Back to Search Start Over

Spectral Characteristics and Photosensitization of TiO2 Nanoparticles in Reverse Micelles by Perylenes

Authors :
Jesse J. Bergkamp
Rodrigo E. Palacios
Thomas A. Moore
Gerdenis Kodis
Robert Godin
Ana L. Moore
Sonia G. Bertolotti
Laura Hernandez
Dalvin D. Méndez-Hernández
John Tomlin
Benjamin D. Sherman
Ernesto Mariño-Ochoa
Manuel J. Llansola Portolés
Gonzalo Cosa
Carlos A. Chesta
Source :
The Journal of Physical Chemistry B. 117:4568-4581
Publication Year :
2012
Publisher :
American Chemical Society (ACS), 2012.

Abstract

We report on the photosensitization of titanium dioxide nanoparticles (TiO2 NPs) synthesized inside AOT (bis(2-ethylhexyl) sulfosuccinate sodium salt) reverse micelles following photoexcitation of perylene derivatives with dicarboxylate anchoring groups. The dyes, 1,7-dibromoperylene-3,4,9,10-tetracarboxy dianhydride (1), 1,7-dipyrrolidinylperylene-3,4,9,10-tetracarboxy dianhydride (2), and 1,7-bis(4-tert-butylphenyloxy)perylene-3,4,9,10-tetracarboxy dianhydride (3), have considerably different driving forces for photoinduced electron injection into the TiO2 conduction band, as estimated by electrochemical measurements and quantum mechanical calculations. Fluorescence anisotropy measurements indicate that dyes 1 and 2 are preferentially solubilized in the micellar structure, creating a relatively large local concentration that favors the attachment of the dye to the TiO2 surface. The binding process was followed by monitoring the hypsochromic shift of the dye absorption spectra over time for 1 and 2. Photoinduced electron transfer from the singlet excited state of 1 and 2 to the TiO2 conduction band (CB) is indicated by emission quenching of the TiO2-bound form of the dyes and confirmed by transient absorption measurements of the radical cation of the dyes and free carriers (injected electrons) in the TiO2 semiconductor. Steady state and transient spectroscopy indicate that dye 3 does not bind to the TiO2 NPs and does not photosensitize the semiconductor. This observation was rationalized as a consequence of the bulky t-butylphenyloxy groups which create a strong steric impediment for deep access of the dye within the micelle structure to reach the semiconductor oxide surface. Fil: Hernández, Laura. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Godin, Robert. McGill University; Canadá Fil: Bergkamp, Jesse J.. Arizona State University; Estados Unidos Fil: Llansola Portolés, Manuel Jose. Arizona State University; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Sherman, Benjamin D.. Arizona State University; Estados Unidos Fil: Tomlin, John. Arizona State University; Estados Unidos Fil: Kodis, Gerdenis. Arizona State University; Estados Unidos Fil: Méndez Hernández, Dalvin D.. Arizona State University; Estados Unidos Fil: Bertolotti, Sonia Graciela. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Chesta, Carlos Alberto. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Mariño Ochoa, Ernesto. Tecnológico de Monterrey; México Fil: Moore, Ana L.. Arizona State University; Estados Unidos Fil: Moore, Thomas A.. Arizona State University; Estados Unidos Fil: Cosa, Gonzalo. McGill University; Canadá Fil: Palacios, Rodrigo Emiliano. Universidad Nacional de Río Cuarto. Facultad de Ciencias Exactas Fisicoquímicas y Naturales; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina

Details

ISSN :
15205207 and 15206106
Volume :
117
Database :
OpenAIRE
Journal :
The Journal of Physical Chemistry B
Accession number :
edsair.doi.dedup.....e5e56fd8062ac1e85a88f39ee6d8cd72
Full Text :
https://doi.org/10.1021/jp3086792