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. 2020 Dec 18;10:22288. doi: 10.1038/s41598-020-79017-3

Field-dependent specific heat of the canonical underdoped cuprate superconductor YBa2Cu4O8

Jeffery L Tallon 1,, John W Loram 2
PMCID: PMC7749183  PMID: 33339851

Abstract

The cuprate superconductor YBa2Cu4O8, in comparison with most other cuprates, has a stable stoichiometry, is largely free of defects and may be regarded as the canonical underdoped cuprate, displaying marked pseudogap behaviour and an associated distinct weakening of superconducting properties. This cuprate ‘pseudogap’ manifests as a partial gap in the electronic density of states at the Fermi level and is observed in most spectroscopic properties. After several decades of intensive study it is widely believed that the pseudogap closes, mean-field like, near a characteristic temperature, T, which rises with decreasing hole concentration, p. Here, we report extensive field-dependent electronic specific heat studies on YBa2Cu4O8 up to an unprecedented 400 K and show unequivocally that the pseudogap never closes, remaining open to at least 400 K where T is typically presumed to be about 150 K. We show from the NMR Knight shift and the electronic entropy that the Wilson ratio is numerically consistent with a weakly-interacting Fermion system for the near-nodal states. And, from the field-dependent specific heat, we characterise the impact of fluctuations and impurity scattering on the thermodynamic properties.

Subject terms: Materials science, Physics


Both the pseudogap13 and the origins of superconductivity in the cuprates remain enigmatic and a source of continuing dispute, especially the former4. Still there is no consensus as to the pseudogap’s phenomenology, at what doping the ground-state pseudogap ultimately vanishes, whether it really does close at T, whether this closure might be a thermodynamic phase transition511 and whether it is causatively related to superconductivity4. The electronic specific heat captures the entire spectrum of low-energy excitations and in principle can adjudicate in all these matters. The key experimental challenge is to separate the electronic term from the much larger phonon term. In many previous experiments1214 and in the present report this can be done using a differential technique in which the specific heat is measured relative to a reference sample which, if closely related to the sample itself, automatically backs off most of the phonon contribution. The residual phonon contribution can be identified and removed by measuring a series of doping states in which the residual is found to scale linearly with the mass change of the doping process, usually changing oxygen content. Further details are given under “Methods”.

Electronic specific heat coefficient

The measured electronic specific heat coefficient, γ(T)CP(T)/T is shown in Fig. 1a for YBa2Cu4O8 (Y124) with 0%, 2% and 4% planar Zn concentration at nine different applied fields, as annotated. As discussed later, the data extends to an unprecedented 400 K but we focus first on the transitions into the superconducting state. Because Zn substitutes only on the CuO2 planes and not on the chains15 these compositions correspond to YBa2Cu4-yZnyO8 with y= 0, 0.04 and 0.08. It is immediately evident that Tc is rapidly suppressed by Zn substitution (as observed previously in other cuprates16) and along with this a rapid reduction in the jump height at Tc, Δγc. At the same time there is a rapid suppression in Δγc with applied field that becomes more extreme in the Zn-substituted samples. Further, at low T, γ(T) fans out to higher values with applied field in the ‘pure’ sample but not appreciably in the doped samples. This is due to the Volovik effect17—the field-induced pairbreaking at the nodes due to Doppler shift of quasiparticle energies, as discussed below.

Figure 1.

Figure 1

(a) The measured electronic specific heat coefficient γ(T) for YBa2Cu4O8 for 0%, 2% and 4% planar Zn concentration at 0, 1, 2, 3, 5, 7, 9, 11 and 13 tesla. The same colour coding is used for each sample. Inset: the same data plotted versus ln(T) highlighting the impurity scattering term (dotted lines). (b) the same data with the impurity term subtracted. The black dashed curve is the fitted normal-state specific heat coefficient, γn which satisfies entropy balance.

The most notable feature, however, is the low-T upturn due to impurity scattering. The inset to Fig. 1a shows γ(T) plotted versus ln(T) and this reveals a common underlying energy scale given by the convergence of the dashed lines at 38 K. The dashed lines are subtracted from the raw data to give the γ(T) versus T plot in panel (b) and it is this that we proceed to analyze. (There is a small anomaly at 18 K, present in the Zn-doped samples but very weak in the pure; and another at 120 K, present only in the pure sample. The sample variability indicates unidentified impurities and these anomalies are ignored in the following).

Our first task is to identify the normal-state coefficient, γn, that would occur in the absence of superconductivity. This is very much constrained by the displayed data for γ(T) because γn must follow each of the three data sets above their respective Tc values. This is the black dashed curve. It is further tightly constrained by the requirement for entropy balance. Because the area under a γ(T) curve is entropy then integrating γ(T) from T=0 to some T0>Tc must give the same result as integrating γn(T) from T=0 to T0. The fit function which satisfies these two requirements is

γn(T)=1.931-0.913tanhαE2kBTln[cosh(E/2kBT)]E/2kBT 1

where E=13.44 meV (or T=E/kB=156 K) and the exponent α=1.7. The general form of this equation for γ(T) arises analytically from inserting into Eq. (3), below, a triangular gap in the density of states (DOS) with a finite DOS at the Fermi level3. The amplitude 0.913 (being less than unity) reflects the finite DOS at EF. This residual DOS is manifested in the finite value of γn(0)=0.183 mJ/g.at.K2 and is a signature of the ungapped Fermi arcs, or hole pockets, of a reconstructed Fermi surface18,19.

T=156 K is typical of values reported for Y124 from transport20 and NMR relaxation21 measurements but we emphasize this reflects an energy scale not a temperature4. An important implication of Fig. 1 is that there is no coupling between superconductivity and the pseudogap in the sense that the onset of superconductivity does not weaken the pseudogap. This is evident from the fact that a single γn(T) curve fits all three samples i.e. γn(T) is the same for 4% and 0% Zn even in the temperature range below Tc for 0% Zn so that the onset of superconductivity in the latter case does not alter the underlying pseudogap energy scale, E. Close scrutiny of the k-dependent gap in Bi2212, as measured by angle-resolved photoelectron spectroscopy (ARPES)22, (which allows separation of the antinodal pseudogap from the nodal superconducting gap on the Fermi arcs) confirms that the pseudogap amplitude does not alter on cooling below Tc.

NMR Knight shift and entropy

Next, we note that the spin susceptibility and electronic entropy are closely related. To see this consider the entropy for a weakly-interacting Fermi liquid23:

Sn=-2kB-[fln(f)+(1-f)ln(1-f)]N(E)dE 2

where f(E) is the Fermi function and N(E) is the electronic DOS for one spin direction. This is just a weighted integral of the DOS with the ‘Fermi window’ [fln(f)+(1-f)ln(1-f)].

On the other hand, the spin susceptibility for a weakly-interacting Fermion system is:

χs=-2μB2-f(E)EN(E)dE, 3

Therefore, like the entropy, the susceptibility is an integral of the DOS where the Fermi window is now the function f/E. It turns out that Tf/E is essentially identical to [fln(f)+(1-f)ln(1-f)] if χs in the former is stretched in temperature by a factor 1.18724. It is therefore not surprising that S/T and χs are related. This relationship is expressed by the Wilson ratio, aW, such that S(T)/T=aWχs(T), where

aW=13μ0πkB2μB2 4

We will now test this relationship in the present case of Y124. By integrating γn(T) from T=0 to T we obtain the normal-state entropy and this is plotted as Sn(T)/T by the black dashed curve in Fig. 2. For fully-oxygenated Y123 Sn(T)/T is essentially independent of temperature25, reflecting the fact that the pseudogap has closed at maximal doping (p0.19 holes/Cu). But for Y124 there is a large pseudogap present which suppresses S/T at low T. This is also seen in the T-dependent NMR Knight shift which is linearly related to the spin susceptibility. To illustrate, we show in Fig. 2 the 17O Knight shift, referenced to the chemical shift, as reported by Tomeno et al.26. These authors also report the bulk susceptibility as a function of the Knight shift, thus enabling calibration of the spin susceptibility from the Knight shift. As a final step we multiply the spin susceptibility by the Wilson ratio, aW, in order to express the T-dependent part of the Knight shift in entropy/T units.

Figure 2.

Figure 2

Dashed curve: the normal-state entropy coefficient, Sn(T)/T, obtained by integrating the dashed curve for γn(T) in Fig. 1b. Red and black data points: the spin susceptibility, χs(T), calculated from the planar oxygen Knight shifts 17K2,c and 17K3,c associated with the O2 and O3 oxygen sites. χs(T) is expressed in entropy units by multiplying by the Wilson ratio, aW, for weakly interacting Fermions. The green connected data points are the difference in O2 and O3 spin susceptibilities obtained from 17K2,c-17K3,c, showing the abrupt onset of nematic splitting at 200 K within the pseudogap state. The inset shows the cuprate phase diagram with the three red data points of Sato et al.10 marking the onset of nematicity in Y123. The blue star marks the onset of nematic splitting of the O2 and O3 Knight shifts in Y124.

It can be seen in Fig. 2 that, not only the shape, but the absolute magnitude concurs remarkably well with the derived Sn(T)/T suggesting, as already noted for the bulk susceptibility27, that the near-nodal states are consistent with a weakly interacting Fermionic system. Of especial interest is the fact that the O2 and O3 Knight shifts begin to diverge below 200 K. The difference in shift, 17K2,c-17K3,c, expressed in entropy units, is also shown in the figure (10×). This shows an abrupt onset in nematicity, consistent with that reported by the Matsuda group10 using torque magnetometry. Its location at (p = 0.13, T = 200) is precisely consistent with the three data points in the (p, T) plane reported by the Matsuda group for Y123. (For the doping state of 0.13 see “Materials”). These are plotted in the inset to Fig. 2 by the red data points. Their susceptibility data was presented as evidence for a thermodynamic “phase transition at the onset of the pseudogap” however it is clear from Fig. 2 that the pseudogap is already open far above Tnematic, having already depleted half of the spin susceptibility. We observe no anomaly in γ(T) at or near 200 K to suggest a phase transition. It must be very weak. We will see below that the pseudogap in fact extends at least to well above 400 K. Consequently this nematic phase transition occurs within a preexisting pseudogap state that extends far above and is not a transition into the pseudogap state, contrary to what has been claimed10.

Volovik effect

We now consider the field-dependent low-T behaviour of γ(T) for the pure sample. Figure 3 shows γ(T,H) plotted as a function of μ0H for T = 6, 8, 10, 12 and 14 K. Above 1 tesla the behaviour is linear, consistent with the expected phenomenology of the Volovik effect. Such behaviour has been seen in the specific heats of single-crystal Y12328 and La2-xSrxCuO429, and in interlayer tunneling in Bi221230. For d-wave symmetry, in the superconducting state the finite ground-state specific heat coefficient is29

Δγ(H,0)=4kB23ħπϕ0nVM15daħkF2Δ0μ0H, 5

in units of mJ/g.at.K2, where VM is the molar volume, d the unit cell length, ϕ0 the flux quantum, Δ0 is the antinodal amplitude of the d-wave gap, and kF the Fermi wave vector at the node along the (π,π) direction. For Δ0= 30 meV the dash/dot line in Fig. 3 shows the expected slope. The data is very consistent with this expectation. The averaged slope of 0.0443 mJ/g.at.K2T1/2 implies a gap amplitude of Δ0= 34 meV. We have used the value kF=0.436×1010 m-131.

Figure 3.

Figure 3

The measured low-temperature specific heat coefficient, γ(T,H) for pure Y124 plotted as a function of field for T = 6, 8, 10, 12 and 14 K. Above 1 tesla the data is essentially linear, consistent with the Volovik effect17. The black dash/dot line shows the expected slope for Δ0=30 meV.

Free energy and superconducting gap

Figure 4a shows the normal-state and superconducting state entropy below 100 K obtained by integrating γn(T) and γs(T), respectively (as displayed in Fig. 1b) from 0 to T. The curves shown are for pure Y124 in zero field and they are denoted Sn(T) and Ss(T), respectively. The difference is the condensation entropy ΔSns=Sn(T)-Ss(T). This is plotted underneath for fields of μ0H = 0, 1, 3, 5, 7, 9, 11 and 13 T, colour-coded as in panel (b). Clearly the condensation entropy is rapidly suppressed in field. Another feature of note is the presence of fluctuations around Tc which broaden the transition somewhat. This will be discussed later.

Figure 4.

Figure 4

(a) The normal-state entropy, Sn(T), obtained by integrating the black dashed curve in Fig. 1b and the measured entropy, Ss(T), for pure Y124 in zero field. The condensation entropy, ΔSns=Sn(T)-Ss(T) is shown underneath for μ0H = 0, 1, 3, 5, 7, 9, 11 and 13 T colour-coded as in (b). (b) The T-dependence of the condensation free energy ΔFns=Fn-Fs for pure Y124 obtained by integrating ΔSns(T) from above Tc for each field as annotated. Below these are shown the condensation energy for the 2% Zn and 4% Zn samples showing a rapid suppression with scattering and applied field. The condensation energy for fully-oxygenated Y123 is also shown and is much higher.

By integrating ΔSns(T) from a temperature T0, sufficiently above the fluctuation regime that ΔSns(T0)=0, down to a temperature, T, one obtains the condensation free energy ΔFns(T). However, a more efficient way of calculating the condensation free energy using just a single integration is given by:

-ΔFns(T)=T0TTΔγns(T)dT-TT0TΔγns(T)dT, 6

where the first term is the condensation internal energy, -ΔUns(T), and the second term is the condensation entropy term, TΔSns(T). The condensation free energy calculated in this way is plotted in Fig. 4b for 0%, 2% and 4% Zn and for the various annotated fields. ΔFns(T) and its components ΔUns(T) and -TΔSns(T) are plotted in Fig. 5. Also plotted in Fig. 4b is the condensation energy for fully oxygenated Y123 which rises to a ground-state value of 3400 mJ/g.at—a full six-fold greater than for pure Y124. This shows the full impact of the pseudogap for Y124 in weakening superconductivity. Also evident is the dramatic effect of impurity scattering in further reducing the condensation energy (which is particularly marked in underdoped cuprates where the pseudogap is present16). ΔFns(0) for the 4% Zn-doped sample in zero field is just 28 mJ/g at—125 times smaller than for pure Y123. The curves for 2% Zn are dashed below 30 K and this is because ΔSns(T) is a little noisy at low T and in some cases does not fall exactly to zero, as it must. We find the first 20 K of the data scales precisely with ΔSns(T) for the 0% Zn sample, and so we assumed that this scaling continues down to T=0 thus enforcing ΔSns(T) to fall to zero as T0. Any errors introduced are very small—of the order of the thickness of the curves and of no consequence in the following analysis.

Figure 5.

Figure 5

(a) The T-dependence of ΔFns(T) and its components ΔUns(T) and -TΔSns(T) calculated from Eq. (6) using γn-γs as given in Fig. 1. Most notable is the persistence of fluctuations high above Tc in both ΔUns(T) and -TΔSns(T) and the almost complete suppression in ΔFns(T). (b) The superconducting order parameter, Δ(T), calculated from 2ΔUns(T)-TΔSns(T) using Eq. (7) for 0% and 2% Zn at fields given by the colour coding in panel (a).

As mentioned, Fig. 5a shows ΔFns(T) and its components ΔUns(T) and -TΔSns(T). It is striking that fluctuations persist high above Tc in both ΔUns(T) and -TΔSns(T) while they are almost completely cancelled in ΔFns(T). The superconducting gap function Δ(T) may be calculated from these components of the free energy using32

ζN(0)Δ(T)2=2ΔFns(T)+TΔSns(T)2ΔUns(T)-TΔSns(T) 7

where ζ = 1 for s-wave and 1/2 for d-wave. The calculated Δ(T) values are plotted in Fig. 5b. The gap is the magnitude of the order parameter, Δ, rather than the spectral gap, Δ, which is higher13. Roughly speaking, Δ0=Δ02-E213. From the impurity suppression of superfluid density40 we estimate Δ023.4 meV while from the high-T entropy suppression we determine E19.1 meV. The quadratic relation above then implies Δ0=13.5 meV, very consistent with the values in Fig. 5b. The values of Δ(T) are seen to descend towards zero at Tc then persist with a more slow decline above Tc. Here the pairing is incoherent33,34 and is a feature of the strong superconducting fluctuations above Tc.

Comparison of Y124 with Y123

It is highly instructive to compare the measured data for Y124 with that for Y123. This is shown for γ(T) in Fig. 6a and for S(T) in Fig. 6b. The Y123 data is taken from ref.24 which, in contrast to earlier reports13,35, includes a small correction for the background DOS in the undoped state. We also show the entropy-conserving normal-state functions as well. Two features are prominent. (1) the size of the specific heat jump for Y124 is much smaller than for Y123 due to the presence of the pseudogap in the former. (2) while the γ(T) curves converge above Tc the S(T) curves remain separated and parallel to the highest temperature. This is clear evidence that the pseudogap remains present in Y124 to the highest temperatures measured—here 400 K.

Figure 6.

Figure 6

Comparison of (a) γ(T) and (b) S(T) for Y124 with nearly fully-oxygenated Y123. At highest oxygenation, x=0.97, a double transition (see side-hump) is observed while a small depletion, x=0.92, sees these merge into a single transition with a larger peak size. Above Tc the γ(T) curves merge while for S(T) they remain separated. The inset in (a) shows the double-peaked Fermi window, F/T, for calculating γ(T) using Eq. (2), where F(E,T)=[fln(f)+(1-f)ln(1-f)]. The window is centred on a normal-state triangular gap in the DOS (red lines) located at EF. The blue, purple and olive-green curves show F/T for temperatures kBT=0.1E, 0.3E and 1.0E, respectively. The inset in (b) shows the single-peaked Fermi window, F(E,T), for calculating entropy, again centred on a triangular gap in the DOS.

To see this, consider the Fermi window for the entropy given in Eq. (2). This is the single-peaked function shown in the inset to Fig. 6b. Three different temperatures of 0.1, 0.3 and 1.0 E/kB are displayed, where E is the magnitude of the triangular gap shown in the figure as a representation of the pseudogap. Provided that the pseudogap remains open, this Fermi window always sees the gap and at higher temperatures loses a fixed fraction of states so that S(T) is displaced down in parallel fashion relative to that for Y123—as evidenced in Fig. 6b, and again in Fig. 7b. In contrast, because γS/T, the Fermi window for γ(T) is the T-derivative of that for S(T). This is a double-peaked function as shown in the inset to Fig 6a. It can be seen that at high enough temperature this Fermi window falls outside of the gap. Therefore γ(T) recovers its full ungapped magnitude at high T, despite the presence of the gap. The data in Fig. 6a,b are entirely consistent with this picture. The two systems have essentially the same background DOS. In the normal-state Y123 is ungapped while Y124 is gapped to the highest temperature as evidenced by the parallel suppression of S(T). If the gap were to close with increasing T then S(T) for Y124 would recover to that for Y123. It does not. By extrapolating S(T) back to the ordinate axis one can read off the normal-state gap magnitude. For a triangular gap, as in the insets to Fig. 6, but with a finite DOS of N1 at EF and a constant DOS of N0 above E this negative intercept is 2ln2kB(N0-N1)VME, where VM is the molar volume. The finite value of γn at T=0 is given by γn0=4ln2×2.374kB2N1VM, while at high T we have γn=(2/3)π2kB2N0VM. From these we obtain E=19.1 meV and N0=6.14×10-3 states/meV/cell.

Figure 7.

Figure 7

(a) 89Y NMR Knight shift for YBa2Cu3O6+x as reported by Alloul et al.36 with x values annotated. Also shown is the MAS 89Y NMR Knight shift and the scaled T variation of 1/T1 for YBa2Cu4O8 as reported by Williams et al.39. (b) Y123: Entropy S (blue solid curve24), aW89χsT (purple squares36) and bulk susceptibility aWχsT (purple dashed curve24) for Y123 at nearly full oxygenation. Y124: entropy S (red solid curve—this work), aW89χsT (red spheres37) and T/63T1 (open black triangles21,39) for Y124. Then, as a proxy for Y124: aW89χsT for Y123 with x=0.75 (solid green triangles—Alloul36); and aWχsT for Y123 with x=0.73 (dashed green curve—Loram24).

High-temperature susceptibility and entropy

We now extend this comparison to 400 K, a range never previously achieved in differential measurements. We combine this data with 89Y Knight shift data, bulk susceptibility measurements and 1/63T1 data in such a way that demonstrates, individually and collectively, the persistence of the pseudogap to 400 K and beyond. 89Ks(T) probes the spin susceptibility of the CuO2 planes that sandwich the Y atom in Y123 and Y12436. The 89Y nucleus has the additional benefit of having no quadrupole moment so there is no quadrupole splitting of the resonance arising from electric field gradients. Further, the use of magic-angle spinning (MAS) enables extremely narrow line widths as will be used below37. The 1/63T1 relaxation rate is a weighted sum over q of the imaginary part of the spin susceptibility, χ(q,ω), where, for the 63Cu nucleus, the weighting form factor is strongly enhanced near the antiferromagnetic wave vector, q=(π,π)38 and hence 1/63T1 is dominated by the antinodal pseudogap.

Figure 7a shows the 89Y Knight shift 89Ks(T) for YBa2Cu3O6+x as reported by Alloul et al.36, with values of x annotated. Also plotted is MAS 89Ks for samples of Y124 from our laboratory39 (red spheres), along with the 1/63T1 data from Raffa et al.21 (up triangles) which we showed39 scales precisely with 89Ks, as can be seen. (The conversion scale is 89Ks=48.8×1/63T1-164.5.) Notably, there is an excellent match over the entire temperature range with Alloul’s data for x=0.75 (green up-triangles) where the doping state (0.13) and Tc for Y123 are much the same as those of Y124. As in Fig. 2, we convert 89Ks to spin susceptibility using the calibration of Alloul et al.36 (see “Methods” for more detail) and multiply by aW to express in S/T units. We find an excellent agreement between Alloul’s 89Ks and the measured entropy for Y123 across a wide range of doping and temperature (see Fig. S4 in Supplementary Information, SI).

In Fig. 7b, we assemble four distinct data sets (S, 89Ks, 1/63T1, and χs from the bulk susceptibility) for Y123 at near full oxygenation (x=0.97), and for Y124. All are expressed in entropy units, in this case using the factor aWT to convert susceptibilities (including the 1/63T1 data expressed as a susceptibility). The χs data is shown for Y123 with x=0.97 and x=0.73 (purple and green dashed curves, respectively, the latter as a proxy for Y124) and is taken from Loram et al.24. Evidently S (blue solid curve), aW89χsT (purple squares) and aWχsT (purple dashed curve) for Y123 at full oxygenation all track linearly to the origin indicating the absence of the pseudogap. For Y124 on the other hand, S (red solid curve—this work), aW89χsT (red spheres) and T/63T1 (open black triangles), together with Alloul’s aW89χsT (solid green triangles) for Y123 with x=0.75 and aWχsT (dashed green curve) for Y123 with x=0.73, both as proxies for Y124, all reveal a linear high-temperature behaviour that extrapolates to a negative intercept on the y-axis indicating the presence of a gap—the pseudogap. For Y124 the entropy curve almost completely overlays the bulk susceptibility green-dashed curve which is barely visible, so the figure is reproduced in the SI with the green-dashed curve overlaying the entropy. Evidently, the agreement over the full temperature range is excellent. Importantly, our entropy data extends to 400 K as does the χs data, and the 89Ks data extends to 370 K. Figure 7b represents the central result of this work. There is no indication, at any temperature, of the entropy recovering to the gap-less curve observed for fully-oxygenated Y123 that would signify the closing of the pseudogap at, or around, some T value. The small upturn in S(T) near 400 K simply represents the limitations of the present differential technique at such a high temperature and is not seen in the χs data. We conclude that the pseudogap does not close at some postulated T in the range 150–200 K but remains open to the highest temperature investigated—400 K. A similar conclusion has recently been drawn from 1/17T1 planar oxygen NMR relaxation data for a number of cuprates41. We showed the same long ago3 for the in-plane resistivity and similarly for the c-axis resistivity4,42.

Scattering resonance

Finally, we wish to discuss the upturn in the raw γ(T) data at low T seen in Fig. 1a. This is in fact a peak rather than an upturn and may be identified with an impurity resonance43. Scanning tunneling spectroscopy (STS) measurements in lightly Zn-doped Bi2Sr2CaCu2O8+δ reveal resonance spots in spatial maps at low energy and low temperature43. Away from these spots, tunneling spectra reveal a well-formed d-wave superconducting gap with sharp coherence peaks. Tunneling spectra collected on the spots (the location of individual Zn atoms) show a nearly full suppression of both the gap and the coherence peaks with, instead, a sharp resonance appearing at εr=-1.5 meV. To calculate the entropy contribution arising from this resonance we replace the DOS in Eq. (2) by a delta function, N(E)=Nrδ(ε-εr). The equation integrates to give:

Δγres=Aresεr2kBT3cosh-2εr2kBT 8

where the amplitude Ares=4kB2/εrNr.

In view of the relationship between entropy and spin susceptibility discussed above, it is highly instructive to contrast this resonance component of γ(T) with that of the susceptibility. Again, replacing the DOS in Eq. (3) by N(E)=Nrδ(ε-εr) we find:

χs,res=Bresεr2kBTcosh-2εr2kBT 9

where the amplitude Bres=μB2/2εrNr. The interesting point in relation to Eqs. (8) and  (9) is that Δγres falls off rapidly as T-3 while χs,res falls off more slowly as T-1. This is borne out by our experimental data. Experimental evidence from the magnetic susceptibility for a Zn-induced resonance within the pseudogap was discussed previously in relation to Y12415 and La2-xSrxCuO444.

Figure 8 shows the as-measured field-induced change in specific heat coefficient, Δγ(13,T)=γ(13,T)-γ(0,T). Recall that this difference contains no correction for the residual phonon contribution so is free of any imposed model. As well as the suppression of fluctuations around the specific heat anomaly near Tc the low-temperature resonance is evident. We fit this using Eq. (8) with the parameters Ares=0.61 mJ/g.at.K2 and εr=-1.55 meV, the latter value being nicely consistent with the STS result for Bi2Sr2CaCu2O8+δ43. This fit is the red curve in Fig. 8 and the difference is shown by the blue curve. The calculated resonance response is an excellent fit and shows the rapid decay at higher temperatures associated with the T-3 tail. The difference is close to entropy conserving and requires a straightforward extrapolation below 2.8 K of its trend above 2.8 K to achieve exact entropy conservation. This rapid decay of the resonance in γ(T) contrasts the predicted much slower T-1 decay in the resonance part of the spin susceptibility. We have previously investigated the 89Y NMR Knight shift in Zn-doped Y12415. The Zn resonance contribution to the spin susceptibility is seen in a satellite peak which has a slowly-decaying Curie temperature dependence observable all the way up to 300 K, thus nicely confirming the behaviour predicted by Eq. (9).

Figure 8.

Figure 8

Black curve: the as-measured field-induced differential specific heat coefficient, Δγ(13,T)=γ(13,T)-γ(0,T). Red curve: resonance γ(T) as calculated using Eq. (8). The blue curve is the difference, which, below 2.8 K, is extrapolated to a finite value as T0 to ensure overall entropy conservation.

Conclusions

In conclusion, we have measured the electronic specific heat of YBa2Cu4-xZnxO8 using a precision differential technique that allows separation of the electronic term from the lattice term up to an unprecedented 400 K. The pure sample reveals the expected Volovik effect which is fully suppressed in the Zn-doped samples. We show that the pseudogap, characteristic of underdoped cuprates, always remains open to above 400 K, far above the nominal pseudogap onset temperature usually proposed, T 150–200 K. Weak thermodynamic transitions reported at T, for example the onset of susceptibility nematicity, occur within the already fully established pseudogap and are not transitions into the pseudogap state as widely claimed. The spin susceptibility, derived from the 17O and 89Y Knight shift and expressed in entropy units, is numerically the same as the electronic entropy divided by temperature, indicating that the near-nodal states are those of weakly-interacting Fermions. We derive the field-dependent condensation energy and superconducting energy gap. These expose the presence of strong pairing fluctuations extending well above Tc as well as canonical impurity scattering behaviour, including the expected low-temperature resonance response which in the entropy channel decays rapidly as T-3, but in the spin channel decays slowly as T-1. The measurements and analysis reveal the remarkable utility of the differential specific heat technique in exposing the rich physics of strongly-correlated electronic materials.

Methods

Materials

The samples were prepared from stoichiometric proportions of high purity Y2O3, dried Ba(NO3)2, ZnO and CuO, pressed as pellets and reacted for 16 h at 935C under an oxygen pressure of 60 bar. The samples were ground finely and the process repeated three more times. X-ray diffraction revealed single-phase YBa2Cu4O8 (see Supplementary Fig. S1) with impurity less than 2% (only CuO identified). Lattice parameters were found to be a=0.3842 nm, b=0.3870 nm, and c=2.7235 nm under Ammm symmetry with a preferred alignment of the c-axis normal to the plane of the pellets. The Tc values, determined from sharp diamagnetic onset were 81.2 K (0% Zn), 51.8 K (2% Zn) and 29.2 K (4% Zn). The quoted Zn concentrations are those referred to the CuO2 plane as essentially no Zn resides on the chains. Thus 2% Zn refers to the composition YBa2Cu3.96Zn0.04O8 and 4% refers to YBa2Cu3.92Zn0.08O8. Thermoelectric power measurements at 290 K give 6.95 μV/K (0% Zn), 6.89 μV/K (2% Zn) and 6.93 μV/K (4% Zn). From the correlation of thermoelectric power with doping45 this amounts to essentially identical doping states of 0.130 holes/Cu for each.

The suppression of Tc with Zn substitution is very much in line with that for underdoped Y123 at the same doping state. Supplementary Fig. S2 shows Tc as a function of doping for 0, 2, 4 and 6% planar Zn substitution for Y0.8Ca0.2Ba2Cu3O7-δ while the red stars show the data for Zn-substituted Y124. They are very consistent. The rapid suppression of Tc for underdoped samples (open symbols) compared with overdoped (filled symbols) is a signature of the pseudogap which lowers the DOS at the Fermi level and hence raises the scattering rate16. Supplementary Fig. S3 shows Tc as a function of planar Zn concentration for Y0.8Ca0.2Ba2Cu3O7-δ at various doping states while red stars show the same data for Y124. Again they are very consistent. Typically, for higher Zn concentrations, the Tc value sits higher than that expected from Abrikosov–Gorkov pairbreaking due to the statistical overlap of nearest neighbours to the Zn substituent16.

Spin susceptibility and Knight shift

The spin susceptibility, χs, is related to the bulk magnetic susceptibility, χm, by χm=χs+χ0 where the constant χ0 comprises diamagnetic and van Vleck terms and is evaluated for Y123 by Alloul et al.36. The measured Knight shift, 89Ks, is given by 89Ks = σ0(x)+a(x)89χs, where σ0(x) is the T-independent chemical shift and a(x) is the relevant hyperfine coupling constant and, as indicated, both change only with oxygen content, x. For each x therefore, χs, χm and 89Ks are linearly related to within an additive constant. We used values of a(x) reported by Alloul36, while for each x the additive constant was determined by matching the 89χs data to our bulk susceptibility data, χs24. This fixed the value of the constant σ0(x) which differed somewhat from those of Alloul but other literature values also reflect those differences39. The overall T-dependence (independent of σ0(x)) was an excellent match.

Supplementary information

Supplementary material 1 (375.1KB, pdf)

Acknowledgements

We are grateful to Dr. J. R. Cooper for helpful comments on the Knight shift and spin susceptibility. We also thank Dr. Martin Ryan for assistance with the X-ray diffraction analysis.

Author contributions

J.L.T. synthesized and characterized the samples, J.W.L. carried out the specific heat measurements and the initial analysis to extract the electronic specific heat. J.L.T. analyzed the data and wrote the paper.

Competing interests

The authors declare no competing interests.

Footnotes

Publisher's note

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

John W. Loram is deceased.

Supplementary Information

The online version contains supplementary material available at 10.1038/s41598-020-79017-3.

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