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Strain engineering is an effective way to modify functional properties of thin films. Recently, the importance of octahedral rotations in pervoskite films has been recognized in discovering and designing new functional phases. Octahedral behavior of SrRuO3 film as a popular electrode in heterostructured devices is of particular interest for its probable interfacial coupling of octahedra with the functional overlayers. Here we report the strain engineering of octahedral rotations and physical properties that has been achieved in SrRuO3 films in response to the substrate-induced misfit strains of almost the same amplitude but of opposite signs. It shows that the compressively strained film on NdGaO3 substrate displays a rotation pattern of a tetragonal phase whilst the tensilely strained film on KTaO3 substrate has the rotation pattern of the bulk orthorhombic SrRuO3 phase. In addition, the compressively strained film displays a perpendicular magnetic anisotropy while the tensilely strained film has the magnetic easy axis lying in the film plane. The results show the prospect of strain engineered octahedral architecture in producing desired property and novel functionality in the class of perovskite material.

BaTiO3 thin films' self‐polarization can be tuned upward or downward, depending on both the substrate termination and the flexoelectric effect upon varying its thickness. Different atomic stacking sequence leads to different self‐polarization direction of fully strained BaTiO3 films, whereas the internal electric field produced by flexoelectric effect becomes the dominating factor in determining the self‐polarization direction of relaxed BaTiO3 films.

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We present a stoichiometry-dependent structural phase transition in SrRuO3 film on SrTiO3 substrate. The oxygen stoichiometry in the films was varied by changing the oxygen partial pressure P(O2) during the deposition process. For SrRuO3 films with P(O2) ≥ 60 mTorr, they exhibited a pseudo-orthorhombic structure with in-plane uniaxial magnetic anisotropy. On the other hand for films with P(O2) ≤ 45 mTorr, the tetragonal SrRuO3 phase with a perpendicular uniaxial magnetic anisotropy was stabilized at room temperature. The big difference in the magnetic anisotropy of these two SrRuO3 phases was shown to be closely linked to their respective RuO6 octahedral rotation patterns: the RuO6 octahedra rotate differently along the two orthogonal in-plane directions in the pseudo-orthorhombic phase, whereas in the tetragonal phase only octahedral rotations around z-axis are present and the octahedral tilts along the in-plane axes are diminished. First-principles calculations show that such a suppression of the RuO6 octahedra tilting in the tetragonal phase arises from the oxygen vacancies at the octahedral apex (along z-axis). This work demonstrates that the stoichiometry plays an important role in determining the octahedral rotations and tilts in the perovskite materials, which may induce new phases with distinctively different structural symmetry and physical property.

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Epitaxial SrRuO3 films were grown under different oxygen partial pressures inducing different amounts of oxygen vacancies. In spite of microstructural disorders, a considerable improvement in the conductivity was observed at ambient temperature with increasing the oxygen vacancies. The oxygen vacancies are responsible for the conductivity improvement by enhancing the orbital overlap between Ru dz2 and O pz orbitals. The finding indicates that the oxygen vacancy plays an important role in determining the transport properties of perovskite oxides, by modifying their electronic structures.