Advanced oxidation process using titanium dioxide as a photocatalyst under solar irradiation is one of the most attractive technologies to eliminate atrazine, an endocrine disrupting and carcinogen contaminant. The N, S-codoped TiO 2nanowires at the calcination of 600°C obtained by a facile hydrothermal method revealed the best photocatalytic performance for the degradation of atrazine under visible light irradiation compared to N, S-codoped TiO 2nanoparticles and S-doped TiO 2nanowires. TOC removal experiment also exhibited the similar result and achieved 63% of atrazine mineralization within 6 h. The degradation of atrazine was driven mainly by •OH and holes during the photocatalytic process. Reactive species quantities such •OH and generated by N, S-codoped TiO 2nanowires under visible light irradiation were much more than those of S-doped TiO 2nanowires and N, S-codoped TiO 2nanoparticles. These results were mainly attributed to the synergistic effect of N and S doping in narrowing the band gap, remarkable increase in electron-hole separation, extending the anatase-to-rutile transformation temperature above 600°C, and preferentially exposing high reactive crystal facets of anatase.