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One of the oldest concepts in tribology is stick-slip dynamics, where a disruptive sequence of stick and slip phases determine the overall resistance in sliding friction. While the mechanical energy dissipates in the sudden slip phase, the stick phase has been shown to be characterized by contact strengthening mechanisms, also termed contact aging. We present experiments of sliding nanoparticles, where friction is measured as a function of sliding velocity and interface temperature. The resulting complex interdependence is in good agreement with Monte Carlo simulations, in which the energy barrier for contact breaking increases logarithmically with time, at a rate governed by thermal activation.

"Structural lubricity" refers to a unique friction state in which two flat surfaces are sliding past each other with ultralow resistance due to incommensurate atomic lattice structures. In this case, theory anticipates sublinear scaling for the area dependence of friction. Here, we experimentally confirm these predictions by measuring the sliding resistance of amorphous antimony and crystalline gold nanoparticles on crystalline graphite. For the amorphous particles a square root relation between friction and contact area is observed. For crystalline gold particles we find a more complex scaling behavior related to variations in particle shape and orientation. These results allow us to link mesoscopic friction to atomic principles.

In the ongoing effort to miniaturize the functional elements in electronic devices, molecular dimensions are currently approached. Scanning probe microscopy has demonstrated fascinating capabilities for bottom-up fabrication of atomically defined prototype structures. However, little is known about the underlying interactions during the manipulation of functional organic molecules with a scanning probe tip. Here, we demonstrate the use of noncontact atomic force microscopy at cryogenic temperatures for the lateral displacement of the organic prototype molecule 3,4,9,10-perylene-tetracarboxylicacid-dianhydride on the Ag(111) surface. During repeated manipulation cycles, we measure the precise lateral and vertical tip-molecule force profiles as well as the energy dissipation before and during the manipulation process. The jump of the molecule to an adjacent equivalent substrate lattice site occurs in the regime of repulsive lateral forces, thus constituting a "pushing" mechanism.

We report on a bottom-up approach of the selective and precise growth of subnanometer wide straight and chevron-type armchair nanoribbons (GNRs) on a stepped Au(788) surface using different specific molecular precursors. This process creates spatially well-aligned GNRs, as characterized by STM. High-resolution direct and inverse photoemission spectroscopy of occupied and unoccupied states allows the determination of the energetic position and momentum dispersion of electronic states revealing the existence of band gaps of several electron volts for straight 7-armchair, 13-armchair, and chevron-type GNRs in the electronic structure.

We report experiments of atomic stick-slip friction on graphite as an explicit function of surface temperature between 100 and 300 K under ultrahigh vacuum conditions. A statistical analysis of the individual stick-slip events as a function of the velocity reveals an agreement with the thermally activated Prandtl-Tomlinson model at all temperatures. Taking into account an explicit temperature-dependence of the attempt frequency all data points collapse onto one single master curve.

One of the most fundamental questions in tribology concerns the area dependence of friction at the nanoscale. Here, experiments are presented where the frictional resistance of nanoparticles is measured by pushing them with the tip of an atomic force microscope. We find two coexisting frictional states: While some particles show finite friction increasing linearly with the interface areas of up to 310 000 nm(2), other particles assume a state of frictionless sliding. The results further suggest a link between the degree of surface contamination and the occurrence of this duality.

Most chemical reactions require activation which is conventionally supplied by heat. In stark contrast, mechanical activation by applied external forces opens intriguing novel possibilities. Here, the first direct comparison of mechanical versus thermal activation of bond breaking is provided. Studying both thiolate-copper interfaces and junctions provides evidence for vastly different reaction pathways and product classes. This is understood in terms of directional mechanical manipulation of coordination numbers and system fluctuations in the process of mechanical activation.

The hopping movements of mobile ions in a nanostructured LiAlSiO4 glass ceramic are characterized by time-domain electrostatic force spectroscopy (TDEFS). While the macroscopic conductivity spectra are governed by a single activation energy, the nanoscopic TDEFS measurements reveal three different dynamic processes with distinct activation energies. Apart from the ion transport processes in the glassy and crystalline phases, we identify a third process with a very low activation energy, which is assigned to ionic movements at the interfaces between the crystallites and glassy phase. Such interfacial processes are believed to play a key role for obtaining high ionic conductivities in nanostructured solid electrolytes.

We report a generally applicable method to pattern organic molecules on mesoscopic scales. In our method, organic molecular beam deposition was conducted on substrate surfaces prepatterned with materials to which the organic molecules have larger binding energies in comparison to the substrate. Fully uniform nucleation control at these predefined locations can be achieved by an appropriate selection of the growth parameters including temperature and deposition rate. The physical mechanisms involved are studied by Monte Carlo simulations and stand in good agreement with the experimental findings.

The lateral forces during stick-slip motion of an atomic force microscope cantilever on highly oriented pyrolytic graphite are measured and analyzed. We identify the regimes where thermally activated interstitial hopping of the cantilever tip proceeds according to a single-step reaction scheme and extract the corresponding force-dependent transition rates directly from the experimental data. We find that such a single-step reaction scenario is valid only at relatively high velocities, while at slower pulling speeds, a more complicated hopping mechanism must be at work. We suggest formation of multiple bonds of the tip-sample contact as a possible candidate for this mechanism.

A key element of functionalizing nanocrystals with organic molecules is the nontemplated selective adsorption of different molecules on different facets. Here we report scanning-tunneling-microscopy images of perylene-3,4,9,10-tetracarboxylic-dianhydride and 2,5-dimethyl-N,N'-dicyanoquinonediimine on silver, demonstrating selective adsorption on different facets. We also report first-principles calculations that account for the data and show that bonding, which controls selectivity, occurs via the end atoms, while the molecule's midregion arches away from the substrate. The results are also consistent with data that have been interpreted in terms of bonding via the midregion.

The potential energy landscape of surfaces governs the dynamics of adsorbed molecules, as well as atomic scale friction processes. We measure the potential energy landscape of a single-atom tip interacting with a vicinal nonconducting NaCl(100) surface in real space using noncontact atomic force microscopy. We find that the shape of the potential energy profile is of sinusoidal form with a barrier height of 48 meV. Furthermore, we observe a discontinuity in the force curves at specific lattice sites, indicating the onset of reversible yet hysteretic mechanical relaxations.

We use low energy electron diffraction, scanning tunneling microscopy, first-principles density-functional theory, and molecular mechanics calculations to analyze the adsorption and growth of quinacridone derivatives (QA) with alkyl chains of 4 and 16 carbon atoms on a Ag(110) substrate. Surprisingly, we find that the alkyl chains determine the orientation of the molecular overlayers. While the interaction of QA and the Ag substrate is primarily due to chemical bonding of oxygen to the silver substrate, determining the molecular orientation and preferred adsorption site, the intermolecular arrangement can be adjusted via the length of alkyl chains. We are thus able to fabricate uniform QA films with very well controlled physical properties.

The atomic-scale stability of clean silicon tips used in noncontact atomic force microscopy (NC-AFM) is simulated by ab initio calculations based on density functional theory. The tip structures are modeled by silicon clusters with and termination. For the often assumed Si(111)-type tip we observe the sharpening of the initially blunt tip via short-range chemical forces during the first approach and retraction cycle. The structural changes corresponding to this intrinsic process are irreversible and lead to stable NC-AFM imaging conditions. In opposition to the picture used in literature, the Si(001)-type tip does not exhibit the so-called "two-dangling bond" feature as a bulklike termination suggests.

We present a probe concept for scanning near-field optical microscopy combining the excellent background suppression of aperture probes with the superior light confinement of apertureless probes. A triangular aperture at the tip of a tetrahedral waveguide (full taper angle approximately 90 degrees ) shows a strong field enhancement at only one rim when illuminated with light of suitable polarization. Compared to a circular aperture of equivalent size, the resolution capability is doubled without loss of brightness. For a approximately 60 nm sized triangular aperture, we measured an optical resolution <40 nm and a transmission of approximately 10(-4).

Car-Parrinello molecular dynamics simulations demonstrate that pulling a single thiolate molecule anchored on a stepped gold surface does not preferentially break the sulfur-gold chemical bond. Instead, it is found that this process leads to the formation of a monoatomic gold nanowire, followed by breaking a gold-gold bond with a rupture force of about 1.2 nN. The simulations also indicate that previous single-molecule thiolate-gold and gold-gold rupture experiments both probe the same phenomenon, namely, the breaking of a gold-gold bond within a gold nanowire.

The conservative and dissipative interaction between an aluminum tip and a gold (111) surface were investigated using dynamic force spectroscopy in UHV. Complete force vs distance curves and friction coefficient vs distance curves were obtained quantitatively. The force curves were compared to the model by Muller, Yushenko, and Derjaguin, and long and short range interactions were subsequently quantified without fit parameters. A short range conservative interaction was separated from longer range van der Waals forces. The long range behavior of the damping coefficient obeys an inverse power law of third order.