arXiv subjects

Karin Jacobs

Publications and source records attributed to Karin Jacobs.

At least 19 recordsLinked to original sources

arXiv2023

Impact of geometry on chemical analysis exemplified for photoelectron spectroscopy of black silicon

For smooth surfaces, chemical composition can be readily analyzed using various spectroscopic techniques, a prominent example is X-ray photoelectron spectroscopy (XPS), where the relative proportions of the elements are mainly determined by the intensity ratio of the element-specific photoelectrons. However, this analysis becomes more complex for nanorough surfaces like black silicon (b-Si) due to the geometry's steep slopes, which mimic local variations in emission angles. In this study, we explicitly quantify this effect through an integral geometric analysis using Minkowski tensors, correlating XPS chemical data with topographical information from Atomic Force Microscopy (AFM). This approach yields reliable estimates of layer thicknesses for nanorough surfaces. For b-Si, we found that the oxide layer is approximately 50% thicker than the native oxide layer on a standard Si wafer. This study underscores the significant impact of nanoscale geometries on chemical property analysis.

cond-mat.mes-hall↗

arXiv2017

Unwanted electroless zinc plating on current collectors in zinc air batteries

The occurrence of metallic film deposition without external power supply on the copper current collector of a zinc air battery half-cell containing zinc slurry is investigated. Therefore, test specimens of miscellaneous materials representing the current collector are immersed in a commercial available zinc slurry as well as an in self-prepared zinc slurry. In case of copper and metals which are more noble (silver and gold), a coating on the respective specimen is obtained. An element mapping of the coated copper specimen is performed by means of scanning electron microscopy (SEM) and energy dispersive x-ray spectroscopy (EDX) identifying that the coating layer consists of zinc and oxygen. In order to clarify the crystal structure and the exact composition, focused ion beam (FIB) and x-ray photoelectron spectroscopy (XPS) measurements are applied, proving that the layer consists of elemental zinc, which, is merely oxidized on the surface. Finally, a reaction mechanism for the reversible zinc film deposition is proposed.

cond-mat.mtrl-sci↗

arXiv2017

Nucleated dewetting in supported ultra-thin liquid films with hydrodynamic slip

This study reveals the influence of the surface energy and solid/liquid boundary condition on the breakup mechanism of dewetting ultra-thin polymer films. Using silane self-assembled monolayers, SiO$_2$ substrates are rendered hydrophobic and provide a strong slip rather than a no-slip solid/liquid boundary condition. On undergoing these changes, the thin-film breakup morphology changes dramatically -- from a spinodal mechanism to a breakup which is governed by nucleation and growth. The experiments reveal a dependence of the hole density on film thickness and temperature. The combination of lowered surface energy and hydrodynamic slip brings the studied system closer to the conditions encountered in bursting unsupported films. As for unsupported polymer films, a critical nucleus size is inferred from a free energy model. This critical nucleus size is supported by the film breakup observed in the experiments using high speed \emph{in situ} atomic force microscopy.

cond-mat.soft↗

arXiv2016

Influence of bidisperse self-assembled monolayer structure on the slip boundary condition of thin polymer films

Alkylsilane self-assembled monolayers (SAMs) are often used as model substrates for their ease of preparation and hydrophobic properties. We have observed that these atomically smooth monolayers also provide a slip boundary condition for dewetting films composed of unentangled polymers. This slip length, an indirect measure of the friction between a given liquid and different solids, is switchable and can be increased [Fetzer et al., Phys. Rev. Lett. 2005; Bäumchen et al. J. Phys.: Cond. Matt. 2012] if the alkyl chain length is changed from 18 to 12 backbone carbons, for example. Typically, this change in boundary condition is affected in a quantized way, using one or the other alkyl chain length, thus obtaining one or the other slip length. Here, we present results in which this SAM structure is changed in a continuous way. We prepare SAMs containing bidisperse mixed SAMs of alkyl silanes, with the composition as a control parameter. We find that all the mixed SAMs we investigated show an enhanced slip boundary condition as compared to the single-component SAMs. The slip boundary condition is accessed using optical and atomic force microscopy, and we describe these observations in the context of X-ray reflectivity measurements. The slip length, varying over nearly two orders of magnitude, of identical polymer melts on chemically similar SAMs is found to correlate with the density of exposed alkyl chains. Our results demonstrate the importance of a well characterized solid/liquid pair, down to the angstrom level, when discussing friction between a liquid and a solid.

cond-mat.soft↗

arXiv2016

Enhanced Adhesion of S. Mutans to Hydroxyapatite after Inoculation in Saliva

Streptococcus mutans cells form robust biofilms on human teeth and are strongly related to caries incidents. Hence, understanding the adhesion of S. mutans in the human oral cavity is of major interest for preventive dentistry. In this study, we report on AFM-based single cell force spectroscopy measurements of S. mutans cells to hydroxyapatite surfaces. We observe a significant increase of adhesion strength if S. mutans cells were exposed to human saliva before adhesion. In contrast, Staphylococcus carnosus cells are almost unaffected by the pre-treatment. Our results demonstrate that S. mutans cells are well-adapted to their natural environment, the oral cavity. This ability promotes the biofilm-forming capability of that species and hence the production of caries-provoking acids. In consequence, understanding the fundamentals of this mechanism may pave a way towards more effective caries-reducing techniques.

physics.bio-ph↗

arXiv2016

Slip-Mediated Dewetting of Polymer Microdroplets

Classical hydrodynamic models predict that infinite work is required to move a three-phase contact line, defined here as the line where a liquid/vapor interface intersects a solid surface. Assuming a slip boundary condition, in which the liquid slides against the solid, such an unphysical prediction is avoided. In this article, we present the results of experiments in which a contact line moves and where slip is a dominating and controllable factor. Spherical cap shaped polystyrene microdroplets, with non-equilibrium contact angle, are placed on solid self-assembled monolayer coatings from which they dewet. The relaxation is monitored using \textit{in situ} atomic force microscopy. We find that slip has a strong influence on the droplet evolutions, both on the transient non-spherical shapes and contact line dynamics. The observations are in agreement with scaling analysis and boundary element numerical integration of the governing Stokes equations, including a Navier slip boundary condition.

cond-mat.soft↗

arXiv2015

Influence of Slip on the Plateau-Rayleigh Instability on a Fibre

The Plateau-Rayleigh instability of a liquid column underlies a variety of fascinating phenomena that can be observed in everyday life. In contrast to the case of a free liquid cylinder, describing the evolution of a liquid layer on a solid fibre requires consideration of the solid-liquid interface. In this article, we revisit the Plateau-Rayleigh Instability of a liquid coating a fibre by varying the hydrodynamic boundary condition at the fibre-liquid interface, from no-slip to slip. While the wavelength is not sensitive to the solid-liquid interface, we find that the growth rate of the undulations strongly depends on the hydrodynamic boundary condition. The experiments are in excellent agreement with a new thin film theory incorporating slip, thus providing an original, quantitative and robust tool to measure slip lengths.

physics.flu-dyn↗

arXiv2012

Solid Surface Structure Affects Liquid Order at the Polystyrene/SAM Interface

We present a combined x-ray and neutron reflectivity study characterizing the interface between polystyrene (PS) and silanized surfaces. Motivated by the large difference in slip velocity of PS on top of dodecyl-trichlorosilane (DTS) and octadecyl-trichlorosilane (OTS) found in previous studies, these two systems were chosen for the present investigation. The results reveal the molecular conformation of PS on silanized silicon. Differences in the molecular tilt of OTS and DTS are replicated by the adjacent phenyl rings of the PS. We discuss our findings in terms of a potential link between the microscopic interfacial structure and dynamic properties of polymeric liquids at interfaces.

cond-mat.soft↗

arXiv2012

Self-assembled silane monolayers: A step-by-step high speed recipe for high-quality, low energy surfaces

Silanization bases on the adsorption, selfassembly and covalent binding of silane molecules onto surfaces, resulting in a densely packed self-assembled monolayer (SAM). Following standard recipes, however, the quality of the monolayer is often variable and therefore unsatisfactory. The process of self-assembly is highly affected by the chemicals involved in the wet-chemical process, by the ambient parameters during preparation such as humidity or temperature and by possibly present contaminants (or impurities). Here, we present a reliable, efficient, and wet-chemical recipe for the preparation of ultra-smooth, highly ordered alkylterminated silane SAMs on Si wafers.

cond-mat.mtrl-sci↗

arXiv2012

Is adhesion superficial? Silicon wafers as a model system to study van der Waals interactions

Adhesion is a key issue for researchers of various fields, it is therefore of uppermost importance to understand the parameters that are involved. Commonly, only surface parameters are employed to determine the adhesive forces between materials. Yet, van der Waals forces act not only between atoms in the vicinity of the surface, but also between atoms in the bulk material. In this review, we describe the principles of van der Waals interactions and outline experimental and theoretical studies investigating the influence of the subsurface material on adhesion. In addition, we present a collection of data indicating that silicon wafers with native oxide layers are a good model substrate to study van der Waals interactions with coated materials.

cond-mat.mtrl-sci↗

arXiv2012

Slippage and Nanorheology of Thin Liquid Polymer Films

Thin liquid films on surfaces are part of our everyday life, they serve e.g. as coatings or lubricants. The stability of a thin layer is governed by interfacial forces, described by the effective interface potential, and has been subject of many studies in the last decades. In recent years, the dynamics of thin liquid films came into focus since results on the reduction of the glass transition temperature raised new questions on the behavior of especially polymeric liquids in confined geometries. The new focus was fired by theoretical models that proposed significant implication of the boundary condition at the solid/liquid interface on the dynamics of dewetting and the form of a liquid front. Our study reflects these recent developments and adds new experimental data to corroborate the theoretical models. To probe the solid/liquid boundary condition experimentally, different ways are possible, each bearing advantages and disadvantages, which will be discussed. Studying liquid flow on a variety of different substrates entails a view on the direct implications of the substrate, the experimental focus of this study is the variation of the polymer chain length: The results demonstrate that inter-chain entanglements and in particular their density close to the interface, originating from non-bulk conformations, govern liquid slip of a polymer.

cond-mat.soft↗

arXiv2008

Elemental depth profiling of fluoridated hydroxyapatite by X-ray photoelectron spectroscopy

Structural and chemical changes that arise from a fluoridation of synthetic hydroxyapatite in neutral and acidic fluoridation agents are investigated. For synthetic hydroxyapatite (Ca5(PO4)3OH = HAp), the elemental depth profiles were determined by X-ray photoelectron spectroscopy (XPS) to reveal the effect of fluoridation in nearly neutral (pH = 6.2) and acidic agents (pH = 4.2). Due to the high surface sensitivity of the technique, the depth profiles have a resolution on the nm scale. With respect to the chemical composition and the crystal structure XPS depth profiling revealed very different effects of the two treatments. In both cases, however, the fluoridation affects the surface only on the nm scale which is in contrast to recent literature, where a penetration depth up to several microns was reported. Moreover, evidence is given that the actual fluoridation depth depends on the pH value. Recently, a qualitative three layer model was proposed for the fluoridation of HAp in an acidic agent. In addition to the elemental depth profile, as presented also by various other authors, we present a quantitative depth profile of the compounds CaF2, Ca(OH)2 and fluorapatite (FAp) that are predicted by the three layer model. The analysis of our experimental data exactly reproduces the structural order of the model, however, on a scale that differs by nearly two orders of magnitude from previous predictions. Our results also reveal that the amount of Ca(OH)2 and FAp is small as compared to that of CaF2. Therefore, it has to be questioned whether such narrow Ca(OH)2 and FAp layers really can act as protective layers for the enamel.

cond-mat.mtrl-sci↗

arXiv2008

Comprehensive Analysis of Dewetting Profiles to Quantify Hydrodynamic Slip

Hydrodynamic slip of Newtonian liquids is a new phenomenon, the origin of which is not yet clarified. There are various direct and indirect techniques to measure slippage. Here we describe a method to characterize the influence of slippage on the shape of rims surrounding growing holes in thin polymer films. Atomic force microscopy is used to study the shape of the rim; by analyzing its profile and applying an appropriate lubrication model we are able to determine the slip length for polystyrene films. In the experiments we study polymer films below the entanglement length that dewet from hydrophobized (silanized) surfaces. We show that the slip length at the solid/liquid interface increases with increasing viscosity. The correlation between viscosity and slip length is dependent on the type of silanization. This indicates a link between the molecular mechanism of the interaction of polymer chains and silane molecules under flow conditions that we will discuss in detail.

cond-mat.soft↗

arXiv2008

Stability and dewetting of thin liquid films

The stability of thin liquid coatings is of fundamental interest in every- day life. Homogeneous and non-volatile liquid coatings may dewet either by heterogeneous nucleation, thermal nucleation, or spinodal dewetting. Wetting and dewetting is explained on a fundamental level, including a discussion of relevant interactions. The article will also address the various dewetting scenarios and explain how the effective interface potential governs the behavior obtained for various stratified substrates and film thicknesses.

cond-mat.soft↗

arXiv2007

Impact of Short- and Long-range Forces on Protein Conformation and Adsorption Kinetics

We have studied the adsorption kinetics of the protein amylase at solid/liquid interfaces. Offering substrates with tailored properties, we are able to separate the impact of short- and long-range interactions. By means of a colloidal Monte Carlo approach including conformational changes of the adsorbed proteins induced by density fluctuations, we develop a scenario that is consistent with the experimentally observed three-step kinetics on specific substrates. Our observations show that not only the surface chemistry determines the properties of an adsorbed protein layer but also the van der Waals contributions of a composite substrate may lead to non-negligible effects.

cond-mat.soft↗

arXiv2002

Generic morphologies of viscoelastic dewetting fronts

A simple model is put forward which accounts for the occurrence of certain generic dewetting morphologies in thin liquid coatings. It demonstrates that by taking into account the elastic properties of the coating, a morphological phase diagram may be derived which describes the observed structures of dewetting fronts. It is demonstrated that dewetting morphologies may also serve to determine nanoscale rheological properties of liquids.

cond-mat.soft↗

arXiv2001

Dynamical pattern formation upon dewetting

Dewetting of thin liquid films is monitored in situ by atomic force microscopy, results are compared with simulations. The experimental setting is mimicked as close as possible using the experimental parameters including the effective interface potential. Numerics for the thin film equation are based on recently developed schemes which are up to now the only methods convergent in all relevant space dimensions. Temporal evolution and morphology of experiment and simulation are compared quantitatively. Our results explain the origin of complex generic patterns that evolve upon dewetting.

cond-mat.soft↗

arXiv2001

Nucleation Induced Undulative Instability in Thin Films of nCB Liquid Crystals

A surface instability is reported in thin nematic films of 5CB and 8CB, occurring near the nematic--isotropic phase transition. Although this instability leads to patterns reminiscent of spinodal dewetting, we show that it is actually based on a nucleation mechanism. Its characteristic wavelength does not depend markedly on film thickness, but strongly on the heating rate.

cond-mat.soft↗