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      Co 2+ and Ho 3+ doped CuS nanocrystals with improved photocatalytic activity under visible light irradiation

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          Abstract

          Co 2+ and Ho 3+ doped CuS nanostructures have been synthesized by a hydrothermal method. The nature of dopants influence the morphology, photocatalytic performance and the band gap values.

          Abstract

          In this work, Co 2+ and Ho 3+ doped CuS nanostructured assemblies have been synthesized by means of a surfactant free hydrothermal method and investigated as photocatalysts in the degradation of methylene blue (MB) dye under visible light irradiation in the presence of H 2O 2. Firstly, it is found that the nature of dopants (M = Co 2+, Ho 3+) plays an important role in controlling the morphology of CuS structures as observed in FESEM and TEM analysis. Secondly, the band gap values of the M doped CuS structures showed a red shift. As a result, the M doped CuS structures exhibited enhanced photocatalytic activities compared to the pristine CuS structures. Among the different photocatalysts tested, 2.5 mol% cobalt doped CuS (CC samples) showed the best activity (∼52% more than CuS) in the photocatalytic degradation of dyes (almost complete degradation (∼99%) of MB dye in 20 min). In addition, these CC samples showed good catalyst stability for the degradation of dyes. The overall differences in the catalytic activity of the samples tested are discussed in terms of their band gap, surface area, porosity, defect surface, and morphology.

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          Self-doped Ti3+ enhanced photocatalyst for hydrogen production under visible light.

          Through a facile one-step combustion method, partially reduced TiO(2) has been synthesized. Electron paramagnetic resonance (EPR) spectra confirm the presence of Ti(3+) in the bulk of an as-prepared sample. 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. It is worth noting that the Ti(3+) 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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            ZnO Hierarchical Micro/Nanoarchitectures: Solvothermal Synthesis and Structurally Enhanced Photocatalytic Performance

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              New materials for tunable plasmonic colloidal nanocrystals.

              We present a review on the emerging materials for novel plasmonic colloidal nanocrystals. We start by explaining the basic processes involved in surface plasmon resonances in nanoparticles and then discuss the classes of nanocrystals that to date are particularly promising for tunable plasmonics: non-stoichiometric copper chalcogenides, extrinsically doped metal oxides, oxygen-deficient metal oxides and conductive metal oxides. We additionally introduce other emerging types of plasmonic nanocrystals and finally we give an outlook on nanocrystals of materials that could potentially display interesting plasmonic properties.
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                Author and article information

                Journal
                RSCACL
                RSC Advances
                RSC Adv.
                Royal Society of Chemistry (RSC)
                2046-2069
                2016
                2016
                : 6
                : 48
                : 42581-42588
                Affiliations
                [1 ]Department of Inorganic Chemistry
                [2 ]Faculty of Chemistry
                [3 ]University of Tabriz
                [4 ]51666-14766 Tabriz
                [5 ]Iran
                [6 ]UNISA Africa Chair in Nanosciences-Nanotechnology
                [7 ]College of Graduate Studies
                [8 ]University of South Africa
                [9 ]Pretoria
                [10 ]South Africa
                [11 ]Department of Nanochemistry
                [12 ]Istituto Italiano di Tecnologia
                [13 ]16163 Genova
                [14 ]Italy
                Article
                10.1039/C6RA03647C
                1eaec22e-701c-47aa-a33d-11c42e027587
                © 2016
                History

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