Synthetic polymers are widely used materials, as attested by a production of more than 200 millions of tons per year, and are typically composed of linear repeat units. They may also be branched or irregularly crosslinked. Here, we introduce a two-dimensional polymer with internal periodicity composed of areal repeat units. This is an extension of Staudinger's polymerization concept (to form macromolecules by covalently linking repeat units together), but in two dimensions. A well-known example of such a two-dimensional polymer is graphene, but its thermolytic synthesis precludes molecular design on demand. Here, we have rationally synthesized an ordered, non-equilibrium two-dimensional polymer far beyond molecular dimensions. The procedure includes the crystallization of a specifically designed photoreactive monomer into a layered structure, a photo-polymerization step within the crystal and a solvent-induced delamination step that isolates individual two-dimensional polymers as free-standing, monolayered molecular sheets.

Sheets and rational synthesis are not like fire and water! Hexafunctional terpyridine monomers can be laterally connected by metal salts to result in a mechanically stable, sheetlike entity that can be transferred from the air/water interface to a solid substrate (see the folded, ca. 1.4 nm thin film) and spanned over micrometer‐sized holes. This result is considered an important step on the way to 2D polymers.

Key in powder-bed-based additive manufacturing is the use of appropriate powder materials that fit to the process conditions. There are many parameters affecting the build process and the corresponding quality of the parts being built. Therefore, an accurate assessment of the powders becomes important. Such an assessment involves, besides others, the powder flowability, which should be sufficient in order to create good-quality powder layers. The current study aims at the development of suitable parameters and values for the qualification of metal powders for selective laser melting (SLM) with regard to their flowability. The powder flowability is assessed by the statistical analysis of the measured powder avalanche angles and the powder surface fractal, which give valuable information about the significance of inter-particle forces. A set of 21 different Fe-and Ni-based powders has been analysed and good correlations between the powder avalanche angles, the surface fractal and the particle shape with the optically evaluated flowability could be derived. The method allows a quantitative powder flowability assessment, which correlates with the experiences for powders for powder-bed-based additive manufacturing, especially for SLM.

Lipid domains in supported lipid layers serve as a popular model to gain insight into the processes associated with the compartmentalization of biological membranes into so-called lipid rafts. In this paper, we present reproducible tip-enhanced Raman spectra originating from a very small number of molecules in a lipid monolayer on a gold surface, probed by the apex of a nanometer-sized silver tip. For the first time, we show large (128 × 128 pixels), high-resolution (< 50 nm) tip-enhanced Raman images of binary lipid mixtures with full spectral information at each pixel.

Oligofunctional terpyridine-based monomers are spread at an air/water interface, where they are connected with transition metal salts such as Fe(II) into mechanically coherent monolayer sheets of macroscopic dimension. The conversions of these processes are determined by XPS for several monomer/metal ion combinations. The sheets are transferred onto TEM grids, the 20 × 20 square micrometer sized holes of which can be spanned. AFM indentation experiments provide in-plane elastic moduli which are compared with naturally occurring sheets such as graphene. The new organometallic sheets are also used to create multilayer assemblies on square centimeter length scales on solid substrates. Finally some directions are provided where this research can lead to in future and where its application potential lies.