Atomic Force Microscopy Observations Research Articles

Resistive Memristors Using Robust Electropolymerized Porous Organic Polymer Films as Switchable Materials.

Porous organic polymers (POPs) with inherent porosity, tunable pore environment, and semiconductive property are ideally suitable for application in various advanced semiconductor-related devices. However, owing to the lack of processability, POPs are usually prepared in powder forms, which limits their application in advanced devices. Herein, we demonstrate an example of information storage application of POPs with film form prepared by an electrochemical method. The growth process of the electropolymerized films in accordance with the Volmer-Weber model was proposed by observation of atomic force microscopy. Given the mechanism of the electron transfer system, we verified and mainly emphasized the importance of porosity and interfacial properties of porous polymer films for memristor. As expected, the as-fabricated memristors exhibit good performance on low turn-on voltage (0.65 ± 0.10 V), reliable data storage, and high on/off current ratio (104). This work offers inspiration for applying POPs in the form of electropolymerized films in various advanced semiconductor-related devices.

Effect of high sodium ion level on the interaction of AmB with a cholesterol-rich phospholipid monolayer.

Invasive fungal infections are a primary reason for high mortality in immunocompromised people, especially in critically ill patients, such as intensive care unit (ICU) patients, advanced cancer patients, or severe burn patients. Hypernatremia also can increase mortality in severely ill patients. Amphotericin B (AmB) is the gold standard for treating infections, but in severely ill patients, AmB can cause hematotoxicity when administered intravenously due to its interaction with cholesterol on red blood cell membranes. This results in limited doses of AmB and affects the treatment of infections. The proportion of cholesterol molecules in membrane lipids in red blood cells is as high as 50mol%, and the sodium ions can influence the interaction between AmB and lipids on the membrane. Therefore, in the complex clinical situation of a severely ill patient with a fungal infection and hypernatremia, the interaction between amphotericin B and the red blood cell membranes is worth studying in depth. In this work, the interaction between AmB and the dipalmitoyl phosphatidylcholine (DPPC)/cholesterol mixed monolayer in the presence of high sodium ion levels was studied when the proportion of cholesterol was 50%. The results show that the effect of AmB on reducing the monolayer's area at a high level of sodium ions is slightly stronger at 30mN/m. The effect of AmB on reducing the elastic modulus of the DPPC/Chol monolayer is significantly weakened by a high sodium ion level, compared with the level of sodium ions at normal physiological concentration. The higher the sodium ion concentration, the weaker the intermolecular force of the DPPC/Chol/AmB mixed monolayers. The scanning electron microscope (SEM) and atomic force microscopy (AFM) observations suggest that at a high sodium ion level, the presence of AmB significantly reduces the surface roughness of the DPPC/Chol monolayer. AmB may bind to cholesterol molecules, and it isolates cholesterol from the monolayer, resulting in a reduced height of the cholesterol-rich monolayer and an increasingly dispersed monolayer region. The results are beneficial to understanding the mechanism of impact of a high sodium ion level on the relationship between AmB and red blood cell membranes rich in cholesterol and are valuable for understanding the hemolytic toxicity of AmB to red blood cells at a high sodium ion level.

The Effect of Lubricity of Calcium Sulfonate on ZnDTP and MoDTC

Reduction of friction and wear by lubrication is necessary to improve the efficiency and prolong the lifespan of industrial machinery. However, several aspects regarding the lubrication effects in additive-combined oil are still unresolved. This study focuses on the effects of combining zinc dialkyldithiophosphate (ZnDTP), molybdenum dithiocarbamate (MoDTC), and Ca sulfonate on the frictional behavior of poly-α-olefin 4 (PAO4) lubricant oils. Ball-on-disk friction tests demonstrated that the exclusive addition of high-base Ca sulfonate solution reduced friction and wear of the lubricating oil. When combined with ZnDTP and MoDTC, the friction coefficients of PAO with high-base and low-base Ca sulfonate are affected by competitive reactions on the sliding surface. Quartz crystal microbalance with dissipation monitoring measurements suggests that high-base Ca sulfonate forms a stronger adsorption film than low-base Ca sulfonate. Atomic force microscope observations confirmed that the addition of low-base Ca sulfonate reduced friction and wear, whereas high-base Ca sulfonate induced competitive reactions with ZnDTP and MoDTC. This study provides valuable insights into the effects of the combination of additives on the lubricity of PAO and their impact on friction and wear characteristics, which are valuable for the design of suitable lubricants for industrial machinery.

A Rapid Self-Assembling Peptide Hydrogel for Delivery of TFF3 to Promote Gastric Mucosal Injury Repair.

Self-assembled peptide-based nanobiomaterials exhibit promising prospects for drug delivery applications owing to their commendable biocompatibility and biodegradability, facile tissue uptake and utilization, and minimal or negligible unexpected toxicity. TFF3 is an active peptide autonomously secreted by gastric mucosal cells, possessing multiple biological functions. It acts on the surface of the gastric mucosa, facilitating the repair process of gastric mucosal damage. However, when used as a drug, TFF3 faces significant challenges, including short retention time in the gastric mucosal cavity and deactivation due to degradation by stomach acid. In response to this challenge, we developed a self-assembled short peptide hydrogel, Rqdl10, designed as a delivery vehicle for TFF3. Our investigation encompasses an assessment of its properties, biocompatibility, controlled release of TFF3, and the mechanism underlying the promotion of gastric mucosal injury repair. Congo red/aniline blue staining revealed that Rqdl10 promptly self-assembled in PBS, forming hydrogels. Circular dichroism spectra indicated the presence of a stable β-sheet secondary structure in the Rqdl10 hydrogel. Cryo-scanning electron microscopy and atomic force microscopy observations demonstrated that the Rqdl10 formed vesicle-like structures in the PBS, which were interconnected to construct a three-dimensional nanostructure. Moreover, the Rqdl10 hydrogel exhibited outstanding biocompatibility and could sustainably and slowly release TFF3. The utilization of the Rqdl10 hydrogel as a carrier for TFF3 substantially augmented its proliferative and migratory capabilities, while concurrently bolstering its anti-inflammatory and anti-apoptotic attributes following gastric mucosal injury. Our findings underscore the immense potential of the self-assembled peptide hydrogel Rqdl10 for biomedical applications, promising significant contributions to healthcare science.

Excess Conductivity Analysis of an YBCO Foam Strut and Its Microstructure.

Struts of a superconducting YBa2Cu3Oy (YBCO) foam prepared by the infiltration growth method on the base of commercial polyurethane foams were extracted from the bulk, and thoroughly characterized concerning the microstructure and the magnetoresistance, measured by the four-point technique. Optical microscopy, electron microscopy, electron backscatter diffraction and atomic force microscopy observations indicate a unique microstructure of the foam struts which shows a large amount of tiny Y2BaCuO5 (Y-211) particles (with diameters between 50 and 100 nm) being enclosed in channel-like grain boundaries between the YBCO grains and a one-of-a-kind surface of the struts covered with Ba3Cu5Oy-particles. The resistance data obtained at temperatures in the range 4.2 K ≤T≤ 150 K (applied magnetic fields ranging from 0 to 7 T) were analyzed in the framework of the fluctuation-induced conductivity (FIC) approach using the models of Aslamazov-Larkin (AL) and Lawrence-Doniach (LD). The resulting FIC curves reveal the presence of five distinct fluctuation regimes, namely, the short-wave (SWF), one-dimensional (1D), two-dimensional (2D), three-dimensional (3D), and critical (CR) fluctuation domains. The analysis of the FIC data enable the coherence length in the direction of the c-axis at zero-temperature (ξc(0)), the irreversibility field (Birr), the upper critical magnetic field (Bc2), the critical current density at T= 0 K (Jc(0)) and several other parameters describing the the material's superconducting properties to be determined. The present data reveal that the minuscule Y-211 particles found along the YBCO grain boundaries alter the excess conductivity and the fluctuation behavior as compared to conventional YBCO samples, leading to a quite high value for Jc(0) for a sample with a non-optimized pinning landscape.

Substantial improvement in photocatalysis performance of N-TiO2 immobilized on PMMA: Exemplified by inactivation of Staphylococcus aureus and Escherichia coli

Photocatalysis is an efficient process for degrading organic pollutants and inactivating pathogenic microorganisms. However, this process constantly suffers from turbidity shading and particle aggregation in a catalyst suspension system, thereby reducing its photocatalytic activity. Immobilizing the photocatalyst on the light-transmissible surface is a viable solution to the obstacles. So far, the photo-inactivation efficacy between the immobilized photocatalyst and suspension systems has yet to be compared and investigated. In this study, N-TiO2 (NT) immobilized on poly-methyl-methacrylate (PMMA) was fabricated via a dip-coating method, which has a high transmittance rate of 92 % - better than all of the previous works (50 %). By immobilizing N-TiO2 on PMMA, up to 60 % and 19 % improvements in inactivation efficiencies against Gram-positive Staphylococcus aureus (S. aureus) and Gram-negative Escherichia coli (E. coli) are achieved, respectively, relative to a photocatalyst suspension. Notably, reactive oxygen species (ROSs) detection results indicate that 5 g/L NT coated PMMA ((NT-PMMA)5) has higher intensities of singlet oxygen (1O2), hydroxyl radicals (HO•), and higher concentration of hydrogen peroxide (H2O2) than the NT suspension. The as-made NT-PMMA sustains a 99.99 % inactivation efficiency (5-log-inactivation) against S. aureus through five consecutive photocatalysis cycles of reuse. The inactivation kinetics of S. aureus and E. coli fit well with the modified Hom model. Atomic force microscopy observations indicate that the NT-PMMA inactivation causes more severe damage to S. aureus's cell wall than E. coli due to the different susceptibility of cell wall structure to ROSs. This study paves a substantial way for scaling up the immobilizing catalyst on PMMA for the effective photocatalytic inactivation of pathogens under visible light.

In Situ Real-Time Atomic Force Microscopy Observations of Chain Mobility at Polymer/Water Interfaces of Poly(methyl methacrylate), Poly(2-hydroxyethyl methacrylate), and Poly(2-methoxyethyl methacrylate) Films in Water.

Polymer materials are widely used in water or in contact with an aqueous environment. However, evaluating the chain mobility, a crucial parameter, at a polymer-water interface is challenging. In this study, we, for the first time, observed poly(methyl methacrylate) (PMMA), poly(2-hydroxyethyl methacrylate) (PHEMA), and poly(2-methoxyethyl methacrylate) (PMEMA) film surfaces in water via in situ real-time atomic force microscopy (AFM) in tapping mode and quantified the chain mobility. The average displacement between adjacent images (nm/8.75 min) was evaluated using particle image velocimetry. The displacement of PMMA, which has a high bulk glass-transition temperature (Tg) (108 °C) and exhibits limited water absorption, was low both in air (0.54 nm/8.75 min) and water (0.86), while PHEMA, which has a high bulk Tg (99 °C) and exhibits high water absorption, exhibited low mobility in air (0.40) but two orders of magnitude higher mobility in water (60). PMEMA, which has a low bulk Tg (14 °C) and exhibits limited water absorption, already started to move in air (4.5), and its mobility moderately increased in water (20). These behaviors were reasonable, considering the bulk Tg and water absorption characteristics of the polymers. Further, the chain mobility in water was compared with that of dried samples at high temperatures in air. The mobility of PMMA, PHEMA, and PMEMA in water corresponded to that of the dried samples observed in air below the surface Tg (97 °C) for PMMA, at ∼125 °C for PHEMA, and at ∼35 °C for PMEMA. In situ real-time AFM analysis of polymer materials in water is an effective method for evaluating the chain mobility at the polymer/water interface.

Ionic Liquid Interface as a Cell Scaffold.

In sharp contrast to conventional solid/hydrogel platforms, water-immiscible liquids, such as perfluorocarbons and silicones, allow the adhesion of mammalian cells via protein nanolayers (PNLs) formed at the interface. However, fluorocarbons and silicones, which are typically used for liquid cell culture, possess only narrow ranges of physicochemical parameters and have not allowed for a wide variety of cell culturing environments. In this paper, it is proposed that water-immiscible ionic liquids (ILs) are a new family of liquid substrates with tunable physicochemical properties and high solvation capabilities. Tetraalkylphosphonium-based ILs are identified as non-cytotoxic ILs, whereon human mesenchymal stem cells are successfully cultured. By reducing the cation charge distribution, or ionicity, via alkyl chain elongation, the interface allows cell spreading with matured focal contacts. High-speed atomic force microscopy observations of the PNL formation process suggest that the cation charge distribution significantly altered the protein adsorption dynamics, which are associated with the degree of protein denaturation and the PNL mechanics. Moreover, by exploiting dissolution capability of ILs, an ion-gel cell scaffold is fabricated. This enables to further identify the significant contribution of bulk subphase mechanics to cellular mechanosensing in liquid-based culture scaffolds.

Promising way for enhancing light absorption in silicon via silver nanoparticles: experimental and numerical study

Silver nanoparticles (Ag-Nps) were grown on the surface of a p-type crystalline silicon (C-Si) substrate using electroless metal deposition. It was found that the Ag-Nps distribution on C-Si was controlled by the silver nitrate (AgNO3) concentrations. Atomic force microscopy observations revealed the formation of a continuous layer at high concentration. In contrast, a distribution of Ag-Nps with a spherical shape was obtained at lower concentration. The samples were also examined by optical microscopy under dark field illumination. The light reflected from Ag-Nps was obtained with different colors. This difference indicates a slight change in particle size. It is demonstrated that a silicon substrate with deposited Ag-Nps shows a significant decrease in reflectance and an increase of the absorption in the region from 200 to 800 nm. Moreover, the behavior of small Ag-Nps while interacting with light (absorbed or scattered light) is theoretically described using the Mie theory based on the Drude model. The introduction of silver nanoparticles on silicon surface is used to improve the efficiency of solar cells by reducing reflection and increasing the light absorption.

Research on the method of loading exosomes onto absorbable stents

To explore a method of loading exosomes onto absorbable stents. By building a stent-(3-aminopropyl) triethoxysilane-1, 2-distearoyl-sn-glycero-3-phosphoethanolamine-N-[methoxy (polyethylene glycol) 5000]-exosomes connection, the exosomes were loaded onto absorbable stents to obtained the exosome-eluting absorbable stents. The surface conditions of the stents and absorption of exosomes were observed by scanning electron microscope and identified through the time-of-flight mass spectrometry; the roughness of the stents' surfaces was observed by atomic force microscope; the appearances and sizes of the stents were observed by stereomicroscope; and the radial force was tested by tensile test machine. The absorbable stents were used as control. The scanning electron microscope observation showed that the exosome-eluting absorbable stents had some small irregular cracks on the surface where many exosomes could be seen. The atomic force microscopy observation showed that within the range of 5 μm 2, the surface roughness of the absorbable stents was ±20 nm, while the surface roughness of the exosome-eluting absorbable stents was ±70 nm. In the results of time-of-flight mass spectrometry, both the exosome-eluting absorbable stents and exosomes had a peak at the mass charge ratio of 81 (m/z 81), while the absorbable stents did not have this peak. The peak of exosome-eluting absorbable stents at m/z 73 showed a significant decrease compared to the absorbable stents. The stereomicroscope observation showed that the sizes of exosome-eluting absorbable stents met standards and the surfaces had no cracks, burrs, or depressions. The radial force results of the exosome-eluting absorbable stents met the strength standards of the original absorbable stent. By applying the chemical connection method, the exosomes successfully loaded onto the absorbable stents. And the sizes and radial forces of this exosome-eluting absorbable stents meet the standards of the original absorbable stents.

In Situ Atomic Force Microscopy Observation of Folded-Chain Crystallization of Single Isolated Isotactic Poly(methyl methacrylate) Chains in Langmuir–Blodgett Monolayers

In Situ Atomic Force Microscopy Observation of Folded-Chain Crystallization of Single Isolated Isotactic Poly(methyl methacrylate) Chains in Langmuir–Blodgett Monolayers

Myosin-independent stiffness sensing by fibroblasts is regulated by the viscoelasticity of flowing actin

The stiffness of the extracellular matrix induces differential tension within integrin-based adhesions, triggering differential mechanoresponses. However, it has been unclear if the stiffness-dependent differential tension is induced solely by myosin activity. Here, we report that in the absence of myosin contractility, 3T3 fibroblasts still transmit stiffness-dependent differential levels of traction. This myosin-independent differential traction is regulated by polymerizing actin assisted by actin nucleators Arp2/3 and formin where formin has a stronger contribution than Arp2/3 to both traction and actin flow. Intriguingly, despite only slight changes in F-actin flow speed observed in cells with the combined inhibition of Arp2/3 and myosin compared to cells with sole myosin inhibition, they show a 4-times reduction in traction than cells with myosin-only inhibition. Our analyses indicate that traditional models based on rigid F-actin are inadequate for capturing such dramatic force reduction with similar actin flow. Instead, incorporating the F-actin network’s viscoelastic properties is crucial. Our new model including the F-actin viscoelasticity reveals that Arp2/3 and formin enhance stiffness sensitivity by mechanically reinforcing the F-actin network, thereby facilitating more effective transmission of flow-induced forces. This model is validated by cell stiffness measurement with atomic force microscopy and experimental observation of model-predicted stiffness-dependent actin flow fluctuation.

Experimental evidence for immiscibility of enantiomeric polymers: Phase separation of high-molecular-weight poly(ʟ-lactide)/poly(ᴅ-lactide) blends and its impact on hindering stereocomplex crystallization

Although polymers tend not to mix, it remains challenging to characterize the immiscibility of enantiomeric poly(ʟ-lactide) (PLLA) and poly(ᴅ-lactide) (PDLA), particularly with equivalent and high molecular weight (high MW), which frustratingly disfavors the exclusive stereocomplexation. By introducing a random copolymer (PLC) of ʟ-lactide and caprolactone to form binary blends with PLLA and PDLA, the phase behavior of high-MW PLLA/PDLA blends was investigated mainly by using differential scanning calorimetry (DSC) and atomic force microscopy (AFM). DSC results showed that PLLA/PLC blends exhibited a single glass transition temperature (Tg), which depended on the blending ratio and precisely corresponded with the theoretical values calculated from the Fox equation. In comparison, PDLA/PLC blends showed composition-dependent heat-capacity increment at two unchanged Tg values of pure PLC and PDLA. AFM observation revealed that PLC is completely miscible with PLLA at high MW but is immiscible with PDLA, logically suggesting immiscibility of high-MW PLLA and PDLA. Moreover, AFM results demonstrated that high-MW PLLA/PDLA blends exhibited spherical droplets in asymmetric blends and bicontinuous interpenetrating worm-like patterns in symmetric counterparts, showing distinct and well-defined interfaces, confirming the microphase separation. Additionally, different MWs fundamentally led to significant differences in miscibility, which consequently affected the crystallization behaviors of PLLA/PDLA blends. This work provides evidence for (im)miscibility and its crucial impact on the crystallization of PLLA/PDLA blends and has important implications for understanding the stereocomplexation of polymers.

Chitosan inhibits Penicillium expansum possibly by binding to DNA and triggering apoptosis

Chitosan is a natural polysaccharide that is abundant, biocompatible and exhibits effective antifungal activity against various pathogenic fungi. However, the potential intracellular targets of chitosan in pathogenic fungi and the way of activity of chitosan are far from well known. The present work demonstrated that chitosan could inhibit Penicillium expansum, the principal causal agent of postharvest blue mold decay on apple fruits, by binding to DNA and triggering apoptosis. UV–visible spectroscopy, fluorescence spectroscopy and electrophoretic mobility assay proved the interaction between chitosan and DNA, while atomic force microscope (AFM) observation revealed the binding morphology of chitosan to DNA. Chitosan could inhibit in vitro DNA replication, and cell cycle analysis employing flow cytometry demonstrated that cell cycle was retarded by chitosan treatment. Furthermore, the reactive oxygen species (ROS) assay and membrane potential analysis showed that apoptosis was induced in P. expansum cells after exposure to chitosan. In conclusion, our results confirmed that chitosan interacts with DNA and induces apoptosis. These findings are expected to provide a feasible theoretical basis and practical direction for the promoting and implementing of chitosan in plant protection and further illuminate the possible antifungal mechanisms of chitosan against fungal pathogens.

Atomic force microscopy observation of surface morphologies and measurements of local contact potential differences of amorphous solid water samples deposited at 15 and 100 K.

We use an ultra-high vacuum cryogenic atomic force microscope to investigate the surface morphology of amorphous solid water (ASW) prepared by oblique deposition of water vapor onto Si(111)7 × 7 substrates at temperatures of 15 and 100 K. Height-height correlation function analysis of topographic images suggests that ASW at 15 K has a columnar structure and that the typical diameter of the column is 5-10 nm. At 100 K, the typical diameter is 10-30 nm, although columnar features are less prominent. The surface roughness (i.e., deviation of the height) is greater at 15 K than at 100 K, indicating that the surface at 100 K exhibits a relatively flat morphology. This result implies that transient diffusion of deposited water molecules affects the surface morphology at 100 K. In addition, measurements of the local contact potential difference between the tip and the ASW surface suggest that the magnitude of the negative surface potential at the microscopic scale, which is attributed to spontaneous polarisation, cannot simply be scaled by the thickness of ASW as predicted in previous experiments with Kelvin probes.

Anodization and nonstructural surface characterizations of fabricated Ti–29Nb–13Ta–7.1Zr alloy for biomedical applications and its mechanical, wettability, tribological, and corrosion properties

Implants subjected to tribocorrosion release metallic ions and solid wear debris, which can cause a peri-implant disease, bone loss, and eventually implant loosening. TiO2 coatings have a wide application range owing to their biocompatibility. In this study, the Ti–29Nb–13Ta–7.1 Zr alloy was fabricated using powder metallurgy technique. The samples were electrochemically oxidized to produce self-standing TiO2 nanotubular arrays followed by annealing for 1 h at 450 °C to improve their crystallinity. The prepared TiO2 coatings were characterized by SEM, X-ray diffraction, and EDX, and the wettability, tribomechanical characteristics, and corrosion behavior of bio-functionalized TiO2 nanotubes were investigated. Atomic force microscopy observations were conducted to examine wear scars, and the wear volume was measured via 2D profilometry. Microhardness and nanoindentation tests were performed to evaluate the mechanical characteristics of TiO2 nanotubes such as microhardness, nanohardness, and modulus of elasticity. The thickness and diameter of the observed TiO2 nanotubes are 2 μm and 90.94 nm, respectively. The obtained results revealed that the deposition of a biofunctionalized Ti/TiO2 nanotube layer enhanced the hydrophilicity, tribomechanical properties, and corrosion resistance of the Ti–29Nb–13Ta–7.1Zr alloy. The COF of Ti alloy was 0.51 and it decreased to 0.28 after anodization and annealing at 450 °C. The contact angle of the Ti sample was 79.9° and it decreased to 45.6° after annealing at 850 °C. However, after the anodic oxidation and annealing at 450 °C, the contact angle decreased to 45.6°.

Strengthening the diffusion of sodium ions by interactions between gum Arabic and oral mucin

In present study, we explored the effect of mucin-gum arabic (GA) interactions on the structural changes of mucin network, as well as on the diffusion behaviors of sodium ions. Diffusion behaviors of sodium ions through the mucin/GA layer with various physicochemical properties were determined. Our results suggested that the introduction of GA induced the phase separation of mucin-GA binary system, which is largely driven by electrostatic interactions (electrostatic repulsion) and followed by the structural changes in the mucin layer. The mucin/GA mixed interconnected network with larger pores was formed, as revealed by transmission electron microscopy and atomic force microscopy observations, which contributed to the diffusion of sodium ions. Our findings might provide a deep understanding of GA for enhancing the salty taste perception.

High-Speed AFM Observation of Electrolytic Nanobubbles Formation on HOPG

IntroductionNanobubbles (NBs) on solid surfaces are an interesting topic for surface and colloid science. Since the diameter of NBs is less than 1 μm, NBs can be morphologically measured by atomic force microscope (AFM) [1]. However, due to the slow scanning speed of conventional atomic force microscope (AFM), the nucleation and growth process is not yet known. We previously applied high-speed AFM (HS-AFM) for NBs’ evolution during water electrolysis [2]. Here, we discuss the NBs’ formation during cyclic voltammetry (CV).ExperimentalThe experimental cell was a three-electrode system at room temperature. The working electrode was highly ordered pyrolytic graphite (HOPG). The counter and reference electrodes were Pt wires. The electrolyte was a sulfuric acid solution (5 mmol L-1). CV was performed by a potentiostat. HS-AFM was operated in dynamic mode. The scanning speed was 0.5 frame s-1 and the size was 1 × 0.75 µm2.Results and discussionWhen the potential was swept to the anode from the open circuit potential, the pancake-like NBs were formed (Fig. 1). The height was ~5 nm, and the surface roughness was very small (< 1 nm). The pancake NBs grew along the step side and moved actively on the surface. They occasionally coalesced with neighboring NBs.On the other hand, when the potential was swept to the cathode, the dynamic process was the opposite. The pancake NBs dissolved. This poster will present the dynamic variation of electrolytic NBs during the CV.Reference[1] X.H. Zhang et al., Langmuir, 23, 1778 (2007).[2] M Mita, H Matsushima, M Ueda, H Ito, J. Colloid Interface Sci., 641, 389 (2022). Figure 1

Predicting the placement of biomolecular structures on AFM substrates based on electrostatic interactions

Atomic force microscopy (AFM) and high-speed AFM allow direct observation of biomolecular structures and their functional dynamics. Based on scanning the molecular surface of a sample deposited on a supporting substrate by a probing tip, topographic images of its dynamic shape are obtained. Critical to successful AFM observations is a balance between immobilization of the sample while avoiding too strong perturbations of its functional conformational dynamics. Since the sample placement on the supporting substrate cannot be directly controlled in experiments, the relative orientation is a priori unknown, and, due to limitations in the spatial resolution of images, difficult to infer from a posteriori analysis, thus hampering the interpretation of measurements. We present a method to predict the macromolecular placement of samples based on electrostatic interactions with the AFM substrate and demonstrate applications to HS-AFM observations of the Cas9 endonuclease, an aptamer-protein complex, the Monalysin protein, and the ClpB molecular chaperone. The model also allows predictions of imaging stability taking into account buffer conditions. We implemented the developed method within the freely available BioAFMviewer software package. Predictions based on available structural data can therefore be made even prior to an actual experiment, and the method can be applied for post-experimental analysis of AFM imaging data.

Large rotating magnetocaloric effects in polycrystalline Ni-Mn-Ga melt-spun ribbons

In this study, the different wheel speeds Ni53Mn23.5Ga23.5 alloy ribbons were prepared by melt-spun method. The morphology and crystal structure, martensitic phase transformation, magnetocrystalline anisotropy, in situ technique magnetization observation and the magnetic refrigeration capacity resulting were tested. The ratio of the length to width for the columnar crystals is approximately 2.5:1.0 in the sample created at a wheel speed of 12 m s−1, and it increases to 5:1 in the sample produced at a wheel speed of 18 m s−1. It is found that a sample with 18 m s−1 ha−1s−1 a large rotating magnetocaloric effect in polycrystalline alloys, with the results of 2 K with different directions. It can be designed as a working substance for rotary refrigeration machines that make full use of their anisotropic characteristics. The in situ atomic force microscope observation of the technological magnetisation has provided an important exploration for a better understanding of the magnetisation.