Sean Vig, Anshul Kogar, Matteo Mitrano, Ali A. Husain, Vivek Mishra, Melinda S. Rak, Luc Venema, Peter D. Johnson, Genda D. Gu, Eduardo Fradkin, Michael R. Norman, Peter Abbamonte
SciPost Phys. 3, 026 (2017) ·
published 6 October 2017
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One of the most fundamental properties of an interacting electron system is its frequency- and wave-vector-dependent density response function, $\chi({\bf q},\omega)$. The imaginary part, $\chi''({\bf q},\omega)$, defines the fundamental bosonic charge excitations of the system, exhibiting peaks wherever collective modes are present. $\chi$ quantifies the electronic compressibility of a material, its response to external fields, its ability to screen charge, and its tendency to form charge density waves. Unfortunately, there has never been a fully momentum-resolved means to measure $\chi({\bf q},\omega)$ at the meV energy scale relevant to modern electronic materials. Here, we demonstrate a way to measure $\chi$ with quantitative momentum resolution by applying alignment techniques from x-ray and neutron scattering to surface high-resolution electron energy-loss spectroscopy (HR-EELS). This approach, which we refer to here as ``M-EELS" allows direct measurement of $\chi''({\bf q},\omega)$ with meV resolution while controlling the momentum with an accuracy better than a percent of a typical Brillouin zone. We apply this technique to finite-{\bf q} excitations in the optimally-doped high temperature superconductor, Bi$_2$Sr$_2$CaCu$_2$O$_{8+x}$ (Bi2212), which exhibits several phonons potentially relevant to dispersion anomalies observed in ARPES and STM experiments. Our study defines a path to studying the long-sought collective charge modes in quantum materials at the meV scale and with full momentum control.
Luca V. Delacrétaz, Blaise Goutéraux, Sean A. Hartnoll, Anna Karlsson
SciPost Phys. 3, 025 (2017) ·
published 29 September 2017
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Bad metals have a large resistivity without being strongly disordered. In many bad metals the Drude peak moves away from zero frequency as the resistivity becomes large at increasing temperatures. We catalogue the position and width of the `displaced Drude peak' in the observed optical conductivity of several families of bad metals, showing that $\omega_\text{peak} \sim \Delta \omega \sim k_BT/\hbar$. This is the same quantum critical timescale that underpins the $T$-linear dc resistivity of many of these materials. We provide a unified theoretical description of the optical and dc transport properties of bad metals in terms of the hydrodynamics of short range quantum critical fluctuations of incommensurate density wave order. Within hydrodynamics, pinned translational order is essential to obtain the nonzero frequency peak.
Milan P. Allan, Mark H. Fischer, Oliver Ostojic, Arjo Andringa
SciPost Phys. 3, 010 (2017) ·
published 10 August 2017
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The quest to create superconductors with higher transition temperatures is as old as superconductivity itself. One strategy, popular after the realization that (conventional) superconductivity is mediated by phonons, is to chemically combine different elements within the crystalline unit cell to maximize the electron-phonon coupling. This led to the discovery of NbTi and Nb3Sn, to name just the most technologically relevant examples. Here, we propose a radically different approach to transform a `pristine' material into a better (meta-) superconductor by making use of modern fabrication techniques: designing and engineering the electronic properties of thin films via periodic patterning on the nanoscale. We present a model calculation to explore the key effects of different supercells that could be fabricated using nanofabrication or deliberate lattice mismatch, and demonstrate that specific pattern will enhance the coupling and the transition temperature. We also discuss how numerical methods could predict the correct design parameters to improve superconductivity in materials including Al, NbTi, and MgB2
Jan Girovsky, Jose L. Lado, Floris E. Kalff, Eleonora Fahrenfort, Lucas J. J. M. Peters, Joaquín Fernández-Rossier, Alexander F. Otte
SciPost Phys. 2, 020 (2017) ·
published 14 June 2017
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The interaction of electrons with a periodic potential of atoms in crystalline solids gives rise to band structure. The band structure of existing materials can be measured by photoemission spectroscopy and accurately understood in terms of the tight-binding model, however not many experimental approaches exist that allow to tailor artificial crystal lattices using a bottom-up approach. The ability to engineer and study atomically crafted designer materials by scanning tunnelling microscopy and spectroscopy (STM/STS) helps to understand the emergence of material properties. Here, we use atom manipulation of individual vacancies in a chlorine monolayer on Cu(100) to construct one- and two-dimensional structures of various densities and sizes. Local STS measurements reveal the emergence of quasiparticle bands, evidenced by standing Bloch waves, with tuneable dispersion. The experimental data are understood in terms of a tight-binding model combined with an additional broadening term that allows an estimation of the coupling to the underlying substrate.
