Research on PbS Nanoparticles Coated with 2,6-O-Diallyl-β-CD

PbS nanoparticles coated with 2.6-O-dial1yl-β-CD were prepared successfully and characterized by transmission electron microscope (TEM), X-ray photoelectron spectrometer (XPS). The sample shows a very rapid induced

Enhancement of photocatalytic and photoelectrochemical properties of TiO_(2) nanotubes sensitized by SILAR-Deposited PbS nanoparticles

The aim of this work is to improve the photocatalytic and photoelectrochemical properties of TiO_(2) nanotubes(TiO_(2)-NTAs)by sensitizing them with PbS nanoparticles(NPs)prepared by the Successive Ionic Layer Adsorption and Reaction method(SILAR).The Microstructure,surface morphology,phase composition and optical properties of the prepared structure were characterized using X-ray diffraction(XRD),scanning electron microscopy(SEM),transmission electron microscopy(TEM and High-resolution mode HRTEM)and X-ray photoelectron spectroscopy(XPS).The TiO_(2) NTAs were loaded by PbS NPs,which contents increase by increasing the number of SILAR cycles.The PbS NPs,which have a size in the order of ~20 nm,were found to be uniformly distributed in the TiO_(2) NTAs without damaging the tubular ordered structure.The photocatalytic activity of the PbS/TiO_(2) NTAs system,toward Amido Black(AB),showed significant enhancement compared to the bare untreated TiO_(2) NTs.At 30 SILAR deposition cycles the PbS-NPs/TiO_(2) NTAs structure is able to remove 75% of BA under simulated solar light,considerably higher than the 40% removal obtained with unloaded TiO_(2) NTAs.A significant improvement of the Photoelectrochemical(PEC)efficiency has been also demonstrated for the PbS-NPs/TiO_(2) NTAs hybrid system.This improvement is mainly related to visible-light harvesting and reduced recombination of photo-generated electron-hole pairs due to the synergistic effect of the heterojunction and to the wellorganized morphology of the TiO_(2) NTAs.

From Two-Dimensional Metal Organic Coordination Networks to Near-Infrared Luminescent PbS Nanoparticle/Layered Polymer Composite Materials

Two-dimensional(2-D)layered metal-organic coordination(lead methacrylate(LDMA))networks have been prepared in aqueous solution under mild conditions and their structure determined by single crystal diffraction.As the ligand used in our experiments is easily polymerized,these metal-organic coordination layers are therefore employed as precursors to fabricate cross-linked polymer layered materials throughγ-irradiated polymerization.The stabilities of the samples are signifi cantly improved afterγ-irradiation.To our knowledge,this is the fi rst time that covalent bonded polymer layered structures have been fabricated without the assistance of added surfactant or template.Such layered polymer materials cannot only act as alternatives to layered inorganic materials in some caustic environments,but also allow the generation of PbS nanoparticles(NPs)without aggregation in the polymer matrix.By exposing the polymer layer to H2S gas at room temperature,uniform PbS nanoparticles with an average size of about 6 nm are generated in situ.In addition,the resulting PbS NPs exhibit near-infrared(NIR)luminescent properties,which suggests the composite materials may be useful as active optical elements at communication wavelengths from 1300 to 1550 nm.