In this work the long-term antibacterial activity of silver doped titania coatings is studied systematically as a function of the titania layer structure (with and without molecular template) and the amount and physical properties of the silver dopant. Silver was incorporated in two different ways into the titania sol-gel films, either by co-deposition, i.e., adding the silver ions directly to the precursor sol of the layer or by postsynthetic impregnation of the mesoporous titania coating. The structure and morphology of the layers were investigated using transmission and scanning electron microscopy, whereas the silver content was determined by Rutherford backscattering spectrometry. Antibacterial properties against Escherichia coli bacteria were studied by colony forming unit assay and agar diffusion method. It was found that directly after preparation, all composite coatings show antibacterial activity both in the dark and under visible light illumination. The antibacterial activity of the co-deposited samples vanished after the first use despite their high and constant remaining silver content (2.597 at%). This type of coating was not effective in agar diffusion tests at all. The antibacterial activity of the impregnated coatings with lower silver contents (0.596 at% and 1.961 at%), however, showed long-lasting antibacterial effect both in the colony forming unit assay and in agar diffusion tests as well. This can be attributed to the fact that the silver content is distributed over the mesoporous network of the titania coating and is effective during the long-term tests. Fig. 2 Toluene adsorption-desorption isotherms at 294 K and normalized pore radius distribution of (a and b) TiO 2 , (c and d) pTiO 2 , and (e and f) TiO 2 -AgNO 3 type titania coatings determined by ellipsometric porosimetry.This journal is

To avoid the restrictions of the captive bubble and the Wilhelmy plate techniques, a method was introduced for contact angle measurements under equilibrium conditions. It enables to determine even ultralow contact angles with high precision without prewetting the investigated surface because in this case, the capillary bridge of the test liquid is formed from a pendant drop and used as a probe. The contact angle is determined from the measured capillary force and liquid bridge geometry by using Delaunay's analytical solution. The method was experimentally proved to be valid. As a demonstration, contact angles less than 1°were measured with the uncertainty down to 0.1°on lightly corroded glass surfaces. Moreover, a new observation was obtained in complete wetting situations: the receding contact line starts to advance again during the increase of the bridge length. The contact angle is much lower in this readvancing phase compared to the advancing and receding values because the contact line finds prewetted surface in front of itself. Further advantage of the method is that the existing contact angle goniometers can be developed further into the presented measurement setup.

We extend the orbital-dependent electron tunnelling model implemented within the three-dimensional (3D) Wentzel-Kramers-Brillouin (WKB) atom-superposition approach for simulating scanning tunnelling microscopy (STM) by including arbitrary tip orientations. The orientation of the tip is characterized by a local coordinate system centred on the tip apex atom obtained by a rotation with respect to the sample coordinate system. The rotation is described by the Euler angles. Applying our method, we highlight the role of the real-space shape of the electron orbitals involved in the tunnelling, and analyse the convergence and the orbital contributions of the tunnelling current above the W(110) surface depending on the orientation of a model tungsten tip. We also simulate STM images at constant-current condition, and find that their quality depends very much on the tip orientation. Some orientations result in protrusions on the images that do not occur above W atoms. The presence of such apparent atom positions makes it difficult to identify the exact position of surface atoms. It is suggested that this tip orientation effect should be considered in the evaluation of experimental STM images on other surfaces as well. The presented computationally efficient tunnelling model could prove to be useful for obtaining more information on the local tip geometry and orientation by comparing STM experiments to a large number of simulations with systematically varied tip orientations.

The validity of various effective medium approximations (EMAs) (Bruggeman, Maxwell-Garnett) was studied for nanostructured systems, where the scale of inhomogeneities is comparable to the wavelength. Langmuir-Blodgett (LB) layers of Stöber silica nanospheres of diameters between 40 and 129 nm are excellent model structures for the experimental verification of the validity of the EMA methods in spectroscopic ellipsometry (SE) evaluation. Nanostructured mono- and multilayered silica films were investigated by SE and reflectance spectroscopy. The effective refractive index and film thickness were determined from the results of multiparameter fitting of SE spectra in the 300-759 nm wavelength region. The distribution of the effective refractive index in the particulate films was calculated assuming an ideal close-packed arrangement of particles. The average deviation from such a structure was deduced from the corrected model by introducing a "fill factor". In the EMA approximation, the spherical shape of the silica particle determines the optical behavior, rather than the "depth distribution" of silica or porosity. Therefore, the shape of particles has a dominant effect on the optical properties of nanoparticulate LB films.

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Micropatterning of living single cells and cell clusters over millimeter–centimeter scale areas is of high demand in the development of cell-based biosensors. Micropatterning methodologies require both a suitable biomimetic support and a printing technology. In this work, we present the micropatterning of living mammalian cells on carboxymethyl dextran (CMD) hydrogel layers using the FluidFM BOT technology. In contrast to the ultrathin (few nanometers thick in the dry state) CMD films generally used in label-free biosensor applications, we developed CMD layers with thicknesses of several tens of nanometers in order to provide support for the controlled adhesion of living cells. The fabrication method and detailed characterization of the CMD layers are also described. The antifouling ability of the CMD surfaces is demonstrated by in situ optical waveguide lightmode spectroscopy measurements using serum modeling proteins with different electrostatic properties and molecular weights. Cell micropatterning on the CMD surface was obtained by printing cell adhesion mediating cRGDfK peptide molecules (cyclo­(Arg-Gly-Asp-d-Phe-Lys)) directly from aqueous solution using microchanneled cantilevers with subsequent incubation of the printed surfaces in the living cell culture. Uniquely, we present cell patterns with different geometries (spot, line, and grid arrays) covering both micrometer and millimeter–centimeter scale areas. The adhered patterns were analyzed by phase contrast microscopy and the adhesion process on the patterns was real-time monitored by digital holographic microscopy, enabling to quantify the survival and migration of cells on the printed cRGDfK arrays.

The electronic properties of graphene can be significantly influenced by mechanical strain. One practical approach to induce strain in graphene is to transfer atomically thin membranes onto pre-patterned substrates with specific corrugations. The possibility of using nanoparticles to impart extrinsic rippling to graphene has not been fully explored yet. Here we study the structure and elastic properties of graphene grown by chemical vapour deposition and transferred onto a continuous layer of SiO2 nanoparticles with diameters of around 25 nm, prepared on a Si substrate by the Langmuir-Blodgett technique. We show that the corrugation of the transferred graphene, and thus the membrane strain, can be modified by annealing at moderate temperatures. The membrane parts bridging the nanoparticles are suspended and can be reversibly lifted by the attractive forces between an atomic force microscope tip and graphene. This allows the dynamic control of the local morphology of graphene nanomembranes.

Ordered porous structures for photonic application were fabricated on p-and n-type silicon by means of masking against ion implantation with Langmuir-Blodgett ͑LB͒ films. LB films from Stöber silica spheres ͓J. Colloid Interface Sci. 26, 62 ͑1968͔͒ of 350 nm diameter were applied in the boron and phosphorus ion-implantation step, thereby offering a laterally periodic doping pattern. Ordered porous silicon structures were obtained after performing an anodic etch and were then removed by alkaline etching resulting in the required two-dimensional photonic arrangement. The LB silica masks and the resulting silicon structures were studied by field emission scanning electron microscope analysis.