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Abstract: Poly(furfuryl alcohol) (PFA) and block copolymer Pluronic F127 were used as pore templates to create mechanically robust silica monoliths with a hierarchical and interconnected macro–mesoporous network in an easy, reproducible bimodal scale templating process. Control over the morphology was obtained by varying the reactant ratios. Phase separation on the submicrometer scale occurred when furfuryl alcohol was cationically polymerized and therefore became immiscible with the solvent and the silica precursor. Upon a subsequent sol–gel reaction, a silica-F127 matrix formed around the PFA spheres, leading to macropore structures with mesoporous walls. Surface areas of the final structures ranged from 500 to 989m2 g−1 and a maximum pore volume of 4.5mLg−1 was achieved. Under mildly acidic conditions, micelle-templated mesopores resulted. Interconnected macropores could be obtained by increasing the pH or the block copolymer concentration. The formation mechanism and the relationship between PFA, Pluronic F127 and acidity are discussed in detail. [Copyright &y& Elsevier]

Abstract: The thermal stability of anatase TiO2 mesoporous thin films has been considerably increased up to 800°C by substituting a fraction of Ti cations by Nb. Mesoporous mixed oxide films Ti1−x Nb x O2, with x =Nb/(Nb+Ti) ranging from 0 to 1, and homogeneous crystalline walls have been successfully prepared from chloride precursors and non-ionic block copolymer templates. They all exhibit a uniaxially distorted Im3m bcc mesostructure with the a lattice parameter ranging from 14 to 19nm. Films have been characterised by simultaneous in situ SAXS and WAXS investigations during thermal treatment. Transmission electron microscopy and UV–visible ellipsometry were used to confirm the structure, the porosity and the good optical quality. A high porosity of 40% (pore size estimated at 7nm) was maintained for the 10% Nb-doped films above the temperature of crystallisation and a bandgap of 3.40eV has been measured after annealing at 500°C. [Copyright &y& Elsevier]