Photocatalytic splitting of water under visible-light irradiation over the NiOx-loaded Sm2InTaO7 with 4f-d10-d0 configuration

A new visible-light-response photocatalyst Sm2InTaO7 with 4f-d10-d0 configuration crystallized in a cubic system with the space group Fd3m was synthesized by a solid-state reaction method. NiOx-loaded Sm2InTaO7 showed high photocatalytic activities for H2 evolution from pure water under visible light irradiation (λ>400 nm). Changes in the photocatalytic activity with the calcination temperature of Sm2InTaO7 and the amount of NiOx loaded indicated that the combination of highly crystallized Sm2InTaO7 and a high dispersion of NiOx particles led to high photocatalytic activity. The high photocatalytic performance of NiOx-loaded Sm2InTaO7 supported the existing view that the photocatalytic activity correlated with the lattice distortion. Density functional theory calculation indicated that strong dispersion from the hybridized In 5s 5p orbitals at the bottom of the conduction band was responsible for the high activity of photocatalyst Sm2InTaO7.

A new visible-light-response photocatalyst Sm2InTaO7 with 4f-d10-d0 configuration was developed. DFT calculation indicated that strong dispersion from the hybridized In 5s 5p orbitals was responsible for the high photocatalytic activity.Figure optionsDownload as PowerPoint slide