RESUMEN
Non-noble metal nanoclusters synthesis is receiving increased attention due to their unique catalytic properties and lower cost. Herein, the synthesis of ligand-free Ni nanoclusters with an average diameter of 0.7â¯nm corresponding to a structure of 13 atoms is presented; they exhibit a zero-valence state and a high stability toward oxidation and thermal treatment. The nanoclusters formation method consists in the electroreduction of nickel ions inside an ordered mesoporous alumina; also, by increasing the current density, other structures can be obtained reaching to nanowires of 10â¯nm diameter. A seed-mediated mechanism is proposed to explain the growth to nanowires inside these mesoporous cavities. The size dependence on the catalytic behavior of these entities is illustrated by studying the reduction of methylene blue where the nanoclusters show an outstanding performance.
RESUMEN
Hierarchical aggregates of gold nanoparticles (NPs) on different length scales were in situ generated at the surface of a bridged silsesquioxane during the process of film formation by polycondensation and solvent evaporation. A precursor of a bridged silsesquioxane based on the reaction product of (glycidoxypropyl)trimethoxysilane (2 mol) with dodecylamine (1 mol) was hydrolytically condensed in a THF solution at room temperature in the presence of formic acid, water, and variable amounts of dodecanethiol-stabilized gold NPs (average diameter of 2 nm). The initial compatibility of the precursor with gold NPs was achieved by the presence of dodecyl chains in both components. Phase separation of gold NPs accompanied by partitioning to the air-polymer interface took place driven by the polycondensation reaction and solvent evaporation. A hierarchical organization of gold NPs in the structures generated at the air-polymer interface was observed. Small body-centered cubic (bcc) crystals of about 20 nm diameter were formed in the first step, in which the 2 nm gold NPs kept their individuality (high-resolution transmission electron microscopy, field emission scanning electron microscopy, and small-angle X-ray diffraction). In the second step, bcc crystals aggregated, forming compact micrometer-sized spherical particles. Under particular evaporation rates a third step of the self-assembly process was observed where micrometer-sized particles formed fractal structures. Increasing the initial concentration of gold NPs in the formulation led to more compact fractal structures in agreement with theoretical simulations. The surface percolation of NPs in fractal structures can be the basis of useful applications.