Spin-Orbit Interactions in Ruddlesden-Popper Phases Srn+1IrnO3n+1 (n = 1, 2, and ∞)

G. Cao, L. DeLong
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Abstract

The Ruddlesden-Popper phases Srn+1IrnO3n+1 (n = 1, 2, and ∞) have been intensively studied, and exhibit many novel behaviors and ground states driven by a rare interplay between strong spin-orbit and Coulomb interactions. One key empirical trend is that most iridates are antiferromagnetic insulators, contrary to conventional wisdom. The spin-orbit-coupled Mott state does not always closely track the magnetic state in iridates. Often, chemical doping can effectively induce a metallic state. Defying expectations, Sr2IrO4, which is the prototypical spin-orbit-coupled Mott insulator, does not become superconducting upon electron doping, but remains insulating under applied pressures extending into the Mbar range, highlighting the extraordinary susceptibility to the lattice degrees of freedom, which is at the heart of the physics driving the iridates.
Ruddlesden-Popper相Srn+1IrnO3n+1 (n = 1,2和∞)的自旋轨道相互作用
Ruddlesden-Popper相Srn+1IrnO3n+1 (n = 1,2和∞)已经被深入研究,并表现出许多新的行为和基态,这些行为和基态是由强自旋轨道和库仑相互作用之间的罕见相互作用驱动的。一个关键的经验趋势是,大多数铱酸盐是反铁磁绝缘体,这与传统观念相反。在铱酸盐中,自旋轨道耦合的莫特态并不总是密切跟踪磁性态。通常,化学掺杂可以有效地诱导金属态。出乎意料的是,Sr2IrO4是典型的自旋轨道耦合Mott绝缘体,在电子掺杂后不会变成超导,但在施加到Mbar范围的压力下仍然保持绝缘,突出了晶格自由度的非凡敏感性,这是驱动铱酸盐的物理核心。
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