A Quenched Disorder in the Quantum-Critical Superconductor CeCoIn5

  • Soon Gil Jung
  • , Harim Jang
  • , Jihyun Kim
  • , Jin Hong Park
  • , Sangyun Lee
  • , Soonbeom Seo
  • , Eric D. Bauer
  • , Tuson Park

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

Emergent inhomogeneous electronic phases in metallic quantum systems are crucial for understanding high-Tc superconductivity and other novel quantum states. In particular, spin droplets introduced by nonmagnetic dopants in quantum-critical superconductors (QCSs) can lead to a novel magnetic state in superconducting phases. However, the role of disorders caused by nonmagnetic dopants in quantum-critical regimes and their precise relation with superconductivity remain unclear. Here, the systematic evolution of a strong correlation between superconductive intertwined electronic phases and antiferromagnetism in Cd-doped CeCoIn5 is presented by measuring current–voltage characteristics under an external pressure. In the low-pressure coexisting regime where antiferromagnetic (AFM) and superconducting (SC) orders coexist, the critical current (Ic) is gradually suppressed by the increasing magnetic field, as in conventional type-II superconductors. At pressures higher than the critical pressure where the AFM order disappears, Ic remarkably shows a sudden spike near the irreversible magnetic field. In addition, at high pressures far from the critical pressure point, the peak effect is not suppressed, but remains robust over the whole superconducting region. These results indicate that magnetic islands are protected around dopant sites despite being suppressed by the increasingly correlated effects under pressure, providing a new perspective on the role of quenched disorders in QCSs.

Original languageEnglish
Article number2304837
JournalAdvanced Science
Volume11
Issue number1
DOIs
StatePublished - 5 Jan 2024

Keywords

  • critical current
  • peak effect
  • pressure
  • quantum-critical superconductor
  • quenched disorder

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