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Photocatalytic reduction of nitrate ( NO 3 − ) is a green and potentially inexpensive technique for reducing NO 3 − pollution in ground water. TiO 2 -based photocatalysts have been studied extensively for this purpose. In the present study, the semiconducting catalyst CuFe 0.7 Cr 0.3 S 2 was applied to NO 3 − reduction. Loading this catalyst with metal co-catalysts (Ru, Au, Cu, Ag, Pt, and Pd) greatly increased the rate of NO 3 − reduction and the N 2 selectivity. In addition, there was a synergistic enhancement of the photocatalytic performance when the catalyst was loaded two co-catalysts. For example, the catalyst loaded with Pd and Au at mass fractions of 0.75% and 3%, respectively, could photocatalyze the complete reduction of NO 3 − in a 100 ppm N aqueous solution with 100% N 2 selectivity in less than 5 h with UV irradiation. However, with an inner irradiation from a full-arc Xe lamp, the NO 3 − conversion rate reduced to 0.065 mg N/h, probably because of the low density of the photoexcited electrons. The results show the potential of metal sulfides for photocatalytic reduction of NO 3 − , and the possibility of use of visible light. [ABSTRACT FROM AUTHOR]

Photocatalytic nitrogen (N 2) fixation provides a green avenue for the production of ammonia (NH 3), which is extremely significant for global biogeochemical cycle. However, there is still lack of highly efficient catalyst to improve the N 2 photofixation efficiency. In this work, oxygen vacancy engineered perovskite SrTiO 3 materials have been prepared by post reduction using lithium alkylamine solution and served as effective catalysts for visible-light-driven N 2 -to-NH 3 conversion. The formation and concentration of oxygen vacancies were confirmed by electron paramagnetic resonance, X-ray photoelectron spectroscopy and thermogravimetric analyses. The SrTiO 3 catalyst with optimized oxygen vacancies concentration exhibited improved photocatalytic N 2 reduction rate of 306.87 μmol·g−1·h−1, which is approach ten-fold higher than that of pristine SrTiO 3. Electrochemical impedance spectroscopy and photoluminescence measurements reveal that optimum amount of oxygen vacancies can promote the effective adsorption of N 2 molecules and improve the photocatalytic performance by facilitating the fast separation of photo-generated charge carriers. Moreover, the as-fabricated defective SrTiO 3 exhibited outstanding stability, which makes it emerge the promising potential for further practical applications. This work offers a feasible method for the design of high performance photocatalysts through defect engineering. • Synthesized defective SrTiO 3 catalysts by lithium alkylamine solution reduction. • Oxygen vacancies regulation to improve the photocatalytic NRR activity for SrTiO 3. • About ten-fold NH 3 formation rate (873.48 μmol·g−1·h−1) to original SrTiO 3. • Defective SrTiO 3 suppressed the recombination of the photogenerated carriers. [ABSTRACT FROM AUTHOR]