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dc.contributor.authorPramod, P-
dc.contributor.authorSoumya, C C-
dc.contributor.authorGeorge Thomas, K-
dc.date.accessioned2013-11-20T10:13:36Z-
dc.date.available2013-11-20T10:13:36Z-
dc.date.issued2011-
dc.identifier.citationJournal of Physical Chemistry Letters 2(7):775-781;07 Apr 2011en_US
dc.identifier.issn1948-7185-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/785-
dc.description.abstractThe modified electronic properties at the heterojunctions of Au nanoparticle-decorated single-walled carbon nanotubes (SWNTs) have been utilized for photoinduced electron transfer by anchoring a photoactive molecule, namely ruthenium trisbipyridine (Ru(bpy)(3)(2+)). A unidirectional electron flow was observed from the excited state of Ru(bpy)(3)(2+) to carbon nanotubes when the chromophores were linked through Au nanoparticles (SWNT-Au-Ru(2+)). In contrast, photoinduced electron transfer was not observed from the excited state of Ru(bpy)(3)(2+) neither to SWNT nor Au nanoparticles when these components were linked directly. The charge equilibration occurring at the SWNT-Au heterojunctions, due to the differences in electrochemical potentials, result in the formation of a localized depletion layer at the bundled carbon nanotube walls, which may act as acceptor sites of electrons from *Ru(bpy)(3)(2+). The charge separation in SWNT-Au-Ru(2+) nanohybrids was sustained for several nanoseconds before undergoing recombination, making these systems promising for optoelectronic and artificial photosynthetic device applications.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectComplexesen_US
dc.subjectInterfaceen_US
dc.subjectCompositesen_US
dc.subjectMetalen_US
dc.subjectPhotochemistryen_US
dc.subjectEnergyen_US
dc.subjectCharge-transferen_US
dc.titleGold nanoparticle-functionalized carbon nanotubes for light-induced electron transfer processen_US
dc.typeArticleen_US
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