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Register a new userObservation of a Three-Dimensional Quasi-Long-Range Electronic Supermodulation in YBa2Cu3O7-x/La0.7Ca0.3MnO3 Heterostructures
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Recent developments in high-temperature superconductivity highlight a generic tendency of the cuprates to develop competing electronic (charge) supermodulations. While coupled to the lattice and showing different characteristics in different materials, these supermodulations themselves are generally conceived to be quasi-two-dimensional, residing mainly in individual CuO2 planes, and poorly correlated along the c-axis. Here we observed with resonant elastic x-ray scattering a distinct type of electronic supermodulation in YBa2Cu3O7-x (YBCO) thin films grown epitaxially on La0.7Ca0.3MnO3 (LCMO). This supermodulation has a periodicity nearly commensurate with four lattice constants in-plane, eight out-of-plane, with long correlation lengths in three dimensions. It sets in far above the superconducting transition temperature and competes with superconductivity below this temperature for electronic states predominantly in the CuO2 plane. Our finding sheds new light on the nature of charge ordering in cuprates as well as a reported long-range proximity effect between superconductivity and ferromagnetism in YBCO/LCMO heterostructures.
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Negative compressibility is a sign of thermodynamic instability of open or non-equilibrium systems. In quantum materials consisting of multiple mutually coupled subsystems, the compressibility of one subsystem can be negative if it is countered by positive compressibility of the others. Manifestations of this effect have so far been limited to low-dimensional dilute electron systems. Here we present evidence from angle-resolved photoemission spectroscopy (ARPES) for negative electronic compressibility (NEC) in the quasi-three-dimensional (3D) spin-orbit correlated metal (Sr1-xLax)3Ir2O7. Increased electron filling accompanies an anomalous decrease of the chemical potential, as indicated by the overall movement of the deep valence bands. Such anomaly, suggestive of NEC, is shown to be primarily driven by the lowering in energy of the conduction band as the correlated bandgap reduces. Our finding points to a distinct pathway towards an uncharted territory of NEC featuring bulk correlated metals with unique potential for applications in low-power nanoelectronics and novel metamaterials.
The electron-phonon interaction is of central importance for the electrical and thermal properties of solids, and its influence on superconductivity, colossal magnetoresistance, and other many-body phenomena in correlated-electron materials is currently the subject of intense research. However, the non-local nature of the interactions between valence electrons and lattice ions, often compounded by a plethora of vibrational modes, present formidable challenges for attempts to experimentally control and theoretically describe the physical properties of complex materials. Here we report a Raman scattering study of the lattice dynamics in superlattices of the high-temperature superconductor $bf YBa_2 Cu_3 O_7$ and the colossal-magnetoresistance compound $bf La_{2/3}Ca_{1/3}MnO_{3}$ that suggests a new approach to this problem. We find that a rotational mode of the MnO$_6$ octahedra in $bf La_{2/3}Ca_{1/3}MnO_{3}$ experiences pronounced superconductivity-induced lineshape anomalies, which scale linearly with the thickness of the $bf YBa_2 Cu_3 O_7$ layers over a remarkably long range of several tens of nanometers. The transfer of the electron-phonon coupling between superlattice layers can be understood as a consequence of long-range Coulomb forces in conjunction with an orbital reconstruction at the interface. The superlattice geometry thus provides new opportunities for controlled modification of the electron-phonon interaction in complex materials.
Exotic phenomenon can be achieved in quantum materials by confining electronic states into two dimensions. For example, relativistic fermions are realised in a single layer of carbon atoms, the quantized Hall effect can result from two-dimensional (2D) systems, and the superconducting transition temperature can be enhanced significantly in a one-atomic-layer material. Ordinarily, 2D electronic system can be obtained by exfoliating the layered materials, growing monolayer materials on substrates, or establishing interfaces between different materials. Herein, we use femtosecond infrared laser pulses to invert the periodic lattice distortion sectionally in a three-dimensional (3D) charge density wave material, creating macroscopic domain walls of transient 2D ordered electronic states with exotic properties. The corresponding ultrafast electronic and lattice dynamics are captured by time- and angle-resolved photoemission spectroscopy and MeV ultrafast electron diffraction. Surprisingly, a novel energy gap state, which might be a signature of light-induced superconductivity, is identified in the photoinduced 2D domain wall near the surface. Such optical modulation of atomic motion is a new path to realise 2D electronic states and will be a new platform for creating novel phases in quantum materials.
High temperature superconductivity in cuprates arises from doping a parent Mott insulator by electrons or holes. A central issue is how the Mott gap evolves and the low-energy states emerge with doping. Here we report angle-resolved photoemission spectroscopy measurements on a cuprate parent compound by sequential in situ electron doping. The chemical potential jumps to the bottom of the upper Hubbard band upon a slight electron doping, making it possible to directly visualize the charge transfer band and the full Mott gap region. With increasing doping, the Mott gap rapidly collapses due to the spectral weight transfer from the charge transfer band to the gapped region and the induced low-energy states emerge in a wide energy range inside the Mott gap. These results provide key information on the electronic evolution in doping a Mott insulator and establish a basis for developing microscopic theories for cuprate superconductivity.
The original proposal to achieve superconductivity by starting from a quantum spin-liquid (QSL) and doping it with charge carriers, as proposed by Anderson in 1987, has yet to be realized. Here we propose an alternative strategy: use a QSL as a substrate for heterostructure growth of metallic films to design exotic superconductors. By spatially separating the two key ingredients of superconductivity, i.e., charge carriers (metal) and pairing interaction (QSL), the proposed setup naturally lands on the parameter regime conducive to a controlled theoretical prediction. Moreover, the proposed setup allows us to customize electron-electron interaction imprinted on the metallic layer. The QSL material of our choice is quantum spin ice well-known for its emergent gauge-field description of spin frustration. Assuming the metallic layer forms an isotropic single Fermi pocket, we predict that the coupling between the emergent gauge-field and the electrons of the metallic layer will drive topological odd-parity pairing. We further present guiding principles for materializing the suitable heterostructure using ab initio calculations and describe the band structure we predict for the case of Y$_2$Sn$_{2-x}$Sb$_x$O$_7$ grown on the (111) surface of Pr$_2$Zr$_2$O$_7$. Using this microscopic information, we predict topological odd-parity superconductivity at a few Kelvin in this heterostructure, which is comparable to the $T_c$ of the only other confirmed odd-parity superconductor Sr$_2$RuO$_4$.
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