APS March Meeting 2014
Volume 59, Number 1
Monday–Friday, March 3–7, 2014;
Denver, Colorado
Session W48: Invited Session: Exotic Phase Transitions in 5d Compounds
2:30 PM–5:30 PM,
Thursday, March 6, 2014
Room: Mile High Ballroom 1A-1B
Sponsoring
Units:
DCMP GMAG
Chair: Sang-Wook Cheong, Rutgers University
Abstract ID: BAPS.2014.MAR.W48.2
Abstract: W48.00002 : Slater and Mott Insulating States in Os- and Ir-Based Transitional Metal Oxides
3:06 PM–3:42 PM
Preview Abstract
Abstract
Author:
A.D. Christianson
(Oak Ridge National Laboratory)
The discovery of a novel J$_{\mathrm{eff}}=$1/2 electronic configuration
and spin-orbit assisted insulating state in
Sr$_{\mathrm{2}}$IrO$_{\mathrm{4}}$ has stimulated a fresh look at
metal-insulator transitions where relativistic effects participate on an
even footing with other energy scales such as crystal field splitting and
electron-electron correlations. There are several view points on the origin
of the insulating state in Sr$_{2}$IrO$_{4}$, but the most
prominent is that spin-orbit coupling modifies the electronic configuration
such that a Mott insulting state emerges despite the relatively modest
electron-electron correlations within the 5$d$ orbitals. An alternative
viewpoint is that magnetic effects enable the opening of the electronic gap
giving rise to the insulating state or a Slater metal-insulator transition.
Here we describe realizations of both Mott and Slater insulators in the
context of Os- and Ir-based 5$d$ transition metal oxides. NaOsO$_{3}$,
exhibits a continuous phase transition at 410 K where antiferromagnetism
appears in conjunction with the onset of insulating behavior. A combination
of neutron diffraction and magnetic resonant x-ray scattering enables the
conclusion that G-type magnetic order occurs at the metal-insulator
transition providing microscopic evidence that NaOsO$_{3}$ is the
first three dimensional realization of a Slater insulator. On the other hand
we have probed the robustness of the J$_{\mathrm{eff}}=$1/2 Mott
insulating state though studies of
Sr$_{2}$Ir$_{\mathrm{1-x}}$T$_{\mathrm{x}}$O$_{4}$
(T$=$Mn, Ru). For both Mn and Ru doping we find that despite qualitative
changes in the magnetic order the J$_{\mathrm{eff}}=$1/2 electronic
configuration remains robust. In particular, for Ru-doping the signatures of
the J$_{\mathrm{eff}}=$1/2 state are observed for all concentrations where
magnetic order is present. Finally, we have investigated
Ca$_{4}$IrO$_{6}$ which appears to exhibit a nearly ideal
J$_{\mathrm{eff}}=$1/2 state which is unperturbed by deviations from cubic
crystal field level splitting.
To cite this abstract, use the following reference: http://meetings.aps.org/link/BAPS.2014.MAR.W48.2