RESUMEN

Nanoparticles of ATO (antimony doped tin oxide) were used to produce thick conductive, free standing mats of nanofibers via electrospinning. These fibrous mats were incorporated into polymer films to produce a transparent conducting polymer foil. Moreover, the fiber mats can serve as porous electrodes for electrodeposition of Prussian Blue and TiO(2) and were tested in dye-sensitized solar cells.

RESUMEN

The modification of platinum nanofibers by silica using the electrochemically-assisted deposition is reported here. Pt nanofibers are obtained by electrospinning and deposited on a glass substrate. The electrochemically-assisted deposition of the sol-gel material then gives the unique possibility to finely tune the silica film thickness around these nanofibers. It also allows the successful encapsulation of a biomolecule (glucose oxidase was chosen here as a model) while retaining its biological activity, as pointed out via the electrochemical monitoring of H(2)O(2) produced upon addition of glucose in the medium. This silica-glucose oxidase composite offers the possibility of comparing systematically the influence of the deposition time on the bioelectrode response and to compare it with the particular features of the deposits. It was found that the film first grew uniformly around the nanofibers and then started to deposit between them, covering the whole sample (fibers and glass substrate), and tended to fully embed the nanofibers for prolonged deposition. The thickness of the silica film is critical for the electroactivity of the biocomposite, the best response being obtained for a silica layer thickness in the range of the fiber diameter (∼50 nm).

Asunto(s)

RESUMEN

A hierarchical system of highly porous nanofibers has been prepared by electrospinning MOF (metal-organic framework) nanoparticles with suitable carrier polymers. Nitrogen adsorption proved the MOF nanoparticles to be fully accessible inside the polymeric fibers.

Asunto(s)

RESUMEN

The new dinuclear nickel-ruthenium complexes [Ni(xbsms)RuCp(L)][PF(6)] (H(2)xbsms = 1,2-bis(4-mercapto-3,3-dimethyl-2-thiabutyl)benzene; Cp(-) = cyclopentadienyl; L = DMSO, CO, PPh(3), and PCy(3)) are reported and are bioinspired mimics of NiFe hydrogenases. These compounds were characterized by X-ray diffraction techniques and display novel structural motifs. Interestingly, [Ni(xbsms)RuCpCO][PF(6)] is stereochemically nonrigid in solution and an isomerization mechanism was derived with the help of density functional theory (DFT) calculations. Because of an increased electron density on the metal centers [Eur. J. Inorg. Chem. 2007, 18, 2613-2626] with respect to the previously described [Ni(xbsms)Ru(CO)(2)Cl(2)] and [Ni(xbsms)Ru(p-cymene)Cl](+) complexes, [Ni(xbsms)RuCp(dmso)][PF(6)] catalyzes hydrogen evolution from Et(3)NH(+) in DMF with an overpotential reduced by 180 mV and thus represents the most efficient NiFe hydrogenase functional mimic. DFT calculations were carried out with several methods to investigate the catalytic cycle and, coupled with electrochemical measurements, allowed a mechanism to be proposed. A terminal or bridging hydride derivative was identified as the active intermediate, with the structure of the bridging form similar to that of the Ni-C active state of NiFe hydrogenases.

Asunto(s)

RESUMEN

Alternating multilayers of ordered mesoporous films of different metal oxides were prepared with the EISA (evaporation-induced self-assembly) method, using block copolymer templates. Selecting certain metal oxides, as exemplified with TiO2 and WO3 in this work, a high mesoscopic order could be achieved and preserved during crystallization. In addition to standard characterizations, the electrochromism of the multilayer film was studied, proving good accessibility of the single layers.

RESUMEN

Replacing the commonly used indium tin oxide (ITO) with a thin metal layer as a quasi-transparent electrode leads to enhancement and acceleration of the electrochromic response of WO(3), as otherwise there is an electronic activation barrier at the interface between WO(3) and the ITO electrode, impeding fast electron transfer.

RESUMEN

Electrospinning of a polyelectrolyte and vapor deposition polymerization were combined to fabricate nanotubes of oxidatively stabilized poly(acrylonitrile) (PANDelta) with an outer diameter of 100 nm, a wall thickness of 14 nm, and centimeter-scale length. Poly(styrene sulfonate) sodium (PSSNa) nanofibers serves as sacrificial cores while vapor deposition polymerization was used to form smooth PAN sheaths of even thickness. After the PAN sheaths had been oxidatively stabilized, the PSSNa cores were etched away with water to form nanotubes of PANDelta. High-temperature carbonization of these nanotubes at 900 degrees C under Ar flow yielded carbon nanotubes with an outer diameter of 80 nm and wall thickness of 10 nm. Raman spectroscopy confirms that the carbon nanotubes were composed of highly disordered graphene sheets, consistent with the carbonization of PAN under similar conditions. These carbon nanotubes have many promising applications as catalyst supports, gas absorbents, and as encapsulants for controlled release of active compounds.

Asunto(s)

RESUMEN

Electrospinning provides a simple approach to fabricating nanofibers and assemblies with controllable hierarchical structures. In this communication, we demonstrate that electrospinning can be combined with calcination to further maneuver the morphology and phase structure of nanofibers. More specifically, single-crystal V2O5 nanorods could be grown on rutile nanofibers by carefully calcining composite nanofibers consisting of amorphous V2O5, amorphous TiO2, and poly(vinylpyrrolidone). The size of the resulting V2O5 nanorods could be conveniently controlled by varying the composition of the nanofibers and/or the calcination temperature. In addition to the nanorod-on-nanofiber hierarchical structure, we believe this approach can also be extended to fabricate other more complex architectures.

Asunto(s)