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Free keywords:
Bond length, Electronic structure, Perovskite, Ruthenium compounds, Strain, Angle-resolved photoemission, Electronic.structure, Layered perovskite, Lifshitz transition, Lower energies, Spectra's, Surface electronic structures, Surface layers, Uni-axial compression, Van Hove singularities, Strontium compounds
Abstract:
We report the evolution of the electronic structure at the surface of the layered perovskite Sr2RuO4 under large in-plane uniaxial compression, leading to anisotropic B1g strains of µxx- µyy=-0.9±0.1%. From angle-resolved photoemission, we show how this drives a sequence of Lifshitz transitions, reshaping the low-energy electronic structure and the rich spectrum of van Hove singularities that the surface layer of Sr2RuO4 hosts. From comparison to tight-binding modeling, we find that the strain is accommodated predominantly by bond-length changes rather than modifications of octahedral tilt and rotation angles. Our study sheds new light on the nature of structural distortions at oxide surfaces, and how targeted control of these can be used to tune density of state singularities to the Fermi level, in turn paving the way to the possible realization of rich collective states at the Sr2RuO4 surface. © 2023 American Physical Society.
