Photocatalytic Activities of Layered Titanates and Niobates Ion-Exchanged with Sn2+ under Visible Light Irradiation

• Published in: Journal of physical chemistry. C Vol. 112; no. 45; pp. 17678 - 17682
• Main Authors: Hosogi, Yasuhiro, Kato, Hideki, Kudo, Akihiko
• Format: Journal Article
• Language: English
• Published: American Chemical Society 13.11.2008
• Subjects: C: Surfaces, Interfaces, Catalysis
• ISSN: 1932-7447; 1932-7455
• DOI: 10.1021/jp805693j

Energy gaps (EG) of Sn2+-exchanged layered metal oxides, Sn2+/KTiNbO5, Sn2+/K4Nb6O17, Sn2+/CsTi2NbO7, Sn2+/K2Ti4O9, Sn2+/K2Ti2O5, and Sn2+/Cs2Ti6O13, were 0.7−1.2 eV narrower than those of the original layered metal oxides. The Sn2+-exchanged layered metal oxides had visible-light absorption bands that were due to the electronic transition from an electron donor level (a valence band maximum) consisting of Sn5s orbitals to conduction bands consisting of Ti3d and Nb4d orbitals. The potential of the electron donor level negatively shifted as the amount of ion-exchanged Sn2+ increased. They showed photocatalytic activities for H2 evolution from an aqueous methanol solution under visible light irradiation. Sacrificial oxidation of Sn2+ also proceeded partly accompanied with the H2 evolution. Sn2+/K4Nb6O17 also showed an activity for O2 evolution from an aqueous silver nitrate solution under visible light irradiation. The stable Sn2+ in Sn2+/K4Nb6O17 to redox reactions contributed to the photocatalytic H2 and O2 evolution reactions in the presence of sacrificial reagents.