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A thin TiO2 semiconductor film embedded between two metal electrodes works as a memristor after being formed by soft breakdown. The forming creates a nano-filament that penetrates through the poorly conducting TiO2 film and connects the electrodes conductively. While previous works characterized the nano-filament properties (shape, composition, and resistivity) by electron microscopy techniques, we present a characterization by electrical measurements. In a typical memristor, both electrodes are made of normal metals. We study the metal/TiO2/metal memristors with a bottom electrode made of a superconducting NbN layer and a top electrode made of a normal (Pt) or superconducting (Nb) metal. The nano-filament connecting the electrodes touches the bottom electrode as a point contact, thus allowing us to perform point-contact Andreev reflection spectroscopy of the NbN superconductor. The spectra, measured below the critical temperature (15 K) of NbN, are analyzed theoretically. The analysis reveals the presence of one nano-filament and determines the nano-filament resistance, Sharvin resistance of the point contact, and Maxwell resistance of the electrodes. Moreover, it shows that the nano-filament is a conical-shaped Ti-like metal point contact with a tip diameter of ∼3–5 nm, Fermi velocity of 2 × 10 6 m / s , and low-temperature resistivity of ∼ 10 − 8 – 10 − 7 Ω m. Thus, the nano-filament in our device is not the Ti4O7 phase observed in previous works. Remarkably, the point contact spectrum of the superconducting NbN layer shows the Andreev peak typical for ballistic transport. This is because the point contact probes the NbN layer through a thin Al layer that mimics superconductivity of NbN via the proximity effect and eliminates the effects of tunneling and disorder. [ABSTRACT FROM AUTHOR]

Oriented polyacrylonitrile (PAN) films were prepared and treated with hot stretching method to obtain higher degree of orientation. The PAN fiber membrane was infiltrated with thermoplastic polyurethane (TPU) to prepare oriented PAN membrane reinforced TPU composite membrane. The tensile properties of the composite material were studied, and the tensile strength, modulus, and toughness all increased with the increase of orientation. The interfacial miscibility between the matrix and nanofibers was observed using Raman spectroscopy, and morphology, properties, and reinforcement mechanism of the composite material were analyzed combining scanning electron microscopy technique. The results indicate as the orientation increases, the compatibility between the matrix and fibers improves, and the mechanical properties of the composite material also improved. [ABSTRACT FROM AUTHOR]

A method to obtain sodium titanate nanoribbons starting from a mixture of brookite and anatase TiO₂ nanopowder is described. As-prepared TiO 2 nanopowder with a major brookite phase was used as a precursor in an alkaline hydrothermal approach, where the temperature was kept at 200 °C. The influence of hydrothermal treatment and consequent annealing temperature (T = 500 °C) on the crystal structure, phase composition, and morphology of samples were investigated by X-ray powder diffraction (XRPD), Raman and FTIR spectroscopy, and electron microscopy techniques (FESEM, HRTEM). All these methods point out that the hydrothermally treated sample, containing the NaTi 3 O 6 (OH)(H 2 O) 2 , Na 2 Ti 3 O 7 , and Na 2 Ti 9 O 19 , is dominated by layer-structured sodium hydroxititanate dihydrate. The annealing leads to the formation of rare sodium titanates, Na 3 Ti 6 O 13 and Na 2 Ti 9 O 19 , with tunnel structures where the hexatitanate with increased sodium content prevails. The photocatalytic activity of synthesized nanostructures was tested in the degradation process of Reactive Orange (RO16) azo-dye upon UV excitation. It appears that photocatalytic activity is lower after hydrothermal treatment, but subsequent annealing makes sodium titanate nanoribbons faster in the degradation of RO16. The research implies that these sodium titanate nanostructures are promising photocatalytic materials and should be considered in the future for removing different pollutants from water. [ABSTRACT FROM AUTHOR]

Prevalent interactions among marine phytoplankton triggered by long‐range climatic stressors are well‐known environmental disturbers of community structure. Dynamic response of phytoplankton physiology is likely to come from interspecies interactions rather than direct climatic effect on single species. However, studies on enigmatic interactions among interspecies, which are induced by bioactive extracellular compounds (BECs), especially between related harmful algae sharing similar shellfish toxins, are scarce. Here, we investigated how BECs provoke the interactions between two notorious algae, Alexandrium minutum and Gymnodinium catenatum, which have similar paralytic shellfish toxin (PST) profiles. Using techniques including electron microscopy and transcriptome analysis, marked disruptions in G. catenatum intracellular microenvironment were observed under BECs pressure, encompassing thylakoid membrane deformations, pyrenoid matrix shrinkage and starch sheaths disappearance. In addition, the upregulation of gene clusters responsible for photosystem‐I Lhca1/4 and Rubisco were determined, leading to weaken photon captures and CO2 assimilation. The redistribution of lipids and proteins occurred at the subcellular level based on in situ focal plane array FTIR imaging approved the damages. Our findings illuminated an intense but underestimated interspecies interaction triggered by BECs, which is responsible for dysregulating photosynthesis and organelle function in inferior algae and may potentially account for fitness alteration in phytoplankton community. Summary statement: The bioactive extracellular compounds of Alexandrium minutum can induce interspecies interaction by affecting the cell physiology of related harmful algae, mainly showing damage to photosynthetic organelles and redistribution of intracellular biomacromolecules. [ABSTRACT FROM AUTHOR]

The Chang 8 formation of the Yanchang Group, located in Yuancheng area of the Ordos Basin, is a typical tight oil reservoir in China. This reservoir is characterized by low porosity, low permeability, strong non-homogeneity, and significant difficulty in evaluating the reservoir parameters. To examine and investigate the microscopic pore structure characteristics of the Chang 8 formation, cast thin section and scanning electron microscopy techniques were utilized in this study, Moreover, tests on the core physical properties were conducted and the data from these tests were integrated into the analysis of basic characteristics of the reservoir rock mineralogy, pore permeability, and other fundamental characteristics. The shapes of piezomercury curves were systematically examined to study the characteristics and features of pore structures for the 17 samples. In accordance with the fractal dimension of the NMR T2 spectrum, the reservoir was classified into four categories, and a conversion model delineating the correlation between the NMR T2 spectrum and the capillary pressure curve was formulated through the application of the segmented power function method. This model was then implemented in the interpretation of NMR logging, facilitating the acquisition of a seamless pseudo-capillary pressure curve spanning the entire well section. Three essential parameters reflecting the microscopic pore structure, namely the expulsion pressure, median pressure, and sorting coefficient of the core samples, were extracted. The association between reservoir parameters and reservoir categorization was then determined through the application of a generalized regression neural network. The pseudo-capillary pressure curve reservoir parameters of the whole well section were processed to derive the classification profile of the reservoir, and the classification results demonstrated a strong alignment with those of the mercury injection experiments. This study highlights that the proposed method can provide crucial foundation for the investigations on pore structures in tight oil reservoirs and the evaluation of reservoir classification. [ABSTRACT FROM AUTHOR]

ABSTRACT The present study aimed to provide comprehensive morphological features of the bronchial and parabronchial systems using cast, histological, histochemical, and scanning electron microscopy techniques, with new insights into the parabronchial topographic distribution system on 22 white Pekin ducks. Casting illustrated that the medioventral secondary bronchi (MVSB) were the largest, but the posterior (POSB) ones were the smallest. The primary (PB) and secondary bronchi (SB) were lined with thin pseudostratified, ciliated columnar epithelium. PB contained discontinuous hyaline cartilage plates interconnected by a membrane of fibrous CT with chondrocytes, while SB had mucous glands. There were two types of hexagonal parabronchi with different lumen shapes: circular in neopulmonic and longitudinal in paleopulmonic. The parabronchi had numerous atria opened into the lumen and guarded by different directed muscles: horizontal in the neopulmonic and vertical or horizontal in the paleopulmonic. The atria were lined with squamous to cuboidal cells, forming the interatrial septum (IAS). A funnel atrial duct connecting the atrium to the infundibulum can be branched. The air capillaries were nearby, at a very short distance from the blood capillaries. Despite their small number, air capillaries, which were found in parabronchi, significantly increased in size and diameter. SEM at the 4th torus level showed a parabronchi distribution with elongated paleopulmonic on the dorsomedial part, hexagonal neopulmonic on the ventrolateral part, and some neopulmonic on the medial part. The parabronchial topography distribution exhibited their unique distribution from the 1st to the 6th torus level. [ABSTRACT FROM AUTHOR]

The actin cytoskeleton is a ubiquitous feature of eukaryotic cells, yet its complexity varies across different taxa. In the parasitic protist Trypanosoma brucei, a rudimentary actomyosin system consisting of one actin gene and two myosin genes has been retained despite significant investment in the microtubule cytoskeleton. The functions of this highly simplified actomyosin system remain unclear, but appear to centre on the endomembrane system. Here, advanced light and electron microscopy imaging techniques, together with biochemical and biophysical assays, were used to explore the relationship between the actomyosin and endomembrane systems. The class I myosin (TbMyo1) had a large cytosolic pool and its ability to translocate actin filaments in vitro was shown here for the first time. TbMyo1 exhibited strong association with the endosomal system and was additionally found on glycosomes. At the endosomal membranes, TbMyo1 colocalised with markers for early and late endosomes (TbRab5A and TbRab7, respectively), but not with the marker associated with recycling endosomes (TbRab11). Actin and myosin were simultaneously visualised for the first time in trypanosomes using an anti-actin chromobody. Disruption of the actomyosin system using the actin-depolymerising drug latrunculin A resulted in a delocalisation of both the actin chromobody signal and an endosomal marker, and was accompanied by a specific loss of endosomal structure. This suggests that the actomyosin system is required for maintaining endosomal integrity in T. brucei. [ABSTRACT FROM AUTHOR]

The article discusses Davian behavior and functional egg fertilization in the Italian Stream Frog Rana italica, focusing on a case of thanatophilia observed in Central Italy. The study highlights the reproductive ecology of the Italian Stream Frog, emphasizing the unique mating habitats and reproductive outcomes of the species. The observation of Davian behavior in R. italica sheds light on the rare occurrence of such behavior in anurans and calls for further research to understand the contextual factors influencing this behavior. [Extracted from the article]

Flaky FeSiCr@Ni0.5Zn0.5Fe2O4 composites are successfully synthesized via ball milling and hydrothermal method. The microstructure, morphology, and phase composition of flaky FeSiCr@Ni0.5Zn0.5Fe2O4 composites are analyzed using X‐Ray diffractometer, energy dispersive spectroscopy, scanning electron microscope, and transmission electron microscope techniques. The electromagnetic wave absorption characteristics of the composite with varying contents of Ni0.5Zn0.5Fe2O4 are comprehensively investigated. The results show that the introduction of Ni0.5Zn0.5Fe2O4 reduces the permittivity, improves the synergistic effect of magnetic loss and dielectric loss, optimizes the impedance matching, and enhances the overall electromagnetic performance of the composites. The sample prepared with a composition of 40 wt% Ni0.5Zn0.5Fe2O4 displays the most pronounced absorption performance. The RLmin (reflection loss) reached −41.3 dB at 4.3 GHz, and the maximum effective absorption bandwidth (EAB) reaches 5.6 GHz which is 7–8 times that of the original sample. Notably, through adjusting the thickness of composites, the EAB could be broadened to 10.5 GHz (2.5–13.0 GHz), encompassing the entire C and X bands. The flaky FeSiCr@Ni0.5Zn0.5Fe2O4 composites have the advantages of wide source of raw materials, strong microwave absorption ability, and wide absorption frequency range, and are expected to become a potential microwave absorption material in the future. [ABSTRACT FROM AUTHOR]

Metal–organic frameworks (MOFs) are lagging in the use of lithium‐ion batteries (LIBs), ascribing to full coordination between metal nodes and organic ligands, to a large extent. By integrating a modulator into a ligand with missing bridging functionality, this study elucidates the role of non‐bridging defect sites in MOFs in tailoring lithium storage performance. A fully bridged pristine MOF (p‐MOF) utilizing the meso‐tetra(4‐carboxylphenyl) porphyrin ligand is compared with a modified MOF containing non‐bridging defects (d‐MOF) introduced by a homologous ligand, tris(4‐carboxyphenyl) porphyrin. Spectroscopic and cryogenic low‐dose electron microscopy techniques verify the presence of non‐bridging defect sites in the d‐MOF and reveal their explicit local structure. Density functional theory calculations show significantly enhanced Li+ adsorption energies and reduced Li+ migration barriers at the non‐bridging sites in the d‐MOF compared to the fully bridging sites in the p‐MOF. As a result, the d‐MOF exhibits exceptional lithium storage performance, achieving a high capacity of 761 mAh g−1 at 0.05 A g−1 and superior rate performance of 203 mAh g−1 at 5 A g−1, which substantially outperform the p‐MOF. This study highlights the potential of modulating MOFs with non‐bridging defects to develop high‐performance LIBs. [ABSTRACT FROM AUTHOR]

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Organisms are able to control material patterning down to the nanometer scale. This is exemplified by the intricate geometrical patterns of the silica cell wall of diatoms, a group of unicellular algae. Theoretical and modeling studies propose putative physical and chemical mechanisms to explain morphogenesis of diatom silica. Nevertheless, direct investigations of the underlying formation process are challenging because this process occurs within the confines of the living cell. Here, a method is developed for in situ 3D visualization of silica development in the diatom Stephanopyxis turris, using electron microscopy slice‐and‐view techniques. The formation of an isotropic hexagonal pattern made of nanoscale pores is documented. Surprisingly, these data reveal a directional process that starts with elongation of silica rods along one of the three equivalent orientations of the hexagonal lattice. Only as a secondary step, these rods are connected by crisscrossing bridges that give rise to the complete hexagonal pattern. These in situ observations combine two known properties of diatom silica, close packing of pores and branching of rods, to a unified process that yields isotropic patterns from an anisotropic background. Future research into diatom morphogenesis should focus on rod elongation and branching as the key for pattern formation. [ABSTRACT FROM AUTHOR]

AbstractThe objective of this study is to investigate the potential of combined pond fly ash (PFA) and flue gas desulfurization gypsum (FGDG) as a partial replacement for cement by mixing them with fine river sand for green mortar development. We studied the physical, mechanical, and microstructural properties of mortars by using techniques such as scanning electron microscopy equipped with energy-dispersive X-ray spectroscopy (SEM-EDXS) and X-ray diffraction (XRD) for chemical component identification of the hydrated phase. These experimental results show that mortar containing pond fly ash, FGDG, and cement concentrations of 5 wt%, 5 wt%, and 90 wt% yields the maximum compressive strength (8.9 MPa) and flexural strength (3.4 MPa) after 28 days. This mortar has 12.6% higher compressive strength and 48% lower shrinkage in comparison with control specimens. A reduction in shrinkage is attributed to the denser structure of the mortar, as the calcium silicate hydrate (C–S–H) gel is found to exist in the SEM image and also identified through XRD studies. It is also concluded that excessive ettringite formation causes expansion in the volume of mortar, voids formation, and results in the reduction of strength. The application of this mortar can be in the internal plaster, bricks, and masonry. [ABSTRACT FROM AUTHOR]

This study developed an electrochemical method for the selective and sensitive detection of Tinidazole (TZ) by modifying a bare carbon nanotube paste electrode (BCNTPE) with electrochemically polymerized l‐Glutamic acid (P(L‐GA)/MCNTPE). The modified carbon nanotube paste electrode (MCNTPE) achieved optimal detection with an irreversible peak in a 0.2 M phosphate buffer solution (PBS) at pH 3.5. Characterization of both the P(L‐GA)/MCNTPE and BCNTPE was carried out using techniques such as scanning electron microscopy (SEM), electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV), and linear sweep voltammetry (LSV). The sensor effectively identified possible interferences from different metals and organic compounds, with scan rate studies indicating that the reaction was controlled by diffusion. The effects of pH and concentration variations were also thoroughly investigated. The active surface area of the P(l‐GA)/MCNTPE and BCNTPE were found to be 0.471 cm2 and 0.217 cm2 respectively. The P(l‐GA)/MCNTPE displayed excellent electrochemical properties, with a limit of detection (LOD) of 0.06 µM and a limit of quantification (LOQ) of 0.2 µM, along with good reproducibility, repeatability, and stability. This study presents a P(l‐GA) MCNTPE that significantly enhances the sensitivity and selectivity for simultaneous detection of TZ and bare carbon nanotube (BCN). The improved electroactive surface area and electron transfer dynamics demonstrate its potential for practical applications in pharmaceutical analysis. [ABSTRACT FROM AUTHOR]

The microstructure evolution of Al0.3FeCoNiCrx (x = 0, 0.3, 0.5, 1, 1.5) high-entropy alloys (HEAs) were studied using X-Ray diffraction technique and scanning electron microscope equipped with energy dispersive spectrometer. The short-term and long-term corrosion behaviours of these alloys in 3.5 wt.% NaCl solution were studied by electrochemical impedance spectroscopy, potentiodynamic polarisation measurement, immersion test and corrosion morphology analysis. The results show that all the designed HEAs present single-phase FCC structure, and the increase in Cr content changes the microstructural morphology from cellular to a typical dendritic–interdendritic state. Without the influence of phase transformation, the corrosion resistance of Al0.3FeCoNiCrx HEAs gradually increases with the increase in Cr content. Our designed alloys exhibit excellent corrosion resistance compared to the existing HEAs in the AlFeCoNiCr composition system. [ABSTRACT FROM AUTHOR]

Graphene oxide-based nanomaterials are garnering significant attention from various fields due to their unique physical and chemical properties, which make them attractive for myriad applications. This feature article stems from Dr. Aicheng Chen's Lecture for the 2023 Ricardo Aroca Award of the Canadian Society for Chemistry and focuses primarily on the synthesis and applications of graphene oxide-based nanomaterials for electrochemical sensing. Graphene oxide (GO), reduced graphene oxide, and functionalized and doped GO-based nanomaterials are emerging as promising enablers of broad applications in electrochemical sensors. This is due to their distinctive functional groups and novel properties, which include high electrical conductivities, large surface areas, and enhanced catalytic activities. Several strategies for the synthesis of these nanomaterials are described in this feature article, encompassing the modified Hummers method, electrochemical, thermal, and microwave reactor methods. The characterization of these GO-based nanomaterials is highlighted, employing techniques such as scanning electron microscopy, transmission electron microscopy, X-ray diffraction, Fourier transform infrared spectroscopy, Raman, and X-ray photoelectron spectroscopy to study their morphologies, structures, and chemical compositions. The development of GO-based electrochemical sensors and their pharmaceutical, medical, environmental, and food safety applications are discussed. Further, the effects of these GO-based nanomaterials and different electrochemical techniques (e.g., cyclic voltammetry, square wave voltammetry, linear sweep voltammetry, and differential pulse voltammetry) on the performance of various electrochemical sensors are addressed. [ABSTRACT FROM AUTHOR]

Biomimetic heterogeneous catalysts were prepared by immobilization of meso‐tetrakis(4‐carboxyphenyl)porphyrinatomanganese(III) acetate (MnTCPP) and meso‐tetrakis(4‐carboxyphenyl)porphyrinatoiron(III) chloride (FeTCPP) on graphitic carbon nitride (g‐C3N4) nanosheets. The anchored catalysts were characterized by various techniques such as scanning electron microscopy, thermogravimetric analysis, powder X‐ray diffraction, ultraviolet visible, photoluminescence, flame atomic absorption, and Fourier transform infrared spectroscopy. The thermogravimetric analysis demonstrated that the prepared catalysts were thermally stable up to almost 350°C, exhibiting high thermal stability. In the following, the catalytic efficiency of the prepared nanocatalyst was also investigated for the oxidation of various olefins with hydrogen peroxide (as a green oxidant) and the effect of various parameters which may affect the catalytic efficiency was optimized. The maximum conversion (100% for α‐methylstyrene and 97% for cyclooctene) was obtained in the presence of MnTCPP@C3N4. The Mn porphyrin nanocatalyst shows higher catalytic efficiency compared to the Fe porphyrin. [ABSTRACT FROM AUTHOR]

This study explores a novel approach to quenching and partitioning (Q&P) heat treatment applied to AISI 9260 spring steel, comprising Fe-0.65C-1.58Mn-1.05Si-0.41Cr (wt.%). Our research focuses on balancing strength and ductility through optimized Q&P pathways, leading to a diverse microstructure that includes martensite, bainite, carbide, and retained austenite. Advanced X-ray diffraction and scanning electron microscopy techniques were employed to analyze the complexities of this microstructure. A key aspect of this study is the precise control of partitioning temperature and time, crucial for modulating lattice distortion and dislocation density within martensitic and bainitic structures. Optimal partitioning temperature promotes carbon distribution into austenite, tempering lattice distortions, and dislocation densities. Concurrently, carbide precipitation and segregation contribute to the refinement of the bainite phase. The sample quenched at 125 °C and partitioned at 350 °C (Q&P-125/350) demonstrates notable mechanical properties: a yield strength of 950 ± 15 MPa, an ultimate tensile strength of 1710 ± 15 MPa, and an elongation of approximately 9.7%. These results are partly attributed to the effect of silicon in preventing cementite coarsening and the effective distribution of carbide. Our findings highlight the potential of Q&P heat treatment in developing tailored microstructures with enhanced mechanical properties in steel, without relying on costly alloying elements. This approach presents new avenues for the design and application of high-performance materials. [ABSTRACT FROM AUTHOR]

Apollo 17 core sample 73001/2 was recently made available to researchers for analysis using state‐of‐the‐art techniques in the framework of a modern understanding of lunar surface processes. In this work, we employ transmission electron microscopic analysis to observe the mineralogy, microstructural, and chemical characteristics of space weathering and solar energetic particle (SEP) track distribution in soil grains in the <20 μm size fraction in core sample 73002. The modal mineralogy and stratigraphic space weathered grain abundance suggests that a geologically recent mixing event affected the top 3 cm of 73002. Surface exposure age distributions derived from SEP tracks demonstrate that individual regolith grains rarely reside on the surface for longer than ∼4 million years. The abundance of surface exposed monomineralic fragments with respect to depth correlates well with bulk measurements of space weathered soils using other techniques, such as ferromagnetic resonance. Exposure age distributions suggest the presence of two unique in situ reworking zones spanning the top 8 cm of the core and median exposure ages decrease with increasing depth for both reworking zones, albeit at different rates. These rates were compared to reworking models and suggest a relationship between median exposure age and reworking rate with respect to depth. Applications of modern transmission electron microscopy to core sample 73001/2 have proven useful in understanding lunar regolith evolution both within the context of the Apollo 17 field site and more broadly via in situ reworking. Plain Language Summary: Space weathering is a process by which lunar soils exposed to the interplanetary space environment are chemically, spectrally, and structurally altered. Apollo 17 lunar core sample 73001/2 was recently released into the scientific community under the Apollo Next Generation Sample Analysis (ANGSA) Program. This core is thought to have sampled a lunar landslide at the base of a mountain. This project utilizes up‐to‐date transmission electron microscopy techniques to understand the space weathering and modal mineralogy within the core sample. Results are compared to regolith mixing models to understand the mechanisms and dynamics of soil mixing. We found elevated numbers of iron and titanium rich components within the top 3 cm of the core relative to layers below it. We also found that individual regolith grains rarely reside on the surface for more than a few million years. Grains with the lowest exposure dominate deeper layers, which suggests a high rate of mixing from small and frequent impacts which forces regolith to migrate below the surface. Key Points: Transmission electron microscopy was used to uncover the mineralogy and space weathering features of soil in Apollo 17 core sample 73002Modal mineralogy and the distribution of space weathered grains indicate frequent and recent mixing in the top 3 cm of the lunar regolithIrradiation damage in grains indicates space weathered soil is reworked beneath the surface in less than a few million years [ABSTRACT FROM AUTHOR]

This article reports the obtention of a new gellan-based hydrogel linked with Fe3+ and loaded with a natural micro/nanostructured carbon designed as a contaminant's removal from wastewater. Hydrogels are known for their water-retaining properties, high binding capacity, and eco-friendly features. The new material is expected to behave as one cost-effective and efficient sorbent, including natural carbon structures with various functional groups. The encapsulation efficiency ranges between 89% and 95%. The obtained hydrogel particles were characterized using FT-IR spectroscopy and scanning electron microscopy techniques. The hydrogel particles' water stability was evaluated by measuring the transmittance for 10 days, and the capacity to retain water was assessed by determining the swelling degree (Q%). The results showed that hydrogel particles are stable (the transmittance value is higher than 97.8% after 10 days), and their properties are influenced by the cross-linking degree, the amount of the carbon particles encapsulated, and the concentration of gellan. For example, the Q% values and encapsulation efficiency increased when the cross-linking degree, the carbon microstructure quantity, and the gellan concentration decreased. The new hybrid material can retain Pb(II) ions and diclofenac molecules, and could be used in different adsorption–desorption cycles. [ABSTRACT FROM AUTHOR]

Steel slag-based glass ceramic for thermal energy storage was first fabricated by quenching method, and then their high temperature corrosion behavior in the eutectic carbonates and related mechanism have been investigated using X-ray diffraction，Raman spectroscopy and scanning electron microscope techniques. The results show that holding time has a significant influence on the corrosion layer thickness at 800oC. As the holding time was extended, the thickness of the corrosion layer with obvious cracks tended to increase. Further EDS analyses disclosed that the divided corrosive layers along the extended directions of the cracks should be similar in both the compositions and microstructure. Based on these observations, the possible corrosion mechanism was discussed after defining phase structure of nonstoichiometric (Fe 0.35 Al 0.20 Mg 0.44) Ca 0.96 (Fe 0.08 Si 0.70 Al 0.20) 2 O 6.12 as a combined system of CaMgSi 2 O 6 (Di)-CaFe3+AlSiO 6 (Es)-CaAl 2 Si 2 O 8 (An). Oxygen offered by the molten carbonates salt is regarded to play a critical role in the corrosion process. In an atmosphere rich in oxygen, both Na+ and K+ ions diffused into the diopside can replace Ca2+ and Mg2+, etc. resulting in polyhedral structural reorganization for electrical neutrality. On the other hand, the bonding stability of the cation-oxygen bonds in diopside was proved to be weaker than that in single oxides. These two aspects contribute to the continuous dissolution of Ca2+ and Mg2+, etc. in the molten carbonates salt. [ABSTRACT FROM AUTHOR]

Wide bandgap orthorhombic polymorph of gallium oxide (κ‐Ga2O3) possessing a high spontaneous polarization grown on wurtzite‐type semiconducting substrates is considered to create a high mobility electron channel suitable for applications. Such κ‐Ga2O3 layers are composed of hexagon microprisms whose properties affect the lateral electric conductance. In this work, the structure and recombination properties of extended defects in individual “suspended” thin microprisms are investigated with transmission and scanning electron microscopy techniques (STEM, HR‐TEM) including cathodoluminescence (CL‐SEM). It is established that the microprism is composed of six equisized orthorhombic domains bounded by twin domain boundaries (TDBs) along the directions <110>. Twin domain contains a parallel array of antiphase boundaries (APB) of a high density stretched in the [010] direction. APBs possess steps or interruption and can form double oppositely shifted spatially separated layers (APB dipoles). TDBs on majority of their length are incoherent and serve as the border for the APB terminations. Panchromatic CL maps reveal either enhanced or reduced intensity of APB without noticeable spectral changes. CL intensity enhancement is proposed to be due to enhanced electron–hole generation caused by excess scattering of primary electron beam by APBs in thin films while, in fact, APB exhibits enhanced nonradiative recombination activity. [ABSTRACT FROM AUTHOR]

In this study, nickel (Ni) nanoparticles were successfully synthesised using two methods: the hot‐injection method and a room temperature colloidal synthesis using dioctyl tartrate as a capping agent. Each approach yielded Ni nanoparticles with unique morphological and electronic properties. The distinct characteristics of these Ni nanoparticles make them promising candidates for unravelling structure/activity relationships, a crucial aspect in developing catalysts with enhanced selectivity. Furthermore, Ni nanoparticles synthesized via these methods were supported on both silica and activated charcoal, with variations in Ni loadings. We explored the impact of nanostructural characteristic of the Ni NPs as well as support effects on the selective hydrogenation of furfural. Using temperature programmed reduction, advanced X‐ray absorption spectroscopy, and atom‐resolved electron microscopy techniques, we established comprehensive structure‐function relationships. Herein, we demonstrate that using a dioctyl tartrate route, foam‐like Ni nanostructures are obtained, yielding higher selectivity towards selective hydrogenation than commercial Ni/Al2O3 and a suppression of the acid‐base catalysed acetalization and etherification reactions. Furthermore, conversions similar to commercial Ni/Al2O3 are achieved using a lower Ni loading. These insights provide valuable guidance for the design of enhanced materials, contributing to the optimization of catalyst performance in selective hydrogenation processes. This research marks a significant step toward the development of more efficient and sustainable catalytic processes. [ABSTRACT FROM AUTHOR]

This article focuses on the fine characterization of steels commonly used in the petrochemical industry damaged by the phenomenon of high temperature hydrogen attack (HTHA). The study was conducted in two steps. To begin with, a damaged 0.5-Mo pearlitic steel from the petroleum refineries, submitted to HTHA for decades, was characterized in detail using multiscale electron microscopy techniques. As part of an upstream study to better understand the onset and the growth of cavities, a brand new SA516 grade 60 low carbon–manganese steel was subsequently exposed to accelerated HTHA conditions through interrupted cycles carried out in autoclaves and then examined. Numerous cavities, plausibly filled with methane, were noticed in both materials. These cavities were mostly located at ferrite–pearlite grain boundaries along carbides and at triple grain boundaries near large carbides. The 0.5-Mo pearlitic steel showed cavities reaching significant sizes, up to 1 µm, but surprisingly no cracks were observed in the depth of the pipe. The major outcome is that 3D focused ion beam–scanning electron microscopy combined with transmission electron microscopy (TEM) analyses unveiled different natures of precipitates as well as in and nearby HTHA cavities for both 0.5-Mo and low carbon–manganese steels. Inclusions, likely AlN, but also Mo- and Cu-rich precipitates were observed in cavities of the industrial steel. These results confirmed a previous study performed on a similar industrial steel that drew a possible correlation between cavities nucleation and the intersection of transgranular inclusion-enriched plane with a grain boundary or carbides in pearlite grains (Flament in Microscopy and Microanalysis 28:1602–1604, 2022). [ABSTRACT FROM AUTHOR]

Background: Investigation of the biochemical profile and storage root yield of three cassava genotypes (H-165, H-226 and TME-419) was carried out. Planting was done at three different seasons: summer, early monsoon and late monsoon. Methods: The storage roots were harvested at intervals of 6, 9 and 12 months after planting to evaluate their yield. Granule morphology of the starches and biochemical characteristics of the flours were examined using electron microscopy and biochemical techniques. Result: Significant variations were observed in the starch content, root yield and size of starch granule, which were mainly dependent on planting dates, while the variations recorded in starch granule morphology, amyloseaa and amylopectin contents were influenced by genotype. The highest starch (33.5%) and amylose content (18.9%) were observed in TME-419 variety. The rate of storage root yield had positive correlation with maximum temperature and sunshine and negative correlation with humidity and rainfall. This study indicated that cultivation season affects starch accumulation and root yield in cassava and can be applied in developing cassava varieties with high starch and root yield, suitable for different planting seasons. [ABSTRACT FROM AUTHOR]

Colloidosomes, pioneering microcapsules composed of coagulated colloidal particles assembled at the interface of emulsion droplets, have garnered significant attention due to their remarkable properties and potential applications in targeted and controlled drug delivery. Their unique core-shell architecture offers unparalleled advantages, including tunable permeability, mechanical strength and encapsulation capabilities for a wide range of therapeutic agents. These versatile carriers have demonstrated remarkable potential in delivering small molecules, biomacromolecules, genetic materials and even living cells, addressing challenges associated with conventional drug delivery systems. Colloidosomes can be fabricated through various techniques, encompassing emulsion-based, nature-of-colloids-based and emerging methods such as microfluidics and 3D printing. Comprehensive characterization, employing techniques like electron microscopy, spectroscopy and rheology, is crucial for understanding their structural, physical and functional properties. Remarkable advancements have been achieved in developing stimuli-responsive, targeted and multi-functional colloidosomes, enabling precise spatiotemporal control, selective accumulation and integrated functionalities for theranostic applications. Despite their immense potential, challenges remain in scaling up production, ensuring long-term stability, navigating regulatory landscapes and facilitating clinical translation. Addressing these obstacles through collaborative efforts, advanced characterization and the integration of emerging technologies is paramount for unlocking the full potential of colloidosomes in revolutionizing drug delivery strategies and realizing personalized medicine. [ABSTRACT FROM AUTHOR]

Background/Objectives: The development of polymer–lipid hybrid nanoparticles (PLNs) is a promising area of research, as it can help increase the stability of cationic lipid carriers. Hybrid PLNs are core–shell nanoparticle structures that combine the advantages of both polymer nanoparticles and liposomes, especially in terms of their physical stability and biocompatibility. Natural polymers such as polyhydroxyalkanoate (PHA) can be used as a matrix for the PLNs' preparation. Methods: In this study, we first obtained stable cationic hybrid PLNs using a cationic liposome (CL) composed of a polycationic lipid 2X3 (1,26-bis(cholest-5-en-3β-yloxycarbonylamino)-7,11,16,20-tetraazahexacosane tetrahydrochloride), helper lipid DOPE (1,2-dioleoyl-sn-glycero-3-phosphoethanolamine), and the hydrophobic polymer mcl-PHA, which was produced by the soil bacterium Pseudomonas helmantisensis P1. Results: The new polymer-lipid carriers effectively encapsulated and delivered model mRNA-eGFP (enhanced green fluorescent protein mRNA) to BHK-21 cells. We then evaluated the role of mcl-PHA in increasing the stability of cationic PLNs in ionic solutions using dynamic light scattering data, electrophoretic mobility, and transmission electron microscopy techniques. Conclusions: The results showed that increasing the concentration of PBS (phosphate buffered saline) led to a decrease in the stability of the CLs. At high concentrations of PBS, the CLs aggregate. In contrast, the presence of isotonic PBS did not result in the aggregation of PLNs, and the particles remained stable for 120 h when stored at +4 °C. The obtained results show that PLNs hold promise for further in vivo studies on nucleic acid delivery. [ABSTRACT FROM AUTHOR]

The aim of this work was the development and morphological/chemical, spectroscopic, and structural characterization of titanium dioxide, niobium pentoxide, and titanium:niobium (Ti:Nb) oxides, as well as materials modified with ruthenium (Ru) with the purpose of providing improvement in photoactivation capacity with visible sunlight radiation. The new materials synthesized using the sol-gel methodology were characterized using the following techniques: scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), photoacoustic spectroscopy (PAS), and X-ray diffraction (XRD). The SEM–EDS analyses showed the high purity of the bases, and the modified samples showed the adsorption of ruthenium on the surface with the crystals' formation and visible agglomerates for higher calcination temperature. The nondestructive characterization of PAS in the ultraviolet visible region suggested that increasing calcination temperature promoted changes in chemical structures and an apparent decrease in gap energy. The separation of superimposed absorption bands referring to charge transfers from the ligand to the metal and the nanodomains of the transition metals suggested the possible absorption centers present at the absorption threshold of the analyzed oxides. Through the XRD analysis, the formation of stable phases such as T-Nb16.8O42, o -Nb12O29, and rutile was observed at a lower temperature level, suggesting pore induction and an increase in surface area for the oxides studied, at a calcination temperature below that expected by the related literature. In addition, the synthesis with a higher temperature level altered the previously existing morphologies of the Ti:Nb, base and modified with Ru, forming the new mixed crystallographic phases Ti2Nb10O29 and TiNb2O7, respectively. As several semiconductor oxide applications aim to reduce costs with photoexcitation under visible light, the modified Ti:Ru oxide calcined at a temperature of 800 °C and synthesized according to the sol-gel methodology used in this work is suggested as the optimum preparation point. This study presented the formation of a stable crystallographic phase (rutile), a significant decrease in gap energy (2.01 eV), and a visible absorption threshold (620 nm). [ABSTRACT FROM AUTHOR]

Seminal studies from the early 20th century defined the structural changes associated with development and regeneration of the gills in goldfish at the gross morphological and cellular levels using standard techniques of light and electron microscopy. More recently, investigations using cell lineage tracing, molecular biology, immunohistochemistry and single-cell RNA-sequencing have pushed the field forward and have begun to reveal the cellular and molecular processes that orchestrate cell proliferation and regeneration in the gills. The gill is a multifunctional organ that mediates an array of important physiological functions, including respiration, ion regulation and excretion of waste products. It is comprised of unique cell types, such as pavement cells, ionocytes, chemoreceptors and undifferentiated stem or progenitor cells that regulate growth and replenish cell populations. The gills develop from the embryonic endoderm and are rich in cell types derived from the neural crest. The gills have the capacity to remodel themselves in response to environmental change, such as in the case of ionocytes, chemoreceptors and the interlamellar cell mass, and can completely regenerate gill filaments and lamellae. Both processes of remodeling and regeneration invariably involve cell proliferation. Although gill regeneration has been reported in only a limited number of fish species, the process appears to have many similarities to regeneration of other organs in fish and amphibians. The present article reviews the studies that have described gill development and growth, and that demonstrate a suite of genes, transcription factors and other proteins involved in cell proliferation and regeneration in the gills. [ABSTRACT FROM AUTHOR]

Simple Summary: Peccaries are distributed from the southern United States to southern South America. Although they were initially described as being from the pig genus Sus, they are very different. This species is currently being used on commercial farms as a source of animal protein; however, there are no studies about their salivary glands, which are important for digestion and in developing feeding strategies. Thus, this work aims to study the major salivary gland morphology of peccaries during their growth. During growth, the parotid enlarges and the mandibular gland loses weight. Histologically, the parotid has serous production, and the sublingual has mucus production, like most species; however, the mandibular gland produces mucus, unlike other animals, including pigs, which produce seromucous secretion. Histochemically, the parotid produces more acidic mucins than pigs and it undergoes maturation during development; the mandibular, especially the sublingual gland, produces more acidic and basic mucopolysaccharides than pigs. The major salivary glands reacted positively to different lecithins and showed a stronger reaction than in pigs. We conclude that peccaries have a salivary secretion that facilitates the digestion of carbohydrates, improving digestibility and performance. Their biometric characteristics and positive reactions to lecithins facilitate adaptation to foods with antinutritional factors, making them a promising production animal. This work aims to study the major salivary gland morphology of peccaries during their growth. The glands were analyzed using macroscopic description, light microscopy, electron microscopy, histochemistry, and immunohistochemistry. Topographically, the salivary glands resemble other animals, including domestic animals and pigs. During growth, the parotid enlarges and mandibular gland loses weight. Histologically, the parotid has serous production, and sublingual has mucous production, resembles most species, however, mandibular gland produces mucous, unlike other animals, including pigs, which produce seromucous secretion. Histochemically, parotid produces more acidic mucins than pigs and it undergoes maturation during development; mandibular, and especially the sublingual gland, produce more acidic and basic mucopolysaccharides than pigs. The results found with transmission and scanning electron microscopy techniques corroborate the histological and histochemistry findings. The major salivary glands were positive to different lecithins (Com-A, BSA-I-B4, WGA and PNA), which were also more positive than in pigs and sheep. We conclude that collared peccaries have a salivary secretion that facilitates the digestion of carbohydrates, and biometric characteristics and positivity to lecithins that facilitate adaptation to foods with antinutritional factors. [ABSTRACT FROM AUTHOR]

Objective: To compare the implant–abutment connection microgap between computer‐aided design and computer‐aided manufacturing (CAD/CAM) milled or laser‐sintered cobalt–chrome custom abutments with or without ceramic veneering and titanium stock abutments with or without crown cementation. Material and Methods: Six groups of six abutments each were prepared: (1) CAD/CAM cobalt–chrome custom abutments: milled, milled with ceramic veneering, laser‐sintered, and laser‐sintered with ceramic veneering (four groups: MIL, MIL‐C, SIN, and SIN‐C, respectively) and (2) titanium stock abutments with or without zirconia crown cementation (two groups: STK and STK‐Z, respectively). Abutments were screwed to the implants by applying 30 Ncm torque. All 36 samples were sectioned along their long axes. The implant–abutment connection microgap was measured using scanning electron microscopy on the right and left sides of the connection at the upper, middle, and lower levels. Data were analyzed using the Kruskal–Wallis test (p <.05). Results: Mean values (μm) of the microgap were 0.54 ± 0.44 (STK), 0.55 ± 0.48 (STK‐Z), 1.53 ± 1.30 (MIL), 2.30 ± 2.2 (MIL‐C), 1.53 ± 1.37 (SIN), and 1.87 ± 1.8 (SIN‐C). Although significant differences were observed between the STK and STK‐Z groups and the other groups (p <.05), none were observed between the milled and laser‐sintered groups before or after ceramic veneering. The largest microgap was observed at the upper level in all groups. Conclusions: Titanium stock abutments provided a closer fit than cobalt–chrome custom abutments. Neither crown cementation nor ceramic veneering resulted in significant changes in the implant–abutment connection microgap. [ABSTRACT FROM AUTHOR]

Herein, we have designed aqueous dispersed self‐assembled nanostructures with diverse morphologies from the zinc tetraphenyl porphyrin (ZnTPP) monomer employing simple solution‐based coprecipitation methods. Detailed morphological studies have been carried out by various electron microscopy techniques. Finally, the structural features were correlated with the underpinning photophysical processes using steady‐state and time‐resolved spectroscopy. Detailed studies suggest that controlled morphology and highly defined intermolecular interactions affect the overall photoinduced charge transfer process. Based on the fundamental investigations, all these different types of nanostructures have been utilized as photocatalysts for solar hydrogen production without using any cocatalysts, and it was found that the spherical nanostructure exhibits significantly higher H2 production rates of ∼1682 μ mole/g, which is a few folds higher than other 1D and 2D nanostructured materials. The experimental findings were further supported by the TD‐DFT study. Furthermore, the detailed computational studies suggest that the spherical aggregates exhibited a more vital interaction between the ZnTPP molecules, causing significant electronic coupling between bright local excited and charge transfer states, which supports our experimental findings. Finally, we have selectively utilized the oxidative half‐reaction for the simultaneous transformation of glycerol to valuable chemicals along with photocatalytic H2 production through reductive half‐reaction. [ABSTRACT FROM AUTHOR]

This article provides an analysis of the physics behind the shattering of glass and ceramic objects when they are dropped or impacted. The study utilizes video analysis to examine the process of fracture propagation and the phenomenon of bouncing before breaking into pieces. The article emphasizes the significance of understanding the resilience of ceramic and glass materials to impacts, particularly in applications such as vehicle and aircraft armor and orthopedic surgery. The experimental setup and results are presented, highlighting the necessity of high-speed cameras to capture crack propagation on a precise timescale. The article also discusses an experiment involving the impact and breakage of ceramic mugs and a wine glass, focusing on the physics of breakage and the conservation of energy. The experiment demonstrates that the speed of crack propagation is limited and that each individual piece of the broken object possesses less kinetic energy than the original object. The article suggests that this experiment can serve as an educational tool for students to comprehend materials and load bearing. Further investigations can be conducted to examine the properties of the materials and the exact failure mechanism during load bearing. [Extracted from the article]

Performance of alumina-supported catalyst systems are significantly affected by how the tetrahedral (Al-O4) and octahedral (Al-O6) coordination are mixed and blended with each other. Characterisation of aluminium-oxygen coordination is thus important to understand how catalysts interact with alumina at the microscopic level. Here we report the application of two advanced electron microscopy techniques on aluminium-oxygen coordination. The first technique is electron energy loss spectroscopy (EELS) that can reveal detailed electronic structure profile of aluminium valence band to analyse how aluminium is coordinated by oxygen. The second technique is pair distribution function (PDF) based on electron diffraction (ED), employed to measure aluminium-oxygen bond lengths associated with the coordination geometry. [ABSTRACT FROM AUTHOR]

The current study is focused on devising treated diatomite interfaces with the robustness and boiling water resistance necessary for high-temperature purposes. This work describes the synthesis methodology of the diatomite-based coatings, which followed the production of a composite formulation composed by treated diatomite powder dispersed in an epoxy resin matrix. After its preparation, the suspension was applied via the dip-coating technique over AISI-304 stainless-steel foils, which, after being air dried, underwent a post-curing treatment. Also, the interfaces were characterized by diverse techniques such as scanning electron microscopy and optical tensiometry. Apart from this, their thermophysical properties like thermal conductivity were also determined. Further, the physical and chemical durability of the interfaces was also evaluated via the elaboration of robustness tests including abrasion resistance, adhesion strength, solid impact resistance, and solvent resistance. The results showed satisfactory resistant interfaces, and with a wettability characterized by contact angles superior to 150°. Also, the interfaces confirmed improved durability when immersed in boiling water at 1 atm, since their wetting characteristics and durability remained nearly unaltered after 762 h of testing. Additionally, the synthesized interfaces possessed self-cleaning ability and chemical and thermal shock aging resistance. Generally, the fundamental outcomes of this work point out the suitability of the produced diatomite-based interfaces to be explored in high-temperature applications like flow boiling, pool boiling, and condensation. In terms of practicality, the method of preparation of the interfaces was a relatively easy and rapid approach to obtaining enhanced wettability and resilient interfaces, and with the required adaptations like the ratios between the raw materials, its suitability for large-scale applications makes this an appealing option. [ABSTRACT FROM AUTHOR]

Antimicrobial medicines serve as the bedrock of modern medical practices. Increasing multidrug resistance compromises surgical processes and increases healthcare costs. Therefore, a combinational approach has become a pre-requisite for sustainable medical care. In recent decade, biologically synthesized metallic nanoparticles have emerged as a class of potent antimicrobials. In this study, green synthesized bimetallic silver–copper oxide (Ag–Cu) nanospheres have been prepared using the culture supernatant of the Bacillus subtilis (MTCC 441) bacteria to effectively target infectious microbes. The hydrodynamic diameter of the nanoparticles as depicted by dynamic light scattering (DLS) was 143.5 nm, while the polydispersity index (PI) of 0.367 and zeta potential of −25.2 mV indicated toward uniform size distribution and excellent colloidal stability. The Ag–Cu nanospheres of diameter 22.24 ± 8.01 nm were prepared using the culture supernatant of B. subtilis MTCC 441. High-end techniques such as transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopy revealed the size (22.24 ± 8.01 nm), spherical morphology, crystal structure and surface functionalization of nanospheres, respectively. The antimicrobial potential of the nanospheres was assessed against multidrug-resistant (MDR) bacterial strains while anti-free radical capacity was evaluated through 2,2-Diphenyl-1-picrylhydrazyl (DPPH) and H 2 O 2 free radical inhibition. The anti-inflammatory study was also performed to investigate the biomedical potential of the synthesized Ag–Cu nanosphere. The comprehensive analysis of antimicrobial, anti-oxidative and anti-inflammatory assays presents Ag–Cu nanospheres spheres as suitable candidates to be used in various biomedical applications. [ABSTRACT FROM AUTHOR]

Because of their full compatibility with CMOS technology, HfO2-based ferroelectrics, and especially Hf0.5Zr0.5O2 (HZO), attract a lot of attention. However, the overwhelming majority of measurement techniques provides only information about the cumulative electrical response of many domains of HZO, i.e., at the macroscopic level. So far, only piezoresponse force microscopy technique was applied to visualize distinct ferroelectric domains in HZO and to analyze the local switching behavior in the microscopic level. This work introduces the possibility of using electron beam-induced current (EBIC) technique in the scanning electron microscope to visualize the gradual polarization reversal of HZO and to obtain the local polarization dynamics. We show that although the local EBIC signal is affected by surrounding domains, studying the variations in the ferroelectric response of individual domains as well as the spread of the local stiffness and local imprint is possible by this method. Besides, we show the connection between the EBIC current and an electric field across passive non-ferroelectric layers at interfaces between HZO and metal electrodes, which opens up additional opportunities to use the EBIC technique for investigations of interface-dependent properties of HZO ferroelectrics in the future. [ABSTRACT FROM AUTHOR]

Because of their full compatibility with CMOS technology, HfO2-based ferroelectrics, and especially Hf0.5Zr0.5O2 (HZO), attract a lot of attention. However, the overwhelming majority of measurement techniques provides only information about the cumulative electrical response of many domains of HZO, i.e., at the macroscopic level. So far, only piezoresponse force microscopy technique was applied to visualize distinct ferroelectric domains in HZO and to analyze the local switching behavior in the microscopic level. This work introduces the possibility of using electron beam-induced current (EBIC) technique in the scanning electron microscope to visualize the gradual polarization reversal of HZO and to obtain the local polarization dynamics. We show that although the local EBIC signal is affected by surrounding domains, studying the variations in the ferroelectric response of individual domains as well as the spread of the local stiffness and local imprint is possible by this method. Besides, we show the connection between the EBIC current and an electric field across passive non-ferroelectric layers at interfaces between HZO and metal electrodes, which opens up additional opportunities to use the EBIC technique for investigations of interface-dependent properties of HZO ferroelectrics in the future. [ABSTRACT FROM AUTHOR]

Inspired by mussels protein adhesives, two series of catechol‐functionalized Linear‐Dendritic Block Copolymer (LDBC) adhesives are synthesized. They show lap shear adhesion strength as high as 7 MPa on aluminum substrates and adhesion up to 3 kPa on porcine skin. These water‐soluble LDBCs are composed of i) either poly(ethylene glycol) (PEG) or poly(ethylene glycol)‐poly(propylene glycol)‐poly(ethylene glycol) triblock copolymer (Pluronic F‐127) as linear polymers, ii) Bis‐MPA dendrons of generation 0, 1, and 2 as dendritic parts, and iii) 2, 4, or 8 terminal catechol moieties. A LDBCs generation comparative test on aluminum reveals a clear dendritic effect: the LDBCs of second generation display higher adhesion than the LDBCs of first generation that also display higher adhesion than the LDBCs of generation 0 for both series, assessing thus a positive dendritic effect in adhesion. Second, a comparative study is carried out between the LDBCs based on PEG and the ones based on Pluronic. The ability of the Pluronic LDBCs to self‐assemble in water appears to reduce adhesion when applied on aluminum whereas it is essential to obtain adhesion on porcine skin, thanks to the formation of hydrogels, as observed by the vial inversion technique and electron microscopy. [ABSTRACT FROM AUTHOR]

Al‐air batteries (AABs) are regarded as a promising future alternative energy source due to their supposedly high energy density. The corrosion of AABs resulting from the hydrogen evolution corrosion and self‐corrosion occurring during their use in alkaline solutions represented a significant obstacle to their development, considerably limiting their commercialization. In this study, we examined the corrosion inhibition efficiency of the hybrid anticorrosive agent composed of potassium stannate (K2SO3) and riboflavin (Rib) when used as an addition in the electrolyte of an alkaline AAB. The experimental results demonstrated that the incorporation of the hybrid corrosion inhibitor leads to an anticorrosion inhibition efficiency of 70.2%, an increase in the discharge specific capacity, and specific energy of the entire battery from 913 mAh g−1 and 1023 Wh kg−1 to 2128 mAh g−1 and 2511 Wh kg−1, respectively. The adsorption behavior of the additives on the surface of the Al alloy was studied using surface characterization techniques such as scanning electron microscopy (SEM), energy‐dispersive X‐ray spectroscopy (EDS), atomic force microscopy (AFM), and X‐ray photoelectron spectroscopy (XPS). It revealed that the incorporation of the hybrid additive leads to the formation of a dense and uniform protective layer on the surface of the Al anode during the discharge process. This film effectively prevents direct contact between the alkaline electrolyte and the Al surface, drastically reducing the formation of possible hydrogen interactions between the electrolyte and the anode. Consequently, the hydrogen evolution reaction (HER) is efficiently inhibited, and the overall performance of the AAB is improved. Thus, this electrolyte regulation strategy presents a novel approach to studying high‐efficiency alkaline AABs. [ABSTRACT FROM AUTHOR]

This study investigates the individual and combined effects of enhancing the radiation shielding properties of waste concrete using the optimal mix design of two waste material powders of different compositions. Marble (MD) and granite (GD) waste dust were individually utilized as partial replacements for cement at a replacement ratio of 6%. Furthermore, two additional mixes were prepared by incorporating 1% by cement weight of nano alumina (NA) to enhance the microstructure of the studied waste concrete. The MGA-concrete was analyzed using X-ray Fluorescence, Energy dispersive X-ray, X-ray diffraction analysis, transmission electron microscopy, and scanning electron microscope techniques. The radiation shielding assets of the examined Concrete samples, such as the linear attenuation coefficient (μ), half value layer (H1/2), tenth value layer (T1/10), and fast neutron removal cross-section were evaluated using the MCS5 Monte Carlo simulation algorithm and Phy-X software. The results showed that the linear attenuation for the GMN-concretes' order is CO < MD < GD < NA < MD + NA < GD + NA. The GD + Na concrete sample presents the best neutron performance. The studied GMN-concrete samples provide the best protection against γ-rays and fast neutrons. Lastly, the excellent performance of the mixes of waste Granite, Marble, and Nano-Alumina on ordinary would pave the way for their employment as radiation shielding in various nuclear and medical facilities. [ABSTRACT FROM AUTHOR]

This paper introduces an innovative microscopy analysis methodology to preserve in situ non-soluble particles within hailstones using a protective porous plastic coating, overcoming previous limitations related to melting the hailstone sample. The method is composed of two techniques: trapping non-soluble particles beneath a plastic coat using the adapted sublimation technique and then analyzing the particles individually with confocal laser scanning microscopy (CLSM) and scanning electron microscopy with energy-dispersive spectroscopy (SEM–EDS). CLSM provides insights into physical attributes like particle size and surface topography, enhancing our understanding of ice nucleation. SEM–EDS complement CLSM by offering detailed information on individual particle elemental chemistry, enabling classification based on composition. Strategies to reduce background noise from glass substrates during EDS spectral analysis are proposed. By combining powerful, high-resolution microscopy techniques, this methodology provides valuable data on hailstone composition and properties. This information can give insights into hail developmental processes by enhancing our understanding of the role of atmospheric particles. [ABSTRACT FROM AUTHOR]

Ferroelectric perovskites are pivotal in diverse technological applications; however, a gap persists in our comprehension of their mechanical properties, emphasizing the need for additional exploration. In the present study, we report on the nanomechanical behavior of BiFeO 3 ceramics in the force range between 200 μN and 2 mN, including the evolution of the hardness and the reduced Young's modulus from (9.9 ± 0.4) GPa and (113.7 ± 6.9) GPa, respectively, with increasing force. A sequence of plastic-deformation mechanisms under the cube-corner probe was revealed through a first pop-in analysis in combination with a variety of electron microscopy techniques, starting with a homogeneous dislocation nucleation, multiplication and rearrangement leading to sub-grain formation, a phenomenon observed in metals but not in ceramics. [ABSTRACT FROM AUTHOR]

The present study describes a set of methodological procedures (seldom applied together), including (i) development of an alternative adsorbent derived from abundant low-cost plant biomass; (ii) use of simple low-cost biomass modification techniques based on physical processing and chemical activation; (iii) design of experiments (DoE) applied to optimize the removal of a pharmaceutical contaminant from water; (iv) at environmentally relevant concentrations, (v) that due to initial low concentrations required determination by ultra-performance liquid phase chromatography coupled to mass spectrometry (UPLC-MS/MS). A central composite rotational design (CCRD) was employed to investigate the performance of vegetable sponge biomass (Luffa cylindrica), physically processed (crushing and sieving) and chemically activated with phosphoric acid, in the adsorption of the antibiotic trimethoprim (TMP) from water. The optimized model identified pH as the most significant variable, with maximum drug removal (91.1 ± 5.7%) achieved at pH 7.5, a temperature of 22.5 °C, and an adsorbent/adsorbate ratio of 18.6 mg µg−1. The adsorption mechanisms and surface properties of the adsorbent were examined through characterization techniques such as scanning electron microscopy (SEM), point of zero charge (pHpzc) measurement, thermogravimetric analysis (TGA), specific surface area, and Fourier-transform infrared spectroscopy (FTIR). The best kinetic fit was obtained by the Avrami fractional-order model. The hypothesis of a hybrid behavior of the adsorbent was suggested by the equilibrium results presented by the Langmuir and Freundlich models and reinforced by the Redlich-Peterson model, which achieved the best fit (R2 = 0.982). The thermodynamic study indicated an exothermic, spontaneous, and favorable process. The maximum adsorption capacity of the material was 2.32 × 102 µg g−1 at an equilibrium time of 120 min. Finally, a sustainable and promising adsorbent for the polishing of aqueous matrices contaminated by contaminants of emerging concern (CECs) at environmentally relevant concentrations is available for future investigations. [ABSTRACT FROM AUTHOR]

Electron microscopy paired with immunogold labeling is the most precise tool for protein localization. However, these methods are either cumbersome, resulting in small sample numbers and restricted quantification, or limited to identifying protein epitopes external to the membrane. Here, we introduce SUB-immunogold-SEM, a scanning electron microscopy technique that detects intracellular protein epitopes proximal to the membrane. We identify four critical sample preparation factors contributing to the method's sensitivity. We validate its efficacy through precise localization and high-powered quantification of cytoskeletal and transmembrane protein distribution. We evaluate the capabilities of SUB-immunogold-SEM on cells with highly differentiated apical surfaces: (i) auditory hair cells, revealing the presence of nanoscale MYO15A-L rings at the tip of stereocilia; and (ii) respiratory multiciliate cells, mapping the distribution of the SARS-CoV-2 receptor ACE2 along the motile cilia. SUB-immunogold-SEM extends the application of SEM-based nanoscale protein localization to the detection of intracellular epitopes on the exposed surfaces of any cell. Nanoscale protein localisation by immunogold-scanning electron microscopy has been restricted to extracellular epitopes. Here, the authors extend this method to sub-membranous epitopes, revealing how transmembrane and cytoplasmic proteins distribute along the surfaces of exposed cells. [ABSTRACT FROM AUTHOR]

The growth of lithium (Li) dendrites, characterized by construction of internal Li substrate and surface solid electrolyte interphase (SEI), represents a significant hurdle for both liquid‐state and solid‐state Li batteries. To better understand the growth behaviors of these dendrites at atomic to device scale, advanced electron microscopy techniques have emerged as a valuable tool, providing high temporal and spatial resolutions for real‐time observations. In this review, the mechanistic aspects of growth of Li dendrites are delved first from both thermodynamic and kinetic perspectives. Then, a systematic overview of the state‐of‐the‐art in‐situ devices is provided that is developed for integration into electron microscopes, detailing the corresponding static and dynamic structures of Li dendrites. Additionally, the utilization of the non‐destructive cryogenic TEM technique is explored to classify and compare the local fine structure information of as‐formed Li deposits, which are influenced by various factors such as current density, temperature, electrolyte composition, solvents, and additives. Overall, this review article offers a comprehensive understanding of the physical origins associated with Li dendrites, spanning from atomic to device scales and encompassing both liquid and all‐solid‐state battery scenarios, then envisioning fundamental principles and strategies for optimizing batteries and overcoming the critical challenges posed by Li dendrites. [ABSTRACT FROM AUTHOR]

Mycelium-bound composites (MBCs) represent a promising advancement in bio-based building materials, offering sustainable alternatives for engineering and construction applications. This review provides a comprehensive overview of the current research landscape, production methodologies, and standardization ideas related to MBCs. A basic search on Scopus revealed over 250 publications on MBCs between 2020 and 2024, with more than 30% focusing on engineering and materials science. Key studies have investigated the physical and mechanical properties of MBCs, optimizing parameters such as substrate type, fungal species, incubation time, and post-processing to enhance material performance. Standardizing the inspection of MBC properties is crucial for ensuring quality and reliability. Various testing standards, including those from the American Society for Testing and Materials (ASTM), the International Organization for Standardization (ISO), the Japanese Industrial Standard (JIS), European Standards (EN), Deutsches Institut für Normung (DIN), and the Thai Industrial Standards Institute (TIS), are utilized to evaluate density, water absorption, compression strength, tensile strength, insulation, and other critical properties. This review highlights the distinction between lab-scale and apply-scale testing methodologies, emphasizing the need for comprehensive evaluation protocols. Additionally, the production process of MBCs involves critical steps like substrate preparation, fungal species selection, and mycelium growth, necessitating the implementation of good manufacturing practices (GMPs) to ensure consistency and quality. The internal and external structures of MBCs significantly influence their performance, necessitating standardized inspection methods using advanced techniques such as scanning electron microscopy (SEM), X-ray computed tomography (CT) scanning, and surface profilometry. By establishing robust inspection protocols and production standards, the industry can enhance the reliability and adoption of MBCs, contributing to innovations in materials science and promoting environmental sustainability. This review underscores the importance of interdisciplinary collaboration, advanced characterization tools, and regulatory frameworks to address challenges and advance the field of MBCs. [ABSTRACT FROM AUTHOR]