4.7 Article

Relationship between Pd oxidation states on TiO2 and the photocatalytic oxidation behaviors of nitric oxide

Journal

CHEMOSPHERE
Volume 77, Issue 2, Pages 264-268

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2009.07.060

Keywords

NO; Photocatalysis; Pd/TiO2; XPS; Adsorption

Funding

  1. National High-Tech Research and Development Program (863) of China [2007AA061701]
  2. Excellent Young Teacher Support Program of Zhejiang University
  3. New Century Excellent Scholar Program of Ministry of Education of China [NCET-04-0549]

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This study has been undertaken to investigate the relationship between I'd oxidation states on TiO2 photocatalysts and their photocatalytic oxidation behaviors of NO. Three types of Pd-modified TiO2 with different Pd oxidation states were prepared by wet impregnation method, neutralization method and photodeposition method, respectively. And these Pd-modified photocatalysts were characterized by X-ray diffraction analysis, X-ray photoelectron spectrum analysis (XPS), UV-Vis diffuse reflectance spectra and temperature programmed desorption (TPD). It was found from XPS results that the dominant oxidation states of Pd on these Pd-modified TiO2 catalysts were Pd2+, PdO, and Pd-0, respectively. NO-TPD results showed that the NO adsorption capacity was improved greatly by the modification of Pd2+ ions. The activity tests showed that Pd-modified TiO2 by a wet impregnation method increased photocatalytic activity compared to pure TiO2 (Degussa P25). It was concluded that Pd2+ ions on as-prepared TiO2 Catalysts provided key contributions to the improvement of photocatalytic activity. However, Pd-0 and PdO deposits on TiO2 almost had no positive effect on NO oxidation. The mechanism of photocatalytic oxidation of NO in gas phase over Pd-modified TiO2 was also proposed. (C) 2009 Elsevier Ltd. All rights reserved.

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