Please use this identifier to cite or link to this item: https://idr.l1.nitk.ac.in/jspui/handle/123456789/10137
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dc.contributor.authorShenoy, S.
dc.contributor.authorJang, E.
dc.contributor.authorPark, T.J.
dc.contributor.authorGopinath, C.S.
dc.contributor.authorSridharan, K.
dc.date.accessioned2020-03-31T08:18:38Z-
dc.date.available2020-03-31T08:18:38Z-
dc.date.issued2019
dc.identifier.citationApplied Surface Science, 2019, Vol.483, , pp.696-705en_US
dc.identifier.urihttp://idr.nitk.ac.in/jspui/handle/123456789/10137-
dc.description.abstractSize 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.en_US
dc.titleCadmium sulfide nanostructures: Influence of morphology on the photocatalytic degradation of erioglaucine and hydrogen generationen_US
dc.typeArticleen_US
Appears in Collections:1. Journal Articles

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