Electronic States and Possible Origin of the Orbital-Glass State in a Nearly Metallic Spinel Cobalt Vanadate: An X-ray Magnetic Circular Dichroism Study
arXiv:1802.07074 · doi:10.1103/PhysRevB.97.205126
Abstract
We have investigated the orbital states of the orbital-glassy (short-range orbital ordered) spinel vanadate CoVO using x-ray absorption spectroscopy (XAS), x-ray magnetic circular dichroism (XMCD), and subsequent configuration-interaction cluster-model calculation. From the sign of the XMCD spectra, it was found that the spin magnetic moment of the Co ion is aligned parallel to the applied magnetic field and that of the V ion anti-parallel to it, consistent with neutron scattering studies. It was revealed that the excess Co ions at the octahedral site take the trivalent low-spin state, and induce a random potential to the V sublattice. The orbital magnetic moment of the V ion is small although finite, suggesting that the ordered orbitals mainly consists of real-number orbitals.
arXiv comment7 pages, 6 figures
References in corpus (14)
- Orbitally-driven Peierls state in spinels
- A different look at the spin state of Co ions in CoO pyramidal coordination
- Magnetic and orbital ordering in the spinel MnV2O4
- Structural, orbital, and magnetic order in vanadium spinels
- Orbital and spin chains in ZnV2O4
- Magnetic transition and orbital degrees of freedom in vanadium spinels
- Spin and Orbital Order of the Vanadium Spinel MgV2O4
- Orbital order in ZnVO
- Proposed Orbital Ordering in MnV2O4 from First-principles Calculations
- Orbital and magnetic transitions in geometrically-frustrated vanadium spinels -- Monte Carlo study of an effective spin-orbital-lattice coupled model --
- Homopolar bond formation in ZnVO close to a metal-insulator transition
- An orbital glass state of a nearly metallic spinel, CoVO
- Structural transition and orbital glass physics in near itinerant CoV2O4
- Strong competition between orbital-ordering and itinerancy in a frustrated spinel vanadate