Abstract
In order to study the visible light photocatalytic activity of nitrogen doped titanium dioxide, the interaction between nitrogen dopant sources and titania precursors during sol-gel synthesis is investigated. N-TiO 2 was synthesised using the sol-gel method using 1,3-diaminopropane as a nitrogen source. Samples were annealed several temperatures and the percentage of rutile present determined by X-ray diffraction to be 0% (500°C), 46% (600°C), and 94% (700°C). The reducing amounts of anatase at higher temperatures are studied using FTIR, which suggests the absence of any polymeric chains formed by the chelating agents, which would normally extend anatase-to-rutile transformation temperatures. Differential scanning calorimetry shows that crystalliation occurs before 500°C, providing the crystalline form determined by XRD at 500°C. Increased temperature also resulted in diminished visible light absorption capability, with only the 500°C sample showing significant absorption in the visible region. XPS studies revealed that nitrogen remained within the TiO 2 lattice at higher temperatures. Consequent with the reduced visible light absorption capacity, photocatalytic activity also reduced with increased annealing temperature. Degradation kinetics of methylene blue, irradiated with a 60W house-bulb, resulted in first order degradation rates constants of 0.40×10 -2, 0.19×10 -2, and 0.22×10 -2min -1 for 500, 600, and 700°C respectively. Degradation of Degussa P25 was minimal under the same conditions, and that of undoped TiO 2 was 0.02×10 -2min -1. Similarly, using 4-chlorophenol under solar irradiation conditions, the N-doped sample at 500°C substantially out-performed the undoped sample. These results are discussed in the context of the effect of increasing temperature on the nature of the band gap. © 2011.
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Nolan, N. T., Synnott, D. W., Seery, M. K., Hinder, S. J., Van Wassenhoven, A., & Pillai, S. C. (2012). Effect of N-doping on the photocatalytic activity of sol-gel TiO 2. Journal of Hazardous Materials, 211–212, 88–94. https://doi.org/10.1016/j.jhazmat.2011.08.074
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