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We have performed density functional VASP calculations of a pure and of a carbon-covered (100) tungsten surface under the presence of an electric field E directed away from the surface. Our aim is to answer the question of an increased penetrability of electrons at the collector side of a nanometric tunnel diode when covered by carbon atoms, a purely quantum mechanical effect related to the value of the workfunction Φ. To obtain Φ at a non-zero electric field we have extrapolated back to the electrical surface the straight line representing the linear increase in the potential energy with distance outside the metal-vacuum interface. We have found that under the presence of E the workfunction Φ = Evac − EF of the (100) pure tungsten surface has a minor dependence on E. However, the carbon-covered tungsten (100) surface workfunction Φ(C − W) has a stronger E dependence. Φ(C − W) decreases continuously with the electric field. This decrease is ΔΦ = 0.08 eV when E = 1 V/nm. This ΔΦ is explained by our calculated changes with electric field of the electronic density of both pure and carbon-covered tungsten. The observed phenomena may be relevant to other surfaces of carbon-covered tungsten and may explain the reported collector dependence of current in Scanning Field Emission Microscopy.

Many tropical residual laterites have relatively poor engineering properties due to the significant percentage of fine-grained soil particles that they contain, which are formed by the soil weathering process. The widespread presence of laterite soils in tropical regions often requires that some form of soil improvement be performed to allow for their use in various civil engineering applications, such as for road base or subbase construction. One of the most commonly utilized stabilization techniques for laterite soils is the application of additives that chemically react with the minerals that are present in soil to enhance its overall strength; effective soil stabilization can allow for the use of site-specific soils, and can consequently result in significant cost savings for a given project. With an increasing focus on the use of more environmentally friendly and sustainable materials in the built and natural environments, there is an emerging interest in eco-friendly additives that are an alternative to traditional chemical stabilizers. The current study examines the viability of xanthan gum as an environmentally friendly stabilizer that can improve the engineering properties of tropical residual laterite soil. Unconfined compressive strength (UCS) tests, standard direct shear tests, Brunauer, Emmett, and Teller (N 2 -BET) surface area analysis tests and field emission scanning electron microscopy (FESEM) tests were used to investigate the effectiveness of xanthan gum for stabilization of a tropical laterite soil. The UCS test results showed that addition of 1.5% xanthan gum by weight yielded optimum stabilization, increasing the unconfined compressive strength of the laterite soil noticeably. Similarly, direct shear testing of 1.5% xanthan gum stabilized laterite specimens showed increasing Mohr–Coulomb shear strength parameters with increases in curing time. From the FESEM results, it was observed that the stabilization process modified the pore-network morphology of the laterite soil, while also forming new white layers on the surface of the clay particles. Analysis of the test results indicated that xanthan gum stabilization was effective for use on a tropical residual laterite soil, providing an eco-friendly and sustainable alternative to traditional soil stabilization additives such as cement or lime.

Biodegradation is an eco-friendly measure to address plastic pollution. This study screened four bacterial isolates that were capable of degrading recalcitrant polymers, i.e., low-density polyethylene, polyethylene terephthalate, and polystyrene. The unique bacterial isolates were obtained from plastic polluted environment. Dermacoccus sp. MR5 (accession no. OP592184) and Corynebacterium sp. MR10 (accession no. OP536169) from Malaysian mangroves and Bacillus sp. BS5 (accession no. OP536168) and Priestia sp. TL1 (accession no. OP536170) from a sanitary landfill. The four isolates showed a gradual increase in the microbial count and the production of laccase and esterase enzymes after 4 weeks of incubation with the polymers (independent experiment set). Bacillus sp. BS5 produced the highest laccase 15.35 ± 0.19 U/mL and showed the highest weight loss i.e., 4.84 ± 0.6% for PS. Fourier transform infrared spectroscopy analysis confirmed the formation of carbonyl and hydroxyl groups as a result of oxidation reactions by enzymes. Liquid chromatography–mass spectrometry analysis showed the oxidation of the polymers to small molecules (alcohol, ethers, and acids) assimilated by the microbes during the degradation. Field emission scanning electron microscopy showed bacterial colonization, biofilm formation, and surface erosion on the polymer surface. The result provided significant insight into enzyme activities and the potential of isolates to target more than one type of polymer for degradation.

Metal oxide nanomaterials are one of the preferences as antibacterial active materials. Due to its distinctive electronic configuration and suitable properties, ZnO is one of the novel antibacterial active materials. Nowadays, researchers are making a serious effort to improve the antibacterial activities of ZnO by forming a composite with the same/different bandgap semiconductor materials and doping of ions. Applying capping agents such as polymers and plant extract that control the morphology and size of the nanomaterials and optimizing different conditions also enhance the antibacterial activity. Forming a nanocomposite and doping reduces the electron/hole recombination, increases the surface area to volume ratio, and also improves the stability towards dissolution and corrosion. The release of antimicrobial ions, electrostatic interaction, reactive oxygen species (ROS) generations are the crucial antibacterial activity mechanism. This review also presents a detailed discussion of the antibacterial activity improvement of ZnO by forming a composite, doping, and optimizing different conditions. The morphological analysis using scanning electron microscopy, field emission-scanning electron microscopy, field-emission transmission electron microscopy, fluorescence microscopy, and confocal microscopy can confirm the antibacterial activity and also supports for developing a satisfactory mechanism.Graphical abstract showing the metal oxides antibacterial mechanism and the fluorescence and scanning electron microscopic images.

As the application requirements of semiconductor lasers continue to increase, severe challenges are brought to the reliability of semiconductor lasers. In order to promote the study of laser failure, this paper proposes an effective failure analysis method for packaged semiconductor lasers with a simple sample preparation and home-made photon emission microscopy (PEM) system. The new simple sample preparation process for failure analysis is presented and the necessary polishing fixture is designed so that sample can be obtained without expensive and complex micro-/nano-processing. Two types of home-made PEM experimental systems were established for observing the failure from the front facet and active region of semiconductor lasers. Experimental results showed that, with the proposed sample preparation flow, the home-made PEM experimental system effectively observed the leakage defects from the front facet and dark spot defects (DSDs) in the active region of semiconductor lasers. The method can help researchers and laser manufactures to perform effective failure analysis of packaged semiconductor lasers.

Tetraglycidyl methylene dianiline (TGMDA) was mixed with 1,4-Butanediol diglycidyl ether (BDE) (in a 4:1 mass ratio) and with a stoichiometric amount of the curing agent diaminodiphenyl sulfone which was solubilized at 120 °C for 20 min in the liquid mixture TGMDA + BDE. The so obtained unfilled epoxy resin matrix, denoted as ER, was blended with glycidyl polyhedral oligomeric silsesquioxane and carbon nanotubes in suitable proportions to obtain binary and ternary mixtures. Characterization of the formulated materials was performed using different experimental techniques, such as Dynamic mechanical analysis, Thermogravimetry (TG), Field emission scanning electron microscopy. Furthermore, the investigation of the flame behavior was carried out by the limiting oxygen index and mass loss calorimeter measurements. Direct current measurements and investigation by Tunneling atomic force microscopy of the conductive nanodomain map allowed the evaluation of the electrical properties of the developed nanofilled systems. The TG data related to thermal decomposition of ER and its binary and ternary mixtures were processed according to isoconversional kinetic analysis by assuming a non-Arrhenian behavior of the temperature function, and lifetime prediction was estimated at suitable relatively low temperatures and possible relation between the thermal stability and the presence of each component was discussed. This method of kinetic analysis paves the way for the possibility of evaluating in a more realistic way, on the basis of thermal stability, the potential application of structural resins with primary load functions in contact with hot areas of aeronautical aircraft engines.

Globally, researchers have devoted consistent efforts to producing excellent coating properties since coating plays an essential role in enhancing electrochemical performance and surface quality. In this study, TiO2 nanoparticles in varying concentrations of 0.5, 1, 2, and 3 wt.% were added into the acrylic-epoxy polymeric matrix with 90:10 wt.% (90A:10E) ratio incorporated with 1 wt.% graphene, to fabricate graphene/TiO2 -based nanocomposite coating systems. Furthermore, the properties of the graphene/TiO2 composites were investigated by Fourier-transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), ultraviolet-visible (UV-Vis) spectroscopy, water contact angle (WCA) measurements, and cross-hatch test (CHT), respectively. Moreover, the field emission scanning electron microscope (FESEM) and the electrochemical impedance spectroscopy (EIS) tests were conducted to investigate the dispersibility and anticorrosion mechanism of the coatings. The EIS was observed by determining the breakpoint frequencies over a period of 90 days. The results revealed that the TiO2 nanoparticles were successfully decorated on the graphene surface by chemical bonds, which resulted in the graphene/TiO2 nanocomposite coatings exhibiting better dispersibility within the polymeric matrix. The WCA of the graphene/TiO2 coating increased along with the ratio of TiO2 to graphene, achieving the highest CA of 120.85° for 3 wt.% of TiO2. Excellent dispersion and uniform distribution of the TiO2 nanoparticles within the polymer matrix were shown up to 2 wt.% of TiO2 inclusion. Among the coating systems, throughout the immersion time, the graphene/TiO2 (1:1) coating system exhibited the best dispersibility and high impedance modulus values (Z0.01 Hz), exceeding 1010 Ω cm2.

We have used field emission scanning electron microscopy (FESEM) to study the high-resolution organization of cellulose microfibrils in onion epidermal cell walls. We frequently found that conventional “rule of thumb” conditions for imaging of biological samples did not yield high-resolution images of cellulose organization and often resulted in artifacts or distortions of cell wall structure. Here we detail our method of one-step fixation and dehydration with 100% ethanol, followed by critical point drying, ultrathin iridium (Ir) sputter coating (3 s), and FESEM imaging at a moderate accelerating voltage (10 kV) with an In-lens detector. We compare results obtained with our improved protocol with images obtained with samples processed by conventional aldehyde fixation, graded dehydration, sputter coating with Au, Au/Pd, or carbon, and low-voltage FESEM imaging. The results demonstrated that our protocol is simpler, causes little artifact, and is more suitable for high-resolution imaging of cell wall cellulose microfibrils whereas such imaging is very challenging by conventional methods.

In this study, it was reported the preliminary results on the chemical and structural composition of decorative elements remains from original Roman mosaic fragments collected from the Roman Mosaic Museum, Constanta (Romania). These investigations were carried out by using non-destructive and micro-invasive techniques such as optical microscopy, X-ray diffraction, field emission - scanning electron microscopy - energy dispersive X-ray spectroscopy, vibrational spectroscopy (i.e., FTIR and Raman). The studied fragments, apart from being beneficial to different restoration opportunities of this Roman mosaic, could be also included in its modification through air pollution. The major and minor phase components of the studied mosaic fragments were determined, the crystal structure of the main phases was analyzed, and their three-dimension spatial arrangement was reconstructed. The similar composition of the major phases of all mosaic fragments can indicate a generic recipe for making mosaic elements, but minor phases were presumably added for coloring of mosaic pieces. Some degradation areas inside the volume of the mosaic fragments were found by means of the X-ray diffraction method. The areas are probably related to the formation of iron hydroxides during chemical interactions of mosaic fragments with the sea and urban polluted atmosphere. The results can also offer important information about the original materials that were used in the Roman period.

The fabrication of high-efficiency GaAsP-based solar cells on GaAs wafers requires addressing structural issues arising from the materials lattice mismatch. We report on tensile strain relaxation and composition control of MOVPE-grown As-rich GaAs1−xPx/(100)GaAs heterostructures studied by double-crystal X-ray diffraction and field emission scanning electron microscopy. Thin (80–150 nm) GaAs1−xPx epilayers appear partially relaxed (within 1−12% of the initial misfit) through a network of misfit dislocations along the sample [011] and [011−] in plane directions. Values of the residual lattice strain as a function of epilayer thickness were compared with predictions from the equilibrium (Matthews–Blakeslee) and energy balance models. It is shown that the epilayers relax at a slower rate than expected based on the equilibrium model, an effect ascribed to the existence of an energy barrier to the nucleation of new dislocations. The study of GaAs1−xPx composition as a function of the V-group precursors ratio in the vapor during growth allowed for the determination of the As/P anion segregation coefficient. The latter agrees with values reported in the literature for P-rich alloys grown using the same precursor combination. P-incorporation into nearly pseudomorphic heterostructures turns out to be kinetically activated, with an activation energy EA = 1.41 ± 0.04 eV over the entire alloy compositional range.