Inspired by the amino acid 2‐chloro‐4,5‐dihydroxyphenylalanine (Cl‐DOPA), present in the composition of the proteinaceous glue of the sandcastle worm Phragmatopoma californica, a simple strategy is presented to confer antifouling properties to polymer surfaces using (but not releasing) a bioinspired biocide. Cl‐Dopamine is used to functionalize polymer materials and hydrogel films easily, to prevent biofilm formation on them.

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The Kelvin equation relates the vapor pressure of a volatile liquid to the curvature of the liquid surface. It describes phenomena such as capillary condensation, capillary adhesion, nucleation, and the adsorption of vapors into porous media. Here we propose an extension of the Kelvin equation, which takes into account changes of the vapor pressure due to electric fields. The presence of electric fields reduces the saturation vapor pressure and leads to field-induced condensation. Field-induced condensation can explain the presence of water bridges in scanning probe nanolithographic methods such as anodic oxidation.

Redox-active, phenothiazine-functionalized polymers were synthesized and employed as a promising cathode-active material (∼3.7 V vs. Li, 77 Ah kg−1) in a rechargeable battery.

To analyze the photothermal ablation of polymers, we designed a temperature measurement setup based on spectral pyrometry. The setup allows to acquire 2D temperature distributions with 1 μm size and 1 μs time resolution and therefore the determination of the center temperature of a laser heating process. Finite element simulations were used to verify and understand the heat conversion and heat flow in the process. With this setup, the photothermal ablation of polystyrene, poly(α-methylstyrene), a polyimide and a triazene polymer was investigated. The thermal stability, the glass transition temperature Tg and the viscosity above Tg were governing the ablation process. Thermal decomposition for the applied laser pulse of about 10 μs started at temperatures similar to the start of decomposition in thermogravimetry. Furthermore, for polystyrene and poly(α-methylstyrene), both with a Tg in the range between room and decomposition temperature, ablation already occurred at temperatures well below the decomposition temperature, only at 30–40 K above Tg. The mechanism was photomechanical, i.e. a stress due to the thermal expansion of the polymer was responsible for ablation. Low molecular weight polymers showed differences in photomechanical ablation, corresponding to their lower Tg and lower viscosity above the glass transition. However, the difference in ablated volume was only significant at higher temperatures in the temperature regime for thermal decomposition at quasi-equilibrium time scales.

We report on adsorption of lysozyme (LYS), ovalbumin (OVA), or ovotransferrin (OVT) on particles of a synthetic smectite (synthetic layered aluminosilicate). In our approach we used atomic force microscopy (AFM) and quartz crystal microbalance (QCM) to study the protein-smectite systems in water solutions at pH ranging from 4 to 9. The AFM provided insights into the adhesion forces of protein molecules to the smectite particles, while the QCM measurements yielded information about the amounts of the adsorbed proteins, changes in their structure, and conditions of desorption. The binding of the proteins to the smectite surface was driven mainly by electrostatic interactions, and hence properties of the adsorbed layers were controlled by pH. At high pH values a change in orientation of the adsorbed LYS molecules and a collapse or desorption of OVA layer were observed. Lowering pH to the value ≤ 4 caused LYS to desorb and swelling the adsorbed OVA. The stability of OVT-smectite complexes was found the lowest. OVT revealed a tendency to desorb from the smectite surface at all investigated pH. The minimum desorption rate was observed at pH close to the isoelectric point of the protein, which suggests that nonspecific interactions between OVT and smectite particles significantly contribute to the stability of these complexes.

The ability to alter surface properties such as morphology and surface energy upon external stimuli makes switchable polymer surfaces a promising field of research. Mixed polymer brushes consisting of two different homopolymers covalently attached to a surface are one system in which surface properties can be switched. In this work the correlation between the change in structure and the resulting surface stress in thin poly(methyl methacrylate)−polystyrene mixed polymer brush film upon exposure to selective solvents is investigated. By measuring the forces acting inside the film, we are able to achieve a deeper understanding of the observed structural changes. To obtain a thorough understanding of the film's morphology, the structure is analyzed by scanning probe microscopy, X-ray reflectivity, and grazing incidence small-angle X-ray scattering (GISAXS). Upon exposure to acetic acid, a selective solvent for PMMA, the film showed a dimple-like structure. This is linked to collapsed domains of polystyrene covered by PMMA chains. Bending experiments resulted in tensile stress, pointing to attractive forces acting inside the polymer film. After exposure to dichloromethane, a good solvent for both polymers, bending experiments revealed a decreased but still high tensile stress, indicating that the microdomains are still present. The results of the experiments enable us to further explain the domain memory effect typically found in these kinds of mixed polymer brush systems.

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