Journal
CHEMICAL ENGINEERING JOURNAL
Volume 325, Issue -, Pages 199-207Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2017.05.080
Keywords
Mesoporous TiO2; Ti3+ self-doping; N doping; Visible-light-driven photocatalysis; Sphere
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Funding
- National Natural Science Foundation of China [21376065, 51672073, 81573134]
- Postdoctoral Science Foundation of China [2017M611399]
- Heilongjiang Postdoctoral Startup Fund [LBH-Q14135]
- University Nursing Program for Young Scholars with Creative Talents in Heilongjiang Province [UNPYSCT-2015014, UNPYSCT-2016018]
- Postdoctoral Science Foundation of Heilongjiang Province [LBH-Z16150]
- Innovative Science Research Project of Harbin Medical University [2016JCZX13]
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Mesoporous black Ti3+/N-TiO2 spheres with high crystallinity are fabricated by a facile evaporation induced self-assembly (EISA) method, using urea as nitrogen resource, combined with a mild calcinations (350 degrees C) after an in-situ hydrogenation under an argon atmosphere. The prepared materials are characterized by X-ray diffraction, Raman, scanning electron microscopy, transmission electron microscopy, and X-ray photoelectron spectroscopy. The results indicate the prepared sample is uniform mesoporous black Ti3+/N-TiO2 spheres with high crystallinity of anatase, high surface area of 100 m(2) g(-1), large pore size of 6.5 nm and narrow band gap of 2.11 eV, could be easily controlled with the diameter from 200 to 800 nm. Meanwhile, the photoresponse extends to near-infrared region owing to Ti3+ and N codoping. The visible-light-driven photocatalytic degradation ratio of methyl orange is up to 96% and photocatalytic hydrogen production rate is similar to 150 mu mol h(-1), which are several times higher than that of pristine TiO2. Besides, the possible photocatalytic mechanism is proposed. The excellent photocatalytic activity can be ascribed to N and Ti3+ doping resulting in high visible light utilization and enhanced separation of photogenerated charge carriers, and the mesoporous networks offering more surface active sites. (C) 2017 Elsevier B.V. All rights reserved.
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