Fabrication of platinum-deposited carbon nitride nanotubes by a one-step solvothermal treatment strategy and their efficient visible-light photocatalytic activity
•Pt/C3N4 NTs were successfully prepared by one-step solvothermal treatment strategy.•Their morphology, structure, and optoelectronic property were well characterized.•Pt/C3N4 NTs exhibit obviously higher visible-light catalytic activity than g-C3N4.•The efficient activity is attributed to tubular st...
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Veröffentlicht in: | Applied catalysis. B, Environmental Environmental, 2015-04, Vol.165, p.428-437 |
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Sprache: | eng |
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Zusammenfassung: | •Pt/C3N4 NTs were successfully prepared by one-step solvothermal treatment strategy.•Their morphology, structure, and optoelectronic property were well characterized.•Pt/C3N4 NTs exhibit obviously higher visible-light catalytic activity than g-C3N4.•The efficient activity is attributed to tubular structure and synergic effect of Pt.
A series of platinum nanoparticles-deposited carbon nitride nanotubes (Pt/C3N4 NTs) was fabricated by a simple one-step solvothermal treatment strategy using graphite carbon nitride (g-C3N4) and chloroplatinic acid (H2PtCl6·6H2O) as precursors. The morphology, porosity, phase and chemical structure, and optical and electronic properties of Pt/C3N4 NTs were well characterized. Compared with bulk g-C3N4, the as-prepared Pt/C3N4 NTs exhibited efficient photocatalytic activity toward hydrogen evolution from water-splitting and aqueous p-chlorophenol degradation under visible-light irradiation (λ>420nm) as a result of their unique tubular nanostructure and the synergic effect of Pt nanoparticles. Subsequently, the activities of simultaneous hydrogen evolution with organic pollutant degradation were also tested using as-prepared Pt/C3N4 NTs under the representative organic pollutants p-chlorophenol, p-nitrophenol, methylene blue, or rhodamine B as electron donors. Finally, the photocatalytic mechanisms in three different photocatalytic systems were discussed. |
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ISSN: | 0926-3373 1873-3883 |
DOI: | 10.1016/j.apcatb.2014.10.039 |