RESUMEN
The effect of an excess of surfactant on the thermophoresis of a sterically stabilized ferrofluid is investigated experimentally by forced Rayleigh scattering (FRS). The experiments are performed with a stable magnetic fluid sample to which controlled amounts of surfactant are added. A decrease in the thermally induced transport of magnetic nanoparticles is observed while increasing the temperature T. The positive Soret coefficient [Formula: see text] decreases by adding 2 vol% of surfactant at room temperature. As shown by FRS relaxation, this decreasing is mainly associated with a reduction of the interaction between the carrier fluid and individual nanoparticles. No significant effect of extra surfactant on the sign of [Formula: see text] is observed at higher T's (up to [Formula: see text]C). Dynamic light scattering at room temperature reveals the presence of a small amount of clusters/aggregates in the samples, which are hardly detectable by FRS relaxation. The presence of these small clusters/aggregates is confirmed by a rheological probing of the fluid properties. Whatever T, a small amount of added surfactant first causes a decrease of the ferrofluid viscosity, associated with a 10% decreasing of the flow activation energy. Further on, viscosity and activation energy both recover at higher excess surfactant concentrations. These results are analyzed in terms of saturation of the surfactant layer, concentration of free surfactant chains and heat of transport of the nanoparticles.
RESUMEN
The mechanism of upconversion enhancement for Li+-doped materials is still contentious. Attempting to settle the debate, here the upconversion emission enhancement of (Y0.97-xYb0.02Er0.01Lix)2O3, x = 0.000-0.123, nanoparticles is studied. Li+ incorporation in the Y2O3 host lattice is achieved via co-precipitation and solid-state reaction routes. In contrast to numerous reports, elemental analysis reveals that the former method does not afford Li+-bearing nanoparticles. The solid-state reaction route accomplishes an effective Li+ doping, as witnessed by inductively coupled plasma atomic emission spectroscopy and X-ray photoelectron spectroscopy (XPS). Transmission electron microscopy and powder X-ray diffraction showed an increase in nanoparticle size with increasing Li+ concentration. Rietveld refinement of powder X-ray diffraction data shows that the cubic lattice parameter decreases with increasing Li+ content. The emission quantum yield increases tenfold with increasing Li+ content up to x = 0.123, reaching a maximal value of 0.04% at x = 0.031. XPS and infrared spectroscopy show that the carbonate groups increase with increasing Li+ content, thus not supporting the prevailing view that the upconversion luminescence enhancement observed upon Li+ nanoparticle's doping is due to the decrease of the number of quenching carbonate groups present. Rather, the particle size increment and the decrease in the lattice parameter of the host crystals are shown to be the prime sources of quantum yield enhancement.
RESUMEN
Low-temperature atomic layer deposition (ALD) of TiO2, SiO2, and Al2O3 was applied to modify the surface and to tailor the diameter of nanochannels in etched ion-track polycarbonate membranes. The homogeneity, conformity, and composition of the coating inside the nanochannels are investigated for different channel diameters (18-55 nm) and film thicknesses (5-22 nm). Small angle x-ray scattering before and after ALD demonstrates conformal coating along the full channel length. X-ray photoelectron spectroscopy and energy dispersive x-ray spectroscopy provide evidence of nearly stoichiometric composition of the different coatings. By wet-chemical methods, the ALD-deposited film is released from the supporting polymer templates providing 30 µm long self-supporting nanotubes with walls as thin as 5 nm. Electrolytic ion-conductivity measurements provide proof-of-concept that combining ALD coating with ion-track nanotechnology offers promising perspectives for single-pore applications by controlled shrinking of an oversized pore to a preferred smaller diameter and fine-tuning of the chemical and physical nature of the inner channel surface.