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dc.contributor.authorNagaraja, C. M.-
dc.contributor.authorKaur, M.-
dc.contributor.authorDhingra, S.-
dc.date.accessioned2021-06-14T23:43:14Z-
dc.date.available2021-06-14T23:43:14Z-
dc.date.issued2021-06-15-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/1820-
dc.description.abstractA facile, one-pot, solvothermal synthesis of MoS2 microflowers (S1) and the heterostructures MoS2/g-C3N4 with varying ratios of 1:1 (S2), 1:2 (S3) and 1:3 (S4) exhibiting enhanced visible-light-assisted H2 generation by water splitting has been reported. The compounds were thoroughly characterized by PXRD, FESEM, HRTEM, EDS, UVevis and XPS techniques. FESEM and HRTEM analyses showed the presence of microflowers composed of nano-sized petals in case of pure MoS2 (S1), while the MoS2 microflowers covered with gC3N4 nanosheets in case of MoS2/g-C3N4 heterostructure, S4. XPS analysis of S2 showed the presence of 2H phase of MoS2 with g-C3N4. The Eosin-Y/dye-sensitized visible-lightassisted photocatalytic investigation of the samples in the absence of any noble metal cocatalyst revealed very good water splitting activity of MoS2/g-C3N4 heterostructure, S2 with hydrogen generation rate of 1787 mmol h1 g1 which is about 6 and 40 times higher than pure MoS2 and g-C3N4 respectively. The relatively higher catalytic activity of the heterostructure, S2 has been ascribed to the efficient spatial separation of photo-induced charge carriers owing to the synergistic interaction between MoS2 and g-C3N4. A possible mechanism for the Eosin-Y-sensitized photocatalytic H2 generation activity of MoS2/g-C3N4 heterostructures has also been presented. The enhanced activity of S2 was furtheren_US
dc.language.isoen_USen_US
dc.subjectMolybdenum disulfideen_US
dc.subjectGraphitic carbon nitrideen_US
dc.subjectVisible-light photocatalysisen_US
dc.subjectDye-sensitizeden_US
dc.subjectH2 generationen_US
dc.titleEnhanced visible-light-assisted photocatalytic hydrogen generation by MoS2/g-C3N4 nanocompositesen_US
dc.typeArticleen_US
Appears in Collections:Year-2020

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