12 research outputs found
Optimizing gold nanoparticle size and shape for the fabrication of sers substrates by means of the langmuir–blodgett technique
The Langmuir–Blodgett technique, in which a layer of nanoparticles is spread at the water/air interface and further transferred onto a solid support, is a versatile approach for the preparation of SERS substrates with a controllable arrangement of hotspots. In a previous work, we demonstrated that fine-tuning the lateral packing and subsequent seed growth of 10 nm gold nanoparticles led to a quasi-resonant enhanced in the SERS signal of a test analyte. Here, we explore further enhancements by modifying the size and shape of the spread gold nanoparticles in order to take advantage of the inherent interparticle repulsion mechanisms present at the interface. We show that the size of the used nanoparticles is also a determinant factor, which cannot be compensated by the subsequent electroless growth. We also show that, although the seeded growth leads to rough hotspots, the sensitivity can be optimized by self-assembling urchin-shaped nanoparticles, with a roughness that is fine-tuned a priori. Our results suggest an intriguing correlation between surface homogeneity and SERS signal enhancement, indicating that regular substrates will have the optimal performance
Colloidal particles at a nematic-isotropic interface: effects of confinement
When captured by a flat nematic-isotropic interface, colloidal particles can
be dragged by it. As a result spatially periodic structures may appear, with
the period depending on a particle mass, size, and interface
velocity~\cite{west.jl:2002}. If liquid crystal is sandwiched between two
substrates, the interface takes a wedge-like shape, accommodating the
interface-substrate contact angle and minimizing the director distortions on
its nematic side. Correspondingly, particles move along complex trajectories:
they are first captured by the interface and then `glide' towards its vertex
point. Our experiments quantify this scenario, and numerical minimization of
the Landau-de Gennes free energy allow for a qualitative description of the
interfacial structure and the drag force.Comment: 7 pages, 9 figure
Active microrheology and simultaneous visualization of sheared phospholipid monolayers
Two-dimensional films of surface-active agents—from phospholipids and proteins to nanoparticles and colloids—stabilize fluid interfaces, which are essential to the science, technology and engineering of everyday life. The 2D nature of interfaces present unique challenges and opportunities: coupling between the 2D films and the bulk fluids complicates the measurement of surface dynamic properties, but allows the interfacial microstructure to be directly visualized during deformation. Here we present a novel technique that combines active microrheology with fluorescence microscopy to visualize fluid interfaces as they deform under applied stress, allowing structure and rheology to be correlated on the micron-scale in monolayer films. We show that even simple, single-component lipid monolayers can exhibit viscoelasticity, history dependence, a yield stress and hours-long time scales for elastic recoil and aging. Simultaneous visualization of the monolayer under stress shows that the rich dynamical response results from the cooperative dynamics and deformation of liquid-crystalline domains and their boundaries
MicroMotility: State of the art, recent accomplishments and perspectives on the mathematical modeling of bio-motility at microscopic scales
Mathematical modeling and quantitative study of biological motility (in particular, of motility at microscopic scales) is producing new biophysical insight and is offering opportunities for new discoveries at the level of both fundamental science and technology. These range from the explanation of how complex behavior at the level of a single organism emerges from body architecture, to the understanding of collective phenomena in groups of organisms and tissues, and of how these forms of swarm intelligence can be controlled and harnessed in engineering applications, to the elucidation of processes of fundamental biological relevance at the cellular and sub-cellular level. In this paper, some of the most exciting new developments in the fields of locomotion of unicellular organisms, of soft adhesive locomotion across scales, of the study of pore translocation properties of knotted DNA, of the development of synthetic active solid sheets, of the mechanics of the unjamming transition in dense cell collectives, of the mechanics of cell sheet folding in volvocalean algae, and of the self-propulsion of topological defects in active matter are discussed. For each of these topics, we provide a brief state of the art, an example of recent achievements, and some directions for future research
Tailoring plasmonic response by Langmuir–Blodgett gold nanoparticle templating for the fabrication of SERS substrates
Nanoparticle self-assembly is a robust and versatile strategy for the development of functional nanostructured materials, offering low-cost and scalable methods that can be fine-tuned for many different specific application. In this work, we demonstrate a pathway for the fabrication of tailorable quasi-two-dimensional lattices of gold nanoparticles to be used in Surface Enhanced Raman Scattering (SERS) detection of biomolecules. As a first step, nanoparticles are spread as a monolayer at the water/air interface, compressed to a target lateral density in a Langmuir–Blodgett technique, and transferred to a properly functionalized substrate surface. Once firmly adhered to the substrate, the lattice of nanoparticles can be directly used or be further processed using electroless gold deposition to let the nanoparticle grow thus tuning the plasmonic response and SERS enhancement. Compared to direct deposition or self-assembly methods, our protocol enables to obtain consistent results and much higher coverage of Au nanoparticles thanks to the active control of the surface pressure of the spread monolayer
Velocity-jump instabilities in Hele-Shaw flow of associating polymer solutions
We study fracturelike flow instabilities that arise when water is injected into a Hele-Shaw cell filled with aqueous solutions of associating polymers. We explore various polymer architectures, molecular weights, and solution concentrations. Simultaneous measurements of the finger tip velocity and of the pressure at the injection point allow us to describe the dynamics of the finger in terms of the finger mobility, which relates the velocity to the pressure gradient. The flow discontinuities, characterized by jumps in the finger tip velocity, which are observed in experiments with some of the polymer solutions, can be modeled by using a nonmonotonic dependence between a characteristic shear stress and the shear rate at the tip of the finger. A simple model, which is based on a viscosity function containing both a Newtonian and a non-Newtonian component, and which predicts nonmonotonic regions when the non-Newtonian component of the viscosity dominates, is shown to agree with the experimental data