Source:http://linkedlifedata.com/resource/pubmed/id/19226135
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2009-3-25
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pubmed:abstractText |
Photoinduced charge transfer events between 3 nm diameter CdSe semiconductor nanocrystals and an electron acceptor, MV2+, have been probed in the subpicosecond-microseconds-seconds time scale by confining the reactants in an AOT/heptane reverse micelle. The probe molecule, methyl viologen (MV2+) interacts with the excited CdSe nanoparticle and quenches its emission effectively. The ultrafast electron transfer to MV2+, as monitored from the exciton bleaching recovery of CdSe and the formation of MV+* radical, is completed with an average rate constant of 2.25x10(10) s(-1). Under steady state irradiation (450 nm) the accumulation of MV+* is seen with a net quantum yield of 0.1. Mediation of the electron transfer through TiO2 nanoparticles is achieved by coupling them with the CdSe-MV2+ system within the reverse micelle. This coupling of two semiconductor nanoparticles increases the quantum yield of MV2+ reduction by a factor of 2. The dual roles of TiO2 as an electron shuttle and a rectifier are elucidated by transient absorption spectroscopy and steady state photolysis. The presence of both TiO2 and MV2+ in the reverse micelle creates a synergistic effect to enhance the electron transfer rate constant by an order of magnitude. The time-resolved events that dictate the production and stabilization of electron transfer product provide an insight into the photocatalytic systems that are potentially important in solar hydrogen production and photocatalytic remediation.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:status |
PubMed-not-MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1936-086X
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
24
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pubmed:volume |
3
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
682-90
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pubmed:year |
2009
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pubmed:articleTitle |
Photocatalysis with CdSe nanoparticles in confined media: mapping charge transfer events in the subpicosecond to second timescales.
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pubmed:affiliation |
Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, Indiana 46556, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.
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