Abstract

The simultaneous production of hydrogen and degradation of organic pollutants (4-chlorophenol, urea, and urine) was successfully achieved using titania photocatalysts which were modified with both anion adsorbates (fluoride or phosphate) and (noble) metals (Pt, Pd, Au, Ag, Cu, or Ni). The dual-function photocatalysis worked only when both components coexisted on the surface of TiO2, whereas TiO2 modified with a single surface component (F–TiO2, P–TiO2, or Pt/TiO2) was inactive under the same experimental condition. Two main surface-modified photocatalysts, F–TiO2/Pt (surface fluorinated and platinized) and P–TiO2/Pt (surface phosphated and platinized), were similarly active for dual-function photocatalysis in the anoxic suspension under UV irradiation. With these catalysts employed, the degradation of 4-chlorophenol (or urea) was accompanied by the concurrent production of H2. The synergistic effect greatly depended on the kind of metal and pH. The activity of F–TiO2/Pt gradually decreased with increasing pH, which makes the application of F–TiO2/Pt limited to the acidic pH region. On the other hand, P–TiO2/Pt exhibited a consistent activity over a wide range of pH, which makes P–TiO2/Pt a more practical dual-function photocatalyst. The synergistic effect of anions and metal deposits on the surface of TiO2 enhanced the interfacial electron transfer and reduced the charge recombination which resulted in a maximum of 20-fold increase of H2 production compared to metal deposited TiO2 in the presence of 4-chlorophenol.

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