4.8 Article

Itinerant Antiferromagnetism in RuO2

Journal

PHYSICAL REVIEW LETTERS
Volume 118, Issue 7, Pages -

Publisher

AMER PHYSICAL SOC
DOI: 10.1103/PhysRevLett.118.077201

Keywords

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Funding

  1. U.S. Department of Energy, Office of Science, Basic Energy Sciences, Materials Sciences and Engineering Division
  2. Gordon and Betty Moore Foundations EPiQS Initiative [GBM F4416]
  3. Scientific User Facilities Division, Office of Basic Energy Sciences
  4. U.S. Department of Energy
  5. Office of Science of the U. S. DOE [DE-AC02-05CH11231]
  6. [NSF-DMR-1350002]
  7. Division Of Materials Research
  8. Direct For Mathematical & Physical Scien [1350002] Funding Source: National Science Foundation

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Bulk rutile RuO2 has long been considered a Pauli paramagnet. Here we report that RuO2 exhibits a hitherto undetected lattice distortion below approximately 900 K. The distortion is accompanied by antiferromagnetic order up to at least 300 K with a small room temperature magnetic moment of approximately 0.05 mu(B) as evidenced by polarized neutron diffraction. Density functional theory plus U (DFT + U) calculations indicate that antiferromagnetism is favored even for small values of the Hubbard U of the order of 1 eV. The antiferromagnetism may be traced to a Fermi surface instability, lifting the band degeneracy imposed by the rutile crystal field. The combination of high Neel temperature and small itinerant moments make RuO2 unique among ruthenate compounds and among oxide materials in general.

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