Thin film networks of multiwalled carbon nanotubes (MWCNTs) were prepared by exerting chemically induced capillary forces upon the nanotubes. During this process MWCNTs undergo a transformation from being a vertically aligned structure to an interlocking resistive network of interconnected nanotubes, whose main feature is a regular three-dimensional (3D) sieve architecture. Due to their structural characteristics at the nanoscale level, 3D-MWCNT-based networks are in principle ideal candidates for scaffolds/matrices in tissue engineering. Their potential application in this field was confirmed by extensive growth, spreading, and adhesion of the common mouse fibroblast cell line L929.
The use of plasmonic metal nanoparticles as photosensitizers has undergone a strong development in the last few years given their ability to increase the activity of semiconductors into the visible and near infrared regions. The present work reports an experimental and theoretical study on the critical influence that shape anisotropy of gold nanoparticles exerts on the photocatalytic performance of Au-TiO2 nanoarchitectures. The obtained results show
A new class of highly fluorescent, photostable, and magnetic core/shell nanoparticles in the submicrometer size range has been synthesized from a modified Stöber method combined with the layer‐by‐layer (LbL) assembly technique. Luminescent magnetic nanoparticles are prepared via two main steps. The first step involves controlled addition of tetraethoxysilane to a dispersion of Fe3O4/γ‐Fe2O3 nanoparticles, which are thereby homogeneously incorporated as cores into monodisperse silica spheres. The second step involves the LbL assembly of polyelectrolytes and luminescent CdTe quantum dots onto the surfaces of the silica‐coated magnetite/maghemite particles, which are finally covered with an outer shell of silica. These spherical particles have a typical diameter of 220 ± 10 nm and a saturation magnetization of 1.34 emu g–1 at room temperature, and exhibit strong excitonic photoluminescence. Nanoparticles with such a core/shell architecture have the added benefit of providing a robust platform (the outer silica shell) for incorporating diverse functionalities into a single nanoparticle.
CdSe and CdSe@CdS semiconductor nanocrystals have been synthesized in aqueous solutions, using sodium
citrate as a stabilizer. Although initially these quantum dots display photoluminescence with very low quantum
yields, upon prolonged illumination with visible light, enhancements up to 5000% have been measured. This
leads to aqueous quantum dots with high luminescence, which can have important implications in biological
and other applications. A distinct correlation between the photocorrosion process and the photoactivation
process is observed. The primary reason for luminescence enhancement is considered to be the smoothing of
the CdSe core surface. Importantly, even stronger activation was observed in silica- and CdS-coated
nanocolloids where the CdSe core was expected to be shielded from photocorrosion. Preferential adsorption
of oxygen molecules in the porous silicate shell accelerates the photocorrosion process. In CdS-coated particles,
incomplete coating of the original particles is postulated, which is accompanied by the reforming of the CdS
coat because of ionic diffusion at the interface on the newly opening areas with smoother surfaces.
Indiscriminate adsorption of nanoparticles (NPs) significantly complicates the preparation of mesoscale NP patterns considered as enabling technology for many devices and processes. Instead of selected chemical functionalization of the substrate surface prior to the assembly of nanocolloids, the required optical properties - in our case, high quantum yield luminescence - are imparted to the layer-by-layer assembled films by spatially selected photoactivation. The films are made by sequential adsorption of a positively charged polyelectrolyte and a negatively charged CdSe/CdS aqueous dispersion with an initial quantum yield of 0.5-2%. The photoactivation process takes place in the presence of oxygen and may be accompanied by photoetching. A 50-500-fold increase in the luminescence intensity of CdSe/CdS citrate-stabilized particles (quantum yield 25-45%) after visible light illumination provides excellent pattern contrast. Micron scale luminescence patterns were produced from NPs of various CdSe core diameters with red, yellow, and green emission. It was also demonstrated that different emission colors such as orange and green can be combined in one image by taking advantage of spatially selective photoetching. The presented optical patterning technique significantly simplifies the preparation of luminescence patterns as compared to conventional methods. The high signal-to-noise ratio associated with it is essential for optical devices, information processing, and biophotonics. The most immediate use of this approach is expected in cryptography and cell monitoring.
The alignment of multiwalled carbon nanotubes (MWNTs) has been accomplished through deposition of uniform layers of magnetite/maghemite nanoparticles (diameter = 6-10 nm) and use of an external magnetic field. The coating of CNTs with magnetic nanoparticles was performed by combining the polymer wrapping and layer-by-layer (LbL) assembly techniques. The particle-coated MWNTs are superparamagnetic and can be aligned at room temperature on any substrate by deposition from an aqueous solution in an external field B = 0.2 T. The volume magnetization of the particle coated MWNTs is found to be enhanced by 17% compared to the pure particles in a powder indicating that either the adsorption process onto the CNTs changes the particle magnetization, or the MWNTs carry an intrinsic magnetization due to remaining Ni used as a catalyst for the growth process.
This Review article ponders core/shell structured nanoparticles that can be prepared with features that combine properties of different materials, including ligands that enhance their biocompatibility. These nanocomposites are not classified in terms of synthesis, but rather by how these features are distributed in the final morphology, attending to connected or isolated materials that end up in interacting or not‐interacting functionalities. In particular, we have focused on magnetic core/shell‐structured particles with a directly connected, coupled, or isolated second functionality. The current progress on methods in colloidal solution that have allowed the great development of these multifunctional magnetic and active spheres on biological and biomedical fields is reported.
With strings attached: Gold nanorods undergo uniform electrostatic assembly on multiwall carbon nanotubes (MWNTs) to form strings of rods with end‐to‐end contacts (see picture, PSS=polystyrene sulfonate, PDDA=poly(diallyldimethyl)ammonium chloride). This arrangement results in uniaxial plasmon coupling, and the polarization‐dependent optical response has been used to monitor the degree of alignment of carbon nanotubes within polymer films.
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