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Title: Influence of electron doping on the ground state of (Sr1-xLax)2IrO4

Journal Article · · Physical Review. B, Condensed Matter and Materials Physics
 [1];  [1];  [2];  [2];  [2];  [2];  [3];  [3];  [4];  [5];  [2];  [6];  [7];  [1]
  1. Univ. of California, Santa Barbara, CA (United States)
  2. Boston College, Chestnut Hill, MA (United States)
  3. Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)
  4. National Inst. of Standards and Technology (NIST), Gaithersburg, MD (United States); Univ. of Maryland, College Park, MD (United States)
  5. National Inst. of Standards and Technology (NIST), Gaithersburg, MD (United States). Center for Neutron Research
  6. National Inst. of Standards and Technology (NIST), Gaithersburg, MD (United States)
  7. Univ. of Illinois, Urbana-Champaign, IL (United States)

The evolution of the electronic properties of electron-doped (Sr1-xLax)2IrO4 is experimentally explored as the doping limit of La is approached. As electrons are introduced, the electronic ground state transitions from a spin-orbit Mott phase into an electronically phase separated state, where long-range magnetic order vanishes beyond x = 0:02 and charge transport remains percolative up to the limit of La substitution (x =0:06). In particular, the electronic ground state remains inhomogeneous even beyond the collapse of the parent state's long-range antiferromagnetic order, while persistent short-range magnetism survives up to the highest La-substitution levels. Furthermore, as electrons are doped into Sr2IrO4, we observe the appearance of a low temperature magnetic glass-like state intermediate to the complete suppression of antiferromagnetic order. Universalities and di erences in the electron-doped phase diagrams of single layer and bilayer Ruddlesden-Popper strontium iridates are discussed.

Research Organization:
Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States). Spallation Neutron Source (SNS)
Sponsoring Organization:
USDOE
Grant/Contract Number:
AC05-00OR22725; AC02-06CH11357
OSTI ID:
1286907
Alternate ID(s):
OSTI ID: 1211566
Journal Information:
Physical Review. B, Condensed Matter and Materials Physics, Vol. 92, Issue 7; ISSN 1098-0121
Publisher:
American Physical Society (APS)Copyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 86 works
Citation information provided by
Web of Science

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Cited By (15)

Symmetry breaking of in-plane anisotropic magnetoresistance with temperature in La-doped S r 2 Ir O 4 films journal August 2019
Unidirectional spin density wave state in metallic (Sr1−xLax)2IrO4 journal January 2018
The challenge of spin–orbit-tuned ground states in iridates: a key issues review journal February 2018
Correlation transports at p- / n- types in electron metastable perovskite family of rare-earth nickelates journal February 2020
Quasistatic antiferromagnetism in the quantum wells of SmTiO3/SrTiO3 heterostructures journal February 2018
Two dimensional electron gas in the $\delta$ -doped iridates with strong spin–orbit coupling: La$_\delta$ Sr 2 IrO 4 journal July 2019
Atomic-scale fragmentation and collapse of antiferromagnetic order in a doped Mott insulator journal October 2019
First-principles calculation of spin and orbital contributions to magnetically ordered moments in Sr 2 IrO 4 journal April 2020
The J eff = 1/2 Antiferromagnet Sr 2 IrO 4 : A Golden Avenue toward New Physics and Functions journal October 2019
Synthesis and physical properties of the new iridium oxyfluoride S r 2 Ir ( O , F ) 6 δ using a topochemical reaction method journal January 2020
Structure, magnetism, and transport properties for Ca doping in Sr 2 IrO 4 journal May 2017
Decoupling of magnetism and electric transport in single-crystal (Sr1-xAx)2IrO4 (A = Ca or Ba) text January 2017
Stability of the Antiferromagnetic State in the Electron Doped Iridates text January 2018
Atomic-scale fragmentation and collapse of antiferromagnetic order in a doped Mott insulator text January 2019
The Jeff=1/2 antiferromagnet Sr2IrO4: A golden avenue toward new physics and functions text January 2021

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