Surfactant-free CZTS nanoparticles as building blocks for low-cost solar cell absorbers.

A process route for the fabrication of solvent-redispersible, surfactant-free Cu2ZnSnS4 (CZTS) nanoparticles has been designed with the objective to have the benefit of a simple sulfide source which advantageously acts as (i) a complexing agent inhibiting crystallite growth, (ii) a surface additive providing redispersion in low ionic strength polar solvents and (iii) a transient ligand easily replaced by an carbon-free surface additive. This multifunctional use of the sulfide source has been achieved through a fine tuning of ((Cu²âº)(a)(Zn²âº)(b)(Sn4⁺)(c)(Tu)(d)(OH⁻)(e))(t⁺), Tu = thiourea) oligomers, leading after temperature polycondensation and S²â» exchange to highly concentrated (c > 100 g l⁻¹), stable, ethanolic CZTS dispersions. The good electronic properties and low-defect concentration of the sintered, crack-free CZTSe films resulting from these building blocks was shown by photoluminescence investigation, making these building blocks interesting for low-cost, high-performance CZTSe solar cells.

Highly-crystallized quaternary chalcopyrite nanocrystals via a high-temperature dissolution-reprecipitation route.

Quaternary chalcopyrite (Cu(2)CoSnS(4), Cu(2)ZnSnS(4)) nanocrystals displaying high crystallization and controlled morphology were synthesized via a high-temperature growth regime achieved by dissolution-reprecipitation of tailored ultrafine precursors in the temperature range 400-500 °C.

A quantitative morphological analysis of nanostructured ceria-silica composite catalysts.

This study aims at examining the morphology of different catalysts, which are based on a dispersion of ceria nanoparticles embedded in a high surface area mesoporous silica framework. In order to fully describe the mesostructured composite material, we propose here a quantitative description of the microstructure based on a quantitative analysis of micrographs that were obtained via high-resolution transmission electron microscopy. We have therefore developed an automatic image analysis process in order to automatically and efficiently extract all the components of the catalyst images. A statistical and a morphological analysis of the spatial arrangement of the components of the catalyst are also presented. The study shows clear differences between the materials analysed in terms of the spatial arrangement and the total surface area of the ceria phase emerging into the pores, parameters of prime importance for the catalytic properties. Thus, the silica-ceria nanostructured composite materials, displaying large surface area up to 300 m(2) g(-1) are shown to exhibit highly rugged surfaces resulting from ceria nanoparticles emerging in the pores.

Colloidal and monocrystalline Ln3+ doped apatite calcium phosphate as biocompatible fluorescent probes.

Ultrafine individualised mono crystalline Ca(10-x)(PO4)(6-x)(HPO4)x(OH)(2-x) deficient calcium hydroxyapatite nanocrystals displaying fluorescence under visible excitation are proposed for utilisation as biocompatible biological probes.

Polynuclear lanthanide hydroxo complexes: new chemical precursors for coordination polymers.

The synthesis of hexanuclear lanthanide hydroxo complexes by controlled hydrolysis led to polymorphic compounds. The hexanuclear entities crystallize in four different ways that depend on the extent of their hydration. The four structures can be described as hexanuclear lanthanide entities with formula [Ln(6)(mu(6)-O)(mu(3)-OH)(8)(NO(3))(6)(H(2)O)(12)](2+). Two additional NO(3)(-) ions intercalate between the hexanuclear entities in order to ensure the electroneutrality of the crystal structure. Some crystallization water molecules fill the intermolecular space. The three first families of compounds (1-3) exhibit crystal structures that have previously been reported. The fourth family of compounds (4) is described here for the first time. Its chemical formula is [Ln(6)(mu(6)-O)(mu(3)-OH)(8)(NO(3))(6)(H(2)O)(12)](NO(3))(2).2H(2)O (Ln = Gd, Er, and Y). In this paper, the chemical and thermal stabilities of the hexanuclear lanthanide compounds are reported together with the magnetic properties of the Gd(III)-containing species. To use these entities as precursors for new materials, the substitution of the nitrato groups by chloride ions has been studied. Two byproduct compounds have so been obtained: The first (compound 5) is a nitrato/chloride hexanuclear compound of chemical formula [Er(6)(mu(6)-O)(mu(3)-OH)(8)(NO(3))(6)(H(2)O)(12)](NO(3))Cl.2H(2)O. The second one (compound 6) is a polymeric compound in which the hexanuclear entities are linked by an unexpected and original N(2)O(4) bridge. Its chemical formula is [Er(6)(mu(6)-O)(mu(3)-OH)(8)(NO(3))(4)(H(2)O)(11)(OH)(ONONO(2))]Cl(3).2H(2)O. Its crystal structure can be described as the juxtaposition of chainlike molecular motifs. To the best of our knowledge, this is the first example of a coordination polymer synthesized from an isolated polylanthanide hydroxo complex.

Surface characterization and properties of ordered arrays of CeO2 nanoparticles embedded in thin layers of SiO2.

We demonstrated the surface composite character down to the nanometer scale of SiO(2)-CeO(2) composite high surface area materials, prepared using 5 nm colloidal CeO(2) nanoparticle building blocks. These materials are made of a homogeneous distribution of CeO(2) nanoparticles in thin layers of SiO(2), arranged in a hexagonal symmetry as shown by small-angle X-ray scattering and transmission electron microscopy. Since the preparation route of these composite materials was selected in order to produce SiO(2) wall thickness in the range of the CeO(2) nanoparticle diameter, these materials display surface nanorugosity as shown by inverse chromatography. Accessibility through the porous volume to the functional CeO(2) nanoparticle surfaces was evidenced through an organic acid chemisorption technique allowing quantitative determination of CeO(2) surface ratio. This surface composite nanostructure down to the nanometer scale does not affect the fundamental properties of the functional CeO(2) nanodomains, such as their oxygen storage capacity, but modifies the acid-base properties of the CeO(2) surface nanodomains as evidenced by Fourier transform IR technique. These arrays of accessible CeO(2) nanoparticles displaying high surface area and high thermal stability, along with the possibility of tuning their acid base properties, will exhibit potentialities for catalysis, sensors, etc.