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Spin-orbit-driven magnetic structure and excitation in the 5d pyrochlore Cd2Os2O7

2016, Calder, S., Vale, J.G., Bogdanov, N.A., Liu, X., Donnerer, C., Upton, M.H., Casa, D., Said, A.H., Lumsden, M.D., Zhao, Z., Yan, J.-Q., Mandrus, D., Nishimoto, S., van den Brink, J., Hill, J.P., McMorrow, D.F., Christianson, A.D.

Much consideration has been given to the role of spin-orbit coupling (SOC) in 5d oxides, particularly on the formation of novel electronic states and manifested metal-insulator transitions (MITs). SOC plays a dominant role in 5d5 iridates (Ir4þ), undergoing MITs both concurrent (pyrochlores) and separated (perovskites) from the onset of magnetic order. However, the role of SOC for other 5d configurations is less clear. For example, 5d3 (Os5þ) systems are expected to have an orbital singlet with reduced effective SOC. The pyrochlore Cd2Os2O7 nonetheless exhibits a MIT entwined with magnetic order phenomenologically similar to pyrochlore iridates. Here, we resolve the magnetic structure in Cd2Os2O7 with neutron diffraction and then via resonant inelastic X-ray scattering determine the salient electronic and magnetic energy scales controlling the MIT. In particular, SOC plays a subtle role in creating the electronic ground state but drives the magnetic order and emergence of a multiple spin-flip magnetic excitation.

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Spin-orbit coupling control of anisotropy, ground state and frustration in 5d2 Sr2MgOsO6

2016, Morrow, Ryan, Taylor, Alice E., Singh, D.J., Xiong, Jie, Rodan, Steven, Wolter, A.U.B., Wurmehl, Sabine, Büchner, Bernd, Stone, M.B., Kolesnikov, A.I., Aczel, Adam A., Christianson, A.D., Woodward, Patrick M.

The influence of spin-orbit coupling (SOC) on the physical properties of the 5d2 system Sr2MgOsO6 is probed via a combination of magnetometry, specific heat measurements, elastic and inelastic neutron scattering, and density functional theory calculations. Although a significant degree of frustration is expected, we find that Sr2MgOsO6 orders in a type I antiferromagnetic structure at the remarkably high temperature of 108 K. The measurements presented allow for the first accurate quantification of the size of the magnetic moment in a 5d2 system of 0.60(2) μB –a significantly reduced moment from the expected value for such a system. Furthermore, significant anisotropy is identified via a spin excitation gap, and we confirm by first principles calculations that SOC not only provides the magnetocrystalline anisotropy, but also plays a crucial role in determining both the ground state magnetic order and the size of the local moment in this compound. Through comparison to Sr2ScOsO6, it is demonstrated that SOC-induced anisotropy has the ability to relieve frustration in 5d2 systems relative to their 5d3 counterparts, providing an explanation of the high TN found in Sr2MgOsO6.