Electronic nematic order in the normal state of strontium ruthenate

Abstract

Despite significant achievements in characterizing the properties of Sr2RuO4 over the last three decades, the precise nature of its electronic ground state is still unresolved. In this work, we provide a missing piece of the puzzle by uncovering evidence of electronic nematic order in the normal state of Sr2RuO4, revealed by ultrafast time-resolved optical dichroism measurements of uniaxially strained thin films. This nematic order, whose domains are aligned by the strain, spontaneously breaks the four-fold rotational symmetry of the crystal. The temperature dependence of the dichroism resembles an Ising-like order parameter, and optical pumping induces a coherent oscillation of its amplitude mode. A microscopic model of intra-unit-cell nematic order is presented, highlighting the importance of Coulomb repulsion between neighboring oxygen p-orbitals. The existence of electronic nematic order in the normal state of Sr2RuO4 may have consequences for the form and mechanism of superconductivity in this material.

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