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Molybdate-based inorganic-organic hybrid disks with a highly ordered layered structure were synthesized via an acid-base reaction of white molybdic acid (MoO 3 $H 2 O) with n-octylamine (C 8 H 17 NH 2 ) in ethanol at room temperature. The thermal treatment of the as-obtained molybdatebased inorganic-organic hybrid disks at 550 C in air led to formation of orthorhombic a-MoO 3 nanoplates. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), thermal analysis (TG-DTA), Fourier-transform infrared (FT-IR) spectra, Raman spectra, and a laser-diffraction grain-size analyzer were used to characterize the starting materials, the intermediate hybrid precursors and the final a-MoO 3 nanoplates. The XRD, FT-IR and TG-DTA results suggested that the molybdate-based inorganic-organic hybrid compound, with a possible composition of (C 8 H 17 NH 3 ) 2 MoO 4 , was of a highly ordered lamellar structure with an interlayer distance of 2.306(1) nm, and the n-alkyl chains in the interlayer places took a double-layer arrangement with a tilt angle of 51 against the inorganic MoO 6 octahedra layers. The SEM images indicated that the molybdate-based inorganic-organic hybrids took on a well-dispersed disk-like morphology, which differed distinctly from the severely aggregated morphology of their starting MoO 3 $H 2 O powders. During the calcining process, the disk-like morphology of the hybrid compounds was well inherited into the orthorhombic a-MoO 3 nanocrystals, showing a definite plate-like shape. The a-MoO 3 nanoplates obtained were of a single-crystalline structure, with a side-length of 1-2 mm and a thickness of several nanometres, along a thickness direction of [010]. The above a-MoO 3 nanoplates were of a loose aggregating texture and high dispersibility. The chemical sensors derived from the as-obtained a-MoO 3 nanoplates showed an enhanced and selective gas-sensing performance towards ethanol vapors. The a-MoO 3 nanoplate sensors reached a high sensitivity of 44-58 for an 800 ppm ethanol vapor operating at 260-400 C, and their response times were less than 15 s.

The hierarchical photocatalysts of Ag/AgCl@plate-WO₃ have been synthesized by anchoring Ag/AgCl nanocrystals on the surfaces of single-crystalline WO₃ nanoplates that were obtained via an intercalation and topochemical approach. The heterogeneous precipitation process of the PVP-Ag⁺-WO₃ suspensions with a Cl⁻ solution added drop-wise was developed to synthesize AgCl@WO₃ composites, which were then photoreduced to form Ag/AgCl@WO₃ nanostructures in situ. WO₃ nanocrystals with various shapes (i.e., nanoplates, nanorods, and nanoparticles) were used as the substrates to synthesize Ag/AgCl@WO₃ photocatalysts, and the effects of the WO₃ contents and photoreduction times on their visible-light-driven photocatalytic performance were investigated. The techniques of TEM, SEM, XPS, EDS, XRD, N₂ adsorption-desorption and UV-vis DR spectra were used to characterize the compositions, phases and microstructures of the samples. The RhB aqueous solutions were used as the model system to estimate the photocatalytic performance of the as-obtained Ag/AgCl@WO₃ nanostructures under visible light (λ ≥ 420 nm) and sunlight. The results indicated that the hierarchical Ag/AgCl@plate-WO₃ photocatalyst has a higher photodegradation rate than Ag/AgCl, AgCl, AgCl@WO₃ and TiO₂ (P25). The contents and morphologies of the WO₃ substrates in the Ag/AgCl@plate-WO₃ photocatalysts have important effects on their photocatalytic performance. The related mechanisms for the enhancement in visible-light-driven photodegradation of RhB molecules were analyzed.

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