Inverse effects of lanthanide co-doping on the photocatalytic hydrogen production and dye degradation activities of Cu doped sol-gel TiO2

•Ti3+ sites formed by Cu doping increases the photocatalytic reduction activity of TiO2.•Lanthanide co-doping decreases the photocatalytic reduction activity of Cu doped TiO2.•Lanthanide co-doping increases the photocatalytic oxidation activity of Cu doped TiO2.•Lanthanide doping modifies pore struc...

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Veröffentlicht in:Materials science & engineering. B, Solid-state materials for advanced technology Solid-state materials for advanced technology, 2023-12, Vol.298, p.116882, Article 116882
Hauptverfasser: Yurtsever, Hüsnü Arda, Erzin, Kubilay, Çiftçioğlu, Muhsin
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Sprache:eng
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Zusammenfassung:•Ti3+ sites formed by Cu doping increases the photocatalytic reduction activity of TiO2.•Lanthanide co-doping decreases the photocatalytic reduction activity of Cu doped TiO2.•Lanthanide co-doping increases the photocatalytic oxidation activity of Cu doped TiO2.•Lanthanide doping modifies pore structure and improves dye adsorption on TiO2 surface. Copper doped and lanthanide-copper co-doped titania powders were prepared by sol–gel technique and the effects of co-doping on the photocatalytic reduction and oxidation activities of titania were investigated in this work. Characterization studies indicated that a reduced structure was formed due to the presence of Ti3+ species in copper doped titania powder and a more stable structure was formed when lanthanides were used as co-dopants. Copper doped powder had a significantly higher activity in photocatalytic hydrogen production (1037 μmol/g/h) than the co-doped powders (∼400 μmol/g/h). The oxidation activities of co-doped powders however were determined to be about 2 times higher than that of the copper doped powder. The decrease in the reduction activity was attributed to the decrease in the number of Ti3+ sites, whereas the increase in oxidation activity was probably a result of the increase in the surface area and dye adsorption due to lanthanide co-doping.
ISSN:0921-5107
1873-4944
DOI:10.1016/j.mseb.2023.116882