Surface States in Template Synthesized Tin Oxide Nanoparticles

Tin–oxide nanoparticles with controlled narrow size distributions are synthesized while physically encapsulated inside silica mesoporous templates. By means of ultraviolet-visible spectroscopy, a redshift of the optical absorbance edge is observed. Photoluminescence measurements corroborate the existence of an optical transition at 3.2 eV. The associated band of states in the semiconductor gap is present even on template-synthesized nanopowders calcined at 800 °C, which contrasts with the evolution of the gap states measured on materials obtained by other methods. The gap states are thus considered to be surface localized, disappearing with surface faceting or being hidden by the surface-to-bulk ratio decrease

Distributions of Noble Metal Pd and Pt in Mesoporous Silica

Mesoporous silica nanostructures have been synthesized and loaded with Pd and Pt catalytic noble metals. It is found that Pd forms small nanoclusters (3–5 nm) on the surface of the mesoporous structure whereas Pt impregnation results in the inclusion of Pt nanostructures within the silica hexagonal pores (from nanoclusters to nanowires). It is observed that these materials have high catalytic properties for CO–CH4 combustion, even in a thick film form. In particular, results indicate that the Pt and Pd dispersed in mesoporous silica are catalytically active as a selective filter for gas sensors

Distributions of Nobel Metal Pd and Pt in Mesoporous Silica

Mesoporous silicananostructures have been synthesized and loaded with Pd and Pt catalytic noble metals. It is found that Pd forms small nanoclusters (3–5 nm) on the surface of the mesoporous structure whereas Pt impregnation results in the inclusion of Pt nanostructures within the silica hexagonal pores (from nanoclusters to nanowires). It is observed that these materials have high catalyticproperties for CO–CH4CO–CH4CO–CH4 combustion, even in a thick film form. In particular, results indicate that the Pt and Pd dispersed in mesoporous silica are catalytically active as a selective filter for gas sensors

Copper oxide nanowires prepared by thermal oxidation for chemical sensing

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Synthesis of Tin Oxide Nanostructures with Controlled Particle Size Using Mesoporous Frameworks

Tin oxide nanostructures with controlled narrow particle size distribution were synthesized inside silica mesoporous templates. In this way, particle growth was blocked by physically corseting the tin compound inside the silica frameworks, the pore diameter of which determines the final tin oxide crystallite size distribution. Template structures were subsequently eliminated by chemical methods to collect the unsupported semiconductor nanoparticles. Thus obtained tin oxed nanopowders, with particle sizes in the range between 6 and 10 nm, were structurally, chemically, and electically characterized. The results are compared with those obtained from the characterization of larger crystallite materials

Synthesis and gas-sensing properties of pd-doped SnO2 nanocrystals. A case study of a general methodology for doping metal oxide nanocrystals

Pd-modified SnO2 nanocrystals, with a Pd/Sn nominal atomic ratio of 0.025, were prepared by injecting SnO2 sols and a Pd precursor solution into tetradecene and dodecylamine at 160 degrees C. Two different doping procedures were investigated: in co-injection, a Pd acetylacetonate solution in chloroform was mixed with the SnO2 sol before the injection; in sequential injection, the Pd solution was injected separately after the SnO2 sol. The obtained suspensions were heated at the resulting 80 degrees C temperature, then the product was collected by centrifugation and dried at 80 degrees C. When using co-injection, in the dried products PdO and Pd nanoparticles were observed by high-resolution transmission electron microscopy. Only SnO2 nanocrystals were observed in dried products prepared by sequential injection. After heat-treatment at 500 degrees C, no Pd species were observed for both doping procedures. Moreover, X-ray photoelectron spectroscopy showed that, in both the doping procedures, after heat-treatment Pd is distributed only into the SnO2 nanocrystal structure. This conclusion was reinforced by the measurement of the electrical properties of Pd-doped nanocrystals, showing a remarkable increase of the electrical resistance if compared with pure SnO2 nanocrystals. This result was interpreted as Pd insertion as a dopant inside the cassiterite lattice of tin dioxide. The addition of Pd resulted in a remarkable improvement of the gas-sensing properties, allowing the detection of carbon monoxide concentrations below 50 ppm and of very low concentrations (below 25 ppm) of other reducing gases such as ethanol and acetone