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Switching magnetic spin states using small magnetic fields in compositionally complex Sm(Ti,Cr,Mn,Fe,Co,Ni,Cu)O3

R. K. Dokala1,*,†, M. Geers2, P. Nordblad1, R. Clulow2,‡, and R. Mathieu1,§

  • 1Department of Materials Science and Engineering, Uppsala University, Box 35, 751 03 Uppsala, Sweden
  • 2Department of Chemistry - Ångström Laboratory, Uppsala University, Box 538, 751 21 Uppsala, Sweden

  • *Present address: Department of Physics, Stockholm University, 106 91 Stockholm, Sweden.
  • †Contact author: ravi.kiran.dokala@fysik.su.se
  • ‡Contact author: rebecca.clulow@kemi.uu.se
  • §Contact author: roland.mathieu@angstrom.uu.se

Phys. Rev. B 114, 034404 – Published 6 July, 2026

DOI: https://doi.org/10.1103/b77s-6l6d

Abstract

High-entropy perovskites offer a unique platform for exploring magnetic phenomena arising from extreme B-site chemical disorder. In Sm(M7)O3, where there are seven cations in equal amounts at the B site (M=Ti, Cr, Mn, Fe, Co, Ni, Cu), we observe long-range antiferromagnetic ordering near 105 K accompanied by a small but robust excess magnetic moment intrinsic to the chemically disordered lattice. This uncompensated moment is evident from zero-field-cooled – field-cooled irreversibility, shifts in the isothermal M(H) loops, and discrete remanent states identified through direct-current–demagnetization measurements. Remarkably, cooling fields as small as ±20 Oe are sufficient to select the direction of the excess moment, and the chosen magnetic state remains stable against applied fields up to 50 kOe. A low-temperature anomaly in the remanent magnetization further reveals a secondary contribution from the Sm3+ sublattice, although the primary origin of the excess moment resides in the B-site antiferromagnetic sublattice.

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