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Ferromagnetism on an atom-thick & extended 2D metal-organic coordination network.

Jorge Lobo-ChecaLeyre Hernández-LópezMikhail M OtrokovIgnacio Piquero-ZulaicaAdriana E CandiaPierluigi GargianiDavid SerrateFernando DelgadoManuel ValvidaresJorge CerdáAndrés ArnauFernando Bartolomé
Published in: Nature communications (2024)
Ferromagnetism is the collective alignment of atomic spins that retain a net magnetic moment below the Curie temperature, even in the absence of external magnetic fields. Reducing this fundamental property into strictly two-dimensions was proposed in metal-organic coordination networks, but thus far has eluded experimental realization. In this work, we demonstrate that extended, cooperative ferromagnetism is feasible in an atomically thin two-dimensional metal-organic coordination network, despite only ≈ 5% of the monolayer being composed of Fe atoms. The resulting ferromagnetic state exhibits an out-of-plane easy-axis square-like hysteresis loop with large coercive fields over 2 Tesla, significant magnetic anisotropy, and persists up to T C  ≈ 35 K. These properties are driven by exchange interactions mainly mediated by the molecular linkers. Our findings resolve a two decade search for ferromagnetism in two-dimensional metal-organic coordination networks.
Keyphrases
  • room temperature
  • ionic liquid
  • molecularly imprinted
  • water soluble
  • magnetic resonance
  • molecular dynamics
  • transcription factor
  • mass spectrometry
  • single molecule
  • metal organic framework
  • aqueous solution