<p>The spin-1/2 Heisenberg antiferromagnet on an anisotropic triangular lattice (ATL) is an archetypal spin system hosting exotic quantum magnetism and dimensional crossover. However, the progress in experimental research on this field has been limited due to the scarcity of ideal model materials. Here, we show that rhenium oxyhalides <i>A</i><sub>3</sub>ReO<sub>5</sub><i>X</i><sub>2</sub>, where spin-1/2 Re<sup>6+</sup> ions form a layered structure of ATLs, allow for flexible chemical substitution in both cation <i>A</i><sup>2+</sup> (<i>A</i> = Ca, Sr, Ba, Pb) and anion <i>X</i><sup>−</sup> (<i>X</i> = Cl, Br) sites, leading to seven synthesizable compounds. By combining magnetic susceptibility and high-field magnetization measurements with theoretical calculations using the orthogonalized finite-temperature Lanczos method, we find that the anisotropy <InlineEquation ID="IEq1"> <InlineMediaObject> <ImageObject Color="BlackWhite" FileRef="41467_2025_65913_Article_IEq1.gif" Format="GIF" Height="19" Rendition="HTML" Resolution="72" Type="Linedraw" Width="37" /> </InlineMediaObject> <EquationSource Format="TEX">\({J}^{{\prime} }/J\)</EquationSource> <EquationSource Format="MATHML"><math> <msup> <mrow> <mi>J</mi> </mrow> <mrow> <mo>′</mo> </mrow> </msup> <mo>/</mo> <mi>J</mi> </math></EquationSource> </InlineEquation> ranges from 0.25 to 0.45 depending on the chemical composition. Our findings demonstrate that <i>A</i><sub>3</sub>ReO<sub>5</sub><i>X</i><sub>2</sub> is an excellent platform for realizing diverse effective spin Hamiltonians that differ in the strength of the anisotropy <InlineEquation ID="IEq2"> <InlineMediaObject> <ImageObject Color="BlackWhite" FileRef="41467_2025_65913_Article_IEq1.gif" Format="GIF" Height="19" Rendition="HTML" Resolution="72" Type="Linedraw" Width="37" /> </InlineMediaObject> <EquationSource Format="TEX">\({J}^{{\prime} }/J\)</EquationSource> <EquationSource Format="MATHML"><math> <msup> <mrow> <mi>J</mi> </mrow> <mrow> <mo>′</mo> </mrow> </msup> <mo>/</mo> <mi>J</mi> </math></EquationSource> </InlineEquation> as well as the relevance of perturbation terms such as the Dzyaloshinskii-Moriya interaction and interlayer exchange coupling.</p>

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Chemically tunable quantum magnetism on the anisotropic triangular lattice in rhenium oxyhalides

  • Masaki Gen,
  • Daigorou Hirai,
  • Katsuhiro Morita,
  • Kazuhiro Nawa,
  • Satoshi Kogane,
  • Naofumi Matsuyama,
  • Takeshi Yajima,
  • Mitsuaki Kawamura,
  • Kazuhiko Deguchi,
  • Akihiro Koda,
  • Maiko Kofu,
  • Seiko Ohira-Kawamura,
  • Taku J. Sato,
  • Akira Matsuo,
  • Koichi Kindo,
  • Yoshimitsu Kohama,
  • Zenji Hiroi

摘要

The spin-1/2 Heisenberg antiferromagnet on an anisotropic triangular lattice (ATL) is an archetypal spin system hosting exotic quantum magnetism and dimensional crossover. However, the progress in experimental research on this field has been limited due to the scarcity of ideal model materials. Here, we show that rhenium oxyhalides A3ReO5X2, where spin-1/2 Re6+ ions form a layered structure of ATLs, allow for flexible chemical substitution in both cation A2+ (A = Ca, Sr, Ba, Pb) and anion X (X = Cl, Br) sites, leading to seven synthesizable compounds. By combining magnetic susceptibility and high-field magnetization measurements with theoretical calculations using the orthogonalized finite-temperature Lanczos method, we find that the anisotropy \({J}^{{\prime} }/J\) J / J ranges from 0.25 to 0.45 depending on the chemical composition. Our findings demonstrate that A3ReO5X2 is an excellent platform for realizing diverse effective spin Hamiltonians that differ in the strength of the anisotropy \({J}^{{\prime} }/J\) J / J as well as the relevance of perturbation terms such as the Dzyaloshinskii-Moriya interaction and interlayer exchange coupling.