondo gap is provided by the finding of a Schotte–Schotte anomaly in the specific heat in Fig. 3 (see also Supplementary Fig. 5), which undergoes a continuous change in shape in an applied magnetic field. A Schotte–Schotte50,51 anomaly occurs under circumstances in which a peak in the electronic density-of-states in the shape of a Lorentzian is offset from the chemical potential by a gap (see Supplementary Fig. 6 and Methods). Fits (see Fig. 3a) to the heat capacity measured at B=0 yield Δ= 1.7 ± 0.2 meV, which is in excellent agreement with Δ estimated from Hall effect measurements (see Fig. 4a). On considering B0 and fixing all parameters except geff, we find that the evolution of the Schotte–Schotte anomaly under a magnetic field can be explained solely in terms of Zeeman splitting, where geff 2.9 ±  0.3 is an effective g-factor for pseudospins of ±12. The critical magnetic field Bc therefore roughly corresponds to geffμBBΔkBTK. As a further consistency check, a similar value of the gap (Δ= 1.5 ± 0.2 meV) qualitatively accounts for the maximum in the magnetic susceptibility as a function of temperature (see Methods and Supplementary Fig. 7) and its shifting to lower temperatures under a magnetic field.

Discussion

The signatures of strongly enhanced electronic correlations in the vicinity of the critical magnetic field Bc 11 T in Figs. 1, 4, 5 and 6, and their association with an insulator-to-metal transition, are strikingly similar to those recently identified in SmB6 as a function of pressure28,31. In SmB6, the entry into the metallic phase with increasing pressure can be qualitatively understood in terms of increased tendency for magnetism accompanying a continuous increase in the valence towards a trivalent value2731. In Ce3Bi4Pd3, the polarization of the f-electron moments by a magnetic field causes the magnetic field to behave like an effective negative pressure; the lattice volume invariably increases under a magnetic field in Ce compounds52,53, causing a reduction in the valence towards a trivalent value. The relative ease by which f-electron moments are polarized by a magnetic field in Ce3Bi4Pd3 (see inset to Fig. 6a) compared to Ce3Bi4Pt354 suggests that the smaller Kondo temperature and gap in the former is a likely consequence of it lying closer to integer valence than the latter37.

While a peak in the magnetic susceptibility at Bc has been predicted to occur on closing the gap in a Kondo insulator55, along with signatures of quantum criticality, other scenarios are possible at Bc, including the case found in itinerant electron metamagnets5658. Here, quantum criticality may occur in the absence of broken symmetry due to the tuning of the highest temperature end point of a notional line of first order phase transitions to absolute zero56. Our finding of a peak in the susceptibility that becomes increasingly sharp on lowering the temperature suggests that Ce3Bi4Pd3 remains in the crossover regime, however, with the end point remaining inaccessible in the limit T0. It has yet to be determined whether this is an intrinsic property of the metal-insulator transition in Ce3Bi4Pd3 or whether it is caused by the broadening of the quasiparticle bands by defects and impurities.

An alternative possibility, given the suppression of the Kondo coupling in strong magnetic fields, is that the Kondo coupling vanishes completely at Bc59,60—in effect causing the f-electrons to behave in a more localized fashion for B>Bc. Indeed, one of the predicted consequences of a localization of the f-electrons in Ce3Bi4Pd3 (and Ce3Bi4Pt3) is a metallic state37. The metallic state induced by the localization of the f-electrons has also recently been identified by way of dynamical mean field-theory as a strong candidate for a line-node semimetal46, in which case Bc would correspond to a insulator-to-line-node semimetal transition or, potentially, a topological quantum critical point61. The collapse of the Hall resistivity to a small value for BBc is indeed consistent with the Fermi liquid regime also being semimetallic.

The contiguity between a vanishing carrier density for B<Bc and suppressed Kondo coupling for B>Bc has the potential to make the nature of the magnetic field-tuned transition somewhat unique compared to that in other d- and f-electron systems. Whether the strong correlations are caused by proximity to a metamagnetic end point or a magnetic field-induced localization of the f-electrons, in both cases the reduction in electronic correlations beyond Bc is generally expected to result in a gradual reduction in the effective mass m*57,62, or equivalently the A coefficient56,63, with increasing magnetic field. The reduction in A with increasing field in Ce3Bi4Pd3 is indeed qualitatively similar to that previously observed in d- and f-electron metamagnets (for example, Sr3Ru2O7 and CeRu2Si2)56,62,63.

Finally, there is the question of whether strong electronic correlations in proximity to a magnetic field-tuned quantum critical point contribute to the growth of the electronic contribution to the heat capacity in the vicinity of the field-induced transitions into the metallic states of the Kondo insulators Ce3Bi4Pt3 and YbB1220,21, or to the temperature dependence of the quantum oscillation amplitudes within the insulating phases of SmB6 and YbB1213,15. Our findings suggest, at the very least, that a growth of electronic interactions at the expense of a declining hybridization needs to be taken into consideration in future more complete models of the insulating state in strong magnetic fields. A further possibility is that the Kondo insulator gradually transforms into an excitonic insulator64 in advance of metallization.

Methods

Sample preparation

Ce3Bi4Pd3 crystallizes in a cubic structure of space group I4¯3d with a noncentrosymmetric unit cell that contains four formula units and a lattice parameter of a= 10.05 Å26. The crystals are grown by the Bi-flux technique with starting composition Ce:Pd:Bi = 1:1:1.8. The reagents are put in an alumina crucible placed inside an evacuated quartz tube. The quartz tube is then heated to 1050 °C at 100 °C/h and is kept there for 8 h. The solution is then cooled down to 450 °C at 2 °C/h. The excess of Bi is removed by spinning the tube in a centrifuge. The crystallographic structure is verified by single-crystal diffraction at room temperature using Mo radiation in a Bruker D8 Venture diffractometer.

The upturn in the magnetic susceptibility at low temperature indicates the presence of uncompensated Ce moments and magnetic impurities (such as other rare earths)1,3,3234, which are frequently seen in Kondo insulators. However, inclusions of other crystalline phases such as CePdBi2, which has a sharp antiferromagnetic transition at TN 6 K65, and superconducting Bi-Pd binary compounds, which have a variety of different transition temperatures Tc, can also be present. The latter include tetragonal PdBi2 (Tc= 4.25 K), BiPd (Tc= 3.7 K) and monoclinic PdBi2 (Tc= 1.73 K). The absence of a sharp feature in the heat capacity at  6 K rules out a significant presence of CePdBi2. On fitting the magnetic susceptibility to a Kondo gap plus a low-temperature Curie–Weiss term to model uncompensated Ce moments and isolated magnetic impurities (see simulations of the magnetic susceptibility below), we estimate their concentration to be equivalent to ~2% per Ce. In the case of Tb impurities, which are determined from a chemical analysis of Ce to be the leading impurity, the larger moment would imply a significantly lower concentration of 0.1%. In samples that have been polished, no significant negative contribution to the susceptibility is found that would indicate a significant presence of superconducting impurity phases within the bulk, suggesting that superconductivity seen in electrical transport measurements occurs mostly on the surface (see electrical transport experimental details below).

At this early stage of sample growth, the electrical resistivity becomes higher with improved sample quality (see e.g., the difference between early work on these samples40, this work and more recent work by another group43).

Electrical transport experimental details

Samples of Ce3Bi4Pd3 are cut into rectangular shapes and polished for electrical transport measurements. All resistivity measurements, including those in static and pulsed magnetic fields are performed using the four wire technique. Whereas freshly polished samples (green line in Supplementary Fig. 4) exhibit insulating behavior down to  2 K, thermally cycled samples exhibit additional superconductivity (red line in Supplementary Fig. 3). After re-polishing, most of the additional superconductivity is removed (blue line in Supplementary Fig. 3).

Despite the opening of a gap in the energy spectrum, Kondo insulators are prone to in-gap states that can reside either at the surface or the bulk and generally cause the electrical resistivity to acquire a finite value in the limit T 0. In a similar manner to SmB645, Ce3Bi4Pd3 is found to have an inverse resistivity ρxx1 that varies linearly in T at low temperatures (see Supplementary Fig. 4), suggesting that scattering from defects may be responsible for the departure from activated behavior at the lowest temperatures (at least down to  2 K) 45.

To delineate regions of the phase diagram where insulating ρxxT<0 and metallic ρxxT<0 are observed, the data in Fig. 5 are differentiated (see Supplementary Fig. 1) and the points where ρxxT=0 are plotted in Fig. 1.

Magnetic susceptibility experimental details

Magnetic susceptibility measurements in pulsed magnetic fields are performed using an extraction magnetometer66. Magnetic susceptibility measurements in static magnetic fields are performed using a Quantum Design vibrating sample magnetometer. Owing to isolated impurities giving rise to an upturn in the susceptibility at low temperatures1,3,3234, and the small energy scale associated with the Kondo gap in Ce3Bi4Pd3, a steady magnetic field of B 4 T is required to uncover the maximum in the susceptibility. Only a shoulder is observed at lower magnetic fields (see simulations of the magnetic susceptibility below). In a similar manner to Ce3Bi4Pt354, the magnetic susceptibility of Ce3Bi4Pd3 continues to remain large as the magnetic field is increased, which is suggestive of a band Van Vleck paramagnetism effect23.

Heat capacity experimental and modeling details

Heat capacity measurements on Ce3Bi4Pd3, made using a Quantum Design Physical Properties Measuring System, reveal a peak in the overall heat capacity centered at 5 K (see Supplementary Fig. 5). In Ce3Bi4Pt3, by contrast, a peak is observed in the heat capacity centered at 50 K20,23. The heat capacity is found to be reproducible in different samples for T 1.5 K. Features that appear below 1.5 K are sample-dependent, suggesting them to be of extrinsic origin.

A Schotte–Schotte anomaly occurs when a peak in the electronic density-of-states in the shape of a Lorentzian is offset by an energy gap Δ relative to the chemical potential (see Supplementary Fig. 6a). In the single impurity limit, the width 2W of the Lorentzian is compared to the Kondo temperature. However, it will also include the effect of quasiparticle scattering from nonmagnetic defects and impurities. While earlier it had been assumed that the Kondo gap is symmetric with respect to the chemical potential (at ε=0)20, band structure calculations of Ce3Bi4Pt3 and Ce3Bi4Pd3 have indicated an asymmetric gap with flat bands situated just below the chemical potential37. Flat bands are also situated above the chemical potential, but are considerably further away in energy. Given what is known about the electronic structure, we model the Schotte–Schotte anomaly using an electronic density of states of the form

D(ε)=D0σ=±12Wπ(W2+(ε+Δ+σgeffμBB)2), 1

where σgeffμBB represents Zeeman splitting. Here, σ represents pseudospins of ±12 while geff is an effective g-factor. The free energy given by F=kBTD(ε)ln[1+exp(εkBT)]dε while the heat capacity given by CpCv=T2FT2v, which we calculate numerically67 and fit to the experimental data over the temperature range 1.5 T 10 K. During fitting, we assume a phonon contribution CphT=βT2 where β= 1 mJ mol–1 Ce–1 K–4. It is important to note, that on fitting to the Schotte–Schotte model, one cannot distinguish whether Δ is positive (corresponding to a peak below the chemical potential) or whether it is negative (corresponding to a peak above the chemical potential), or whether there are peaks located at both ±Δ as has sometimes been assumed20.

We initially fit the data only at B=0, from which we obtain Δ= 1.7 ± 0.2 meV, which is comparable to the value estimated from Hall effect measurements (see Fig. 4a), and W= 1.1 ± 0.2 meV. For B0, we hold D0, W, and Δ constant and allow only geff to vary. Zeeman splitting alone, with geff= 2.9 ± 0.3, is able to explain the evolution of the Schotte–Schotte peak under a magnetic field. ΔW 0.6 meV (7 K) is of comparable order to the reduced gap estimated from the slope of the Arrhenius plot in the inset to Fig. 2a.

A distinguishing feature of the Schotte–Schotte anomaly that appears to be present in the experimental data (see Fig. 3 and ref. 40) is an electronic contribution to the heat capacity of the form

CelTγ0+(ββ)T2 2

(see Supplementary Fig. 5b) in the limit T0, where (ββ)T2 exceeds the contribution βT2 from phonons and where γ0 is the Sommerfeld coefficient characterizing in-gap states (that also depends on the strength of the magnetic field)67. Supplementary Fig. 5b shows that Ce3Bi4Pd3 exhibits the form given by Eq. (2) in the limit T0, with γ0 increasing by 30 mJmol1K2 on increasing the magnetic field from 0 to 4 T. A comparable increase was reported in Ce3Bi4Pt3 on increasing the magnetic field from 0 to 40 T20.

The observed consistency with the Schotte–Schotte model therefore includes (i) a peak at 5 T, (ii) a residual electronic contribution γ0 and (iii) a magnetic field-dependent low- temperature behavior of the form CelTγ0+(ββ)T2 (see Supplementary Fig. 5 and Methods). It remains to be determined to what extent the Lorentzian line-shape (of halfwidth W= 1.1 ± 0.2 meV) is intrinsic (e.g., related to the Kondo coupling and electronic bandwidths) or affected by quasiparticles scattering from defects and impurities.

Simulations of the magnetic susceptibility

As a further consistency check, we show that similar parameters as used in the modeling of the heat capacity also provide a qualitative explanation for the approximate location of the peak in the susceptibility as a function of temperature and its suppression to lower temperatures as the magnetic field is increased. We calculate the susceptibility using

χ=CD(ε)fFD(ε)dε, 3

(valid for low-magnetic fields) where fFD(ε) is the derivative of the Fermi-Dirac distribution function and C is a constant renormalized to the experimental susceptibility at 300 K, the results of which are plotted in Supplementary Fig. 7. Equation (3) does not include the low-temperature Curie–Weiss-like contribution from impurities and defects. Partly for this reason, it overestimates the the initial growth in the susceptibility with increasing field. The model performs poorly once B~Bc, however, which is likely a consequence of electronic correlations not being included. Electrical transport measurements indicate electronic correlations to be important in the vicinity of Bc. On comparing the calculated peaks in the susceptibility (B<Bc) with those obtained in Fig. 6b, we estimate Δ= 1.5 ± 0.2 meV and geff= 2.7 ± 0.2 from the susceptibility.

To obtain a rough estimate of the concentration of uncompensated Ce moments and magnetic impurities, we fit the low-temperature portion of the magnetic susceptibility at 0.1 T (inset to Supplementary Fig. 7) to χfit=(1f)χ+fχimp, where f is the volume fraction of impurities, χ is the susceptibility given by Eq. (3) and χimp corresponds to the impurity concentration. We model this by assuming a modified version of χ in which D(ε) is replaced by a delta function (for simplicity, we assume the total number of states D(ε)dε and effective g-factor are the same as used in modeling the Kondo gap). We estimate f~ 2%.

Anomalous Hall effect estimate

We estimate the anomalous Hall effect contribution from skew scattering within the high-magnetic field metallic phase using ρxyA=γχ~ρxx47, where γ~ 0.08 KT–1 is a typical value of the coefficient for Ce compounds47. At B=0, the reduced susceptibility is χ~χ5TpeakC 0.03 K–1, but this falls to 0.014 K–1 at 60 T. Using ρxx 160 μΩcm at 60 T, we obtain ρxyA~ 1.5 × 10–8Ωm at 60 T, which is ~10% of ρxy.

Supplementary information

Peer Review File (163.3KB, pdf)

Acknowledgements

This high-magnetic field work was supported by the US Department of Energy “Science of 100 tesla” BES program. S.K.K. acknowledges support of the LANL Directors Postdoctoral Funding LDRD program. Sample characterization at Los Alamos National Laboratory was performed under the auspices of the U.S. Department of Energy, Office of Basic Energy Sciences, Division of Materials Sciences and Engineering, “Quantum Fluctuations in Narrow Band Systems” project. The high-magnetic field facilities of the National High-Magnetic Field Laboratory—PFF facility and related technical support are funded by the National Science Foundation Cooperative Agreement Number DMR-1157490 and DMR-1644779, the State of Florida and the U.S. Department of Energy. We acknowledge helpful discussions with Mucio Continentino, Peter Riseborough, Chao Cao, Jianxin Zhu, Qimiao Si. and Peter Wölfle. M.K.C. acknowledges support by the Laboratory Directed Research and Development program of Los Alamos National Laboratory under project number 20180137ER in conducting experiments on Kondo insulators. N.H. acknowledges support from the Los Alamos National Laboratory LDRD program: project number 20180025DR.

Author contributions

S.K.K., M.K.C., J.P., S.M.T., and N.H. performed the measurements. P.F.S.R. and E.D.B. grew and characterized the samples. S.K.K., N.H., and P.F.S.R. wrote the manuscript. J.D.T. and F.R. assisted with the interpretation of the experimental data.

Data availability

The data presented in this manuscript is available from the corresponding author on reasonable request.

Competing interests

There are no competing interests.

Footnotes

Peer review information Nature Communications thanks Andrea Bianchi, Toshiro Takabatake and the other, anonymous, reviewer(s) for their contribution to the peer review of this work. Peer reviewer reports are available.

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Supplementary information is available for this paper at 10.1038/s41467-019-13421-w.

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Supplementary Materials

Peer Review File (163.3KB, pdf)

Data Availability Statement

The data presented in this manuscript is available from the corresponding author on reasonable request.


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