Microstructures of the materials (e.g., crystallinitiy, defects, and composition, etc.) determine their properties, which eventually lead to their diverse applications. In this contribution, the properties, especially the electrochemical properties, of cubic silicon carbide (3C-SiC) films have been engineered by controlling their microstructures. By manipulating the deposition conditions, nanocrystalline, microcrystalline and epitaxial (001) 3C-SiC films are obtained with varied properties. The epitaxial 3C-SiC film presents the lowest double-layer capacitance and the highest reversibility of redox probes, because of its perfect (001) orientation and high phase purity. The highest double-layer capacitance and the lowest reversibility of redox probes have been realized on the nanocrystalline 3C-SiC film. Those are ascribed to its high amount of grain boundaries, amorphous phases and large diversity in its crystal size. Based on their diverse properties, the electrochemical performances of 3C-SiC films are evaluated in two kinds of potential applications, namely an electrochemical capacitor using a nanocrystalline film and an electrochemical dopamine sensor using the epitaxial 3C-SiC film. The nanocrystalline 3C-SiC film shows not only a high double layer capacitance (43-70 μF/cm(2)) but also a long-term stability of its capacitance. The epitaxial 3C-SiC film shows a low detection limit toward dopamine, which is one to 2 orders of magnitude lower than its normal concentration in tissue. Therefore, 3C-SiC film is a novel but designable material for different emerging electrochemical applications such as energy storage, biomedical/chemical sensors, environmental pollutant detectors, and so on.

Supraballs of various sizes and compositions can be fabricated via drying of drops of aqueous colloidal dispersions on super-liquid-repellent surfaces with no chemical waste and energy consumption. A "supraball" is a particle composed of colloids. Many properties, such as mechanical strength and porosity, are determined by the ordering of a colloidal assembly. To tune such properties, a colloidal assembly needs to be controlled when supraballs are formed during drying. Here, we introduce a method to control a colloidal assembly of supraballs by adjusting the dispersity of the colloids. Supraballs are fabricated on superamphiphobic surfaces from colloidal aqueous dispersions of polystyrene microparticles carrying pH-responsive poly[2-(diethylamino)ethyl methacrylate]. Drying of dispersion drops at pH 3 on superamphiphobic surfaces leads to the formation of spherical supraballs with densely packed colloids. The pH 10 supraballs are more oblate and consist of more disordered colloids than the pH 3 supraballs, caused by particle aggregates with random sizes and shapes in the pH 10 dispersion. Thus, the shape, crystallinity, porosity, and mechanical properties could be controlled by pH, which allows broader uses of supraballs.

The contact mechanics of individual, very small particles with other particles and walls is studied using a nanoindenter setup that allows normal and lateral displacement control and measurement of the respective forces. The sliding, rolling and torsional forces and torques are tested with borosilicate microspheres, featuring radii of about 10 µm. The contacts are with flat silicon substrates of different roughness for pure sliding and rolling and with silicon based, ion-beam crafted rail systems for combined rolling and torsion. The experimental results are discussed and compared to various analytical predictions and contact models, allowing for two concurrent interpretations of the effects of surface roughness, plasticity and adhesion. This enables us to determine both rolling and torsion friction coefficients together with their associated length scales. Interestingly, even though normal contacts behave elastically (Hertzian), all other modes of motion display effects due to surface roughness and consequent plastic deformation. The influence of adhesion is interpreted in the framework of different models and is very different for different degrees of freedom, being largest for rolling.

Cotton is a promising basis for wearable smart textiles. Current approaches that rely on fiber coatings suffer from function loss during wear. We present an approach that allows biological incorporation of exogenous molecules into cotton fibers to tailor the material's functionality. In vitro model cultures of upland cotton () are incubated with 6-carboxyfluorescein-glucose and dysprosium-1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid-glucose, where the glucose moiety acts as a carrier capable of traveling from the vascular connection to the outermost cell layer of the ovule epidermis, becoming incorporated into the cellulose fibers. This yields fibers with unnatural properties such as fluorescence or magnetism. Combining biological systems with the appropriate molecular design offers numerous possibilities to grow functional composite materials and implements a material-farming concept.

Surfaces with self‐cleaning properties are desirable for many applications. Conceptually, super liquid‐repellent surfaces are required to be highly porous on the nano‐ or micrometer scale, which inherently makes them mechanically weak. Optimizing the balance of mechanical strength and liquid repellency is a core aspect toward applications. However, quantitative mechanical testing of porous, super liquid‐repellent surfaces is challenging due to their high surface roughness at different length scales and low stress tolerance. For this reason, mechanical testing is often performed qualitatively. Here, the mechanical responses of soot‐templated super liquid‐repellent surfaces are studied qualitatively by pencil and finger scratching and quantitatively by atomic force microscopy, colloidal probe force measurements, and nanoindentation. In particular, colloidal probe force measurements cover the relevant force and length scales. The effective elastic modulus, the plastic work Wplastic and the effective adhesive work Wadhesive are quantified. By combining quantitative information from force measurements with measurements of surface wetting properties, it is shown that mechanical strength can be balanced against low wettability by tuning the reaction parameters.