Effect of Amorphous-Crystalline Phase Transition on Superlubric Sliding.

Structural superlubricity describes the state of greatly reduced friction between incommensurate atomically flat surfaces. Theory predicts that, in the superlubric state, the remaining friction sensitively depends on the exact structural configuration. In particular the friction of amorphous and crystalline structures for, otherwise, identical interfaces should be markedly different.

Nanoscale Friction across the First-Order Charge Density Wave Phase Transition of 1T-TaS.

Nanotribology using atomic force microscopy (AFM) can be considered as a unique approach to analyze phase transition materials by localized mechanical interaction. In this work, we investigate friction on the lamellar transition metal dichalcogenide 1T-TaS, which can undergo first-order charge density wave (CDW) phase transitions. Based on temperature-dependent atomic force microscopy under ultrahigh vacuum conditions (UHV), we can characterize the general friction levels across the first-order phase transitions and for the different phases.

Characterization of Vegard strain related to exceptionally fast Cu-chemical diffusion in Cu[Formula: see text]Mo[Formula: see text]S[Formula: see text] by an advanced electrochemical strain microscopy method.

Electrochemical strain microscopy (ESM) has been developed with the aim of measuring Vegard strains in mixed ionic-electronic conductors (MIECs), such as electrode materials for Li-ion batteries, caused by local changes in the chemical composition. In this technique, a voltage-biased AFM tip is used in contact resonance mode. However, extracting quantitative strain information from ESM experiments is highly challenging due to the complexity of the signal generation process.

Thermal Activation of Nanoscale Wear.

Nanoscale wear tracks on ionic crystals are created by reciprocating single asperity scratch tests using atomic force microscopy. The wear characteristics are analyzed by the scratch depth as a function of surface temperature from 25 to 300 K. The average wear depth shows a nonmonotonic behavior as a function of temperature, with a transition between two different regimes characterized by the occurrence of quasiperiodic ripple formation.

Single-asperity sliding friction across the superconducting phase transition.

In sliding friction, different energy dissipation channels have been proposed, including phonon and electron systems, plastic deformation, and crack formation. However, how energy is coupled into these channels is debated, and especially, the relevance of electronic dissipation remains elusive. Here, we present friction experiments of a single-asperity sliding on a high- superconductor from 40 to 300 kelvin.

Lattice Discontinuities of 1T-TaS across First Order Charge Density Wave Phase Transitions.

Transition metal dichalcogenides are lamellar materials which can exhibit unique and remarkable electronic behavior due to effects of electron-electron and electron-phonon coupling. Among these materials, 1T-tantalum disulfide (1T-TaS) has spurred considerable interest, due to its multiple first order phase transitions between different charge density wave (CDW) states. In general, the basic effects of charge density wave formation in 1T-TaS can be attributed to in plane re-orientation of Ta-atoms during the phase transitions.

Nanoscale Characterization of Ion Mobility by Temperature-Controlled Li-Nanoparticle Growth.

Detailed understanding of electrochemical transport processes on the nanoscale is considered not only as a topic of fundamental scientific interest but also as a key to optimize material systems for application in electrochemical energy storage. A prominent example is solid-state electrolytes, where transport properties are strongly influenced by the microscopic structure of grain boundaries or interface regimes. However, direct characterization of ionic transport processes on the nanoscale remains a challenge.

Limitations of Structural Superlubricity: Chemical Bonds versus Contact Size.

Structural superlubricity describes the state of virtually frictionless sliding if two atomically flat interfaces are incommensurate, that is, they share no common periodicity. Despite the exciting prospects of this low friction phenomenon, there are physical limitations to the existence of this state. Theory predicts that the contact size is one fundamental limit, where the critical size threshold mainly depends on the interplay between lateral contact compliance and interface interaction energies.

Time Strengthening of Crystal Nanocontacts.

We demonstrate how an exponentially saturating increase of the contact area between a nanoasperity and a crystal surface, occurring on time scales governed by the Arrhenius equation, is consistent with measurements of the static friction and lateral contact stiffness on a model alkali-halide surface at different temperatures in ultrahigh vacuum. The "contact ageing" effect is attributed to atomic attrition and is eventually broken by thermally activated slip of the nanoasperity on the surface. The combination of the two effects also leads to regions of strengthening and weakening in the velocity dependence of the friction, which are well-reproduced by an extended version of the Prandtl-Tomlinson model.

Nanotribological Properties of Hexadecanethiol Self-Assembled Monolayers on Au(111): Structure, Temperature, and Velocity.

Self-assembled monolayers (SAM) are promising building blocks for the optimization of a large variety of systems both on the nano- and on the microscale. Among other applications, SAM are often used as protective coating or friction modifiers. In this work, we have used hexadecanethiol SAM on Au(111) as a model system and studied the different mechanisms of energy dissipation during temperature and velocity dependent friction force microscopy (FFM).

Universal Aging Mechanism for Static and Sliding Friction of Metallic Nanoparticles.

The term "contact aging" refers to the temporal evolution of the interface between a slider and a substrate usually resulting in increasing friction with time. Current phenomenological models for multiasperity contacts anticipate that such aging is not only the driving force behind the transition from static to sliding friction, but at the same time influences the general dynamics of the sliding friction process. To correlate static and sliding friction on the nanoscale, we show experimental evidence of stick-slip friction for nanoparticles sliding on graphite over a wide dynamic range.

Influence of contact aging on nanoparticle friction kinetics.

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.

Scaling laws of structural lubricity.

"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.

Spinning and translational motion of Sb nanoislands manipulated on MoS2.

Antimony nanoislands grown on a MoS2 surface in ultra-high vacuum have been manipulated by atomic force microscopy (AFM) in ambient conditions. The island profiles have been digitized and provided as an input to a collisional algorithm based on classical mechanics. Assuming that the islands are rigid and static friction is high enough to prevent further motion after the passage of the probing tip, the direction of motion and the angle of rotation of the islands have been reproduced numerically.

Tuning the instability in static mode atomic force spectroscopy as obtained in an AFM by applying an electric field between the tip and the substrate.

We have investigated experimentally the role of cantilever instabilities in determination of the static mode force-distance curves in presence of a dc electric field. The electric field has been applied between the tip and the sample in an atomic force microscope working in ultra-high vacuum. We have shown how an electric field modifies the observed force (or cantilever deflection)-vs-distance curves, commonly referred to as the static mode force spectroscopy curves, taken using an atomic force microscope.

Understanding frictional duality and bi-duality: Sb-nanoparticles on HOPG.

Antimony nanoparticles deposited under UHV conditions on HOPG are found to exhibit an intriguing frictional behavior characterized by a distinct clearly separated double dual behavior of dependence of the frictional force on contact area. We present the first realistic simulations, density functional modeling adapted to accommodate van der Waals interactions, of the (double) dual frictional behavior. The simulations provide insights into the physics/chemistry of all the frictional branches in terms of incommensurable interfaces, mobile spacer molecules as well as a novel concept of mobile oxidized multi-nanoasperities.

The effect of intrinsic instability of cantilever on static mode atomic force spectroscopy.

We show that the static force spectroscopy curve taken in an atomic force microscope is significantly modified due to presence of intrinsic cantilever instability which occurs as a result of its movement in a nonlinear force field. This instability acts in tandem with such instabilities as water bridge or molecular bond rupture and makes the static force spectroscopy curve (including 'jump-off-contact') dependent on the step size of data collection. A theoretical model has been proposed to explain the data.

Frictional duality observed during nanoparticle sliding.

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.