AI Article Synopsis

  • MgMn(OH)Cl is identified as a significant example of a kagome antiferromagnet, showing strong spin frustration characteristics similar to herbertsmithite.
  • The study involved synthesizing nanosheets of MgMn(OH)Cl and conducting low-temperature magnetic tests, which revealed two distinct antiferromagnetic transitions at around 8 K and 55 K.
  • High-pressure experiments demonstrated that at pressures over 7.8 GPa, MgMn(OH)Cl undergoes a structural phase transition due to Jahn-Teller distortions, shifting from rhombohedral to monoclinic, which was further supported by changes observed in Raman and UV-visible absorption spectra.

Article Abstract

MgMn(OH)Cl serves readily as the classical Heisenberg kagome antiferromagnet lattice spin frustration material, due to its similarity to herbertsmithite in composition and crystal structure. In this work, nanosheets of MgMn(OH)Cl are synthesized through a solid-phase reaction. Low-temperature magnetic measurements revealed two antiferromagnetic transitions, occurring at ∼8 and 55 K, respectively. Utilizing high-pressure synchrotron radiation X-ray diffraction techniques, the topological structural evolution of MgMn(OH)Cl under pressures up to 24.8 GPa was investigated. The sample undergoes a second-order structural phase transition from the rhombohedral phase to the monoclinic phase at pressures exceeding 7.8 GPa. Accompanying the disappearance of the Fano-like line shape in the high-pressure Raman spectra were the emergence of new Raman active modes and discontinuities in the variations of Raman shifts in the high-frequency region. The phase transition to a structure with lower symmetry was attributed to the pressure-induced enhancement of cooperative Jahn-Teller distortion, which is caused by the mutual substitution of Mn ions from the kagome layer and Mg ions from the triangular interlayer. High-pressure ultraviolet-visible absorption measurements support the structural evolution. This research provides a robust experimental approach and physical insights for further exploration of classical geometrical frustration materials with kagome lattice.

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Source
http://dx.doi.org/10.1021/acs.inorgchem.4c00967DOI Listing

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