4.6 Article

Mott versus Slater-type metal-insulator transition in Mn-substituted Sr3Ru2O7

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PHYSICAL REVIEW B
卷 86, 期 4, 页码 -

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AMER PHYSICAL SOC
DOI: 10.1103/PhysRevB.86.041102

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资金

  1. Max Plank-UBC Centre for Quantum Materials
  2. Killam Steacie Fellowship Program
  3. Sloan Steacie Fellowship Program
  4. NSERC's Steacie Fellowship Program
  5. CRC
  6. ALS
  7. NSERC
  8. CFI
  9. CIFAR Quantum Materials
  10. BCSI
  11. US DOE [DE-AC02-05CH11231]

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We present a temperature-dependent x-ray-absorption (XAS) and resonant elastic x-ray scattering (REXS) study of the metal-insulator transition (MIT) in Sr-3(Ru1-xMnx)(2)O-7. The XAS results reveal that the MIT drives the onset of local antiferromagnetic correlations around the Mn impurities, a precursor of the long-range antiferromagnetism detected by REXS at T-order < T-MIT. This establishes that the MIT is of the Mott type (electronic correlations) as opposed to Slater type (magnetic order). While this behavior is induced by Mn impurities, the (1/4, 1/4, 0) order exists for a wide range of Mn concentrations, and points to an inherent instability of Sr3Ru2O7.

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