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Andrea Vanossi

Publications and source records attributed to Andrea Vanossi.

At least 19 recordsLinked to original sources

Striped twisted state in the orientational epitaxy on quasicrystals

The optimal "twisted" geometry of a crystalline layer on a crystal is long known, but that on a quasicrystal is still unknown and open. We predict analytically that the layer equilibrium configuration will generally exhibit a nonzero misfit angle. The theory perfectly agrees with numerical optimization of a colloid monolayer on a quasiperiodic decagonal optical lattice. Strikingly different from crystal-on-crystal epitaxy, the structure of the novel emerging twisted state exhibits an unexpected stripe pattern. Its high anisotropy should reflect on the tribomechanical properties of this unconventional interface.

cond-mat.mes-hall

Can Neural Networks Learn Nanoscale Friction?

Current nanofriction experiments on crystals, both tip-on-surface and surface-on-surface, provide force traces as their sole output, typically exhibiting atomic size stick-slip oscillations. Physically interpreting these traces is a task left to the researcher. Historically done by hand, it generally consists in identifying the parameters of a Prandtl-Tomlinson (PT) model that best reproduces these traces. This procedure is both work-intensive and quite uncertain. We explore in this work how machine learning (ML) could be harnessed to do that job with optimal results, and minimal human work. A set of synthetic force traces is produced by PT model simulations covering a large span of parameters, and a simple neural network (NN) perceptron is trained with it. Once this trained NN is fed with experimental force traces, it will ideally output the PT parameters that best approximate them. By following this route step by step, we encountered and solved a variety of problems which proved most instructive and revealing. In particular, and very importantly, we met unexpected inaccuracies with which one or another parameter was learned by the NN. The problem, we then show, could be eliminated by proper manipulations and augmentations operated on the training force traces, and that without extra efforts and without injecting experimental informations. Direct application to the sliding of a graphene coated AFM tip on a variety of 2D materials substrates validates and encourages use of this ML method as a ready tool to rationalise and interpret future stick-slip nanofriction data.

cond-mat.mes-hall

Emerging chirality and moiré dynamics in twisted layered material heterostructures

Moiré superstructures arising at twisted 2D interfaces have recently attracted the attention of the scientific community due to exotic quantum states and unique mechanical and tribological behaviors that they exhibit. Here, we predict the emergence of chiral distortions in twisted layered interfaces of finite dimensions. This phenomenon originates in intricate interplay between interfacial interactions and contact boundary constraints. A metric termed the fractional chiral area, is introduced to quantify the overall chirality of the moiré superstructure and to characterize its spatial distribution. Despite the equilibrium nature of the discovered energetic and structural chirality effects they are shown to be manifested in the twisting dynamics of layered interfaces, which demonstrates a continuous transition from stick-slip to smooth rotation with no external trigger.

cond-mat.mes-hall

Effective stick-slip parameter for structurally lubric 2D interface friction

The wear-free sliding of layers or flakes of graphene-like 2D materials, important in many experimental systems, may occur either smoothly or through stick-slip, depending on driving conditions, corrugation, twist angles, as well as edges and defects. No single parameter has been so far identified to discriminate a priori between the two sliding regimes. Such a parameter, $η$, does exist in the ideal (Prandtl-Tomlinson) problem of a point particle sliding across a 1D periodic lattice potential. In that case $η>1$ implies mechanical instability, generally leading to stick-slip, with $η= \frac{2π^2 U_0}{K_\mathrm{p} a^2}$, where $U_0$ is the potential magnitude, $a$ the lattice spacing, and $K_\mathrm{p}$ the pulling spring constant. Here we show, supported by a repertoire of graphene flake/graphene sliding simulations, that a similar stick-slip predictor $η_\mathrm{eff}$ can be defined with the same form but suitably defined $U_\mathrm{eff}$, $a_\mathrm{eff}$ and $K_\mathrm{eff}$. Remarkably, simulations show that $a_\mathrm{eff} = a$ of the substrate remains an excellent approximation, while $K_\mathrm{eff}$ is an effective stiffness parameter, combining equipment and internal elasticity. Only the effective energy barrier $U_\mathrm{eff}$ needs to be estimated in order to predict whether stick-slip sliding of a 2D island or extended layer is expected or not. In a misaligned defect-free circular graphene sliding island of contact area $A$, we show that $U_\mathrm{eff}$, whose magnitude for a micrometer size diameter is of order 1 eV, scales as $A^{1/4}$, thus increasing very gently with size. The PT-like parameter $η_\mathrm{eff}$ is therefore proposed as a valuable tool in 2D layer sliding.

cond-mat.mtrl-sci

Sliding friction and superlubricity of colloidal AFM probes coated by tribo-induced graphitic transfer layers

Colloidal probe Atomic Force Microscopy (AFM) allows to explore sliding friction phenomena in graphite contacts of nominal lateral size up to hundreds of nanometers. It is known that contact formation involves tribo-induced material transfer of graphite flakes from the graphitic substrate to the colloidal probe. In this context, sliding states with nearly-vanishing friction, i.e. superlubricity, may set in. A comprehensive investigation of the transfer layer properties is mandatory to ascertain the origin of superlubricity. Here we explore the friction response of micrometric beads, of different size and pristine surface roughness, sliding on graphite under ambient conditions. We show that such tribosystems undergo a robust transition towards a low-adhesion, low-friction state dominated by mechanical interactions at one dominant tribo-induced nanocontact. Friction force spectroscopy reveals that the nanocontact can be superlubric or dissipative, in fact undergoing a load-driven transition from dissipative stick-slip to continuous superlubric sliding. This behavior is excellently described by the thermally-activated, single-asperity Prandtl-Tomlinson model. Our results indicate that upon formation of the transfer layer, friction depends on the energy landscape experienced by the topographically-highest tribo-induced nanoasperity. Consistently we find larger dissipation when the tribo-induced nanoasperity is sled against surfaces with higher atomic corrugation than graphite, like MoS2 and WS2, in prototypical Van der Waals layered hetero-junctions.

cond-mat.mes-hall

Rheological softening of metal nanocontacts sheared under oscillatory strains

The way metal interfaces evolve during frictional sliding, and how that evolution can be externally influenced under external drivers are important questions, hard to investigate experimentally because the contacts themselves are generally difficult to access. Here we focus on an elementary constituent of a general metal-metal interface, namely an ultra-thin individual nanocontact, where recent rheological studies of crystalline gold nanocontacts [Nature 569, 393 (2019)] showed a dramatic and unexpected mechanical softening as a result of external oscillatory tensile stress. The question which we address through realistic nonequilibrium molecular dynamics simulations is to what extent such mechanical softening might influence the shearing habit of gold nanocontacts at room temperature. It is found that the shearing evolution, which occurs through a series of discrete slips, is indeed rheologically softened, even though not completely, by the oscillations. Differences also emerge for different types of external oscillation, tensile or rotational. The relevance of these results for future experiments will be discussed.

cond-mat.mtrl-sci

Bending Stiffness Collapse, Buckling, Topological Bands of Freestanding Twisted Bilayer Graphene

The freestanding twisted bilayer graphene (TBG) is unstable, below a critical twist angle θ_c~3.7 degrees, against a moire (2 \times 1) buckling distortion at T=0. Realistic simulations reveal the concurrent unexpected collapse of the bending rigidity, an unrelated macroscopic mechanical parameter. An analytical model connects bending and buckling anomalies at T=0, but as temperature rises the former fades, while buckling persists further. The (2 \times 1) electronic properties are also surprising. The magic twist angle narrow bands, now eight in number, fail to show zone boundary splittings despite the new periodicity. Symmetry shows how this is dictated by an effective single valley physics. These structural, critical, and electronic predictions promise to make the freestanding state of TBG especially interesting.

cond-mat.mes-hall

Graphite superlubricity enabled by triboinduced nanocontacts

Colloidal probe Atomic Force Microscopy allows to explore sliding states of vanishing friction, i.e. superlubricity, in mesoscopic graphite contacts. Superlubricity is known to appear upon formation of a triboinduced transfer layer, originated by material transfer of graphene flakes from the graphitic substrate to the colloidal probe. Previous studies suggest that friction vanishes due to crystalline incommensurability at the newly formed interface. However this picture still lacks several details, such as the roles of the tribolayer roughness and of loading conditions. Hereafter we gain deeper insight into the tribological response of micrometric silica beads sliding on graphite under ambient conditions. We show that the tribotransferred flakes behave as lubricious nanoasperities with a twofold role. First, they decrease the silica-graphite true contact area, in fact causing a breakdown of adhesion and friction by one order of magnitude. Second, they govern mechanical dissipation through the specific energy landscape experienced by the topographically-highest triboinduced nanoasperity. Remarkably, such contact junctions can undergo a load-driven atomic-scale transition from continuous superlubric sliding to dissipative stick-slip, that agrees with the single-asperity Prandtl-Tomlinson model. Superlubricity in mesoscopic silica-graphite junctions may therefore arise from the load-controlled competition between interfacial crystalline incommensurability and contact pinning effects at one dominant nanoasperity.

cond-mat.mes-hall

Solid lubrication by wet-transferred solution-processed graphene flakes: dissipation mechanisms and superlubricity in mesoscale contacts

Solution-processed few-layers graphene flakes, dispensed to rotating and sliding contacts via liquid dispersions, are gaining increasing attention as friction modifiers to achieve low friction and wear at technologically-relevant interfaces. Vanishing friction states, i.e. superlubricity, have been documented for nearly-ideal nanoscale contacts lubricated by individual graphene flakes; there is however no clear understanding if superlubricity might persist for larger and morphologically-disordered contacts, as those typically obtained by graphene wet transfer from a liquid dispersion. In this study we address the friction performance of solution-processed graphene flakes by means of colloidal probe Atomic Force Microscopy. We use an additive-free aqueous dispersion to coat micrometric silica beads, which are then sled under ambient conditions against prototypical material substrates, namely graphite and the transition metal dichalcogenides (TMDs) MoS2 and WS2. High resolution microscopy proves that the random assembly of the wet-transferred flakes over the silica probes results into an inhomogeneous coating, formed by graphene patches that control contact mechanics through tens-of-nanometers tall protrusions. Atomic-scale friction force spectroscopy reveals that dissipation proceeds via stick-slip instabilities. Load-controlled transitions from dissipative stick-slip to superlubric continuous sliding may occur for the graphene-graphite homojunctions, whereas single- and multiple-slips dissipative dynamics characterizes the graphene-TMD heterojunctions. Systematic numerical simulations demonstrate that the thermally-activated single-asperity Prandtl-Tomlinson model comprehensively describes friction experiments involving different graphene-coated colloidal probes, material substrates and sliding regimes.

cond-mat.mes-hall

Electric-field frictional effects in confined zwitterionic molecules

We theoretically explore the effect of a transverse electric field on the frictional response of a bi-layer of packed zwitterionic molecules. The dipole-moment reorientation promoted by the electric field can lead to either stick-slip or smooth sliding dynamics, with average shear stress values varying over a wide range. A structure-property relation is revealed by investigating the array of molecules and their mutual orientation and interlocking. Moreover, the thermal friction enhancement previously observed in these molecules is shown to be suppressed by the electric field, recovering the expected thermolubricity at large-enough fields. The same holds for other basic tribological quantities, such as the external load, which can influence friction in opposite ways depending on the strength of the applied electric field. Our findings open a route for the reversible control of friction forces via electric polarization of the sliding surface.

cond-mat.soft

Anisotropic Rheology and Friction of Suspended Graphene

Graphene is a powerful membrane prototype for both applications and fundamental research. Rheological phenomena including indentation, twisting, and wrinkling in deposited and suspended graphene are actively investigated to unravel the mechanical laws at the nanoscale. Most studies focused on isotropic set-ups, while realistic graphene membranes are often subject to strongly anisotropic constraints, with important consequences for the rheology, strain, indentation, and friction in engineering conditions.

cond-mat.mtrl-sci

Sliding and Pinning in Structurally Lubric 2D Material Interfaces

A plethora of two-dimensional (2D) materials entered the physics and engineering scene in the last two decades. Their robust, membrane-like sheet permit -- mostly require -- deposition, giving rise to solid-solid dry interfaces whose bodily mobility, pinning, and general tribological properties under shear stress are currently being understood and controlled, experimentally and theoretically. In this Colloquium we use simulation case studies of twisted graphene system as a prototype workhorse tool to demonstrate and discuss the general picture of 2D material interface sliding. First, we highlight the crucial mechanical difference, often overlooked, between small and large incommensurabilities, corresponding e.g., to small and large twist angles in graphene interfaces. In both cases, focusing on flat, structurally lubric, "superlubric" geometries, we elucidate and review the generally separate scaling with area of static friction in pinned states and of kinetic friction during sliding, tangled as they are with the effects of velocity, temperature, load, and defects. Including the role of island boundaries and of elasticity, and corroborating when possible the existing case-by-case results in literature beyond graphene, the overall picture proposed is meant for general 2D material interfaces, that are of importance for the physics and technology of existing and future bilayer and multilayer systems.

cond-mat.mtrl-sci

Frictionless nanohighways on crystalline surfaces

The understanding of friction at nano-scales, ruled by the regular arrangement of atoms, is surprisingly incomplete. Here we provide a unified understanding by studying the interlocking potential energy of two infinite contacting surfaces with arbitrary lattice symmetries, and extending it to finite contacts. We categorize, based purely on geometrical features, all possible contacts into three different types: a structurally lubric contact where the monolayer can move isotropically without friction, a corrugated and strongly interlocked contact, and a newly discovered directionally structurally lubric contact where the layer can move frictionlessly along one specific direction and retains finite friction along all other directions. This novel category is energetically stable against rotational perturbations and provides extreme friction anisotropy. The finite-size analysis shows that our categorization applies to a wide range of technologically relevant materials in contact, from adsorbates on crystal surfaces to layered two-dimensional materials and colloidal monolayers.

cond-mat.soft

The Smallest Archimedean Screw: Facet Dynamics and Friction in Multi-Walled Nanotubes

We identify a new material phenomenon, where minute mechanical manipulations induce pronounced global structural reconfigurations in faceted multi-walled nanotubes. This behavior has strong implications on the tribological properties of these systems and may be the key to understand the enhanced inter-wall friction recently measured for boron-nitride nanotubes with respect to their carbon counterparts. Notably, the fast rotation of helical facets in these systems upon coaxial sliding may serve as a nanoscale Archimedean screw for directional transport of physisorbed molecules.

cond-mat.mes-hall

Multiwalled nanotube faceting unravelled

Nanotubes show great promise for miniaturizing advanced technologies. Their exceptional physical properties are intimately related to their morphological and crystal structure. Circumferential faceting of multiwalled nanotubes reinforces their mechanical strength and alters their tribological and electronic properties. Here, the nature of this important phenomenon is fully rationalized in terms of interlayer registry patterns. Regardless of the nanotube identity (that is, diameter, chirality, chemical composition), faceting requires the matching of the chiral angles of adjacent layers. Above a critical diameter that corresponds well with experimental results, achiral multiwalled nanotubes display evenly spaced extended axial facets whose number equals the interlayer difference in circumferential unit cells. Elongated helical facets, commonly observed in experiment, appear in nanotubes that exhibit small interlayer chiral angle mismatch. When the wall chiralities are uncorrelated, faceting is suppressed and outer layer corrugation, which is induced by the moiré superlattice, is obtained in agreement with experiments. Finally, we offer an explanation for the higher incidence of faceting in multiwalled boron nitride nanotubes with respect to their carbon-based counterparts.

cond-mat.mes-hall

Critical Peeling of Tethered Nanoribbons

The peeling of an immobile adsorbed membrane is a well known problem in engineering and macroscopic tribology. In the classic setup, picking up at one extreme and pulling off results in a peeling force that is a decreasing function of the pickup angle. As one end is lifted, the detachment front retracts to meet the immobile tail. At the nanoscale, interesting situations arise with the peeling of graphene nanoribbons (GNRs) on gold, as realized, e.g., by atomic force microscopy. The nanosized system shows a constant-force steady peeling regime, where the tip lifting h produces no retraction of the ribbon detachment point, and just an advancement h of the free tail end. This is opposite to the classic case, where the detachment point retracts and the tail end stands still. Here we characterise, by analytical modeling and numerical simulations, a third, experimentally relevant, setup where the nanoribbon, albeit structurally lubric, does not have a freely moving tail end, which is instead elastically tethered. Surprisingly, novel nontrivial scaling exponents appear that regulate the peeling evolution. As the detachment front retracts and the tethered tail is stretched, power laws of h characterize the shrinking of the adhered length the growth of peeling force and the peeling angle. These exponents precede the final total detachment as a critical point, where the entire ribbon eventually hangs suspended between the tip and tethering spring. These analytical predictions are confirmed by realistic MD simulations, retaining the full atomistic description, also confirming their survival at finite experimental temperatures.

cond-mat.mes-hall

Moiré-pattern evolution couples rotational and translational friction at crystalline interfaces

The sliding motion of objects is typically governed by their friction with the underlying surface. Compared to translational friction, however, rotational friction has received much less attention. Here, we experimentally and theoretically study the rotational depinning and orientational dynamics of two-dimensional colloidal crystalline clusters on periodically corrugated surfaces in the presence of magnetically exerted torques. We demonstrate that the traversing of locally commensurate areas of the moiré pattern through the edges of clusters, which is hindered by potential barriers during cluster rotation, controls its rotational depinning. The experimentally measured depinning thresholds as a function of cluster size strikingly collapse onto a universal theoretical curve which predicts the possibility of a superlow-static-torque state for large clusters. We further reveal a cluster-size-independent rotation-translation depinning transition when lattice-matched clusters are driven jointly by a torque and a force. Our work provides guidelines to the design of nanomechanical devices that involve rotational motions on atomic surfaces.

cond-mat.soft

Thermal Friction Enhancement in Zwitterionic Monolayers

We introduce a model for zwitterionic monolayers and investigate its tribological response to changes in applied load, sliding velocity, and temperature by means of molecular-dynamics simulations. The proposed model exhibits different regimes of motion depending on temperature and sliding velocity. We find a remarkable increase of friction with temperature, which we attribute to the formation and rupture of transient bonds between individual molecules of opposite sliding layers, triggered by the out-of-plane thermal fluctuations of the molecules' orientations. To highlight the effect of the molecular charges, we compare these results with analogous simulations for the charge-free system. These findings are expected to be relevant to nanoscale rheology and tribology experiments of locally-charged lubricated systems such as, e.g., experiments performed on zwitterionic monolayers, phospholipid micelles, or confined polymeric brushes in a surface force apparatus.

cond-mat.soft