Controlling the synergistic effect of oxygen vacancies and N dopants to enhance photocatalytic activity of N-doped TiO<sub>2sub> by H<sub>2sub> reduction
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摘要
This paper focuses on improving photocatalytic activity of N-doped TiO<sub>2sub> photocatalyst for efficiently utilizing solar energy. A simple H<sub>2sub> reduction is found to remarkably enhance the photocatalytic activity of N-doped TiO<sub>2sub> for ethylene oxidation under visible light or simulated solar light irradiation. Ultraviolet/visible diffuse reflectance spectra (UV/vis DRS), X-ray photoelectron spectra (XPS) and electron paramagnetic resonance (EPR) spectra were employed to characterize the surface properties and chemical states of nitrogen dopants in H<sub>2sub>-reduced N-doped TiO<sub>2sub>. The results reveal that H<sub>2sub> reduction facilitates the creation of oxygen vacancies and Ti<sup>3+sup> species in N-doped TiO<sub>2sub> but without removal of nitrogen species from catalyst surface. The formed oxygen vacancies and Ti<sup>3+sup> species seriously influence electron excitation from doped nitrogen species and subsequently tune the generation of active oxygen species O<sub>2sub><sup>鈭?/sup> radicals on N-doped TiO<sub>2sub>. The synergistic effect of oxygen vacancies and doped nitrogen species contributes to the enhancement of photocatalytic activity of N-doped TiO<sub>2sub> samples, but the formed Ti<sup>3+sup> ions largely suppress the photocatalytic activity.

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