Abstract
Revealing the activation mechanism of nitrate (NO3−) reduction is crucially important to design high-efficiency photocatalysts for NO3− removal. In this work, the performance of photoreduction NO3− has been thoroughly studied over different crystalline phases TiO2. Photodegradation rate of NO3− over anatase TiO2 is found to be higher than that of rutile TiO2 at simulated sunlight, which can achieve high NO3− conversion of 94% and 100% nitrogen selectivity (original concentration of 50 mg/L NO3−-N) at reaction time of 4 h. With the aid of in situ Fourier Transform Infrared (FTIR) and density functional theory (DFT) calculations, the possible reaction paths of photoreduction NO3− over anatase TiO2 was verified from theory and practice sides. NO3− was adsorbed on surface Ti site to form bridging nitrate (M − O)2NO model. Then, monodentate nitrite (M-O-N-O) model was the dominant intermediate in the reduction process of NO3−. This study presents a new opinion of photoreduction NO3− reaction paths.
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