It has recently been established that the high temperature (high-Tc(between atomic and macroscopic scale). Here we report micro X-ray diffraction imaging of the spatial distribution of both the charge-density-wave 'puddles' (domains with only a few wavelengths) and quenched disorder in HgBa 2 CuO 4+y , the single layer cuprate with the highest T c , 95 kelvin [26][27][28] . We found that the charge-density-wave puddles, like the steam bubbles in boiling water, have a fat-tailed size distribution that is typical of selforganization near a critical point 19 . However, the quenched disorder, which arises from oxygen interstitials, has a distribution that is contrary to the usual assumed random, uncorrelated distribution 12, 13 . The interstitials-oxygen-rich domains are spatially anticorrelated with the charge-density-wave domains, leading to a complex emergent geometry of the spatial landscape for superconductivity. 2Although it is known that the incommensurate charge-density-wave (CDW) order in cuprates (copper oxides) is made of ordered, stripy, nanoscale puddles with an average of only 3-4 oscillations, information about the size distribution and spatial organization of these puddles has so far not been available. We present experiments that demonstrate that CDW puddles, have a complex spatial distribution and coexist with, but are spatially anticorrelated to, quenched disorder in HgBa 2 CuO 4+y (Hg1201). The sample we studied is a layered perovskite at optimum doping with oxygen interstitials y=0.12, tetragonal symmetry P4/mmm and a low misfit strain [14][15][16] . The X-ray diffraction (XRD) measurements (see Methods) show diffuse CDW satellites (secondary peaks surrounding a main peak) at q CDW =(0.23a*, 0.16c*), in the b*=0 plane and q CDW =(0.23b*, 0.16c*) in the a*=0 plane (where a*, b*, and c* are the reciprocal lattice units) around specific Bragg peaks, such as (1 0 8), below the onset temperature T CDW =240 K (see Fig. 1a). The component of the momentum transfer q CDW in the CuO 2 plane (0.23a*) in this case is smaller than it is in the underdoped case (0.28a*) 5 . The temperature evolution of CDW-peak profile along a* (in the h direction; Fig. 1b) shows a smeared, glassy-like evolution below T CDW .The CDW-peak intensity reaches a maximum at T=100 K, followed by a drop associated with the onset of superconductivity at T=T c . We investigated the isotropic character of the CDW, in the a-b plane using azimuthal scans, as shown in Fig. 1c. We observed an equal probability of vertical and horizontally striped CDW puddles.Our main result is the discovery of the statistical spatial distribution of the CDW-puddle size and density throughout the sample, which shows an emergent complex network geometry for the superconducting phase. We performed scanning micro X-ray diffraction (SµXRD) measurements (see Methods) to extend the imaging of spatial inhomogeneity previously obtained by scanning tunneling microscopy [7][8][9] , from the surface to the bulk of the sample and from nanoscale to mesoscale spatial inh...
We report scanning tunneling spectroscopy imaging of the vortex lattice in single crystalline MgB2. By tunneling parallel to the c axis, a single superconducting gap (Delta=2.2 meV) associated with the pi band is observed. The vortices in the pi band have a large core size compared to estimates based on H(c2) and show an absence of localized states in the core. Furthermore, superconductivity between the vortices is rapidly suppressed by an applied field. These results suggest that superconductivity in the pi band is, at least partially, induced by the intrinsically superconducting sigma band.
The anisotropy gamma of the superconducting state of high quality single crystals of MgB2 was determined, using torque magnetometry with two different methods. The anisotropy of the upper critical field was found to be temperature dependent, decreasing from gamma approximately 6 at 15 K to 2.8 at 35 K. Reversible torque data near T(c) reveal a field dependent anisotropy, increasing nearly linearly from gamma approximately equal to 2 in zero field to 3.7 in 10 kOe. The unusual temperature dependence is a true bulk property and can be explained by nonlocal effects of anisotropic pairing and/or the k--> dependence of the effective mass tensor.
The ab-plane thermal conductivity κ of single-crystalline hexagonal MgB2 has been measured as a function of magnetic field H with orientations both parallel and perpendicular to the c-axis and at temperatures between 0.5 and 300 K. In the mixed state, κ(H) measured at constant temperatures reveals features that are not typical for common type-II superconductors. The observed behavior may be associated with the field-induced reduction of two superconducting energy gaps, significantly different in magnitude. A nonlinear temperature dependence of the electronic thermal conductivity is observed in the field-induced normal state at low temperatures. This behavior is at variance with the law of Wiedemann and Franz, and suggests an unexpected instability of the electronic subsystem in the normal state at T ≈ 1 K.
The growth of carbon-substituted magnesium diboride Mg͑B 1−x C x ͒ 2 single crystals with 0 ഛ x ഛ 0.15 is reported, and the structural, transport, and magnetization data are presented. The superconducting transition temperature decreases monotonically with increasing carbon content in the full investigated range of substitution. By adjusting the nominal composition, T c of substituted crystals can be tuned in a wide temperature range between 10 and 39 K. Simultaneous introduction of disorder by carbon substitution and significant increase of the upper critical field H c2 is observed. Comparing with the nonsubstituted compound, H c2 at 15 K for x = 0.05 is enhanced by more than a factor of 2 for H oriented both perpendicular and parallel to the ab plane. This enhancement is accompanied by a reduction of the H c2 -anisotropy coefficient ␥ from 4.5 ͑for the nonsubstituted compound͒ to 3.4 and 2.8 for the crystals with x = 0.05 and 0.095, respectively. At temperatures below 10 K, the single crystal with larger carbon content shows H c2 ͑defined at zero resistance͒ higher than 7 and 24 T for H oriented perpendicular and parallel to the ab plane, respectively. Observed increase of H c2 cannot be explained by the change in the coherence length due to the disorder-induced decrease of the mean free path only.
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