An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
In this article, a ternary WO3/g-C3N4@ BiVO4 composites were prepared using eco-friendly hydrothermal method to produce efficient hydrogen energy through water in the presence of sacrificial agents. The prepared samples were characterized by scanning electron microscopy (SEM), scanning transmission electron microscopy (STEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), ultraviolet-visible (UV-vis), Brunauer-Emmett-Teller (BET) surface area, and photoluminescence spectroscopy (PL) emission spectroscopy. The experimental study envisages the formation of 2-D nanostructures and observed that such kinds of nanostructures could provide more active sites for photocatalytic reduction of water and their inherent reactive-species mechanism. The results showed the excellent photocatalytic performance (432 μmol h−1 g−1) for 1.5% BiVO4 nanoparticles in WO3/g-C3N4 composite when compared with pure WO3 and BiVO4. The optical properties and photocatalytic activity measurement confirmed that BiVO4 nanoparticles in WO3/g-C3N4 photocatalyst inhibited the recombination of photogenerated electron and holes and enhanced the reduction reactions for H2 production. The enhanced photocatalytic efficiency of the composite nanostructures may be attributed to wide absorption region of visible light, large surface area, and efficient separation of electrons/holes pairs owing to synergistic effects between BiVO4 and WO3/g-C3N4. The prepared samples would be a precise optimal photocatalyst to increase their suppliers for worldwide applications especially in energy harvesting.
In the title mol-ecule, C(18)H(12)N(2)OS, the dihedral angle between the two fused-ring systems is 7.2 (1)°. The hydr-oxy group forms an intra-molecular hydrogen bond with the imino group.
In this paper, polypyrrole was prepared using the vapor phase polymerization process on membrane filter. The resulting membrane filter is flexible with electrical conductivity of 6.7 S/cm. When used as a binder-free threedimensional porous electrode for supercapacitor, such membrane filter delivers high specific capacitances of 310 and 130 F/g at current densities of 1 and 5 A/g, respectively, with excellent cycling stability.
Electroreduction of carbon dioxide (CO<sub>2</sub>) in a flow electrolyzer represents a promising carbon-neutral technology with efficient production of valuable chemicals. In this work, the catalytic performance of polycrystalline copper (Cu), Cu<sub>2</sub>O-derived copper (O(I)D-Cu), and CuO-derived copper (O(II)D-Cu) toward CO<sub>2</sub> reduction is unraveled in a custom-designed flow cell. A peak Faradaic efficiency of >70% and a production rate of ca. -250 mA cm<sup>-2</sup> toward C<sub>2+</sub> products have been achieved on all the catalysts. In contrast to previous studies that reported a propensity for C<sub>2+</sub> products on OD-Cu in conventional H-cells, the selectivity and activity of ethylene-dominated C<sub>2+</sub> products are quite similar on the three types of catalysts at the same current density in our flow reactor. Our analysis also reveals current density to be a critical factor determining the C-C coupling in a flow cell, regardless of Cu catalyst's initial oxidation state and morphology.