Explore the vast range of titles available.

Molybdenum disulfide (MoS2) was grown on a laser-processed periodic-hole sapphire substrate through chemical vapor deposition. The main purpose was to investigate the mechanism of MoS2 growth in substrate with a periodic structure. By controlling the amount and position of the precursor, adjusting the growth temperature and time, and setting the flow rate of argon gas, MoS2 grew in the region of the periodic holes. A series of various growth layer analyses of MoS2 were then confirmed by Raman spectroscopy, photoluminescence spectroscopy, and atomic force microscopy. Finally, the growth mechanism was studied by transmission electron microscopy (TEM). The experimental results show that in the appropriate environment, MoS2 can be successfully grown on substrate with periodic holes, and the number of growth layers can be determined through measurements. By observing the growth mechanism, composition analysis, and selected area electron diffraction diagram by TEM, we comprehensively understand the growth phenomenon. The results of this research can serve as a reference for the large-scale periodic growth of MoS2. The production of periodic structures by laser drilling is advantageous, as it is relatively simpler than other methods.

Developing low‐cost biosensing platforms for robust detection response and sensitivity at low concentrations is of great interest. This work reports synthesizing 1D ZnO nanostructured materials (1DZnO) with controllable properties utilizing a metal catalyst‐assisted vapor phase growth technique (VLS). The obtained materials are functionalized with (3‐aminopropyl) trimetoxysilane (APTMS) and immobilized with anti‐Escherichia coli enteropathogenic (EPEC) antibodies. Characterization results show changes in the optical and structural properties of 1DZnO that are correlated with the biofunctionalization methodologies. Further, the biofunctionalization process is assessed on 1DZnO surface platforms to obtain acceptable antibody immobilization efficiencies (52%, 96%, and 100%) using a low‐concentration antibody solution (30 µg ml−1). Special techniques such as focused ion beam micromachining and scanning tunneling electron microscopy are proposed to appreciate the semiconductor biofunctionalization layer around 1DZnO and explain the physics of the interaction process. It is found that morphology obtained from distinct synthesis methods, solvents, and functionalization agents can generate functional groups for biomolecule attachment. Remarkably, it is demonstrated that biofunctionalization on 1DZnO takes place all over a single nanostructure. This work presents a proof‐of‐concept focused on generating pathogen sensing platforms using 1DznO semiconducting materials, providing new insights into bio‐analytes interaction with structures at the nanoscale. This work presents a proof‐of‐concept focused on generating pathogen sensing platforms using 1DZnO semiconducting materials and provides new insights into bio‐analytes interaction with structures at the nanoscale. Comprehension of antibody immobilization mechanisms on ZnO nanostructured morphologies could directly impact the enhancement of biosensors by improving surface chemical modification.

Prepared by powder metallurgy process incorporating atomization and hot isostatic pressing (HIP) sintering at six different temperatures from 600 to 1160 °C, borated stainless steel (BSS) containing boron content of 1.86 wt% was studied. The phase of BSS, relative density of different temperature, microstructure, elemental distribution, and mechanical properties were tested and analyzed. The phases of the alloy were calculated by the Thermo-Calc (2021a, Thermo-Calc Software, Solna, Sweden) and studied by quantitative X-ray diffraction phase analysis. The distributions of boron, chromium, and iron in grains of the alloy were analyzed by scanning electron microscopy and transmission electron microscope. The grain size distributions and average grain sizes were calculated for the boron-containing phases at 900, 1000, 1100, and 1160 °C, as well as the average grain size of the austenite phase at 700 and 1160 °C. After undergoing HIP sintering at 900, 1000, 1100, and 1160 °C, respectively, the tensile strength and ductility of the alloy were tested, and the fracture surfaces were analyzed. It was found that the alloy consisted of two phases (austenite and boron-containing phase) when HIP sintering temperature was higher than 900 °C, and the relative density of the prepared alloys was higher than 99% when HIP temperature was higher than 1000 °C. According to the boron-containing phase grain size distribution and microstructure analysis, the boron-containing phase precipitated both inside the austenite matrix and at the grain boundaries and its growth mechanism was divided into four steps. The tensile strength and elongation of alloy were up to 776 MPa and 19% respectively when the HIP sintering was at 1000 °C.

In a hydrothermal preparation of crystalline magnetite (Fe3O4) nanoparticles, the influence of the experimental parameters (initial molar ratio of ferrous/ferric ions, initial concentration of ferrous ions, and heating time), and their interactions, on the particle formation was studied using response surface methodology (RSM), based on a statistical design of experiments (DOE). As indices indicating particle formation and crystallization, the variation in the particle diameter and crystallite size with the synthesis conditions was examined. The crystallite size was greatly affected by both the initial ferrous/ferric ion molar ratio and the heating time, whereas the particle diameter strongly depended on the heating time, and on the interaction between the initial ferrous/ferric ion molar ratio and the initial concentration of ferrous ions. The results from a statistical analysis suggest that the polycrystalline Fe3O4 nanoparticles form via crystal growth and/or thermal aggregation, after nucleation during hydrothermal treatment.

The 2D van der Waals crystals have shown great promise as potential future electronic materials due to their atomically thin and smooth nature, highly tailorable electronic structure, and mass production compatibility through chemical synthesis. Electronic devices, such as field effect transistors (FETs), from these materials require patterning and fabrication into desired structures. Specifically, the scale up and future development of “2D”-based electronics will inevitably require large numbers of fabrication steps in the patterning of 2D semiconductors, such as transition metal dichalcogenides (TMDs). This is currently carried out via multiple steps of lithography, etching, and transfer. As 2D devices become more complex (e.g., numerous 2D materials, more layers, specific shapes, etc.), the patterning steps can become economically costly and time consuming. Here, we developed a method to directly synthesize a 2D semiconductor, monolayer molybdenum disulfide (MoS₂), in arbitrary patterns on insulating SiO₂/Si via seed-promoted chemical vapor deposition (CVD) and substrate engineering. This method shows the potential of using the prepatterned substrates as a master template for the repeated growth of monolayer MoS₂ patterns. Our technique currently produces arbitrary monolayer MoS₂ patterns at a spatial resolution of 2 μm with excellent homogeneity and transistor performance (room temperature electron mobility of 30 cm² V−1 s−1 and on–off current ratio of 10⁷). Extending this patterning method to other 2D materials can provide a facile method for the repeatable direct synthesis of 2D materials for future electronics and optoelectronics.

Zeolite crystallization predominantly occurs by nonclassical pathways involving the attachment of complex (alumino)silicate precursors to crystal surfaces, yet recurrent images of fully crystalline materials with layered surfaces are evidence of classical growth by molecule attachment. Here we use in situ atomic force microscopy to monitor three distinct mechanisms of two-dimensional (2D) growth of zeolite A where we show that layer nucleation from surface defects is the most common pathway. Direct observation of defects was made possible by the identification of conditions promoting layered growth, which correlates to the use of sodium as an inorganic structure-directing agent, whereas its replacement with an organic results in a nonclassical mode of growth that obscures 2D layers and markedly slows the rate of crystallization. In situ measurements of layered growth reveal that undissolved silica nanoparticles in the synthesis medium can incorporate into advancing steps on crystal surfaces to generate defects (i.e., amorphous silica occlusions) that largely go undetected in literature. Nanoparticle occlusion in natural and synthetic crystals is a topic of wide-ranging interest owing to its relevance in fields spanning from biomineralization to the rational design of functional nanocomposites. In this study, we provide unprecedented insight into zeolite surface growth by molecule addition through time-resolved microscopy that directly captures the occlusion of silica nanoparticles and highlights the prevalent role of defects in zeolite crystallization.

With the development of society and the economy, there is an increasing demand for surface treatment techniques that can efficiently utilize metal materials to obtain good performances in the fields of mechanical engineering and the aerospace industry. The laser metal deposition (LMD) technique for cladding has become a research focus in recent years because of its lower dilution rate, small heat-effect zone and good metallurgical bonding between the coating and substrate. This paper reviews the simulation technology for the melt pool’s grain growth mechanism, temperature and stress distribution that are directly related to defect formation in LMD technology. At the same time, the defect suppression method and the performance improvement method of the cladded layer in LMD technology are introduced. Finally, it is pointed out that the active selection of materials according to the required performance, combined with the controllable processing technology, to form the corresponding microstructure, and finally, to actively realize the expected function, is the future development direction of LMD technology.

Understanding nanoparticle growth mechanisms is crucial for the synthesis of nanocrystals with desired biological and chemical properties. Growth of nanocrystals by oriented attachment (OA) is frequently reported as a method supplementary to the classical growth by Ostwald ripening (OR) process. In this work, ZnO nanoparticles (NPs) were prepared by wet chemical method. Size/shape evolution of ZnO NPs in ethanol solution was systematically studied using transmission electron microscopy (TEM), dynamic light scattering (DLS), and X-ray diffraction (XRD). In addition, a detailed process of the nanoparticle growth-based OA mechanism is discussed. Results revealed that reaction conditions affect size/shape of NPs and change their surface structure: prior to OA, the surface of adjacent particles transformed into their “rough” states. We proved that stability of the solution was significantly improved in this state. Such a state is important to design nanoparticles with high stability and as nano-suspensions with special physical and/or chemical properties. This state is a critical step in enhancing OA process.

Graphene and its derivatives hold a great promise for widespread applications such as field‐effect transistors, photovoltaic devices, supercapacitors, and sensors due to excellent properties as well as its atomically thin, transparent, and flexible structure. In order to realize the practical applications, graphene needs to be synthesized in a low‐cost, scalable, and controllable manner. Plasma‐enhanced chemical vapor deposition (PECVD) is a low‐temperature, controllable, and catalyst‐free synthesis method suitable for graphene growth and has recently received more attentions. This review summarizes recent advances in the PECVD growth of graphene on different substrates, discusses the growth mechanism and its related applications. Furthermore, the challenges and future development in this field are also discussed. Plasma‐enhanced chemical vapor deposition (PECVD) is one of the promising methods for controllable synthesis of graphene with the advantages of low growth temperature and being catalyst‐free. This review summarizes recent advance in the PECVD growth of graphene on different substrates, and discusses the growth mechanism and its related applications in electrical devices, supercapacitors, sensors, and so on.

Airborne particles play critical roles in air quality, health effects, visibility, and climate. Secondary organic aerosols (SOA) formed from oxidation of organic gases such as α-pinene account for a significant portion of total airborne particle mass. Current atmospheric models typically incorporate the assumption that SOA mass is a liquid into which semivolatile organic compounds undergo instantaneous equilibrium partitioning to grow the particles into the size range important for light scattering and cloud condensation nuclei activity. We report studies of particles from the oxidation of α-pinene by ozone and NO3 radicals at room temperature. SOA is primarily formed from low-volatility ozonolysis products, with a small contribution from higher volatility organic nitrates from the NO3 reaction. Contrary to expectations, the particulate nitrate concentration is not consistent with equilibrium partitioning between the gas phase and a liquid particle. Rather the fraction of organic nitrates in the particles is only explained by irreversible, kinetically determined uptake of the nitrates on existing particles, with an uptake coefficient that is 1.6% of that for the ozonolysis products. If the nonequilibrium particle formation and growth observed in this atmospherically important system is a general phenomenon in the atmosphere, aerosol models may need to be reformulated. The reformulation of aerosol models could impact the predicted evolution of SOA in the atmosphere both outdoors and indoors, its role in heterogeneous chemistry, its projected impacts on air quality, visibility, and climate, and hence the development of reliable control strategies.