SrRuO 3 (SRO) is widely used as an electrode in oxide electronic device applications due to its excellent material properties such as metallic conductivity, chemical stability, good lattice match with multifunctional oxides, and atomically smooth and welldefined surfaces. [1][2][3][4][5][6] Especially in the fabrication of epitaxial thin-film heterostructures, the crystal symmetry and domain structure of the overlayer thin film are strongly dependent on those of the bottom electrode. Thus, it is critical to investigate the crystal symmetry and domain structure of the bottom electrode at the growth temperature and during cooling of the epitaxial heterostructures to room temperature if the bottom electrode undergoes structural transitions.In ABO 3 perovskite materials, the ideal cubic symmetry can be distorted by several mechanisms such as distortions of the octahedra, cation displacements within the octahedra, and tilting of the octahedra. The first two mechanisms are driven by electronic instabilities of the octahedral metal ion as exemplified by the Jahn-Teller distortion in KCuF 3 or the ferroelectric displacement of titanium in BaTiO 3 . [7,8] The third and most common mechanism, octahedral tilting, can be realized by tilting essentially rigid BO 6 octahedra while maintaining their corner-sharing connectivity. This type of distortion is typically observed when the A cation is too small for the cubic BO 3 corner-sharing octahedral network.At room temperature bulk SRO exhibits orthorhombic symmetry (Pbnm).[9] Figure 1 shows the sequence of phase transitions in unstrained bulk SRO from orthorhombic to tetragonal and then cubic symmetry with increasing temperature.[10] According to the Glazer notation, octahedral tilting in orthorhombic SRO is described by a À a À c þ , implying that RuO 6 octahedra are rotated in opposite directions by equivalent magnitude along [100] and [010] and in the same direction about [001]. [11,12] Tetragonal SRO is a one-tilt system, where RuO 6 octahedra are rotated only about the [001] direction (a 0 a 0 c À ). The tetragonal phase of SRO is stable within the very narrow temperature range from 547 to 677 8C and, finally, high-symmetry cubic perovskite (Pm3m) becomes stable above 677 8C.[10]Enormous strains exist in thin films when one material is deposited onto a substrate due to differences in crystal symmetry, lattice parameters, and thermal expansion coefficients between the film and the underlying substrate. [2,14] As a result, the properties of thin films can be differ widely from the intrinsic properties of the unstrained bulk counterparts. For example, recent experiments have shown strain-induced ferroelectricity in SrTiO 3 (STO) films at room temperature [15] and huge changes in the ferroelectric transition temperature in both BaTiO 3 . [16] Several groups have reported on the structural phase transition of SRO in thin-film form. The structural transition temperature of an epitaxial SRO thin film on (001) STO substrates, investigated using in situ transmission electron micro...