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Two-dimensional Sn2Ta2O7 nanosheets with a thickness of ~ 10 nm were successfully prepared through a novel tantalic acid-based solid-state reaction method at reduced temperature. The as-obtained samples were characterized by powder X-ray diffraction (XRD), ultraviolet–visible (UV–Vis) diffuse reflectance spectra, scanning electron microscopy (SEM), transmission electron microscopy (TEM) and Brunauer–Emmett–Teller (BET) analysis. The photocatalytic performance of Sn2Ta2O7 nanosheets was evaluated by photocatalytic water splitting for hydrogen evolution under visible light irradiation (λ ≥ 400 nm). The Sn2Ta2O7 nanosheets with a large surface area of 25.9 m2·g−1 showed higher H2 production activity, which was about 4.4 times higher than that of bulk Sn2Ta2O7 in lactic acid aqueous solutions using Pt as a co-catalyst. The improved photocatalytic performance mainly benefited from the nanosheet structure, which provided abundant surface active sites and facilitated the photogenerated charge carrier separation efficiently. This work may open up new opportunity to develop novel nanostructured tantalum-based semiconductors with improved catalytic performance for solar energy conversion. [ABSTRACT FROM AUTHOR]

A new photochromic film was prepared based on the Keggin type H3PW12O40 (PW12) with polyacrylamide (PAM) matrix. The microstructure, photochromic behavior and mechanism were investigated with FT-Infrared spectroscopy (FT-IR), atomic force microscopy (AFM), transmission electron microscopy (TEM), ultraviolet–visible absorption spectroscopy (UV–VIS), and electron resonance spectroscopy (ESR). FT-IR results showed that the Keggin geometry of PW12 was still preserved inside the matrix, and a charge-transfer bridge was built between PW12 and PAM via hydrogen bond. AFM images indicated that the surface topography of the polymer matrix changed after adding PW12. In the hybrid films, the PW12 particles had regular microstucture in nanoscale shown in TEM image. Under UV irradiation, the film was reduced photochemically to yield a blue species. With the increase of irradiation time, the photoreduction proceeded from one-electron to two-electron blue stage. The characteristic signals of W (V) and radical in ESR spectra indicated that the photoreduced process was in accordance with the radical mechanism. [Copyright &y& Elsevier]

Semiconducting heterostructures with type-II band structure have attracted much attention due to their novel physical properties and wide applications in optoelectronics. Herein, we report, for the first time, a controlled synthesis of type-II ZnS/SnO2 heterostructured ribbon composed of SnO2 nanoparticles that uniformly cover the surface of ZnS ribbon via a simple and versatile thermal evaporation approach. Structural analysis indicated that the majority of SnO2 nanoparticles have an equivalent zone axis, i.e., <-313> of rutile SnO2, which is perpendicular to ±(2-1-10) facets (top/down surfaces) of ZnS ribbon. For those SnO2 nanoparticles decorated on ±(01-10) facets (side surfaces) of ZnS ribbon, an epitaxial relationship of (01-10)ZnO//(020)SnO2 and [2-1-10]ZnO//[001]SnO2 was identified. To explore their electronic and optoelectronic properties, we constructed field-effect transistors from as-prepared new heterostructures, which exhibited an n-type characteristic with an on/off ratio of ∼10(3) and a fast carrier mobility of ∼33.2 cm2 V(-1) s(-1). Owing to the spatial separation of photogenerated electron-hole pairs from type-II band alignment together with the good contacts between electrodes and ribbon, the resultant photodetector showed excellent photoresponse properties, including large photocurrent, high sensitivity (external quantum efficiency as high as ∼2.4×10(7)%), good stability and reproducibility, and relatively fast response speed. Our results suggest great potential of ZnS/SnO2 heterostructures for efficient UV light sensing, and, more importantly, signify the advantages of type-II semiconducting heterostructures for construction of high-performance nano-photodetectors.