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On the connection between magnetic interactions and the spin-wave gap of the insulating phase of NaOsO$_{3}$

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 Added by Manuel Pereiro
 Publication date 2021
  fields Physics
and research's language is English




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The scenario of a metal-insulator transition driven by the onset of antiferromagnetic order in NaOsO$_3$ calls for a trustworthy derivation of the underlying effective spin Hamiltonian. To determine the latter we rely on {it ab initio} electronic-structure calculations, linear spin-wave theory, and comparison to experimental data of the corresponding magnon spectrum. We arrive this way to Heisenberg couplings that are $lesssim$45% to$lesssim$63% smaller than values presently proposed in the literature and Dzyaloshinskii-Moriya interactions in the region of 15% of the Heisenberg exchange $J$. These couplings together with the symmetric anisotropic exchange interaction and single-ion magnetocrystalline anisotropy successfully reproduce the magnon dispersion obtained by resonant inelastic X-ray scattering measurements. In particular, the spin-wave gap fully agrees with the measured one. We find that the spin-wave gap is defined from a subtle interplay between the single-ion anisotropy, the Dzyaloshinskii-Moriya exchange and the symmetric anisotropic exchange interactions. The results reported here underpin the local-moment description of NaOsO$_3$, when it comes to analyzing the magnetic excitation spectra. Interestingly, this comes about from a microscopic theory that describes the electron system as Bloch states, adjusted to a mean-field solution to Hubbard-like interactions.



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NaOsO3 hosts a rare manifestation of a metal-insulator transition driven by magnetic correlations, placing the magnetic exchange interactions in a central role. We use resonant inelastic x-ray scattering to directly probe these magnetic exchange interactions. A dispersive and strongly gapped (58 meV) excitation is observed indicating appreciable spin-orbit coupling in this 5d3 system. The excitation is well described within a minimal model Hamiltonian with strong anisotropy and Heisenberg exchange (J1=J2=13.9 meV). The observed behavior places NaOsO3 on the boundary between localized and itinerant magnetism.
Chiral magnets with topologically nontrivial spin order such as Skyrmions have generated enormous interest in both fundamental and applied sciences. We report broadband microwave spectroscopy performed on the insulating chiral ferrimagnet Cu$_{2}$OSeO$_{3}$. For the damping of magnetization dynamics we find a remarkably small Gilbert damping parameter of about $1times10^{-4}$ at 5 K. This value is only a factor of 4 larger than the one reported for the best insulating ferrimagnet yttrium iron garnet. We detect a series of sharp resonances and attribute them to confined spin waves in the mm-sized samples. Considering the small damping, insulating chiral magnets turn out to be promising candidates when exploring non-collinear spin structures for high frequency applications.
A pressure and temperature dependent Raman study of the vibrational and spin dynamics in CuGeO3 is presented. A new low temperature, high pressure phase has been identified, and a pressure-temperature phase-diagram is proposed for CuGeO3. The pressure dependence of the effective exchange interaction, of the spin-Peierls gap, and of the spin-Peierls temperature strongly supports a model in which next nearest neighbor interactions stabilise the SP ground state. The Raman data allow for a quantitative estimate of the pressure dependence of the next nearest neighbor interactions.
Motivated by the presence of an unquenched orbital angular momentum in CoO, a team at Chalk River, including a recently hired research officer Roger Cowley, performed the first inelastic neutron scattering experiments on the classic Mott insulator [Sakurai $textit{et al.}$ 1968 Phys. Rev. $mathbf{167}$ 510]. Despite identifying magnon modes at the zone boundary, the team was unable to parameterise the low energy magnetic excitation spectrum below $Trm{_{N}}$ using conventional pseudo-bosonic approaches. It would not be for another 40 years that Roger, now at Oxford and motivated by the discovery of the high-$T_{c}$ cuprate superconductors [Bednorz & Muller 1986 Z. Phys. B $mathbf{64}$ 189], would make another attempt at the parameterisation of the magnetic excitation spectrum that had previously alluded him. Upon his return to CoO, Roger found a system embroiled in controversy, with some of its most fundamental parameters still remaining undetermined. Faced with such a formidable task, Roger performed a series of inelastic neutron scattering experiments in the early 2010s on both CoO and a magnetically dilute structural analogue MgO. These experiments would prove instrumental in the determination of both single-ion [Cowley $textit{et al.}$ 2013 Phys. Rev. B $mathbf{88}$ 205117] and cooperative magnetic parameters [Sarte $textit{et al.}$ 2018 Phys. Rev. B $mathbf{98}$ 024415] for CoO. Both these sets of parameters would eventually be used in a spin-orbit exciton model [Sarte $textit{et al.}$ 2019 Phys. Rev. B $mathbf{100}$ 075143], developed by his longtime friend and collaborator Bill Buyers, to successfully parameterise the complex spectrum that both measured at Chalk River almost 50 years prior. The story of CoO is of one that has come full circle, one filled with both spectacular failures and intermittent, yet profound, little victories.
139 - N.Matsunaga , A.Ayari , P.Monceau 2002
Magnetoresistance measurements have been carried out along the highly conducting a axis in the FISDW phase of hydrogened and deuterated (TMTSF)$_2$ClO$_4$ for various cooling rates through the anion ordering temperature. With increasing the cooling rate, a) the high field phase boundary $beta_{rm {HI}}$, observed at 27 T in hydrogened samples for slowly cooled, is shifted towards a lower field, b) the last semimetallic SDW phase below $beta_{rm {HI}}$ is suppressed, and c) the FISDW insulating phase above $beta_{rm {HI}}$ is enhanced in both salts. The cooling rate dependence of the FISDW transition and of $beta_{rm {HI}}$ in both salts can be explained by taking into account the peculiar SDW nesting vector stabilized by the dimerized gap due to anion ordering.
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