Evolution of in-gap spectral weight in electron- and hole-doped Sr<sub>2</sub>IrO<sub>4</sub> studied by time-resolved optical reflectivity
ORAL
Abstract
The 5d transition metal oxide Sr2IrO4 realizes an unusual Jeff = 1/2 antiferromagnetic Mott insulating ground state that is stabilized by an interplay of strong spin-orbit coupling and on-site Coulomb repulsion. Motivated by its structural and magnetic similarities to La2CuO4 - the parent compound of cuprate high-Tc superconductors - there have recently been intensive efforts to study the electron-doped (Sr1-xLax)2IrO4 series and the hole-doped Sr2Ir1-xRhxO4 series. In both cases, light substitution levels trigger a collapse of long-range antiferromagnetic order and an emergence of unusual metallic states with residual pseudogaps. Here we study the doping evolution of the electronic density of states in both (Sr1-xLax)2IrO4 and Sr2Ir1-xRhxO4 using ultrafast time-resolved optical reflectivity. Our results reveal a similar development of in-gap states and a shifting of the chemical potential upon crossing over from Mott insulator to metal on both electron- and hole-doped sides of the phase diagram.
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Presenters
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Hao Chu
- California Institute of Technology