Search Results
Tomonaga–Luttinger liquid behavior and spinon confinement in YbAlO 3
2019, Wu, L.S., Nikitin, S.E., Wang, Z., Zhu, W., Batista, C.D., Tsvelik, A.M., Samarakoon, A.M., Tennant, D.A., Brando, M., Vasylechko, L., Frontzek, M., Savici, A.T., Sala, G., Ehlers, G., Christianson, A.D., Lumsden, M.D., Podlesnyak, A.
Low dimensional quantum magnets are interesting because of the emerging collective behavior arising from strong quantum fluctuations. The one-dimensional (1D) S = 1/2 Heisenberg antiferromagnet is a paradigmatic example, whose low-energy excitations, known as spinons, carry fractional spin S = 1/2. These fractional modes can be reconfined by the application of a staggered magnetic field. Even though considerable progress has been made in the theoretical understanding of such magnets, experimental realizations of this low-dimensional physics are relatively rare. This is particularly true for rare-earth-based magnets because of the large effective spin anisotropy induced by the combination of strong spin–orbit coupling and crystal field splitting. Here, we demonstrate that the rare-earth perovskite YbAlO3 provides a realization of a quantum spin S = 1/2 chain material exhibiting both quantum critical Tomonaga–Luttinger liquid behavior and spinon confinement–deconfinement transitions in different regions of magnetic field–temperature phase diagram.
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.
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.