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Abstract: Nickel phosphide nanocrystals with various phases have been successfully synthesized via a simple solvothermal route at 180°C for 16h, employing nickel chloride and white phosphorus (WP) as starting reactants in the presence of sodium dodecylbenzene sulfonate (SDBS). X-ray powder diffraction (XRD) research showed that the pure Ni12P5 phase with a high yield could be obtained in an ethanol solution, and the pure Ni2P form was prepared in a mixed system with the volume ratio of water/ethanol of 10:10. Namely, the presence of water molecules induced the phase conversion of nickel phosphides. Furthermore, in order to investigate the correlation between properties and phases, as a case, the photocatalytic degradation abilities of two nickel phosphide phases for organic dyes were compared. [Copyright &y& Elsevier]

Abstract: In the present paper, novel t-Se microspheres with holes were successfully prepared via a facile solution-phase approach at 150°C for 20h, employing SeO2 and glucose as reagents, poly(vinylpyrrolidone) (PVP) as the surfactant. The phase and morphology of the product were characterized by means of powder X-ray diffraction (XRD), energy dispersive spectrometry (EDS), transmission electron microscopy (TEM), and scanning electron microscopy (SEM). The conversion from α-Se to t-Se was investigated by a series of experiments and a possible formation process was suggested based on the experimental results. [Copyright &y& Elsevier]

Abstract: In the present paper, we successfully prepared PbTe nanocrystals in a simple aqueous system via the hydrothermal route employing PbO, Te powders and N2H4·H2O as the starting reactants at 150°C for 14h. Some factors affecting the morphologies of the PbTe nanocrystals, such as the reaction temperature, time, the amount of NaOH, sorts of reductants and Pb2+ ion sources, were systematically investigated. Experimental results indicated that, under keeping the other experimental conditions constant: raising the reaction temperature, the shapes of the as-obtained PbTe hardly changed, while decreasing the temperature, some PbTe dendrites were obtained; the short reaction time availed to obtain cubes with a hole in the center of each face; more amounts of NaOH were favorable to the formation of regular PbTe nanocuboids. When NaBH4 was used as the reductant, a large amount of near spherical PbTe nanocrystals was produced; while NaH2PO2 was used, many PbTe crystals with hollow framework structures were obtained. When Pb(CH3COO)2 was used as the Pb2+ ion source, some dendrites made of many irregular particles were generated; while PbSO4 was employed, many PbTe nanocuboids were produced. A possible formation mechanism of PbTe nanocrystals was proposed based on the experimental results. [Copyright &y& Elsevier]

Abstract: In the current paper, we successfully prepared lead sulfide (PbS) microcrystals with various shapes in a simple aqueous system using the hydrothermal synthesis route. Experimental results indicated that the change of the molar ratio of Pb2+/S2O3 2− could significantly influence the morphology of the product while keeping the other experimental conditions constant: with the decrease of the molar ratio of Pb2+/S2O3 2− from 1:1 to 1:4, the shape of the products varied from tri-prism, cube to magic-square structure. Changing the reaction temperature had big effect on the shape of the product: flower-shaped product was obtained at 80°C and cube-shaped products were produced at 120°C. When the reaction time varied, the shapes of the as-obtained PbS crystals also changed. At the same time, SEM observations showed that the counter-anions for Pb2+ could influence the shape of the product: Pb(NO3)2 being used as lead ion sources, most flower-shaped and few cubic PbS crystals were produced; while PbSO4 as lead ion source, the PbS cubes were obtained. An evolution process was described based on experimental facts. [Copyright &y& Elsevier]

ZnS nanoparticles about 3 nm in size were prepared by a simple, rapid and reliable route under microwave irradiation in a heterogeneous system, using ZnAc2·2H2O (Ac&z.dbnd6;CH3COO) and Na2S·9H2O as the starting materials, ethylene glycol (EG) as the medium. The product was characterized with X-ray powder diffraction (XRD), transmission electron microscopy (TEM) and ED, respectively. The optical properties of ZnS nanoparticles were studied. [Copyright &y& Elsevier]

Highlights: [•] La-doped ZnO nanoparticles were successfully prepared via a simple solution-combustion route. [•] The integration of La3+ ions into ZnO decreased the band-gap of ZnO nanoparticles. [•] La-doped ZnO nanoparticles could remove more Pb and Cu ions from water resources than undoped ZnO. [ABSTRACT FROM AUTHOR]

Abstract: In this paper, we report the hydrothermal preparation of Cd(OH)2 nanowires and further conversion to CdO nanobelts, CdS nanowires and CdSe nanoparticles through thermal treatment, solvothermal and mixed-solvothermal routes, respectively. The as-obtained products were characterized by means of powder X-ray diffraction (XRD), transmission electron microscopy (TEM), and field emission scanning electron microscopy (FEMSEM). Research showed that four cadmium compounds were good photocatalysts for the degradation of organic dyes such as Safranine T and Pyronine B, under irradiation of 365nm UV light. The order of catalytic activity of different materials was found to be Cd(OH)2

Large-scale of long NbS2 nanowire strands were successfully synthesized by a catalyzed transport reaction involving C60. The strands have a diameter of 1–2 μm and length up to 0.5 mm, which are composed of single nanowire. The diameter of single nanowire is 1.6–20 nm. The products were characterized by powder X-ray diffraction, transmission electron microscopy, selected area electron diffraction, high-resolution transmission electron microscopy, scanning electron microscopy, and X-ray photoelectron spectroscopy. Probable mechanisms for catalytic growth were proposed. [Copyright &y& Elsevier]