Water Splitting into H2 and O2 over ALa4Ti4O15 (A=Ca, Sr, and Ba) Photocatalysts with Layered Perovskite Structure
Development of active photocatalysts for water splitting into H2 and O2 is an important topic. In the present study, photophysical and photocatalytic properties of ALa4Ti4O15 (A=Ca, Sr, and Ba) with layered perovskite structure were investigated. ALa4Ti4O15 (A=Ca, Sr, and Ba) powder was prepared by a polymerizable complex method. Water splitting reactions were carried out in a gas-closed circulation system equipped. In an inner irradiation reaction cell made of quartz equipped with a 400-W high-pressure mercury lamp. The amounts of evolved H2 and O2 were determined using on-line gas chromatography. Diffuse reflection spectra indicated that the band gaps of ALa4Ti4O15 (A=Ca, Sr, and Ba) were 3.8~3.9eV. Native BaLa4Ti4O15 showed no activity for water splitting. In contrast, NiO/BaLa4Ti4O15 showed high activity for water splitting when the pretreatment of H2 reduction at subsequent O2 oxidation was carried out. The activity of NiO/BaLa4Ti4O15 was higher than that of NiO/CaLa4Ti4O15. This is due to difference in distribution alkaline earth cations and La between CaLa4Ti4O15 and BaLa4Ti4O15 at perovskite slab and interlayer space. The optimized NiO (0.5 wt %)/BaLa4Ti4O15 photocatalyst steadily produced H2 and O2 at the rates of 2.4 and 1.2 mmol/h, respectively. The apparent quantum yield was 15% at 270 nm. In conclusion, ALa4Ti4O15 (A=Ca, Sr, and Ba) with layered perovskite structure was found to be new photocatalyst materials for water splitting.