Tongfei Qi

Evidence of an odd-parity hidden order in a spin-orbit coupled correlated iridate

A rare combination of strong spin–orbit coupling and electron–electron correlations makes the iridate Mott insulator Sr_2IrO_4 a promising host for novel electronic phases of matter. The resemblance of its crystallographic, magnetic and electronic structures to La_2CuO_4, as well as the emergence on doping of a pseudogap region and a low-temperature d-wave gap, has particularly strengthened analogies to cuprate high-T_c superconductors. However, unlike the cuprate phase diagram, which features a plethora of broken symmetry phases in a pseudogap region that includes charge density wave, stripe, nematic and possibly intra-unit-cell loop-current orders, no broken symmetry phases proximate to the parent antiferromagnetic Mott insulating phase in Sr_2IrO_4 have been observed so far, making the comparison of iridate to cuprate phenomenology incomplete. Using optical second-harmonic generation, we report evidence of a hidden non-dipolar magnetic order in Sr_2IrO_4 that breaks both the spatial inversion and rotational symmetries of the underlying tetragonal lattice. Four distinct domain types corresponding to discrete 90°-rotated orientations of a pseudovector order parameter are identified using nonlinear optical microscopy, which is expected from an electronic phase that possesses the symmetries of a magneto-electric loop-current order. The onset temperature of this phase is monotonically suppressed with bulk hole doping, albeit much more weakly than the Neel temperature, revealing an extended region of the phase diagram with purely hidden order. Driving this hidden phase to its quantum critical point may be a path to realizing superconductivity in Sr_2IrO_4.

Hallmarks of the Mott-metal crossover in the hole-doped pseudospin-1/2 Mott insulator Sr2IrO4

The physics of doped Mott insulators remains controversial after decades of active research, hindered by the interplay among competing orders and fluctuations. It is thus highly desired to distinguish the intrinsic characters of the Mott-metal crossover from those of other origins. Here we investigate the evolution of electronic structure and dynamics of the hole-doped pseudospin-1/2 Mott insulator Sr2IrO4. The effective hole doping is achieved by replacing Ir with Rh atoms, with the chemical potential immediately jumping to or near the top of the lower Hubbard band. The doped iridates exhibit multiple iconic low-energy features previously observed in doped cuprates—pseudogaps, Fermi arcs and marginal-Fermi-liquid-like electronic scattering rates. We suggest these signatures are most likely an integral part of the materials proximity to the Mott state, rather than from many of the most claimed mechanisms, including preformed electron pairing, quantum criticality or density-wave formation.

Dimensionality-controlled Mott transition and correlation effects in single-layer and bilayer perovskite iridates

We studied Sr2IrO4 and Sr3Ir2O7 using angle-resolved photoemission spectroscopy (ARPES), making direct experimental determinations of intra- and inter-cell coupling parameters as well as Mott correlations and gap sizes. The results are generally consistent with LDA+U+Spin-orbit coupling (SOC) calculations, though the calculations missed the momentum positions of the dominant electronic states and neglected the importance of inter-cell coupling on the size of the Mott gap. The calculations also ignore the correlation-induced spectral peak widths, which are critical for making a connection to activation energies determined from transport experiments. The data indicate a dimensionality-controlled Mott transition in these 5d transition-metal oxides (TMOs).

A Low Temperature Nonlinear Optical Rotational Anisotropy Spectrometer for the Determination of Crystallographic and Electronic Symmetries

Nonlinear optical generation from a crystalline material can reveal the symmetries of both its lattice structure and underlying ordered electronic phases and can therefore be exploited as a complementary technique to diffraction based scattering probes. Although this technique has been successfully used to study the lattice and magnetic structures of systems such as semiconductor surfaces, multiferroic crystals, magnetic thin films, and multilayers, challenging technical requirements have prevented its application to the plethora of complex electronic phases found in strongly correlated electron systems. These requirements include an ability to probe small bulk single crystals at the μm length scale, a need for sensitivity to the entire nonlinear optical susceptibility tensor, oblique light incidence reflection geometry, and incident light frequency tunability among others. These measurements are further complicated by the need for extreme sample environments such as ultra low temperatures, high magnetic fields, or high pressures. In this review we present a novel experimental construction using a rotating light scattering plane that meets all the aforementioned requirements. We demonstrate the efficacy of our scheme by making symmetry measurements on a μm scale facet of a small bulk single crystal of Sr2IrO4 using optical second and third harmonic generation.

The magnetic and crystal structures of Sr2IrO4: A neutron diffraction study

We report a single-crystal neutron diffraction study of the layered

Correlated giant dielectric peaks and antiferromagnetic transitions near room temperature in pure and alkali-doped BaMnO3−δ

\rm Sr_2IrO_4

Magnetic and Crystal Structures of Sr 2 IrO 4 : A Neutron Diffraction Study

. This work unambiguously determines the magnetic structure of the system and reveals that the spin orientation rigidly tracks the staggered rotation of the

X-ray Absorption Spectroscopy Study of the Effect of Rh doping in Sr2IrO4

\rm IrO_6

High-energy electronic excitations in Sr 2 IrO 4 observed by Raman scattering

octahedra in

Experimental electronic structure of the metallic pyrochlore iridate Bi2Ir2O7

\rm Sr_2IrO_4