A general route to the synthesis of surfactant-free, solvent-dispersible ternary and quaternary chalcogenide nanocrystals

A general route to the synthesis of surfactant-free CuInS2 (CIS), Cu2CoSnS4 (CCTS) and Cu2ZnSnS4 (CZTS) nanocrystals dispersible in low boiling point solvents is proposed. These nanocrystal inks should be of great interest to the fabrication of thin film absorbers of chalcogenide solar cells

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

Quaternary chalcopyrite (Cu2CoSnS4, Cu2ZnSnS4) 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

Synthesis and Optical Properties of Cu2CoSnS4 Colloidal Quantum Dots

Monodisperse quaternary chalcopyrite Cu2CoSnS4 colloidal quantum dots have been synthesized by acid peptization of a tailored Cu2CoSnS4 precursor displaying loosely packed, ultrafine primary crystallites. Well-defined peaks shifted to higher energy compared to the Cu2CoSnS4 bulk band gap value were observed on the UV-Vis absorption curve consistent with a quantum confinement behavior. First investigations by room temperature time resolved photoluminescence (TRPL) spectroscopy suggest that the photoluminescence emission does not arise from a donor–acceptor recombination.

Nanostructured materials with highly dispersed Au–Ce0.5Zr0.5O2 nanodomains: A route to temperature stable Au catalysts?

Our strategy to inhibit Au(0) growth with temperature involves the preparation of ultrafine Au clusters that are highly dispersed and strongly interacting with a thermally stable high-surface-area substrate. Temperature-stable Au-cluster-based catalysts were successfully prepared through the controlled synthesis of 3.5 nm Ce0.5Zr0.5O2 colloidal building blocks containing tailored strongly bound Au-cluster precursors. With the objective of stabilizing these Au clusters with temperature, grain growth of Ce0.5Zr0.5O2 nanodomains was inhibited by their dispersion through Al2O3 nanodomains. High surface area Au–Ce0.5Zr0.5O2–Al2O3 nanostructured composites were thus designed highlighting the drastic effect of Au cluster dispersion on Au(0) cluster growth. High thermal stability of our Au(0)-cluster-based catalysts was shown with the surprising catalytic activity for CO conversion observed on our nanostructured materials heated to temperatures as high as 800 C for 6 h

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

Ultrafine individualised mono crystalline Ca102x(PO4)62x-(HPO4)x(OH)22x deficient calcium hydroxyapatite nanocrystals displaying fluorescence under visible excitation are proposed for utilisation as biocompatible biological probes

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 SiO2-CeO2 composite high surface area materials, prepared using 5 nm colloidal CeO2 nanoparticle building blocks. These materials are made of a homogeneous distribution of CeO2 nanoparticles in thin layers of SiO2, 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 SiO2 wall thickness in the range of the CeO2 nanoparticle diameter, these materials display surface nanorugosity as shown by inverse chromatography. Accessibility through the porous volume to the functional CeO2 nanoparticle surfaceswasevidenced throughanorganic acid chemisorption technique allowing quantitative determination of CeO2 surface ratio. This surface composite nanostructure down to the nanometer scale does not affect the fundamental properties of the functional CeO2 nanodomains, such as their oxygen storage capacity, but modifies the acid-base properties of the CeO2 surface nanodomains as evidenced by Fourier transform IR technique. These arrays of accessible CeO2 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

3D rGO aerogel with superior electrochemical performance for K – Ion battery

As one possible alternative metal to lithium in ion batteries, potassium has recently attracted considerable attention as a result of its geochemical abundance and low cost. In this work, a detailed study of the electrochemical properties of potassium ion storage was performed using reduced graphene oxide (rGO) aerogel as a negative electrode material. The influence of the nature of the electrolyte and the drying methods used were investigated in order to optimize the electrochemical performance of freeze-dried rGO in potassium-ion batteries (PIBs). Electrochemical impedance spectroscopy (EIS) were used to assess the performance of our rGO material in PIBs. Used as the negative electrode, freeze-dried rGO can deliver a high capacity of 267 mA h/g at C/3 rate together with 78% capacity retention during 100 cycles, combined with high rate capability (92 mA h/g at 6.7C). This set of results makes rGO aerogel a promising electrode material for PIBs

Structural characterization of dense reduced BaTiO3 and Ba0.95La0.05TiO3 nanoceramics showing colossal dielectric values

BaTiO3−x and Ba0.95La0.05TiO3−x nanoceramics showing colossal permittivity values have been characterized. While starting powders are of cubic symmetry, X-ray and Neutron Diffraction techniques and Raman Spectroscopy measurements show that the one-step processed ceramics obtained by Spark Plasma Sintering (SPS) contain cubic and tetragonal phases. Rather large oxygen deficiency determined in such ceramics by Electron Micro Probe analysis and Electron Energy Loss Spectroscopy analyzes is explained by the presence of Ti3+, as evidenced by X-ray Photoelectron Spectroscopy measurements. Transmission Electron Microscopy and High Resolution Transmission Electron Microscopy show that these ceramics contain 50–300 nm grains, which have single-domains, while grain boundaries are of nanometer scale. Colossal permittivity values measured in our dense nanoceramics are explained by a charge hopping mechanism and an interfacial polarization of a large number of polarons generated after sample reduction in SPS apparatus

Sol–gel synthesis and sintering of submicronic copper molybdate (α-CuMoO4) powders

A sol–gel method was proposed to prepare copper II molybdate α-CuMoO4 powders. A gel was first obtained via the polymerizable complex method, using citric acid as complexing and polymerizing agent, dried at 120 °C and decomposed at 300 °C. A calcination in the temperature range 400–500 °C for 2 h led to the pure phase α-CuMoO4. The different powders obtained were characterized by X ray diffraction analysis and by transmission (TEM) and scanning (SEM) electron microscopies. Ceramics were prepared using conventional sintering and spark plasma sintering (SPS) techniques. A maximal relative density of 94.8% was reached after conventional sintering at 520 °C for 2 h. In the case of SPS, the densification was optimized by varying the temperature, the time and the applied pressure. Higher densities, up to 98.7%, were obtained at very low temperature, i.e., 300 °C, for 5 min only under a pressure of 225 MPa

A high temperature route to the formation of highly pure quaternary chalcogenide particles

A process route to the fabrication of quaternary chalcogenides (Cu2CoSnS4, Cu2ZnSnS4) particles is proposed in molten KSCN at 400 °C. This high temperature route allows the formation of highly pure and highly crystallized quaternary chalcogenides particles. Control of primary crystallites size is demonstrated by altering the chemical homogeneity of the precursors. This method could be exploited to prepare building blocks for the fabrication of low-cost solar cell absorbers