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Gold nanoparticle-functionalized carbon nanotubes for light-induced electron transfer process

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dc.contributor.author Pramod, P
dc.contributor.author Soumya, C C
dc.contributor.author George Thomas, K
dc.date.accessioned 2013-11-20T10:13:36Z
dc.date.available 2013-11-20T10:13:36Z
dc.date.issued 2011
dc.identifier.citation Journal of Physical Chemistry Letters 2(7):775-781;07 Apr 2011 en_US
dc.identifier.issn 1948-7185
dc.identifier.uri http://ir.niist.res.in:8080/jspui/handle/123456789/785
dc.description.abstract The 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.iso en en_US
dc.publisher American Chemical Society en_US
dc.subject Complexes en_US
dc.subject Interface en_US
dc.subject Composites en_US
dc.subject Metal en_US
dc.subject Photochemistry en_US
dc.subject Energy en_US
dc.subject Charge-transfer en_US
dc.title Gold nanoparticle-functionalized carbon nanotubes for light-induced electron transfer process en_US
dc.type Article en_US


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