Layer-by-Layer Photocatalytic Assembly for Solar Light-Activated Self-Decontaminating Textiles

Novel photocatalytic nanomaterials that can be used to functionalize textiles, conferring to them efficient solar-light-activated properties for the decontamination of toxic and lethal agents, are described. Textiles functionalized with one-dimensional (1D) SnS₂-based nanomaterials were used for photocatalytic applications for the first time. We showed that 1D SnS₂/TiO₂ nanocomposites can be easily and strongly affixed onto textiles using the layer-by-layer deposition method. Ultrathin SnS₂ nanosheets were associated with anatase TiO₂ nanofibers to form nano-heterojunctions with a tight interface, considerably increasing the photo-oxidative activity of anatase TiO₂ due to the beneficial interfacial transfer of photogenerated charges and increased oxidizing power. Moreover, it is easy to process the material on a larger scale and to regenerate these functionalized textiles. Our findings may aid the development of functionalized clothing with solar light-activated photocatalytic properties that provide a high level of protection against chemical warfare agents

Titania-Decorated Silicon Carbide-Containing Cobalt Catalyst for Fischer–Tropsch Synthesis

The metal–support interactions of titanium dioxide decorated silicon carbide (β-SiC)-supported cobalt catalyst for Fischer–Tropsch synthesis (FTS) were explored by a combination of energy-filtered transmission electron microscopy (EFTEM), ⁵⁹Co zero-field nuclear magnetic resonance (⁵⁹Co NMR), and other conventional characterization techniques. From the 2D elemental maps deduced by 2D EFTEM and ⁵⁹Co NMR analyses, it can be concluded that the nanoscale introduction of the TiO₂ into the β-SiC matrix significantly enhances the formation of small and medium-sized cobalt particles. The results revealed that the proper metal–support interaction between cobalt nanoparticles and TiO₂ led to the formation of smaller cobalt particles (<15 nm), which possess a large fraction of surface atoms and, thus, significantly contribute to the great enhancement of conversion and the reaction rate. The cobalt time yield of the catalyst after modification increased to 7.5 × 10^–5 mol_CO g_Co^–1 s^–1 at 230 °C, whereas the C₅₊ selectivity maintained a high level (>90%). In addition, the adequate meso- and macro-pores of the SiC-based support facilitated intimate contact between the reactants and active sites and also accelerated the evacuation of the intermediate products. It was also worth noting that a superior and stable FTS specific rate of 0.56 g_C₅₊ g_catalyst^–1 h^–1 together with high C₅₊ selectivity of 91% were obtained at common industrial content of 30 wt % cobalt