Evidence for strong electron correlations in a nonsymmorphic Dirac semimetal

Metallic iridium oxides (iridates) provide a fertile playground to explore new phenomena resulting from the interplay between topological protection, spin-orbit and electron-electron interactions. To date, however, few studies of the low energy electronic excitations exist due to the difficulty in synthesising crystals with sufficiently large carrier mean-free-paths. Here, we report the observation of Shubnikov-de Haas quantum oscillations in high-quality single crystals of monoclinic SrIrO3 in magnetic fields up to 35 T. Analysis of the oscillations reveals a Fermi surface comprising multiple small pockets with effective masses up to 4.5 times larger than the calculated band mass. Ab-initio calculations reveal robust linear band-crossings at the Brillouin zone boundary, due to its non-symmorphic symmetry, and overall we find good agreement between the angular dependence of the oscillations and the theoretical expectations. Further evidence of strong electron correlations is realized through the observation of signatures of non-Fermi liquid transport as well as a large Kadowaki-Woods ratio. These collective findings, coupled with knowledge of the evolution of the electronic state across the Ruddlesden-Popper iridate series, establishes monoclinic SrIrO3 as a topological semimetal on the boundary of the Mott metal-insulator transition.

Iridium Oxide Enabled Sensors Applications

There have been numerous studies applying iridium oxides in different applications to explore their proton-change-based reactions since the 1980s. Iridium oxide can be fabricated directly by applying electrodeposition, sputter-coating method, or oxidation of iridium wire. Generally, there have been currently two approaches in applying iridium oxide to enable its sensing applications. One was to improve or create different electrolytes with (non-)electrodeposition method for better performance of Nernst Constant with the temperature-related system. The mechanism behind the scenes were summarized herein. The other was to change the structure of iridium oxide through different kinds of templates such as photolithography patterns, or template-assisted direct growth methods, etc. to improve the sensing performance. The detection targets varied widely from intracellular cell pH, glucose in an artificial sample or actual urine sample, and the hydrogen peroxide, glutamate or organophosphate pesticides, metal-ions, etc. This review paper has focused on the mechanism of electrodeposition of iridium oxide in aqueous conditions and the sensing applications towards different biomolecules compounds. Finally, we summarize future trends on Iridium oxide based sensing and predict future work that could be further explored.

The origin of the high electrochemical activity of pseudo-amorphous iridium oxides

Combining high activity and stability, iridium oxide remains the gold standard material for the oxygen evolution reaction in acidic medium for green hydrogen production. The reasons for the higher electroactivity of amorphous iridium oxides compared to their crystalline counterpart is still the matter of an intense debate in the literature and, a comprehensive understanding is needed to optimize its use and allow for the development of water electrolysis. By producing iridium-based mixed oxides using aerosol, we are able to decouple the electronic processes from the structural transformation, i.e. Ir oxidation from IrO2 crystallization, occurring upon calcination. Full characterization using in situ and ex situ X-ray absorption spectroscopy, X-ray photoelectron spectroscopy, X-ray diffraction and transmission electron microscopy allows to unambiguously attribute their high electrochemical activity to structural features and rules out the iridium oxidation state as a critical parameter. This study indicates that short-range ordering, corresponding to sub-2nm crystal size for our samples, drives the activity independently of the initial oxidation state and composition of the calcined iridium oxides.

Insights into the Spin–Orbital Entanglement in Complex Iridium Oxides from High-Field ESR Spectroscopy

Complex iridium oxides have attracted recently a substantial interdisciplinary attention due to an intimate entanglement of spin and orbital degrees of freedom which may give rise to a novel spin–orbital Mott insulating behavior and exotic quantum spin liquid phases. Electron spin resonance (ESR) spectroscopy is known to be an instructive tool for studying the spin–orbital coupling (SOC) effects as it can directly access the relevant parameters sensitive to SOC, such as the g factor tensor, magnetic anisotropy gaps and spin dynamics. In this article, a systematic study at the Leibniz IFW Dresden of the static and dynamic properties of selected Ir-based materials with multi-frequency high-field ESR spectroscopy will be reviewed. Specifically, evidence for a surprisingly isotropic antiferromagnetic spin dynamics and the inversion of the orbital states in the prototypical spin–orbital Mott insulator $$\text {Sr}_2\text {IrO}_4$$ Sr 2 IrO 4 , observation of the collective resonance modes in the family of double perovskites $$\text {La}_2$$ La 2 B$$\text {IrO}_6$$ IrO 6 (B = Cu, Co) and the origin of the unexpected magnetism in the double perovskite $$\text {Ba}_2\text {YIrO}_6$$ Ba 2 YIrO 6 will be highlighted.

Recent advances in understanding oxygen evolution reaction mechanisms over iridium oxide

Recent spectroscopic and computational studies concerning the oxygen evolution reaction over iridium oxides are reviewed to provide the state-of-the-art understanding of its reaction mechanism.