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Author: search.filters.author.Shenoy, S.Subject: search.filters.subject.Cadmium sulfide

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    Cadmium sulfide nanostructures: Influence of morphology on the photocatalytic degradation of erioglaucine and hydrogen generation
    (Elsevier B.V., 2019) Shenoy, S.; Jang, E.; Park, T.J.; Gopinath, C.S.; Sridharan, K.
    Size and shape of inorganic materials are known to have great effects on their physical and chemical properties. Here, for the first time we report the visible light driven photocatalytic degradation of erioglaucine – a stable organic dye molecule in the presence of chemically synthesized nanoscale CdS with 1D (nanorods), 2D (nanosheets) and 3D (hierarchical) morphology. Visible light driven photocatalytic degradation efficiency of both 1D and 3D CdS in the removal of erioglaucine are identical. Surprisingly, with 5 min of sonication, the highly crystalline 3D CdS stacked with many thin nanowires containing numerous active surface sites exhibited four-fold enhanced photodegradation efficiency in comparison to 1D and 2D CdS. Scavenger studies revealed that electrons and superoxide radicals are primary reactive species involved in the photodegradation of erioglaucine, while cyclic photodegradation studies revealed the good stability of 3D CdS against photocorrosion. Further, the photocatalytic hydrogen evolution studies also revealed the excellent activity of 3D CdS in comparison to 1D and 2D CdS. Thus, we find that the morphology indeed influences the photocatalytic activity. These results reveal that 3D CdS nanostructures investigated in the present work are efficient photocatalysts that could be fine-tuned for both environmental remediation and hydrogen generation applications. © 2019 Elsevier B.V.
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    Enhanced photocatalytic efficiency of layered CdS/CdSe heterostructures: Insights from first principles electronic structure calculations
    (Institute of Physics Publishing helen.craven@iop.org, 2020) Shenoy, S.; Tarafder, K.
    Metal sulfides are emerging as an important class of materials for photocatalytic applications, because of their high photo responsive nature in the wide visible light range. In this class of materials, CdS with a direct band gap of 2.4 eV, has gained special attention due to the relative position of its conduction band minimum, which is very close to the energies of the reduced protons. However, the photogenerated holes in the valence band of CdS are prone to oxidation and destroy its structure during photocatalysis. Thus constructing a CdS based heterostructure would be an effective strategy for improving the photocatalytic performance. In this work we have done a detail theoretical investigation based on hybrid density functional theory calculation to get insight into the energy band structure, mobility and charge transfer across the CdS/CdSe heterojunction. The results indicate that CdS/CdSe forms type-II heterostructure that has several advantages in improving the photocatalytic efficiency under visible light irradiation. © 2020 IOP Publishing Ltd.
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    Graphitic C3N4/CdS composite photocatalyst: Synthesis, characterization and photodegradation of methylene blue under visible light
    (Elsevier B.V., 2020) Shenoy, S.; Tarafder, K.; Sridharan, K.
    Design and development of heterojunction photocatalysts is one among the main strategies for improving the photocatalytic activity of semiconductor materials. Here, we report the synthesis of a heterojunction photocatalyst by the embedment of cadmium sulphide (CdS) nanoparticles on the surface of graphitic carbon nitride (g-C3N4) layers through hydrothermal approach. The g-C3N4/CdS heterojunction photocatalyst exhibited two-fold and three-fold enhancement in the photodegradation efficiency in comparison to pristine CdS and g-C3N4, respectively in the removal of 20 ppm methylene blue dye molecules under visible light irradiation. The enhanced photocatalytic activity can be attributed to the formation of heterojunction and the synergistic effect of g-C3N4 and CdS in the promotion of charge separation and charge mobility that was tracked through photoluminescence spectroscopy. © 2020 Elsevier B.V.