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

Conducting polymer wires in mesopore hosts

Nanometer-size conducting structures are of great interest in view of fundamental issues and potential applications. We explore the inclusion chemistry of conjugated polymers and graphite-like materials as a means to create such structures. Novel mesoporous materials with pore diameters in the 3 nm range (MCM-41) are used as hosts. Monomer molecules are introduced via vapor or solution transfer and polymerized either by included or external reagents. The properties of the conjugated systems are studied while encapsulated or after dissolution of the host. In the case of polyaniline formed on oxidation of aniline with persulfate, microwave absorption shows the presence of conducting filaments in the host channels. The above systems are compared with graphite-type material encapsulated in MCM-41 by first forming a precursor polymer such as polyacrylonitrile that is pyrolyzed at 500-800°C. These polymer chains are the first nanometer-size conducting filaments stabilized in a well-defined channel host

Crack fronts and damage in glass at the nanometer scale

We have studied the low speed fracture regime for different glassy materials with variable but controlled length scales of heterogeneity in a carefully mastered surrounding atmosphere. By using optical and atomic force microscopy (AFM) techniques we tracked in real-time the crack tip propagation at the nanometer scale on a wide velocity range (mm/s - pm/s and below). The influence of the heterogeneities on this velocity is presented and discussed. Our experiments reveal also -for the first time- that the crack progresses through nucleation, growth and coalescence of nanometric damage cavities within the amorphous phase. This may explain the large fluctuations observed in the crack tip velocities for the smallest values. This behaviour is very similar to what is involved, at the micrometric scale, in ductile fracture. The only difference is very likely due to the related length scales (nanometric instead of micrometric). Consequences of such a nano-ductile fracture mode observed at a temperature far below the glass transition temperature in glass is finally discussed.Comment: 12 pages, 8 figures, submitted to Journal of Physics: Condensed Matter; Invited talk at Glass and Optical Materials Division Fall 2002 Meeting, Pittsburgh, Pa, US

Characterization methods dedicated to nanometer-thick hBN layers

Hexagonal boron nitride (hBN) regains interest as a strategic component in graphene engineering and in van der Waals heterostructures built with two dimensional materials. It is crucial then, to handle reliable characterization techniques capable to assess the quality of structural and electronic properties of the hBN material used. We present here characterization procedures based on optical spectroscopies, namely cathodoluminescence and Raman, with the additional support of structural analysis conducted by transmission electron microscopy. We show the capability of optical spectroscopies to investigate and benchmark the optical and structural properties of various hBN thin layers sources