The Influence of Long-Range Surface Forces on the Contact Angle of Nanometric Droplets and Bubbles

For a droplet or a bubble of dimensions below 100 nm, long-range surface forces such as long-range van der Waals forces can compete with capillarity, which leads to a size dependence of the contact angle. This is discussed in this work, where we also show that the effect cannot simply be described by a normalized line tension. We calculate interfacial profiles for typical values of van der Waals forces and discuss the role of long-range surface forces on the contact angle of nanobubbles and nanodrops

Surpassingly Competitive Electromagnetic Field Enhancement at the Silica/Silver Interface for Selective Intracellular Surface Enhanced Raman Scattering Detection

A thin plasmonic nanofilm is formed by preformed silver nanoparticles (30 nm) in the matrix of poly(vinyl alcohol) adsorbed on silica microparticles (1.5 μm) (SiO₂@Ag-PVA). By applying finite element method (FEM) analysis the surface enhanced Raman spectroscopy (SERS) enhancement factors (EFs) can reach 10⁵ with higher values from 10⁹ to 10¹¹ in the silver layer of 5 nm thickness. Nanoparticles in the SiO₂@Ag-PVA nanofilm need at least 15 nm radius to exhibit SERS EFs greater than 10⁷. High values of this enhancement at the silver/silica interface of spherical geometry can be reached faster by using a 532 nm compared to 785 nm excitation wavelength. By this approach different SERS spectral features can be distinguished between live fibroblasts with spread (“healthy” state) or round (“unhealthy” state) shapes. Characteristic features of secondary protein structures, detection of different acidic conditions and cholesterol with at least a 3-fold higher sensitivity are examined. Moreover, a greater amount of glucose (glucogen) and also tyrosine can be monitored in real time. This is important in identification of higher risk of diabetes as well as in several genetic metabolic disorders (<i>e.g.</i>, phenylketonuria, tyrosinaemia type II and tyrosinosis)

Influence of Embedded Nanocontainers on the Efficiency of Active Anticorrosive Coatings for Aluminum Alloys Part II: Influence of Nanocontainer Position

The present work contributes to the coating design of active anticorrosive coatings for the aluminum alloy, AA2024-T3. Part II is a continuation of Part I: Influence of Nanocontainer Concentration and describes further surprising aspects of the design of nanocontainer based active anticorrosive coatings, which influence their performance. The studied coating system consists of a passive sol–gel (SiO_<i>x</i>/ZrO_<i>x</i>) matrix and inhibitor (2-mercaptobenzothiazole) loaded mesoporous silica nanocontainers (MBT@NCs), which are dispersed only in half of the coating volume. Varying position and concentration of MBT@NCs the synergetic effect of inhibitor amount and path length on the metal surface were analyzed, considering the balance between optimum barrier properties, active protection and adhesion. The impact of MBT@NC position on passive and active corrosion resistance was investigated by electrochemical impedance spectroscopy and scanning vibrating electrode technique. Increasing the distance between MBT@NCs and metal surface led to better barrier properties but worse active corrosion inhibition. These findings improve the understanding of the factors influencing the overall performance of active anticorrosive coatings and enable the development of a coating system with optimum anticorrosion efficiency

Influence of Embedded Nanocontainers on the Efficiency of Active Anticorrosive Coatings for Aluminum Alloys Part I: Influence of Nanocontainer Concentration

This work presents an effective anticorrosive coating for the industrially important aluminum alloy, AA2024-T3. The protective coating was designed by dispersing mesoporous silica nanocontainers, loaded with the nontoxic corrosion inhibitor, 2-mercaptobenzothiazole, in a hybrid sol–gel (SiO_<i>x</i>/ZrO_<i>x</i>) layer. The concentration of the embedded nanocontainers was varied (0.04–1.7 wt %) to ascertain the optimum conditions for anticorrosion performance. Attaining high efficiency was found to be a compromise between delivering sufficient corrosion inhibitor and preserving the coating barrier properties. The impact of nanocontainer concentration on the thickness and adhesion of freshly cured coatings was also investigated. The barrier properties of the intact coatings were assessed by electrochemical impedance spectroscopy. The active corrosion inhibition was evaluated during a simulated corrosion process by the scanning vibrating electrode technique. This study has led to a better understanding of the factors influencing the anticorrosion performance and properties of active anticorrosive coatings with embedded nanocontainers

Plasmonic Nanochemistry Based on Nanohole Array

We show that the growth of Ag nanoparticles (NPs) follows the areas of maximum plasmonic field in nanohole arrays (NAs). We thus obtain Ag NP rings not connected to the metallic rim of the nanoholes. The photocatalytic effect resulting from the enhanced <i>E</i>-field of NAs boosts the reaction and is responsible for the site selectivity. The strategy, using plasmonics to control a chemical reaction, can be expanded to organic reactions, for example, synthesis of polypyrrole. After the NA film is removed, ordered ring-shaped Ag NPs are easily obtained, inspiring a facile micropatterning method. Overall, the results reported in this work will contribute to the control of chemical reactions at the nanoscale and are promising to inspire a facile way to pursue patterned chemical reactions

One-Pot Synthesis of Polypeptide–Gold Nanoconjugates for <i>in Vitro</i> Gene Transfection

We present a general strategy to create polypeptide–gold nanoconjugates by a one-pot synthesis approach, where polypeptides act not only as capping agents but also as reductants for the formation of gold nanoparticles without the need of an additional reducing agent. The present approach is environmentally benign, facile, and flexible for the design of functional polypeptide–gold nanoconjugates. As a demonstration of as-synthesized nanoconjugates for biomedical applications, the resulting positively charged polypeptide-conjugated gold nanoparticles are applied for gene delivery. A gradual and prolonged intracellular uptake and transfection is achieved, and transfection activity is maintained for almost two weeks with no obvious cytotoxicity. The biologically based method presented in this work will provide a new alternative in creating a variety of multifunctional polypeptide–metallic nanoconjugates in a simple and straightforward manner, which will be more advantageous for their applications in biomedicine

Laser-Induced Cell Detachment, Patterning, and Regrowth on Gold Nanoparticle Functionalized Surfaces

We report on the selective cell detachment from nanoengineered gold nanoparticle (AuNP) surfaces triggered by laser irradiation, which occurs in a nonthermal manner. The gold nanoparticle-based surfaces reveal good adhesion of NIH3T3 fibroblast cells. Patterning is achieved by lithographic microcontact printing, selective gold nanoparticle deposition, and by laser beam profiling. It is shown that the effectiveness of fibroblast cell detachment depends on the cell age, laser power, and AuNP patterning profile. Heat distribution and temperature rise around gold nanoparticle functionalized surfaces is modeled, revealing low heating of nanoparticles by laser illumination. The nonthermal photochemical mechanism of cell detachment due to production of reactive oxygen species under illumination of gold nanoparticles by green laser light is studied. We also demonstrate that cells migrate from unirradiated areas leading to their reattachment and surface recovery which is important for controlled spatial organization of cells in wound healing and tissue engineering. Research presented in this work is targeted at designing biointerfaces for cell cultures

Effect of Linear Elongation on Carbon Nanotube and Polyelectrolyte Structures in PDMS-Supported Nanocomposite LbL Films

Polyelectrolyte (PE) multilayer (PEM) thin films prepared by layer-by-layer self-assembly on flexible substrates are exposed to elongation in many fields of technology. Upon elongation, these types of films are showing interesting, but not understood, phenomena, such as controlled wetting, stimuli-responsive nanovalves, and lithography-free surface structuring. To investigate the mechanisms causing these interesting phenomena, we employed spectroscopic investigations of supported PEM films that were prepared from polystyrene sulfonate (PSS)-wrapped single-walled carbon nanotubes (SWNTs) or pyrene-labeled PSS (PSS-PY) and polydiallyldiammonium chloride. Our results show that the SWNTs agglomerated upon deposition into the PEM and showed a strong change in orientation upon uniaxial elongation of the PEM. Upon release of elongation, the resulting wrinkling pattern was changing its wavelength upon time, in the case of the SWNT-containing PEM. Fluorescence measurements of the PSS-PY in the PEM showed that the PEs changed their orientation due to constant mechanical force from elongation up to a time scale of 2 days after beginning the elongation. The results prove that elongated and released PEM films, until now considered static structures, possess strong kinetics, which has to be taken into account for their application

Different Microtubule Structures Assembled by Kinesin Motors

The microtubule–kinesin system is used to form microtubule-based structures via microtubule gliding motility. On the kinesin-coated surface, the microtubules can be easily assembled into stable micro- and nanostructures like circles and microtubule bundles using the streptavidin–biotin system. Furthermore, these microtubules structures can still retain performance with kinesin motor movement in spite of different velocities. Collisions bear responsibility for the majority of events leading to circle formation. By taking advantage of biological substances, some micro- or nanostructures, which are difficult to fabricate by artificial processes, can be easily obtained

Silica/Polymer Double-Walled Hybrid Nanotubes: Synthesis and Application as Stimuli-Responsive Nanocontainers in Self-Healing Coatings

We report the development of silica/polymer double-walled hybrid nanotubes, which consist of a hollow cavity, a porous silica inner wall, and a stimuli-responsive (pH, temperature, and redox) polymeric outer wall, as a novel nanocontainer system. The length, diameter, wall thickness, and aspect ratio of the hybrid nanotubes are precisely controlled in the range of 48–506 nm, 41–68 nm, 3–24 nm, and 1.2–7.6, respectively. The hybrid nanotubes loaded with active molecules exhibit morphology-dependent release and pH-, temperature-, redox-responsive release, which enable a wide range of applications from energy storage to drug delivery and self-healing coatings for metal corrosion protection