Abstract
In conventional BCS superconductors, the quantum condensation of superconducting electron pairs is understood as a Fermi surface instability, in which the low-energy electrons are paired by attractive interactions. Whether this explanation is still valid in high-Tc superconductors such as cuprates and iron-based superconductors remains an open question. In particular, a fundamentally different picture of the electron pairs, which are believed to be formed locally by repulsive interactions, may prevail. Here we report a high-resolution angle-resolved photoemission spectroscopy study on LiFe1−xCoxAs. We reveal a large and robust superconducting gap on a band sinking below the Fermi level on Co substitution. The observed Fermi-surface-free superconducting order is also the largest over the momentum space, which rules out a proximity effect origin and indicates that the order parameter is not tied to the Fermi surface as a result of a surface instability.
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Introduction
Two main categories of theoretical descriptions arise when trying to describe the high-Tc superconductivity of the iron-based superconductors (IBSCs): the weak coupling approach, which involves only the low-energy electronic structure near the Fermi level (EF) (refs 1, 2, 3, 4, 5), and the strong coupling approach, which emphasizes the local magnetic moments and strong Coulomb interactions6,7,8,9,10. In the former, superconductivity emerges as a Fermi surface (FS) instability and is, in principle, sensitive to FS changes. In particular, the superconducting (SC) gap is tied to the FS and its amplitude is strongly influenced by the nesting conditions. In the latter, the pairing is caused by local antiferromagnetic exchange couplings, well defined in the real space, which lead to a SC order parameter (OP) that is fixed in the momentum space and relatively insensitive to small changes of the electronic structure near the FS.
In principle, one can distinguish between these two approaches and get critical information on the pairing mechanism of IBSCs by tracking precisely the evolution of the SC OP on bands for which the contributions to the FS vary drastically. In this respect, LiFe1−xCoxAs offers a perfect platform for this study because it undergoes a Lifshitz transition with one FS disappearing at small Co substitution11,12.
Here we show a high-resolution angle-resolved photoemission spectroscopy (ARPES) study on SC LiFe1−xCoxAs. We reveal a large and robust SC gap with 2Δα/kBTc~7 on the inner hole band that is sinking below the Fermi level on Co substitution. The observed FS-free SC gap is also the largest over the momentum space, which rules out a proximity effect origin and indicates that the SC OP is not tied to the FS as a result of a FS instability.
Results
FS topology of pristine LiFeAs and LiFe0.97Co0.03As
We first look at the FS topologies of pristine LiFeAs and LiFe0.97Co0.03As, which are illustrated in Fig. 1. In agreement with previous studies, the substitution of Co introduces electron carriers and effectively moves the chemical potential upwards11,12,13,14. Since the inner hole-like FS (the α FS) shown in Fig. 1a only barely crosses EF in pristine LiFeAs15,16, a slight substitution of Fe by Co removes this tiny FS pocket at the Γ(0,0) point, and thus the system undergoes a Lifshitz transition12. The remnant intensity at EF around Γ in Fig. 1b is attributed to the limited energy resolution setting (~14 meV) for this normal state (NS) measurement (T=30 K), which broadens the spectral width beyond EF.
Band dispersions of LiFe1−xCoxAs near EF
To accurately determine the band top of the α band, we performed high-resolution (~3 meV) ARPES measurements in the vicinity of Γ for samples at three doping levels (x=0, 1%, 3%, with onset Tc≈18, 16, 15 K, correspondingly, as shown in Supplementary Figs 1 and 2). As seen in Fig. 2d–f, the band top shifts to 4 and 8 meV below EF at Co contents of 1 and 3%, respectively. This shift is also clearly demonstrated by the energy distribution curves (EDCs) shown in Fig. 2m–o. While the low-energy quasiparticle peaks of pristine LiFeAs are clearly cutoff by the Fermi-Dirac (FD) function, those of the 1% Co and 3% Co samples shift below EF with small spectral weight at EF due the finite peak width.
Although the electronic structure of LiFe1−xCoxAs is quite two dimensional, previous studies indicate that the α band has a small dispersion along kz (refs 11, 12, 16). To quantify the kz effect of the α band and confirm that it does not cross EF along kz, we extract the NS dispersion of the α band at kz=0 and π. Figure 3a,c shows the ARPES intensity plots of 3% Co at 51 eV (kz=0) and 35 eV (kz=π), respectively. The data are recorded at 20 K with linearly polarized light to enhance the intensity of the α band11,17. The intensity plots and EDCs show that the band top of the α band has tiny dispersion along kz and prove that at least for 3% Co, the α band is completely sinking below EF all over the momentum space. The disappearance of the α FS reduces the density-of-states near EF and hence significantly suppresses the interband scattering between the α band and the electron FSs at the M point (π,0), as seen from Fig. 2m–o.
In the SC state, electrons are gapped towards higher binding energies and form a well-defined Bogoliubov quasiparticle peak. Figure 2m compares the representative EDCs of pristine LiFeAs across the Γ point above and below Tc. The electronic states within the SC gap are significantly altered, while the states at higher binding energies are only slightly modified by the Bogoliubov dispersion:
where Ek is the energy of the Bogoliubov quasiparticle, which will not show clear deviation from the NS energy ξk when ξk is much larger than the SC gap Δk. Interestingly, we find that near the band top, the electronic states of the 1% Co and 3% Co samples are slightly shifted to higher binding energies as shown in Fig. 2n,o, indicating the opening of a SC gap on the α band, even though this α band is located below EF at these doping levels (Supplementary Fig. 3).
Extraction of the SC gap
To see how the SC condensation affects the electronic states away from EF, we show the simulated EDCs without FD distribution in the NS and SC state in Fig. 4b, corresponding to the vertical line at the Γ point in the simulated NS intensity plot in Fig. 4a. The band tops are set at 8 and 20 meV below EF, respectively, in agreement with the real band positions in this material. With a 5-meV SC gap turned on, the low-energy peak (P1) is shifted by 2 meV, while the high-energy peak (P2) is almost unchanged. Moreover, due to the particle–hole mixing, a small peak above EF develops in the EDC of the SC state. Back to the experimental data, in Fig. 4c,e,g, the EDCs at the BZ centre exhibit a coherent peak developing at all three doping levels below Tc. Figure 4d,f,h shows the same data but divided by the FD function convoluted with the system resolution. To extract the SC gap, the EDCs in the NS and SC state are fitted by the BCS spectral function plus a constant background (Supplementary Table 1). The extracted SC gap keeps almost constant, while the line width of the coherent peak becomes broader at higher doping levels. This indicates that the Co substitution introduces impurity potentials, which is believed to play a destructive role in sign-reversal pairing, at least in the weak coupling regime1.
Following the procedure shown in Fig. 4, we extract the low-energy band dispersion below and above Tc. Figure 5a–d show the extracted data of the 1% Co and 3% Co samples in wide and narrow energy ranges. In agreement with equation (1), the band shift is the largest near the band top and quickly vanishes at higher binding energies. By using the NS data to fit the dispersion in the SC state, we extract the SC gaps of pristine LiFeAs, 1% Co and 3% Co and plot them as a function of the Co concentration in Fig. 5e. The SC gap on the α band remains almost constant, while the associated FS topology undergoes a Lifshitz transition with the substitution of Co.
Since LiFe1−xCoxAs is a multi-orbital superconductor, the large SC gap observed on the α band, in principle, can be induced via proximity to other bands, which are crossing EF at all doping levels. In this scenario, the SC gap on the α band is expected to be smaller than the other bands and to give a negligible contribution to the SC pairing. To justify this point, we show the SC gap on the β, γ and δ bands of 3% Co in Fig. 6. The extracted SC gap on the β, δ and γ bands are 3.3, 3.5 and 4 meV, respectively (Supplementary Table 2). Since the cut on the γ band measures the largest gap on the electron FSs15,16, our results prove that the SC gap on the α band is the largest over the momentum space and thus rule out the possibility of a proximity effect causing by the pairing on other FS sheets.
Discussion
As discussed before, the interband scattering in the particle–particle channel is dramatically reduced due to the Lifshitz transition. According to the weak coupling nesting scenarios, the SC gap on the α band is expected to exponentially decrease when the contribution of this band to the density-of-states at EF goes to zero18,19, as shown in Fig. 5e. This is clearly in contradiction with our experimental observation that the SC gap on the α band is robust and the largest over the momentum space.
Recent inelastic neutron scattering and NMR studies have demonstrated that low-energy spin fluctuations are relatively weak and incommensurate for pristine LiFeAs20,21,22. Combined with ARPES data, the incommensurate inelastic neutron scattering peaks were attributed to the interband scattering between the β FS and the electron FSs23. However, ARPES and STM studies demonstrate that the largest SC gap is indeed on the α band, which is clearly incompatible with the low-energy spin fluctuations scenario15,16,24,25. Although this discrepancy can be removed by subtle modifications involving orbital fluctuations or small-q interband scattering26,27, our observation of strong SC pairing on the band without FS is beyond any reasonable mending within the weak coupling approach. Instead, it is naturally consistent with many strong coupling approaches6,7,8,9,10,28,29, in particular with the J1–J2 model that predicts the strongest pairing at the zone centre6,7,8,9. Indeed, the ratio 2Δα/kBTc~7 observed in the LiFe1−xCoxAs is twice larger than the predicted BCS value, which also suggests a strong coupling pairing mechanism.
Finally, it is interesting to compare the observed SC gap with εF, here defined as the energy difference from the band top to the chemical potential30, as illustrated in Fig. 5a. Previous studies on the iron-chalcogenide superconductor FeTe1−xSex (refs 30, 31) show that the SC gap is comparable with εF and consistent with a BCS–BEC crossover scenario29,30. In LiFe1−xCoxAs, as shown in Fig. 5e, the value of εF drops from +2 to −8 meV with 3% Co substitution, while the SC gap remains almost unchanged and is immune to the Lifshitz transition. We note that due to the multi-orbital nature of the IBSCs, the value of the Fermi energy might be much larger than we defined here, and whether the LiFe1−xCoxAs lays in the BCS–BEC crossover regime needs further experimental and theoretical investigations.
Methods
Sample preparation and experimental setup
Single crystals of LiFe1−xCoxAs were synthesized by the self-flux method using Li3As, Fe1–xCoxAs and As powders as starting materials. The Li3As, Fe1−xCoxAs and As powders were weighed according to the element ratio of Li(Fe1−xCox)0.3As. The mixture was grounded and put into an alumina crucible and sealed in Nb crucibles under 1 atm of Argon gas. The Nb crucible was then sealed in an evacuated quartz tube, heated to 1,100 °C and slowly cooled down to 700 °C at a rate of 3 °C per hour. High-energy-resolution ARPES data were recorded at the Institute of Physics, Chinese Academy of Sciences, using the He Iα (hν=21.218 eV) resonance line of a helium discharge lamp. The angular and momentum resolutions were set to 0.2° and 3 meV, respectively. ARPES polarization-dependent measurements were performed at Beamline I05 of Diamond Light Source using a Scienta R4000 with energy and momentum resolutions set to 0.2° and 10 meV, respectively. To select the α band, we employed linearly polarized light with the potential vector perpendicular to the mirror plane of the sample. All samples were cleaved in situ. The data were taken in a vacuum better than 3 × 10−11 Torr with discharge lamp and 1 × 10−10 Torr with synchrotron light source.
Extraction of the SC gap
To extract the SC gap from EDCs, we use the functions:
Here we assume a BCS spectral function in the occupied states, with the Γk parameter not changing with binding energy. ai is a fitting constant, which is proportional to Γk and uk2. The fitting parameters are summarized in Supplementary Tables 1 and 2. Equations (2)–(4), , are used to fit the SC gap of the α, β and γ/δ FSs, respectively. The first and second BCS spectral function in equation (2) are used to fit the α band and α′ band, respectively11. Since the γ and δ bands are close to each other, we use a polynomial function to remove the large background, and we assume the background has an even symmetry with respect to EF (ref. 32). Since the BCS spectral function can be derived from the Bogoliubov formalism, it can be applied to the strong coupling regime31,33,34,35.
Additional information
How to cite this article: Miao, H. et al. Observation of strong electron pairing on bands without Fermi surfaces in LiFe1-xCoxAs. Nat. Commun. 6:6056 doi: 10.1038/ncomms7056 (2015).
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Acknowledgements
We thank A. Chubukov, Y.M. Dai, W. Ku and X.R. Liu for useful discussions. This work was supported by grants from CAS (2010Y1JB6 and XDB07000000), MOST (2010CB923000, 2011CBA001000 and 2013CB921700) and NSFC (11234014 and 11274362).
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H.M. and H.D. designed the experiments; H.M., T.Q., X.S., P.R., T.K.K. and M.H. carried out the experiments; H.M. analysed the data; L.Y.X., X.-C.W. and C.-Q.J. provided the samples; H.M., T.Q., P.R., J.-P.H. and H.D. wrote the manuscript. All authors discussed the results and commented on the manuscript.
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Supplementary Figures 1-3 and Supplementary Tables 1-2. (PDF 391 kb)
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Miao, H., Qian, T., Shi, X. et al. Observation of strong electron pairing on bands without Fermi surfaces in LiFe1−xCoxAs. Nat Commun 6, 6056 (2015). https://doi.org/10.1038/ncomms7056
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DOI: https://doi.org/10.1038/ncomms7056
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