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Title: Coexisting charge and magnetic orders in the dimer-chain iridate Ba5AlIr2O11

Journal Article · · Physical Review. B, Condensed Matter and Materials Physics
 [1];  [2];  [3];  [4];  [1];  [1];  [1];  [5];  [6];  [1]
  1. Univ. of Kentucky, Lexington, KY (United States). Center for Advanced Materials. Dept. of Physics and Astronomy
  2. Univ. of Kentucky, Lexington, KY (United States). Center for Advanced Materials. Dept. of Physics and Astronomy; Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Quantum Condensed Matter Division; Renmin Univ. of China, Beijing (China). Dept. of Physics
  3. Univ. of Kentucky, Lexington, KY (United States). Center for Advanced Materials. Dept. of Physics and Astronomy; Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Quantum Condensed Matter Division
  4. Univ. of Kentucky, Lexington, KY (United States). Center for Advanced Materials. Dept. of Physics and Astronomy; Chinese Academy of Sciences (CAS), Hefei (China). Inst. of Solid State Physics
  5. Inst. of Metal Physics, Ekaterinburg (Russian Federation); Ural Federal Univ., Ekaterinburg (Russian Federation). Dept. of Physics
  6. Univ. of Cologne (Germany). Inst. of Physics II

In this paper, we have synthesized and studied single-crystal Ba5AlIr2O11 that features dimer chains of two inequivalent octahedra occupied by tetravalent Ir4+(5d5) and pentavalent Ir5+(5d4) ions, respectively. Ba5AlIr2O11 is a Mott insulator that undergoes a subtle structural phase transition near TS=210K and a magnetic transition at TM=4.5K; the latter transition is surprisingly resistant to applied magnetic fields μoH≤12T but more sensitive to modest applied pressure (dTM/dp ≈ +0.61K/GPa). All results indicate that the phase transition at TS signals an enhanced charge order that induces electrical dipoles and strong dielectric response near TS. It is clear that the strong covalency and spin-orbit interaction (SOI) suppress double exchange in Ir dimers and stabilize a novel magnetic state that is neither S=3/2 nor J=1/2, but rather lies in an “intermediate” regime between these two states. Finally, the novel behavior of Ba5AlIr2O11 therefore provides unique insights into the physics of SOI along with strong covalency in competition with double-exchange interactions of comparable strength.

Research Organization:
Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES); National Science Foundation (NSF); Civil Research and Development Foundation (CRDF) (United States); Russian Foundation of Basic Research; China Scholarship Council
Grant/Contract Number:
AC05-00OR22725; DMR-1265162; 13-02-00374; FSCX-14-61025-0
OSTI ID:
1324136
Alternate ID(s):
OSTI ID: 1198602
Journal Information:
Physical Review. B, Condensed Matter and Materials Physics, Vol. 91, Issue 23; ISSN 1098-0121
Publisher:
American Physical Society (APS)Copyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 27 works
Citation information provided by
Web of Science

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Cited By (9)

Covalent bonds against magnetism in transition metal compounds journal September 2016
The challenge of spin–orbit-tuned ground states in iridates: a key issues review journal February 2018
Ground state in the novel dimer iridate B a 13 I r 6 O 30 with I r 6 + ( 5 d 3 ) ions journal August 2019
Frustration-induced non-Curie-Weiss paramagnetism in La 3 Ir 3 O 11 : A fractional valence state iridate journal November 2019
Block excitonic condensate at n = 3.5 in a spin-orbit coupled t 2 g multiorbital Hubbard model journal April 2019
Non-Kitaev spin liquids in Kitaev materials journal May 2019
Covalent bonds against magnetism in transition metal compounds text January 2016
Models and Materials for Generalized Kitaev Magnetism text January 2017
Density matrix renormalization group study of a three-orbital Hubbard model with spin-orbit coupling in one dimension text January 2017

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