Yq. Wang et al., Mesoporous titanium dioxide: sonochemical synthesis and application in dye-sensitized solar cells, J MAT CHEM, 11(2), 2001, pp. 521-526
A novel method for shortening the synthesis time of mesoporous TiO2 to 6 h
is reported. Low-angle XRD and TEM showed that mesoporous TiO2 with short-r
ange ordered structures was synthesized when octadecylamine was used as a s
tructure-directing agent and when Ti(OPri)(4) was used as a precursor. The
highest surface area (853 m(2) g(-1)) was obtained after extraction with a
dilute solution of nitric acid. The material maintained a high surface area
(467 m(2) g(-1)) after calcination at 350 degreesC, but the short-range or
dered structures collapsed. XPS showed the interaction between TiO2 and oct
adecylamine, while DSC, TGA, and FT-IR spectra showed the removal of octade
cylamine by extraction and calcination. A mechanism for the fast formation
of mesoporous TiO2 is proposed. It is attributed to the formation of mesopo
rous material at high temperatures formed in the interface between the gas
and bulk solutions resulting from ultrasound irradiation. Electrodes made f
rom the mesoporous TiO2 were tested in a dye-sensitized solar cell. The sho
rt-circuit photocurrent, open-circuit photovoltage and fill factor increase
d with an increase in the sintering temperature, having a performance thres
hold at 450 degreesC, showing that the more ordered structures are required
for high solar cell conversion efficiencies.