Issue 10, 2015

Metal and F dual-doping to synchronously improve electron transport rate and lifetime for TiO2 photoanode to enhance dye-sensitized solar cells performances

Abstract

A general strategy to synchronously improve electron transport rate and lifetime for TiO2 photoanode by metal and F dual doping is proposed and demonstrated for dye-sensitized solar cells (DSSCs) for the first time. Tin and fluorine dual-doped TiO2 nanoparticles are prepared and X-ray photoelectron spectroscopy (XPS) analysis indicates that the Sn atoms and the F atoms locate mainly in the TiO2 lattice and on the TiO2 particles surface, respectively. The DSSC based on Sn/F–TiO2 sample shows a high photoconversion efficiency of 8.89% under an AM 1.5 solar condition (100 mW cm−2), which is higher than those for the undoped TiO2 nanoparticles (7.12%) and the solely Sn (8.14%) or F doped (8.31%) samples. This improvement is attributed to the combined effects of a faster electron transport rate and a longer electron lifetime in the dual-doped TiO2 film. Following this strategy, we also prepare Ta/F, Nb/F, and Sb/F dual-doped TiO2 nanoparticles and find that the performance of DSSCs based on all the dual-doped samples is further improved compared with the single doping cases. Finally, through density functional theory (DFT) calculations, the mechanism behind the improvement by tin and fluorine dual-doping is discussed in detail.

Graphical abstract: Metal and F dual-doping to synchronously improve electron transport rate and lifetime for TiO2 photoanode to enhance dye-sensitized solar cells performances

Supplementary files

Article information

Article type
Paper
Submitted
23 Dec 2014
Accepted
27 Jan 2015
First published
28 Jan 2015

J. Mater. Chem. A, 2015,3, 5692-5700

Author version available

Metal and F dual-doping to synchronously improve electron transport rate and lifetime for TiO2 photoanode to enhance dye-sensitized solar cells performances

Y. Duan, J. Zheng, M. Xu, X. Song, N. Fu, Y. Fang, X. Zhou, Y. Lin and F. Pan, J. Mater. Chem. A, 2015, 3, 5692 DOI: 10.1039/C4TA07068B

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