This research demonstrates enhanced photocatalytic activity of orthorhombic Sn3O4 films compared to monoclinic variants, suggesting potential applications in hydrogen production.
Although visible-light-responsive Sn3O4 is known to be synthesized by a hydrothermal method, its reported crystal structure is limited to the monoclinic phase. Recently, orthorhombic Sn3O4 has been reported as a new polymorph of tin oxides; however, its photocatalytic properties have not been examined. This paper reports the thin film synthesis of orthorhombic Sn3O4 and its photocatalytic properties under visible-light irradiation. We synthesized films and powders of orthorhombic and conventional monoclinic Sn3O4 and evaluated their crystal structures, morphologies, and physical properties by using X-ray diffraction (XRD), scanning electron microscope (SEM), hard X-ray photoemission spectroscopy (HAXPES) for core levels and valence bands, and ultraviolet-visible light (UV-vis) spectroscopy. Further, we compared photoelectrochemical and photocatalytic properties of the monoclinic Sn3O4 and those of the orthorhombic Sn3O4. A comparison between the film and powder showed that the orthorhombic Sn3O4 film had higher crystallinity with a strong crystal orientation and exhibited higher photocatalytic activity than the orthorhombic powder form. By comparison between the orthorhombic film and the monoclinic film, the orthorhombic Sn3O4 film was responsive to longer wavelength photons and exhibited higher internal quantum efficiency for hydrogen production than the monoclinic Sn3O4 film. Orthorhombic Sn3O4 exhibited a rod-like structure with clear crystal facets, where rectangular (110) facets were exposed on the side faces, and the (001) facet was exposed at the edge of the rod. In the orthorhombic Sn3O4 rod, photoexcited electron-hole pairs are efficiently separated because of the high crystallinity and different surface energies of the crystal facets, yielding high photocatalytic activity toward hydrogen production. Orthorhombic Sn3O4 films are expected to be applied as visible-light-sensitive photocatalysts.
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Uchida et al. (2025) studied this question.
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