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Solvent-free hydrothermal synthesis of anatase TiO2 nanoparticles with enhanced photocatalytic hydrogen production activity
•TiO2 anatase nanoparticles exhibiting large surface area were readily synthesized.•A water soluble titanium precursor was employed.•The photocatalytic hydrogen production from aqueous EDTA solutions was measured.•The effect of different parameters on the hydrogen production rate was investigated.•T...
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Published in: | Applied catalysis. A, General General, 2013-09, Vol.466, p.32-37 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | •TiO2 anatase nanoparticles exhibiting large surface area were readily synthesized.•A water soluble titanium precursor was employed.•The photocatalytic hydrogen production from aqueous EDTA solutions was measured.•The effect of different parameters on the hydrogen production rate was investigated.•The prepared TiO2 nanoparticles showed higher activity than TiO2 P25 and TiO2 UV100.
TiO2 nanoparticles exhibiting large surface area were synthesized by the hydrothermal treatment of the water soluble titanium(IV) bis(ammoniumlactato) dihydroxide (TALH) complex in the presence of aqueous ammonia. The obtained powders were characterized by X-ray diffraction, scanning electron microscopy, diffuse reflectance spectroscopy, and nitrogen adsorption. Their photocatalytic activities were assessed by the photocatalytic hydrogen evolution from aqueous EDTA solutions. The effects of Pt- and photocatalyst loading, EDTA concentration, light intensity, pH, and temperature on the H2 evolution rate were studied in detail. The highest reaction rate was obtained for the TiO2 photocatalyst loaded with 0.4–0.5wt.% Pt at pH 5 and this was found to be 18 and 34% higher than that of TiO2 P25 and TiO2 UV100, respectively. The reaction rate increased substantially with increasing the temperature from 5°C to 45°C. |
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ISSN: | 0926-860X 1873-3875 |
DOI: | 10.1016/j.apcata.2013.06.033 |