Citation: ZHANG Xiao-Ru, LIN Yan-Hong, ZHANG Jian-Fu, HE Dong-Qing, WANG De-Jun. Photoinduced Charge Carrier Properties and Photocatalytic Activity of N-Doped TiO2 Nanocatalysts[J]. Acta Physico-Chimica Sinica, ;2010, 26(10): 2733-2738. doi: 10.3866/PKU.WHXB20101007 shu

Photoinduced Charge Carrier Properties and Photocatalytic Activity of N-Doped TiO2 Nanocatalysts

  • Received Date: 21 May 2010
    Available Online: 27 September 2010

    Fund Project: 国家重点基础研究发展规划项目(973) (2007CB613303) (973) (2007CB613303)国家自然科学基金(20703020, 20873053) (20703020, 20873053)吉林大学科学前沿与交叉学科创新项目(421031401412)资助 (421031401412)

  • Nitrogen-doped TiO2 (N-TiO2) photocatalysts with different amounts of N doping were successfully synthesized by the hydrothermal method using urea as the nitrogen source. The samples were characterized by X-ray diffraction (XRD), UV-Vis diffuse reflectance spectroscopy (UV -Vis DRS),X -ray photoelectron spectroscopy (XPS), and photoluminescence (PL) spectroscopy. The photodegradation of rhodamineB (RhB) and methyl orange (MO) solutions was used to evaluate the photocatalytic activity of the catalysts under UV and visible light irradiation. Surface photovoltage (SPV) and transient photovoltage (TPV) techniques were used to investigate the separation and transport mechanism of the photogenerated charge carriers of the N-doped TiO2 nanoparticles. The relationship between the photogenerated charge carriers and photocatalytic activity was also discussed. The results showed that the SPV threshold values shifted to the visible region and a stronger photovoltaic response in the visible region was observed with an increase in N doping. We also found that the maximum TPV response time was different for N-TiO2. These results indicate that with an appropriate amount of N doping, the photoinduced charge carriers separate efficiently, the transmission time increases, and the lifetime of the photoinduced charge carriers increases. Therefore, the photocatalytic activity is enhanced. However, excessive N acts as recombination centers for photoinduced electrons and holes, which reduces their photocatalytic activity.

     

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