Competition between magnetism and the kinetic energy of mobile carriers (typically holes) in doped antiferromagnets may lead to ‘stripe’ phases1,2,3,4, which are charged rivers separating regions of oppositely phased antiferromagnetism. In copper oxides the main experimental evidence for such coexisting static spin and charge order comes from neutron scattering in La1.48Nd0.4Sr0.12CuO4 (LNSCO; ref. 5) and La1.875Ba0.125CuO4 (LBCO; ref. 6). However, as a neutron is neutral, it does not detect charge but rather its associated lattice distortion7, so it is not known whether the stripes involve ordering of the doped holes. Here we present a study of the charge order in LBCO with resonant soft X-ray scattering (RSXS). We observe giant resonances near the Fermi level as well as near the correlated gap8,9, demonstrating significant modulation in both the doped-hole density and the ‘Mottness’, or the degree to which the system resembles a Mott insulator10. The peak-to-trough amplitude of the valence modulation is estimated to be 0.063 holes, which suggests11 an integrated area of 0.59 holes under a single stripe, close to the expected 0.5 for half-filled stripes.
The charge/spin superstructure in LNSCO5 and LBCO6 appears only in the low-temperature tetragonal (LTT) phase, is most stable at x=1/8 and coincides with an anomalous suppression of the critical temperature Tc (ref. 12). This phase is frequently interpreted as (quasi) static stripes that have been pinned by the LTT distortion. The charge reflections observed with neutron scattering are weak (∼6 times less intense than the magnetic reflections) as neutrons only detect the lattice distortion, which was estimated to be only about 0.004 Å (ref. 7). However, one assumes that the hole modulation itself is significant. We point out, however, that the spin-density wave in elemental Cr also exhibits half-wavelength charge reflections that are weaker by about a factor of 4.1 and represent a distortion of similar size13. So, in the neutron Bragg peaks alone there is no clear difference between the phenomenon in LNSCO and a simple spin-density wave. To determine whether the doped holes are actually involved we have studied LBCO with RSXS near the O K (1s→2p) and Cu L3/2 (2p3/2→3dx2−y2) edges, which provide direct sensitivity to valence electron ordering14,15,16,17,18,19,20.
Single crystals of La2−xBaxCuO4 with x=1/8 were grown by the floating-zone method21. The sample used in this study had Tc=2.5 K indicating suppressed superconductivity and stabilized spin/charge order. The sample was cleaved in air revealing a surface with (0,0,1) orientation. RSXS measurements were performed on beam line X1B at the National Synchrotron Light Source, Brookhaven, using a 10-axis, ultrahigh-vacuum-compatible diffractometer. The sample was cooled with a He flow cryostat connected through Cu braids, providing a base temperature of 18 K. X-ray absorption spectra (XAS) were measured in situ in fluorescence yield mode at the O K and Cu L3/2 edges and found to be consistent with previous studies8 (see Figs 1, 3a). We will denote reciprocal space with Miller indices (H,K,L), which represent a momentum transfer Q=(2π/a H,2π/b K,2π/c L) where a=b=3.788 Å, c=13.23 Å. The incident X-ray polarization depends on Q but was approximately 60∘ from the Cu–O bond for measurements at both edges.
The O K XAS in the cuprates exhibits a mobile carrier peak (MCP) at 528.6 eV, corresponding to transitions into the doped hole levels, and an upper Hubbard band (UHB) peak at 530.4 eV, corresponding to transitions into the d level of a neighbouring Cu (see Figs 1 and 3). As the hole density increases, spectral weight is transferred from the UHB to the MCP as the number of sites opposing electron addition decreases8,9,22. In this letter we take the spectral weight in the MCP to be a measure of the local hole density and that in the UHB to be a measure of the ‘Mottness’10, that is, the degree to which there is a functioning Hubbard U, the degree to which the system resembles a Mott insulator. The Cu L3/2 edge exhibits a main peak at 933 eV and ligand hole side band at 934.3 eV, which grows with doping. We take the sideband to be a measure of the hole density, similar to the MCP, and the main peak to be a measure of distortions in the Cu sublattice.
Static charge ‘stripe’ correlations were initially detected at the Cu L3/2 resonance and mapped in the (H,0,L) plane, shown in Fig. 2. In agreement with hard X-ray studies23,24, the scattering was sharp along H but rod-like along L (correlation lengths ξa≈127a, ξc≈2c), indicating quasi-long-range order in the CuO2 plane but weak coupling between planes. A maximum intensity of 175 Hz on a fluorescence background of 425 Hz was observed at (0.251,0,3/2). Owing to differences in beam refraction a slightly different value H=0.245 was observed at the O K edge. The half-integer L indicates that charge order is offset by 2a between successive unit cells, presumably to minimize Coulomb repulsion. No scattering could be detected off-resonance above the fluorescence background.
In Fig. 1 we display a ‘resonance profile’, that is, the intensity of charge scattering as a function of energy compared with XAS. For geometric convenience the O K and Cu L3/2 data were taken with L=0.72 and 1.47, respectively. The charge scattering at the Cu L3/2 edge is offset from the absorption maximum by 0.2 eV and probably arises from distortions in the Cu sublattice. The O K scattering exhibits strong resonances at both the MCP and UHB features, indicating that the carrier density and the degree of Mottness are both modulated in real space. This shows that this phase exhibits real charge order and, perhaps more significantly, is associated with a periodic restoration of a Mott state.
The charge modulation seems to be substantial but it is important to estimate its size. The integrated intensity of a Bragg reflection is proportional to the square of its structure factor, ρQmn(ω)=(1/Vcell)Σjfjmn(ω)exp(i Q · rj), where Vcell is the unit cell volume, fjmn(ω) is the X-ray form factor of atom j, rj its position, ω is the photon energy, and m and n are incoming and outgoing polarization indices25. So to estimate the hole amplitude one must first define the X-ray form factor for a doped hole.
For this purpose we separate the oxygen form factor fOmn(ω,p)=fR(ω)+p fDmn(ω), where fR is a ‘raw’ component common to all oxygen atoms, that is, fR→8 as ω→∞, and fDmn(ω) describes the polarization-dependent spectral changes with the doped-hole density, p. fDmn has units of electrons per hole and can be interpreted as the doped hole form factor. A form factor is related to the absorptive part of the index of refraction by Im[nm(ω;p)]=−reλ2/2πVcellIm[Σifimm (ω,p)], where re is the classical electron radius and λ is the X-ray wavelength, so fDmn may be determined from doping-dependent XAS. Using this relationship and data from ref. 8 (Fig. 3a) we extracted the diagonal components Im[fDmm(ω)] by solving a system of equations at each energy and retrieving the real parts by Kramers–Kronig transform. The off-diagonal components were assumed to be small. For an x-oriented hole we find |fDxx|=82 electrons per hole on the resonance maximum, that is, a doped hole scatters as strongly as a Pb atom.
A stripe structure factor ρstripesmn was constructed based on the orbital pattern from a previous three-band Hubbard calculation11 to relate fDmn(ω) to the scattered intensity (Fig. 3c). This pattern was stacked in alternating fashion as proposed in ref. 7 and, accounting for the incident and scattered polarizations, the structure factor was computed analytically to be |ɛf*· ρstripes· ɛi|=A·(0.00475 Å−3) (where ɛi and ɛf* are the incident and scattered (or ‘final’) polarizations, respectively). A is a fit variable that may be interpreted as the number of holes contained in one stripe a single unit cell in length (A=0.5 would be consistent with half-filled stripes).
The integrated intensity of resonant scattering was determined in the ellipsoidal approximation by tuning to the MCP and carrying out linear scans along three orthogonal directions, and taking the product I=Ipeak×ΔqxΔqyΔqz, where Ipeak is the peak count rate in hertz and Δqn is the width along direction n. We measured Δqx=0.0133 Å−1 and Δqy=0.0169 Å−1. The limited Q range of RSXS prevented complete determination of Δqz so we use the value from ref. 6 of Δqz=0.256 Å−1, giving Istripes=0.101 Hz Å−3. To determine the absolute scale, the same measurement was done 10 eV below the O K edge on the (0,0,2) Bragg reflection from a cleaved single crystal of Bi2Sr2CaCu2O8+δ, which has a known structure factor. Comparing the two, correcting for differences in absorption, we arrive at |ɛf*· ρstripes· ɛi|=0.00282 Å−3 or A=0.59 holes. This number is only an estimate but is close to the value 0.5 expected for half-filled stripes. The estimated occupancies for various orbitals are shown in Fig. 3c. Note that despite the large integral the peak-to-trough amplitude is only 0.063 holes, as the doped holes are distributed over many sites.
To search for a difference between the ordering of holes and the lattice, angular scans through the charge scattering were performed at different temperatures at both the MCP and Cu L3/2 resonances (Fig. 4). Charge correlations were visible at both edges below the LTT transition at 60 K, which is higher than previously published6 because the x value for our sample is closer to 1/8 (ref. 26). No difference in temperature dependence was detected between the two edges, suggesting that the holes and lattice order simultaneously.
The reader may wonder about the relationship between this study and the negative result reported in ref. 12 for optimally doped La2CuO4+y (LCO), in which the stripe order is sometimes said to be ‘dynamic’. It is well known that a fluctuating density can give rise to diffuse, elastic scattering, a common example being Rayleigh scattering by the atmosphere. In ref. 14 we showed that the resonant diffuse scattering from such fluctuations in LCO is negligible, that is, such correlations may be valid excited states but are not thermally occupied, therefore translational symmetry is not broken even on short timescales. By contrast the charge ordering in LBCO is static and, as evident from the large amplitude and the broad spectral width, a macroscopic fraction of the doped holes are modulated. The amplitude of 0.063 is similar to an estimate for Nickelate stripes20 even though the lattice in LBCO is only weakly involved. The associated modulation of high-energy spectral weight is strong evidence that this phase is driven instead by a desire of the system to restore a Mott state in some regions of the sample.
Our results do not establish whether this phase is truly nematic or is, for example, a ‘checkerboard’ Wigner crystal27. Forthcoming measurements will address this issue. In the meantime, we point out the similarity of this phenomenon to the ‘hole crystal’ observed in Sr14Cu24O41 (ref. 17). The importance of Umklapp processes for the stability of a Wigner crystal on a lattice may explain the stability charge order at the commensurate doping x=1/8.
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We acknowledge T. Valla for assistance with sample cleaving and discussions with S. K. Sinha, J. M. Tranquada, C. Schüßler-Langheine, P. A. Lee and W. Ku. This work was supported by the US Department of Energy, NWO (Dutch Science Foundation) and FOM (Netherlands Organization for Fundamental Research on Matter).
The authors declare no competing financial interests.
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Abbamonte, P., Rusydi, A., Smadici, S. et al. Spatially modulated 'Mottness' in La2-xBaxCuO4. Nature Phys 1, 155–158 (2005). https://doi.org/10.1038/nphys178
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