On the structure of thin4He films on solid hydrogen

We have investigated the adsorption of4He onto a quench-condensed H2 film by means of surface state electrons. Oscillations in the surface state electron conductivity clearly reveal the layerwise character of the adsorption. At temperatures below 2K we have observed an anomaly in the conductivity around the completion of the first monolayer. This new feature is interpreted as an indication of a liquid-to-solid phase transition in the first layer

Step roughness on Ag(111) investigated by STM: a systematic study of tip influence

We have investigated monatomic steps on Ag(111) by STM at different temperatures. At room temperature, the rough appearance of these steps is usually attributed to thermal step fluctuations. We have investigated the influence of the tip systematically. Applying a new test, we demonstrate that even subtle influences can lead to wrong results in statistical analysis

A simple, ultrahigh vacuum compatible scanning tunneling microscope for use at variable temperatures

We present the construction of a very compact scanning tunneling microscope (STM) which can be operated at temperatures between 4 and 350 K. The tip and a tiny tip holder are the only movable parts, whereas the sample and the piezoscanner are rigidly attached to the body of the STM. This leads to an excellent mechanical stability. The coarse approach system relies on the slip-stick principle and is operated by the same piezotube which is used for scanning. As an example of the performance of the device, images of a NbSe2 surface with atomic resolution are obtained

Influence of confinement by smooth and rough walls on particle dynamics in dense hard-sphere suspensions

We used video microscopy and particle tracking to study the dynamics of confined hard-sphere suspensions. Our fluids consisted of 1.1-μm-diameter silica spheres suspended at volume fractions of 0.33–0.42 in water-dimethyl sulfoxide. Suspensions were confined in a quasiparallel geometry between two glass surfaces: a millimeter-sized rough sphere and a smooth flat wall. First, as the separation distance (H) is decreased from 18 to 1 particle diameter, a transition takes place from a subdiffusive behavior (as in bulk) at large H, to completely caged particle dynamics at small H. These changes are accompanied by a strong decrease in the amplitude of the mean-square displacement (MSD) in the horizontal plane parallel to the confining surfaces. In contrast, the global volume fraction essentially remains constant when H is decreased. Second, measuring the MSD as a function of distance from the confining walls, we found that the MSD is not spatially uniform but smaller close to the walls. This effect is the strongest near the smooth wall where layering takes place. Although confinement also induces local variations in volume fraction, the spatial variations in MSD can be attributed only partially to this effect. The changes in MSD are predominantly a direct effect of the confining surfaces. Hence, both the wall roughness and the separation distance (H) influence the dynamics in confined geometries

Measuring Advection and Diffusion of Colloids in Shear Flow

An analysis of the dynamics of colloids in shear flow can be challenging because of the superposition of diffusion and advection. We present a method that separates the two motions, starting from the time-dependent particle coordinates. The restriction of the tracking to flow lanes and the subtraction of estimated advective displacements are combined in an iterative scheme that eventually makes the spatial segmentation redundant. Tracking errors due to the neglect of lateral diffusion are avoided, while drifts parallel and perpendicular to the flow are eliminated. After explaining the principles of our method, we validate it against both computer simulations and experiments. A critical overall test is provided by the mean square displacement function at high Peclet numbers (up to 50). We demonstrate via simulations how the measurement accuracy depends on diffusion coefficients and flow rates, expressed in units of camera pixels and frames. Also, sample-specific issues are addressed: inaccuracies in the velocity profile for dilute suspensions (volume fraction ≤0.03) and tracking errors for concentrated ones (VF ≥ 0.3). An analysis of experiments with colloidal spheres flowing through microchannels corroborates these findings and indicates perspectives for studies on transport, mixing, or rheology in microfluidic environments

Charge inversion and colloidal stability of carbon black in battery electrolyte solutions

Colloids and Surfaces A: Physicochemical and Engineering Aspects is an international journal devoted to the science of the fundamentals, engineering fundamentals, and applications of colloidal and interfacial phenomena and processes. The journal aims at publishing research papers of high quality and lasting value. In addition, the journal contains critical review papers by acclaimed experts, brief notes, letters, book reviews, and announcements. Basic areas of interest include the following: theory and experiments on fluid interfaces; adsorption; surface aspects of catalysis; dispersion preparation, characterization and stability; aerosols, foams and emulsions; surfaces forces; micelles and microemulsions; light scattering and spectroscopy; detergency and wetting; thin films, liquid membranes and bilayers; surfactant science; polymer colloids; rheology of colloidal and disperse systems; electrical phenomena in interfacial and disperse systems. These and related areas are rich and broadly applicable to many industrial, biological and agricultural systems. Of interest are applications of colloidal and interfacial phenomena in the following areas: separation processes; materials processing; biological systems (see also companion publication Colloids and Surfaces B: Biointerfaces); environmental and aquatic systems; minerals extraction and metallurgy; paper and pulp production; coal cleaning and processing; oil recovery; household products and cosmetics; pharmaceutical preparations; agricultural, soil and food engineering; chemical and mechanical engineering

Extracting local surface charges and charge regulation behavior from atomic force microscopy measurements at heterogeneous solid-electrolyte interfaces

We present a method to determine the local surface charge of solid–liquid interfaces from Atomic Force Microscopy (AFM) measurements that takes into account shifts of the adsorption/desorption equilibria of protons and ions as the cantilever tip approaches the sample. We recorded AFM force distance curves in dynamic mode with sharp tips on heterogeneous silica surfaces partially covered by gibbsite nano-particles immersed in an aqueous electrolyte with variable concentrations of dissolved NaCl and KCl at pH 5.8. Forces are analyzed in the framework of Derjaguin–Landau–Verwey–Overbeek (DLVO) theory in combination with a charge regulation boundary that describes adsorption and desorption reactions of protons and ions. A systematic method to extract the equilibrium constants of these reactions by simultaneous least-squared fitting to experimental data for various salt concentrations is developed and is shown to yield highly consistent results for silica-electrolyte interfaces. For gibbsite-electrolyte interfaces, the surface charge can be determined, yet, an unambiguous identification of the relevant surface speciation reactions is not possible, presumably due to a combination of intrinsic chemical complexity and heterogeneity of the nano-particle surfaces