Abstract

Visible-light-driven nitrogen-doped TiO 2 was synthesized using a novel nitrogen-ion donor of hydrazine hydrate. Low-concentration (∼0.2 at%) nitrogen species and Ti 3+ were detected in the TiO 2-based photocatalyst by X-ray photoelectron spectroscopy (XPS) and electron paramagnetic resonance (EPR) spectroscopy. The trace amount of Ti–N would contribute to the minor band-gap narrowing of about 0.02 eV. Those nitrogen-containing species, especially the NO 2 2− species, form surface states, which make the catalysts possible to degrade 4-chlorophenol (4-CP) under visible irradiation ( λ>400 nm). Moreover, Ti 3+ species induce oxygen vacancy states between the valence and the conduction bands, which would also contribute to the visible response. The photocatalytic activity of the nitrogen-doped TiO 2 catalyst was thought to be the synergistic effect of nitrogen and Ti 3+ species. The catalysts showed higher photocatalytic activity for degradation of 4-CP than pure TiO 2 under not only visible but also UV irradiation. The visible response and the higher UV activity of the nitrogen-doped TiO 2 make it possible to utilize solar energy efficiently to execute photocatalysis processes.

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