Atomic Force Microscopy Probe Research Articles

Nano-spherical tip-based smoothing with minimal damage for 2D van der Waals heterostructures.

Two-dimensional materials and their heterostructures have significant potential for future developments in materials science and optoelectronics due to their unique properties. However, their fabrication and transfer process often introduce impurities and contaminants that degrade their intrinsic qualities. To address this issue, current atomic force microscopy (AFM) probe contact mode methods provide a solution by allowing in situ cleaning and real-time observation of the nanoscale cleaning process. Nevertheless, existing pyramidal probes may scratch surfaces and damage heterostructures during force application. Therefore, we proposed a method based on the nano-spherical probe contact mode to clean residual and polymer contamination for minimum damage cleaning of MoS2/hBN substrates. Comparative experiments with pyramidal probes in 2DM morphology and photoluminescence (PL) have shown that nano-spherical probes are exceptionally effective in cleaning bubbles of various sizes, compared to uncleaned MoS2, where PL full width at half maximum (FWHM) averages 0.115 eV, nano-spherical probes reduce it by 30% to 0.08 eV. Pyramidal probes, however, only clean smaller bubbles and leave residuals in larger ones, resulting in less optimal PL mapping data with values in both the 0.09 eV and 0.0115 eV regions. We also collected the standard deviation of the FWHM data points for the uncleaned region and the regions cleaned by the pyramidal and nano-spherical probes, which were 0.02773, 0.01895, and 0.00531, respectively. Notably, the standard deviation of the FWHM in the nano-spherical probe-cleaned region is only 28% of that in the pyramidal probe-cleaned region. Then, increasing the applied force leads to damage in the crystal structure, resulting in potential inconsistencies across different areas, as evidenced by KPFM and SEM observations. In contrast, nano-spherical probes demonstrate a uniform potential in KPFM and consistently maintain a smooth surface morphology in SEM throughout the process. This approach highlights the potential of nano-spherical probes to advance minimum-damage cleaning techniques in 2D material research and applications.

MXene Nanoconfinement of SAM-Modified Molecularly Imprinted Electrochemical Biosensor for Point-of-Care Monitoring of Carcinoembryonic Antigen.

The high rate of cancer worldwide and the heavy costs imposed on governments and humanity have always motivated researchers to develop point-of-care (POC) biosensors for easy diagnosis and monitoring of cancer treatment. Herein, we report on a label-free impedimetric biosensor based on Ti3C2Tx MXene and imprinted ortho-phenylenediamine (o-PD) for the detection of carcinoembryonic antigen (CEA), a biomarker for various cancers surveillance, especially colorectal cancer (CRC). Accordingly, MXene was drop-casted on the surface of a disposable silver electrode to increase the sensitivity and create high-energy nanoareas on the surface, which are usable for protein immobilization and detection. A self-assembled monolayer (SAM) was exploited for oriented CEA immobilization on the MXene-modified electrode. The monomer-protein interaction and successful protein removal were confirmed by molecular docking and atomic force microscopy (AFM) investigations to evaluate the quality of the fabricated molecularly imprinted polymer (MIP). Also, the role of MXene in increasing the electrical field inside the nanoareas was simulated using COMSOL Multiphysics software. A suitable limit of detection (9.41 ng/mL), an appropriate linear range of detection (10 to 100 ng/mL) in human serum, and a short detection time (10 min) resulted from the use of SAM/MIP next to MXene. This biosensor presented outstanding repeatability (97.60%) and reproducibility (98.61%). Moreover, acceptable accuracy (between 93.04 and 116.04%) in clinical serum samples was obtained compared with immunoassay results, indicating the high potential of our biosensor for real sample analysis. This biomimetic and disposable sensor provides a cost-effective method for facile and POC monitoring of cancer patients during treatment.

Effect of film thickness on phase structure of epitaxial non-doped hafnium oxide films

HfO2 has been widely used in the electronics industry as a dielectric material with excellent properties. It has attracted much attention since HfO2 was first reported to be ferroelectric in 2011. With the continuous advancement of research, various methods such as oxygen vacancy control and interface control have been proven to be able to stabilize the metastable polar o-phase structure in doped hafnium oxide thin films. However, there are still some shortcomings in the relevant issues concerning non-doped hafnium oxide thin film materials. Here, polycrystalline non-doped HfO2 thin films were grown on SrTiO3 substrates by pulsed laser deposition (PLD). Atomic force microscopy investigation suggests that the surface roughness of HfO2 thin films increases as the film thickness increases. X-ray photoelectron spectroscopy analyses indicate that the HfO2 thin film has a high purity and contain only Hf4+ ions. The band gap of HfO2 was measured by valence EELS and UV–visible spectra. Atomic structures of the HfO2/SrTiO3 heterointerface have been studied by the aberration-corrected transmission electron microscopy and energy-dispersive X-ray spectroscopy. The HfO2/SrTiO3 heterointerface is atomically abrupt and incoherent. Our findings suggest that non-doped HfO2 films with o-phase structure through PLD technology.

Finite element modelling of atomic force microscopy imaging on deformable surfaces.

Atomic force microscopy (AFM) provides a three-dimensional topographic representation of a sample surface, at nanometre resolution. Computational simulations can aid the interpretation of such representations, but have mostly been limited to cases where both the AFM probe and the sample are hard and not compressible. In many applications, however, the sample is soft and therefore deformed due to the force exerted by the AFM tip. Here we use finite element modelling (FEM) to study how the measured AFM topography relates to the surface structures of soft and compressible materials. Consistent with previous analytical studies, the measured elastic modulus in AFM is generally found to deviate from the elastic modulus of the sample material. By the analysis of simple surface geometries, the FEM modelling shows how measured mechanical and topographic features in AFM images depend on a combination of tip-sample geometry and indentation of the tip into the sample. Importantly for the interpretation of AFM data, nanoparticles may appear larger or smaller by a factor of two depending on tip size and indentation force; and a higher spatial resolution in AFM images does not necessarily coincide with a more accurate representation of the sample surface. These observations on simple surface geometries also extend to molecular-resolution AFM, as illustrated by comparing FEM results with experimental data acquired on DNA. Taken together, the FEM results provide a framework that aids the interpretation of surface topography and local mechanics as measured by AFM.

Enhancing the Pressure-Sensitive Electrical Conductance of Self-Assembled Monolayers.

The inherent large HOMO-LUMO gap of alkyl thiol (CnS) self-assembled monolayers (SAMs) has limited their application in molecular electronics. This work demonstrates significant enhancement of mechano-electrical sensitivity in CnS SAMs by external compression, achieving a gauge factor (GF) of approximately 10 for C10S SAMs. This GF surpasses values reported for conjugated wires and DNA strands, highlighting the potential of CnS SAMs in mechanosensitive devices. Conductive atomic force microscopy (cAFM) investigations reveal a strong dependence of GF on the alkyl chain length in probe/CnS/Au junctions. This dependence arises from the combined influence of molecular tilting and probe penetration, facilitated by the low Young's modulus of alkyl chains. Theoretical simulations corroborate these findings, demonstrating a shift in the electrode Fermi level toward the molecular resonance region with increasing chain length and compression. Introducing a rigid graphene interlayer prevents probe penetration, resulting in a GF that is largely independent of the alkyl chain length. This highlights the critical role of probe penetration in maximizing mechano-electrical sensitivity. These findings pave the way for incorporating CnS SAMs into mechanosensitive and mechanocontrollable molecular electronic devices, including touch-sensitive electronic skin and advanced sensor technologies. This work demonstrates the potential of tailoring mechanical and electrical properties of SAMs through molecular engineering and interface modifications for optimized performance in specific applications.

High-Resolution Atomic Force Microscopy Investigation of Alginate Hydrogel Materials in Aqueous Media.

Alginate hydrogels are frequently used in 3D bioprinting and tissue repair and regeneration. Establishing the structure-property-performance correlation of these materials would benefit significantly from high-resolution structural characterization in aqueous environments from the molecular level to continuum. This study overcomes technical challenges and enables high-resolution atomic force microscopy (AFM) imaging of hydrated alginate hydrogels in aqueous media. By combining a new sample preparation protocol with extremely gentle tapping mode AFM imaging, we characterized the morphology and regional mechanical properties of the hydrated alginate. Upon cross-linking, basic units of these hydrogel materials consist of egg-box dimers, which assemble into long fibrils. These fibrils congregate and pile up, forming a sponge-like structure, whose pore size and distribution depend on the cross-linking conditions. At the exterior, surface tension impacts the piling of fibrils, leading to stripe-like features. These structural features contribute to local, regional, and macroscopic mechanics. The outcome provides new insights into its structural characteristics from nanometers to tens of micrometers, i.e., at the dimensions pertaining to biomaterial and hydrogel-cell interactions. Collectively, the results advance our knowledge of the structure and mechanics from the nanometer to continuum, facilitating advanced applications in hydrogel biomaterials.

Tunable macroscopic self-healing of supramolecular gel through host–guest inclusion

Supramolecular gels (SGs) consisted of noncovalent cross-linking network structures are fascinating due to their efficient energy dissipation and reversible self-healing properties. However, it is unknown how the noncovalent interactions alter the macroscopic self-healing and mechanical properties of SGs. Herein, the peculiar nature of SGs manufactured by combining covalent and noncovalent (host–guest inclusion of β-cyclodextrin and C16 hydrophobic chain) cross-linking structures was studied and compared with covalent cross-linking preformed particle gels. The macroscopic self-healing behaviors, rheology, mechanical tensile properties, as well as the tunable mechanisms of self-healing were explored by visual inspection, rheological, and atomic force microscopy probing methods. The results show that the SGs exhibit excellent self-healing efficiency and mechanical strength after interfacial cutting. Moreover, the SGs exhibited excellent mechanical tensile properties, including loading–unloading, successive loading–unloading, and recovery loading–unloading tensile performances. Notably, the macroscopic self-healing of SGs has good tunability by changing the covalent and noncovalent crosslinker contents and salt contents. This peculiar phenomenon is attributed to certain host–guest inclusion forces (4.7 and 0.3 nN) between different SGs under the distilled and high-salinity water conditions, respectively. This study is beneficial for the development of stimuli–response supramolecular gels in different applications, such as oil recovery in fractured reservoirs.

Reversible Light-Triggered Stretching of Small-Molecule Photochromic Organic Nanoparticles.

Functional organic nanomaterials are nowadays largely spread in the field of nanomedicine. In situ modulation of their morphology is thus expected to considerably impact their interactions with the surroundings. In this context, photoswitchable nanoparticles that are manufactured, amenable to extensive disassembling upon illumination in the visible, and reversible reshaping under UV exposure. Such reversibility turns to be strongly impaired for photochromic nanoparticles in close contact with a substrate. In situ atomic force microscopy investigations at the nanoscale actually reveal progressive disintegration of the organic nanoparticles under successive UV-vis cycles of irradiation, in the absence of intrinsic elastic forces. These results point out the dramatic interactions exerted by surfaces on the cohesion of non-covalently bonded organic nanoparticles. They invite to harness such systems, often used as biomarkers, to also serve as photoactivatable drug delivery nanocarriers.

Single-molecule Magnets (SMM) spin channels connecting FeMn antiferromagnet and NiFe ferromagnetic electrodes of a tunnel junction

The integration of single-molecule magnets (SMMs) into magnetic tunnel junctions (MTJs) offers significant potential for advancing molecular spintronics, particularly for next-generation memory devices, quantum computing, and energy storage technologies such as solar cells. In this study, we present the first demonstration of SMM-induced spin-dependent properties in an antiferromagnet-based MTJ molecular spintronic device (MTJMSD). We engineered cross-junction-shaped devices comprising FeMn/AlOx/NiFe MTJs. The AlOx barrier thickness where the exposed junction edges meet was comparable to the SMM length, facilitating the incorporation of SMM molecules as spin channels for spin-dependent transport. The SMM channels enabled long-range magnetic moment ordering around molecular junctions, which were precisely engineered via fabrication processes. The SMM, composed of a [Mn6(μ3-O)2(H2N-sao)6(6-atha)2(EtOH)6] (H2N-saoH = salicylamidoxime, 6-atha = 6-acetylthiohexanoate) complex, featured thioester groups at the ends that upon hydrolysis they form bonds with the magnetic electrodes. SMM-treated junctions demonstrated a significant current enhancement, reaching up to 7 μA at an input voltage of 60 mV. Furthermore, SMM-doped junctions exhibited current stabilization in the μA range at lower temperatures, whereas the bare electrodes showed current suppression to the picoampere range. Magnetization measurements conducted at 55 K and 300 K on pillar-shaped devices revealed a reduction in magnetic moment at low temperatures. Additionally, Kelvin probe atomic force microscopy (KPAFM) measurements confirmed that SMM integration transformed the electronic properties over long ranges.These findings are attributed to the spin channels formed between magnetic metal electrodes, which enhance spin polarization at each magnetic electrode. Our research highlights the potential of using antiferromagnetic materials, characterized by minimal stray fields and zero net magnetization, to transform MTJMSD devices.

Investigating Gold Deposition with High-Power Impulse Magnetron Sputtering and Direct-Current Magnetron Sputtering on Polystyrene, Poly-4-vinylpyridine, and Polystyrene Sulfonic Acid.

Fabricating thin metal layers and particularly observing their formation process in situ is of fundamental interest to tailor the quality of such a layer on polymers for organic electronics. In particular, the process of high power impulse magnetron sputtering (HiPIMS) for establishing thin metal layers has sparsely been explored in situ. Hence, in this study, we investigate the growth of thin gold (Au) layers with HiPIMS and compare their growth with thin Au layers prepared by conventional direct current magnetron sputtering (dcMS). Au was chosen because it is an inert noble metal and has a high scattering length density. This allows us to track the growing nanostructures via grazing incidence scattering. In particular, Au deposition on the polymer polystyrene (PS) with the respective structural analogues poly-4-vinlypyridine (P4VP) and polystyrene sulfonic acid (PSS) is studied. Additionally, the nanostructured layers on these different polymer films are further probed by field emission scanning electron microscopy (FESEM), atomic force microscopy (AFM), X-ray reflectometry (XRR), and four-point probe measurements. We report that HiPIMS leads to smaller island-to-island distances throughout the whole sputter process. Moreover, an increased cluster density and an earlier percolation threshold are achieved compared to dcMS. Additionally, in the early stage, we observe a significant increase in coverage by HiPIMS, which is favorable for the improvement of the polymer-metal interface.

Enhancing copper corrosion resistance in highly caustic environments: Evaluation of environmentally friendly inorganic inhibitors and mechanistic insights

During this study, two inorganic glasses materials with chemical compositions of (1−x) (2Bi2 O3 ⋅B2 O3)–x BaO (with x=0.2 (BiB-Ba0.2) and x=0.6 and (BiB-Ba0.6)) were synthetized characterized and investigated as viable, ecofriendly, and sustainable inhibitors to mitigate copper corrosion in a highly caustic solution containing 0.5 M H2SO4 solution. To evaluate inhibition processes, several techniques were employed, including potentiodynamic polarization (PDP), electrochemical impedance spectroscopy (EIS), X-ray diffraction (XRD), Fourier transforms infrared spectroscopy (FTIR), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), and atomic force microscopy (AFM). Furthermore, the results show that the two inhibitors studied, BiB-Ba0.2 and BiB-Ba0.6, have higher corrosion inhibition efficiencies at the optimum concentration (10−3 M), reaching 91.2 % and 90.8 %, respectively. Moreover, these findings suggest that the two inorganic compounds elaborated possess inhibitors of mixed types. Copper oxide (Cu2O) production is markedly delayed when the two inhibitors are added to the acid medium, according to the findings of the XRD, FTIR, SEM/EDS, and AFM investigations. This outcome is explained by the development of a shield that lessens surface damage to copper metal, producing a smoother surface morphology.

Novel hybrid interference and atomic force microscopy

Abstract A novel hybrid microscope which combines an interference microscopic (IM) and an atomic force microscopic (AFM) measurement mode is introduced. It is realised by adding an AFM probe to an IM, where the AFM probe can be mechanically switched in or out of the beam path of the IM. When the AFM cantilever is out of the beam path, the system works in the IM measurement mode for noncontact and fast optical measurements. When the AFM cantilever is in the beam path, it works in the AFM measurement mode, where the AFM tip interacts with sample surfaces for measurements. The deformation of the AFM cantilever induced by the tip-sample interaction force is detected from interference fringes, which are formed by the interference of the light beam reflected from the backside of the AFM cantilever and a reference beam in the IM. This novel design has a high-level synergy of AFM and IM technologies and provides several promising application potentials. For instance, it can bring high-resolution AFM measurements whenever and wherever needed in IM measurements, thus, to complement the lateral resolution limits of IM; The AFM measurement mode can provide measurement results with higher topography fidelity, thus, to offer in-situ reference areal surface metrology for IM measurements. In the paper, design concept, realisation of a prototype instrument, and experimental results illustrating the performance of the prototype instrument are detailed. 

Automated High-Throughput Atomic Force Microscopy Single-Cell Nanomechanical Assay Enabled by Deep Learning-Based Optical Image Recognition.

Mechanical forces are essential for life activities, and the mechanical phenotypes of single cells are increasingly gaining attention. Atomic force microscopy (AFM) has been a standard method for single-cell nanomechanical assays, but its efficiency is limited due to its reliance on manual operation. Here, we present a study of deep learning image recognition-assisted AFM that enables automated high-throughput single-cell nanomechanical measurements. On the basis of the label-free identification of the cell structures and the AFM probe in optical bright-field images as well as the consequent automated movement of the sample stage and AFM probe, the AFM probe tip could be accurately and sequentially moved onto the specific parts of individual living cells to perform a single-cell indentation assay or single-cell force spectroscopy in a time-efficient manner. The study illustrates a promising method based on deep learning for achieving operator-independent high-throughput AFM single-cell nanomechanics, which will benefit the application of AFM in mechanobiology.

In-situ investigation into the atomic-scale removal behavior of gallium nitride

The process of elimination at the atomic level stands as the paramount step in crafting ultra-smooth gallium nitride (GaN) substrates. However, this delicate removal mechanism presents a notable challenge. In this study, we employed a scraping technique utilizing atomic force microscope (AFM) probe manipulation to conduct an in-situ examination of atomic-scale removal behaviors. Through in-situ regular imaging, we uncovered the principles underlying atomic-scale removal. We systematically explored how scraping and imaging techniques impacted surface topography and the behavior of atomic step-terraces removal. Our findings indicated that abrasives knocking facilitates the emergence of atomic step-terraces, while sliding removal techniques hinder the structure. During the scraping process, both the upper and lower sections of the atomic step-terraces were simultaneously eliminated, with material removal rate (MRR) being slower at the bottom. To validate our in-situ observations, we conducted polishing experiments. Furthermore, the coefficient of friction (COF) recorded during chemical mechanical polishing offered insights into the frictional disparities of abrasives on the GaN surface, thereby shedding light on the atomic-scale removal mechanism.

Physicochemical Changes of Apoferritin Protein during Biodegradation of Magnetic Metal Oxide Nanoparticles.

The biodegradation of therapeutic magnetic-oxide nanoparticles (MONPs) in the human body raises concerns about their lifespan, functionality, and health risks. Interactions between apoferritin proteins and MONPs in the spleen, liver, and inflammatory macrophages significantly accelerate nanoparticle degradation, releasing metal ions taken up by apoferritin. This can alter the protein's biological structure and properties, potentially causing health hazards. This study examines changes in apoferritin's shape, electrical surface potential (ESP), and protein-core composition after incubation with cobalt-ferrite (CoFe2O4) oxide nanoparticles. Using atomic force microscopy (AFM) and scanning Kelvin probe force microscopy (SKPFM), we observed changes in the topography and ESP distribution in apoferritin nanofilms over time. After 48 h, the characteristic apoferritin hole (∼1.35 nm) vanished, and the protein's height increased from ∼3.5 to ∼7.5 nm due to hole filling. This resulted in a significant ESP increase on the filled-apoferritin surface, attributed to the formation of a heterogeneous chemical composition and crystal structure (γ-Fe2O3, Fe3O4, CoO, CoOOH, FeOOH, and Co3O4). These changes enhance electrostatic interactions and surface charge between the protein and the AFM tip. This approach aids in predicting and improving the MONP lifespan while reducing their toxicity and preventing apoferritin deformation and dysfunction.

Probing the interactions between asphaltenes and a PEO-PPO demulsifier at oil–water interface: Effect of temperature

HypothesisAsphaltenes are primary stabilizers in water-in-oil (W/O) emulsions that cause corrosion and fouling issues. In oil sands industry, oil/water separation processes are generally conducted at high temperatures. A high temperature is expected to impact the interactions between asphaltenes and emulsion breakers (EBs), consequently influencing demulsification performance. ExperimentsThe adsorption and interactions of asphaltenes and a PEO-PPO type EB (Pluronic F68) at the oil–water interface were investigated at various temperatures, using tensiometer, quartz crystal microbalance with energy dissipation (QCM-D), and atomic force microscopy (AFM). The effect of temperature on EB’s demulsification performance was explored through bottle tests. Additionally, demulsification mechanisms were studied using direct force measurements with the droplet probe AFM technique. FindingsDynamic interfacial tension and QCM-D results demonstrate that the PEO-PPO type EB exhibits higher interfacial activity than asphaltenes and can disrupt rigid asphaltene films at the oil–water interfaces. Elevated temperatures accelerate the displacement of adsorbed asphaltenes by EB molecules, leading to sparse interfacial films, rapid droplet coalescence, and improved demulsification efficiency (supported by AFM and bottle test results). This work provides valuable insights into interfacial interactions between asphaltenes and EB at different temperatures, enhancing the understanding of demulsification mechanisms and offering useful implications for the development of efficient EBs to enhance oil/water separation performance.

Optimizing the thermoelectric performance of Bi-Sb-Te thin films through compositional engineering

The objective of the present investigation was to systematically investigate the structural and thermoelectric (TE) properties of BixSb2-xTe3 thin films with varying content of Bi. We investigated the impact of different atomic percentages of Bi (4, 6, 8 at. %) on the properties of carrier transport and TE performance. In general, the Seebeck coefficient remained consistent across the thin films. For the 8 at. % Bi thin film, the Seebeck coefficient and electrical conductivity were measured at 230 μV/K and 730 S/cm, respectively, at room temperature. These values were more than 20 times greater than the electrical conductivity observed in the thin films with compositions of 6 and 4 at. % Bi. As a result, the Bi-Sb-Te compound exhibited a TE power factor (PF) of 38x10−4 W/mK2 at 40 °C, surpassing the PFs observed in previous compositions. The analysis of surface microstructure, combined with atomic force microscopy and Kelvin probe microscopy images, revealed that the transport of carriers in films with high Bi content was impeded by the size of particles and scattering sites. On the other hand, an augmentation in Bi content promoted the transfer of charge through crystalline regions, hence improving the mobility of carriers and the total electrical conductivity. The aforementioned results emphasize the significant influence of Bi content on the electrical properties of semiconductors and demonstrate the effectiveness of compositional engineering based on Bi content in the development of TE materials with superior performance. The present study investigates the influence of Bi content on the electrical properties of Bi-Sb-Te thin films, demonstrating that compositional adjustments based on Bi content can impact the performance of TE materials. These findings contribute to the understanding of material optimization in the field of TE.

Effects of adhesive and frictional contacts on the nanoindentation of two-dimensional material drumheads

Nanoindentation of suspended circular thin films, dubbed drumhead nanoindentation, is a widely adopted technique for characterizing the mechanical properties of micro- or nano-membranes, including atomically thin two-dimensional (2D) materials. This method involves suspending an ultrathin specimen over a circular microhole and applying a precise indenting force at the center using an atomic force microscope (AFM) probe. Classical solutions assuming a point load and a fixed edge, which are referred to as Schwerin-type solutions, are commonly used to estimate Young’s modulus of the membrane material out of load–deflection measurements. However, given the widespread experimental evidence for adhesive and frictional contacts between the probe tip and the membrane, as well as sliding between the membrane and its supporting substrate, quantitative investigations of the effects of these interactions are required. In this paper, we formulate a boundary value problem to rigorously model such effects, ensuring relevance to experimental operations. Our numerical analyses reveal that the adhesive effect at the tip-membrane interface diminishes as the indentation depth increases or the tip size decreases. Furthermore, frictional interactions at this interface shift the maximum membrane stress from the center to the tip-membrane contact line with increasing indentation depth and interfacial shear stress. At large indentation depths, the size of the indenter tip and the sliding of the membrane-substrate are found to have a large effect on the indentation load–deflection relationship. Thus, we propose a new approximate formula for this relationship assuming a non-adhesive and frictionless spherical tip of a finite radius and a slippery contact with the supporting substrate. This formula is more accurate than the widely used Schwerin-type solution. It can be used to simultaneously extract the in-plane stiffness of the membrane and the shear strength at the membrane-substrate interface.

Anisotropic Stick-Slip Frictional Surfaces via Titania Nanorod Patterning.

Nanoscale or microscale surface texturing is an effective technique to tailor the tribological properties between two surfaces that are rubbed against each other. In order to achieve the desired frictional properties by a patterned surface, one needs an in-depth understanding of the underlying mechanisms. Here, we demonstrate anisotropic stick-slip friction achieved via a nanotextured surface of tilted titania nanorods (TiNRs). The surface was developed by using the glancing angle deposition (GLAD) technique, and exhibited load-dependent variations in stick-slip friction as well as frictional anisotropy in different sliding directions. For studying the frictional properties of the newly developed surface, lateral force microscopy (LFM) was performed in three different reciprocal orientations (0° rotated, 45° rotated, 90° rotated) using a custom-made colloidal alumina atomic force microscopy (AFM) probe. The frictional behavior was found to vary significantly with the orientation. At 0° rotated position) a prominent "stick-slip" was observed when scanning opposite to the tilt direction, whereas the phenomenon reduced significantly when the nanotextured surface was scanned along the tilt direction or rotated to different angles (45 and 90°) with respect to the sliding direction of the AFM cantilever supporting the probe. The experimental findings were interpreted based on the classical solution for large deflections of tilted elastic rods. Overall, the textured surface, LFM-based frictional measurement, and the quantitative analysis presented here provide a fundamental understanding of how friction can be significantly varied on a surface patterned with tilted TiNRs at a length scale of about 1 μm, which can be comprehensively applied to nanorod patterns of other materials on different substrates.

A new mechanical engineering strategy based on microsphere probe and its application in transition metal dichalcogenides

Mechanical engineering of 2D materials allows continuous and reversible modulation of their electronic and photonic properties. Although photoluminescence (PL) measurement is an effective way to monitor the effects of mechanical forces on 2D semiconductors, there is currently a lack of techniques to enhance PL signals during stress application. This study presents an innovative mechanical engineering approach that integrates a dielectric microsphere as an atomic force microscopy (AFM) probe into a Raman-AFM system. Force–distance curve tests and COMSOL simulations were performed to analyze and estimate the compressive stress exerted by the microsphere. Importantly, the PL signals of transition metal dichalcogenides subjected to microsphere probe's force were enhanced and reveal distinct mechanical responses depending on the substrate rigidity: compressive pressures for rigid substrates and tensile strains for flexible ones. Notably, this strategy not only amplifies spectral signals in real time but also achieves fine stress modulation in the precise targeted material region, demonstrating its superiority in sensitive mechanical engineering applications. Our work offers a new avenue for the deliberate design of mechanical strains in 2D materials, which is crucial for optimizing the performance of related devices.