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Journal ArticleDOI

Self-Doped Ti3+ Enhanced Photocatalyst for Hydrogen Production under Visible Light

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TLDR
The UV-vis spectra show that the Ti(3+) here extends the photoresponse of TiO(2) from the UV to the visible light region, which leads to high visible-light photocatalytic activity for the generation of hydrogen gas from water.
Abstract
Through a facile one-step combustion method, partially reduced TiO2 has been synthesized. Electron paramagnetic resonance (EPR) spectra confirm the presence of Ti3+ in the bulk of an as-prepared sample. The UV−vis spectra show that the Ti3+ here extends the photoresponse of TiO2 from the UV to the visible light region, which leads to high visible-light photocatalytic activity for the generation of hydrogen gas from water. It is worth noting that the Ti3+ sites in the sample are highly stable in air or water under irradiation and the photocatalyst can be repeatedly used without degradation in the activity.

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Citations
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Journal ArticleDOI

A novel TiO2 composite for photocatalytic wastewater treatment

TL;DR: In this paper, a novel TiO2 composite consisting of Anatase interacting with a Ti3+-containing Rutile phase was synthesized by heating a mixture of Hombikat and Ti2O3 in air at different temperatures ranging from 300 °C up to 900 °C.
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Ice–Water Quenching Induced Ti3+ Self-doped TiO2 with Surface Lattice Distortion and the Increased Photocatalytic Activity

TL;DR: In this paper, the authors reported a facile strategy to prepare Ti3+ self-doped TiO2 with increased photocatalytic activity, which was directly thrown into ice-water for rapid quenching.
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Fluorine- and Niobium-Doped TiO2: Chemical and Spectroscopic Properties of Polycrystalline n-Type-Doped Anatase

TL;DR: In this article, the optical band gap transition is slightly red-shifted (by a few tenths of an electronvolt) for all samples containing fluorine, and the Fermi level lies, depending on the material, at the boundary or even in the lower region of the conduction band.
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A direct charger transfer from interface to surface for the highly efficient spatial separation of electrons and holes: The construction of Ti–C bonded interfaces in TiO2-C composite as a touchstone for photocatalytic water splitting

TL;DR: In this article, using one-dimensional TiO 2 -C composite nanorods with a chemically bonded interface as a touchstone, which was prepared through a simple carbonized process, the above strategy for better semiconductor photocatalytic water splitting property has been realized.
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Super-hydrophobic fluorination mesoporous MCF/TiO2 composite as a high-performance photocatalyst

TL;DR: In this article, NH4F was used instead of conventional organic silylation agent as the hydrophobic modifier to synthesize the super-hydrophobic mesocellular foams (MCF) loaded with nano-sized TiO2 photocatalysts in its pore channels, which could be considered as an extractant for organics.
References
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Journal ArticleDOI

Visible-Light Photocatalysis in Nitrogen-Doped Titanium Oxides

TL;DR: Film and powders of TiO2-x Nx have revealed an improvement over titanium dioxide (TiO2) under visible light in optical absorption and photocatalytic activity such as photodegradations of methylene blue and gaseous acetaldehyde and hydrophilicity of the film surface.
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Efficient photochemical water splitting by a chemically modified n-TiO2.

TL;DR: A chemically modified n-type TiO2 is synthesized by controlled combustion of Ti metal in a natural gas flame and performs water splitting with a total conversion efficiency of 11% and a maximum photoconversion efficiency of 8.35% when illuminated at 40 milliwatts per square centimeter.
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Inorganic Materials as Catalysts for Photochemical Splitting of Water

TL;DR: A review of the known inorganic catalysts with a focus on structure-activity relationships is given in this article, where the first water splitting system based on TiO2 and Pt was proposed by Fujishima and Honda in 1972.
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Infrared Absorption of Reduced Rutile Ti O 2 Single Crystals

TL;DR: In this paper, the infrared absorption of a series of plane parallel plates having electrical resistivities ranging from 3 to 0.01 ohm-m has been examined and it is postulated that the electrical conductivity arises from the ionization of either one or two trapped electrons from each oxygen vacancy.
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