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      TiO 2 Fibers Supported β-FeOOH Nanostructures as Efficient Visible Light Photocatalyst and Room Temperature Sensor

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          Abstract

          Hierarchical heterostructures of beta-iron oxyhydroxide (β-FeOOH) nanostructures on electrospun TiO 2 nanofibers were synthesized by a facile hydrothermal method. This synthesis method proves to be versatile to tailoring of β-FeOOH structural design that cuts across zero-dimensional particles (TF-P), one-dimensional needles (TF-N) to two-dimensional flakes (TF-F). In addition, synthesizing such oxyhyroxide nanostructures presents the advantage of exhibiting similar functional performances to its oxides counterpart however, without the need to undergo any annealing step which leads to undesirable structural collapse or sintering. The as-prepared hierarchical heterostructures possess high surface area for dye adsorptivity, efficient charge separation and visible photocatalytic activity. Also, for the first time, hydrogen gas sensing has been demonstrated on β-FeOOH nanostructures at room temperature. The reported hierarchical heterostructures of β-FeOOH on TiO 2 nanofibers afford multiple functions of photocatalysis and sensing which are highly promising for environment monitoring and clean up applications.

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          Branched TiO₂ nanorods for photoelectrochemical hydrogen production.

          We report a hierarchically branched TiO(2) nanorod structure that serves as a model architecture for efficient photoelectrochemical devices as it simultaneously offers a large contact area with the electrolyte, excellent light-trapping characteristics, and a highly conductive pathway for charge carrier collection. Under Xenon lamp illumination (UV spectrum matched to AM 1.5G, 88 mW/cm(2) total power density), the branched TiO(2) nanorod array produces a photocurrent density of 0.83 mA/cm(2) at 0.8 V versus reversible hydrogen electrode (RHE). The incident photon-to-current conversion efficiency reaches 67% at 380 nm with an applied bias of 0.6 V versus RHE, nearly two times higher than the bare nanorods without branches. The branches improve efficiency by means of (i) improved charge separation and transport within the branches due to their small diameters, and (ii) a 4-fold increase in surface area which facilitates the hole transfer at the TiO(2)/electrolyte interface.
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            Preparation and photocatalytic behavior of MoS2 and WS2 nanocluster sensitized TiO2.

            A new approach has been developed for the fabrication of visible light photocatalysts. Nanoclusters of MoS2 and WS2 are coupled to TiO2 by an in situ photoreduction deposition method taking advantage of the reducing power of the photogenerated electrons from TiO2 particles. The photocatalytic degradation of methylene blue and 4-chlorophenol in aqueous suspension has been employed to evaluate the visible light photocatalytic activity of the powders. The blue shift in the absorption onset confirms the size quantization of MS2 nanoclusters, which act as effective and stable sensitizers, making it possible to utilize visible light in photocatalysis. Quantum size effects alter the energy levels of the conduction and valence band edges in the coupled semiconductor systems, which favors the interparticle electron transfer. In addition, the coupled systems are believed to act in a cooperative manner by increasing the degree of charge carrier separation, which effectively reduces recombination.
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              Preparation and visible light photocatalytic activity of Ag/TiO₂/graphene nanocomposite.

              Great efforts have been made to develop efficient visible light-activated photocatalysts in recent years. In this work, a new nanocomposite consisting of anatase TiO(2), Ag, and graphene was prepared for use as a visible light-activated photocatalyst, which exhibited significantly increased visible light absorption and improved photocatalytic activity, compared with Ag/TiO(2) and TiO(2)/graphene nanocomposites. The increased absorption in visible light region is originated from the strong interaction between TiO(2) nanoparticles and graphene, as well as the surface plasmon resonance effect of Ag nanoparticles that are mainly adsorbed on the surface of TiO(2) nanoparticles. The highly efficient photocatalytic activity is associated with the strong adsorption ability of graphene for aromatic dye molecules, fast photogenerated charge separation due to the formation of Schottky junction between TiO(2) and Ag nanoparticles and the high electron mobility of graphene sheets, as well as the broad absorption in the visible light region. This work suggests that the combination of the excellent electrical properties of graphene and the surface plasmon resonance effect of noble metallic nanoparticles provides a versatile strategy for the synthesis of novel and efficient visible light-activated photocatalysts.
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                Author and article information

                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group
                2045-2322
                01 June 2015
                2015
                : 5
                : 10601
                Affiliations
                [1 ]Department of Electrical and Computer Engineering, National University of Singapore , 4 Engineering Drive 3, 117583, Singapore
                [2 ]Engineering Science Programme, National University of Singapore , 9 Engineering Drive 1, 117575, Singapore
                [3 ]Institute of Materials Research and Engineering, A*STAR (Agency for Science, Technology and Research) , 3 Research Link, 117602, Singapore
                Author notes
                [*]

                These authors contributed equally to this work.

                Article
                srep10601
                10.1038/srep10601
                4450542
                26030002
                56e1e010-b37a-41e4-9bd9-3ea4e08d94a9
                Copyright © 2015, Macmillan Publishers Limited

                This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

                History
                : 10 December 2014
                : 20 April 2015
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