Tapping Mode Atomic Force Microscopy Research Articles

Molecular dynamics models of tapping mode atomic force microscopy

Macro-mechanical simulation software cannot easily simulate the atomic resolution of the tapping mode atomic force microscope (TM-AFM), so the accuracy of the corresponding mechanical model is questioned. In this paper, a TM-AFM simulation model is established using classical molecular dynamics (MD). The model simulated the tapping of gold (Au) and aluminum (Al) by probes with various amplitudes. The simulation yielded the z-direction force curves, trajectory curves and indentation curves of the probe. The amplitude change and the phase shift of the probe at various amplitudes were calculated from the direct measurement results. A contact jump and detachment jump become evident and are significant to energy and force results. The recovery ability of Al after indenting is smaller than that of Au. The energy calculations can be fitted to a high goodness of fit, reaching 0.99 and better; hence, the amplitude and phase shift variations of the probe can be used to fit the stored and dissipated energies, the sample energies when the sample is tapped. In this way, the TM-AFM is able to calculate the mechanical properties of the sample, and thus characterize the sample.

Blunting and wear of AFM tips during dynamic lithography

Mechanical scanning probe lithography using AFM tips has been applied to the fabrication of nanostructures on material surfaces. Particularly, the dynamic lithography under the AFM tapping mode is promising in fabricating the surface nanostructures at the width of around 20 nm. However, tip blunting and gradual atom-by-atom wear occurred during the process although the tip tapping motion has largely reduced the tip-surface interaction force and time. This study aims to investigate the blunting rate and mechanism of such AFM tips. It was found that the maximum contact stress was in the range of 0.7 to 1.0 GPa when a silicon AFM tip (initial tip radius under 20 nm) was tapped on a PMMA thin-film surface. And the contact stress was mainly attributed to the tip radius, which was the key factor to limit machinability and machining efficiency of the dynamic lithography. Furthermore, the mechanism of the tip blunting was through its plastic deformation and tip wear. A stress analysis indicated that it was the large stress gradient that contributed to the high density of wrinkles in the tips, and that ninety percent of the blunting of a tip were caused by the plastic deformation, leading to a significant increase of the tip radius.

Probing the morphological and mechanical changes in a C. elegans model of Huntington's disease.

Huntington's Disease (HD) is a fatal neurodegenerative disease caused by a mutation in the huntingtin gene, in which CAG nucleotides are excessively repeated. In turn, translated huntingtin protein (htt) contains an expanded polyglutamine (polyQ) domain, which triggers toxic protein aggregation, the hallmark feature of this disease. Common symptoms of HD, such as chorea, muscle atrophy, and behavioral and neurological decline, continue to worsen as the disease progresses. This study aims to investigate the relationship between polyQ domain length and age-dependent morphological and mechanical changes in a Caenorhabditis elegans model of HD. C. elegans are an established model species to investigate aging, as morphological and mechanical changes—such as epidermal roughening and whole body decrease in Young's modulus, respectively—occur as a function of age. Moreover, worm mobility exhibits a deficit as a result of such changes. We expect to observe age-dependent morphological changes much earlier in the pathogenic C. elegans (Q128), as opposed to age-matched, non-pathogenic C. elegans (Q15). Morphological analysis was performed using tapping mode atomic force microscopy (AFM), and images were processed using custom MATLAB scripts to determine RMS roughness. Further studies will be conducted to investigate the role of age-dependent changes in mechanical properties, such as Young's modulus, as they relate to polyQ domain length. In-situ contact mode AFM will be used to achieve this. We expect to observe age-dependent mechanical changes much earlier in the Q128 worms, in comparison to the Q15 worms. Pending results, additional studies may be conducted to determine if these changes serve as a peripheral biomarker of HD, as well as the role of such a biomarker in diagnostic, prognostic, and therapeutic strategies.

Highly Efficient Ternary Near-Infrared Organic Photodetectors for Biometric Monitoring.

Near-infrared (NIR) small-molecule acceptors that absorb at wavelengths of up to 1000 nm are attractive for applications in organic photodetectors (OPDs) and biometrics. In this study, we incorporated IEICO-4F as the third component for PffBT4T-2OD:PC71BM-based OPDs to provide an efficient NIR response while greatly suppressing the leakage current at reverse bias. By varying the blend ratio and thickness (250-600 nm), we obtained an NIR OPD displaying an ultralow dark-current density (JD = 2.62 nA cm-2), ultrahigh detectivity [D* = 7.2 × 1012 Jones (850 nm)], high sensitivity, and photoresponsivity covering the region from the ultraviolet to the NIR. We used tapping-mode atomic force microscopy, optical microscopy, grazing-incidence wide-angle X-ray scattering, and contact angle measurements to investigate the effect of IEICO-4F on the performance of the ternary OPDs. The low compatibility of PffBT4T-2OD and IEICO-4F, originating from weak intermolecular interactions, allowed us to manipulate the degree of phase separation between the donor and acceptor in the ternary blends, leading to an optimized blend morphology featuring efficient charge separation, transport, and collection. To demonstrate its applicability, we integrated our OPD with two light-emitting diodes and used the system for precisely calculated transmissive pulse oximetry.

Strengthening Polylactic Acid by Salification: Surface Characterization Study.

Polylactic acid (PLA) is one of the market's most commonly used biodegradable polymers, with diverse applications in additive manufacturing, specifically fused deposition modeling (FDM) 3D printing. The use of PLA in complex and sophisticated FDM applications is continually growing. However, the increased range of applications requires a better understanding of the material properties of this polymer. For example, recent studies have shown that PLA has the potential to be used in artificial heart valves. Still, the durability and longevity of this material in such a harsh environment are unknown, as heart valve failures have been attributed to salification. Additionally, there is a gap in the field for in situ material characterization of PLA surfaces during stiffening. The present study aims to benchmark different dynamic atomic force microscopy (AFM) techniques available to study the salification phenomenon of PLA at micro-scales using different PLA thin films with various salt concentrations (i.e., 10%, 15%, and 20% of sodium chloride (NaCl)). The measurements are conducted by tapping mode AFM, bimodal AFM, the force spectroscopy technique, and energy quantity analysis. These measurements showed a stiffening phenomenon occurring as the salt solution is increased, but the change was not equally sensitive to material property differences. Tapping mode AFM provided accurate topographical information, while the associated phase images were not considered reliable. On the other hand, bimodal AFM was shown to be capable of providing the topographical information and material compositional mapping through the higher eigenmode's phase channel. The dissipated power energy quantities indicated that how the polymers become less dissipative as salt concentration increases can be measured. Lastly, it was shown that force spectroscopy is the most sensitive technique in detecting the differences in properties. The comparison of these techniques can provide a helpful guideline for studying the material properties of PLA polymers at micro- and nano-scales that can prove beneficial in various fields.

Friction hysteretic behavior of supported atomically thin nanofilms

Hysteretic friction behavior has been observed on varied 2D nanofilms. However, no unanimous conclusion has yet been drawn on to the exact mechanism or relative contribution of each mechanism to the observed behavior. Here we report on hysteretic friction behavior of supported atomically thin nanofilms studied using atomic force microscopy (AFM) experiments and molecular dynamics (MD) simulations. Load dependent friction measurements were conducted on unheated and heated samples of graphene, h-BN, and MoS2 supported by silica substrates. Two diverging friction trends are reported: the unheated samples showed higher friction during unloading than during loading, and the heated samples showed a reversed hysteresis. Further, the friction force increased sub-linearly with normal force for heated samples, compared with unheated samples. Tapping mode AFM suggested that the interaction strength of the substrate was increased with heating. Roughened substrates in the MD simulations that mimicked strong/weak interaction forces reproduced the experimental observations and revealed that the evolution of real contact area in different interface interaction situation caused the diverging behaviors. Surface roughness and interaction strength were found to be the key parameters for controlling the out-of-plane deformation of atomically thin nanofilms.

Insights and guidelines to interpret forces and deformations at the nanoscale by using a tapping mode AFM simulator: dForce 2.0.

Amplitude modulation (tapping mode) AFM is the most versatile AFM mode for imaging surfaces at the nanoscale in air and liquid environments. However, it remains challenging to estimate the forces and deformations exerted by the tip. We introduce a new simulator environment to predict the values of the observables in tapping mode AFM experiments. The relevant feature of dForce 2.0 is the incorporation of contact mechanics models aimed to describe the properties of ultrathin samples. These models were essential to determine the forces applied on samples such as proteins, self-assembled monolayers, lipid bilayers, and few-layered materials. The simulator incorporates two types of long-range magnetic forces. The simulator is written in an open-source code (Python) and it can be run from a personal computer.

CuAAC-methacrylate interpenetrating polymer network (IPN) properties modulated by visible-light photoinitiation.

Interpenetrating polymer networks (IPNs) are a class of materials with interwoven polymers that exhibit unique blended or enhanced properties useful to a variety of applications, ranging from restorative protective materials to conductive membranes and hydrophobic adhesives. The IPN formation kinetics can play a critical role in the development of the underlying morphology and in turn the properties of the material. Dual photoinitiation of copper-catalyzed azide-alkyne (CuAAC) and radical mediated methacrylate polymerization chemistries enable the manipulation of IPN microstructure and properties by controlling the kinetics of IPN formation via the intensity of the initiating light. Specifically, azide and alkyne-based polyethylene glycol monomers and tetraethylene glycol dimethacrylate (TEGDMA) were polymerized in a single pot to form IPNs and the properties were evaluated as a function of the photoinitiating light intensity. Morphological differences as a function of intensity were observed in the IPNs as determined by thermomechanical properties and phase-contrast imaging in tapping mode atomic force microscopy (AFM). At moderate intensities (20 mW/cm2) of visible light (470 nm), the TEGDMA polymerization gels first and therefore forms the underlying network scaffold. At low intensities (0.2 mW/cm2), the CuAAC polymerization can gel first. The ability to switch sequence of gelation and IPN trajectory (simultaneous vs. sequential), affords control over phase separation behavior. Thus, light not only allows for spatial and temporal control over the IPN formation but also provides control over their thermomechanical properties, representing a route for facile IPNs design, synthesis, and application.

Morphological Effects of Strain Localization in the Elastic Region of Magnetorheological Elastomers.

Strain localization is a significant issue that poses interesting research challenges in viscoelastic materials because it is difficult to accurately predict the damage evolution behavior. Over time, the damage mechanism in the amorphous structure of viscoelastic materials leads to subsequent localization into a shear band, gradually jeopardizing the materials' elastic sustainability. The primary goal of this study is to further understand the morphological effects and the role of shear bands in viscoelastic materials precipitated by strain localization. The current study aims to consolidate the various failure mechanisms of a sample and its geometry (surface-to-volume ratio) used in torsional testing, as well as to understand their effects on stress relaxation durability performance. A torsional shear load stress relaxation durability test was performed within the elastic region on an isotropic viscoelastic sample made of silicon rubber and a 70% weight fraction of micron-sized carbonyl iron particles. Degradation was caused by a shear band of localized plasticity that developed microscopically due to stress relaxation durability. The failure pattern deteriorated as the surface-to-volume ratio decreased. A field-emission scanning electron microscope (FESEM) and a tapping-mode atomic force microscope (AFM) were used for further observation and investigation of the sample. After at least 7500 cycles of continuous shearing, the elastic sustainability of the viscoelastic materials microstructurally degraded, as indicated by a decline in stress performance over time. Factors influencing the formation of shear bands were observed in postmortem, which was affected by simple micromanipulation of the sample geometry, making it applicable for practical implementation to accommodate any desired performance and micromechanical design applications.

Manipulating Trapped Nanobubbles Moving and Coalescing with Surface Nanobubbles.

Trapped nanobubbles are observed nucleating at nanopits on a pitted substrate, while surface nanobubbles are usually formed on the smooth solid surface in water. In this work, trapped nanobubbles and surface nanobubbles were captured by a tapping-mode atomic force microscope (AFM) on a nanopitted substrate based on the temperature difference method. A single trapped nanobubble was manipulated to change into a surface nanobubble, then to change into the trapped nanobubble again. At the same time, surface nanobubbles can be moved to merge into a trapped nanobubble. Our results show that the scan load and the size of the scan area were the main factors that significantly affect the mobility of surface/trapped nanobubbles. The coalescence and mutual transformation of the two kinds of nanobubbles indicate that trapped nanobubbles and surface nanobubbles have the same chemical nature, which also provides vital experimental proof of the existence of nanobubbles in the course of contact line depinning. Our results are of great significance for understanding nanobubble stability and providing guidelines in some industrial applications.

(Digital Presentation) Investigation of Microstructure Dependent Inhibitor Adsorption Mechanism on Carbon Steel By in Situ Atomic Force Microscopy

In the petroleum industry, organic surfactant type inhibitors have been widely applied in the oil and gas industry considering their high efficiency. Carbon steels with various carbide contents have also been used extensively as pipeline materials during the transport and storage of crude oil due to their excellent mechanical properties and low cost. The previous investigation of inhibition mechanism on carbon steel is limited by lack of surface characterization techniques at a molecular level. Atomic force microscopy (AFM) can not only provide localized visual observation, but can also achieve the detection of mechanical properties of an inhibitor film. In this study, in situ AFM contact mode friction imaging and in situ AFM tapping mode phase imaging techniques have been applied to investigate the influence of the ferritic-pearlitic microstructure of carbon steel on inhibitor adsorption mechanisms during CO2 corrosion under different inhibitor concentrations. At concentration above surface saturation, AFM contact mode friction images show a large friction contrast between inhibitor covered cementite structures and ferrite structures, while in the absence of inhibitor, this friction contrast almost disappears, indicating the inhibitor adsorption induced this difference. AFM tapping mode phase images indicate uniform adsorption of inhibitor on both cementite and ferrite structures.The differences observed in these AFM analyses indicate that the adhesion force of inhibitor molecules on cementite could be smaller than on ferrite, or the molecular orientations of inhibitor molecules adsorbed on cementite and ferrite structures could be different. The special adsorption behavior of inhibitor molecules on cementite means the carbide component of the microstructure could directly influence inhibitor adsorption and may decrease inhibitor efficiency. Simultaneous linear polarization resistance tests in electrochemical AFM (EC-AFM) cell indicates a maximum inhibition efficiency at concentration above saturation.Keywords : Contact mode AFM, friction contrast, tapping mode AFM, phase contrast, cementite, ferrite, organic inhibitor, adhesion force.Statement of importance:Studies related to inhibitor adsorption mechanisms on ferritc-pearlitic carbon steels can be connected with the practical issues that iron carbide can impair the corrosion inhibitor performance on carbon steels. This AFM work connects the corrosion inhibition effect with the carbon steel components at a molecular level for the first time. Physical explanations regarding the interactions between inhibitor molecules and carbon steel microstructures can also be provided with the assistance of molecular simulations.Figure caption: Contact and tapping mode AFM images of inhibitor film formed on UNS G1018 steel at 2 CMC (100ppm) tetradecyldimethylbenzylammonium inhibitor + 1 wt% NaCl. The contact mode friction image indicates a large friction contrast between inhibitor covered cementite and ferrite structure, while the tapping mode phase image indicates a negligible softness contrast between cementite and ferrite structure. Figure 1

Poloxamer-Based Hydrogel as Drug Delivery System: How Polymeric Excipients Influence the Chemical-Physical Properties.

Thermogelling amphiphilic block copolymers have been widely investigated in the development of pharmaceutical drug carriers. In particular, thermosensitive gels based on poloxamer 407 (P407) have great potential for periodontal disease treatment, thanks to their ability to be liquid at room temperature and become viscous gels at body temperature. However, some problems, related to short in situ residence time, reduce their feasible clinical use. Thus, in order to improve the effective applicability of these materials, we studied how P407 thermogels are affected by the pH and by the inclusion of different hydrophilic polymers, used as excipients for increasing the gel stiffness. For this scope, a complete chemical-physical characterization of the synthesized gels is provided, in terms of determination of sol-gel transition temperature, viscosity and erosion degree. The data are correlated according to a statistical multivariate approach based on Principal Component Analysis and their mucoadhesion properties are also tested by Tapping mode-Atomic Force Microscopy (TM-AFM) imaging. Finally, we studied how the different P407 formulations are able to influence the release pathway of two antibacterial drugs (i.e., chlorhexidine digluconate and doxycycline hyclate) largely used in oral diseases.

Tip-enhanced Raman spectroscopy with amplitude-controlled tapping-mode AFM

Tip-enhanced Raman spectroscopy (TERS) is a powerful tool for analyzing chemical compositions at the nanoscale owing to near-field light localized at a metallic tip. In TERS, atomic force microscopy (AFM) is commonly used for tip position control. AFM is often controlled under the contact mode for TERS, whereas the tapping mode, which is another major operation mode, has not often been employed despite several advantages, such as low sample damage. One of the reasons is the low TERS signal intensity because the tip is mostly away from the sample during the tapping motion. In this study, we quantitatively investigated the effect of the tapping amplitude on the TERS signal. We numerically evaluated the dependence of the TERS signal on tapping amplitude. We found that the tapping amplitude had a significant effect on the TERS signal, and an acceptable level of TERS signal was obtained by reducing the amplitude to a few nanometers. We further demonstrated amplitude-controlled tapping-mode TERS measurement. We observed a strong dependence of the TERS intensity on the tapping amplitude, which is in agreement with our numerical calculations. This practical but essential study encourages the use of the tapping mode for further advancing TERS and related optical techniques.

Subsurface phase imaging of tapping-mode atomic force microscopy at phase resonance.

The phase image of tapping-mode atomic force microscopy (TM-AFM) contains energy dissipation, which is related to the sample information on the physical properties such as the sample Young's modulus, adhesion, surface morphology and subsurface morphology. When TM-AFM is used for sample measurement, the frequency near the first resonance peak of probe is usually selected to drive the probe vibration. When the probe vibration is driven by the frequency, the probe has a high amplitude sensitivity, but the phase sensitivity is relatively low. In this paper, the frequency at the probe phase resonance peak was selected for driving the probe vibration to measure the sample, which improved the image resolution. Phase imaging was performed on three uniform photoresist samples with different thicknesses and the same structure. When the scanning parameters were fixed and the probe setpoint value was changed alone, it was found that with the decrease of setpoint value the horizontal resolution of the phase subsurface image was decreased, and the depth sensitivity was increased first and then decreased. The result shows that TM-AFM working at the phase resonance peak can better realise the subsurface imaging of samples at different depths. Phase subsurface imaging at the resonance can be used to quantitatively obtain subsurface phase images of different depths.

High resolution atomic force microscopy with an active piezoelectric microcantilever.

Active microcantilevers with on-chip sensing and actuation provide significant advantages in tapping mode Atomic Force Microscopy (AFM). Collocated transduction allows for effective manipulation of cantilever dynamics through feedback control, enabling higher scan rates. However, the adjacency of the sensing and actuation electrodes is known to result in a high level of feedthrough, leading to a low imaging resolution. Readout circuit noise further deteriorates the imaging precision. Here, we investigate the noise sources that affect AFM microcantilevers with collocated aluminum nitride (AlN) actuator-sensor pairs. We reported these cantilevers in earlier work and demonstrated that they display a very low level of feedthrough between the actuation and sensing electrodes. We present a high signal-to-noise ratio (SNR) sensing method that enables us to demonstrate high-resolution AFM on a calibration grating with nm-step silicon carbide (SiC) terraces. Measuring the Lorentzian response of the cantilever's Brownian motion with the on-chip active sensor at resonance enables us to calibrate the dynamic stiffness at the first fundamental resonance mode, without utilizing an optical sensor.

Design and Synthesis of 6-O-Phosphorylated Heparan Sulfate Oligosaccharides to Inhibit Amyloid β Aggregation.

Dysregulation of amyloidogenic proteins and their abnormal processing and deposition in tissues cause systemic and localized amyloidosis. Formation of amyloid β (Aβ) fibrils that deposit as amyloid plaques in Alzheimer's disease (AD) brains is an earliest pathological hallmark. The polysulfated heparan sulfate (HS)/heparin (HP) is one of the non‐protein components of Aβ deposits that not only modulates Aβ aggregation, but also acts as a receptor for Aβ fibrils to mediate their cytotoxicity. Interfering with the interaction between HS/HP and Aβ could be a therapeutic strategy to arrest amyloidosis. Here we have synthesized the 6‐O‐phosphorylated HS/HP oligosaccharides and reported their competitive effects on the inhibition of HP‐mediated Aβ fibril formation in vitro using a thioflavin T fluorescence assay and a tapping mode atomic force microscopy.

Machine learning to probe modal interaction in dynamic atomic force microscopy

Modal interactions are pervasive effects that commonly emerge in nanomechanical systems. The coupling of vibrating modes can be leveraged in many ways, including to enhance sensing or to disclose complex phenomenologies. In this work we show how machine learning and data-driven approaches could be used to capture intermodal coupling. We employ a quasi-recurrent neural network (QRNN) for identifying mode coupling and verify its applicability on experimental data obtained from tapping mode atomic force microscopy (AFM). Hidden units of the QRNN are monitored to trace fingerprints of modes activation and to quantify their contributions over the global distortion of orbits in the phase space. To demonstrate the broad applicability of the method, the trained model is re-applied over different experiments and on diverse materials. Over a range of tip-sample configurations, dynamic AFM possesses features general enough to be seized by the QRNN and it is not required an ad-hoc re-training for the identification of interacting modes. Our study opens up a route for utilizing established machine learning techniques for rapid recognition of nonlinear complex effect such as internal resonances in nanotechnology. The QRNN analysis is meant to assist AFM sensing operations when exploiting modal interaction to enhance the signal-to-noise ratio of higher harmonics and provide high resolution compositional contrast in multi-frequency AFM applications.

Internal topology and water transport in tetrafunctional epoxy resins

AbstractWater sorption into epoxy resins limits the performance lifetime of many composites, adhesives, and coatings. One hypothesis for the well‐known hygroscopicity of epoxies is that the well‐known internal nodular topology of epoxy networks enhances permeability. This theory has however remained untested to date, since previous attempts to manipulate the internal topology have been accompanied by changes in the hydrogen bonding capability of resins, which dominates water uptake. Here, the nanostructure of highly cross‐linked network polymers based on tetra glycidyl diaminodiphenyl methane is varied in the absence of significant polarity effects by careful optimization of the cure schedule. The internal morphology of resins cured at 100, 150, and 200°C are characterized using Peakforce tapping mode atomic force microscopy, whilst the cure progression at each temperature is analyzed using in‐situ transmission mode infrared spectroscopy. Distinct nodular morphologies are found to form at high cure temperatures (150 and 200°C), where spectroscopic analysis demonstrates that excess epoxy consumption occurs prior to the gel point, as a result of intra‐cluster cross‐linking and reduced reaction selectivity. Surprisingly, the establishment of an internal nanostructure is, however, found to have negligible effect on the extent and kinetics of moisture sorption.

Atomic resolution with high-eigenmode tapping mode atomic force microscopy

Atomic surface structure imaging is instrumental for the understanding of surface-related phenomena. Here, we show that conventional tapping mode atomic force microscopy with high cantilever eigenmodes and subnanometer amplitudes allow routine atomic imaging at atmospheric pressures. We identify the reasons for failure of atomic resolution imaging employing low eigenmodes. Strong tip-surface interactions cause significant differences between the oscillatory behaviors of the inclination of the cantilever as detected by conventional instruments and of the vertical position of the tip, which prevents correct functioning of instrumental feedback control loops. However, high effective spring constants of high eigenmodes make it possible to overcome the problem. Furthermore, the combination of high effective elastic constants of high cantilever eigenmodes with the high flexibility of the cantilever substantially enhances the imaging stability, thereby universally allowing atomic imaging of solid surfaces in gaseous environments and at elevated temperatures. Demonstrated imaging examples include single sulfur vacancies at the surface of ${\mathrm{MoS}}_{2}$ crystals imaged at temperatures ranging from room temperature to 250\ifmmode^\circ\else\textdegree\fi{}C and potassium ions on hydrophilic and highly adhesive muscovite mica surfaces. Moreover, the high imaging stability allows knocking atoms off the ${\mathrm{MoS}}_{2}$ surface by hard tapping, indicating the potential for ultrahigh resolution lithography.

Moiré Modulation of Van Der Waals Potential in Twisted Hexagonal Boron Nitride.

When a twist angle is applied between two layered materials (LMs), the registry of the layers and the associated change in their functional properties are spatially modulated, and a moiré superlattice arises. Several works explored the optical, electric, and electromechanical moiré-dependent properties of such twisted LMs but, to the best of our knowledge, no direct visualization and quantification of van der Waals (vdW) interlayer interactions has been presented, so far. Here, we use tapping mode atomic force microscopy phase-imaging to probe the spatial modulation of the vdW potential in twisted hexagonal boron nitride. We find a moiré superlattice in the phase channel only when noncontact (long-range) forces are probed, revealing the modulation of the vdW potential at the sample surface, following AB and BA stacking domains. The creation of scalable electrostatic domains, modulating the vdW potential at the interface with the environment by means of layer twisting, could be used for local adhesion engineering and surface functionalization by affecting the deposition of molecules or nanoparticles.