Abstract
The exploitation of interface effects turned out to be a powerful tool for generating exciting material properties. Such properties include magnetism, electronic and ionic transport and even superconductivity. Here, instead of using conventional homogeneous doping to enhance the hole concentration in lanthanum cuprate and achieve superconductivity, we replace single LaO planes with SrO dopant planes using atomic-layer-by-layer molecular beam epitaxy (two-dimensional doping). Electron spectroscopy and microscopy, conductivity measurements and zinc tomography reveal such negatively charged interfaces to induce layer-dependent superconductivity (Tc up to 35 K) in the space-charge zone at the side of the planes facing the substrate, where the strontium (Sr) profile is abrupt. Owing to the growth conditions, the other side exhibits instead a Sr redistribution resulting in superconductivity due to conventional doping. The present study represents a successful example of two-dimensional doping of superconducting oxide systems and demonstrates its power in this field.
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Introduction
Interface effects in complex oxide heterostructures have received great attention because of the emergence of functional properties such as magnetism1,2,3,4, metallicity5,6,7, superconductivity8,9 and high-temperature superconductivity10 that are not shown by the phases individually. This rationale has been applied to ionic and mixed electronic/ionic conductors (‘heterogeneous doping’)11,12,13, where this powerful technique, relying on the introduction of space-charge zones, has been proven to be on a par, if not superior, to the classic homogeneous (bulk) doping (see Supplementary Note 1). While superconducting electronic accumulation layers have been created at heterojunctions between two phases or at grain boundaries (for example refs 8, 9, 10, 14), the insertion of an atomic plane of defined interfacial charge (here substitutional insertion) yielding local high-temperature superconductivity has not been achieved so far. This is not only exciting in terms of generating space-dependent superconductivity without dopant disorder but also for purposeful functional structuring.
As well known, homogeneously doped La2−xSrxCuO4, in which the resulting strontium (Sr) dopants ( in Kröger–Vink notation) give rise to a significant concentration of electron holes [], exhibits high-temperature superconductivity with critical temperatures (Tc) up to ≈40 K (for the optimal doping x=0.16). For a higher doping level (‘overdoping’), Tc decreases and the structure eventually becomes metallic15,16. This is attributed to an interplay of electronic and structural reasons, since for a high Sr-content defect chemistry predicts a tendency to oxygen vacancy () compensation (because of double-positive charge), association between and and between and (refs 17, 18; see Supplementary Fig. 1 and Supplementary Note 2).
Unlike forming La2−xSrxCuO4 solid solutions, we use here unconventional heterogeneous doping11,12,13 to enhance the hole concentration and thus trigger superconductivity. Inspired by the so-called delta-doping technique19,20,21, we replace single LaO planes with SrO ones, with the aim of creating two-dimensional (2D) and atomically confined charged layers within the undoped La2CuO4 matrix. So far, delta-doping in oxides referred to either the insertion of one (or more) complete unit cells of a doped material in a matrix of the same but undoped material22,23,24 or , in few cases dealing with the formation of 2D electronic gases or local modification of magnetic properties, the successful substitution of single atomic planes in perovskites (LaO for SrO planes5,25,26,27, SrO for GdO planes28). None of them used delta-doping for obtaining high-temperature superconductivity. Either comparatively thick layers were inserted9,29 or, in the few cases where 2D doping was employed5,25,26,27,28, superconductivity was not achieved.
Here the Sr-to-La substitution targets a single atomic layer of La2CuO4 and yields a layer of high effective negative charge density. Such an approach is expected to yield a local space-charge redistribution of and mobile ionic charges12. While the possibility of cation redistribution deserves a closer inspection (see below), oxygen diffusion kinetics18 (Supplementary Fig. 2) certainly allow oxygen interstitials () and vacancies () to redistribute on the nm scale.
The rationale of this contribution is depicted in Fig. 1, which compares the two cases of homogeneously (zero-dimensional) doped with heterogeneously (2D) doped La2CuO4. While, in the first case (Fig. 1a,c), at equilibrium all positive (negative) defects are increased (depressed) on Sr-doping in correspondence to the randomly distributed Sr point defects, in the second case (Fig. 1b,d) the interfacial charge dictates the charge-wise similar but spatially very different behaviour in the space-charge zones. A SrO layer substituting one LaO layer in the La2CuO4 cell acts as a negatively charged interface, analogously to a charged grain-boundary case in a bicrystal11, yet with a priori known interfacial charge, resulting in an enhancement of the positively charged mobile defects (particularly holes) in the adjacent layers.
In the classical doping case, the probability of finding the excess hole in the local environment of a Sr-dopant is enhanced; yet, owing to the disorder, a high concentration of Cooper pairs in a given layer cannot build up. The transition to an ordered 2D situation corresponds to a transition from a Debye–Hückel to a Gouy–Chapman situation, in which the very high local interfacial charge, whose sign is known a priori, produces a sharp hole accumulation enabling measurability (see below), percolation efficiency and structurability.
Qualitatively, the effects of homogeneous and heterogeneous doping can be described by the following rules30:
where ck and zk are the concentration of the charge carrier k and its charge number, respectively, and qdop the charge of the dopant. This expression indicates that on homogeneous addition of acceptors into a host material (for strontium substituting lanthanum qdop<0)) the concentrations of all positively (negatively) charged carriers ck are increased (decreased), as long as they are mobile and can attain distribution equilibrium. This follows from charge conservation and the electroneutrality of the disorder reactions. In the case of heterogeneous doping :
where ∑int represents the effective charge density of the 2D dopant. Equation (2) follows from the fact that all charge carriers perceive the same electrical potential30.
By employing atomic-layer-by-layer oxide molecular beam epitaxy technique (ALL-oxide MBE), which allows for a definition of the nominal composition of each atomic layer31,32, we synthesized more than 100 epitaxial superlattices, in which single LaO layers in the La2CuO4 structure were substituted by SrO layers with the desired periodicity (see Supplementary Methods and Supplementary Figs 3–5 for preparation and structural characterization). Ignoring oxygen defects, the resulting composition of the heterostructures is described as (Fig. 2a):
with R representing the number of superlattice unit repetitions and N the spacing between the SrO layers (expressed in number of constituting La2CuO4 units, which corresponds to half a unit cell).
The two sides of each SrO plane (the downward side facing the substrate and the upward side oriented towards the free surface) exhibit remarkably different properties. At the downward side, a clear decoupling between hole and Sr concentration, whose profile is here abrupt, is detected. This finding proves space-charge effect as the key mechanism yielding superconductivity. At the upward side instead, where Sr redistribution occurs, superconductivity arises because of conventional homogeneous doping.
Results
Resistivity measurements reveal confined superconductivity
The in-plane resistivity data collected from a set of samples having comparable total thicknesses (≈400 Å) and different spacing N between subsequent SrO layers is shown in Fig. 2b. Notably, the samples exhibit high-Tc superconductivity, with Tc (Fig. 2c) reaching a maximum value of ∼35 K for 5≤N≤9 (see Supplementary Methods as well as Supplementary Figs 6 and 7 for the definition and analysis of Tc). For higher spacing N, Tc saturates at only ≈25 K and the in-plane resistivity drastically increases. This lowering of the Tc for large N is connected with a lower orthorhombicity32, a trend that is observed also in the case of conventional doping. These results suggest that conducting layers are formed in the proximity of each SrO layer. For short distances between two subsequent SrO layers (namely for N<5), Tc and resistivity decrease, suggesting ‘overdoping’ or structural distortions. For N≤1, a non-superconducting phase is formed.
Abrupt Sr profile at the downward side of the interface
To elucidate the local microstructure and composition, high-resolution transmission electron microscopy, together with analytical characterizations, was systematically performed employing aberration-corrected scanning transmission electron microscopy (TEM, see also Supplementary Methods). The high-angle annular dark-field (HAADF) micrograph in Fig. 3a reveals that the superlattice exhibits perfect epitaxy, illustrating the absence of any extended structural defects such as misfit dislocations or antiphase boundaries. A high-resolution micrograph is presented in Fig. 3e, showing the atomic arrangement in greater detail. In the intensity profile obtained from the HAADF image (averaged perpendicularly to the growth direction), the intensity drop is connected with the Sr-containing layers (compare Fig. 3a,b). It is noteworthy that, such a change of intensity involves more than a single atomic plane indicating a certain Sr redistribution into the La2CuO4 matrix. Highly spatial-resolved spectroscopic analyses (Fig. 3c,d) provide more precise information revealing a pronouncedly asymmetric character of the Sr profile: virtually abrupt at the side facing the substrate (downward side) with an extent of 0.9±0.2 nm and smeared over 2.3±0.4 nm at the upward side, a feature that will be explained below. Results from energy-dispersive X-ray spectroscopy (EDXS) allows for a quantitative estimation of the La3+/Sr2+ concentration ratio (Fig. 3c and Supplementary Fig. 8). The maximum estimated ratio, obtained by averaging the maximum intensities of the different peaks, is 0.21±0.02. Electron energy-loss spectroscopy (EELS; Fig. 3d) provides further robust evidence of the asymmetric Sr distribution, ensuring single atomic layer resolution (step size≈2 Å)33,34.
By averaging the different EELS Sr-L2,3 intensity profiles from several Sr-containing atomic slabs, and applying an appropriate scaling factor to satisfy the nominal overall composition of the compound, one can accurately define the Sr level (x) that can be assigned to each ‘constituting block’ (namely a single CuO2 plane and the two surrounding (La,Sr)O layers) in proximity of the layer where Sr was initially inserted (see Fig. 3f and also Supplementary Methods, Supplementary Figs 9 and 10). Obviously, we have realized a rather abrupt profile, but only at the downward side, while at the other side (upward) there is a pronounced redistribution of the aliovalent cation. According to our rationale, we expect the space-charge mode to be active at the downward side and a usual homogeneous mode at the upward side (cf. Supplementary Note 3 and Supplementary Fig. 11). Taking both these mechanisms into account, the expected hole profile is sketched in Fig. 4.
Zn tomography specifies layer-dependent superconductivity
Further complementary tests relying on the Zn-doping tomography technique21 were carried out on structures containing one single SrO layer (Fig. 5a). The method consists of substituting ∼3% of Cu with Zn and thus suppressing Tc of specific CuO2 planes (Supplementary Fig. 12 and Supplementary Methods). In this way, spatial information is available, which allows us to identify which particular CuO2 planes are responsible for high-Tc superconductivity. To determine the contribution to superconductivity of each single CuO2 plane at the downward side of the interface, we proceeded as follows: all the CuO2 planes at the upward side were Zn-doped but on the downward side selected single CuO2 planes were Zn-doped and the electrical transport properties measured. Analogously, the same procedure was applied to determine the contribution of each single CuO2 layer of the upward side, after that the P=−2 CuO2 plane of the downward side had been Zn-doped.
The results are summarized in Fig. 5b, in which Tc obtained after having placed Zn in the different CuO2 planes is shown (see also Supplementary Fig. 13). The two sides exhibit similar Tc (orange and green areas in Fig. 5b for downward and upward sides, respectively), in contrast to what one would expect according to a simple homogeneous doping picture (see section above). Moreover, while no remarkable effect coming from Zn substitution in single CuO2 planes could be observed for the upward side (consistent with a homogeneous doping situation predicting several CuO2 planes to be superconducting, cf. Fig. 3f), for the downward side, we found Tc to stay almost unaffected when Zn was put in each plane P (−4≤P≤0), except for P=−2. In this case, the insertion of Zn leads to a drastic Tc reduction (Tc<4 K), allowing us to identify this CuO2 plane (P=−2) as the main source of high-Tc superconductivity of the downward side. Owing to the very low local Sr content (x ≈0.02), this undoubtedly demonstrates that superconductivity at the downward side does not arise from homogeneous doping. Rather, one has to refer to the heterogeneous case as sketched in Fig. 1d, which results in a hole accumulation, up to the optimal for superconductivity, for P=−2. Please note again that, in all the samples, which were prepared to investigate the role of the downward side of the interface by Zn tomography, all the P≥1 planes were doped by Zn with the purpose of suppressing any contribution to Tc stemming from the upward side.
Electrical properties of the La2CuO4/SrO bilayer
To confirm the minor role of the La3+/Sr2+ intermixing in the definition of the electrical properties at the downward side, we also considered a structure consisting of a bilayer of La2CuO4 and a 10-unit-cell-thick SrO film (Fig. 6a). Here the growth dynamics for the downward side follows a similar sequence compared with the structure depicted in Fig. 5a, with the only difference that several SrO layers are deposited in succession. If cation intermixing was responsible for the observed superconductivity at the backward side of the SrO planes, then we would expect to detect superconductivity also in this bilayer as long as we can neglect serious accommodation problems of the replaced La. Nevertheless, no sign of metallicity or superconductivity could be found (Fig. 6b, Supplementary Note 4 and Supplementary Fig. 14), confirming the relevance space-charge effects induced by the heterogeneous doping mechanism.
STEM–EELS confirms the predicted hole profile
A further nice corroboration of the findings described above stems from the intensity profile of the oxygen-K-edge pre-peak35, which is attributed to electronic transitions from the O1s-core level to hole states with p symmetry in the valence band (cf. Supplementary Fig. 15). As these data are averaged over each (La,Sr)O-CuO2-(La,Sr)O-constituting block, we compare it with the averaged Sr profile obtained from EELS analysis in Fig. 3f. The scaling was performed to satisfy global electroneutrality (ignoring oxygen point defects—see Supplementary Methods). The results are shown in Fig. 7. One clearly recognizes local electroneutrality on the right-hand side (upward side) and space-charge accumulation on the left-hand side (downward side). The qualitative agreement with the prediction given in Fig. 4 is remarkable. In addition, the absolute value of the hole concentration [] is reasonable: to plane P=−2 corresponds a hole concentration ≈0.1 per CuO2 plane, which for single phase thin films on LaSrAlO4 (001) substrates has Tc≈25 K (refs 15, 21), as indeed estimated by the Zn-doping experiment (cf. Fig. 5b). This agreement in absolute numbers may be partially coincidental because of possible structure distortions36, and to the fact that the high-Tc behaviour in space-charge zones may differ from the bulk situation.
Discussion
The most fascinating of the above described results regards the realization of a space-dependent superconductivity induced, as a consequence of a space-charge effect, by the Sr abrupt profile at the downward side of the SrO plane. While EDXS and EELS Sr-L2,3 intensity profiles reveal the Sr concentration profile to abruptly decrease even in close proximity of the SrO plane, the analysis of the pre-peak of the oxygen-K-edge indicates a substantial accumulation of within the same region. Electrical transport measurements carried out according to the Zn tomography technique corroborate these findings by demonstrating that the CuO2 plane-labelled P=−2 is the main source of high-Tc superconductivity at the downward side. Such hole accumulation (decoupled from Sr), due to the excess negative charge of the SrO layer, leads to a highly space-dependent Tc. The decay length of the hole profile is consistent with the bulk defect chemistry of pure La2CuO4 governed by 217.
It is noteworthy that, while in the case of homogeneous doping a rather large volume is necessary for inducing percolating superconductivity22,37, a space-charge-induced two-dimensional layer serves for highest volume concentration in terms of Cooper pairs. (As to the influence of dimensionality on superconductivity cf. ref. 38). Moreover, heterogeneous doping offers the advantage of experimentally probing the space-charge-induced superconductivity by means of different and complementary techniques, including STEM–EELS (scanning transmission electron microscopy–EELS) and Zn-doping tomography. In the literature, there is only one report on a possible decoupling between and at the interface between metallic La2−xSrxCuO4 and insulating La2CuO4 (ref. 10), yet also at the upward side (in growth direction) of the interface where we rather observe Sr redistribution.
At this side, the situation is dominated by non-negligible dopant redistribution leading to locally neutralizing diffused point defects. Such mixing effects have been seen in MBE-grown δ-doped semiconductors19,39 and, in some cases, in PLD-grown complex oxide systems40,41. Its occurrence is due to the specific kinetics of the atomic-layer-by-layer deposition process (Supplementary Methods), assuming intermixing to occur only between the last atomic layers on the film surface and the incoming species of high-kinetic energy. This may also be connected with the observed roughness of the film (Supplementary Fig. 16) and the high surface atomic mobility during growth. In such a nonequilibrium situation, cation exchange occurs in the growth direction only42, whereas it is limited in the downward direction because of sluggish diffusion. Finally, dopant segregation to the surface of the heterostructure43, which has been theoretically predicted for La2CuO4 (ref. 44), provides an additional, mainly energetic, driving force for the formation of such a Sr profile.
In summary, this study demonstrates the significance of heterogeneous doping in the field of superconductivity. It represents not simply an alternative to the homogenous doping approach but rather it offers a series of unique features. First, in the case of 2D doping, one can tune the local charge distribution (and thus local superconductivity) without affecting the chemical composition of the host material and without introducing local crystallographic disorder resulting from the dopant solid solution. This allows for a clear space-charge effect and for structuring the matrix material at wish, that is, we are able to insert active layers in the matrix and control their number, position and relative distance. From an operational point of view, it is certainly desired and will be attempted in the future to arrive at a two-sided abruptness of such profiles rather than an asymmetric situation.
Second, one can induce layer-dependent high-temperature superconductivity, while conventional doping leads to a homogeneous situation. Third, such superconductivity induced by a 2D charge distribution yields the formation of a layer of high Cooper pair concentration unlike the case of induction by homogeneously distributed dopant atoms. Fourth, the technique may be applied to situations where the solubility of the dopant is limited (and conventional doping is not possible) and/or a large volume is required for a sufficient percolation.
Last, our findings can be used to shed light on the influence of dimensionality on superconductivity38 but also on the importance of typically neglected effects of defect chemistry and ionic mobility in the field of high-temperature superconductivity.
Methods
ALL-oxide MBE synthesis
Thin films of 2D Sr-doped lanthanum cuprate were grown on LaSrAlO4 (001) substrates (Crystec GmbH), using ozone-assisted MBE31,32. The deposition conditions used for synthesizing the samples are temperature T≈620 °C and pressure p≈2.5 × 10−5 Torr (of mixed ozone, molecular and atomic oxygen). It is worth noting that, after the growth, all the samples were cooled under vacuum starting from a temperature T=200°C, which ensures that no contribution to electrical conductivity of La2CuO4 can be ascribed to extrinsic doping by interstitial oxygen (cf. ref. 32). A more detailed description of the growth method and sample structural characterization can be found in the Supplementary Methods.
Conductivity measurements
Electrical properties of the films were probed using direct current (DC)-electrical conductivity measurements as a function of temperature, using a Keithley 2,000 multimeter and a Keithley 2,400 sourcemeter implemented in a home-built system. The measurements were performed by warming up the sample from ≈4 K to room temperature, with a rate<0.1 K s−1, applied by a motorized dipstick whose motion was controlled via the customized LABVIEW software. Pt contacts were deposited on sample corners by sputtering, and measurements were carried out in a four-point (Van Der Pauw) configuration. To minimize any contribution due to possible sample inhomogeneities, several measurements were carried out on the same sample on rotation.
Electron microscopy and spectroscopy
The cross-section specimens for STEM experiments were thinned to electron transparency by tripod polishing down to ≈10 μm and argon ion beam milling in a stage cooled with liquid nitrogen. The electron microscopy and spectroscopy measurement were performed on a JEOL ARM 200CF microscope equipped with a cold field-emission electron source, a probe Cs corrector, a large solid-angle SDD-type JEOL Centurio EDX detector and a Gatan GIF Quantum ERS spectrometer. The microscope was operated at 200 kV, a semiconvergence angle (α) of 21 mrad, giving rise to a probe size of 0.8 Å (1 Å for the analytical analysis). Collection angle (109–270 mrad) was used to obtain the HAADF images. A collection semi-angle (β) of 68.5 mrad was used for EELS measurements. The STEM analysis was carried out at the specimen region where thickness is below 30 nm (t/λ<0.4 measured by low loss EELS using a log-ratio method). A detailed analysis about EELS data evaluation can be found in the Supplementary Methods and Supplementary Figs 9 and 10.
Additional information
How to cite this article: Baiutti, F. et al. High-temperature superconductivity in space-charge regions of lanthanum cuprate induced by two-dimensional doping. Nat. Commun. 6:8586 doi: 10.1038/ncomms9586 (2015).
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Acknowledgements
We thank Jochen Mannhart for critically reading the manuscript and for the helpful comments, P. Specht and B. Stuhlhofer for the technical support on the Oxide MBE system, B. Stuhlhofer, Y. Link and S. Schmid for contact deposition, H. Hoier for XRR measurements and U. Salzberger for TEM specimen preparation. Y.W., W.S. and P.A.v.A. acknowledge funding from the European Union Seventh Framework Program (FP7/2007-2013) under grant agreement no. 312483 (ESTEEM2).
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F.B., G.L., G.G. and J.M. conceived the experiments. Samples were synthetized by F.B., G.L. and G.C.; atomic force microscopy and X-ray diffraction characterization were performed by F.B., electrical measurements by F.B., G.L. and G.C. Electron microscopy and related spectroscopy measurements were carried out by Y.W., W.S. and P.A.v.A. The initial draft was prepared by F.B, G.G. and J.M. All the authors contributed to the interpretation and discussion of the experimental data and to editing the initial draft.
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Supplementary Figures 1-16, Supplementary Notes 1-4, Supplementary Methods and Supplementary References (PDF 974 kb)
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Baiutti, F., Logvenov, G., Gregori, G. et al. High-temperature superconductivity in space-charge regions of lanthanum cuprate induced by two-dimensional doping. Nat Commun 6, 8586 (2015). https://doi.org/10.1038/ncomms9586
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DOI: https://doi.org/10.1038/ncomms9586
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