Stuart Calder

Magnetically Driven Metal-Insulator Transition in NaOsO3

The metal-insulator transition (MIT) is one of the most dramatic manifestations of electron correlations in materials. Various mechanisms producing MITs have been extensively considered, including the Mott (electron localization via Coulomb repulsion), Anderson (localization via disorder), and Peierls (localization via distortion of a periodic one-dimensional lattice) mechanisms. One additional route to a MIT proposed by Slater, in which long-range magnetic order in a three dimensional system drives the MIT, has received relatively little attention. Using neutron and x-ray scattering we show that the MIT in NaOsO(3) is coincident with the onset of long-range commensurate three dimensional magnetic order. While candidate materials have been suggested, our experimental methodology allows the first definitive demonstration of the long predicted Slater MIT.

Magnetic order and electronic structure of 5d3 double perovskite Sr2ScOsO6

The magnetic susceptibility, crystal and magnetic structures, and electronic structure of double perovskite Sr2ScOsO6 are reported. Using both neutron and x-ray powder diffraction we find that the crystal structure is monoclinic P21/n from 3.5 to 300 K. Magnetization measurements indicate an antiferromagnetic transition at TN=92 K, one of the highest transition temperatures of any double perovskite hosting only one magnetic ion. Type I antiferromagnetic order is determined by neutron powder diffraction, with an Os moment of only 1.6(1) muB, close to half the spin-only value for a crystal field split 5d electron state with t2g^3 ground state. Density functional calculations show that this reduction is largely the result of strong Os-O hybridization, with spin-orbit coupling responsible for only a ~0.1 muB reduction in the moment.

Magnetic structural change of Sr2IrO4 upon Mn doping

The layered 5d transition metal oxide Sr2IrO4 has been shown to host a novel Jeff=1/2 Mott spin orbit insulating state with antiferromagnetic ordering, leading to comparisons with the layered cuprates. Here we study the effect of substituting Mn for Ir in single crystals of Sr2Ir0.9Mn0.1O4 through an investigation involving bulk measurements and resonant x-ray and neutron scattering. We observe a new long range magnetic structure emerge upon doping through a reordering of the spins from the basal plane to the c-axis with a reduced ordering temperature compared to Sr2IrO4. The strong enhancement of the magnetic x-ray scattering intensity at the L3 edge relative to the L2 edge indicates that the Jeff=1/2 state is robust and capable of hosting a variety of ground states.

Magnetic structure and phase stability of the van der Waals bonded ferromagnet Fe3-xGeTe2

The magnetic structure and phase diagram of the layered ferromagnetic compound

Spin-orbit coupling controlled ground state in Sr2ScOsO6

{\mathrm{Fe}}_{3}{\mathrm{GeTe}}_{2}

Magnetism and electronic structure of La2ZnIrO6 and La2MgIrO6: Candidate Jeff = 1/2 Mott insulators

has been investigated by a combination of synthesis, x-ray and neutron diffraction, high-resolution microscopy, and magnetization measurements. Single crystals were synthesized by self-flux reactions, and single-crystal neutron diffraction finds ferromagnetic order with moments of

Jeff=12Mott spin-orbit insulating state close to the cubic limit inCa4IrO6

1.11(5){\ensuremath{\mu}}_{B}/\mathrm{Fe}

Stripe antiferromagnetic spin fluctuations in SrCo2As2.

aligned along the

Enhanced spin-phonon-electronic coupling in a 5d oxide

c

Spin glass and semiconducting behavior in one-dimensional BaFe2 Se3 ( 0.2) crystals

axis at 4 K. These flux-grown crystals have a lower Curie temperature