RESUMO
A simple method based on sputtering deposition of Pd onto mesoporous SiO2 (SBA-15) was employed to produce supported Pd nanoparticles (NPs) that can be used as hydrogenation catalysts. The use of sputtering deposition eliminates contaminants and avoids additional drawbacks of traditional chemical methods applied to prepare heterogeneous supported metal catalysts. A mechanical resonant stirrer was used to revolve the SBA-15 powder and ensure homogeneous distribution of the Pd NPs over the support. The SBA-15 pores act as templates for Pd NPs and drive nanostructure growth. Consequently, the NPs obtained have the same diameter as that of the SBA-15 channels (~5 nm) and elongated particles are formed as sputtering deposition increases. The SBA-15 supported Pd NPs (Pd NPs/SBA-15) were tested in a probe hydrogenation of cyclohexene reaction to evaluate the catalytic activity of the Pd NPs. Turnover frequency (TOF) of 2000 min-1 were achieved with the lower Pd NPs concentration (0.15 wt%) catalyst.
RESUMO
Highly ordered TiO2 NT arrays were easily decorated with CdSe via RF magnetron sputtering. After deposition thermal annealing at different temperatures was performed to obtain an improved TiO2/CdSe interface. The heterostructures were characterized by RBS, SEM, XRD, HRTEM, UV-Vis, EIS, IPCE and current versus voltage curves. The sensitized semiconducting electrodes display an enhanced photocurrent density of ca. 2 mA cm(-2) at 0.6 V (vs. Ag/AgCl) under visible light (λ > 400 nm). The sensitized photoelectrodes displayed 3 and 535-fold enhanced photocurrent when compared to bare TiO2 NTs under 1 sun and under visible light illumination, respectively. IES results confirmed the improved charge transfer across the TiO2/CdSe/electrolyte interface after annealing at 400 °C. Incident photon-to-electron conversion efficiency measurements confirmed the efficient sensitization by allowing photoresponse in the visible range.
RESUMO
Sputtering deposition of gold onto the 1-(butyronitrile)-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (BCN)MI·N(Tf)(2) ionic liquid (IL) has generated colloidal and stable gold nanospheres (AuNS) and gold nanodisks (AuND) in a bimodal size distribution. Upon increasing the sputtering discharge voltage, three distinct phenomena were observed: (i) the mean diameter of both AuNS and AuND decreased; (ii) the population with lower diameters increased and (iii) the formation of AuND disappeared at voltages higher than 340 V. By dissolving the colloidal gold nanoparticles (AuNPs) in isopropanol and dropping the product onto carbon-coated Cu grids, 2D and 3D superlattices tended to be formed, as observed by transmission electron microscopy (TEM). Therefore, the formation of AuND is probably related to a strong interaction between sputtered Au atoms of low kinetic energy and the nitrile groups orientated to the vacuum phase of the IL surface, which drives the preferential anisotropic lateral growth.
RESUMO
The Conventional anodization of commercial aluminum sheets with a phosphoric acid electrolyte was employed for the preparation of alumina nanopore and/or nanotube structures. Modifying the system geometry (the ratio of platinum to aluminum electrode areas) controlled the nature of the anodization process (mild to hard). Nanotube formation was observed after low temperature preferential chemical etching of the defective corners of the hexagonal alumina cells using the same solution from the anodization process. Electrode geometry can be used to combine mild and hard anodization with low temperature etching to tune the alumina morphology from 100% nanopores to 100% nanotubos coverage.
Assuntos
Óxido de Alumínio/química , Galvanoplastia/métodos , Nanotubos/química , Nanotubos/ultraestrutura , Cristalização/métodos , Eletrodos , Galvanoplastia/instrumentação , Substâncias Macromoleculares/química , Teste de Materiais , Conformação Molecular , Nanotecnologia/métodos , Tamanho da Partícula , Porosidade , Propriedades de SuperfícieRESUMO
A simple one-step method based on the sputtering deposition of Ni nanoparticles (NP) has been developed for the production of magnetic biocatalysts, avoiding the complications and drawbacks of methods based on chemical functionalisation or coating of magnetic NP. This new technique provided high levels of recovery, reusability and catalytic activity for the lipase-Ni biocatalyst.
Assuntos
Biocatálise , Lipase/química , Lipase/metabolismo , Fenômenos Magnéticos , Nanopartículas Metálicas/química , Níquel/química , Burkholderia cepacia/enzimologia , Esterificação , Hidrólise , Propriedades de SuperfícieRESUMO
Self-organized TiO(2) nanotube (NT) arrays were produced by anodization in ethylene glycol (EG) electrolytes containing 1-n-butyl-3-methyl-imidazolium tetrafluoroborate (BMI.BF(4)) ionic liquid and water. The morphology of the as-formed NTs was considerably affected by changing the anodization time, voltage, and water and ionic liquid electrolyte concentrations. In general, a nanoporous layer was formed on the top surface of the TiO(2) NTs, except for anodization at 100 V with 1 vol % of BMI.BF(4), where the NT's mouth was revealed. The length and bottom diameter of the NTs as well as the pore diameter of the top layer showed a linear relationship with increased anodization voltage. These TiO(2) NTs were tested as photocatalysts for methyl orange photodegradation and hydrogen evolution from water/methanol solutions by UV light irradiation. The results show that the TiO(2) NTs obtained by anodization in EG/H(2)O/BMI.BF(4) electrolytes are active and efficient for both applications.
Assuntos
Nanotubos/química , Titânio , Compostos Azo/metabolismo , Hidrogênio/metabolismo , Líquidos Iônicos , Nanotubos/ultraestrutura , Processos FotoquímicosRESUMO
Micro- and nanostructures of Ti-γCu (γ = 0, 30, 50, 70, and 100 wt %) intermetallic alloys were produced through a single anodization step. It was found that the original alloy composition influences the final oxide morphology obtained after anodization which presented formation of a microstructure with nanotubes, nanoparticles or nanopillars on the surface. Pure Ti and Cu oxide metals and their alloys presented hydrophilic or superhydrophilic properties immediately after anodization. When the anodized pure metal and/or Ti-γCu surfaces were functionalized with trimethoxypropylsilane (TPMSi), by dipping and coating with a thin perfluorinated layer, the treated substrates became in all cases superhydrophobic (water contact angles in the range of 152-166°), showing excellent self-cleaning properties with hysteresis below 3°. These results can be explained by a combination of nanomicro morphologies with low surface energy compounds in the topmost monolayers. The decrease in hysteresis was associated with a higher M-OH bond concentration on the anodized surfaces, which allowed for more complete TMPSi coating coverage. This study also indicates that easy and effective fabrication of superhydrophobic surfaces in pure metals and alloys is possible without involving traditional multistep processes.
RESUMO
This work presents a novel way to introduce gold nanoparticles (Au NPs) in a multilayer polymer produced by the layer-by-layer (LbL) assembling technique. The technique chosen shows that, depending on the pH used, different morphological structures can be obtained from monolayer or bilayer Au NPs. The MEIS and RBS techniques allowed for the modelling of the interface polymer-NPs, as well as the understanding of the interaction of LbL system, when adjusting the pH in weak polyelectrolytes. The process reveals that the optical properties of multilayer systems could be fine-tuned by controlling the addition of metallic nanoparticles, which could also modify specific polarization responses.
Assuntos
Ouro/química , Nanoestruturas/química , Nanoestruturas/ultraestrutura , Substâncias Macromoleculares/química , Teste de Materiais , Conformação Molecular , Tamanho da Partícula , Propriedades de SuperfícieRESUMO
The sputtering of Au targets onto castor oil generates stable spherical gold nanoparticles (AuNPs) of 2.4 to 3.8 nm. The AuNP size increases with the discharge voltage and the mechanism of nucleation and growth are related to the energy of the atoms/clusters ejected from the target.