Abstract
Central to the understanding of high-temperature superconductivity is the evolution of the electronic structure as doping alters the density of charge carriers in the CuO2 planes. Superconductivity emerges along the path from a normal metal on the overdoped side to an antiferromagnetic insulator on the underdoped side. This path also exhibits a severe disruption of the overdoped normal metal’s Fermi surface1,2,3. Angle-resolved photoemission spectroscopy (ARPES) on the surfaces of easily cleaved materials such as Bi2Sr2CaCu2O8+δ shows that in zero magnetic field the Fermi surface breaks up into disconnected arcs4,5,6. However, in high magnetic field, quantum oscillations7 at low temperatures in YBa2Cu3O6.5 indicate the existence of small Fermi surface pockets8,9,10,11,12,13,14,15,16,17,18. Reconciling these two phenomena through ARPES studies of YBa2Cu3O7−δ (YBCO) has been hampered by the surface sensitivity of the technique19,20,21. Here, we show that this difficulty stems from the polarity and resulting self-doping of the YBCO surface. Through in situ deposition of potassium atoms on cleaved YBCO, we can continuously control the surface doping and follow the evolution of the Fermi surface from the overdoped to the underdoped regime. The present approach opens the door to systematic studies of high-temperature superconductors, such as creating new electron-doped superconductors from insulating parent compounds.
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In the heavily overdoped regime, angular magnetoresistance oscillation1 and angle-resolved photoemission spectroscopy (ARPES) experiments2,3 on Tl2Ba2CuO6+δ have arrived at a quantitative consensus in observing a large hole-like Fermi surface. On reducing the number of holes in the CuO2 planes, the Fermi surface volume decreases in the manner expected by Luttinger’s theorem, but below optimal doping the single-particle Fermi surface seems to reduce to four disconnected nodal Fermi arcs. This scenario was suggested from ARPES studies of Bi cuprates4,5 and Ca2−xNaxCuO2Cl2 (ref. 6), and is thought to be connected to the existence of the pseudogap. The detection of quantum oscillations in oxygen-ordered ortho-II YBa2Cu3O6.5 (YBCO6.5) suggests a different scenario involving Fermi surface reconstruction into hole and/or electron pockets7,9,10. These two pictures are derived from quite different measurement techniques, carried out on different materials, and under conditions of high magnetic field in one case, but zero field in the other. Owing to the complex multiband and correlated character of the electronic structure of YBCO6.5 (ref. 11), the determination of the nature of these pockets and their generality to the underdoped cuprates requires connecting transport and single-particle spectroscopy information on the same underdoped system. The study of YBCO6.5 by ARPES is thus crucial. Unfortunately, this material is complicated by the lack of a natural [001] cleavage plane (Fig. 1a) and also by the presence of CuO-chain layers. More specifically, YBCO cleaves between the CuO-chain layer and the BaO layer, leaving on the cleaved surface relatively large regions (>100 Å) of either CuO or BaO terminations. Scanning tunnelling microscopy shows that the CuO-chain terraces are characterized by prominent surface density waves22 and differ substantially from the bulk: as also seen in ARPES19, they exhibit surface states and unavoidable doping disorder. Recent ARPES studies of nearly optimally doped YBCO indicated that surfaces terminating in either a CuO and BaO layer give different contributions to the total photoemission intensity21, and that the doping of the topmost CuO2 planes is p=0.3, almost irrespective of the nominal bulk doping. This corresponds to heavy overdoping, all the way into the non-superconducting regime (Fig. 4), and is actually not achievable in bulk, fully oxygenated YBCO7.0 for which p=0.194 (ref. 23). Similar problems have been encountered in the ARPES study of YBa2Cu4O8 (ref. 24).
Overcoming these problems requires, first of all, recognizing that the cleaved surface of YBCO is actually polar. This can lead to overdoped-like Fermi surfaces (Fig. 1b) due to reconstruction of the electronic states25. A wide momentum-distribution map of the Fermi surface from ‘as-cleaved’ YBCO6.5 is shown in Fig. 2a (see the Methods section). The ARPES data are a superposition of features from the BaO- and CuO-terminated regions: because of the few ångström electron escape depth at these photon energies, the ARPES intensity from the BaO-terminated regions is dominated by the CuO2-bilayer bands and that from the CuO-terminated regions by the chain band. The comparison with Fig. 1b enables us to identify the Fermi surface features originating from the CuO2-plane bonding and antibonding bands (FSB and FSAB) and the one-dimensional (1D) CuO-chain band (FSCh). Note that the strong momentum-dependent intensity modulation of the ARPES features, which seems inconsistent with the sample symmetry, is simply a manifestation of the matrix element effects associated with the photon/crystal/electron geometry changing across the field of view (no symmetrization was carried out). In addition, this particular ortho-II sample happened to be twinned, in the bulk and not just on the surface, as confirmed by X-ray diffraction (this has an effect on FSCh but not on the discussion of the four-fold symmetric Fermi arcs). Most importantly, the fit of the 2D ARPES Fermi surfaces over multiple zones returns the following areas, counting electrons, relative to the Brillouin zone area ABZ=4π2/a b: the bonding Fermi surface area FSB=46.2%, the antibonding FSAB=26.0% and the chain surface FSCh=13.8%. From the average of bonding and antibonding Fermi surface areas, we can calculate the hole doping p=0.28±0.01 per planar copper (p=0 for the 1/2-filled Mott insulator with 1 hole per Cu atom). As summarized in the phase diagram of Fig. 4, this indicates that the self-doping of the YBCO6.5 polar surface is that of a heavily overdoped, non-superconducting cuprate.
The next step is that of actively controlling the self-doping of the surface, to reduce its hole content to that of underdoped, bulk YBCO6.5. This can be achieved by in situ evaporation of potassium onto the cleaved surface (see the Methods section): owing to the low ionization potential, K1+ ions are adsorbed on the surface and electrons are doped into the topmost layers. As a consequence, we would anticipate the evolution of all detected features towards the underdoped regime of hole-doped cuprates, which is precisely what can be observed in Fig. 2, from a to c, on increasing the K1+ concentration (decreasing the hole doping). The doping is indeed changing according to an increase in electron filling (all data were acquired on the same sample after subsequent K evaporations). This is demonstrated by the continuous FSCh area increase (counting electrons), which evolves from FSCh=13.8% for the as-cleaved surface to FSChK1=14.7% and FSChK2=16.6% for the increasingly K-deposited YBCOK1 (Fig. 2b) and YBCOK2 (Fig. 2c). By comparing the carrier concentration per chain Cu measured by the FSCh area with the results of ab initio local density approximation (LDA) band-structure calculations11, we can estimate the corresponding hole doping per planar Cu. This way we find good agreement with the value p=0.28 already estimated for as-cleaved YBCO6.5 from the average of FSB and FSAB. Most importantly, however, we obtain a hole doping pK1=0.20 and pK2=0.11 for YBCOK1 and YBCOK2, which means that the surface of YBCOK2 is very close to the doping level p=0.097 of bulk oxygen-ordered ortho-II YBCO6.5.
The most interesting aspect of the data in Fig. 2 is the evolution of the CuO2-plane features. For heavy K deposition (Fig. 2c), the LDA-like CuO2-bilayer bonding and antibonding Fermi surfaces of overdoped YBCO have collapsed into four nodal Fermi arcs, consistent with other underdoped cuprates 4,5,6. This is accompanied by the complete suppression of CuO2 antinodal spectral intensity as well as nodal bilayer splitting, which in contrast were clearly resolved for as-cleaved YBCO6.5 (Fig. 2a). Their disappearance with K deposition suggests a severe loss of coherence on underdoping. Correspondingly, the CuO2 nodal Fermi wave vectors, relative to the Brillouin zone diagonal (0,0)–(π,π), have evolved from kFAB=0.29 and kFB=0.36 for ‘overdoped’ as-cleaved YBCO6.5, to a single kFK2=0.40 for ‘underdoped’ YBCOK2. These numbers compare well to what has been observed on other cuprates at similar dopings (note that the following are both single CuO2-layer systems): kF=0.36 and 0.41, respectively, for overdoped (p=0.26) Tl2Ba2CuO6+δ (ref. 2) and underdoped (p=0.12) Ca2−xNaxCuO2Cl2 (ref. 6).
The transfer of electrons to the surface of YBCO on K deposition is also confirmed by an inspection of the electronic dispersions along the (−π,−2π)–(−π,2π) direction (corresponding momentum-distribution curves are shown in the Supplementary Information). On p=0.28 as-cleaved YBCO6.5 (Fig. 3a), we detect well-defined bonding and antibonding CuO2 bands crossing EF at the antinodes, as well as the BaO band with a maximum binding energy at the zone corners (−π,±π). On underdoped p=0.11 YBCOK2 (Fig. 3b), the BaO band is located ∼100 meV deeper in energy. This indicates a shift of the chemical potential consistent with the transfer of electrons from adsorbed K atoms to the topmost BaO-plane, CuO-chain and CuO2-plane layers. On YBCOK2, the only coherent feature detected at the antinodes is the 1D CuO-chain band; the antinodal CuO2-plane spectral weight has now become fully incoherent. The nodal and antinodal energy-distribution curves (EDCs) in Fig. 3c–e clearly show that the progressive loss of quasiparticle coherence with K deposition is very similar to what is observed on other cuprates on hole underdoping2,4,5,6. Most importantly, whereas metallic behaviour is observed on as-cleaved YBCO6.5, a leading-edge antinodal gap Δ∼10 and 80 meV is detected for YBCOK1 and YBCOK2, respectively. This is consistent with YBCO being superconducting for p=0.11 and 0.20 but not 0.28 (Fig. 4—the experiments were all carried out at T=20 K), and enables us to conclude that the properties of the K-deposited YBCO surfaces are representative of bulk YBCO.
We now summarize our findings, illustrated by the phase diagram and symmetrized Fermi surface data for YBCOK2 and as-cleaved YBCO6.5 in Fig. 4. Our study demonstrates that the self-hole-doping of the cleaved polar surfaces of YBCO can be controlled by the in situ evaporation of alkali metals, in the present case K. This novel approach paves the way for the study of this important material family—-across the whole phase diagram—by single-particle spectroscopies. As this material has been the gold standard in a number of seminal bulk-sensitive studies of the normal and superconducting properties, the direct connection with single-particle spectroscopy can lead to an understandable underdoped anchor point, analogous to Tl2Ba2CuO6+δ in the overdoped regime3. The results obtained for p=0.11 YBCOK2 establish that the ARPES Fermi surface of underdoped YBCO consists of the superposition of 1D CuO-chain Fermi surface and CuO2-plane-derived nodal Fermi arcs. It is thus consistent, with the extra complication of the chains, to what has already been observed in oxychloride6 and Bi cuprates4,5. In this sense, the disruption of the large hole-like coherent Fermi surface in underdoped cuprates is a truly universal phenomenon.
Having obtained the first momentum-resolved Fermi surface data for underdoped YBCO, it becomes crucial to understand the connection between ARPES and quantum oscillation results7,10. First, the detection of the BaO-band maximum at ∼0.5 eV below EF rules out the scenario coming from LDA band-structure calculations, which suggested that the small Fermi surface found in the quantum oscillation measurements might originate from small pockets produced by BaO–Cuchain bands at (±π,±π) 11,12. We also did not observe any signature of CuO2-derived band folding arising from the ortho-II oxygen-ordering of the chains11,12, which is possibly consistent with the loss of three-dimensional coherence demonstrated by the suppression of bilayer band splitting on underdoping. Recent measurements of the Hall resistance in high magnetic field have noted a sign change with decreasing temperature9, suggesting that the quantum oscillations seen on top of a negative Hall coefficient might come from small electron pockets, rather than the hole pockets originally proposed 7. However, there is no sign of such electron pockets in our ARPES data from underdoped YBCOK2, nor are there signs of extra zone-folding due to the kinds of density wave instabilities that might give rise to such a Fermi surface reconstruction8,9,15.
If any pocket had to be postulated on the basis of the present ARPES data, the most obvious possibility would be that the Fermi arcs are in fact hole-like nodal Fermi pockets, as obtained for light doping of the antiferromagnetic parent compound in self-consistent Born calculations26 and already speculated from the study of other underdoped cuprates4,5,6. The lack of a finite ARPES intensity on the outer side of the pockets would be consistent with the strong drop in the quasiparticle coherence Zk expected beyond the antiferromagnetic zone boundary13,27. To estimate an area for these ostensible nodal pockets, we can fold the detected arc profile, either with respect to the antiferromagnetic zone boundary or the end points of the arc itself, obtaining values of either 2.6% or 1.3%, relative to the full Brillouin zone area ABZ=4π2/a b. These numbers compare relatively well to the pocket area of 1.9% suggested on the basis of quantum oscillation experiments on bulk YBCO6.5 (refs 7, 10). However, these are hole, not electron pockets. Thus, the interpretation of high field measurements in terms of electron and hole pockets differs markedly from single-particle spectroscopy on the same material, suggesting that the high magnetic field might be inducing a state different from that being studied in zero field.
Whatever the solution to the puzzle outlined above, it should be emphasized that the present approach, based on the in situ alkaline metal evaporation on freshly cleaved surfaces, opens the door to this type of manipulation of other cuprates and complex oxides, not only to control the self-doping of polar surfaces but also to reach doping levels otherwise precluded in the bulk. For instance, we could try to underdope the surface of Tl2Ba2CuO6+δ, which grows naturally overdoped3, or even to obtain an electron-doped superconductor starting from the insulating parent compounds.
Methods
Sample preparation
YBa2Cu3O6+x single crystals were grown in non-reactive BaZrO3 crucibles using a self-flux technique. The CuOx-chain oxygen content was set to x=0.51 by annealing in a flowing O2:N2 mixture and homogenized by further annealing in a sealed quartz ampoule, together with ceramic at the same oxygen content. After mounting for the cleave required in an ARPES measurement, the samples were cooled from 100 ∘C to room temperature over several days to establish the ortho-II superstructure ordering of the CuOx-chain layer28. The particular sample used here was twinned, as confirmed by X-ray diffraction after the ARPES measurements.
ARPES experiments
ARPES measurements were carried out on the Electronic Structure Factory endstation at Beamline 7.01 of the Advanced Light Source. The data were measured with linearly polarized 110 eV photons and a Scienta R4000 electron analyser in angle-resolved mode. YBCO6.5 single crystals were cleaved in situ at a base pressure better than 2.5×10−11 torr and then oriented by taking fast Fermi surface scans. Several procedures were tried on these samples in an attempt to suppress the surface contribution to the total photoemission intensity and gain direct insight into the bulk electronic structure. For instance, samples were temperature-cycled between 20 and 100 K or were cleaved at higher temperature (∼80 K) and then cooled to 20 K (ref. 29), to age and/or vary the characteristics of the cleaved surfaces. Whereas both procedures have proved successful in measuring the bulk dispersion and Fermi surface of layered Sr2RuO4 (ref. 29), no effect was observed in the case of YBCO6.5. Successful control of the self-doping of the cleaved surfaces was achieved by in situ deposition of submonolayers of potassium, with a commercial SAES getter source30, on freshly cleaved YBCO6.5. In this last case, the samples were kept at 20 K at all times during the cleaving, K-deposition and ARPES measurements (temperature-dependent measurements could not be carried out because of the need to maintain the most stable experimental conditions over extended time, during and between subsequent K evaporations). All ARPES data shown in Figs 2–4 were obtained on the same sample, that is, as-cleaved, and after two subsequent K evaporations. Energy and angular resolutions were set to ∼ 30 meV and 0.2∘ (±15∘ angular window) for the data in Figs 2 and 3, and to ∼ 30 meV and 0.1∘ (±7∘ angular window) for the higher-quality Fermi surface mappings in Fig. 4. The Fermi surface maps of Figs 2 and 4 were obtained by integrating the ARPES intensity over a 30 meV energy window about EF, and then by normalizing the intensity maps relative to one another for display purposes. A more quantitative comparison of the ARPES intensity for as-cleaved and K-deposited surfaces is given in the Supplementary Information on the basis of the analysis of momentum-distribution curves, which shows an overall intensity suppression by a factor of 4.4 and 7.2 for low and high K coverage, with respect to the as-cleaved surface.
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Acknowledgements
We gratefully acknowledge J. van den Brink for insightful discussions. This work was supported by the Alfred P. Sloan Foundation (A.D.), an ALS Doctoral Fellowship (M.A.H.), the CRC Program (A.D. and G.A.S), NSERC, CFI, CIFAR Quantum Materials and BCSI. The Advanced Light Source is supported by the Director, Office of Science, Office of Basic Energy Sciences, of the US Department of Energy under Contract No. DE-AC02-05CH11231.
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Hossain, M., Mottershead, J., Fournier, D. et al. In situ doping control of the surface of high-temperature superconductors. Nature Phys 4, 527–531 (2008). https://doi.org/10.1038/nphys998
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DOI: https://doi.org/10.1038/nphys998
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