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dc.contributor.authorGeorge, Leenaen_US
dc.contributor.authorSappati, Subrahmanyamen_US
dc.contributor.authorGHOSH, PRASENJITen_US
dc.contributor.authorDevi, R. Nandinien_US
dc.date.accessioned2019-03-15T11:24:15Z
dc.date.available2019-03-15T11:24:15Z
dc.date.issued2015-02en_US
dc.identifier.citationJournal of Physical Chemistry C, 119 (6), 3060-3067.en_US
dc.identifier.issn1932-7447en_US
dc.identifier.issn1932-7447en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2204-
dc.identifier.urihttps://doi.org/10.1021/jp511996zen_US
dc.description.abstractSurface modification of ZnO nanoparticles is identified as a method of modulating surface sites advantageously. ZnO nanoparticles of two different sizes are surface modified with a conjugated organic moiety to enable electron conduction and transfer. Enhanced H2 evolution from water–methanol mixtures was observed in the composite systems compared to pristine ZnO under visible light irradiation without any cocatalyst. The system is also marginally active in water splitting in pure water without any sacrificial agents. Photophysical characterization indicates that even though reducing size into the nanoregime affects the band gap detrimentally, modifications by simple conjugated organic molecules assist in enhanced visible light activity. The experimental observations are corroborated with computational studies, which also point to a localization of valence band maximum of the interface on the organic moiety and conduction band minimum on ZnO.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectConjugated Organic Moleculesen_US
dc.subjectVisible Light Activityen_US
dc.subjectZnO Nanostructuresen_US
dc.subjectPhotocatalytic Water Splittingen_US
dc.subject2015en_US
dc.titleSurface Site Modulations by Conjugated Organic Molecules To Enhance Visible Light Activity of ZnO Nanostructures in Photocatalytic Water Splittingen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleJournal of Physical Chemistry Cen_US
dc.publication.originofpublisherForeignen_US
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