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Charge-ordered state satisfying the Anderson condition in LiRh2O4 arising from local dimer order

M. Shiomi1, K. Kojima1, N. Katayama1,*, S. Maeda1, J. A. Schneeloch2, S. Yamamoto3, K. Sugimoto4, Y. Ohta3, D. Louca2 et al.

Y. Okamoto1 and H. Sawa1

  • 1Department of Applied Physics, Nagoya University, Furo-cho, Chikusa-ku, Nagoya, Aichi 464-8603, Japan
  • 2Department of Physics, University of Virginia, Charlottesville, Virginia 22904, USA
  • 3Department of Physics, Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba 263-8522, Japan
  • 4Department of Physics, Keio University, 3-14-1 Hiyoshi, Kohoku-ku, Yokohama, Kanagawa 223-8522, Japan

  • *katayama.naoyuki@b.mbox.nagoya-u.ac.jp

Phys. Rev. B 105, L041103 – Published 5 January, 2022

DOI: https://doi.org/10.1103/PhysRevB.105.L041103

Abstract

We report on the charge-ordered structure of LiRh2O4 arising below the metal-insulator transition at 170 K. Structural studies using synchrotron x rays have revealed that the charge-ordered states of Rh3+ and Rh4+ with dimerization are realized in the low-temperature phase below 170 K. Although the low-temperature ground state resembles that of CuIr2S4, a charge-ordering pattern satisfying the Anderson condition is realized in LiRh2O4. Based on structural information such as the short-range order of dimers appearing above the transition temperature and the weakening of the correlation between rhodium one-dimensional chains appearing in the crystal structure, we argue that the Coulomb interaction plays an important role in determining the charge-ordering patterns.

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