@article {Mora-Ser{\'o}20106755,
	title = {Fast regeneration of CdSe quantum dots by ru dye in sensitized TiO 2 electrodes},
	journal = {Journal of Physical Chemistry C},
	volume = {114},
	number = {14},
	year = {2010},
	note = {cited By 40},
	pages = {6755-6761},
	abstract = {Interacting properties of colloidal CdSe quantum dots (QDs) and polypyridyl ruthenium dyes employed as cosensitizers of mesoporous TiO2 electrodes as well as the effect of QDs coating and anchoring mode (direct and linker adsorption) have been investigated by photoluminesce (PL), Raman, and transient absorption (TAS) spectroscopies. Direct adsorption of QDs on TiO 2 leads to a more efficient PL quenching compared to that of QDs attached by means of a molecular linker (cysteine). This fact suggests higher electron injection for the former anchoring mode. Coating of ZnS on CdSe QDs sensitized TiO2 electrodes passivates the QDs surface states and partially releases quantum confinement effects, as is observed in colloidal core-shell nanoparticles. Subsequent cosensitization with a ruthenium molecular dye dramatically quenches the PL of the QDs/TiO2 electrodes, even in the presence of ZnS coating, indicating the presence of strong photoinduced charge transfer between the CdSe QDs and the dye molecules. This is firmly supported by TAS spectroscopy on the interfacial recombination kinetics that points to the fast hole transfer from the photoexcited QDs to the dye. The regenerating action of molecular dyes for QD sensitizers can have important implications in the development of efficient photovoltaic devices based on the synergistic action of dye-QD-TiO2 heterostructures. {\textcopyright} 2010 American Chemical Society.},
	doi = {10.1021/jp100591m},
	url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-77951077909\&doi=10.1021\%2fjp100591m\&partnerID=40\&md5=5ac44892ad0de49def0b0967a22dd26e},
	author = {Mora-Ser{\'o}, I. and V. Likodimos and Gim{\'e}nez, S. and Mart{\'\i}nez-Ferrero, E. and Albero, J. and Palomares, E. and A. G. Kontos and P. Falaras and Bisquert, J.}
}
