The nonconventio
nal bottom-up growth of TiO
2 was first demonstrated in the preparation of hierarchical TiO
2 electrodes for use in highly efficient dye-sensitized solar cells. The simple immersion of a substrate in a precursor solution e
nabled the growth of TiO
2 particulate films. Here, we
have implemented a hierarchical growth strategy in which two stages of controlled growth yielded first macroscale TiO
2 particles, followed by mesoscale TiO
2 particles. We successfully fabricated electrode films up to 20 渭m thick via a growth rate of 0.3 渭m/min. The specific area of the electrodes was controlled via the deposition of mesoscale TiO
2 particles. The deposited particles displayed a rutile p
hase with an average size of several tens of
nanometers in diameter, as confirmed by XRD and high-resolution TEM imaging. After depositing the second layer of mesoscale TiO
2 particles, the photocurrent density increased by a factor of 3. A maximum efficiency of 6.84% was obtained for the hierarchically structured TiO
2 electrodes under 1 sun illumi
nation. The hierarchical TiO
2 electrodes were compared with macroporous TiO
2 electrodes, revealing t
hat the higher photocurrent density could be attributed to a longer electron recombi
nation lifetime and a high specific area. The longer recombi
nation lifetime was supported by the presence of fewer defective TiO
2 surfaces, as confirmed by the XPS spectrum.
Keywords:
hierarchical structures; solution deposition; TiO2; macroporous; nation+lifetime&qsSearchArea=searchText">recombination lifetime; dye-sensitized solar cells