Preparation Mico/Nano Composite Particles and their Applications for Dye-Sensitized Solar Cells

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Abstract:

This study investigated the applicability of TiO2/Au (or TiO2/Ag) composite particles, which probably have the plasmon resonance effect, on FTO-glass substrate of the working electrode of a DSSC. The dry particle coating technique was utilized to coat the surfaces of TiO2 particle with nano-sized Au (or Ag) powder particles. A layer of TiO2/Au (or TiO2/Ag) composite particles was deposited on the FTO-glass substrate of the working electrode, and it was then sintered in a high-temperature furnace. The working electrode covered with a TiO2/Au (or TiO2/Ag) thin film was kept immersed in a solution of N-719 (Ruthenium) dye for 12 h. Finally, the DSSC was assembled, and the short-circuit photocurrent; the open-circuit photovoltage, and the power conversion efficiency η of DSSC were measured using a home-made I-V measurement system. This study also examined the effects of the mass ratio of TiO2 to Au (or Ag) and the duration of dry coating on the η of the DSSC. If the duration of dry coating is adequate, the η of the DSSC with TiO2/Au (or TiO2/Ag) composite particles increased with increase in the percentage of Au (or Ag) in the composite particles. Most importantly, this study shows that the power conversion efficiency η of the DSSC with a film of TiO2/Au (or TiO2/Ag) on the working electrode always exceeds that of the conventional DSSC due to presence of the Schottky barrier, which is probably created in the TiO2/Au (or TiO2/Ag) composite particle.

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Advanced Materials Research (Volumes 239-242)

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202-205

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May 2011

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© 2011 Trans Tech Publications Ltd. All Rights Reserved

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[1] B. O ' Regan et al., Nature, Vol. 353 (1991), p.737–739.

Google Scholar

[2] M. Grätzel et al., Journal of Photochemistry & Photobiology A: Chemistry, Vol. 164 (2004), p.3–14.

Google Scholar

[3] A. Hauch et al., Journal of The Electrochemical Society, Vol. 149 (2002), p. H159–H163.

Google Scholar

[4] T.S. Kang et al., Journal of The Electrochemical Society, Vol. 149 (2002), p. E155–E158.

Google Scholar

[5] M. Adachi et al., Journal of The Electrochemical Society, Vol. 150 (2003), p. G488–G493.

Google Scholar

[6] J. Jiu et al., Journal of The Electrochemical Society, Vol. 151 (2004), p. A1653–A1658.

Google Scholar

[7] B.S. Richards et al., Journal of The Electrochemical Society, Vol. 152 (2005), p. F71–F74.

Google Scholar

[8] H. Han et al., Journal of The Electrochemical Society, Vol. 152 (2005), p. A164–A166.

Google Scholar

[9] M. Wei et al., Journal of The Electrochemical Society, Vol. 153 (2006), p. A1232–A1236.

Google Scholar

[10] G. S. Kim et al., Electrochemistry Communications, Vol. 8 (2006), p.961–966.

Google Scholar

[11] A. Kongkanand et al., Nano Letter, Vol. 7 (2007), p.676–680.

Google Scholar

[12] C. S. Chou et al., Powder Technology, Vol. 187 (2008), p.181–189.

Google Scholar

[13] Y. H. Su et al., Applied Physics A, Vol. 88 (2007), p.173–178.

Google Scholar

[14] E.W. McFarland et al., Nature, Vol. 421 (2003), p.616–618.

Google Scholar

[15] C.S. Chou et al., Powder Technology, Vol. 194 (2009), pp.95-105.

Google Scholar

[16] A. Zaban et al., Journal of Physical Chemistry B, Vol. 102 (1998), p.452–460.

Google Scholar