Influence of cysteine adsorption on the performance of CdSe quantum dots sensitized solar cells
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Otros documentos de la autoría: XU, XUEQING; Gimenez, Sixto; Mora-Sero, Ivan; Abate, Antonio; Bisquert, Juan; Xu, Gang
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Mostrar el registro completo del ítemcomunitat-uji-handle:10234/9
comunitat-uji-handle2:10234/2507
comunitat-uji-handle3:10234/6973
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http://dx.doi.org/10.1016/j.matchemphys.2010.07.041 |
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Título
Influence of cysteine adsorption on the performance of CdSe quantum dots sensitized solar cellsFecha de publicación
2010Editor
ElsevierISSN
0254-0584Cita bibliográfica
Materials Chemistry and Physics, 124, 1, p. 709-712Tipo de documento
info:eu-repo/semantics/articleVersión
info:eu-repo/semantics/publishedVersionPalabras clave / Materias
Resumen
The surface of mesoporous TiO<sub>2</sub> electrodes has been functionalized with cysteine using different solutions for the subsequent attachment of colloidal CdSe QDs solved in toluene. The adsorption behavior of ... [+]
The surface of mesoporous TiO<sub>2</sub> electrodes has been functionalized with cysteine using different solutions for the subsequent attachment of colloidal CdSe QDs solved in toluene. The adsorption behavior of both cysteine and CdSe QDs on the TiO<sub>2</sub> nanoparticles has been investigated by Attenuated Total Reflectance-Fourier Transform Infrared (ATR-FTIR) Spectroscopy. The photoelectrochemical properties of the CdSe QDs sensitized TiO<sub>2</sub> electrode have been characterized by using UV-vis spectroscopy, photocurrent-potential measurement, open-circuit voltage decay, and cyclic voltammetry. It is found that the amount of adsorbed cysteine becomes excessive when highly concentrated aqueous solutions were adopted instead of toluene solutions, leading to a blocking for the diffusion and adsorption of the CdSe QDs. This is translated into a decrease of light harvesting and short circuit current (J<sub>sc</sub>) in the solar cell devices. On the other hand, it is suggested that the large amount of adsorbed cysteine on the surface of the TiO<sub>2</sub> electrode could reduce the electron recombination at the interface between the TiO<sub>2</sub> electrode and the electrolyte. As a consequence, the charge transfer resistance and fill factor became larger, and the electron lifetime became longer. © 2010 Elsevier B.V. All rights reserved. [-]
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