Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2011-2-9
pubmed:abstractText
Charge transfer dynamics between an adsorbed molecule and a rutile TiO(2)(110) surface have been investigated in three organometallic dyes related to multicenter water splitting dye complexes: Ru 535 (cis-bis(isothiocyanato)bis(2,2'-bipyridyl-4,4'-dicarboxylato)-ruthenium(II)), Ru 455 (cis-bis(2,2'-bipyridyl)-(2,2'-bipyridyl-4,4'-dicarboxylic acid)-ruthenium(II)), and Ru 470 (tris(2,2'-bipyridyl-4,4'-dicarboxylic acid)-ruthenium(II)). The adsorption of the dye molecules on the rutile TiO(2)(110) surface has been studied using core-level and valence photoemission. Dye molecules were deposited in situ using ultrahigh vacuum electrospray deposition. Core-level photoemission spectra reveal that each complex bonds to the surface via deprotonation of two carboxylic groups. All three dye complexes show evidence of ultrafast charge transfer to the TiO(2) substrate using the core-hole clock implementation of resonant photoemission spectroscopy.
pubmed:language
eng
pubmed:journal
pubmed:status
PubMed-not-MEDLINE
pubmed:month
Feb
pubmed:issn
1089-7690
pubmed:author
pubmed:issnType
Electronic
pubmed:day
7
pubmed:volume
134
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
054705
pubmed:year
2011
pubmed:articleTitle
Charge transfer dynamics of model charge transfer centers of a multicenter water splitting dye complex on rutile TiO2(110).
pubmed:affiliation
School of Physics and Astronomy, and Nottingham Nanotechnology and Nanoscience Centre (NNNC), University of Nottingham, Nottingham NG7 2RD, United Kingdom.
pubmed:publicationType
Journal Article