Issue 4, 2013

Enhanced charge collection efficiency of dye-sensitized solar cells based on size-tunable hierarchically structured TiO2 beads

Abstract

Hierarchically structured mesoporous TiO2 beads (HS-TBs), which are used as photoelectrodes in highly efficient dye-sensitized solar cells (DSCs), were prepared by an electrostatic spray (e-spray) technique. To prepare different sized HS-TBs, the electric field and the concentration of TiO2 particles were carefully controlled, because they are critical factors in preparing size-controlled TiO2 beads. Four different HS-TBs were formulated with average diameters of 250, 450, 700, and 1200 nm as high-quality photoelectrodes for use in DSCs. In this study, we found that the zero-dimensional HS-TBs were the most promising photoelectrode for DSCs due to enhanced charge collection efficiency and better penetration of electrolytes through relatively large pores among the HS-TBs. The HS-TBs were characterized by intensity modulated photocurrent spectroscopy (IMPS), the scanning electron microscopy (SEM), transmission electron microscopy (TEM), Brunauer–Emmett–Teller (BET) method, Barrett–Joyner–Halenda (BJH) method, and electrochemical analysis. The conversion efficiency of HS-TB photoelectrodes improved with increasing bead size due to the enhanced electron transport through electrodes. The present HS-TB cells exhibit a noticeable improvement in the overall efficiency: maximum 9.54% (1200 nm) versus 5.83% for the reference cell made of a TiO2 nanocrystalline film.

Graphical abstract: Enhanced charge collection efficiency of dye-sensitized solar cells based on size-tunable hierarchically structured TiO2 beads

Supplementary files

Article information

Article type
Paper
Submitted
13 Sep 2012
Accepted
13 Nov 2012
First published
13 Nov 2012

J. Mater. Chem. A, 2013,1, 1359-1367

Enhanced charge collection efficiency of dye-sensitized solar cells based on size-tunable hierarchically structured TiO2 beads

D. Hwang, H. Lee, Y. Seo, D. Kim, S. M. Jo and D. Y. Kim, J. Mater. Chem. A, 2013, 1, 1359 DOI: 10.1039/C2TA00292B

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