Photocatalytic property of partially substituted Pt-intercalated layered perovskite, ASr2TaxNb3−xO10 (A=K, H; x=0, 1, 1.5, 2 and 3)

A series of layered perovskite photocatalysts, ASr2TaxNb3−xO10 (A=K, H; x=0, 1, 1.5, 2 and 3), were synthesized by conventional solid-state reaction followed by an ion-exchange reaction. Pt was incorporated in the interlayer of HSr2TaxNb3−xO10 by the stepwise intercalation reaction. The HSr2TaxNb3−xO10 showed hydrogen production activity and the activities were greatly enhanced by Pt co-incorporating. The x value in HSr2TaxNb3−xO10 had an important effect on the photocatalytic activity of the catalyst. When the x=1, the HSr2TaNb2O10/Pt photocatalyst showed a photocatalytic activity of 208 cm3 g−1 h−1 hydrogen evolution rate in 10 vol% methanol solution under irradiation with wavelength more than 290 nm from a 100-W mercury lamp at 333 K. The HSr2TaNb2O10/Pt photocatalyst exhibited much higher photocatalytic activity than the well-known TiO2/Pt photocatalyst under the same conditions.

Graphical AbstractWe have synthesized a series of layered perovskite photocatalysts, ASr2TaxNb3-xO10 (A = K, H; x = 0, 1, 1.5, 2 and 3) by conventional solid-state reaction followed by an ion-exchange reaction. Pt was incorporated in the interlayer of HSr2TaxNb3-xO10 by the stepwise intercalation reaction. The x value in HSr2TaxNb3-xO10 had an important effect on the photocatalytic activity of the catalyst. When the x = 1, the HSr2TaNb2O10/Pt photocatalyst showed a photocatalytic activity of 208 cm3·g−1·h−1 hydrogen evolution rate in 10 vol. % methanol solution under irradiation with wavelength more than 290 nm from a 100-W mercury lamp at 333 K.Figure optionsDownload full-size imageDownload as PowerPoint slide