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      Enhanced photoelectrochemical and photocatalytic behaviors of MFe 2O 4 (M = Ni, Co, Zn and Sr) modified TiO 2 nanorod arrays

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          Abstract

          Modified TiO 2 nanomaterials are considered to be promising in energy conversion and ferrites modification may be one of the most efficient modifications. In this research, various ferrites, incorporated with various cations (MFe 2O 4, M = Ni, Co, Zn, and Sr), are utilized to modify the well aligned TiO 2 nanorod arrays (NRAs), which is synthesized by hydrothermal method. It is found that all MFe 2O 4/TiO 2 NRAs show obvious red shift into the visible light region compared with the TiO 2 NRAs. In particular, NiFe 2O 4 modification is demonstrated to be the best way to enhance the photoelectrochemical and photocatalytic activity of TiO 2 NRAs. Furthermore, the separation and transfer of charge carriers after MFe 2O 4 modification are clarified by electrochemical impedance spectroscopy measurements. Finally, the underlying mechanism accounting for the enhanced photocatalytic activity of MFe 2O 4/TiO 2 NRAs is proposed. Through comparison among different transition metals modified TiO 2 with the same synthesis process and under the same evaluating condition, this work may provide new insight in designing modified TiO 2 nanomaterials as visible light active photocatalysts.

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          Most cited references12

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          Ni(x)Co(3-x)O(4) nanowire arrays for electrocatalytic oxygen evolution.

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            Comparing graphene-TiO₂ nanowire and graphene-TiO₂ nanoparticle composite photocatalysts.

            We demonstrate that uniform dispersion of TiO(2) on graphene is critical for the photocatalytic effect of the composite. The hydrothermal method was employed to synthesize TiO(2) nanowires (NW) and then fabricate graphene-TiO(2) nanowire nanocomposite (GNW). Graphene oxide (GO) reduction to graphene and hybridization between TiO(2) NWs and graphene by forming chemical bonding was achieved in a one-step hydrothermal process. Graphene-TiO(2) nanoparticle (NP) nanocomposite (GNP) was also synthesized. Photocatalytic performance and related properties of NP, NW, GNP, and GNW were comparatively studied. It was found that by incorporation of graphene, GNP and GNW have higher performance than their counterparts. More importantly, it was found that NWs, in comparison with NPs, have more uniform dispersion on graphene with less agglomeration, resulting in more direct contact between TiO(2) and graphene, and hence further improved electron-hole pairs (EHPs) separation and transportation. The adsorbability of GNW is also found to be higher than GNP. The result reveals that the relative photocatalytic activity of GNW is much higher than GNP and pure NWs or NPs.
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              Monodisperse M(x)Fe(3-x)O4 (M = Fe, Cu, Co, Mn) nanoparticles and their electrocatalysis for oxygen reduction reaction.

              Sub-10 nm nanoparticles (NPs) of M(II)-substituted magnetite MxFe3-xO4 (MxFe1-xO•Fe2O3) (M = Mn, Fe, Co, Cu) were synthesized and studied as electrocatalysts for oxygen reduction reaction (ORR) in 0.1 M KOH solution. Loaded on commercial carbon support, these MxFe3-xO4 NPs showed the M(II)-dependent ORR catalytic activities with MnxFe3-xO4 being the most active followed by CoxFe3-xO4, CuxFe3-xO4, and Fe3O4. The ORR activity of the MnxFe3-xO4 was further tuned by controlling x and MnFe2O4 NPs were found to be as efficient as the commercial Pt in catalyzing ORR. The MnFe2O4 NPs represent a new class of highly efficient non-Pt catalyst for ORR in alkaline media.
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                Author and article information

                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group
                2045-2322
                28 July 2016
                2016
                : 6
                : 30543
                Affiliations
                [1 ]High-Tech Institute of Xi’an , Xi’an, 710025, China
                Author notes
                [*]

                These authors contributed equally to this work.

                Article
                srep30543
                10.1038/srep30543
                4964351
                27464888
                dfc04c8e-3570-4dd1-94eb-236e8465f904
                Copyright © 2016, The Author(s)

                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
                : 05 April 2016
                : 06 July 2016
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