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dc.contributor.authorSuyana, P.
dc.contributor.authorSneha, K. R.
dc.contributor.authorNair, Balagopal N.
dc.contributor.authorKarunakaran, V.
dc.contributor.authorMohamed, A.
dc.contributor.authorWarrier, K.
dc.contributor.authorHareesh, U.
dc.date.accessioned2017-01-30T13:04:32Z
dc.date.available2017-01-30T13:04:32Z
dc.date.created2016-11-21T19:30:21Z
dc.date.issued2016
dc.identifier.citationSuyana, P. and K R, S. and Nair, B. and Karunakaran, V. and Mohamed, A. and Warrier, K. and Hareesh, U. 2016. A facile one pot synthetic approach for C3N4-ZnS composite interfaces as heterojunctions for sunlight-induced multifunctional photocatalytic applications. RSC Advances. 6 (22): pp. 17800-17809.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/28342
dc.identifier.doi10.1039/c5ra27427c
dc.description.abstract

Herein, we report a facile one pot synthetic protocol for the creation of C3N4-ZnS composite interfaces by the co-pyrolysis of a precursor mix containing zinc nitrate, melamine, and thiourea at 550°C in air. The organic-inorganic semiconductor heterojunctions thus formed displayed increased absorbance in the longer wavelength region and facilitated broad absorption of visible light compared to pure ZnS, C3N4 and conventionally synthesized hybrid samples. The decreased emission intensity, increased photocurrent generation and decreased fluorescence lifetime revealed reduced exciton recombinations in the co-pyrolysed sample containing C3N4-ZnS heterostructures. The samples displayed sunlight driven photocatalytic reduction of nitrophenol as well as hydrogen generation (4 mmol g-1 h-1) by water splitting. © The Royal Society of Chemistry 2016.

dc.publisherRoyal Society of Chemistry
dc.titleA facile one pot synthetic approach for C3N4-ZnS composite interfaces as heterojunctions for sunlight-induced multifunctional photocatalytic applications
dc.typeJournal Article
dcterms.source.volume6
dcterms.source.number22
dcterms.source.startPage17800
dcterms.source.endPage17809
dcterms.source.titleRSC Advances
curtin.departmentNanochemistry Research Institute
curtin.accessStatusOpen access


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