Study of phenomena induced by interfacial oxygen octahedra coupling in La<sub>0.5</sub>Sr<sub>0.5</sub>CoO<sub>3-δ</sub>/SrTiO<sub>3</sub> heterostructures using Cryo-STEM

ORAL

Abstract

In recent years epitaxial transition metal oxide thin films with broken symmetry have been studied extensively due to their novel magnetization and transport properties. Ferromagnetic La0.5Sr0.5CoO3-δ (LSCO) thin films grown on SrTiO3 exhibit oxygen vacancy ordering which is absent in bulk, while SrTiO3 undergoes antiferrodistortive phase transition at 105 K being triggered by rotations of the TiO6 octahedra. This structural symmetry breaking accommodated by interfacial lattice mismatch modifies the Ti-O-Co bond angle at the interface, and hence distorts both CoO6 octahedral and CoO4 tetrahedral structures in LSCO thin films. Here, we use aberration-corrected scanning transmission electron microscopy combined with an in situ TEM cryo-holder to compare the atomic/electronic structure and magnetic properties of La0.5Sr0.5CoO3-δ thin films grown on SrTiO3, below and above 105 K. Atomic-resolution imaging and electron energy-loss spectroscopy (EELS) are used to examine variations in the local density of states and magnetic moments as a function of sample temperature.

*This work is supported by a grant from NSD (DMR-1408427). Support from the UIC Research Resources Center (RRC), in particular A.W. Nicholls and F. Shi is acknowledged. Work at UMN is supported by the DOE.

Presenters

  • Xue Rui

    • Univ of Illinois - Chicago
    • Department of Physics, University of Illinois at Chicago

Authors

  • Xue Rui

    • Univ of Illinois - Chicago
    • Department of Physics, University of Illinois at Chicago
  • Jeffery Walter

    • University of Minnesota
    • Chemical Engineering and Materials Science, University of Minnesota
  • Chris Leighton

    • University of Minnesota
    • Chemical Engineering and Materials Science, University of Minnesota
    • Chemical Engineering and Materials Science, Univ of Minnesota - Twin Cities
  • Robert Klie

    • Department of Physics, University of Illinois at Chicago
    • Univ of Illinois - Chicago
    • University of Illinois at Chicago