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Artículos SCI



2008


Nanotecnología en Superficies y Plasma

Influence of the chemical and electronic structure on the electrical behavior of zirconium oxynitride films

Carvalho, P; Chappe, JM; Cunha, L; Lanceros-Mendez, S; Alpuim, P; Vaz, F; Alves, E; Rousselot, C; Espinos, JP; Gonzalez-Elipe, AR
Journal of Applied Physics, 103 (2008) 104907

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This work is devoted to the investigation of decorative zirconium oxynitride, ZrOxNy, films prepared by dc reactive magnetron sputtering, using a 17:3 nitrogen-to-oxygen-ratio gas mixture. The color of the films changed from metallic-like, very bright yellow pale, and golden yellow, for low gas mixture flows [from 0 to about 9 SCCM (SCCM denotes cubic centimeter per minute at STP)] to red brownish for intermediate gas flows (values up to 12 SCCM). Associated to this color change there is a significant decrease of brightness. With further increase of the reactive gas flow, the color of the samples changed from red brownish to dark blue (samples prepared with 13 and 14 SCCM). The films deposited with gas flows above 14 SCCM showed only apparent colorations due to interference effects. This change in optical behavior from opaque to transparent (characteristic of a transition from metallic to insulating-type materials), promoted by the change in gas flow values, revealed that significant changes were occurring in the film structure and electronic properties, thus opening new potential applications for the films, beyond those of purely decorative ones. Taking this into account, the electrical behavior of the films was investigated as a function of the reactive gas flow and correlated with the observed chemical, electronic, and structural features. The variations in composition disclosed the existence of four different zones, which were correlated to different crystalline structures. For the so-called zone I, x-ray diffraction revealed the development of films with a B1 NaCl face-centered cubic zirconium nitride-type phase, with some texture changes. Increasing the reactive gas flow, the structure of the films is that of a poorly crystallized overstoichiometric nitride phase, which may be similar to that of Zr3N4, but with some probable oxygen inclusions within nitrogen positions. This region was characterized as zone II. Zone III was indexed as an oxynitride-type phase, similar to that of gamma-Zr2ON2 with some oxygen atoms occupying some of the nitrogen positions. Finally, occurring at the highest flow rates, zone IV was assigned to a ZrO2 monoclinic-type structure. The composition/structure variations were consistent with the chemical bonding analysis carried out by x-ray photoelectron spectroscopy, which showed oxygen doping in both Zr3N4- and ZrN-type grown films. The electronic properties of the films exhibited significant changes from zone to zone. Resistivity measurements revealed a very wide range of values, varying from relatively highly conductive materials (for zone I) with resistivity values around few hundreds of mu Omega cm to highly insulating films within zones III and IV, which presented resistivity values in the order of 10(15) mu Omega cm. Regarding zone II, corresponding to oxygen doped Zr3N4-type compounds, the observed behavior revealed resistivity values increasing steeply from about 10(3) up to 10(15) mu Omega cm, indicating a systematic transition from metallic to insulating regimes. 


Mayo, 2008 | DOI: 10.1063/1.2927494

Nanotecnología en Superficies y Plasma

Ar+NO microwave plasmas for Escherichia coli sterilization

Hueso, JL; Rico, VJ; Frias, JE; Cotrino, J; Gonzalez-Elipe, AR
Journal of Physics D-Applied Physics, 41 (2008) 092002

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Ar + NO microwave discharges are used for sterilization and the results are compared with additional experiments with Ar, O(2) and N(2)-O(2) plasma mixtures. The NO* species produced in the Ar - NO mixtures remain up to long distances from the source, thus improving the sterilization efficiency of the process. E. coli individuals exposed to the Ar + NO plasma undergo morphological damage and cell lysis. Combined effects of etching ( by O* and Ar* species) and UV radiation ( from deactivation of NO* species) are responsible for the higher activity found for this plasma mixture.


Mayo, 2008 | DOI: 10.1088/0022-3727/41/9/092002

Materiales Nanoestructurados y Microestructura - Tribología y Protección de Superficies

Tribological behaviour of titanium carbide/amorphous carbon nanocomposite coatings: From macro to the micro-scale

Sanchez-Lopez, JC; Martinez-Martinez, D; Lopez-Cartes, C; Fernandez, A
Surface & Coatings Technology, 202 (2008) 4011-4018

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The tribological behaviour of nanocomposite coatings made of nanocrystalline metal carbides and amorphous carbon (a-C) prepared by PVD/CVD techniques is found to be very dependant on the film deposition technique, synthesis conditions and testing parameters. Focusing in the TiC/amorphous carbon-based nanostructured system, this paper is devoted to an assessment of the factors governing the tribological performance of this family of nanocomposites using a series of TiC/a-C films prepared by magnetron sputtering technique varying the power applied to each target (titanium or graphite) as model system to establish correlations between film microstructure and chemical compositions and tribological properties measured by a pin-on-disk tribometer. The film microstructure goes from a quasi -polycrystalline TiC to a nanocomposite formed by nanocrystals of TiC embedded in an amorphous carbon matrix as observed by transmission electron microscopy (TEM). The nanocrystalline/amorphous ratio appears to be the key-parameter to control the tribological properties and its quantification has been done by electron energy-loss spectroscopy (EELS). A significant change in the tribological performance is observed for nanocomposites with amorphous carbon phase contents above 60-65%. The friction coefficient decreases from 0.3 to 0.1 and the film wear rates by a factor of 10. Examination of the wear scars on ball and film surfaces by laser micro-Raman spectroscopy has allowed to determine the presence of metallic oxides and carbonaceous compounds responsible of the observed friction behaviour. The revision of the literature results in view of the conclusions obtained enabled to explain their apparent dispersion in the tribological performance.


Mayo, 2008 | DOI: 10.1016/j.surfcoat.2008.02.012

Fotocatálisis Heterogénea: Aplicaciones - Materiales y Procesos Catalíticos de Interés Ambiental y Energético

Study of the synergic effect of sulphate pre-treatment and platinisation on the highly improved photocatalytic activity of TiO2

Hidalgo, MC; Maicu, M; Navio, JA; Colon, G
Applied Catalysis B-Environmental, 81 (2008) 49-55

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An important improvement of the photocatalytic activity of sol-gel prepared TiO2 has been achieved by sulphate pre-treatment, calcination at high temperature and further platinisation of the samples.
The presence of sulphuric acid clearly stabilised TiO2 surface area against sintering, maintaining at the same time anatase phase until higher calcination temperatures than in non-sulphated samples. Platinisation of the samples with different nominal amounts of platinum (from 0.5 to 2.5 wt%) was performed and the influence of sulphate treatment on the dispersion and deposit size of platinum on the TiO2 surface was studied.
Characterisation results and photocatalytic activity of these catalysts were compared with those of unmodified TiO2. Simultaneously sulphated and platinised TiO2 samples were highly active for phenol degradation, used as model reaction for the photocatalytic studies, having higher activities than only platinised or only sulphated samples. The activity of these samples were several orders of magnitude higher than that of the commercial TiO2 Degussa P25 (platinised or unmodified) as well, with independence of the nominal amount of platinum of the samples.
A wide characterisation of the samples was performed and correlations between characterisation results and activity properties are reported.


Mayo, 2008 | DOI: 10.1016/j.apcatb.2007.11.036

Química de Superficies y Catálisis

CO and VOCs oxidation over Pt/SiO2 catalysts prepared using silicas obtained from stainless steel slags

Dominguez, MI; Barrio, I; Sanchez, M; Centeno, MA; Montes, M; Odriozola, JA
Catalysis Today, 133 (2008) 467-474

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Stainless steels slags are mainly composed of low specific surface area calcium silicates together with a variable amount of metallic cations dispersed in such silicate matrix. These silicates due to their heavy metals content have to be considered as hazardous wastes that cannot be reclaimed easily. An alternative to reclamation is the production of valuable materials designed to accomplish processes without economic profit as the abatement of VOCs. In this paper we describe a method for obtaining high specific surface area (up to 290 m(2) g(-1)) metal-doped SiO2 and SiO2/ Al2O3 supports for catalytic applications using as raw materials stainless steel slags. The acid digestion of these slags followed by a hydrothermal treatment results in transition metal oxides doped silicas and silica-aluminas that are used as support for platinum catalysts. The prepared catalysts are active in the total oxidation of CO and toluene, showing comparable activities to those shown by Pt catalysts supported on commercial SiO2.(


Abril, 2008 | DOI: 10.1016/j.cattod.2007.11.033

 

 

 

 

 

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