Magnetic properties and pairing tendencies of the iron-based superconducting ladder BaFe2 S3: Combined ab initio and density matrix renormalization group study

  • Niravkumar D. Patel
  • , Alberto Nocera
  • , Gonzalo Alvarez
  • , Ryotaro Arita
  • , Adriana Moreo
  • , Elbio Dagotto

Research output: Contribution to journalArticlepeer-review

39 Scopus citations

Abstract

The recent discovery of superconductivity under high pressure in the two-leg ladder compound BaFe2S3 [H. Takahashi, Nat. Mater. 14, 1008 (2015)1476-112210.1038/nmat4351] opens a broad avenue of research, because it represents the first report of pairing tendencies in a quasi-one-dimensional iron-based high-critical-temperature superconductor. Similarly, as in the case of the cuprates, ladders and chains can be far more accurately studied using many-body techniques and model Hamiltonians than their layered counterparts, particularly if several orbitals are active. In this publication, we derive a two-orbital Hubbard model from first principles that describes individual ladders of BaFe2S3. The model is studied with the density matrix renormalization group. These first reported results are exciting for two reasons: (i) at half-filling, ferromagnetic order emerges as the dominant magnetic pattern along the rungs of the ladder, and antiferromagnetic order along the legs, in excellent agreement with neutron experiments; and (ii) with hole doping, pairs form in the strong coupling regime, as found by studying the binding energy of two holes doped on the half-filled system. In addition, orbital selective Mott phase characteristics develop with doping, with only one Wannier orbital receiving the hole carriers while the other remains half-filled. These results suggest that the analysis of models for iron-based two-leg ladders could clarify the origin of pairing tendencies and other exotic properties of iron-based high-critical-temperature superconductors in general.

Original languageEnglish
Article number075119
JournalPhysical Review B
Volume94
Issue number7
DOIs
StatePublished - Aug 10 2016

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