Effect of Thermal Treatment on the Textural Properties of CeO2 Powders Synthesized in Near- and Supercritical Alcohols.

CeO2 nanocrystals (NCs) have attracted increasing interest over the past few years, in particular for their use in catalytic reactions. Syntheses mediated by near- and supercritical alcohols have proven to be innovative ways to obtain CeO2 NCs with controlled crystallite sizes (from 3 to 8 nm depending on the alcohol) and surface functionalities, with alcohol moieties. When submitted to a thermal treatment at 500 °C, required to desorb/degrade surface organic species, these powders displayed different behaviors depending on the alcohol used during the synthesis. Cerium oxide powders synthesized in sc-MeOH, sc-EtOH and sc-iPrOH undergo sintering during treatment at 500 °C, with a decrease of their specific surface area. Conversely, those synthesized in sc-BuOH, nc-PentOH and nc-HexOH keep their initial crystallite sizes and morphology, but show a great enhancement of their specific surface area (up to 200 m(2) g(-1)), which is unprecedented after such a thermal treatment.

CeO2 nanocrystals from supercritical alcohols: new opportunities for versatile functionalizations?

The fast and controlled synthesis of surface-modified cerium oxide nanoparticles was carried out in supercritical {ethanol + alcohol derivative} mixtures. The newly found ability of supercritical alcohols to graft onto cerium oxide nanocrystals (CeO2 NCs) during their synthesis was exploited to control their surface chemistry via the addition of three aminoalcohols: ethanolamine, 3-amino-1-propanol and 6-amino-1-hexanol. Although the ethanol to aminoalcohol ratio was consistent (285:1), the successful grafting of these alcohol derivatives onto CeO2 NCs was identified based on Fourier transform infrared (FTIR) and thermogravimetric analysis-mass spectrometry (TGA-MS) measurements. Smaller crystallite size of CeO2 NCs synthesized in the presence of aminoalcohols, compared to those synthesized in supercritical ethanol alone, were also noticed and attributed to a possible intervention of amine groups helping the grafting of the alcohols, allowing one to stop the growth of the CeO2 NCs faster. The use of supercritical alcohol mixture-ethanol with hexanol, dodecanol, or octadecanol, with a 285:1 ratio-was also investigated. Such mixtures allow accessing a finer control in CeO2 NCs crystallite size compared to pure alcohols, according to calculation made from X-ray diffraction measurements. Finally, fluorescent molecules (fluorescein isothiocyanate) were grafted onto amine-modified CeO2 NCs. The powders displayed a fluorescent behavior under UV light, confirming the suitability and interest of CeO2 NCs surface modification by such technique.

Near- and supercritical alcohols as solvents and surface modifiers for the continuous synthesis of cerium oxide nanoparticles.

Supercritical fluids offer fast and facile routes toward well-crystallized tailor-made cerium oxide nanoparticles. However, the use of surfactants to control morphology and surface properties remains essential. Therefore, although water, near-critical (nc) or supercritical (sc), is a solvent of choice, the poor water solubility of some surfactants could require other solvent systems such as alcohols, which could themselves behave as surface modifiers. In here, the influence of seven different alcohols, MeOH, EtOH, PrOH, iPrOH, ButOH, PentOH, and HexOH, in alcothermal conditions (300 °C, 24.5 MPa) over CeO(2) nanocrystals (NCs) size, morphology, and surface properties was investigated. The crystallite size of the CeO(2) nanocrystals can be tuned in the range 3-7 nm depending on the considered alcohol, and their surface has been modified by these solvents without the use of surfactants. Mechanisms are proposed for the interaction of primary and secondary alcohols with CeO(2) surface and its functionalization during the synthesis based on FTIR and TGA-MS studies. This study allows apprehending the role of alcohols during the synthesis and may lead to an informed choice of solvent as a function of the required size and surface properties of CeO(2) NCs. It also opens new route to CeO(2) functionalization using supercritical alcohol derivatives.

Nanoscaled tin dioxide films processed from organotin-based hybrid materials: an organometallic route toward metal oxide gas sensors.

Nanocrystalline tin dioxide (SnO(2)) ultra-thin films were obtained employing a straightforward solution-based route that involves the calcination of bridged polystannoxane films processed by the sol-gel process from bis(triprop-1-ynylstannyl)alkylene and -arylene precursors. These films have been thoroughly characterized by FTIR, contact angle measurements, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), atomic force (AFM) and scanning electron (SEM) microscopies. Annealing at a high temperature gave 30-35 nm thick cassiterite SnO(2) films with a mean crystallite size ranging from 4 to 7 nm depending on the nature of the organic linker in the distannylated compound used as a precursor. In the presence of H(2) and CO gases, these layers led to highly sensitive, reversible and reproducible responses. The sensing properties were discussed in regard to the crystallinity and porosity of the sensing body that can be tuned by the nature of the precursor employed. Organometallic chemistry combined with the sol-gel process therefore offers new possibilities toward metal oxide nanostructures for the reproducible and sensitive detection of combustible and toxic gases.

A new route towards nanoporous TiO2 as powders or thin films from the thermal treatment of titanium-based hybrid materials.

Calcination of cyclopentadienyltitanium-based organic-inorganic hybrid materials at 450-500 °C led to the formation of anatase titanium dioxide as white powders consisting of a porous network of aggregated nanoparticles, the nanoporosity detected being related to the inter-particle space. Depending on the calcination temperatures, the surface area of the titanium dioxide particles varied from 65 to 158 m(2) g(-1).