From the discovery of photoinduced water splitting on titanium dioxide (TiO 2 ) electrodes in 1972, 1 TiO 2 has attracted many researchers due to its potential usage in industry. 2,3 The strong oxidation power of the photogenerated holes, the chemical inertness, and nontoxicity of TiO 2 have made it a superior photocatalyst and thus it has been extensively studied first in powder form and then in film form. [4][5][6][7][8][9] In recent years, environmental cleanup has become one of the most active topics in photocatalysis. [10][11][12] Conversely, we have found that the UV illumination of TiO 2 produces a highly hydrophilic surface, exhibiting a water contact angle of zero de-gree. 13,14 On the basis of investigations with friction force microscopy (FFM), Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS), we have suggested that these hydrophilic surfaces are caused by a surface structural change on TiO 2 , the production of surface oxygen vacancies, leading to preferential adsorption of water. [14][15][16] Here we compare photoinduced processes proceeding on TiO 2 and strontium titanate (SrTiO 3 ) films. Like TiO 2 , SrTiO 3 is known as an efficient photocatalyst for the production of gaseous hydrogen from water and for the decomposition of various organic compounds. [17][18][19][20] Moreover the electronic structure of SrTiO 3 resembles that of TiO 2 , i.e., the valence and conduction bands of these metal oxides consist mainly of O-2p-like orbitals and Ti-3dlike orbitals, respectively, with band gaps of about 3 eV. [21][22][23] It is also reported that the SrTiO 3 surface is composed of Ti-O, and no Sr 2+ ions are exposed. 24,25 However, it should be noted that the crystal structure of SrTiO 3 is neither rutile nor anatase, but is perovskite which contains only corner-sharing TiO 6 octahedra, not edge-shared octahedra.Both TiO 2 and SrTiO 3 polycrystalline films were prepared on SiO 2 -coated glass plates, by a spin-coating method and using commercial alkoxide solutions [NDH-510C (Nihon Soda, Ltd.) for TiO 2 and DSRT150 (GELEST, Inc.) for SrTiO 3 , respectively], followed by a calcination at 500 °C for 30 min in air. Such coating steps were repeated twice, yielding thin films of ∼350 nm. XRD showed sharp diffraction patterns of anatase and perovskite for TiO 2 and SrTiO 3 , respectively. The UV-vis spectra showed that the main absorption edges for both TiO 2 and SrTiO 3 are situated at ∼380 nm, corresponding to a band gap of 3.2 eV.The activities of photocatalytic oxidation of these films were determined by the decomposition rate of methylene blue adsorbed on the film surface. The amounts of the dye adsorbed on the surface were evaluated by measuring the average absorbance of the film in the range