Competition of defect ordering and site disproportionation in strained LaCoO3_{3} on SrTiO3_3(001)

preprint2020arXivOpen access

Abstract

The origin of the 3×13 \times 1 reconstruction observed in epitaxial LaCoO3_{3} films on SrTiO3(001)_3(001) is assessed by using first-principles calculations including a Coulomb repulsion term. We compile a phase diagram as a function of the oxygen pressure, which shows that (3×13 \times 1)-ordered oxygen vacancies (LaCoO2.67_{2.67}) are favored under commonly used growth conditions, while stoichiometric films emerge under oxygen-rich conditions. Growth of further reduced LaCoO2.5_{2.5} brownmillerite films is impeded by phase separation. We report two competing ground-state candidates for stoichiometric films: a semimetallic phase with 3×13 \times 1 low-spin/intermediate-spin/intermediate-spin magnetic order and a semiconducting phase with intermediate-spin magnetic order. This demonstrates that tensile strain induces ferromagnetism even in the absence of oxygen vacancies. Both phases exhibit an intriguing (3×13 \times 1)-reconstructed octahedral rotation pattern and accordingly modulated La-La distances. In particular, charge and bond disproportionation and concomitant orbital order of the t2gt_{2g} hole emerge at the Co sites that are also observed for unstrained bulk LaCoO3_3 in the intermediate-spin state and explain structural data obtained by x-ray diffraction at elevated temperature. Site disproportionation drives a metal-to-semiconductor transition that reconciles the intermediate-spin state with the experimentally observed low conductivity during spin-state crossover without Jahn-Teller distortions.

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