Prof. Dr. Tobias Kraus

Under the right process conditions, nanoparticles can cluster together to form defined particular structures, which can be termed supraparticles. Controlling the size, shape, and morphology of such entities is a central step in various fields of science and technology, ranging from colloid chemistry and soft matter physics to powder technology and pharmaceutical and food sciences. These diverse scientific communities have been investigating formation processes and structure/property relations of such supraparticles under completely different boundary conditions. On the fundamental side, the field is driven by the desire to gain maximum control of the assembly structures using very defined and tailored colloidal building-blocks, while more applied disciplines focus on optimizing the functional properties from rather ill-defined starting materials. With this review article, we aim to provide a connecting perspective by outlining fundamental principles that govern the formation and functionality of supraparticles. We discuss the formation of supraparticulates as a result of colloidal properties interplaying with external process parameters. We then outline how the structure of the supraparticles gives rise to different functional properties. They can be a result of the structure itself (emergent properties), of the colocalization of different, functional building-blocks, or of coupling between individual particles in close proximity. Taken together, we aim to establish structure-property and process-structure relationships that provide unifying guidelines for the rational design of functional supraparticles with optimized properties. Finally, we aspire to connect the different disciplines by providing a categorized overview of the existing, diverging nomenclature of seemingly similar supraparticle structures.

Coinage-metal nanoparticles are key components of many printable electronic inks. They can be combined with polymers to form conductive composites and have been used as the basis of molecular electronic devices. This review summarizes the multidimensional role of surface ligands that cover their metal cores. Ligands not only passivate crystal facets and determine growth rates and shapes; they also affect size and colloidal stability. Particle shapes can be tuned via the ligand choice while ligand length, size, ω-functionalities, and chemical nature influence shelf-life and stability of nanoparticles in dispersions. When particles are deposited, ligands affect the electrical properties of the resulting film, the morphology of particle films, and the nature of the interfaces. The effects of the ligands on sintering, cross-linking, and self-assembly of particles in electronic materials are discussed.

A semicontinuous process is used to nanoimprint a nanowire ink and form transparent conductive electrodes. Ultrathin gold nanowires are confined in the features of an elastomeric stamp, where they spontaneously assemble upon drying into hierarchical, percolating superstructures. This templated self-organization yields grids with defined line widths down to 0.9 µm and high pattern fidelity. Metal grids with square, hexagonal, and linear features are printed over 30 cm2 on different substrates and gently sintered in hydrogen plasma. Meshes on polyethylene terephthalate foil show high optical transmittances (>92%) and low sheet resistances (106–168 Ω sq−1). Their resistance is changed by only 10% after 500 bending cycles at a radius of 5 mm. The printed electrodes are used to build capacitive and resistive touch sensor devices.

Ionic liquids (ILs) exhibit tunable behaviour and properties that are due to their supramolecular structure. We synthesized a series of alkylated and fluorinated phosphonium dicyanamide ILs to study the relation between molecular structure and assembly with a focus on the roles of cation chain length and fluorination. Small angle X-ray scattering indicated a lamellar structure with long-range order for all fluorinated ILs, while alkylated ILs showed only the general structures of ILs, i.e., alternating a polar ionic-zone and a nonpolar alkyl-zone. "Fluorophobic" interactions caused microphase segregation between perfluorinated and other molecular segments, "fluorophilic" interactions among the perfluorinated segments stabilized the microphase structure, and the coupling of "fluorophobic" and "fluorophilic" interactions resulted in a stable mesophase structure. The perfluorinated segments packed more densely than the alkylated analogues; the fluorinated versions (except for F2) liquefied at temperatures considerably above that of alkylated ILs. The lamellar structures strongly affected the rheology of the ILs. Fluorinated ILs had higher viscosities and exhibited non-Newtonian shear thinning; the alkylated ILs of the same length had an order of magnitude lower viscosities and were purely Newtonian. We propose that the disruption of lamellar structure in the shear flow causes the non-Newtonian flow behaviour.

Hierarchical structures lend strength to natural fibers made of soft nanoscale building blocks. Intermolecular interactions connect the components at different levels of hierarchy, distribute stresses, and guarantee structural integrity under load. Here, we show that synthetic ultrathin gold nanowires with interacting ligand shells can be spun into biomimetic, free-standing microfibers. A solution spinning process first aligns the wires, then lets their ligand shells interact, and finally converts them into a hierarchical superstructure. The resulting fiber contained 80 vol % organic ligand but was strong enough to be removed from the solution, dried, and mechanically tested. Fiber strength depended on the wire monomer alignment. Shear in the extrusion nozzle was systematically changed to obtain process–structure–property relations. The degree of nanowire alignment changed breaking stresses by a factor of 1.25 and the elongation at break by a factor of 2.75. Plasma annealing of the fiber to form a solid metal shell decreased the breaking stress by 65%.

We show that the use of oriented linear arrays of smectic A defects, the so-called smectic oily streaks, enables the orientation of gold nanorods (GNRs) for a large range of GNR diameters, ranging from 7 to 48 nm, and for various ligands. For the small GNRs it enables oriented end-to-end small chains of GNRs when the density is increased from around 2 GNRs/μm2 to around 6 GNRs/μm2. We have characterized the orientation of single GNRs by spectrophotometry and two-photon luminescence (TPL). A strongly anisotropic absorption of the composites and an on–off switching of GNR luminescence, both controlled by incident light polarization, are observed, revealing an orientation of the GNRs mostly parallel to the oily streaks. A more favorable trapping of GNRs by smectic dislocations with respect to ribbon-like defects is thus demonstrated. The dislocations appear to be localized at a specific localization, namely, the summit of rotating grain boundaries. Combining plasmonic absorption measurements, TPL measurements, and simulation of the plasmonic absorption, we show that the end-to-end GNR chains are both dimers and trimers, all parallel to each other, with a small gap between the coupled GNRs, on the order of 1.5 nm, thus associated with a large red-shift of 110 nm of the longitudinal plasmonic mode. A motion of the GNRs along the dislocations appears as a necessary ingredient for the formation of end-to-end GNR chains, the gap value being driven by the balance between the attracting van der Waals interactions and the steric repulsion between the GNRs and leading to interdigitation of the neighboring ligands. We thus obtain electromagnetic coupling of nanorods controlled by light polarization.

We study the molecular origins of anisotropy in a semicrystalline polymer nanocomposite that is caused by aligned, elongated filler nanoparticles. Our study is based on spatially resolved 2D WAXS/SAXS data that indicates the arrangement of molecules, lamellae, and filler particles in the composite. Isotactic polypropylene (IPP) samples filled with anisotropic TiO2 nanoparticles were prepared by injection molding. The nanocomposite contained IPP crystals with preferential alignment, while neat IPP formed crystals with random orientation under the same preparation conditions. We studied the mechanism through which anisotropic TiO2 nanoparticles change the molecular assembly in the polymer melt and cause preferential alignment. Our hypothesis is that shear forces during injection molding align the long axis of the nanoparticles parallel to the melt flow direction, and the particles align the adjacent IPP molecules. The aligned IPP molecules in the melt then serve as nuclei in crystal growth during solidification. This templating increases the elastic modulus compared to that of neat IPP.

The extraordinary adherence and climbing agility of geckos on rough surfaces has been attributed to the multiscale hierarchical structures on their feet. Hundreds of thousands of elastic hairs called setae , each of which split into several spatulae , create a large number of contact points that generate substantial adhesion through van der Waals interactions. The hierarchical architecture provides increased structural compliance on surfaces with roughness features ranging from micrometers to millimeters. We review synthetic adhesion surfaces that mimic the naturally occurring hierarchy with an emphasis on microfabrication strategies, material choice and the adhesive performance achieved.

The oxides of the transition metal molybdenum exhibit excellent antimicrobial properties. We present the preparation of molybdenum trioxide dihydrate (MoO3 × 2H2O) by an acidification method and demonstrate the thermal phase development and morphological evolution during and after calcination from 25 °C to 600 °C. The thermal dehydration of the material was found to proceed in two steps. Microbiological roll-on tests using Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa were performed and exceptional antimicrobial activities were determined for anhydrous samples with orthorhombic lattice symmetry and a large specific surface area. The increase in the specific surface area is due to crack formation and to the loss of the hydrate water after calcination at 300 °C. The results support the proposed antimicrobial mechanism for transition metal oxides, which based on a local acidity increase as a consequence of the augmented specific surface area.