A novel photocatalyst, PbBi2Nb2O9 has been discovered that shows high activities for degradation of organic pollutants, generation of photocurrent, and water decomposition into O2 or H2, all under visible right irradiation (λ ≥ 420 nm). This is the first example of an undoped, single-phase oxide photocatalyst that shows such reactivity. Its quantum yields are much higher than those for most of the previously reported materials, especially in water decomposition to generate oxygen (29%). Since it is an oxide, there is much less concern for stability under light irradiation.

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CdS/TiO 2 composite photocatalysts were platinized by different methods such as photodeposition (PD), wet impregnation (WI), and chemical reduction (CR), and studied for hydrogen production from water under visible light. All Pt species were in the metallic state, yet PD and WI photocatalysts contained electrondeficient Pt. In particular, Pt-Ti formation was identified in the WI catalyst, which contributed to electron deficiency of Pt. These two photocatalysts of electron-deficient Pt exhibited higher rates of hydrogen evolution due to favorable diffusion of photoelectrons from excited CdS toward the Pt. Between PD and WI photocatalysts, the PD catalyst showed a lower rate because part of the Pt in the catalyst resided on CdS, whereas all Pt species were located on TiO 2 nanoparticles for WI and CR catalysts. The results indicate that the location as well as the electronic state of Pt is important for the high performance of platinized CdS/TiO 2 photocatalysts in hydrogen production from water.

In the search for efficient photocatalysts working under visible light, we have investigated the effect of cation substitution on a layered perovskite, La2Ti2O7. Among various metal dopants, only Cr and Fe induced intense absorption of visible light (lambda > 400 nm), and only these catalysts produced H2 photocatalytically from water in the presence of methanol under visible light irradiation (lambda > 420 nm). The polymerized complex method was found to be more efficient for fabrication of the present catalysts producing a more homogeneous structure than the solid-state reaction. The characterization by XRD, UV-vis DRS, XPS, and XANES revealed that doped Cr and Fe were present in the Cr3+ and Fe3+ states substituting for Ti sites in the La2Ti2O7 lattice. The theoretical calculation indicated that the most significant feature in the electronic band structure of the metal-doped La2Ti2O7 was the formation of a partially filled 3d band in the band gap of La2Ti2O7, while the contribution of these dopants on the valence band was negligible. Excitation of electrons from this localized interband to the conduction band of La2Ti2O7 was responsible for visible light absorption and the H2 evolution from water under visible light.