Structural modifications in strain-engineered bilayer nickelate thin films.

Abstract

The discovery of high-temperature superconductivity in bulk La₃Ni₂O₇ under high hydrostatic pressure^1-4 and biaxial compression in epitaxial thin films^5-8 has ignited significant interest in understanding the interplay between atomic and electronic structure in these compounds. Subtle changes in the nickel-oxygen bonding environment are thought to be key drivers for stabilizing superconductivity, but specific details of which bonds and which modifications are most relevant remains so far unresolved. While direct, atomic-scale structural characterization under hydrostatic pressure is beyond current experimental capabilities, static stabilization of strained La₃Ni₂O₇ films provides a platform well-suited to investigation with new picometer-resolution electron microscopy methods. Here, we use multislice electron ptychography (MEP)^9,10 to directly measure the atomic-scale structural evolution of La₃Ni₂O₇ thin films across a wide range of biaxial strains tuned via substrate choice. By resolving both the cation and oxygen sublattices, we study the strain-dependent evolution of atomic bonds, providing the opportunity to isolate and disentangle the effects of specific structural motifs for stabilizing superconductivity. We identify the lifting of crystalline symmetry through modification of the nickel-oxygen octahedral distortions under compressive strain as a key structural ingredient for superconductivity and identify in-plane lattice compression as a common attribute between bulk and thin film superconductivity. Building upon the detailed structures obtained by MEP, we introduce a theoretical framework to disentangle coupled structural distortions in corner-sharing octahedra¹¹, which suggest that both known superconducting geometries of La₃Ni₂O₇ (hydrostatic pressure and compressive strain) suppress local t_2g orbital mixing in the low-energy Ni bands by raising the octahedral symmetry.