Atomic Force Microscopy Probe Research Articles

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.

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.

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.

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. 

Mechanical properties of freestanding few-layer graphene/boron nitride/polymer heterostacks investigated with local and non-local techniques.

van der Waals two-dimensional materials and heterostructures combined with polymer films continue to attract research attention to elucidate their functionality and potential applications. This study presents the fabrication and mechanical testing of 2D material heterostacks, consisting of few-layer boron nitride and graphene heterostructures synthesized via chemical vapor deposition, capped with a polymethyl methacrylate layer and suspended across ∼200 μm wide trenches using a combined wet-dry transfer method. The mechanical characterization of the heterostacks was performed using two independent approaches: (a) non-local testing with a custom-built tensile testing platform and (b) local load-displacement testing employing atomic force microscopy probes, complemented by finite element simulations. Both approaches provided new results, which are in good agreement with each other. Overall, our findings offer new insights into a combined load capacity in complex multi-material two-dimensional systems, and can contribute to advancing micro and nano-scale device designs and implementations.

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.

Electrified Nano-Gaps Under AC Field: A Molecular Dynamics Study

Solid-Liquid Interfaces (SLIs) hold immense significance in various areas such as materials science, chemistry, physics, biology and medicine [1]. Many studies aim to decipher the molecular details of SLIs through analytical, computational or experimental methods [2]-[3], each optimized for different aspects of SLIs. Analytical methods are mainly based on the mean field approximation and work best for dilute solutions. Computational methods are bound by their maximum accessible time and length scales, while the limitation of experimental approach tend to lie in minimum values accessible of these scales. The concomitant deployment of both the approaches is a powerful tool in studying SLIs.In the current study both the computational and experimental tools are employed to study the interface of silica with aqueous saline solutions under electric fields. Molecular Dynamics (MD) simulation are utilized to investigate the relative response of the ions and waters exposed to an external AC field in a nanoscale silica-elecrolyte-gold system. Complementary experimental measurements are conducted with atomic force microscopy (AFM) which measures the dielectric force exerted on the nanoscale AFM probe. The impact of external factors such as salt concentration, AC voltage frequency and the system size is systematically investigated.Simulations reveal both the transient and stable response of water and ions as the main component of the system to the AC field. In the transient response, the water electric dipole increases monotonically with the voltage at the first cycle while it takes longer for ions to react to the field, limited by their diffusion time. When the ionic response becomes large enough to screen the field, the dipole moment of water molecules decreases and lead the phase of the applied field. The lag in the ionic response is owing to the time required for the ionic diffusion, while the lead in the water response is due to ionic lag.To obtain the stable response through MD simulation, Fourier transform was deployed with the results showing that electric dipole of ions and water have a periodic behavior with a frequency similar to the AC field and waters in lead and ions in lag. The dipole-voltage plots for ions and waters depicted an energy transfer between water and ions in each cycle. Decreasing the frequency to 10MHz, no energy exchange was observed concomitant to the removal of water lead. Besides, in the frequency range of 100MHz-200MHz in which the water phase lead reaches its maximum value, there is also a maximum in the energy exchange. Thus, there is a direct relation between the water-ion energy exchange and lead in the water response.The stable response is affected by various factors including the separation distance between the surfaces, the ionic concentration and the AC frequency. The MD observations of a decrease in the water lead and ionic lag with reducing the electrolyte gap could explain AFM measurements where the dielectric force appears to decrease for small gaps, a counter-intuitive result if bulk electrolyte properties are assumed. The simulation results also show that the sum of the electric dipole of water and ions is always in phase with the applied voltage implying that the field is totally screened by the combination of both of them. To provide the same amount of screening in larger separation distance the electric dipole of ions has to increase to counteract its larger lag which is observed in the ionic dipole values. As the ionic dipole despite water molecules are caused by translational entropy, larger ionic dipole translates to larger forces which is observed in the AFM experiments.[1] Taketoshi et al. Japanese Journal of Applied Physics (2021).[2] T. Fukuma and R. Garcia, ACS nano (2018).[3] J.M. Andanson and A. Baiker, Chemical Society Reviews (2010).

Application of the nuclear tracks methodology for the validation of atomic force microscope probe tips

Atomic force microscopy (AFM) is a well-established technique for studying materials at nanoscale dimensions. The resolution of this instrument strongly relies on the sharpness of its tip, which can become compromised through wear and breakage, often due to contamination at the AFM tip apex. To evaluate the condition of both new and used tips, scanning electron microscopy (SEM) inspection is commonly employed. However, SEM services may not always be readily available or in high demand. In this study, we present an AFM tip calibration device that utilizes a pattern of etched tracks on CR-39 material. To construct this device, you will require a radioactive alpha particle source, typically Americium-241, as well as a controlled temperature bath set at 60 degrees Celsius, which contains a 6.25 M KOH solution. This endeavor serves as another intriguing and practical application of the nuclear tracks methodology.

An Infrared Nanospectroscopy Technique for the Study of Electric-Field-Induced Molecular Dynamics.

Static electric fields play a considerable role in a variety of molecular nanosystems as diverse as single-molecule junctions, molecules supporting electrostatic catalysis, and biological cell membranes incorporating proteins. External electric fields can be applied to nanoscale samples with a conductive atomic force microscopy (AFM) probe in contact mode, but typically, no structural information is retrieved. Here we combine photothermal expansion infrared (IR) nanospectroscopy with electrostatic AFM probes to measure nanometric volumes where the IR field enhancement and the static electric field overlap spatially. We leverage the vibrational Stark effect in the polymer poly(methyl methacrylate) for calibrating the local electric field strength. In the relevant case of membrane protein bacteriorhodopsin, we observe electric-field-induced changes of the protein backbone conformation and residue protonation state. The proposed technique also has the potential to measure DC currents and IR spectra simultaneously, insofar enabling the monitoring of the possible interplay between charge transport and other effects.

Atomic force microscopic investigations of transient early-stage bacterial adhesion and antibacterial activity of silver and ceria modified bioactive glass

Bioactive glass 58S (BG58S) is widely recognised for its bioactivity and antibacterial properties, making it a promising material for orthopaedic implant applications. This study investigates the effects of incorporating silver (BG58S-2.5Ag) and cerium oxide (BG58S-5C) into BG58S on early-stage bacterial adhesion and subsequent bacterial growth inhibition. Using a high-intensity ball milling approach, BG58S was modified with 5% cerium oxide (CeO2) and 2.5% silver (Ag) nanoparticles to create homogeneous BG58S-2.5Ag and BG58S-5C nanocomposites. Custom-made biomineral probes were employed to measure the bacterial adhesion within one second of contact with Gram-negative Escherichia coli and Gram-positive Staphylococcus aureus, using Atomic Force Microscopy (AFM). The results demonstrated that BG58S-2.5Ag showed significantly stronger transient adhesion to bacteria compared to BG58S, leading to a more effective long-term antibacterial response. Additionally, it was observed that the antibacterial effect of Ag commenced within one second of contact. These findings indicate a potential correlation between the rate of bond strengthening and cell wall penetration. This study highlights the potential for enhancing the effectiveness of antibacterial implant surfaces for various biomaterial applications.Graphical abstract

Magnetic imaging of individual magnetosome chains in magnetotactic bacteria

While significant advances have been made in exploring and uncovering the promising potential of biomagnetic materials, persistent challenges remain on various fronts, notably in the characterization of individual elements. This study makes use of advanced modes of Magnetic Force Microscopy (MFM) and tailored MFM probes to characterize individual magnetotactic bacteria in different environments. The characterization of these elements posed a significant challenge, as the magnetosomes, besides presenting low magnetic signal, are embedded in bacteria of much larger size. To overcome this, customed Atomic Force Microscopy probes are developed through various strategies, enhancing sensitivity in different environments, including liquids. Furthermore, employing MFM imaging under an in-situ magnetic field provides an opportunity to gather quantitative data regarding the critical fields of these individual chains of nanoparticles. This approach marks a substantial advancement in the field of MFM for biological applications, enabling the detection of magnetosomes under different conditions.

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.