Mesoporous TiO 2 films treated with N 2 /argon plasma were studied for ultraviolet and visible light induced photocatalytic water oxidation activity. Compared to pristine TiO 2 films, plasma treated TiO 2 films showed remarkable enhancement of photocurrents (up to 80-240 times) in both ultraviolet light and visible light, greatly surpassing enhancements previously reported in the literature. The cubic ordered mesoporous TiO 2 thin films were prepared by a surfactanttemplated sol-gel method and were treated with N 2 /argon plasma, an approach hypothesized to capitalize on the high degree of disorder in the material and the high energy of the plasma species to achieve efficient nitrogen doping. The effects of reaction gas pressure and N 2 gas flow rate on photoelectrochemical (PEC) response were investigated. UV-vis absorbance spectra indicated that the incorporated N atoms significantly reduced the band gap of TiO 2 with the enhancement of visible light absorption, and XPS analysis showed primarily substitutional N atoms incorporation rather than interstitial. The photocatalytic activity of nitrogen-doped TiO 2 (N-TiO 2 ) films was evaluated by chronoamperometry and linear sweep voltammetry. The effect of light sources on PEC performance was explored using UV (365 nm), blue (455 nm) and green (530 nm) LEDs. N-TiO 2 films showed 242x and 240x enhancement of photocurrent, compared to undoped TiO 2 films under UV and blue LED irradiation, respectively. The N-doped films also showed overall enhancement of up to 70x and 92x with a broad spectrum Xe arc lamp and halogen bulb, respectively, and photocatalytic activity even with green LED illumination, compared to no measurable activity without doping. The present study shows that plasmainduced doping of sol-gel materials enables the efficient incorporation of heteroatoms into disordered metal oxide nanostructures, thereby leading to remarkable enhancement in visiblelight driven photoelectrochemical water oxidation.