Repository logo
English
  • English
  • Català
  • Čeština
  • Deutsch
  • Español
  • Français
  • Gàidhlig
  • Italiano
  • Latviešu
  • Magyar
  • Nederlands
  • Polski
  • Português
  • Português do Brasil
  • Suomi
  • Svenska
  • Türkçe
  • Tiếng Việt
  • Қазақ
  • বাংলা
  • हिंदी
  • Ελληνικά
  • Yкраї́нська
  • Log In
    or
    New user? Click here to register.Have you forgotten your password?
Repository logo
  • Communities & Collections
  • All of R-3
English
  • English
  • Català
  • Čeština
  • Deutsch
  • Español
  • Français
  • Gàidhlig
  • Italiano
  • Latviešu
  • Magyar
  • Nederlands
  • Polski
  • Português
  • Português do Brasil
  • Suomi
  • Svenska
  • Türkçe
  • Tiếng Việt
  • Қазақ
  • বাংলা
  • हिंदी
  • Ελληνικά
  • Yкраї́нська
  • Log In
    or
    New user? Click here to register.Have you forgotten your password?
  1. Home
  2. Browse by Author

Browsing by Author "Yin, Z.P."

Now showing 1 - 2 of 2
Results Per Page
Sort Options
  • Loading...
    Thumbnail Image
    Item
    Correlation-driven metal-insulator transition in proximity to an iron-based superconductor
    (American Physical Society, 2017) Charnukha, A.; Yin, Z.P.; Song, Y.; Cao, C.D.; Dai, Pengcheng; Haule, K.; Kotliar, G.; Basov, D.N.
    We report the direct spectroscopic observation of a metal to correlated-insulator transition in the family of iron-based superconducting materials. By means of optical spectroscopy we demonstrate that the excitation spectrum of NaFe1−xCuxAs develops a large gap with increasing copper substitution. Dynamical mean-field theory calculations show a good agreement with the experimental data and suggest that the formation of the charge gap requires an intimate interplay of strong on-site electronic correlations and spin-exchange coupling, revealing the correlated Slater-insulator nature of the antiferromagnetic ground state. Our calculations further predict the high-temperature paramagnetic state of the same compound to be a highly incoherent correlated metal. We verify this prediction experimentally by showing that the doping-induced weakening of antiferromagnetic correlations enables a thermal crossover from an insulating to an incoherent metallic state. Redistribution of the optical spectral weight in this crossover uncovers the characteristic energy of Hund's-coupling and Mott-Hubbard electronic correlations essential for the electronic localization. Our results demonstrate that NaFe1−xCuxAs continuously transitions from the typical itinerant phases of iron pnictides to a highly incoherent metal and ultimately a correlated insulator. Such an electronic state is expected to favor high-temperature superconductivity.
  • Loading...
    Thumbnail Image
    Item
    Critical quadrupole fluctuations and collective modes in iron pnictide superconductors
    (American Physical Society, 2016) Thorsmølle, V.K.; Khodas, M.; Yin, Z.P.; Zhang, Chenglin; Carr, S.V.; Dai, Pengcheng; Blumberg, G.
    The multiband nature of iron pnictides gives rise to a rich temperature-doping phase diagram of competing orders and a plethora of collective phenomena. At low dopings, the tetragonal-to-orthorhombic structural transition is closely followed by a spin-density-wave transition both being in close proximity to the superconducting phase. A key question is the nature of high-Tc superconductivity and its relation to orbital ordering and magnetism. Here we study the NaFe1−xCoxAs superconductor using polarization-resolved Raman spectroscopy. The Raman susceptibility displays critical enhancement of nonsymmetric charge fluctuations across the entire phase diagram, which are precursors to a d-wave Pomeranchuk instability at temperature θ(x). The charge fluctuations are interpreted in terms of quadrupole interorbital excitations in which the electron and hole Fermi surfaces breathe in-phase. Below Tc, the critical fluctuations acquire coherence and undergo a metamorphosis into a coherent in-gap mode of extraordinary strength.
  • About R-3
  • Report a Digital Accessibility Issue
  • Request Accessible Formats
  • Fondren Library
  • Contact Us
  • FAQ
  • Privacy Notice
  • R-3 Policies

Physical Address:

6100 Main Street, Houston, Texas 77005

Mailing Address:

MS-44, P.O.BOX 1892, Houston, Texas 77251-1892