Abstract

The influence of nitrogen-source on the photocatalytic properties of nitrogen-doped titanium dioxide is herein first investigated from the perspective of the chemical bond form of the nitrogen element in the nitrogen-source. The definitive role of groups such as NN from the nitrogen-source on the surface of as-prepared samples in the selectivity of the dominant product of photocatalytic reduction is demonstrated. Well-crystallized one-dimensional NTiO2 nanorod arrays with a preferred orientation of the rutile (310) facet are manufactured via a hydrothermal treatment using hydrazine and ammonia variously as the source of nitrogen. Significant selectivity of the dominant reduced products has been exhibited for NTiO2 prepared from different nitrogen-sources in carbon dioxide photocatalytic reduction under visible light illumination. CH4 is the main product with N2H4-doped NTiO2, while CO is the main product with NH3-doped NTiO2, which can be attributed to the existence of the reducing NN groups in the N2H4-doped NTiO2 surfaces after the hydrothermal treatment. Compared with the approaches previously reported, the facile one-step route utilized here accomplishes the fabrication of NTiO2 possessing visible-light activity and attainment of selectivity of dominant photocatalytic reduction product simultaneously by choosing a nitrogen-source with appropriate chemical bond form, which provides a completely new approach to understanding the effects of doping treatment on photocatalytic properties.

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