It is well known that the microstructures of the transition-metal oxides, including the high-transition-temperature (high-T(c)) copper oxide superconductors, are complex. This is particularly so when there are oxygen interstitials or vacancies, which influence the bulk properties. For example, the oxygen interstitials in the spacer layers separating the superconducting CuO(2) planes undergo ordering phenomena in Sr(2)O(1+y)CuO(2) (ref. 9), YBa(2)Cu(3)O(6+y) (ref. 10) and La(2)CuO(4+y) (refs 11-15) that induce enhancements in the transition temperatures with no changes in hole concentrations. It is also known that complex systems often have a scale-invariant structural organization, but hitherto none had been found in high-T(c) materials. Here we report that the ordering of oxygen interstitials in the La(2)O(2+y) spacer layers of La(2)CuO(4+y) high-T(c) superconductors is characterized by a fractal distribution up to a maximum limiting size of 400 mum. Intriguingly, these fractal distributions of dopants seem to enhance superconductivity at high temperature.

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...

Advanced synchrotron radiation focusing down to a size of 300 nm has been used to visualize nanoscale phase separation in the K 0.8 Fe 1.6 Se 2 superconducting system using scanning nanofocus single-crystal X-ray diffraction. The results show an intrinsic phase separation in K 0.8 Fe 1.6 Se 2 single crystals at T< 520 K, revealing coexistence of i) a magnetic phase characterized by an expanded lattice with superstructures due to Fe vacancy ordering and ii) a non-magnetic phase with an in-plane compressed lattice. The spatial distribution of the two phases at 300 K shows a frustrated or arrested nature of the phase separation. The space-resolved imaging of the phase separation permitted us to provide a direct evidence of nanophase domains smaller than 300 nm and different micrometer-sized regions with percolating magnetic or nonmagnetic domains forming a multiscale complex network of the two phases.

The disposition of defects in metal oxides is a key attribute exploited for applications from fuel cells and catalysts to superconducting devices and memristors. The most typical defects are mobile excess oxygens and oxygen vacancies, and can be manipulated by a variety of thermal protocols as well as optical and dc electric fields. Here we report the X-ray writing of high-quality superconducting regions, derived from defect ordering 1 , in the superoxygenated layered cuprate, La 2 CuO 4+y . Irradiation of a poor superconductor prepared by rapid thermal quenching results first in growth of ordered regions, with an enhancement of superconductivity becoming visible only after a waiting time, as is characteristic of other systems such as ferroelectrics 2,3 where strain must be accommodated for order to become extended. However, in La 2 CuO 4+y , we are able to resolve all aspects of the growth of (oxygen) intercalant order, including an extraordinary excursion from low to high and back to low anisotropy of the ordered regions. We can also clearly associate the onset of high quality superconductivity with defect ordering in two dimensions. Additional experiments with small beams demonstrate a photoresist-free, single-step strategy for writing functional materials.