Atomic Force Microscopy Techniques Research Articles

Mechanical properties of tunneling nanotube and its mechanical stability in human embryonic kidney cells.

Tunneling nanotubes (TNTs) are thin membrane tubular structures that interconnect physically separated cells. Growing evidence indicates that TNTs play unique roles in various diseases by facilitating intercellular transfer of signaling and organelles, suggesting TNTs as a potential target for disease treatment. The efficiency of TNT-dependent communication is largely determined by the number of TNTs between cells. Though TNTs are physically fragile structures, the mechanical properties of TNTs and the determinants of their mechanical stability are still unclear. Here, using atomic force microscope (AFM) and microfluidic techniques, we investigated the mechanical behavior and abundance of TNTs in human embryonic kidney (HEK293) cells upon the application of forces. AFM measurements demonstrate that TNTs are elastic structures with an apparent spring constant of 79.1 ± 16.2 pN/μm. The stiffness and membrane tension of TNTs increase by length. TNTs that elongate slower than 0.5 μm/min display higher mechanical stability, due to the growth rate of F-actin inside TNTs being limited at 0.26 μm/min. Importantly, by disturbing the cytoskeleton, membrane, or adhesion proteins of TNTs, we found that F-actin and cadherin connection dominantly determines the tensile strength and flexural strength of TNTs respectively. It may provide new clues for screening TNT-interfering drugs that alter the stability of TNTs.

Use of Nanoparticles to Prevent Resistance to Antibiotics-Synthesis and Characterization of Gold Nanosystems Based on Tetracycline.

Antimicrobial resistance (AMR) is a serious public health problem worldwide which, according to the World Health Organization (WHO), requires research into new and more effective drugs. In this work, both gold nanoparticles covered with 16-3-16 cationic gemini surfactant (Au@16-3-16) and DNA/tetracycline (DNA/TC) intercalated complexes were prepared to effectively transport tetracycline (TC). Synthesis of the Au@16-3-16 precursor was carried out by using trihydrated gold, adding sodium borohydride as a reducing agent and the gemini surfactant 16-3-16 as stabilizing agent. Circular dichroism and atomic force microscopy techniques were then used to ascertain the optimal R range of the relationship between the concentrations of Au@16-3-16 and the DNA/TC complex (R = CAu@16-3-16/CDNA) that allow the obtainment of stable and compact nanosystems, these characteristics being fundamental for their use as antibiotic transporters. Stability studies over time were carried out for distinct selected Au@16-3-16 and Au@16-3-16/DNA-TC nanoformulations using the ultraviolet–visible spectrophotometry technique, checking their stability for at least one month. In addition, in order to know the charge and size distribution of the nanocomplexes, DLS and zeta potential measurements were performed in the solution. The results showed that the characterized nanosystems were highly charged, stable and of a reduced size (<100 nm) that allows them to cross bacterial membranes effectively (>1 μm). Once the different physicochemical characteristics of the gold nanosystems were measured, Au@16-3-16 and Au@16-3-16/DNA-TC were tested on Escherichia coli and Staphylococcus aureus to study their antibacterial properties and internalization capacity in microbes. Differences in the interaction of the precursors and the compacted nanosystems generated were observed in Gram-positive and Gram-negative bacteria, possibly due to membrane damage or electrostatic interaction with internalization by endocytosis. In the internalization experiments, depending on the treatment application time, the greatest bacterial destruction was observed for all nanoformulations explored at 18 h of incubation. Importantly, the results obtained demonstrate that both new nanosystems based on TC and Au@16-3-16 precursors have optimal antimicrobial properties and would be beneficial for use in patients, avoiding possible side effects.

Morphology-Tuned Electrochemical Immunosensing of a Breast Cancer Biomarker Using Hierarchical Palladium Nanostructured Interfaces.

Metallic nanostructures are considered attractive candidates for designing novel biosensors due to their enormously significant surface area, accelerated kinetics, and improved affinity. Controllable morphological tuning of metallic nanostructures on sensing interfaces is crucial for attaining clinically relevant sensitivity and exquisite selectivity in a complex biological environment. Therefore, a facile, convenient, and robust one-step electroreduction method was employed to develop different morphological variants of palladium (Pd) nanostructures supported onto oxidized carbon nanotubes to facilitate label-free electrochemical immunosensing of HER2. The morphological and structural attributes of the synthesized Pd nanostructures were thoroughly investigated using scanning electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and atomic force microscopy techniques. In-depth electrochemical investigations revealed an intimate correlation between the nanostructured sensor and electrochemical response, suggesting the suitability of hierarchical palladium nanostructures supported onto carbon nanotubes [Pd(−0.1 V)/CNT] for sensitive detection of HER2. The high surface area of hierarchical Pd nanostructures enabled an ultrasensitive electrochemical response toward HER2 (detection limit: 1 ng/mL) with a wide detection range of 10 to 100 ng/mL. The ease of surface modification, sensitivity, and reliable electrochemical response in human plasma samples suggested the enormous potential of Pd nanostructuring for chip-level point-of-care screening of HER2-positive breast cancer patients.

Biochemistry and Nanomechanical Properties of Human Colon Cells upon Simvastatin, Lovastatin, and Mevastatin Supplementations: Raman Imaging and AFM Studies.

One of the most important areas of medical science is oncology, which is responsible for both the diagnostics and treatment of cancer diseases. Over the years, there has been an intensive development of cancer diagnostics and treatment. This paper shows the comparison of normal (CCD-18Co) and cancerous (CaCo-2) cell lines of the human gastrointestinal tract on the basis of nanomechanical and biochemical properties to obtain information on cancer biomarkers useful in oncological diagnostics. The research techniques used were Raman spectroscopy and imaging and atomic force microscopy (AFM). In addition, the studies also included the effect of the statin compounds—mevastatin, lovastatin, and simvastatin—and their influence on biochemical and nanomechanical changes of cell properties using Raman imaging and AFM techniques. The cytotoxicity of statins was determined using XTT tests.

Unraveling Nanoscale Elastic and Adhesive Properties at the Nanoparticle/Epoxy Interface Using Bimodal Atomic Force Microscopy.

The addition of a small fraction of solid nanoparticles to thermosetting polymers can substantially improve their fracture toughness, while maintaining various intrinsic thermomechanical properties. The underlying mechanism is largely related to the debonding process and subsequent formation of nanovoids at a nanoscale nanoparticle/epoxy interface, which is thought to be associated with a change in the structural and mechanical properties of the formed epoxy network at the interface compared with the matrix region. However, a direct characterization of the local physical properties at this nanoscale interface remains significantly challenging. Here, we employ a recently developed bimodal atomic force microscopy technique for the direct mapping of nanoscale elastic and adhesive responses of an amine-cured epoxy resin filled with ∼50 nm diameter silica nanoparticles. The obtained elastic modulus and dissipated energy maps with high spatial resolution evidence the existence of a ∼20-nm-thick interfacial epoxy layer surrounding the nanoparticles, which exhibits a reduced modulus and weaker adhesive response in comparison with the matrix properties. While the presence of such a soft and weak-adhesive interfacial layer is found not to affect the architecture of structural heterogeneities in the epoxy matrix, it conceivably supports the toughening mechanism related to the debonding and plastic nanovoid growth at the silica/epoxy interface. The incorporation of this soft interfacial layer into the Halpin-Tsai model also provides a good explanation for the effect of the silica fraction on the tensile modulus of cured epoxy nanocomposites.

Antibacterial Studying of Silver Nanoparticles Synthesized by Chemical Reduction Method Using Different Stabilized Concentrations

Silver nanoparticles were prepared by the chemical reduction method. Silver nitrate was taken as a metal precursor and sodium borohydride as a reducing agent with polyvinyl alcohol (PVA) stabilizers of different concentrations, polyvinylpyrrolidone (PVP). X-ray diffraction (XRD), transmission electron microscopy (TEM), and atomic force microscopy (AFM) techniques have been used, these measurement results showed that the prepared material is silver nanoparticles. The average size of silver nanoparticles using the Scherrer equation with values ranging from 8.49-12.15nm. TEM images showed that the silver nanoparticles are spherical in size between 5-47nm. Nanoscale distribution of silver nanoparticles (AgNPs) prepared at different concentrations was studied by AFM. Silver nanoparticles showed high antimicrobial and antibacterial activity against Gram-positive bacteria such as Escherichia Coli and Gram-negative Staphylococcus aureus, whose bacterial activity was dependent on the concentration of PVA and PVP and the degree of intramolecular accumulation. Low concentrations of PVP lead to increase the activity, while high concentrations of PVA give better activity.

Cu and Zn Interactions with Peptides Revealed by High-Resolution Mass Spectrometry.

Alzheimer’s disease (AD) is a progressive neurodegenerative disease characterized by abnormal extracellular amyloid-beta (Aβ) peptide depositions in the brain. Among amorphous aggregates, altered metal homeostasis is considered a common risk factor for neurodegeneration known to accelerate plaque formation. Recently, peptide-based drugs capable of inhibiting amyloid aggregation have achieved unprecedented scientific and pharmaceutical interest. In response to metal ions binding to Aβ peptide, metal chelation was also proposed as a therapy in AD. The present study analyzes the interactions formed between NAP octapeptide, derived from activity-dependent neuroprotective protein (ADNP), amyloid Aβ(9–16) fragment and divalent metal ions such as Cu and Zn. The binding affinity studies for Cu and Zn ions of synthetic NAP peptide and Aβ(9–16) fragment were investigated by matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS), electrospray ion trap mass spectrometry (ESI-MS) and atomic force microscopy (AFM). Both mass spectrometric methods confirmed the formation of metal–peptide complexes while the AFM technique provided morphological and topographic information regarding the influence of metal ions upon peptide crystallization. Our findings showed that due to a rich histidine center, the Aβ(9–16) fragment is capable of binding metal ions, thus becoming stiff and promoting aggregation of the entire amyloid peptide. Apart from this, the protective effect of the NAP peptide was found to rely on the ability of this octapeptide to generate both chelating properties with metals and interactions with Aβ peptide, thus stopping its folding process.

Formulation and Development of Bioadhesive Oral Films Containing Usnea barbata (L.) F.H.Wigg Dry Ethanol Extract (F-UBE-HPC) with Antimicrobial and Anticancer Properties for Potential Use in Oral Cancer Complementary Therapy.

Medical research explores plant extracts’ properties to obtain potential anticancer drugs. The present study aims to formulate, develop, and characterize the bioadhesive oral films containing Usnea barbata (L.) dry ethanol extract (F-UBE-HPC) and to investigate their anticancer potential for possible use in oral cancer therapy. The physicochemical and morphological properties of the bioadhesive oral films were analyzed through Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), Atomic Force Microscopy (AFM), thermogravimetric analysis (TG), and X-ray diffraction techniques. Pharmacotechnical evaluation (consisting of the measurement of the specific parameters: weight uniformity, thickness, folding endurance, tensile strength, elongation, moisture content, pH, disintegration time, swelling rate, and ex vivo mucoadhesion time) completed the bioadhesive films’ analysis. Next, oxidative stress, caspase 3/7 activity, nuclear condensation, lysosomal activity, and DNA synthesis induced by F-UBE-HPC in normal blood cell cultures and oral epithelial squamous cell carcinoma (CLS-354) cell line and its influence on both cell types’ division and proliferation was evaluated. The results reveal that each F-UBE-HPC contains 0.330 mg dry extract with a usnic acid (UA) content of 0.036 mg. The bioadhesive oral films are thin (0.093 ± 0.002 mm), reveal a neutral pH (7.10 ± 0.02), a disintegration time of 118 ± 3.16 s, an ex vivo bioadhesion time of 98 ± 3.58 min, and show a swelling ratio after 6 h of 289 ± 5.82%, being suitable for application on the oral mucosa. They displayed in vitro anticancer activity on CLS-354 tumor cells. By considerably increasing cellular oxidative stress and caspase 3/7 activity, they triggered apoptotic processes in oral cancer cells, inducing high levels of nuclear condensation and lysosomal activity, cell cycle arrest in G0/G1, and blocking DNA synthesis. All these properties lead to considering the UBE-loaded bioadhesive oral films suitable for potential application as a complementary therapy in oral cancer.

Methine initiated polypropylene-based disposable face masks aging validated by micromechanical properties loss of atomic force microscopy

The contagious coronavirus disease-2019 pandemic has led to an increasing number of disposable face masks (DFMs) abandoned in the environment, when they are exposed to the air condition, the broken of chemical bond induced aging is inevitably occurred which meantime would cause a drastic decrease of the mechanical flexibility. However, the understanding of between chemical bond change related to aging and its micromechanical loss is limited due to the lack of refined techniques. Herein, the atomic force microscopy (AFM) technique was firstly used to observe the aging process induced by methine of the polypropylene-based DFMs. By comparing the micromechanical properties loss, the influences of humidity and light density on the DFM aging were systematically studied in the early 72 h, and it revealed that the increasing scissions number of the easiest attacked methine (Ct-H) can gradually decrease the micromechanical properties of the polypropylene (PP)-based DFM. Furthermore, the results are also validated by the in- situ FTIR and XPS analysis. This work discloses that an aging process can be initially estimated with the micromechanical changes observed by AFM, which offers fundamental data to manage this important emerging plastic pollution during COVID-19 pandemic.

Phytofabrication of silver nanoparticles from Limonia acidissima leaf extract and their antimicrobial, antioxidant and its anticancer prophecy

Green synthesis of nanoparticles by eco-friendly methods is a recent technique which draws the attention of researchers because of the reward over many conventional chemical methods. The present work focuses on aqueous Limonia acidissima leaf extract in synthesizing silver nanoparticles and its applications in a simple way. The silver nanoparticles formed were characterized by Infrared, Ultra violet-visible, X-ray diffraction, transmission electron microscopic, and atomic force microscopic techniques. The powder X-ray diffraction studies and transmission electron microscopic images reveal that the silver nanoparticles synthesized were approximately 10–40 nm and have a spherical structure. The nanoparticles were assayed for their antibacterial, antifungal and antioxidant activity. The antimicrobial studies for the silver nanoparticles show a maximum zone of inhibition of 8.8 mm for Bacillus subtilis bacteria and 8.5 mm for Candida albicans fungi at 3 and 1 μg/mL respectively. In-silico ADMET studies reveal that the toxicity, bioactivity, pharmacokinetics and drug-likeness properties of Limonia acidissima leaf extract is good. The molecular docking studies show that the microbial activity is high for Bacillus subtilis and Candida albicans showing the coincidence of the in silico and in vitro studies as expected. The free radical scavenging activity of nanoparticles is 80 for 100 μg/mL. The 50% of inhibition of silver nanoparticles against human breast cancer cell lines is 18 μg/mL. It is evident that silver nanoparticles would be helpful in treating cancer cell lines and have great perspectives in the biomedical sector.

Photovoltaic and photothermal effects induced by visible laser radiation in atomic force microscopy probes

Excitation of electrons into higher energy states in solid state materials can be induced by absorption of visible light, a physical process generally studied by optical absorption spectroscopy. A promising approach for improving the spatial resolution of optical absorption spectroscopy beyond the diffraction limit is the detection of photoinduced forces by an atomic force microscope operating under wavelength-dependent light irradiation. Here, we report on a combined photovoltaic/photothermal effect induced by the absorption of visible light by the microscope probes. By monitoring the photoinduced modifications of the oscillation of the probes, it is found that the oscillation phase-voltage parabolic signals display specific fingerprints which depend on light intensity and the nature of the materials composing the probes. In particular, a localized surface photovoltage (SPV) is evidenced at the tip apex of uncoated Si probes, while none is observed on Au-coated Si probes. The photothermal effects are distinguished from photovoltaic effects by specific shifts of the phase-voltage parabolas. The findings are relevant for the whole range of atomic force microscopy techniques making use of visible light as an additional means of local optical characterization.

Surface Characterization of Current Dental Ceramics Using Scanning Electron Microscopic and Atomic Force Microscopic Techniques

Dental ceramics is a highly esthetic material and its surface properties can impact its roughness, bonding properties, as well as strength and wear. The aim of the study is to analyze the surface characteristics by the determination of the roughness parameters of three dental ceramics used in computer-aided design/computer-aided manufacturing (CAD/CAM) technique: lithium disilicate (LS2), zirconium oxide-reinforced lithium silicate (ZLS), and zirconium oxide (ZrO2), prepared using two different processing techniques, polishing (self-glaze) and glazing with three different glazes. Both glass ceramics, pre-crystallized LS2 and crystallized ZLS, were cut into disks, and the surface was ground and polished. Crystallization was performed for LS2 samples, while ZrO2 samples were fabricated using CAD/CAM and sintered. Then, the glaze was applied and the samples were reheated as per the manufacturer’s instructions. The contact surface topographies of the tested ceramics were measured by atomic force microscopy (AFM) and the roughness parameters: average surface roughness (Ra), root-mean-square roughness (Rq), and surface area difference (SAD) were evaluated. Changes in the morphological characteristics of the tested ceramics were examined by scanning electron microscopy (SEM), and the surface chemical composition was determined by attenuated total reflection Fourier-transform infrared spectroscopy (FT—IR). In the spectroscopic analysis, a characteristic signal for ZrO2 was obtained for ZLS samples. A significant decrease in surface roughness was observed after glazing in all tested ceramics (p &lt; 0.05). The abstract should be an objective representation of the article and it must not contain results that are not presented and substantiated in the main text and should not exaggerate the main conclusions.

Surface Planarization of CdZnTe Wafers: Effect of Slurry Formulation and CMP Processing Parameters on Surface Planarity

This study investigates the effect of chemical mechanical planarization (CMP) processing parameters such as platen velocity, the concentration of the oxidizer and abrasive nanoparticle, slurry pH and surfactant types on the surface roughness of cadmium zinc telluride (CdZnTe) substrate. It was found that these parameters have a significant effect on the quality of the polished surfaces. It was found that lower platen velocity, lesser concentration of abrasive particles, basic slurry pH, and addition of anionic surfactant (SDS) into the CMP slurry solution showed improved surface planarity. Optical Surface Profiler and atomic force microscopy (AFM) techniques were used to monitor the surface topography before and after polishing. A notable root-mean-square surface roughness, (Rq), ∼0.9 nm, has been obtained on the polished CdZnTe (CZT) surface over a scan area of 481 × 361 μm2 under the optimized conditions of 60 rpm relative velocity, slurry pH of 9, 3.75 vol% of oxidizer (H2O2) and 1.25 wt% of abrasive (SiO2 nanoparticle). A probable mechanism of the present CMP surface planarization of CZT substrate has been proposed. Unlike the conventional surface planarization processes, which involve two-step lapping followed by CMP for the CZT surfaces, we have developed a single step CMP process to obtain good surface planarity.

Corrosion inhibition of Pichia sp. biofilm against mild steel corrosion in 1 M H2SO4

Pichia sp. was isolated from rotten gooseberry (Phyllanthus emblica) and monitored for corrosion inhibition properties by means of biofilm-forming ability. The corrosion inhibition potential of Pichia sp. was evaluated against mild steel corrosion in 1 M H2SO4 via standard weight loss, electrochemical impedance spectroscopy (EIS), and potentiodynamic polarization (PP) techniques. Further, Fourier transform infrared (FT-IR) spectroscopy, X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM) with energy dispersive X-ray (EDX), X-ray photoelectron (XPS) spectroscopy, and atomic force microscopic (AFM) techniques were employed for confirming the biofilm accumulation on the mild steel (MS) surface. The weight loss investigation was carried out at varying temperatures (283 K−303 K), which showed the increasing trend of inhibition efficiency (IE%), and decreasing trend of corrosion rate, along with increasing Pichia sp. isolate’s concentrations. Pichia sp. isolate has shown maximum corrosion inhibition efficiency (>90%) at 283 K with an optimum concentration of 9 × 106 (CFU/mL). However, temperature studies insisted on the physical adsorption of corrosion inhibitor molecules over the metal surface. EIS data revealed enhanced values of charge transfer resistance (Rct), when increasing Pichia sp. isolate concentrations. Potentiodynamic polarization (Tafel curve) investigation revealed that Pichia sp. isolate exhibited mixed-type corrosion inhibition, while predominantly controlling the anodic reaction. The surface analysis data revealed the adherence and anticorrosive nature of Pichia sp. isolate on the MS surface, and a possible corrosion inhibition mechanism has also been discussed.

Furan functionalized naphthalenediimide semiconductors with different N-alkyl chains for n-type organic thin-film transistor applications

Development of n-type organic semiconductors (OSCs) is necessary in order to develop complementary electronics based on organic thin-film transistors (OTFTs). In this investigation, we designed and synthesized a series of four novel imide- and core-substituted naphthalene diimide (NDI) molecules. The molecular architecture was altered via introduction of different alkyl side chains (octyl and 2-ethylhexyl) to the imide-N positions and 2-dicyanomethylene-3-cyano-4,5,5-trimethyl-2,5-dihydrofuran (TCF) to the NDI core. The NDI-TCF derivatives are abbreviated as NDI-TCF1A, NDI-TCF1B, NDI-TCF2A, and NDI-TCF2B, using a “1” or “2” to indicate the number of TCF subunits at the NDI core, and an “A” or a “B” to indicate an octyl or a 2-ethylhexyl alkyl chain at the imide-N position, respectively. All four compounds displayed similar photophysical properties but exhibited different electrochemical properties with lower LUMO levels of −4.25 eV, −4.33 eV, −4.27 eV and −4.35 eV for NDI-TCF1A, NDI-TCF1B, NDI-TCF2A, and NDI-TCF2B, respectively. These LUMO levels suggest a capacity for electron transport. Furthermore, the NDI-TCF chromophores were incorporated into OTFTs and systematically studied on the relationship between the NDI-TCF molecular architecture and electron transport properties. NDI-TCF1A and NDI-TCF1B displayed more consistent OTFT performance than NDI-TCF2A and NDI-TCF2B. NDI-TCF1A and NDI-TCF1B exhibited low threshold voltages (VT) of −0.43 V ± 4.78 V and 6.12 V ± 6.63 V, respectively, electron mobilities (μe) of ca. 3 × 10−5 cm2V−1s−1, and on/off (ION/OFF) ratios of ca. 103. Insofar that TCF facilitates electron transport, the OTFT data suggest that the number of TCF subunits affect OTFT performance via thin-film morphology. The thin-film morphology of NDI-TCF1A, NDI-TCF1B, NDI-TCF2A, and NDI-TCF2B was studied using atomic force microscopy (AFM) technique and supported by X-ray diffraction measurements.

Effect of Ultrasonic Surface Mechanical Attrition Treatment-Induced Nanograins on the Mechanical Properties and Biocompatibility of Pure Titanium.

Commercially pure titanium (Ti) is widely used in bio-implants due to its high corrosion resistance. However, Ti exhibits marginally low mechanical and tribological properties, which limit its applications in some orthopedic implants. In this work, the Ti samples were subjected to ultrasonic surface mechanical attrition treatment (SMAT) for various durations to improve their surface properties such as hardness, strength and surface energy. SMAT-induced grain refinement was analyzed using optical, scanning electron and atomic force microscopy techniques. A Vickers hardness test was performed to determine the through-thickness hardness. Mechanical testing was carried out to measure the yield strength, ultimate tensile strength and ductility of the specimens. Corrosion tests were performed on a Gamry Potentiostat. The surface energy of SMAT-modified samples was calculated using the Owens–Wendt method. It was observed that SMAT reduced the average grain size from 50 μm to as low as 100 nm. The grain refinement and the corresponding grain boundary density led to a significant improvement in mechanical properties and biocompatibility in terms of increased hardness, yield and tensile strengths, surface energy, corrosion rate and hydrophilicity.

Direct and Sensitive Electrochemical Evaluation of Pramipexole Using Graphitic Carbon Nitride (gCN) Sensor.

Pramipexole (PMXL) belongs to the benzothiazole class of aromatic compounds and is used in treating Parkinson’s disease; however, overdosage leads to some abnormal effects that could trigger severe side effects. Therefore, it demands a sensitive analytical tool for trace level detection. In this work, we successfully developed an electrochemical sensor for the trace level detection of PMXL, using the voltammetric method. For the analysis, graphitic carbon nitride (gCN) was opted and synthesized by using a high-temperature thermal condensation method. The synthesized nanoparticles were employed for surface characterization, using transmission electron microscopy (TEM), X-ray diffraction (XRD), and atomic force microscopy (AFM) techniques. The electrochemical characterization of the material was evaluated by using the electrochemical impedance spectroscopy (EIS) technique to evaluate the solution–electrode interface property. The cyclic voltammetry (CV) behavior of PMXL displayed an anodic peak in the forward scan, indicating that PMXL underwent electrooxidation, and an enhanced detection peak with lower detection potential was achieved for gCN-modified carbon paste electrode (gCN·CPE). The influence of different parameters on the electrochemical behavior was analyzed, revealing the diffusion governing the electrode process with an equal number of hydronium ions and electron involvement. For the fabricated gCN·CPE, good linearity range was noticed from 0.05 to 500 µM, and a lower detection limit (LD) of 0.012 µM was achieved for the selected concentration range (0.5 to 30 µM). Selectivity of the electrode in PMXL detection was investigated by conducting an interference study, while the tablet sample analysis demonstrates the sensitive and real-time application of the electrode. The good recovery values for the analysis illustrate the efficiency of the electrode for PMXL analysis.

An Inquiry-Based Introduction to Atomic Force Microscopy Techniques through Optical Storage Disc Surface Imaging

Scanning probe microscopy such as atomic force microscopy has become increasingly integrated and relevant in undergraduate laboratory investigations. As the “hands and eyes of the nanoworld”, atomic force microscopes (AFMs) continue to be used to innovate the nanowriting process for data storage and in the exploration of novel materials suitable for ultrafast, nonvolatile, high density memory storage. Optical storage discs (OSDs) coevolved with AFM technology, are relatively inexpensive, and are easily available for purchase. They can, consequently, serve as a relevant phenomenon for undergraduate students to explore nanoscale material structure and macroscopic function through an AFM. The guided inquiry investigation presented here introduces students to the design and basic functions of an AFM through their identification of three unknown OSD samples (CD, DVD, or Blu-ray). The surface of each OSD is explored through students’ collection and interpretation of topographic and force curve data using an AFM to identify differences in the structure of the grooves containing pits and lands, estimation of theoretical storage capacity, and finally distinguish OSD types by comparing their data and calculations to known structures and capacities.

Assessment of the corrosion behaviour of untreated and chemically treated pure magnesium in simulated body fluid

The corrosion behaviour of pure Mg in simulated body fluid (SBF) and the effect of chemical treatment on the corrosion resistance property were investigated using DEIS (dynamic electrochemical impedance spectroscopy), EIS (electrochemical impedance spectroscopy), PDP (potentiodynamic polarization), SEM (scanning electron microscopy), AFM (atomic force microscope), and pH measurement techniques for 30 h. NaOH or H2O2 were utilized for the chemical treatment. The DEIS was used for the first time in the investigation of Mg corrosion in SBF. Results obtained disclosed that the chemical treatment benefitted the anticorrosion property immensely. Results from both the electrochemical and surface analysis techniques are consistent.

Elucidating Evidence for the In Situ Reduction of Graphene Oxide by Magnesium Hydride and the Consequence of Reduction on Hydrogen Storage

The current study highlights important information regarding how graphene oxide (GO) additive interacts with magnesium hydride (MgH2) and transforms to reduced graphene oxide (rGO). A mild reduction occurs during mechanical milling itself, whereas a strong reduction of GO happens concurrently with the oxidation of Mg formed during the dehydrogenation of MgH2. Owing to the in situ transformation of GO to rGO, the dehydrogenation temperature of MgH2 reduces by about 60 °C, whereas the hydrogen ab/desorption reaction kinetics of MgH2 increases by two orders of magnitude and the dehydrogenation activation energy decreases by about 20 kJ/mol. We have thoroughly scrutinized the transformation of GO to rGO by differential scanning calorimetry (DSC), X-ray diffraction (XRD), Raman spectroscopy, Fourier transform infrared (FTIR) spectroscopy and atomic force microscopy (AFM) techniques. Interestingly, the GO to rGO transformation triggered by magnesium hydride in the current study further paves the way for the facile preparation of rGO- and MgO-decked rGO composites, which are important materials for energy storage applications.