5 research outputs found

    Pressure Induced Quantum Phase Transitions in Metallics Oxides and Pnictides

    No full text
    Quantum phase transitions occur as a result of competing ground states. The focus of the present work is to understand quantum criticality and its consequences when the competition is between insulating and metallic ground states. Metal-insulator transitions are studied by means of electronic transport measurements and quantum critical points are approached by applying hydrostatic pressure in two different compounds namely Eu2_2Ir2_2O7_7 and FeCrAs. The former is a ternary metal oxide and the latter is a ternary metal pnictide. A major component of this work was the development of the ultra-high pressure measurements by means of Anvil cells. A novel design is introduced which minimizes the alignment accessory components hence, making the cell more robust and easier to use. Eu2_2Ir2_2O7_7 is a ternary metal oxide and a member of the pyrochlore iridate family. Resistivity measurements under pressure in moissanite anvil cells show the evolution of the ground state of the system from insulating to metallic. The quantum phase transition at Pc∼6P_c\sim6 GPa appears to be continuous. A remarkable correspondence is revealed between the effect of the hydrostatic pressure on Eu2_2Ir2_2O7_7 and the effect of chemical pressure by changing the R size in the R2_2Ir2_2O7_7 series. This suggests that in both cases the tuning parameter controls the t2gt_{2\textrm{g}} bandwidth of the iridium 5d5d electrons. Moreover, hydrostatic pressure unveils a curious cross-over from incoherent to conventional metallic behaviour at a T∗>T^* > 150 K in the neighbourhood of PcP_c, suggesting a connection between the high and low temperature phases. The possibility of a topological semi-metallic ground state, predicted in recent theoretical studies, is explained. FeCrAs is a ternary metal pnictide with Fermi liquid specific heat and susceptibility behaviour but non-metallic non-Fermi liquid resistivity behaviour. Characteristic properties of the compound are explained and compared to those of superconducting pnictides. Antiferromagnetic (AFM) order sets in at ∼125\sim125 K with the magnetic moments residing on the Cr site. Pressure measurements are carried out in moissanite and diamond anvil cells in order to suppress the AFM order and resolve the underlying electronic transport properties. While AFM order is destroyed by pressure, the non-metallic non-Fermi liquid behaviour is shown to be robust against pressure.Ph

    Trivalent Iridium Oxides: Layered Triangular Lattice Iridate K<sub>0.75</sub>Na<sub>0.25</sub>IrO<sub>2</sub> and Oxyhydroxide IrOOH

    No full text
    Solid oxides with transition-metal ions in unusual oxidation states attract enormous attention due to their electronic, magnetic, and catalytic properties. Yet, no crystalline oxide compounds based on purely trivalent iridium have been characterized to date. Here, we present the synthesis and thorough investigation of the properties of the compounds K<sub>0.75</sub>Na<sub>0.25</sub>IrO<sub>2</sub> and IrOOH, both containing trivalent iridium on a triangular lattice in layers of [IrO<sub>2</sub>]<sup>−</sup>. K<sub>0.75</sub>Na<sub>0.25</sub>IrO<sub>2</sub> crystallizes in a P2-structure with the space group <i>P</i>6<sub>3</sub>/<i>mmc</i>, while the crystal structure of IrOOH adopts the direct maximal subgroup <i>P</i>3̅<i>m</i>1. The trivalent state of the iridium ion is discussed with regards to the iridium–oxygen bond length from X-ray diffraction, the chemical composition, the electronic and magnetic behavior of the material, and X-ray photoemission spectroscopy. The discovery of a new valence state in ternary crystalline iridium oxides is not only of interest from a fundamental perspective, but also has far-reaching implications for such diverse fields as electrochromism, solid-state magnetism, and especially heterogeneous catalysis
    corecore