Marcel Richter

Inner structure of adsorbed ionic microgel particles.

Microgel particles of cross-linked poly(NIPAM-co-acrylic acid) with different acrylic acid contents are investigated in solution and in the adsorbed state. As a substrate, silicon with a poly(allylamine hydrochloride) (PAH) coating is used. The temperature dependence of the deswelling of the microgel particles was probed with atomic force microscopy (AFM). The inner structure of the adsorbed microgel particles was detected with grazing incidence small angle neutron scattering (GISANS). Small angle neutron scattering (SANS) on corresponding microgel suspensions was performed for comparison. Whereas the correlation length of the polymer network shows a divergence in the bulk samples, in the adsorbed microgel particles it remains unchanged over the entire temperature range. In addition, GISANS indicates changes in the particles along the surface normal. This suggests that the presence of a solid surface suppresses the divergence of internal fluctuations in the adsorbed microgels close to the volume phase transition.

The impact of the cononsolvency effect on poly (N-isopropylacrylamide) based microgels at interfaces

The paper addresses the effect of solid interfaces on the cononsolvency effect for poly(N-iso propylacrylamide) based microgels containing different contents of the co-monomer allyl acetic acid (AAA). The cononsolvency effect is studied by dynamic light scattering (DLS) in solution and with atomic force microscopy (AFM) at surfaces against different mixtures of water and organic solvent (ethanol, iso-propanol, and tetrahydrofuran). For the studies at interfaces, the microgels are spin coated on silicon wafers that are precoated with poly(allylamine hydrochloride) (PAH). The minimum in particle volume due to cononsolvency shows a pronounced shift from 10–20 % of organic solvent to 40–50 % after deposition at the Si/PAH wafer. The strong shift indicates an increase of water to organic solvent ratio within the gel at the surface with respect to the bulk solution. In order to understand the increase of water to organic solvent ratio, shrinking/reswelling AFM experiments for different spin-coating conditions and under ambient conditions are carried out. Spin coating from water instead from different solvent mixtures has no effect on the cononsolvency. In ambient conditions, the cononsolvency effect disappears

Responsive Microgels at Surfaces and Interfaces

Abstract Stimuli responsive surface structures attract increasing attention due to a large variety of envisioned applications. The controlled organization of poly(N-isopropyl acrylamid), PNIPAM microgel particles at solid surfaces inspired numerous research activities. In this review article, we briefly discuss the swelling/deswelling properties of adsorbed microgel particles in comparison to the behavior in the bulk phase. The presence of the solid interface highly influences and changes their behavior with respect to the properties in solution. Furthermore, the confinement on a solid substrate allows the direct and in-situ investigation of the mechanical properties of the microgel particles. Additionally, we briefly review the research on microgel particles at liquid interfaces. At these interfaces new interesting effects occur. Moreover, we discuss some interesting work on potential applications. In this context, microgel particles are often used as an active component for responsive coatings of various functionality envisioning applications, e.g. in medicine, biotechnology, and nanooptics.

Externally Triggered Oscillatory Structural Forces

This paper addresses triggering of oscillatory structural forces via temperature variation across an aqueous dispersion of thermoresponsive poly( N-isopropylacrylamide) (PNIPAM) nanogels confined between silica surfaces. Oscillatory structural forces are a well-known phenomenon in colloidal science, caused by interactions between molecules or colloids. Modulation of these forces usually requires changing the internal parameters of the dispersion, such as ionic strength, particle concentration, and surface charge, or changing the properties of the confining walls, such as surface roughness, potential, or elasticity. All of these parameters are usually fixed and can only be changed via exchange of the sample or the complete experimental setup. Here, a new approach is presented, combining the characteristics of smart materials with the properties of nanoparticles, using negatively charged PNIPAM nanogels. Aqueous dispersions of these nanogels express no oscillatory structural forces in the initial state (20 °C), below the volume phase transition temperature (32 °C). Heating (60 °C) reduces the nanogel size and leads to a more negative ζ-potential, which triggers the onset of oscillatory structural forces.